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  <VOL>76</VOL>
  <NO>147</NO>
  <DATE>Monday, August 1, 2011</DATE>
  <UNITNAME>Contents</UNITNAME>
  <CNTNTS>
    <AGCY>
      <EAR>Agriculture</EAR>
      <PRTPAGE P="iii"/>
      <HD>Agriculture Department</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Animal and Plant Health Inspection Service</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Forest Service</P>
      </SEE>
    </AGCY>
    <AGCY>
      <EAR>Alcohol Tobacco Firearms</EAR>
      <HD>Alcohol, Tobacco, Firearms, and Explosives Bureau</HD>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Agency Information Collection Activities; Proposals, Submissions, and Approvals:</SJ>
        <SJDENT>
          <SJDOC>Firearms Transaction Record, Part 1, Over-the-Counter,</SJDOC>
          <PGS>45863</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19370</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Animal</EAR>
      <HD>Animal and Plant Health Inspection Service</HD>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Agency Information Collection Activities:</SJ>
        <SJDENT>
          <SJDOC>Pork and Poultry Products From Mexico Transiting the United States,</SJDOC>
          <PGS>45769-45770</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19363</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Army</EAR>
      <HD>Army Department</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Privacy Act; Systems of Records,</DOC>
          <PGS>45783-45785</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19364</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR/>
      <HD>Arts and Humanities, National Foundation</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>National Foundation on the Arts and the Humanities</P>
      </SEE>
    </AGCY>
    <AGCY>
      <EAR/>
      <HD>Blind or Severely Disabled, Committee for Purchase From  People Who Are</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Committee for Purchase From People Who Are Blind or Severely Disabled</P>
      </SEE>
    </AGCY>
    <AGCY>
      <EAR/>
      <HD>Bureau of Consumer Financial Protection</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Privacy Act; Systems of Records,</DOC>
          <PGS>45757-45769</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19424</FRDOCBP>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19425</FRDOCBP>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19426</FRDOCBP>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19427</FRDOCBP>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19428</FRDOCBP>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19429</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Coast Guard</EAR>
      <HD>Coast Guard</HD>
      <CAT>
        <HD>RULES</HD>
        <SJ>Drawbridge Operation Regulations:</SJ>
        <SJDENT>
          <SJDOC>Raritan River, Arthur Kill and their Tributaries, Staten Island, NY and Elizabeth, NJ,</SJDOC>
          <PGS>45690-45693</PGS>
          <FRDOCBP D="3" T="01AUR1.sgm">2011-19322</FRDOCBP>
        </SJDENT>
        <SJ>Safety Zones:</SJ>
        <SJDENT>
          <SJDOC>San Diego POPS Fireworks, San Diego, CA,</SJDOC>
          <PGS>45693-45695</PGS>
          <FRDOCBP D="2" T="01AUR1.sgm">2011-19321</FRDOCBP>
        </SJDENT>
      </CAT>
      <CAT>
        <HD>PROPOSED RULES</HD>
        <SJ>International Convention on Standards of Training, Certification and Watchkeeping for Seafarers:</SJ>
        <SJDENT>
          <SJDOC>Implementation of Amendments and Changes to Domestic Endorsements; Public Meetings,</SJDOC>
          <PGS>45908-46081</PGS>
          <FRDOCBP D="173" T="01AUP2.sgm">2011-17093</FRDOCBP>
        </SJDENT>
        <SJ>Regulated Navigation Areas:</SJ>
        <SJDENT>
          <SJDOC>Pacific Sound Resources and Lockheed Shipyard EPA Superfund Cleanup Sites, Elliott Bay, Seattle, WA,</SJDOC>
          <PGS>45738-45741</PGS>
          <FRDOCBP D="3" T="01AUP1.sgm">2011-19320</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Commerce</EAR>
      <HD>Commerce Department</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Foreign-Trade Zones Board</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>International Trade Administration</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>National Oceanic and Atmospheric Administration</P>
      </SEE>
    </AGCY>
    <AGCY>
      <EAR>Committee for Purchase</EAR>
      <HD>Committee for Purchase From People Who Are Blind or Severely Disabled</HD>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Agency Information Collection Activities; Proposals, Submissions, and Approvals:</SJ>
        <SJDENT>
          <SJDOC>Nonprofit Agency Recordkeeping Requirements,</SJDOC>
          <PGS>45782-45783</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19379</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Commodity Futures</EAR>
      <HD>Commodity Futures Trading Commission</HD>
      <CAT>
        <HD>RULES</HD>
        <DOCENT>
          <DOC>Provisions Common to Registered Entities; Correction,</DOC>
          <PGS>45666</PGS>
          <FRDOCBP D="0" T="01AUR1.sgm">2011-19385</FRDOCBP>
        </DOCENT>
      </CAT>
      <CAT>
        <HD>PROPOSED RULES</HD>
        <DOCENT>
          <DOC>Clearing Member Risk Management,</DOC>
          <PGS>45724-45730</PGS>
          <FRDOCBP D="6" T="01AUP1.sgm">2011-19362</FRDOCBP>
        </DOCENT>
        <DOCENT>
          <DOC>Customer Clearing Documentation and Timing of Acceptance for Clearing,</DOC>
          <PGS>45730-45738</PGS>
          <FRDOCBP D="8" T="01AUP1.sgm">2011-19365</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Copyright Royalty Board</EAR>
      <HD>Copyright Royalty Board</HD>
      <CAT>
        <HD>RULES</HD>
        <DOCENT>
          <DOC>Use of Sound Recordings Under Statutory License,</DOC>
          <PGS>45695-45696</PGS>
          <FRDOCBP D="1" T="01AUR1.sgm">2011-19306</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Defense Department</EAR>
      <HD>Defense Department</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Army Department</P>
      </SEE>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Meetings:</SJ>
        <SJDENT>
          <SJDOC>Missile Defense Advisory Committee,</SJDOC>
          <PGS>45783</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19395</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR/>
      <HD>Department of Transportation</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Pipeline and Hazardous Materials Safety Administration</P>
      </SEE>
    </AGCY>
    <AGCY>
      <EAR>Drug</EAR>
      <HD>Drug Enforcement Administration</HD>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Denial of Applications:</SJ>
        <SJDENT>
          <SJDOC>Shannon L. Gallentine, D.P.M.,</SJDOC>
          <PGS>45864-45867</PGS>
          <FRDOCBP D="3" T="01AUN1.sgm">2011-19381</FRDOCBP>
        </SJDENT>
        <SJ>Suspension of Registrations:</SJ>
        <SJDENT>
          <SJDOC>Michael S. Moore, M.D.,</SJDOC>
          <PGS>45867-45878</PGS>
          <FRDOCBP D="11" T="01AUN1.sgm">2011-19376</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Employment and Training</EAR>
      <HD>Employment and Training Administration</HD>
      <CAT>
        <HD>RULES</HD>
        <SJ>Wage Methodology for the Temporary Non-agricultural Employment H-2B Program:</SJ>
        <SJDENT>
          <SJDOC>Amendment of Effective Date,</SJDOC>
          <PGS>45667-45673</PGS>
          <FRDOCBP D="6" T="01AUR1.sgm">2011-19319</FRDOCBP>
        </SJDENT>
      </CAT>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Amended Certifications Regarding Eligibility to Apply for Worker Adjustment Assistance:</SJ>
        <SJDENT>
          <SJDOC>Alticor, Inc., et al.,</SJDOC>
          <PGS>45878</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19343</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>Cinram Manufacturing, LLC, et al., Olyphant, PA,</SJDOC>
          <PGS>45879</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19339</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>West, A Thomson Reuters Legal, Eagan, MN,</SJDOC>
          <PGS>45879</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19342</FRDOCBP>
        </SJDENT>
        <DOCENT>
          <DOC>Determinations Regarding Eligibility to Apply for Worker Adjustment Assistance and Alternative Trade Adjustment Assistance,</DOC>
          <PGS>45879-45881</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19341</FRDOCBP>
        </DOCENT>
        <DOCENT>
          <DOC>Investigations Regarding Certifications of Eligibility to Apply for Worker Adjustment Assistance and Alternative Trade Assistance,</DOC>
          <PGS>45881</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19340</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Energy Department</EAR>
      <HD>Energy Department</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Energy Efficiency and Renewable Energy Office</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Federal Energy Regulatory Commission</P>
      </SEE>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Meetings:</SJ>
        <SJDENT>
          <SJDOC>Advanced Scientific Computing Advisory Committee,</SJDOC>
          <PGS>45786</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19439</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Energy Efficiency</EAR>
      <HD>Energy Efficiency and Renewable Energy Office</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Agency Information Collection Activities; Proposals, Submissions, and Approvals,</DOC>
          <PGS>45786</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19437</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Environmental Protection</EAR>
      <PRTPAGE P="iv"/>
      <HD>Environmental Protection Agency</HD>
      <CAT>
        <HD>RULES</HD>
        <SJ>Approvals and Promulgations of Air Quality Implementation Plans:</SJ>
        <SJDENT>
          <SJDOC>Pennsylvania; Diesel-Powered Motor Vehicle Idling Act,</SJDOC>
          <PGS>45705-45709</PGS>
          <FRDOCBP D="4" T="01AUR1.sgm">2011-19276</FRDOCBP>
        </SJDENT>
      </CAT>
      <CAT>
        <HD>PROPOSED RULES</HD>
        <SJ>Approvals and Promulgations of Air Quality Implementation Plans:</SJ>
        <SJDENT>
          <SJDOC>Pennsylvania; Diesel-Powered Motor Vehicle Idling Act,</SJDOC>
          <PGS>45741-45742</PGS>
          <FRDOCBP D="1" T="01AUP1.sgm">2011-19275</FRDOCBP>
        </SJDENT>
        <DOCENT>
          <DOC>Secondary National Ambient Air Quality Standards for Oxides of Nitrogen and Sulfur,</DOC>
          <PGS>46084-46147</PGS>
          <FRDOCBP D="63" T="01AUP3.sgm">2011-18582</FRDOCBP>
        </DOCENT>
      </CAT>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Proposed Reissuance of a General NPDES Permit for Facilities Related to Oil and Gas Extraction,</DOC>
          <PGS>45792</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19127</FRDOCBP>
        </DOCENT>
        <DOCENT>
          <DOC>Proposed Settlement Agreements, Clean Air Act Citizen Suits,</DOC>
          <PGS>45793-45794</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19397</FRDOCBP>
        </DOCENT>
        <DOCENT>
          <DOC>Public Water System Supervision Program Revision for the State of Louisiana,</DOC>
          <PGS>45794</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19396</FRDOCBP>
        </DOCENT>
        <DOCENT>
          <DOC>Sixty-Eighth Report of the TSCA Interagency Testing Committee,</DOC>
          <PGS>46174-46180</PGS>
          <FRDOCBP D="6" T="01AUN2.sgm">2011-19414</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR/>
      <HD>Executive Office of the President</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Presidential Documents</P>
      </SEE>
    </AGCY>
    <AGCY>
      <EAR>Federal Aviation</EAR>
      <HD>Federal Aviation Administration</HD>
      <CAT>
        <HD>RULES</HD>
        <SJ>Airworthiness Directives:</SJ>
        <SJDENT>
          <SJDOC>Cessna Aircraft Co. (Cessna) Models 337, 337A (USAF 02B), 337B, 337C, 337D, 337E, etc., Airplanes,</SJDOC>
          <PGS>45657-45666</PGS>
          <FRDOCBP D="9" T="01AUR1.sgm">2011-18242</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>Superior Air Parts and Lycoming Engines (Formerly Textron Lycoming) Fuel-Injected Engines,</SJDOC>
          <PGS>45655-45657</PGS>
          <FRDOCBP D="2" T="01AUR1.sgm">2011-18168</FRDOCBP>
        </SJDENT>
      </CAT>
      <CAT>
        <HD>PROPOSED RULES</HD>
        <SJ>Airworthiness Directives:</SJ>
        <SJDENT>
          <SJDOC>Bombardier Inc. Model DHC-8-400 Series Airplanes,</SJDOC>
          <PGS>45713-45715</PGS>
          <FRDOCBP D="2" T="01AUP1.sgm">2011-19330</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Federal Communications</EAR>
      <HD>Federal Communications Commission</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Agency Information Collection Activities; Proposals, Submissions, and Approvals,</DOC>
          <PGS>45794-45797</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19408</FRDOCBP>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19409</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Federal Election</EAR>
      <HD>Federal Election Commission</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Filing Dates for the New York Special Election in the 9th Congressional District,</DOC>
          <PGS>45797-45798</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19311</FRDOCBP>
        </DOCENT>
        <DOCENT>
          <DOC>Meetings; Sunshine Act,</DOC>
          <PGS>45798</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19547</FRDOCBP>
        </DOCENT>
        <SJ>Policy Statements:</SJ>
        <SJDENT>
          <SJDOC>Program for Requesting Consideration of Legal Questions by the Commission,</SJDOC>
          <PGS>45798-45799</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19312</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Federal Energy</EAR>
      <HD>Federal Energy Regulatory Commission</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Combined Filings,</DOC>
          <PGS>45787-45792</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19347</FRDOCBP>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19348</FRDOCBP>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19349</FRDOCBP>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19350</FRDOCBP>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19351</FRDOCBP>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19352</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Federal Mine</EAR>
      <HD>Federal Mine Safety and Health Review Commission</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Meetings; Sunshine Act,</DOC>
          <PGS>45799</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19462</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Federal Trade</EAR>
      <HD>Federal Trade Commission</HD>
      <CAT>
        <HD>PROPOSED RULES</HD>
        <DOCENT>
          <DOC>Appliance Labeling,</DOC>
          <PGS>45715-45724</PGS>
          <FRDOCBP D="9" T="01AUP1.sgm">2011-19041</FRDOCBP>
        </DOCENT>
      </CAT>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Agency Information Collection Activities; Proposals, Submissions, and Approvals,</DOC>
          <PGS>45799-45801</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19367</FRDOCBP>
        </DOCENT>
        <SJ>Analysis of Agreement Containing Consent Orders to Aid Public Comments:</SJ>
        <SJDENT>
          <SJDOC>Perrigo Co. and Paddock Laboratories, Inc.,</SJDOC>
          <PGS>45801-45804</PGS>
          <FRDOCBP D="3" T="01AUN1.sgm">2011-19422</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Financial</EAR>
      <HD>Financial Crimes Enforcement Network</HD>
      <CAT>
        <HD>RULES</HD>
        <SJ>Financial Crimes Enforcement Network:</SJ>
        <SJDENT>
          <SJDOC>Repeal of Final Rule and Withdrawal of Finding of Primary Money Laundering Concern Against VEF Banka,</SJDOC>
          <PGS>45689-45690</PGS>
          <FRDOCBP D="1" T="01AUR1.sgm">2011-19118</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Fish</EAR>
      <HD>Fish and Wildlife Service</HD>
      <CAT>
        <HD>RULES</HD>
        <SJ>Financial Assistance:</SJ>
        <SJDENT>
          <SJDOC>Wildlife Restoration, Sport Fish Restoration, Hunter Education and Safety,</SJDOC>
          <PGS>46150-46171</PGS>
          <FRDOCBP D="21" T="01AUR2.sgm">2011-19206</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Food and Drug</EAR>
      <HD>Food and Drug Administration</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Animal Drug User Fee Rates and Payment Procedures for Fiscal Year 2012,</DOC>
          <PGS>45811-45814</PGS>
          <FRDOCBP D="3" T="01AUN1.sgm">2011-19336</FRDOCBP>
        </DOCENT>
        <DOCENT>
          <DOC>Animal Generic Drug User Fee Rates and Payment Procedures for Fiscal Year 2012,</DOC>
          <PGS>45814-45818</PGS>
          <FRDOCBP D="4" T="01AUN1.sgm">2011-19334</FRDOCBP>
        </DOCENT>
        <DOCENT>
          <DOC>Burden of Food and Drug Administration Food Safety Modernization Act Fee Amounts on Small Business,</DOC>
          <PGS>45818-45820</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19333</FRDOCBP>
        </DOCENT>
        <SJ>Food Safety Modernization Act:</SJ>
        <SJDENT>
          <SJDOC>Domestic and Foreign Facility Reinspections, Recall, and Importer Reinspection User Fee Rates for Fiscal Year 2012,</SJDOC>
          <PGS>45820-45825</PGS>
          <FRDOCBP D="5" T="01AUN1.sgm">2011-19331</FRDOCBP>
        </SJDENT>
        <SJ>Institute of Medicine Report; Availability:</SJ>
        <SJDENT>
          <SJDOC>Medical Devices and the Public's Health, The FDA 510(k) Clearance Process at 35 Years,</SJDOC>
          <PGS>45825-45826</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19353</FRDOCBP>
        </SJDENT>
        <DOCENT>
          <DOC>Medical Device User Fee Rates for Fiscal Year 2012,</DOC>
          <PGS>45826-45831</PGS>
          <FRDOCBP D="5" T="01AUN1.sgm">2011-19335</FRDOCBP>
        </DOCENT>
        <DOCENT>
          <DOC>Prescription Drug User Fee Rates for Fiscal Year 2012,</DOC>
          <PGS>45831-45838</PGS>
          <FRDOCBP D="7" T="01AUN1.sgm">2011-19332</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Foreign Trade</EAR>
      <HD>Foreign-Trade Zones Board</HD>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Applications for Manufacturing Authority:</SJ>
        <SJDENT>
          <SJDOC>Makita Corp. of America, Foreign-Trade Zone 26, Atlanta, GA,</SJDOC>
          <PGS>45771-45772</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19405</FRDOCBP>
        </SJDENT>
        <SJ>Proposed Foreign-Trade Zones:</SJ>
        <SJDENT>
          <SJDOC>Brunswick, ME,</SJDOC>
          <PGS>45772</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19404</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Forest</EAR>
      <HD>Forest Service</HD>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Meetings:</SJ>
        <SJDENT>
          <SJDOC>Glenn/Colusa County Resource Advisory Committee,</SJDOC>
          <PGS>45771</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19368</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>Plumas County Resource Advisory Committee,</SJDOC>
          <PGS>45771</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19354</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>Tehama County Resource Advisory Committee,</SJDOC>
          <PGS>45770-45771</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19366</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Health and Human</EAR>
      <HD>Health and Human Services Department</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Food and Drug Administration</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>National Institutes of Health</P>
      </SEE>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Agency Information Collection Activities; Proposals, Submissions, and Approvals,</DOC>
          <PGS>45804-45805</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19323</FRDOCBP>
        </DOCENT>
        <DOCENT>
          <DOC>Calculation of Annual Federal Medical Assistance Percentages for Indian Tribes for Use in the Title IV-E Foster Care, Adoption Assistance, and Kinship Guardianship Assistance Programs,</DOC>
          <PGS>45805-45810</PGS>
          <FRDOCBP D="5" T="01AUN1.sgm">2011-19358</FRDOCBP>
        </DOCENT>
        <SJ>Meetings:</SJ>
        <SJDENT>
          <SJDOC>National Committee on Vital and Health Statistics,</SJDOC>
          <PGS>45810-45811</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19359</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Homeland</EAR>
      <PRTPAGE P="v"/>
      <HD>Homeland Security Department</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Coast Guard</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>U.S. Citizenship and Immigration Services</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>U.S. Customs and Border Protection</P>
      </SEE>
    </AGCY>
    <AGCY>
      <EAR>Interior</EAR>
      <HD>Interior Department</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Fish and Wildlife Service</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Land Management Bureau</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>National Park Service</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Surface Mining Reclamation and Enforcement Office</P>
      </SEE>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Meetings:</SJ>
        <SJDENT>
          <SJDOC>Vendor Outreach Workshop for Small Businesses in New Mexico,</SJDOC>
          <PGS>45847-45848</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19360</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Internal Revenue</EAR>
      <HD>Internal Revenue Service</HD>
      <CAT>
        <HD>RULES</HD>
        <DOCENT>
          <DOC>Methods of Accounting Used by Corporations that Acquire Assets of Other Corporations,</DOC>
          <PGS>45673-45689</PGS>
          <FRDOCBP D="16" T="01AUR1.sgm">2011-19256</FRDOCBP>
        </DOCENT>
      </CAT>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Agency Information Collection Activities; Proposals, Submissions, and Approvals,</DOC>
          <PGS>45906</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19398</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>International Trade Adm</EAR>
      <HD>International Trade Administration</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Antidumping or Countervailing Duty Order, Finding, or Suspended Investigation; Administrative Review,</DOC>
          <PGS>45773-45775</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19411</FRDOCBP>
        </DOCENT>
        <DOCENT>
          <DOC>Antidumping or Countervailing Duty Order, Finding, or Suspended Investigations; Sunset Reviews,</DOC>
          <PGS>45775</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19413</FRDOCBP>
        </DOCENT>
        <SJ>Final Results of Antidumping Duty New Shipper Reviews:</SJ>
        <SJDENT>
          <SJDOC>Certain Frozen Warmwater Shrimp from the Socialist Republic of Vietnam,</SJDOC>
          <PGS>45775-45777</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19388</FRDOCBP>
        </SJDENT>
        <SJ>Initiation of Antidumping Duty New Shipper Reviews:</SJ>
        <SJDENT>
          <SJDOC>Tapered Roller Bearings and Parts Thereof, Finished and Unfinished from the People's Republic of China,</SJDOC>
          <PGS>45777-45778</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19407</FRDOCBP>
        </SJDENT>
        <DOCENT>
          <DOC>Initiation of Five Year (Sunset) Review,</DOC>
          <PGS>45778-45780</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19402</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>International Trade Com</EAR>
      <HD>International Trade Commission</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Complaints,</DOC>
          <PGS>45850-45851</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19355</FRDOCBP>
        </DOCENT>
        <SJ>Institution of  Five-Year Reviews Concerning Countervailing Duty Orders:</SJ>
        <SJDENT>
          <SJDOC>Certain Bearings from China, France, Germany, and Italy,</SJDOC>
          <PGS>45853-45856</PGS>
          <FRDOCBP D="3" T="01AUN1.sgm">2011-19318</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>Certain Lined Paper School Supplies from China, India, and Indonesia,</SJDOC>
          <PGS>45851-45853</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19314</FRDOCBP>
        </SJDENT>
        <SJ>Institution of Five-Year Review Concerning the Antidumping Duty Orders:</SJ>
        <SJDENT>
          <SJDOC>Silicomanganese from Brazil, China, and Ukraine,</SJDOC>
          <PGS>45856-45859</PGS>
          <FRDOCBP D="3" T="01AUN1.sgm">2011-19315</FRDOCBP>
        </SJDENT>
        <SJ>Investigations:</SJ>
        <SJDENT>
          <SJDOC>Certain Electronic Devices, Including Wireless Communication Devices, Portable Music And Data Processing Devices, And Tablet Computers,</SJDOC>
          <PGS>45860-45861</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19356</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>Certain Video Analytics Software, Systems, Components Thereof, and Products Containing Same,</SJDOC>
          <PGS>45859-45860</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19357</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Justice Department</EAR>
      <HD>Justice Department</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Alcohol, Tobacco, Firearms, and Explosives Bureau</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Drug Enforcement Administration</P>
      </SEE>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Agency Information Collection Activities; Proposals, Submissions, and Approvals:</SJ>
        <SJDENT>
          <SJDOC>Customer Outreach and Information,</SJDOC>
          <PGS>45861-45862</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19371</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>Semi-Annual Progress Report for Grantees from the Children and Youth Exposed to Violence,</SJDOC>
          <PGS>45861</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19345</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>Semi-Annual Progress Report for Grantees from the Services, Training, Education and Policies to Reduce Domestic Violence, etc.,</SJDOC>
          <PGS>45862-45863</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19346</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Labor Department</EAR>
      <HD>Labor Department</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Employment and Training Administration</P>
      </SEE>
    </AGCY>
    <AGCY>
      <EAR>Land</EAR>
      <HD>Land Management Bureau</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Application for Withdrawal of National Forest System Lands, Oregon,</DOC>
          <PGS>45848</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19302</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Library</EAR>
      <HD>Library of Congress</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Copyright Royalty Board</P>
      </SEE>
    </AGCY>
    <AGCY>
      <EAR/>
      <HD>Mine Safety and Health Federal Review Commission</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Federal Mine Safety and Health Review Commission</P>
      </SEE>
    </AGCY>
    <AGCY>
      <EAR>National Foundation</EAR>
      <HD>National Foundation on the Arts and the Humanities</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Agency Information Collection Activities; Proposals, Submissions, and Approvals,</DOC>
          <PGS>45881-45882</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19298</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>National Institute</EAR>
      <HD>National Institutes of Health</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Government-Owned Inventions; Availability for Licensing,</DOC>
          <PGS>45838-45841</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19377</FRDOCBP>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19378</FRDOCBP>
        </DOCENT>
        <SJ>Meetings:</SJ>
        <SJDENT>
          <SJDOC>Center for Scientific Review,</SJDOC>
          <PGS>45842-45843</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19369</FRDOCBP>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19375</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>National Heart, Lung, and Blood Institute,</SJDOC>
          <PGS>45843</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19373</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>National Library of Medicine,</SJDOC>
          <PGS>45842-45843</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19374</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>National Labor</EAR>
      <HD>National Labor Relations Board</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Meetings; Sunshine Act,</DOC>
          <PGS>45882</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19486</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>National Oceanic</EAR>
      <HD>National Oceanic and Atmospheric Administration</HD>
      <CAT>
        <HD>RULES</HD>
        <SJ>Fisheries of the Exclusive Economic Zone Off Alaska:</SJ>
        <SJDENT>
          <SJDOC>Pacific Ocean Perch in the West Yakutat District of the Gulf of Alaska; Closure,</SJDOC>
          <PGS>45709</PGS>
          <FRDOCBP D="0" T="01AUR1.sgm">2011-19394</FRDOCBP>
        </SJDENT>
      </CAT>
      <CAT>
        <HD>PROPOSED RULES</HD>
        <SJ>Fisheries of Northeastern United States:</SJ>
        <SJDENT>
          <SJDOC>Atlantic Mackerel, Squid, and Butterfish Fisheries; Amendment 11,</SJDOC>
          <PGS>45742-45756</PGS>
          <FRDOCBP D="14" T="01AUP1.sgm">2011-19415</FRDOCBP>
        </SJDENT>
      </CAT>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Environmental Assessments; Availability, etc.:</SJ>
        <SJDENT>
          <SJDOC>Emergency Restoration of Seagrass Impacts from the Deepwater Horizon Oil Spill Response,</SJDOC>
          <PGS>45780</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19403</FRDOCBP>
        </SJDENT>
        <SJ>Meetings:</SJ>
        <SJDENT>
          <SJDOC>Atlantic Highly Migratory Species Advisory Panel,</SJDOC>
          <PGS>45781</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19401</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>South Atlantic Fishery Management Council,</SJDOC>
          <PGS>45780-45781</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19309</FRDOCBP>
        </SJDENT>
        <SJ>Permits:</SJ>
        <SJDENT>
          <SJDOC>Endangered Species; File No. 15552,</SJDOC>
          <PGS>45781-45782</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19399</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>National Park</EAR>
      <HD>National Park Service</HD>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Environmental Impact Statements; Availability, etc.:</SJ>
        <SJDENT>
          <SJDOC>Denali Park Road Vehicle Management Plan, Denali National Park and Preserve,</SJDOC>
          <PGS>45848-45849</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19310</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Personnel</EAR>
      <HD>Personnel Management Office</HD>
      <CAT>
        <HD>PROPOSED RULES</HD>
        <DOCENT>
          <DOC>Pay in Nonforeign Areas,</DOC>
          <PGS>45710-45713</PGS>
          <FRDOCBP D="3" T="01AUP1.sgm">2011-19361</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Pipeline</EAR>
      <PRTPAGE P="vi"/>
      <HD>Pipeline and Hazardous Materials Safety Administration</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Agency Information Collection Activities; Proposals, Submissions, and Approvals,</DOC>
          <PGS>45904-45906</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19383</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Postal Regulatory</EAR>
      <HD>Postal Regulatory Commission</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Post Office Closings,</DOC>
          <PGS>45882-45883</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19380</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Presidential Documents</EAR>
      <HD>Presidential Documents</HD>
      <CAT>
        <HD>PROCLAMATIONS</HD>
        <SJ>Special Observances:</SJ>
        <SJDENT>
          <SJDOC>World Hepatitis Day (Proc. 8696),</SJDOC>
          <PGS>46181-46184</PGS>
          <FRDOCBP D="3" T="01AUD0.sgm">2011-19618</FRDOCBP>
        </SJDENT>
      </CAT>
      <CAT>
        <HD>ADMINISTRATIVE ORDERS</HD>
        <DOCENT>
          <DOC>Lebanon; Continuation of National Emergency with Respect to Actions to Undermine its Sovereignty or Democratic Processes and Institutions,</DOC>
          <PGS>45653</PGS>
          <FRDOCBP D="0" T="01AUO0.sgm">2011-19490</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Securities</EAR>
      <HD>Securities and Exchange Commission</HD>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Self-Regulatory Organizations; Proposed Rule Changes:</SJ>
        <SJDENT>
          <SJDOC>EDGA Exchange, Inc.,</SJDOC>
          <PGS>45896-45899</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19326</FRDOCBP>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19327</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>EDGX Exchange, Inc.,</SJDOC>
          <PGS>45895-45896</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19325</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>Financial Industry Regulatory Authority, Inc.,</SJDOC>
          <PGS>45883-45885</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19324</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>NYSE Amex LLC,</SJDOC>
          <PGS>45899-45902</PGS>
          <FRDOCBP D="3" T="01AUN1.sgm">2011-19328</FRDOCBP>
        </SJDENT>
        <SJDENT>
          <SJDOC>NYSE Arca, Inc.,</SJDOC>
          <PGS>45885-45895</PGS>
          <FRDOCBP D="10" T="01AUN1.sgm">2011-19329</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Social</EAR>
      <HD>Social Security Administration</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Agency Information Collection Activities; Proposals, Submissions, and Approvals,</DOC>
          <PGS>45902-45904</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19406</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Surface Mining</EAR>
      <HD>Surface Mining Reclamation and Enforcement Office</HD>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Agency Information Collection Activities; Proposals, Submissions, and Approvals,</DOC>
          <PGS>45849-45850</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19295</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Transportation Department</EAR>
      <HD>Transportation Department</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Federal Aviation Administration</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Pipeline and Hazardous Materials Safety Administration</P>
      </SEE>
    </AGCY>
    <AGCY>
      <EAR>Treasury</EAR>
      <HD>Treasury Department</HD>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Financial Crimes Enforcement Network</P>
      </SEE>
      <SEE>
        <HD SOURCE="HED">See</HD>
        <P>Internal Revenue Service</P>
      </SEE>
      <CAT>
        <HD>NOTICES</HD>
        <DOCENT>
          <DOC>Agency Information Collection Activities; Proposals, Submissions, and Approvals,</DOC>
          <PGS>45906</PGS>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19344</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>U.S. Citizenship</EAR>
      <HD>U.S. Citizenship and Immigration Services</HD>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Agency Information Collection Activities:</SJ>
        <SJDENT>
          <SJDOC>E-Verify Program,</SJDOC>
          <PGS>45843-45844</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19423</FRDOCBP>
        </SJDENT>
        <DOCENT>
          <DOC>Agency Information Collection Activities; Proposals, Submissions, and Approvals,</DOC>
          <PGS>45844-45845</PGS>
          <FRDOCBP D="1" T="01AUN1.sgm">2011-19316</FRDOCBP>
          <FRDOCBP D="0" T="01AUN1.sgm">2011-19317</FRDOCBP>
        </DOCENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Customs</EAR>
      <HD>U.S. Customs and Border Protection</HD>
      <CAT>
        <HD>NOTICES</HD>
        <SJ>Final Determinations on Country of Origin:</SJ>
        <SJDENT>
          <SJDOC>Certain Patient Transport Chair,</SJDOC>
          <PGS>45845-45847</PGS>
          <FRDOCBP D="2" T="01AUN1.sgm">2011-19400</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <AGCY>
      <EAR>Veteran Affairs</EAR>
      <HD>Veterans Affairs Department</HD>
      <CAT>
        <HD>RULES</HD>
        <SJ>Vocational Rehabilitation and Employment Program:</SJ>
        <SJDENT>
          <SJDOC>Changes to Subsistence Allowance,</SJDOC>
          <PGS>45697-45705</PGS>
          <FRDOCBP D="8" T="01AUR1.sgm">2011-19473</FRDOCBP>
        </SJDENT>
      </CAT>
    </AGCY>
    <PTS>
      <HD SOURCE="HED">Separate Parts In This Issue</HD>
      <HD>Part II</HD>
      <DOCENT>
        <DOC>Homeland Security Department, Coast Guard,</DOC>
        <PGS>45908-46081</PGS>
        <FRDOCBP D="173" T="01AUP2.sgm">2011-17093</FRDOCBP>
      </DOCENT>
      <HD>Part III</HD>
      <DOCENT>
        <DOC>Environmental Protection Agency,</DOC>
        <PGS>46084-46147</PGS>
        <FRDOCBP D="63" T="01AUP3.sgm">2011-18582</FRDOCBP>
      </DOCENT>
      <HD>Part IV</HD>
      <DOCENT>
        <DOC>Interior Department, Fish and Wildlife Service,</DOC>
        <PGS>46150-46171</PGS>
        <FRDOCBP D="21" T="01AUR2.sgm">2011-19206</FRDOCBP>
      </DOCENT>
      <HD>Part V</HD>
      <DOCENT>
        <DOC>Environmental Protection Agency,</DOC>
        <PGS>46174-46180</PGS>
        <FRDOCBP D="6" T="01AUN2.sgm">2011-19414</FRDOCBP>
      </DOCENT>
      <HD>Part VI</HD>
      <DOCENT>
        <DOC>Presidential Documents,</DOC>
        <PGS>46181-46184</PGS>
        <FRDOCBP D="3" T="01AUD0.sgm">2011-19618</FRDOCBP>
      </DOCENT>
    </PTS>
    <AIDS>
      <HD SOURCE="HED">Reader Aids</HD>
      <P>Consult the Reader Aids section at the end of this page for phone numbers, online resources, finding aids, reminders, and notice of recently enacted public laws.</P>
      
      <P>To subscribe to the Federal Register Table of Contents LISTSERV electronic mailing list, go to http://listserv.access.gpo.gov and select Online mailing list archives, FEDREGTOC-L, Join or leave the list (or change settings); then follow the instructions.</P>
    </AIDS>
  </CNTNTS>
  <VOL>76</VOL>
  <NO>147</NO>
  <DATE>Monday, August 1, 2011</DATE>
  <UNITNAME>Rules and Regulations</UNITNAME>
  <RULES>
    <RULE>
      <PREAMB>
        <PRTPAGE P="45655"/>
        <AGENCY TYPE="F">DEPARTMENT OF TRANSPORTATION</AGENCY>
        <SUBAGY>Federal Aviation Administration</SUBAGY>
        <CFR>14 CFR Part 39</CFR>
        <DEPDOC>[Docket No. FAA-2011-0547; Directorate Identifier 2011-NE-13-AD; Amendment 39-16757; AD 2011-15-10]</DEPDOC>
        <RIN>RIN 2120-AA64</RIN>
        <SUBJECT>Airworthiness Directives; Superior Air Parts and Lycoming Engines (Formerly Textron Lycoming) Fuel-Injected Engines</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Federal Aviation Administration (FAA), DOT.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Final rule; request for comments.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>We are adopting a new airworthiness directive (AD) for certain Superior Air Parts and Lycoming (formerly Textron Lycoming) fuel-injected engines. This AD requires removing from service, certain fuel servos. This AD was prompted by an accident involving a Piper PA32R-301. We are issuing this AD to correct the unsafe condition on these products.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>This AD is effective August 16, 2011.</P>
          <P>The Director of the Federal Register approved the incorporation by reference of a certain publication listed in the AD as of August 16, 2011.</P>
          <P>We must receive comments on this AD by September 15, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may send comments, using the procedures found in 14 CFR 11.43 and 11.45, by any of the following methods:</P>
          <P>•<E T="03">Federal eRulemaking Portal:</E>Go to<E T="03">http://www.regulations.gov.</E>Follow the instructions for submitting comments.</P>
          <P>•<E T="03">Fax:</E>202-493-2251.</P>
          <P>•<E T="03">Mail:</E>U.S. Department of Transportation, Docket Operations, M-30, West Building Ground Floor, Room W12-140, 1200 New Jersey Avenue, SE., Washington, DC 20590.</P>
          <P>•<E T="03">Hand Delivery:</E>U.S. Department of Transportation, Docket Operations, M-30, West Building Ground Floor, Room W12-140, 1200 New Jersey Avenue SE., Washington, DC 20590, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays.</P>

          <P>For service information identified in this AD, contact AVStar Fuel Systems, Inc., 1365 Park Lane South, Jupiter, FL 33458; phone: 561-575-1560; Web site:<E T="03">www.avstardirect.com.</E>You may review copies of the referenced service information at the FAA, Engine &amp; Propeller Directorate, 12 New England Executive Park, Burlington, MA 01803. For information on the availability of this material at the FAA, call 781-238-7125.</P>
        </ADD>
        <HD SOURCE="HD1">Examining the AD Docket</HD>
        <P>You may examine the AD docket on the Internet at<E T="03">http://www.regulations.gov;</E>or in person at the Docket Management Facility between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays. The AD docket contains this AD, the regulatory evaluation, any comments received, and other information. The street address for the Docket Office (phone: 800-647-5527) is in the<E T="02">ADDRESSES</E>section. Comments will be available in the AD docket shortly after receipt.</P>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Neil Duggan, Aerospace Engineer, Atlanta Certification Office, FAA, 1701 Columbia Avenue, College Park, GA 30337; phone: 404-474-5576; fax: 404-474-5606; e-mail:<E T="03">neil.duggan@faa.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P/>
        <HD SOURCE="HD1">Discussion</HD>
        <P>On August 10, 2010, a Piper PA32R-301 airplane crashed after reporting a loss of engine power. The subsequent investigation by the National Transportation Safety Board suspects a faulty fuel servo, Bendix model RSA-10ED1. AVStar Fuel Systems (AFS) had overhauled the fuel servo using a new AFS diaphragm, part number (P/N) AV2541803. The diaphragm failed after 19 flight hours (FH) since new due to suspected manufacturing defects. AVStar Fuel Systems produces diaphragms, P/Ns AV2541801 and AV2541803 under a parts manufacturing authorization (PMA). Diaphragms produced from specific lot numbers could have stud threads that don't meet design, incomplete braze between the stud and hub, and studs made from lower temper material. Diaphragms from these lots could fail in fatigue prematurely. About 261 diaphragms, P/Ns AV2541801 and AV2541803, might still be service inside either AFS new or overhauled servos of any manufacturer (Bendix or Precision). Other overhaul facilities may also have purchased AFS diaphragms between the dates of May 21, 2010, and October 19, 2010, and used these diaphragms in their overhauls. This condition, if not corrected, could result in an in-flight engine shutdown due to a failed fuel servo diaphragm and damage to the airplane.</P>
        <HD SOURCE="HD1">Relevant Service Information</HD>
        <P>We reviewed AFS Mandatory Service Bulletin (MSB) AFS-SB6, Revision 2, dated April 6, 2011. The MSB provides P/Ns and serial numbers (S/Ns) of affected servos.</P>
        <HD SOURCE="HD1">FAA's Determination</HD>
        <P>We are issuing this AD because we evaluated all the relevant information and determined the unsafe condition described previously is likely to exist or develop in other products of the same type design.</P>
        <HD SOURCE="HD1">AD Requirements</HD>
        <P>This AD requires, within 5 FH after the effective date of this AD, removing your fuel servo if AFS Diaphragm P/N AV2541801 or AV2541803 was installed at any time after May 20, 2010, as specified in AFS MSB AFS-SB6, Revision 2, dated April 6, 2011.</P>
        <HD SOURCE="HD1">Differences Between the AD and the Service Information</HD>
        <P>AVStar Fuel Systems MSB AFS-SB6, Revision 2, dated April 6, 2011, doesn't specify a compliance time and recommends limiting special flight permits to delivery to a service location. This AD requires performing the required actions within 5 FH and prohibits special flight permits.</P>
        <HD SOURCE="HD1">FAA's Justification and Determination of the Effective Date</HD>

        <P>An unsafe condition exists that requires the immediate adoption of this AD. The FAA has found that the risk to the flying public justifies waiving notice and comment prior to adoption of this rule because of the compliance requirement of 5 FH. Therefore, we find that notice and opportunity for prior<PRTPAGE P="45656"/>public comment are impracticable and that good cause exists for making this amendment effective in less than 30 days.</P>
        <HD SOURCE="HD1">Comments Invited</HD>

        <P>This AD is a final rule that involves requirements affecting flight safety and was not preceded by notice and an opportunity for public comment. However, we invite you to send any written data, views, or arguments about this AD. Send your comments to an address listed under the<E T="02">ADDRESSES</E>section. Include the docket number FAA-2011-0547 and Directorate Identifier 2011-NE-13-AD at the beginning of your comments. We specifically invite comments on the overall regulatory, economic, environmental, and energy aspects of this AD. We will consider all comments received by the closing date and may amend this AD because of those comments.</P>
        <P>We will post all comments we receive, without change, to<E T="03">http://www.regulations.gov,</E>including any personal information you provide. We will also post a report summarizing each substantive verbal contact we receive about this AD.</P>
        <HD SOURCE="HD1">Costs of Compliance</HD>
        <P>We estimate that this AD affects 60,000 engines installed on aircraft of U.S. registry. We also estimate that it will take about 0.5 work-hour per engine to perform the inspection, 2.0 work-hours per engine to remove the servo from 261 engines with discrepant AFS Diaphragm P/N AV2541801 or AV2541803 installed and that the average labor rate is $85 per work-hour. We estimate the parts cost to be $565 per servo. Based on these figures, we estimate the total cost of the AD to U.S. operators to be $2,736,735.</P>
        <HD SOURCE="HD1">Authority for This Rulemaking</HD>
        <P>Title 49 of the United States Code specifies the FAA's authority to issue rules on aviation safety. Subtitle I, section 106, describes the authority of the FAA Administrator. “Subtitle VII: Aviation Programs” describes in more detail the scope of the Agency's authority.</P>
        <P>We are issuing this rulemaking under the authority described in subtitle VII, part A, subpart III, section 44701: “General requirements.” Under that section, Congress charges the FAA with promoting safe flight of civil aircraft in air commerce by prescribing regulations for practices, methods, and procedures the Administrator finds necessary for safety in air commerce. This regulation is within the scope of that authority because it addresses an unsafe condition that is likely to exist or develop on products identified in this rulemaking action.</P>
        <HD SOURCE="HD1">Regulatory Findings</HD>
        <P>This AD will not have federalism implications under Executive Order 13132. This AD will not have a substantial direct effect on the States, on the relationship between the national government and the States, or on the distribution of power and responsibilities among the various levels of government.</P>
        <P>
          <E T="03">For the reasons discussed above, I certify that this AD:</E>
        </P>
        <P>(1) Is not a “significant regulatory action” under Executive Order 12866,</P>
        <P>(2) Is not a “significant rule” under DOT Regulatory Policies and Procedures (44 FR 11034, February 26, 1979),</P>
        <P>(3) Will not affect intrastate aviation in Alaska, and</P>
        <P>(4) Will not have a significant economic impact, positive or negative, on a substantial number of small entities under the criteria of the Regulatory Flexibility Act.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 14 CFR Part 39</HD>
          <P>Air transportation, Aircraft, Aviation safety, Incorporation by reference, Safety.</P>
        </LSTSUB>
        <HD SOURCE="HD1">Adoption of the Amendment</HD>
        <P>Accordingly, under the authority delegated to me by the Administrator, the FAA amends 14 CFR part 39 as follows:</P>
        <REGTEXT PART="39" TITLE="14">
          <PART>
            <HD SOURCE="HED">PART 39—AIRWORTHINESS DIRECTIVES</HD>
          </PART>
          <AMDPAR>1. The authority citation for part 39 continues to read as follows:</AMDPAR>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>49 U.S.C. 106(g), 40113, 44701.</P>
          </AUTH>
        </REGTEXT>
        <REGTEXT PART="39" TITLE="14">
          <SECTION>
            <SECTNO>§ 39.13</SECTNO>
            <SUBJECT>[Amended]</SUBJECT>
          </SECTION>
          <AMDPAR>2. The FAA amends § 39.13 by adding the following new airworthiness directive (AD):</AMDPAR>
          
          <EXTRACT>
            <FP SOURCE="FP-2">
              <E T="04">2011-15-10Superior Air Parts and Lycoming Engines (formerly Textron Lycoming):</E>Amendment 39-16757; Docket No. FAA-2011-0547; Directorate Identifier 2011-NE-13-AD.</FP>
            <HD SOURCE="HD1">(a) Effective Date</HD>
            <P>This AD is effective August 16, 2011.</P>
            <HD SOURCE="HD1">(b) Affected ADs</HD>
            <P>None.</P>
            <HD SOURCE="HD1">(c) Applicability</HD>
            <P>This AD applies to the Superior Air Parts engine models and Lycoming engine models listed in Table 1 of this AD with an AVStar Fuel Systems (AFS) fuel servo diaphragm, part numbers (P/Ns) AV2541801 and AV2541803, installed.</P>
            <GPOTABLE CDEF="xs100,r150" COLS="2" OPTS="L2,i1">
              <TTITLE>Table 1—Affected Lycoming and Superior Air Parts Engines</TTITLE>
              <BOXHD>
                <CHED H="1">Engine manufacturer</CHED>
                <CHED H="1">Engine model</CHED>
              </BOXHD>
              <ROW>
                <ENT I="01">Lycoming Engines</ENT>
                <ENT>AEIO-320-D1B, -D2B, -E1A, -E1B, -E2A, -E2B.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>AIO-320-A1A, -A1B, -A2A, -A2B, -B1B, -C1B.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>IO-320-A1A, -A2A, -B1A, -B1B, -B1C, -B1E, -B1D, -B2A, -C1A, -C1B, -D1A, -D1C, -D1B, -E1A, -E1B, -E2A, -E2B, -F1A.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>LIO-320-B1A, -C1A.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>AEIO-360-A1A, -A1B, -A1B6, -A1E6, -A1C, -A1D, -A1E, -A2A, -A2B, -A2C, -B1B, -B1D, -B1F, -B1F6, -B1G6, -B2F, -B2F6, -B1H, -B4A, -H1A, -H1B.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>AIO-360-A1A, -A1B, -A2A, -A2B, -B1B.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>HIO-360-A1A, -A1B, -B1A, -B1B, -C1A, -C1B, -E1AD, -E1BD, -F1AD, -G1A.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>IO-360-A1A, -A1B, -A1B6, -A1B6D, -A1C, -A1D, -A1D6, -A1D6D, -A2A, -A2B, -A2C, -A3B6, -A3B6D, -A3D6D, -B1A, -B1B, -B1C, -B1D, -B1E, -B1F, -B1F6, -B1G6, -B2E, -B2F, -B2F6, -B4A, -C1A, -C1B, -C1C, -C1C6, -C1D6, -C1E6, -C1E6D, -C1F,-C1G6, -D1A, -E1A, -F1A, -J1AD, -J1A6D, -K2A, -L2A, -M1A, -M1B.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>LIO-360-C1E6, -M1A.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>TIO-360-A1A, -A1B, -A3B6, -C1A6D.</ENT>
              </ROW>
              <ROW>
                <PRTPAGE P="45657"/>
                <ENT I="22"/>
                <ENT>IO-540-A1A5, -B1A5, -B1B5, -B1C5, -C1B5, -C1C5, -C2C, -C4B5, -C4B5D, -C4D5, -C4C5, -C4D5D, -D4A5, -D4B5, -D4C5, -E1A5, -E1B5, -E1C5, -G1A5, -G1B5, -G1C5, -G1D5, -G1E5, -G1F5, -J4A5, -K1A5, -K1A5D, -K1B5, -K1B5D, -K1C5, -K1D5, -K1E5, -K1E5D, -K1F5, -K1F5D, -K1G5, -K1G5D, -K1H5, -K1J5, -K1J5D, -K1K5, -K2A5, -L1A5, -L1A5D, -L1B5D, -L1C5, -M1A5, -M1A5D, -M1B5D, -M1C5, -M2A5D, -N1A5, -P1A5, -R1A5, -S1A5, -T4A5D, -T4B5, -T4B5D, -T4C5D, -U1A5D, -U1B5D, -V4A5D, -V4A5, -W1A5, -W1A5D, -W3A5D, -AA1A5, -AA1B5, -AB1A5, -AC1A5, -AE1A5, -AF1A5.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>IGO-480-A1A6, -A1B6.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>AEIO-540-D4A5, -D4B5, -D4C5, -D4D5, -L1B5D, -L1B5, -L1D5.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>IVO-540-A1A.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>TIO-540-A1A, -A1B, -A2A, -A2B, -A1C, -A2C, -C1A, -E1A, -F2BD, -G1A, -H1A, -J2B, -J2BD, -K1AD, -N2BD, -R2AD, -S1AD, -T2AD, -U2A, -V2AD, -W2A, -AA1AD, -AB1AD, -AB1BD, -AE2A, -AF1A, -AF1B, -AG1A, -AH1A, -AJ1A, -AK1A.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>LTIO-540-F2BD, -J2B, -J2BD, -K1AD, -N2BD, -R2AD, -U2A, -V2AD, -W2A.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>IO-720-A1A, -A1B, -A1BD, -B1A, -B1B, -B1BD, -C1B, -C1BD, -D1B, -D1BD, -D1C, -D1CD.</ENT>
              </ROW>
              <ROW>
                <ENT I="22"/>
                <ENT>TIGO-541-B1A, -C1A, -D1A, -D1B, -E1A, -G1AD.</ENT>
              </ROW>
              <ROW>
                <ENT I="01">Superior Air Parts</ENT>
                <ENT>IO-360-A1A1, A1A2, A2A1, A2A2, A3A1, A3A2, B1A1, B1A2, B2A1, B2A2, B3A1, B3A2, B4A1, B4A2, B5A1, B5A2, B6A1, B6A2, C1A1, C1A2, C2A1, C2A2, C2A1, C3A2, D1A1, D1A2, D2A1, D2A2, D3A1, D3A2, D4A1, D4A2, D5A1, D5A2, D6A1, D6A2, E1A1, E1A2, E2A1, E2A2, E3A1, E3A2.</ENT>
              </ROW>
            </GPOTABLE>
            <HD SOURCE="HD1">(d) Unsafe Condition</HD>
            <P>This AD was prompted by an accident involving a Piper PA32R-301. We are issuing this AD to correct the unsafe condition on these products.</P>
            <HD SOURCE="HD1">(e) Compliance</HD>
            <P>Comply with this AD within the compliance times specified, unless already done.</P>
            <HD SOURCE="HD1">(f) Remove Fuel Servo</HD>
            <P>If an AFS fuel servo diaphragm P/N AV2541801 or AV2541803 was installed in your fuel servo at any time after May 20, 2010, do the following as specified AVStar Fuel Systems (AFS) Mandatory Service Bulletin (MSB) AFS-SB6, Revision 2, dated April 6, 2011:</P>
            <P>(1) Before further flight remove the fuel servo.</P>
            <P>(2) After the effective date of this AD, don't install any affected fuel servo containing a discrepant AVStar fuel servo diaphragm, P/N AV2541801 or AV2541803, as listed in AFS MSB AFS-SB6, Revision 2, dated April 6, 2011.</P>
            <HD SOURCE="HD1">(g) Special Flight Permit</HD>
            <P>We will not issue a special flight permit.</P>
            <HD SOURCE="HD1">(h) Alternative Methods of Compliance (AMOCs)</HD>
            <P>The Manager, Atlanta Aircraft Certification Office, FAA, has the authority to approve AMOCs for this AD, if requested using the procedures found in 14 CFR 39.19.</P>
            <HD SOURCE="HD1">(i) Related Information</HD>

            <P>For more information about this AD, contact Neil Duggan, Aerospace Engineer, Atlanta Certification Office, FAA, 1701 Columbia Avenue, College Park, GA 30337; phone: (404) 474-5576; fax: (404) 474-5606; e-mail:<E T="03">neil.duggan@faa.gov.</E>
            </P>
            <HD SOURCE="HD1">(j) Material Incorporated by Reference</HD>
            <P>(1) You must use AVStar Fuel Systems Mandatory Service Bulletin AFS-SB6, Revision 2, dated April 6, 2011, to do the actions required by this AD, unless the AD specifies otherwise. The Director of the Federal Register approved the incorporation by reference (IBR) under 5 U.S.C. 552(a) and 1 CFR part 51 of the following service information on the date specified:</P>
            <P>(2) The Director of the Federal Register approved the incorporation by reference of AVStar Fuel Systems Mandatory Service Bulletin AFS-SB6, Revision 2, dated April 6, 2011, on September 6, 2011 under 5 U.S.C. 552(a) and 1 CFR part 51.</P>

            <P>(3) For service information identified in this AD, contact AVStar Fuel Systems, Inc., 1365 Park Lane South, Jupiter, FL 33458; 561-575-1560; Web site:<E T="03">http://www.avstardirect.com.</E>
            </P>
            <P>(4) You may review copies of the service information at the FAA, 12 New England Executive Park, Burlington, MA 01803. For information on the availability of this material at the FAA, call 781-238-7125.</P>

            <P>(5) You may also review copies of the service information that is incorporated by reference at the National Archives and Records Administration (NARA). For information on the availability of this material at an NARA facility, call 202-741-6030, or go to<E T="03">http://www.archives.gov/federal_register/code_of_federal_regulations/ibr_locations.html.</E>
            </P>
          </EXTRACT>
        </REGTEXT>
        <SIG>
          <DATED>Issued in Burlington, Massachusetts, on July 13, 2011.</DATED>
          <NAME>Colleen M. D'Alessandro,</NAME>
          <TITLE>Acting Manager, Engine &amp; Propeller Directorate, Aircraft Certification Service.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-18168 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4910-13-P</BILCOD>
    </RULE>
    <RULE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF TRANSPORTATION</AGENCY>
        <SUBAGY>Federal Aviation Administration</SUBAGY>
        <CFR>14 CFR Part 39</CFR>
        <DEPDOC>[Docket No. FAA-2011-0450; Directorate Identifier 2011-CE-010-AD; Amendment 39-16758; AD 2011-15-11]</DEPDOC>
        <RIN>RIN 2120-AA64</RIN>
        <SUBJECT>Airworthiness Directives; Cessna Aircraft Company (Cessna) Models 337, 337A (USAF 02B), 337B, 337C, 337D, 337E, T337E, 337F, T337F, 337G, T337G, M337B, F 337E, FT337E, F 337F, FT337F, F 337G, and FT337GP Airplanes</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Federal Aviation Administration (FAA), DOT.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Final rule.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>We are adopting a new airworthiness directive (AD) for the products listed above. This AD requires inspecting the wings for internal and external damage, repairing any damage, reinforcing the wings, installing operational limitation placards in the cockpit, and adding limitations to the airplane flight manual supplement. This AD was prompted by a review of installed Flint Aero, Inc. wing tip auxiliary fuel tanks, Supplemental Type Certificate (STC) SA5090NM. We are issuing this AD to detect and correct damage in the wings and to prevent overload failure of the wing due to the installation of the STC. Damage in the wing or overload failure of the wing could result in structural failure of the wing, which could result in loss of control.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>This AD is effective September 6, 2011.<PRTPAGE P="45658"/>
          </P>
          <P>The Director of the Federal Register approved the incorporation by reference of certain publications listed in the AD as of September 6, 2011.</P>
        </EFFDATE>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>For service information identified in this AD, contact Flint Aero, Inc., 1942 Joe Crosson Drive, El Cajon, CA 92020; phone: (619) 448-1551; fax: (619)  448-1571; Internet:<E T="03">http://www.flintaero.com.</E>You may review copies of the referenced service information at the FAA, Small Airplane Directorate, 901 Locust, Kansas City, MO 64106. For information on the availability of this material at the FAA, call (816)  329-4148.</P>
        </ADD>
        <HD SOURCE="HD1">Examining the AD Docket</HD>
        <P>You may examine the AD docket on the Internet at<E T="03">http://www.regulations.gov;</E>or in person at the Docket Management Facility between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays. The AD docket contains this AD, the regulatory evaluation, any comments received, and other information. The address for the Docket Office (phone: 800-647-5527) is Document Management Facility, U.S. Department of Transportation, Docket Operations, M-30, West Building Ground Floor, Room W12-140, 1200 New Jersey Avenue, SE., Washington, DC 20590.</P>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Dara Albouyeh, Aerospace Engineer, FAA, Los Angeles Aircraft Certification Office, 3960 Paramount Blvd., Lakewood, CA 90712; phone: (562) 627-5222; fax: (562) 627-5210; e-mail:<E T="03">dara.albouyeh@faa.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">Discussion</HD>

        <P>We issued a notice of proposed rulemaking (NPRM) to amend 14 CFR part 39 to include an AD that would apply to the specified products. That NPRM published in the<E T="04">Federal Register</E>on May 4, 2011 (76 FR 25264). That NPRM proposed to require inspecting the wings for internal and external damage, repairing any damage, reinforcing the wings, installing operational limitation placards in the cockpit, and adding limitations to the Flint Aero, Inc. Airplane Flight Manual Supplement.</P>
        <HD SOURCE="HD1">Comments</HD>
        <P>We gave the public the opportunity to participate in developing this AD. The following presents the comments received on the proposal and the FAA's response to each comment.</P>
        <HD SOURCE="HD1">Request To Remove Certain Steps From Appendix 1</HD>
        <P>Dennis L. Hamblin from Flint Aero, Inc. stated that steps 11, 13, and 14 should be removed from Appendix 1 of this AD. The inspection procedures in Appendix 1 are focused on damage caused by trimming of the close-out rib to allow passage of the fuel line. The Flint Aero, Inc. STC kit provides a close-out rib that replaces the Cessna  close-out rib. This configuration allows for the passage of the fuel line. Additionally, the Flint Aero, Inc. STC kit provides reinforcement doublers for all added inspection openings/cutouts; therefore, there should be no unreinforced cutouts.</P>
        <P>We do not agree with the commenter. All steps in Appendix 1 are required to check for any damage to the affected close-out rib, spar cap, and cut-outs that may have been caused by an overload condition regardless of the STC installation configuration.</P>
        <P>We have not changed the final rule AD action based on this comment.</P>
        <HD SOURCE="HD1">Request To Incorporate Revised Service Information</HD>
        <P>Flint Aero, Inc. issued a revision to Service Bulletin FA2 to correct a part number reference. We inferred that Flint Aero, Inc. wanted the FAA to include reference to the revised service bulletin into the final rule AD action.</P>
        <P>We agree. We have revised the final rule AD action to incorporate the revised service bulletin.</P>
        <HD SOURCE="HD1">Conclusion</HD>
        <P>We reviewed the relevant data, considered the comments received, and determined that air safety and the public interest require adopting the AD with the change described previously and any minor editorial changes. We have determined that these minor changes:</P>
        <P>• Αre consistent with the intent that was proposed in the NPRM for correcting the unsafe condition; and</P>
        <P>• Do not add any additional burden upon the public than was already proposed in the NPRM.</P>
        <P>We also determined that these changes will not increase the economic burden on any operator or increase the scope of the AD.</P>
        <HD SOURCE="HD1">Costs of Compliance</HD>
        <P>We estimate that this AD affects 33 airplanes of U.S. registry.</P>
        <P>We estimate the following costs to comply with this AD:</P>
        <GPOTABLE CDEF="s100,r80,r50,r50,r50" COLS="5" OPTS="L2,i1">
          <TTITLE>Estimated Costs</TTITLE>
          <BOXHD>
            <CHED H="1">Action</CHED>
            <CHED H="1">Labor cost</CHED>
            <CHED H="1">Parts cost</CHED>
            <CHED H="1">Cost per product</CHED>
            <CHED H="1">Cost on U.S.<LI>operators</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Inspection of the wing for damage</ENT>
            <ENT>5 work-hours × $85 per hour = $425 per inspection cycle</ENT>
            <ENT>Not applicable</ENT>
            <ENT>$425 per inspection cycle</ENT>
            <ENT>$14,025 per inspection cycle.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Fabricating and installing placards in the cockpit</ENT>
            <ENT>1 work-hour × $85 per hour = $85</ENT>
            <ENT>Not applicable</ENT>
            <ENT>$85</ENT>
            <ENT>$2,805.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Modifying the Limitations section of the Flint Aero, Inc. Airplane Flight Manual Supplement</ENT>
            <ENT>.5 work-hour × $85 per hour = $42.50</ENT>
            <ENT>Not applicable</ENT>
            <ENT>$42.50</ENT>
            <ENT>$1,402.50.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Reinforcing the upper wing skin, stringer, and wing front spar cap</ENT>
            <ENT>25 work-hours × $85 per hour = $2,125</ENT>
            <ENT>$1,070</ENT>
            <ENT>$3,195</ENT>
            <ENT>$105,435.</ENT>
          </ROW>
        </GPOTABLE>
        <HD SOURCE="HD1">Authority for This Rulemaking</HD>
        <P>Title 49 of the United States Code specifies the FAA's authority to issue rules on aviation safety. Subtitle I, section 106, describes the authority of the FAA Administrator. Subtitle VII: Aviation Programs, describes in more detail the scope of the Agency's authority.</P>

        <P>We are issuing this rulemaking under the authority described in subtitle VII, part A, subpart III, section 44701: “General requirements.” Under that section, Congress charges the FAA with promoting safe flight of civil aircraft in air commerce by prescribing regulations for practices, methods, and procedures the Administrator finds necessary for safety in air commerce. This regulation is within the scope of that authority because it addresses an unsafe condition that is likely to exist or develop on<PRTPAGE P="45659"/>products identified in this rulemaking action.</P>
        <HD SOURCE="HD1">Regulatory Findings</HD>
        <P>This AD will not have federalism implications under Executive Order 13132. This AD will not have a substantial direct effect on the States, on the relationship between the national government and the States, or on the distribution of power and responsibilities among the various levels of government.</P>
        <P>
          <E T="03">For the reasons discussed above, I certify that this AD:</E>
        </P>
        <P>(1) Is not a “significant regulatory action” under Executive Order 12866,</P>
        <P>(2) Is not a “significant rule” under DOT Regulatory Policies and Procedures (44 FR 11034, February 26, 1979),</P>
        <P>(3) Will not affect intrastate aviation in Alaska, and</P>
        <P>(4) Will not have a significant economic impact, positive or negative, on a substantial number of small entities under the criteria of the Regulatory Flexibility Act.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 14 CFR Part 39</HD>
          <P>Air transportation, Aircraft, Aviation safety, Incorporation by reference, Safety.</P>
        </LSTSUB>
        <HD SOURCE="HD1">Adoption of the Amendment</HD>
        <P>Accordingly, under the authority delegated to me by the Administrator, the FAA amends 14 CFR part 39 as follows:</P>
        <REGTEXT PART="39" TITLE="14">
          <PART>
            <HD SOURCE="HED">PART 39—AIRWORTHINESS DIRECTIVES</HD>
          </PART>
          <AMDPAR>1. The authority citation for part 39 continues to read as follows:</AMDPAR>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>49 U.S.C. 106(g), 40113, 44701.</P>
          </AUTH>
        </REGTEXT>
        
        <REGTEXT PART="39" TITLE="14">
          <SECTION>
            <SECTNO>§ 39.13</SECTNO>
            <SUBJECT>[Amended]</SUBJECT>
          </SECTION>
          <AMDPAR>2. The FAA amends § 39.13 by adding the following new airworthiness directive (AD):</AMDPAR>
          
          <EXTRACT>
            <FP SOURCE="FP-2">
              <E T="04">2011-15-11Cessna Aircraft Company:</E>Amendment 39-16758; Docket No. FAA-2011-0450; Directorate Identifier 2011-CE-010-AD.</FP>
            <HD SOURCE="HD1">(a) Effective Date</HD>
            <P>This AD is effective September 6, 2011.</P>
            <HD SOURCE="HD1">(b) Affected ADs</HD>
            <P>AD 2010-21-18, Amendment 39-16478, is related to the subject of this AD.</P>
            <HD SOURCE="HD1">(c) Applicability</HD>
            <P>This AD applies to Cessna Aircraft Company (Cessna) Models 337, 337A (USAF 02B), 337B, 337C, 337D, 337E, T337E, 337F, T337F, 337G, T337G, M337B, F 337E, FT337E, F 337F, FT337F, F 337G, and FT337GP airplanes, all serial numbers, that:</P>
            <P>(1) Are certificated in any category; and</P>
            <P>(2) Are or have ever been modified by Flint Aero, Inc. Supplemental Type Certificate (STC) SA5090NM.</P>
            <HD SOURCE="HD1">(d) Subject</HD>
            <P>Joint Aircraft System Component (JASC)/Air Transport Association (ATA) of America Code 57; Wings.</P>
            <HD SOURCE="HD1">(e) Unsafe Condition</HD>
            <P>This AD was prompted by a review of installed Flint Aero, Inc. wing tip auxiliary fuel tanks, STC SA5090NM. We are issuing this AD to detect and correct damage in the wings and to prevent overload failure of the wing due to the installation of the STC. Damage in the wing or overload failure of the wing could result in structural failure of the wing, which could result in loss of control.</P>
            <HD SOURCE="HD1">(f) Compliance</HD>
            <P>Comply with this AD within the compliance times specified, unless already done.</P>
            <HD SOURCE="HD1">(g) Required Actions</HD>
            <P>(1) Within the next 50 hours time-in-service (TIS) after September 6, 2011 (the effective date of this AD) or within 30 days after September 6, 2011 (the effective date of this AD), whichever occurs first, do a general and focused inspection of the left and right wing for internal and external damage at wing stations (WSTA) 150 and 177. Do the inspections following Appendix 1 of this AD.</P>

            <P>(2) After the inspection required in paragraph (g)(1) of this AD if no damage was found and before the modification required in paragraph (g)(5) of this AD is incorporated, anytime severe and/or extreme turbulence is encountered during flight, before the next flight do a focused inspection of the wing for damage following steps 1, 2, 3, 4, 7, and 10 in Appendix 1 of this AD. Also inspect for signs of distress in the upper front spar in the area around WSTA 150 and 177. The definition of severe and extreme turbulence can be found in table 7-1-9 of the FAA Aeronautical Information Manual (AIM). You may obtain a copy of the FAA AIM at<E T="03">http://www.faa.gov/air_traffic/publications/atpubs/aim/.</E>
            </P>
            <P>(3) For airplanes that have not had the modification specified in paragraphs (g)(4) and (g)(5) incorporated, within the next 50 hours time-in-service (TIS) after September 6, 2011 (the effective date of this AD) or within 30 days after September 6, 2011 (the effective date of this AD), fabricate a placard (using at least<FR>1/8</FR>-inch letters) with the following words and install the placard on the instrument panel within the pilot's clear view:</P>
            <P>(i) “MAINTAIN AT LEAST 12 GAL OF FUEL IN EACH WING TIP FUEL TANK FOR AIRPLANE WEIGHTS BETWEEN 3,400 LBS AND 4,330 LBS.”</P>
            <P>(ii) “MAINTAIN FULL FUEL IN EACH WING TIP FUEL TANK FOR AIRPLANE WEIGHTS AT OR ABOVE 4,330 LBS.”</P>
            <P>(4) If damage or signs of distress are found during the inspections required in paragraphs (g)(1) and (g)(2) of this AD, before further flight do the following:</P>

            <P>(i) Repair all damaged and distressed parts following FAA Advisory Circular (AC) 43.13-1B, Chapter 4, which can be found at<E T="03">http://rgl.faa.gov/;</E>
            </P>
            <P>(ii) Incorporate the modification reinforcement specified in Flint Aero, Inc. Service Bulletin FA2, Rev 2, dated April 8, 2011, or Flint Aero, Inc. Service Bulletin FA2, Rev 3, dated May 3, 2011, following Flint Aero, Inc. Drawing FA2, Rev A, dated April 8, 2011;</P>
            <P>(iii) Remove the placard specified in paragraph (g)(3) of this AD;</P>
            <P>(iv) Fabricate a new placard (using at least<FR>1/8</FR>-inch letters) with the following words and install the placard on the instrument panel within the pilot's clear view: “MAINTAIN AT LEAST 12 GAL OF FUEL IN EACH WING TIP FUEL TANK FOR AIRPLANE WEIGHTS AT OR ABOVE 4,330 LBS”; and</P>
            <P>(v) Incorporate the information from Appendix 2 of this AD into the Limitations section of the Flint Aero, Inc. Airplane Flight Manual Supplement.</P>
            <P>(5) If no damage or signs of distress are found during the inspections required in paragraphs (g)(1) and (g)(2) of this AD, within the next 100 hours TIS after September 6, 2011 (the effective date of this AD) or within 12 months after September 6, 2011 (the effective date of this AD), whichever occurs first, do the following:</P>
            <P>(i) Incorporate the modification reinforcement specified in Flint Aero, Inc. Service Bulletin FA2, Rev 2, dated April 8, 2011, or Flint Aero, Inc. Service Bulletin FA2, Rev 3, dated May 3, 2011, following Flint Aero, Inc. Drawing FA2, Rev A, dated April 8, 2011;</P>
            <P>(ii) Remove the placard specified in paragraph (g)(3) of this AD;</P>
            <P>(iii) Fabricate a new placard (using at least 1/8-inch letters) with the following words and install the placard on the instrument panel within the pilot's clear view: “MAINTAIN AT LEAST 12 GAL OF FUEL IN EACH WING TIP FUEL TANK FOR AIRPLANE WEIGHTS AT OR ABOVE 4,330 LBS”; and</P>
            <P>(iv) Incorporate the information from Appendix 2 of this AD into the Limitations section of the Flint Aero, Inc. Airplane Flight Manual Supplement.</P>
            <P>(6) You may incorporate the modification reinforcement specified in Flint Aero, Inc. Service Bulletin FA2, Rev 2, dated April 8, 2011, or Flint Aero, Inc. Service Bulletin FA2, Rev 3, dated May 3, 2011, following Flint Aero, Inc. Drawing FA2, Rev A, dated April 8, 2011, at any time after the inspection required in paragraph (g)(1) of this AD but no later than the compliance time specified in paragraph (g)(5) of this AD as long as no cracks were found. As required in paragraph (g)(4) of this AD, the modification reinforcement must be incorporated before further flight if damage or signs of distress are found.</P>
            <HD SOURCE="HD1">(h) Alternative Methods of Compliance (AMOCs)</HD>

            <P>(1) The Manager, Los Angeles Aircraft Certification Office (ACO), FAA, has the authority to approve AMOCs for this AD, if requested using the procedures found in 14 CFR 39.19. In accordance with 14 CFR 39.19, send your request to your principal inspector or local Flight Standards District Office, as<PRTPAGE P="45660"/>appropriate. If sending information directly to the manager of the ACO, send it to the attention of the person identified in the Related Information section of this AD.</P>
            <P>(2) Before using any approved AMOC, notify your appropriate principal inspector, or lacking a principal inspector, the manager of the local flight standards district office/certificate holding district office.</P>
            <HD SOURCE="HD1">(i) Related Information</HD>

            <P>For more information about this AD, contact Dara Albouyeh, Aerospace Engineer, FAA, Los Angeles ACO, 3960 Paramount Blvd., Lakewood, CA 90712; phone: (562) 627-5222; fax: (562) 627-5210; e-mail:<E T="03">dara.albouyeh@faa.gov.</E>
            </P>
            <HD SOURCE="HD1">(j) Material Incorporated by Reference</HD>
            <P>(1) You must use the following service information to do the actions required by this AD, unless the AD specifies otherwise. The Director of the Federal Register approved the incorporation by reference (IBR) under 5 U.S.C. 552(a) and 1 CFR part 51 of the following service information on September 6, 2011:</P>
            <P>(i) Flint Aero, Inc. Service Bulletin FA2, Rev 2, dated April 8, 2011;</P>
            <P>(ii) Flint Aero, Inc. Service Bulletin FA2, Rev 3, dated May 3, 2011; and</P>
            <P>(iii) Flint Aero, Inc. Drawing FA2, Rev A, dated April 8, 2011.</P>

            <P>(2) For service information identified in this AD, contact Flint Aero, Inc., 1942 Joe Crosson Drive, El Cajon, CA 92020; phone: (619) 448-1551; fax: (619) 448-1571; Internet:<E T="03">http://www.flintaero.com.</E>
            </P>
            <P>(3) You may review copies of the referenced service information at the FAA, Small Airplane Directorate, 901 Locust, Kansas City, MO 64106. For information on the availability of this material at the FAA, call (816) 329-4148.</P>

            <P>(4) You may also review copies of the service information that is incorporated by reference at the National Archives and Records Administration (NARA). For information on the availability of this material at an NARA facility, call 202-741-6030, or go to<E T="03">http://www.archives.gov/federal_register/code_of_federal_regulations/ibr_locations.html.</E>
            </P>
            <HD SOURCE="HD1">Appendix 1 to AD 2011-15-11</HD>
            <HD SOURCE="HD1">General and Focused Inspection Procedures</HD>

            <P>Perform a general and focused inspection of the wing for internal and external damage from wing station (WSTA) 23 to the wing tip. The general inspection must be performed in accordance with 14 CFR 43.15(c), using a checklist that includes at least the scope and detail of the items contained in Appendix D of 14 CFR part 43. The focused inspection must include the items listed below. Remove all wing access panels to conduct the inspections. Do these inspections following the manufacturer's service information and any other appropriate guidance, such as FAA Advisory Circular (AC) 43.13-1B Acceptable Methods, Techniques, and Practices—Aircraft Inspection and Repair. AC 43.13-1B can be found at<E T="03">http://rgl.faa.gov/.</E>
            </P>
            <P>Focused inspection items to look for:</P>
            <P>(1) Wrinkles in upper wing skins, from the outboard edge on the fuel tank access covers (WSTA 150 or 177) to the WSTA 222 (See View B, Figure 3).</P>
            <P>(2) Wrinkles in the upper wing skins from WSTA 55 to 66, adjacent to the booms (See View E, Figure 6).</P>
            <P>(3) Cracking of the upper wing skins. Pay particular attention to any wrinkles, the radius between stiffeners at WSTA 150 (under fuel tank covers), and unreinforced access holes (See View B, Figure 3).</P>
            <P>(4) Working (smoking) rivets outboard of the wing tank access covers.</P>
            <P>(5) Fasteners with less than two diameters edge distance.</P>
            <P>(6) Fasteners with less than four diameters center to center spacing.</P>
            <P>(7) Looseness of attachments of the tip extension to the wing and wing tip to wing extension when pushing up and down on the tip.</P>
            <P>(8) Any signs of distress along both front and rear spars, particularly in the area around WSTA 177.</P>
            <P>(9) Inspect under any repairs to the upper skins, particularly in the area just outboard of the fuel tank access covers as these may be covering up existing damage.</P>
            <P>(10) Inter-rivet buckling of the stringers attached to the upper surface skin, outboard of the fuel tank access covers (See View F, Figure 7).</P>
            <P>(11) Inspect rib at WSTA 222 for damage. Trimming of the rib may have been done to allow installation of fuel lines (See View A, Figure 2). Repair in accordance with AC 43.13-1B, Chapter 4, paragraph 4-58(g) and Figure 4-14, or by using another FAA-approved method that restores equivalent strength of the wing rib.</P>
            <HD SOURCE="HD1">Appendix 1 to AD 2011-15-11</HD>
            <HD SOURCE="HD1">General and Focused Inspection Procedures (Continued)</HD>
            <P>(12) Inspect and identify screws, installed in tapped (threaded) holes in metal substructure, used to attach wing tips, stall fences, fuel and electrical components, and access doors. For tapped holes, remove fastener and open up the diameter to provide a smooth bore hole, for the smallest oversize fastener, using close tolerance holes noted in AC 43.13-1B, paragraph 7-39 or other FAA-approved scheme. Maintain minimum 2 x fastener diameter edge distance and 4 x fastener diameter center to center spacing. Select and install new, equivalent strength or stronger, fasteners with nuts/collars in accordance with AC 43.13-1B, Chapter 7 and AC 43.13-2B, paragraph 108 or other FAA-approved repair. New fasteners must not have threads in bearing against the sides of the holes.</P>
            <P>(13) Inspect wing skins for unreinforced cutouts. (See View C, Figure 4).</P>
            <P>(14) Inspect the upper spar cap horizontal flanges for open holes (See View D,  Figure 5).</P>
            <BILCOD>BILLING CODE 4910-13-P</BILCOD>
            <GPH DEEP="591" SPAN="3">
              <PRTPAGE P="45661"/>
              <GID>ER01AU11.036</GID>
            </GPH>
            <GPH DEEP="465" SPAN="3">
              <PRTPAGE P="45662"/>
              <GID>ER01AU11.037</GID>
            </GPH>
            <GPH DEEP="407" SPAN="3">
              <PRTPAGE P="45663"/>
              <GID>ER01AU11.038</GID>
            </GPH>
            <GPH DEEP="302" SPAN="3">
              <PRTPAGE P="45664"/>
              <GID>ER01AU11.039</GID>
            </GPH>
            <GPH DEEP="464" SPAN="3">
              <PRTPAGE P="45665"/>
              <GID>ER01AU11.040</GID>
            </GPH>
            <GPH DEEP="387" SPAN="3">
              <PRTPAGE P="45666"/>
              <GID>ER01AU11.041</GID>
            </GPH>
            <HD SOURCE="HD1">Appendix 2 to AD 2011-15-11</HD>
            <P>Airworthiness Limitations for the Flint Aero, Inc. Airplane Flight Manual Supplement.</P>
            <P>“MAINTAIN AT LEAST 12 GAL OF FUEL IN EACH WING TIP FUEL TANK FOR AIRPLANE WEIGHTS AT OR ABOVE 4,330 LBS.”</P>
          </EXTRACT>
        </REGTEXT>
        <SIG>
          <DATED>Issued in Kansas City, Missouri, on July 14, 2011.</DATED>
          <NAME>Earl Lawrence,</NAME>
          <TITLE>Manager, Small Airplane Directorate, Aircraft Certification Service.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-18242 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4910-13-C</BILCOD>
    </RULE>
    <RULE>
      <PREAMB>
        <AGENCY TYPE="N">COMMODITY FUTURES TRADING COMMISSION</AGENCY>
        <CFR>17 CFR Part 40</CFR>
        <RIN>RIN 3038-AD07</RIN>
        <SUBJECT>Provisions Common to Registered Entities; Correction</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Commodity Futures Trading Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Final rule; Correction.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>This document corrects incorrect text published in the<E T="04">Federal Register</E>of July 27, 2011, regarding Provisions Common to Registered Entities.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>
            <E T="03">Effective date:</E>September 26, 2011.</P>
        </EFFDATE>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Bella Rozenberg, Assistant Deputy Director, Division of Market Oversight (“DMO”), at 202-418-5119 or<E T="03">brozenberg@cftc.gov</E>, Riva Spear Adriance, Associate Director, DMO at 202-418-5494 or<E T="03">radriance@cftc.gov</E>, and Joseph R. Cisewski, Attorney Advisor, DMO at 202-418-5718 or<E T="03">jcisewski@cftc.gov</E>, in each case, at the Commodity Futures Trading Commission, Three Lafayette Centre, 1155 21st Street, NW., Washington, DC 20581.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>In FR Doc. 2011-18661 appearing on page 44776 in the<E T="04">Federal Register</E>issue of Wednesday, July 27, 2011, the following correction is made:</P>
        <SECTION>
          <SECTNO>§ 40.6</SECTNO>
          <SUBJECT>[Corrected]</SUBJECT>
          <P>On page 44794, in the right column, in § 40.6(a), the text “other than a rule delisting or withdrawing the certification of a product,” is corrected to read, “other than a rule delisting or withdrawing the certification of a product with no open interest and submitted in compliance with §§ 40.6(a)(1)-(2) and § 40.6(a)(7),”.</P>
        </SECTION>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>David A. Stawick,</NAME>
          <TITLE>Secretary of the Commission.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19385 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE P</BILCOD>
    </RULE>
    <RULE>
      <PREAMB>
        <PRTPAGE P="45667"/>
        <AGENCY TYPE="N">DEPARTMENT OF LABOR</AGENCY>
        <SUBAGY>Employment and Training Administration</SUBAGY>
        <CFR>20 CFR Part 655</CFR>
        <RIN>RIN 1205-AB61</RIN>
        <SUBJECT>Wage Methodology for the Temporary Non-Agricultural Employment H-2B Program; Amendment of Effective Date</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Employment and Training Administration, Labor.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Final rule.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Department of Labor (we or us) is amending the effective date of Wage Methodology for the Temporary Non-agricultural Employment H-2B Program; Final Rule, 76 FR 3452, Jan. 19, 2011 (the Wage Rule). The Wage Rule revised the methodology by which we calculate the prevailing wages to be paid to H-2B workers and United States (U.S.) workers recruited in connection with a temporary labor certification for use in petitioning the Department of Homeland Security to employ a nonimmigrant worker in H-2B status. The effective date of the Wage Rule was set at January 1, 2012. This Final Rule revises the effective date of the Wage Rule to 60 days after the publication date of this Final Rule.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>

          <P>The effective date of the final regulations published in the<E T="04">Federal Register</E>on January 19, 2011, at 76 FR 3452, is September 30, 2011.</P>
        </EFFDATE>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>William L. Carlson, Ph.D., Administrator, Office of Foreign Labor Certification, ETA, U.S. Department of Labor, 200 Constitution Avenue, NW., Room C-4312, Washington, DC 20210; Telephone (202) 693-3010 (this is not a toll-free number). Individuals with hearing or speech impairments may access the telephone number above via TTY by calling the toll-free Federal Information Relay Service at 1-877-889-5627 (TTY/TDD).</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">I. Amendment of Effective Date of the Wage Rule</HD>
        <HD SOURCE="HD2">A. The Prevailing Wage Final Rule</HD>
        <P>We published the Wage Rule on January 19, 2011. Under the Wage Rule, the prevailing wage for the H-2B program is based on the highest of the following: The wage rate established under an agreed-upon collective bargaining agreement; the wage rate established under the Davis-Bacon Act (DBA) or the McNamara O'Hara Service Contract Act (SCA) for that occupation in the area of intended employment; or the arithmetic mean wage rate established by the Occupational Employment Statistics (OES) wage survey for that occupation in the area of intended employment. The Wage Rule also permits the use of private wage surveys in very limited circumstances. Lastly, the Wage Rule required the new wage methodology to apply to all work performed on or after January 1, 2012. We selected the January 1, 2012 effective date because “many employers already may have planned for their labor needs and operations for this year in reliance on the existing prevailing wage methodology. In order to provide employers with sufficient time to plan for their labor needs for the next year and to minimize the disruption to their operations, the Department is delaying implementation of this Final Rule so that the prevailing wage methodology set forth in this Rule applies only to wages paid for work performed on or after January 1, 2012.” 76 FR 3462, Jan. 19, 2011.</P>
        <P>On January 24, 2011, the plaintiffs in<E T="03">CATA</E>v.<E T="03">Solis,</E>Civil No. 2:09-cv-240-LP (E.D. Pa.), filed a motion for an order to require the Department to comply with the court's August 30, 2010 order,<SU>1</SU>

          <FTREF/>arguing that the Wage Rule violated the Administrative Procedure Act (APA) because “it did not provide notice to Plaintiffs and the public that DOL was considering delaying implementation of the new regulation and because DOL's reason for delaying implementation of the new regulation is arbitrary.”<E T="03">CATA</E>v.<E T="03">Solis,</E>Dkt. No. 103-1, Plaintiff's Motion for an Order Enforcing the Judgment at 2 (Jan. 24, 2011). On June 16, 2011, the court issued a ruling that invalidated the January 1, 2012 effective date of the Wage Rule and ordered us to announce a new effective date for the rule within 45 days from June 16. The basis for the court's ruling was twofold: (1) That the almost one-year delay in the effective date was not a “logical outgrowth” of the proposed rule, and therefore violated the APA; and (2) that the Department violated the INA in considering hardship to employers when deciding to delay the effective date. The court held that “it is apparent that in this case the notice of proposed rulemaking was deficient.”<E T="03">CATA</E>v.<E T="03">Solis,</E>Dkt. No. 119, 2011 WL 2414555 at *4. The court noted that the NPRM said nothing about a delayed effective date, and accordingly “the public would * * * be justified in assuming that any delay in the effective date would mirror the minimal delays associated with the issuance of similar wage regulations over the past several decades.”<E T="03">Id.</E>In finding a violation of the INA, the court relied extensively on the 1983 district court decision in<E T="03">NAACP</E>v.<E T="03">Donovan,</E>566 F. Supp. 1202 (D.D.C. 1983), which held that the Department could not phase in a wage regime based upon a desire to alleviate hardship on small businesses, because “ `[in] administering the labor certification program, DOL is charged with protection of workers.' ”<E T="03">CATA</E>v.<E T="03">Solis,</E>Dkt. No. 119, 2011 WL 2414555 at *4 (citing<E T="03">NAACP</E>v.<E T="03">Donovan,</E>566 F. Supp. at 1206).</P>
        <FTNT>
          <P>

            <SU>1</SU>On August 30, 2010, the U.S. District Court for the Eastern District of Pennsylvania in<E T="03">CATA v.</E>
            <E T="03">Solis,</E>2010 WL 3431761 (E.D. Pa.) ruled that the Department had violated the Administrative Procedure Act by failing to adequately explain its reasoning for using skill levels as part of the H-2B prevailing wage determinations, and failing to consider comments relating to the choice of appropriate data sets in deciding to rely on OES data rather than SCA and DBA in setting the prevailing wage rates. The court ordered the Department to “promulgate new rules concerning the calculation of the prevailing wage rate in the H-2B program that are in compliance with the Administrative Procedure Act no later than 120 days from the date of this order.” The order was later amended to provide additional time, until January 18, 2011, to promulgate a final rule.</P>
        </FTNT>
        <P>In response to the court's order, we issued a Notice of Proposed Rulemaking (NPRM) on June 28, 2011, which proposed that the Wage Rule take effect 60 days from the date of publication of a final rule resulting from this rulemaking. Because we anticipated the date of publication of the final rule to be on or about August 1, 2011, we said in the NPRM that the effective date of the Wage Rule would be on or about October 1, 2011. The Wage Rule would be effective for wages paid to H-2B workers and U.S. workers recruited in connection with an H-2B labor certification for all work performed on or after the new effective date.</P>
        <HD SOURCE="HD1">II. Discussion of Comments</HD>
        <HD SOURCE="HD2">A. Overview of Comments Received</HD>
        <P>We received 59 comments in response to the NPRM. Forty-two of the comments were completely unique, one was a duplicate, and the remainder were a form letter or based on a form letter. Commenters represented individual employers, worker advocacy groups, business associations, agents, the Chief Counsel for the Office of Advocacy of the Small Business Administration (Chief Counsel for Advocacy, SBA), Members of Congress, and various interested members of the public. The comments are discussed in greater detail below.</P>

        <P>Some of the comments were outside the scope of the proposed rule. The NPRM proposed a new effective date for the Wage Rule and specifically provided that any comments relating to the merits of the Wage Rule would be deemed out<PRTPAGE P="45668"/>of scope and would not be considered. Furthermore, the NPRM stated that under the court's order, we cannot consider specific examples of employer hardship to delay the effective date of a new wage rule. See<E T="03">CATA</E>v.<E T="03">Solis,</E>Dkt. No. 119, 2011 WL 2414555 at *4. Many comments went well beyond the scope of amending the effective date of the Wage Rule. Among the comments that we deemed out of scope were comments that challenged the merits of the Wage Rule and asserted that the Wage Rule and/or the proposed effective date of the Wage Rule would result in employer hardship, including inadequate time to plan or prepare for the change in wages, cancellation of contracts, lower profits, and financial insolvency. Because the district court was clear that our consideration of hardship to employers when setting the January 1, 2012 effective date was contrary to our responsibilities under the INA to protect the wages and working conditions of U.S. workers, we cannot consider these comments in this rulemaking. We also did not consider comments submitted before the comment period began or after the comment period closed.</P>
        <HD SOURCE="HD2">B. Adequacy of Comment Period</HD>

        <P>Several commenters did not believe that the ten day comment period provided an adequate amount of time for the public to comment on the NPRM, and several specifically requested extending the deadline for submission of comments, including up to 120 days. An agency is only required to provide a “meaningful opportunity” for comments on a proposed rule.<E T="03">See Grand Canyon Air Tour Coalition</E>v.<E T="03">FAA,</E>154 F.3d 455 (D.C. Cir. 1998). In<E T="03">Florida Power &amp; Light Company</E>v.<E T="03">NRC,</E>846 F.2d 765 (D.C. Cir 1988), the court used a reasonableness standard to uphold the agency's 15 day comment period. Although the agency in that case was attempting to meet a Congressional deadline, we are under an analogous constraint here given the judicial requirement of the<E T="03">CATA</E>order that a new effective date be announced within 45 days. As was true in<E T="03">Florida Power,</E>despite the truncated comment period, we received more than 40 substantive comments addressing every aspect of the issue. We issued an NPRM that simply proposed to move up the effective date of the Wage Rule by 3 months. Ten days is ample time for a member of the public to review the NPRM, which only consisted of 4 pages in the<E T="04">Federal Register,</E>and formulate a meaningful response. The shorter timeframe is warranted here, given the limited scope of this rulemaking and the court's June 16, 2011 order that we announce a new effective date within 45 days. Because we had to draft an NPRM, review comments, draft a final rule and submit both the NPRM and the Final Rule for Executive Order 12866 review within the 45-day period ordered by the court, the ten-day comment period is the most generous period that we could provide.</P>
        <HD SOURCE="HD2">C. Authority of CATA Decision</HD>

        <P>An employer expressed its disagreement with the June 16, 2011<E T="03">CATA</E>decision, stating that the Department's consideration of employer hardship was appropriate and that the court misunderstood the procedural requirements of the H-2B program. An employer association chided the Department for its “wholesale endorsement of the decision,” arguing that the court's holding that the Department is not permitted to consider employer hardship was “meaningless dicta,” that the<E T="03">CATA</E>case was not a legitimate case or controversy but more akin to an “advisory opinion” because both the plaintiffs' and our interests were aligned, and that the INA does not make any reference good or bad to employer hardship. While we understand that there may not be agreement with the merits of the June 16, 2011<E T="03">CATA</E>decision, it is binding on the Department and we must act in accordance with it. As to the commenter's claim that the plaintiffs' and our interests are aligned in the<E T="03">CATA</E>litigation, we have vigorously defended our positions at all stages of the<E T="03">CATA</E>case, including opposing the plaintiffs' January 24, 2011 motion.<E T="03">See CATA</E>v.<E T="03">Solis,</E>Dkt. No.105, Defendants' Opposition to Plaintiffs' Motion for Order Enforcing the Judgment.</P>
        <HD SOURCE="HD2">D. Harm to H-2B and U.S. Workers</HD>
        <P>Two employer associations asserted that employers and workers stand and fall together—specifically, that there is no distinction between the benefit of employers and the benefit of workers and that a negative impact on the employer has an immediate negative effect on the workers. In an effort to illustrate that point, a number of employers and employer associations stated that the accelerated effective date would result in having to lay off their H-2B workers because they simply would not be able to afford the increase in wages based on the Wage Rule's new wage methodology. Additionally, some employers commented that as a result of their H-2B worker layoffs, they would be forced to lay off their U.S. workers who are in supervisory, support, and administrative positions.</P>

        <P>Our responsibilities in the H-2B labor certification program first and foremost are to ensure that U.S. workers are given priority for temporary non-agricultural job opportunities and to protect U.S. workers' wages and working conditions from being adversely affected by the employment of foreign workers in such job opportunities.<E T="03">See</E>8 U.S.C. 1101(a)(15)(H)(ii)(b). Only when we certify that U.S. workers capable of performing the services or labor are not available and that the employment of the foreign worker(s) will not adversely affect the wages and working conditions of similarly employed U.S. workers (<E T="03">see</E>8 CFR 214.2(h)(6)) may an employer file an H-2B visa petition to bring in temporary foreign workers. The court was quite clear that “[d]elaying the implementation of the Wage Rule requires, by necessity, the continued payment of a lower, invalid wage to H-2B workers.”<E T="03">CATA</E>v.<E T="03">Solis,</E>Dkt. No. 119, 2011 WL 2414555 at *4. The payment of this lower, invalid wage clearly has an adverse effect on the wages of similarly employed U.S. workers.</P>

        <P>We do not dispute that the implementation of the Wage Rule, whether on the amended or original timeframe, regrettably may result in the layoffs of H-2B workers and possibly U.S. workers in positions that support those that are currently filled by H-2B workers. However, our role in the H-2B program, as further reinforced by the district court in<E T="03">CATA,</E>is to protect the wages and working conditions of similarly employed U.S. workers—a constituency that few, if any, of the commenters acknowledge—but who are the very group the labor certification program was designed to protect.</P>
        <HD SOURCE="HD2">E. Earlier Effective Date</HD>

        <P>Two worker advocacy organizations and a labor organization supported putting the Wage Rule into effect as quickly as possible. A worker advocacy organization specifically requested “the earliest administratively practical effective date” for the Wage Rule and that the effective date be no later than 30 days after the publication of the final rule resulting from this rulemaking—i.e., August 31, 2011. The commenter stated that it disagreed with our suggestion in the NPRM that the fact that the Congressional Review Act (CRA) applied to the Wage Rule provided any basis for delaying the Wage Rule another 60 days from the date of publication of the final rule resulting from this rulemaking. The commenter believes that we have the authority under the APA to set an immediate effective date for the Wage<PRTPAGE P="45669"/>Rule upon publication of the final rule resulting from this rulemaking. The commenter contends that we would have good cause for doing so, as more than six months have passed without any action from Congress to vacate the Wage Rule under the CRA, while “H-2B workers continue to be paid unlawfully low wages.” While the commenter agreed that the Department's “administrative needs in implementation of [the Wage Rule] is an appropriate factor to consider in establishing the effective date,” the commenter believes that:</P>
        
        <EXTRACT>

          <P>It would be administratively practicable for DOL to immediately issue bulk interim prevailing wage determinations by electronic mail notifying all applicants for H-2B prevailing wage determinations submitted since October 1, 2010 that if they employed any H-2B workers after August 1, 2011, they would be immediately required to pay the FLC Data Center Level 3 wage based on 2011 OES data for the SOC (ONET/OES) code on their initial prevailing wage determination for their geographic area until such time as DOL determined if there were higher Service Contract Act (SCA) or Davis Bacon Act (DBA) wage rates for their H-2B workers and other workers in corresponding employment. Employers could be directed to<E T="03">http://www.flcdatacenter.com/OESWizardStart.aspx,</E>the Online Wage Library—FLC Wage Search Wizard, to mathematically calculate the appropriate prevailing wage rate pending an individualized further notice from DOL. Employers for whom SCA or DBA wages might be appropriate could be notified of procedures for submitting further information for determining those wage rates.</P>
        </EXTRACT>
        
        <P>The same commenter also stated that if we have an internal computerized system for tracking H-2B certification applications and decisions, identifying employers with certifications for periods of employment on or after August 1, 2011 should be relatively straightforward. Additionally, the commenter raised the possibility of whether the existing computerized data for the H-2B prevailing wage determinations could be used to automatically recompute new prevailing wage rates at the July 2011 OES Level 3 wage rates, which would relieve employers from having to re-calculate the new wage rates themselves. Lastly, the commenter stated that if we already have a cross reference by SOC (ONET/OES) codes for employment involving potential DBA or SCA wage rates, “that possibility could be specifically flagged only for those codes and a questionnaire seeking additional information in relationship thereto could be generated.”</P>
        
        <P>We still consider the proposed 60 day delayed effective date to be necessary and appropriate, despite the commenter's proposal of various operational measures to implement the Wage Rule in a more expeditious manner. We do not dispute that the 60 day delayed effective date requirement of the CRA applied only to the publication of the Wage Rule in January 2011 and that we are not legally required under the CRA to delay by 60 days from the publication of this rulemaking the effective date of the rule. However, while we agree with the commenter that the Wage Rule should have the “earliest possible administratively practical effective date,” an effective date of 30 days after the publication of the final rule does not provide us with sufficient operational time to issue new prevailing wage determinations (PWDs) under the methodology prescribed by the Wage Rule.</P>
        <P>Because the new wage methodology under the Wage Rule would take effect for all wages paid to H-2B workers and U.S. workers recruited in connection with an H-2B labor certification for all work performed on or after the new effective date, we will have to issue PWDs using the Wage Rule methodology not only for all applications received after the new effective date but also for existing certifications for which work is to be performed on or after the new effective date. What this means is that our National Prevailing Wage Center (NPWC) will have to issue approximately 4,000 supplemental prevailing wage determinations.<SU>2</SU>
          <FTREF/>This is a manual process, as there is no way to automatically link the PWD requests that were submitted and processed in the iCert prevailing wage system with the actual H-2B applications that were subsequently filed and approved for work that will be performed on or after the effective date. Many of these requests involve multiple locations, some including dozens of locations, each of which requires a separate determination.<SU>3</SU>
          <FTREF/>While the NPWC anticipates being able to issue all of these 4,000 supplemental wage determinations before October 1, to do so before August 31 is physically and operationally impossible.</P>
        <FTNT>
          <P>
            <SU>2</SU>It has not been possible to perform recalculations of the prevailing wage before July 1, as the wages in OES are updated on or about that date each year, and were not available before that date for use in the H-2B program.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>3</SU>Until we have reviewed all affected applications some of which are still in the process of adjudication we will not know the exact number of determinations that that the NPWC must issue.</P>
        </FTNT>

        <P>We appreciate the commenter's suggestions for streamlining the PWD process in order to implement the new Wage Rule in the most expeditious manner possible. However, it is imperative that we issue individual PWDs for each employer that has an H-2B labor certification for work being performed on or after the new effective date to ensure the integrity and enforceability of the new prevailing wage. The commenter's suggestion that employers calculate their own prevailing wage would present us with substantial challenges in both implementation and enforcement. NPWC staff provide a level of consistency and accuracy that would not be replicable if responsibility for PWDs were devolved to hundreds, if not thousands, of individual H-2B employers and their various representatives. In the simplest scenario proposed by the commenter, an employer with limited or no previous knowledge of the prevailing wage determination process would have to follow our instructions to use an unfamiliar set of online tools to determine their correct prevailing wage. In addition to possible errors caused by lack of familiarity with the system, further complications could arise for employers with certified occupations that are a blend of two unique occupations or with multiple areas of intended employment. There is potential for employer error at every step that could result in the unintentional payment of an incorrect wage rate to thousands of H-2B workers. Moreover, our ability to enforce an employer's failure to pay the correct wage would be compromised if we could not definitively show that the employer knew what the proper wage was (<E T="03">see</E>20 CFR 655.65(e)), which would be quite difficult, given the practical challenges just discussed.</P>

        <P>Moreover, obtaining the appropriate SCA and DBA wages for the job opportunity is not as simple a process as obtaining the OES wage, since the SCA and DBA wages are determined in a completely different manner and updated on a completely separate timeframe. We make SCA and DBA wage rates available to Federal contracting officers and the public through the<E T="03">http://www.wdol.gov</E>Web site. While it is easy to use this Web site to locate wage determinations, selecting the appropriate occupations or job classification from the wage determination presents additional opportunities for employer error. Occupations under the SCA are determined using the Dictionary of Occupational Titles (DOT). Employers would be required to review the<PRTPAGE P="45670"/>definitions in the DOT and determine the appropriate SCA occupation for their specific job opportunity. For example, an employer seeking to hire H-2B workers for its restaurant could be presented with SCA wage rates for a “Cook I,” “Cook II,” and “Food Service Worker” on the same wage determination. The employer would be required to analyze the DOT to determine the appropriate occupation.</P>

        <P>A similar challenge exists with DBA wage rates. DBA wage rates reflect the area practice concept which makes it difficult for someone inexperienced with those wage rates to determine which rate applies. For example, in some areas of the country, a rate is established for “welders,” and in other areas welders receive the rate prescribed for the craft to which performance of the welding is an incidental operation, depending on whether it is the practice in the area to treat welding as a separate occupation. Therefore, we do not believe that employers could easily select the correct prevailing wage rate for the job opportunity without this specialized knowledge. The commenter implicitly acknowledges this complexity, as it offers no proposal for obtaining those wages in an expedited manner; instead, it proposes that employers be required to immediately begin paying the OES Level 3 wage and that the NPWC would determine the applicability of the SCA or DBA wage at a later date. This would serve further to undermine our ability to enforce the payment of the prevailing wage as of the new effective date if either the SCA or DBA wage eventually were found to be the highest wage (<E T="03">see</E>76 FR 3484 (Jan. 19, 2011) (to be codified at 20 CFR 655.10(b)(2)), because the employer may not have been aware at the time that the work was performed after the new effective date that either the SCA or DBA wage was the prevailing wage.</P>
        <P>We do not think it appropriate to issue “interim” wage determinations and then issue corrected wage determinations at a later date, possibly requiring employers to pay make-up pay at a later date, or for workers to have their pay adjusted downward. Sound program administration and basic fairness require us to provide employers with a prevailing wage determination on which they can rely in time for them to make any needed adjustments in their payroll systems and pay the correct new wages when they are due. Issuing prevailing wage determinations as quickly as possible but in time for employers to implement them on the effective date avoids confusion for both employers and workers, and also reduces the necessity of enforcement actions and the possibility of litigation.</P>
        <HD SOURCE="HD2">F. Later Effective Date</HD>
        <P>Two employer associations asserted that the court in<E T="03">CATA</E>did not mandate an earlier effective date but merely required that the effective date be subject to notice and comment. One employer suggested that any new wage changes apply to H-2B visas released after the new effective date. We do not believe, based on the<E T="03">CATA</E>decision and on our mandate to ensure that the employment of foreign workers in temporary non-agricultural positions does not adversely affect similarly employed U.S. workers, that we can further delay implementing the Wage Rule beyond the time that it takes to issue and implement the new prevailing wage determinations, as described above. While the court did not order us to issue any particular effective date, its decision made it clear that the court was concerned with the “critical importance of avoiding the depression of wages paid to U.S. and to H-2B workers, and * * * the already protracted delay in implementing a valid prevailing wage regime.”<E T="03">CATA</E>v.<E T="03">Solis,</E>Dkt. No. 119<E T="03">,</E>2011 WL 2414555 at *5. Applying the Wage Rule's prevailing wage methodology only to H-2B visas issued after the new effective date would result in what the court in<E T="03">CATA</E>specifically sought to avoid—prolonging the payment of a lower, invalidated wage to H-2B workers. We believe that, under the court's decision, we must do all we can that is administratively and operationally feasible to minimize the period in which these payments continue.</P>
        <HD SOURCE="HD2">G. Impact of Changing the Prevailing Wage for Existing Certifications</HD>
        <P>Several commenters objected to the application of the Wage Rule's prevailing wage methodology to existing certifications. An employer association asserted that we would be acting in conflict with our regulations providing that the prevailing wage would be valid throughout the intended of period employment. Similarly, another employer association claimed that allowing the new prevailing wage methodology to apply to existing certifications would violate the attestation on older versions of the ETA Form 9142, Appendix B.1 that “the offered wage equals or exceeds the highest of the prevailing wage, the applicable, Federal, State, or local minimum wage, and the employer will pay the offered wage during the entire period of the approved labor certification.”</P>
        <P>In the fall of 2010, the<E T="03">CATA</E>plaintiffs moved for additional relief including seeking an order requiring the Department to condition future H-2B certifications on employer agreement to pay the wage rate under the Wage Rule once it became effective. We opposed this order, arguing that the regulation at 20 CFR 655.10(d) meant that once an employer had received a prevailing wage determination in any year, it is entitled to use that prevailing wage throughout the duration of its H-2B certification. In a November 24, 2010 ruling, the court rejected that argument:</P>
        
        <EXTRACT>
          <P>Nothing in § 655.10(d), nor any related regulation, prevents the DOL from devising interim measures to reduce the impact of the deficient methodology. Thus an employer must pay a valid wage for the duration of employment, but it does not follow that an employer must continue paying that wage after it has been deemed to be the product of an invalid regulation.</P>
        </EXTRACT>
        
        <FP>
          <E T="03">CATA</E>v.<E T="03">Solis,</E>Dkt. No. 97, 2010 WL 4823236 at *2 (footnote omitted). Although the court did not order us to take any specific action, we reconsidered our position in light of the court's ruling that the current wage methodology is invalid and that we have the authority to require employers to pay wages other than those issued in a prevailing wage determination. Accordingly, in these special circumstances, we decided that it is not appropriate to allow wage determinations made under the invalidated current methodology to continue to govern the payment of wages beyond the effective date of the Wage Rule.</FP>
        
        <P>While these commenters may not agree with the district court's rationale, as discussed above, the decision is nevertheless binding. As to the commenter's concern that an employer would be in violation of the attestation on the previous version of the ETA Form 9142, Appendix B.1, we do not consider the attestation to be inconsistent with an employer's payment of a higher wage rate once the Wage Rule takes effect. The attestation only requires that the offered wage equal or exceed the highest of the prevailing wage or applicable minimum wage and that the employer pay the offered wage during the time period the work is performed. If the prevailing wage increases as a result of the Wage Rule taking effect, then the employer's offered wage would need to increase in accordance with that change.</P>

        <P>Additionally, a commenter stated that because employers have a protected property interest in the validity of the prevailing wage throughout the period of intended employment, we would be<PRTPAGE P="45671"/>denying the employer due process to take away that right without notice and an opportunity for an individual hearing. The commenter's concerns about due process are not warranted. As a threshold matter, due process applies only to individualized determinations, and not to legislative rulemaking.<E T="03">See United States</E>v.<E T="03">Florida East Coast Railway,</E>410 U.S. 224, 244-46 (1973). We are not required to provide a hearing before taking an action that affects the property interest of a class of individuals or regulated entities.<E T="03">See McMurtray</E>v.<E T="03">Holladay,</E>11 F.3d 499, 504 (5th Cir. 1993). In any event, when employers operating under current certifications are notified of the new prevailing wage, the notice will provide them with appropriate appeal rights under section 655.11, so that they can challenge the correctness of their individualized prevailing wage determination.</P>
        <P>Another employer association claimed that because an employer would have advertised and tested the labor market at a wage rate that is different than the new prevailing wage under the Wage Rule, the employer could be accused of applying a wage that is higher than the wage that was advertised to domestic workers, which could result in a revocation of the employers' petition by DHS. The commenter relies on what it deems to be the Department of State's interpretation that an employer may not pay above the prevailing wage that was advertised at the time the H-2B job was advertised per regulation. Along the same lines, one commenter called for the Department to provide extra time to re-apply to USCIS for continued certification under the new prevailing wage, and another commenter stated that any new changes to the wage rates must not require employers to complete the recruitment phase or obtain a new foreign labor certification once these steps have already been completed.</P>
        <P>The Department of State and USCIS, each of which play a role in the H-2B process, are aware of the unique circumstances of this supplemental wage determination process as outlined in the Wage Rule and in this Final Rule. We contacted each agency about this issue. The Department of State advised us that it might not issue a visa in some circumstances where the visa has not yet been issued but the wage will be higher than stated on the petition. However, because this is a regulatory change mandated by an agency with the authority to do so—namely, the Department—this is not in itself a basis for petition revocation. USCIS advised that, while circumstances vary, they generally cannot deny or revoke a nonimmigrant visa petition for this reason. We will continue to advise both the Department of State and USCIS as the supplemental wage determinations are issued.</P>
        <HD SOURCE="HD1">III. Administrative Information</HD>
        <HD SOURCE="HD2">A. Executive Orders 12866 and 13563</HD>
        <P>Under Executive Order (E.O.) 12866 and E.O. 13563, we must determine whether a regulatory action is significant and therefore, subject to the requirements of the E.O.s and subject to review by the Office of Management and Budget (OMB). Section 3(f) of E.O. 12866 defines a “significant regulatory action” as an action that is likely to result in a rule that: (1) Has an annual effect on the economy of $100 million or more or adversely and materially affects a sector of the economy, productivity, competition, jobs, the environment, public health or safety, or State, local or Tribal governments or communities (also referred to as “economically significant”); (2) creates serious inconsistency or otherwise interferes with an action taken or planned by another agency; (3) materially alters the budgetary impacts of entitlement grants, user fees, or loan programs or the rights and obligations of recipients thereof; or (4) raises novel legal or policy issues arising out of legal mandates, the President's priorities, or the principles set forth in the E.O. Executive Orders 13563 and 12866 direct agencies to assess all costs and benefits of available regulatory alternatives and, if regulation is necessary, to select regulatory approaches that maximize net benefits (including potential economic, environmental, public health and safety effects, distributive impacts, and equity). Executive Order 13563 emphasizes the importance of quantifying both costs and benefits, of reducing costs, of harmonizing rules, and of promoting flexibility.</P>
        <P>We have determined that this Final Rule is not an economically significant regulatory action under sec. 3(f)(1) of E.O. 12866. We have, however, determined that this Final Rule is a significant regulatory action under sec. 3(f)(4) of the E.O. and, accordingly, OMB has reviewed this Final Rule.</P>
        <HD SOURCE="HD2">B. Regulatory Flexibility Act</HD>
        <P>The Regulatory Flexibility Act (RFA) at 5 U.S.C. 603 requires agencies to prepare a regulatory flexibility analysis to determine whether a regulation will have a significant economic impact on a substantial number of small entities. Section 605 of the RFA allows an agency to certify a rule in lieu of preparing an analysis if the regulation is not expected to have a significant economic impact on a substantial number of small entities. Further, under the Small Business Regulatory Enforcement Fairness Act of 1996, 5 U.S.C. 801 (SBREFA), an agency is required to produce a compliance guidance for small entities if the rule has a significant economic impact. The Assistant Secretary of ETA has notified the Chief Counsel for Advocacy, Small Business Administration (SBA), under the RFA at 5 U.S.C. 605(b), and certified that this rule will not have a significant economic impact on a substantial number of small entities.</P>
        <P>We received a comment from the Chief Counsel for Advocacy, SBA, in which the Chief Counsel contended that we did not adequately provide a factual basis for the RFA certification and that the certification did not take into consideration the economic impact that this unexpected change in the effective date of the Wage Rule will have on small businesses. The Chief Counsel for Advocacy, SBA strongly encouraged us to complete an Interim Regulatory Flexibility Analysis of the NPRM. Several associations also asserted that we failed to consider the impact of this rulemaking on small businesses.</P>
        <P>In particular, the Chief Counsel for Advocacy, SBA, claimed that we offered no data or other analysis in support of the factual basis used to support the certification as required by the RFA beyond the statement “[w]hile the change in the effective date of the Wage Rule that is being proposed in this NPRM may change the period in which the total cost burdens for small entities would occur, the Department believes that the amount of the total cost burdens themselves would not change.”<SU>4</SU>
          <FTREF/>An employer association stated that if the effective date moves to October 1, 2011, its average member's payroll would increase from $79,840 to $159,680 and that their “total cost of labor” would likely double or even triple these figures. Another employer association argued that if the period that the Wage Rule is in effect is increasing, the total cost burden would increase along with the extended period, as the difference in implementing the Wage Rule on October 1, 2011 as opposed to January 1, 2012 would be $1,872 per worker.</P>
        <FTNT>
          <P>
            <SU>4</SU>76 FR 37686, 37688-89 (June 28, 2011).</P>
        </FTNT>

        <P>We disagree with the Chief Counsel for Advocacy, SBA's assessment that we did not provide a factual basis for the certification. As we stated in the NPRM, we already established in the Wage Rule that we believed that the Wage Rule was<PRTPAGE P="45672"/>not likely to impact a substantial number of small entities, and we provided an extensive analysis in the Wage Rule to support this conclusion. See 76 FR 3452, 3473-3482 (Jan. 19, 2011). Changing the effective date of the Wage Rule does not change the total cost burden for small entities as calculated under the Wage Rule. The total cost burden for small entities under the Wage Rule accounted for the increase in wage costs as a result of the new wage methodology (e.g., a $4.83 increase in the weighted average hourly wage for H-2B workers (and similarly employed U.S. workers hired in response to the recruitment required as part of the H-2B application))<SU>5</SU>
          <FTREF/>and the cost of reading and reviewing the Wage Rule—neither of which accounted for or were impacted by the original January 1, 2012 effective date of the Wage Rule. While we found that the Wage Rule has a significant economic impact<SU>6</SU>
          <FTREF/>(contrary to a commenter's assertion that we did not make such a finding), we found that the Wage Rule did not impact a substantial number of small entities, as the small entities that have historically applied for H-2B workers represent relatively small proportions of all small businesses—i.e., less than 10% of the relevant universe of small entities in a given industry.<SU>7</SU>
          <FTREF/>The H-2B employers that the commenters cite are already captured by these numbers, as the determination of the number of small entities affected by the Wage Rule neither accounted for, nor was affected by, the original January 1, 2012 effective date of the Wage Rule. We do not dispute that as a result of the Wage Rule, employers may in the short term experience an increase in costs, but the increase in total costs of the H-2B program as a result of the Wage Rule during the first year of its implementation and annually thereafter would be the same, regardless of whether it goes into effect October 1, 2011 or January 1, 2012. Therefore, the RFA analysis in the Wage Rule continues to be an accurate analysis of the impact of the Wage Rule on small businesses and would remain unaffected by the change in the effective date of the Wage Rule.</P>
        <FTNT>
          <P>
            <SU>5</SU>76 FR 3452, 3475 (Jan. 19, 2011).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>6</SU>See<E T="03">id.</E>at 3476.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>7</SU>
            <E T="03">Id.</E>
          </P>
        </FTNT>

        <P>The Chief Counsel, Office of Advocacy, SBA, also stated that “[t]here is nothing cited in the Proposed Rule that negates the agency's previous concern noted in the Wage Rule about the impact of the wage modification on small businesses, other than a court order mandating a new effective date,” a sentiment that was echoed by a number of associations. However, the Chief Counsel is mistaken, as the NPRM clearly states that the need for the rulemaking arose from the<E T="03">CATA</E>litigation under which the court specifically found that we violated the INA in considering hardship to employers (regardless of size) when deciding to delay the effective date. We do not dispute the Chief Counsel's observations that “[s]mall businesses have made plans, commitments, and have expended money for the current year based on the January 1, 2012, effective date announced in the Wage Rule nearly six months ago” but, as we discussed in the Wage Rule's RFA analysis, the rule does not impact a significant number of small businesses. Moreover, the court in<E T="03">CATA</E>has explicitly prohibited us from considering these employer hardships when setting the effective date of the Wage Rule. Additionally, as we have explained above, we continue to rely on the total cost burden provided in the Wage Rule's RFA analysis, as it is not impacted by the change in the effective date of the Wage Rule.</P>
        <HD SOURCE="HD2">C. Unfunded Mandates Reform Act of 1995</HD>
        <P>Title II of the Unfunded Mandates Reform Act of 1995 (2 U.S.C. 1531) directs agencies to assess the effects of Federal regulatory actions on State, local, and tribal governments, and the private sector. The Final Rule has no Federal mandate, which is defined in 2 U.S.C. 658(6) to include either a “Federal intergovernmental mandate” or a “Federal private sector mandate.” A Federal mandate is any provision in a regulation that imposes an enforceable duty upon State, local, or tribal governments, or imposes a duty upon the private sector which is not voluntary.</P>
        <HD SOURCE="HD2">D. Small Business Regulatory Enforcement Fairness Act of 1996</HD>
        <P>We have determined that this rulemaking does not impose a significant impact on a substantial number of small entities under the RFA; therefore, we are not required to produce any compliance guides for small entities as mandated by the SBREFA. We have similarly concluded that this Final Rule is not a major rule requiring review by the Congress under the SBREFA because it will not likely result in: (1) An annual effect on the economy of $100 million or more; (2) a major increase in costs or prices for consumers, individual industries, Federal, State or local government agencies, or geographic regions; or (3) significant adverse effects on competition, employment, investment, productivity, innovation, or on the ability of U.S.-based enterprises to compete with foreign-based enterprises in domestic or export markets. We received two comments that suggested that the earlier effective date of the Wage Rule would exacerbate the already negative impact that higher wages resulting from the Wage Rule would have on competition, employment, and investment and, in particular, the crab meat processing industry, as cheaper foreign crabmeat will completely displace domestically produced crabmeat in local markets. Another employer echoed this concern for the manufacturing industry in general, stating that the change in effective date would result in job losses either because the company fails or moves its operations outside the U.S.</P>
        <P>The only data offered by one of the commenters in support of these statements is an undated study on Maryland's crabmeat processing industry.<SU>8</SU>
          <FTREF/>This study not only appears to challenge the underlying merits of the Wage Rule, which would make it out of scope for purposes of this rulemaking, but also is premised on the assumption that absolutely no U.S. workers would be willing to work in any positions formerly held by H-2B workers, thereby resulting in major job losses in Maryland's crabmeat processing industry and in the loss of related jobs affected by the crabmeat processing industry. Given that the increase in wages not only would ensure against adverse effect but may also have the effect of causing U.S. workers to become more interested in these jobs, the study's assumption that no U.S. workers would ever replace the H-2B workers is fundamentally flawed. Therefore, neither of these commenters makes a sufficient case that changing the effective date of the Wage Rule would result in significant adverse effects on competition, employment, investment, productivity, innovation, or on the ability of U.S.-based enterprises to compete with foreign-based enterprises in domestic or export markets.</P>
        <FTNT>
          <P>
            <SU>8</SU>Lipton, Douglas D. Analysis of Economic Impact of H-2B Worker Program on Maryland's Economy.</P>
        </FTNT>
        <HD SOURCE="HD2">E. Executive Order 13132—Federalism</HD>

        <P>We have reviewed this Final Rule in accordance with E.O. 13132 on federalism and have determined that it does not have federalism implications. The Final Rule does not have substantial direct effects on States, on the relationship between the States, or on the distribution of power and<PRTPAGE P="45673"/>responsibilities among the various levels of government as described by E.O. 13132. Therefore, we have determined that this Final Rule will not have a sufficient federalism implication to warrant the preparation of a summary impact statement.</P>
        <HD SOURCE="HD2">F. Executive Order 13175—Indian Tribal Governments</HD>
        <P>We reviewed this Final Rule under the terms of E.O. 13175 and determined it not to have tribal implications. The Final Rule does not have substantial direct effects on one or more Indian tribes, on the relationship between the Federal Government and Indian tribes, or on the distribution of power and responsibilities between the Federal Government and Indian tribes. As a result, no tribal summary impact statement has been prepared.</P>
        <HD SOURCE="HD2">G. Assessment of Federal Regulations and Policies on Families</HD>
        <P>Section 654 of the Treasury and General Government Appropriations Act, enacted as part of the Omnibus Consolidated and Emergency Supplemental Appropriations Act of 1999 (Pub. L. 105-277, 112 Stat. 2681) requires us to assess the impact of this Final Rule on family well-being. A rule that is determined to have a negative effect on families must be supported with an adequate rationale. We have assessed this Final Rule and determined that it will not have a negative effect on families.</P>
        <HD SOURCE="HD2">H. Executive Order 12630—Government Actions and Interference With Constitutionally Protected Property Rights</HD>
        <P>The Final Rule is not subject to E.O. 12630, Governmental Actions and Interference with Constitutionally Protected Property Rights, because it does not involve implementation of a policy with takings implications.</P>
        <HD SOURCE="HD2">I. Executive Order 12988—Civil Justice</HD>
        <P>The Final Rule has been drafted and reviewed in accordance with E.O. 12988, Civil Justice Reform, and will not unduly burden the Federal court system. The Department has developed the Final Rule to minimize litigation and provide a clear legal standard for affected conduct, and has reviewed the Final Rule carefully to eliminate drafting errors and ambiguities.</P>
        <HD SOURCE="HD2">J. Plain Language</HD>
        <P>We drafted this Final Rule in plain language.</P>
        <HD SOURCE="HD2">K. Paperwork Reduction Act</HD>
        <P>As part of our continuing effort to reduce paperwork and respondent burden, we conduct a preclearance consultation program to provide the general public and Federal agencies with an opportunity to comment on proposed and continuing collections of information in accordance with the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3506(c)(2)(A)). This process helps to ensure that the public understands the collection instructions; that respondents provide requested data in the desired format; that reporting burden (time and financial resources) is minimized; that collection instruments are clearly understood; and that we properly assess the impact of collection requirements on respondents.</P>
        <P>The PRA requires all Federal agencies to analyze proposed regulations for potential time burdens on the regulated community created by provisions within the proposed regulations that require the submission of information. These information collection (IC) requirements must be submitted to the OMB for approval. Persons are not required to respond to a collection of information unless it displays a currently valid OMB control number as required in 5 CFR 1320.11(l) or it is exempt from the PRA.</P>

        <P>The majority of the IC requirements for the current H-2B program are approved under OMB control number 1205-0466 (which includes ETA Form 9141 and ETA Form 9142). There are no burden adjustments that need to be made to the analysis. For an additional explanation of how we calculated the burden hours and related costs, the PRA package for information collection OMB control number 1205-0466 may be obtained at<E T="03">http://www.RegInfo.gov.</E>
        </P>
        <HD SOURCE="HD1">IV. Change of Effective Date of Wage Rule</HD>

        <P>In the final rule published January 19, 2011, 76 FR 3452, under the<E T="02">DATES</E>section, the effective date of the final rule is amended to read as follows:</P>
        <P>This final rule is effective September 30, 2011.</P>
        <SIG>
          <DATED>Signed in Washington, this 26th day of July 2011.</DATED>
          <NAME>Jane Oates,</NAME>
          <TITLE>Assistant Secretary, Employment and Training Administration.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19319 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4510-FP-P</BILCOD>
    </RULE>
    <RULE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF THE TREASURY</AGENCY>
        <SUBAGY>Internal Revenue Service</SUBAGY>
        <CFR>26 CFR Part 1</CFR>
        <DEPDOC>[TD 9534]</DEPDOC>
        <RIN>RIN 1545-BD81</RIN>
        <SUBJECT>Methods of Accounting Used by Corporations That Acquire the Assets of Other Corporations</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Internal Revenue Service (IRS), Treasury.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Final regulations.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>This document contains final regulations relating to the methods of accounting, including the inventory methods, to be used by corporations that acquire the assets of other corporations in certain corporate reorganizations and tax-free liquidations. These regulations clarify and simplify the rules regarding the accounting methods to be used following these reorganizations and liquidations.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>
            <E T="03">Effective date:</E>These regulations are effective on August 31, 2011.</P>
          <P>
            <E T="03">Applicability date:</E>For dates of applicability, see §§ 1.381(a)-1(e), 1.381(c)(4)-1(f), 1.381(c)(5)-1(f), and 1.446-1(e)(4)(iii).</P>
        </EFFDATE>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Cheryl Oseekey at (202) 622-4970 (not a toll-free number).</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">Background</HD>

        <P>This document contains amendments to 26 CFR part 1. On November 16, 2007, the IRS and the Treasury Department published a notice of proposed rulemaking (REG-151884-03) in the<E T="04">Federal Register</E>(72 FR 64545). This notice of proposed rulemaking, while continuing most of the provisions of the regulations originally issued under sections 381(c)(4) and 381(c)(5) of the Internal Revenue Code (Code) regarding the methods of accounting to be used by a corporation that acquires the assets of another corporation in a section 381(a) transaction, proposed to clarify and simplify those existing regulations. The IRS received no comments in response to the notice of proposed rulemaking. No public hearing was requested or held. The proposed regulations, as revised by this Treasury decision, are adopted as final regulations.</P>
        <HD SOURCE="HD1">Explanation of Provisions</HD>

        <P>The final regulations differ somewhat in organization and format from the notice of proposed rulemaking. These changes are intended to be editorial in<PRTPAGE P="45674"/>nature and are not intended to alter the substance and principles of the rules set forth in the notice of proposed rulemaking. The IRS and the Treasury Department made these changes to further advance the objective, as expressed in the preamble to the notice of proposed rulemaking, of reducing uncertainty and controversy by providing regulations under sections 381(c)(4) and 381(c)(5) that are clear, consistent, and administrable. For example, the final regulations under sections 381(c)(4) and 381(c)(5) have been drafted so that the regulations mirror each other to the greatest extent possible, thus highlighting the consistencies of the regulations' provisions. Similarly, many of the examples in the notice of proposed rulemaking have been revised in the final regulations to specify the substantive tax rule in the regulations that the examples illustrate. Additionally, new examples were added to the final regulations to provide further illustrations of the substantive tax rules in these regulations.</P>
        <P>The keystone of the final regulations for sections 381(c)(4) and 381(c)(5) continues to be whether the acquiring corporation operates the trades or businesses of the parties to a section 381(a) transaction as separate and distinct trades or businesses following the date of distribution or transfer. The final regulations continue to provide that when the acquiring corporation operates the trades or businesses of the parties as separate and distinct trades or businesses after the date of distribution or transfer, the acquiring corporation will use a carryover method. In contrast, when the acquiring corporation does not operate the trades or businesses of the parties as separate and distinct trades or businesses after the date of distribution or transfer, the acquiring corporation will use a principal method. These rules do not apply when a carryover method or principal method, as applicable, is not a permissible method, or when the acquiring corporation chooses not to use a carryover method or principal method. In those cases, the general rules under section 446(e) that govern methods of accounting apply.</P>
        <P>The final regulations modify the test for determining a principal method when the acquiring corporation does not operate the trades or businesses of the parties to the section 381(a) transaction as separate and distinct trades or businesses after the date of distribution or transfer. Under the final regulations, the determination of whether the distributor or transferor corporation is larger than the acquiring corporation is made by comparing certain attributes (that is, under section 381(c)(4) the adjusted bases of the assets and gross receipts, and under section 381(c)(5) the fair market value of the inventory) of only the trades or businesses that will be integrated after the date of distribution or transfer rather than comparing the attributes for the entire entity. The IRS and the Treasury Department believe that the attributes of a trade or business that will continue to operate as a separate and distinct trade or business after the date of distribution or transfer should not influence the determination of a principal method that will be used by trades or businesses that will be integrated after the date of distribution or transfer. The IRS and the Treasury Department also believe that applying the test at the trade or business level is consistent with § 1.446-1(d) because methods of accounting are generally determined at the trade or business level.</P>
        <P>The final regulations also provide rules on how an acquiring corporation identifies a principal method when an acquiring corporation or a distributor or transferor corporation operates more than one separate and distinct trade or business on the date of distribution or transfer, has more than one method of accounting used in the trades or businesses, and the acquiring corporation combines the trades or businesses after the date of distribution or transfer. While the IRS and the Treasury Department do not think these situations occur frequently, the final regulations are revised to provide certainty for an acquiring corporation and to obviate the need to obtain a ruling in these situations.</P>

        <P>The final regulations under sections 381(c)(4) and 381(c)(5) clarify the definition of “cut-off basis.” The final regulations provide that<E T="03">cut-off basis</E>generally means a manner in which a change in method of accounting is made without a section 481(a) adjustment and under which only the items arising after the beginning of the year of change (or, in the case of a change made to a principal method, only the items arising after the date of distribution or transfer) are accounted for under the new method of accounting. The definition of cut-off basis is expanded in the final regulations under section 381(c)(5) to clarify that a taxpayer that makes a change within the last-in, first-out (LIFO) inventory method from one LIFO method or sub-method to another LIFO method or sub-method does not recompute the cost of its beginning inventories for the year of change under the new LIFO inventory method when it implements the change on a cut-off basis.</P>
        <P>The final regulations under section 381(c)(5) also make certain organizational changes to § 1.381(c)(5)-1(e)(6) of the notice of proposed rulemaking with respect to the integration of inventories after a section 381(a) transaction. These changes do not change the substantive rules in the notice of proposed rulemaking but are intended to clarify that the rules apply whether the inventory method of either the acquiring corporation or the transferor or distributor corporation must be changed to a principal method. The IRS and the Treasury Department are considering issuing additional guidance that would clarify or modify the manner in which inventories must be combined and integrated in a section 381(a) transaction.</P>
        <P>Finally, the final regulations correct the discussion of section 472(d) that was in § 1.381(c)(5)-1(e)(6)(ii)(B) of the notice of proposed rulemaking. Section 1.381(c)(5)-1(e)(6)(ii)(B) of the notice of proposed rulemaking provided that the restoration to cost of any previous write-downs to market value shall be taken into account fully in the year that included the date of distribution or transfer. Consistent with the amendments to section 472(d), the final regulations provide that these restorations shall be taken into account by the acquiring corporation ratably in each of the three taxable years beginning with the taxable year that includes the date of the distribution or transfer.</P>
        <P>The IRS and the Treasury Department are aware that some practitioners were concerned that the notice of proposed rulemaking did not provide audit protection when an acquiring corporation uses a principal method after the date of distribution or transfer. For the reasons expressed in the preamble to the notice of proposed rulemaking, the final regulations continue to deny audit protection in these circumstances. Unlike changes in method of accounting under section 446(e) for which a taxpayer must disclose its use of a method of accounting, proper or improper, as part of the process for obtaining consent to make the change, changes to a principal method pursuant to these final regulations are made on the acquiring corporation's tax return with no disclosure on a Form 3115, “Application for Change in Accounting Method,” that a change in method of accounting occurred.</P>

        <P>The IRS and the Treasury Department are aware that some taxpayers desire to obtain audit protection for a required change to a principal method by filing a Form 3115. However, the IRS and the Treasury Department believe that, given<PRTPAGE P="45675"/>the need for efficient tax administration, filing a Form 3115 merely to obtain audit protection should not be allowed. Although audit protection is not provided for a change to a principal method required under these regulations, audit protection ordinarily is provided for any voluntary change in method of accounting for which a party to a section 381(a) transaction obtains consent under section 446(e) and the generally applicable administrative procedures.</P>
        <HD SOURCE="HD1">Special Analyses</HD>

        <P>It has been determined that this Treasury decision is not a significant regulatory action as defined in Executive Order 12866. Therefore, a regulatory assessment is not required. It is hereby certified that these regulations will not have a significant economic impact on a substantial number of small entities. Therefore, a regulatory flexibility analysis under the Regulatory Flexibility Act (5 U.S.C. chapter 6) is not required. This certification is based on the belief of the IRS and the Treasury Department that the corporate reorganizations and tax-free liquidations described in section 381(a) generally involve large entities. In addition, these final regulations reduce the burden on taxpayers by clarifying and simplifying the existing rules and make the procedures for requesting changes in methods of accounting relating to corporate reorganizations and tax-free liquidations described in section 381(a) consistent with the general rules for requesting changes in methods of accounting. Pursuant to section 7805(f), the notice of proposed rulemaking that preceded these final regulations was submitted to the Chief Counsel for Advocacy of the Small Business Administration for comment on its impact on small business. Consistent with 5 U.S.C. section 553(d), the regulations are effective 30 days after publication of this document in the<E T="04">Federal Register</E>.</P>
        <HD SOURCE="HD1">Drafting Information</HD>
        <P>The principal author of these final regulations is Cheryl Oseekey, Office of Associate Chief Counsel (Income Tax and Accounting). However, other personnel from the IRS and the Treasury Department participated in their development.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 26 CFR Part 1</HD>
          <P>Income taxes, Reporting and recordkeeping requirements.</P>
        </LSTSUB>
        <HD SOURCE="HD1">Adoption of Amendments to the Regulations</HD>
        <P>Accordingly, 26 CFR part 1 is amended as follows:</P>
        <REGTEXT PART="1" TITLE="26">
          <PART>
            <HD SOURCE="HED">PART 1—INCOME TAXES</HD>
          </PART>
          <AMDPAR>
            <E T="04">Paragraph 1.</E>The authority citation for part 1 continues to read in part as follows:</AMDPAR>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>26 U.S.C. 7805 * * *</P>
          </AUTH>
          <EXTRACT>
            <P>Section 1.381(c)(4)-1 also issued under 26 U.S.C. 381(c)(4). * * *</P>
            <P>Section 1.381(c)(5)-1 also issued under 26 U.S.C. 381(c)(5). * * *</P>
          </EXTRACT>
        </REGTEXT>
        <REGTEXT PART="1" TITLE="26">
          
          <AMDPAR>
            <E T="04">Par. 2.</E>In § 1.381(a)-1, paragraph (b)(1)(i) is revised and paragraph (e) is added to read as follows:</AMDPAR>
          <SECTION>
            <SECTNO>§ 1.381(a)-1</SECTNO>
            <SUBJECT>General rule relating to carryovers in certain corporate acquisitions.</SUBJECT>
            <STARS/>
            <P>(b)  * * *</P>
            <P>(1) * * * (i) The complete liquidation of a subsidiary corporation upon which no gain or loss is recognized in accordance with the provisions of section 332;</P>
            <STARS/>
            <P>(e)<E T="03">Effective/applicability date.</E>The rules of paragraph (b)(1)(i) of this section apply to corporate reorganizations and tax-free liquidations described in section 381(a) that occur on or after August 31, 2011.</P>
          </SECTION>
        </REGTEXT>
        <REGTEXT PART="1" TITLE="26">
          <AMDPAR>
            <E T="04">Par. 3.</E>Section 1.381(c)(4)-1 is revised to read as follows:</AMDPAR>
          <SECTION>
            <SECTNO>§ 1.381(c)(4)-1</SECTNO>
            <SUBJECT>Method of accounting.</SUBJECT>
            <P>(a)<E T="03">Introduction</E>—(1)<E T="03">Purpose.</E>This section provides guidance regarding the method of accounting or combination of methods (other than inventory and depreciation methods) an acquiring corporation must use following a distribution or transfer to which sections 381(a) and 381(c)(4) apply and how to implement any associated change in method of accounting. See § 1.381(c)(5)-1 for guidance regarding the inventory method an acquiring corporation must use following a distribution or transfer to which sections 381(a) and 381(c)(5) apply. See § 1.381(c)(6)-1 for guidance regarding the depreciation method an acquiring corporation must use following a distribution or transfer to which sections 381(a) and 381(c)(6) apply.</P>
            <P>(2)<E T="03">Carryover method requirement for separate and distinct trades or businesses.</E>In a transaction to which section 381(a) applies, if an acquiring corporation continues to operate a trade or business of the parties to the section 381(a) transaction as a separate and distinct trade or business after the date of distribution or transfer, the acquiring corporation must use a carryover method as defined in paragraph (b)(5) of this section for each continuing trade or business, unless either the carryover method is impermissible and must be changed under paragraph (a)(4) of this section or the acquiring corporation changes the carryover method in accordance with paragraph (a)(5) of this section. The carryover method requirement applies to the overall method of accounting (for example, an accrual method of accounting) and any special method of accounting (for example, the percentage of completion method of accounting described in section 460) as defined in paragraph (b)(2) of this section used by each trade or business after the date of distribution or transfer. The acquiring corporation need not secure the Commissioner's consent to continue a carryover method.</P>
            <P>(3)<E T="03">Principal method requirement for trades or businesses not operated as separate and distinct trades or businesses.</E>In a transaction to which section 381(a) applies, if an acquiring corporation does not operate the trades or businesses of the parties to the section 381(a) transaction as separate and distinct trades or businesses after the date of distribution or transfer, the acquiring corporation must use a principal method determined under paragraph (c) of this section, unless either the principal method is impermissible and must be changed under paragraph (a)(4) of this section or the acquiring corporation changes the principal method in accordance with paragraph (a)(5) of this section. The principal method requirement applies to the overall method of accounting (for example, the cash receipts and disbursements method of accounting) and any special method of accounting (for example, the installment method under section 453) as defined in paragraph (b)(2) of this section used by each integrated trade or business after the date of distribution or transfer. The acquiring corporation must change to a principal method in accordance with paragraph (d)(1) of this section for each integrated trade or business and need not secure the Commissioner's consent to use a principal method.</P>
            <P>(4)<E T="03">Carryover method or principal method not a permissible method.</E>If a carryover method or principal method is not a permissible method of accounting, the acquiring corporation must secure the Commissioner's consent to change to a permissible method of accounting as provided in paragraph (d)(2) of this section. If the acquiring corporation must use a single method of accounting for a particular item after the date of distribution or transfer regardless of the<PRTPAGE P="45676"/>number of separate and distinct trades or businesses operated on that date, the acquiring corporation must use the principal method for that item as determined under paragraph (c) of this section, unless either the principal method is impermissible and must be changed under this paragraph (a)(4) or the acquiring corporation changes the principal method in accordance with paragraph (a)(5) of this section.</P>
            <P>(5)<E T="03">Voluntary change.</E>Any party to a section 381(a) transaction may request permission under section 446(e) to change a method of accounting for the taxable year in which the transaction occurs or is expected to occur. For trades or businesses that will not operate as separate and distinct trades or businesses after the date of distribution or transfer, a change in method of accounting for the taxable year that includes that date will be granted only if the requested method is the method that the acquiring corporation must use after the date of distribution or transfer. The time and manner of obtaining the Commissioner's consent to change to a different method of accounting is described in paragraph (d)(2) of this section.</P>
            <P>(6)<E T="03">Examples.</E>The following examples illustrate the rules of this paragraph (a). Unless otherwise noted, the carryover method is a permissible method of accounting.</P>
            
            <EXAMPLE>
              <HD SOURCE="HED">Example<E T="01">(1)</E>.</HD>
              <P>
                <E T="03">Carryover method for separate and distinct trades or businesses after the date of distribution or transfer</E>—(i)<E T="03">Facts.</E>X Corporation operates an employment agency that uses the overall cash receipts and disbursements method of accounting. T Corporation operates an educational institution that uses an overall accrual method of accounting. X Corporation acquires the assets of T Corporation in a transaction to which section 381(a) applies. After the date of distribution or transfer, X Corporation operates the employment agency as a trade or business that is separate and distinct from the educational institution.</P>
              <P>(ii)<E T="03">Conclusion.</E>Because after the date of distribution or transfer X Corporation operates the employment agency as a separate and distinct trade or business, under paragraph (a)(2) of this section X Corporation must use the carryover method for each continuing trade or business, unless either the carryover method is impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the carryover method in accordance with paragraph (a)(5) of this section. As defined in paragraph (b)(5) of this section, the carryover method for the employment agency is the cash receipts and disbursements method of accounting and the carryover method for the educational institution is the accrual method of accounting used by T Corporation immediately prior to the date of distribution or transfer. There is no change in method of accounting, and X Corporation need not secure the Commissioner's consent to use either carryover method.</P>
            </EXAMPLE>
            <EXAMPLE>
              <HD SOURCE="HED">Example<E T="01">(2)</E>.</HD>
              <P>
                <E T="03">Carryover method for a special method of accounting</E>—(i)<E T="03">Facts.</E>X Corporation provides personal grooming consulting and T Corporation provides weight management consulting. Both X Corporation and T Corporation use the same overall accrual method of accounting. X Corporation has elected to use the recurring item exception under § 1.461-5. T Corporation does not use the recurring item exception. X Corporation acquires the assets of T Corporation in a transaction to which section 381(a) applies. After the date of distribution or transfer, X Corporation operates the personal grooming consulting business as a trade or business that is separate and distinct from the weight management consulting business.</P>
              <P>(ii)<E T="03">Conclusion.</E>Because after the date of distribution or transfer, X Corporation operates the personal grooming consulting business as a separate and distinct trade or business, under paragraph (a)(2) of this section X Corporation must use a carryover method for each continuing trade or business, unless either the carryover method is impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the carryover method in accordance with paragraph (a)(5) of this section. As defined in paragraph (b)(5) of this section, the carryover method for the overall method of accounting for each trade or business is the accrual method used immediately prior to the date of distribution or transfer. The carryover method for the special method of accounting for the personal grooming consulting business is the recurring item exception under § 1.461-5 while the carryover method for the weight management consulting business is not to use the recurring item exception under § 1.461-5. There is no change in method of accounting, and X Corporation need not secure the Commissioner's consent to use the carryover methods of accounting.</P>
            </EXAMPLE>
            <EXAMPLE>
              <HD SOURCE="HED">Example<E T="01">(3)</E>.</HD>
              <P>
                <E T="03">Carryover method for a special method of accounting not permissible</E>—(i)<E T="03">Facts.</E>X Corporation is an engineering firm that uses the overall cash receipts and disbursements method of accounting and has elected under section 171 to amortize bond premium with respect to its taxable bonds acquired at a premium. T Corporation is a manufacturer that uses an overall accrual method of accounting and has not made a section 171 election to amortize bond premium with respect to its taxable bonds acquired at a premium. X Corporation acquires the assets of T Corporation in a transaction to which section 381(a) applies. After the date of distribution or transfer, X Corporation operates the engineering firm as a trade or business that is separate and distinct from the manufacturing business.</P>
              <P>(ii)<E T="03">Conclusion.</E>Because after the date of distribution or transfer X Corporation operates the engineering firm as a separate and distinct trade or business, under paragraph (a)(2) of this section X Corporation must use a carryover method for each continuing trade or business, unless either the carryover method is impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the carryover method in accordance with paragraph (a)(5) of this section. As defined in paragraph (b)(5) of this section, the carryover method for the overall method of accounting for the engineering firm is the cash receipts and disbursements method used by X Corporation immediately prior to the date of distribution or transfer, and the carryover method for the overall method of accounting for the manufacturing business is the accrual method used by T Corporation immediately prior to the date of distribution or transfer. There is no change in method of accounting, and X Corporation need not secure the Commissioner's consent to use either carryover method. Notwithstanding that after the date of distribution or transfer X Corporation has two separate and distinct trades or businesses, X Corporation is permitted only one method of accounting for amortizable bond premium under section 171. Because after the date of distribution or transfer X Corporation must use a single method of accounting for bond premium for all trades or businesses, X Corporation must use the principal method for that item as determined under paragraph (c) of this section, unless either the principal method is impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes that method in accordance with paragraph (a)(5) of this section. X Corporation must change to the principal method in accordance with paragraph (d)(1) of this section. If amortizing bond premium is not the principal method, X Corporation may make an election to amortize bond premium to the extent permitted by section 171. See paragraph (e)(2) of this section for rules on making elections.</P>
            </EXAMPLE>
            
            <P>(b)<E T="03">Definitions.</E>For purposes of this section—</P>
            <P>(1)<E T="03">Method of accounting.</E>A method of accounting has the same meaning as provided in section 446 and any applicable Income Tax Regulations.</P>
            <P>(2)<E T="03">Special method of accounting.</E>A special method of accounting is a method expressly permitted or required by the Internal Revenue Code, Income Tax Regulations, or administrative guidance published in the Internal Revenue Bulletin that deviates from the normal application of the cash receipts and disbursements method or an accrual method of accounting. The installment method under section 453, the mark-to-market method under section 475, the amortization of bond premium under section 171, the percentage of completion method under section 460, the recurring item exception of § 1.461-5, and the income deferral methods under section 455 and § 1.451-5 are examples of special methods of accounting. See § 1.446-1(c)(1)(iii).</P>
            <P>(3)<E T="03">Adoption of a method of accounting.</E>Adoption of a method of accounting has the same meaning as provided in § 1.446-1(e)(1).<PRTPAGE P="45677"/>
            </P>
            <P>(4)<E T="03">Change in method of accounting.</E>A change in method of accounting has the same meaning as provided in § 1.446-1(e)(2).</P>
            <P>(5)<E T="03">Carryover method.</E>A carryover method for the overall method of accounting is the overall method of accounting that each party to a section 381(a) transaction uses for each separate and distinct trade or business immediately prior to the date of distribution or transfer. The carryover method for a special method of accounting for an item is the special method of accounting for that item that each party to a section 381(a) transaction uses for each separate and distinct trade or business immediately prior to the date of distribution or transfer.</P>
            <P>(6)<E T="03">Principal method.</E>A principal method is an overall or special method of accounting that is determined under paragraph (c) of this section.</P>
            <P>(7)<E T="03">Permissible method of accounting.</E>A permissible method of accounting is a method of accounting that is proper or permitted under the Internal Revenue Code or any applicable Income Tax Regulations.</P>
            <P>(8)<E T="03">Acquiring corporation.</E>An acquiring corporation has the same meaning as provided in § 1.381(a)-1(b)(2).</P>
            <P>(9)<E T="03">Distributor corporation.</E>A distributor corporation means the corporation, foreign or domestic, that distributes its assets to another corporation described in section 332(b) in a distribution to which section 332 (relating to liquidations of subsidiaries) applies.</P>
            <P>(10)<E T="03">Transferor corporation.</E>A transferor corporation means the corporation, foreign or domestic, that transfers its assets to another corporation in a transfer to which section 361 (relating to nonrecognition of gain or loss to corporations) applies, but only if—</P>
            <P>(i) The transfer is in connection with a reorganization described in section 368(a)(1)(A), (a)(1)(C), or (a)(1)(F), or</P>
            <P>(ii) The transfer is in connection with a reorganization described in section 368(a)(1)(D) or (a)(1)(G), provided the requirements of section 354(b) are met.</P>
            <P>(11)<E T="03">Parties to the section 381(a) transaction.</E>Parties to the section 381(a) transaction means the acquiring corporation and the distributor or transferor corporation that participate in a transaction to which section 381(a) applies.</P>
            <P>(12)<E T="03">Date of distribution or transfer.</E>The date of distribution or transfer has the same meaning as provided in section 381(b)(2) and § 1.381(b)-1(b).</P>
            <P>(13)<E T="03">Separate and distinct trades or businesses.</E>Separate and distinct trades or businesses has the same meaning as provided in § 1.446-1(d).</P>
            <P>(14)<E T="03">Gross receipts.</E>Gross receipts means all the receipts, including amounts that are excludible from gross income, that must be taken into account under the method of accounting used in a representative period (determined without regard to this section) for federal income tax purposes. For example, gross receipts includes income from investments, amounts received for services, rents, total sales (net of returns and allowances), and both taxable and tax-exempt interest. See paragraph (e)(5) of this section for rules on determining the representative period.</P>
            <P>(15)<E T="03">Audit protection.</E>Audit protection means, for purposes of paragraph (d)(1) of this section, that the IRS will not require an acquiring corporation that is required to change a method of accounting under paragraph (a)(3) of this section to change that method for a taxable year ending prior to the taxable year that includes the date of distribution or transfer.</P>
            <P>(16)<E T="03">Section 481(a) adjustment.</E>The section 481(a) adjustment means an adjustment that must be taken into account as required under section 481(a) to prevent amounts from being duplicated or omitted when the taxable income of an acquiring corporation is computed under a method of accounting different from the method used to compute taxable income for the preceding taxable year.</P>
            <P>(17)<E T="03">Cut-off basis.</E>A cut-off basis means a manner in which a change in method of accounting is made without a section 481(a) adjustment and under which only the items arising after the beginning of the year of change (or, in the case of a change made under paragraph (d)(1) of this section, after the date of distribution or transfer) are accounted for under the new method of accounting.</P>
            <P>(18)<E T="03">Adjustment period.</E>The adjustment period means the number of taxable years for taking into account the section 481(a) adjustment required as a result of a change in method of accounting.</P>
            <P>(19)<E T="03">Component trade or business.</E>A component trade or business is a trade or business of a party to the section 381(a) transaction that will be combined and integrated with a trade or business of the other party to the section 381 transaction. See paragraph (e)(4)(ii) of this section for the determination of whether a trade or business is operated as a separate and distinct trade or business after the date of distribution or transfer.</P>
            <P>(c)<E T="03">Principal method</E>—(1)<E T="03">In general.</E>For each integrated trade or business, the principal method is generally the method of accounting used by the component trade or business of the acquiring corporation immediately prior to the date of distribution or transfer. If, however, the component trade or business of the distributor or transferor corporation is larger than the component trade or business of the acquiring corporation on the date of distribution or transfer, the principal method is the method used by the component trade or business of the distributor or transferor corporation immediately prior to that date. If the larger component trade or business does not have a special method of accounting for a particular item immediately prior to the date of distribution or transfer, the principal method for that item is the method of accounting used by the component trade or business that does have a special method of accounting for that item. See paragraph (e)(9) of this section for special rules concerning methods of accounting that are elected on a project-by-project, job-by-job, or other similar basis. For each integrated trade or business, the component trade or business of the distributor or transferor corporation is larger than the component trade or business of the acquiring corporation on the date of distribution or transfer if—</P>
            <P>(i) The aggregate of the adjusted bases of the assets held by each component trade or business of the distributor or transferor corporation (determined under section 1011 and any applicable Income Tax Regulations) exceeds the aggregate of the adjusted bases of the assets of each component trade or business of the acquiring corporation immediately prior to the date of distribution or transfer, and</P>
            <P>(ii) The aggregate of the gross receipts for a representative period of each component trade or business of the distributor or transferor corporation exceeds the aggregate of the gross receipts for the same period of each component trade or business of the acquiring corporation. See paragraph (e)(5) of this section for rules on determining the representative period.</P>
            <P>(2)<E T="03">Multiple component trades or businesses with different principal methods.</E>If a party to the section 381(a) transaction has multiple component trades or businesses and more than one principal overall method of accounting or more than one principal special method of accounting for an item, then the acquiring corporation may choose which of the principal methods of accounting used by such component trades or businesses will be the<PRTPAGE P="45678"/>principal methods of the integrated trade or business. The acquiring corporation must choose a principal method that is a permissible method of accounting. In general, a change to a principal method in a transaction to which section 381(a) and paragraph (a)(3) of this section applies is made under paragraph (d)(1) of this section.</P>
            <P>(3)<E T="03">Examples.</E>The following examples illustrate the rules of this paragraph (c). Unless otherwise noted, the principal method is a permissible method of accounting.</P>
            
            <EXAMPLE>
              <HD SOURCE="HED">Example</HD>
              <P>(1).<E T="03">Principal method is the method used by the acquiring corporation</E>—(i)<E T="03">Facts</E>. X Corporation and T Corporation each operate an employment agency. X Corporation uses the overall cash receipts and disbursements method of accounting, and T Corporation uses an overall accrual method of accounting. X Corporation acquires the assets of T Corporation in a transaction to which section 381(a) applies. The adjusted bases of the assets in X Corporation's employment agency immediately prior to the date of distribution or transfer exceed the adjusted bases of the assets in T Corporation's employment agency, and the gross receipts in X Corporation's employment agency for the representative period exceed the gross receipts of T Corporation's employment agency for the period. After the date of distribution or transfer, X Corporation's employment agency will not be operated as a trade or business that is separate and distinct from T Corporation's employment agency.</P>
              <P>(ii)<E T="03">Conclusion</E>. Because after the date of distribution or transfer X Corporation will not operate its employment agency as a separate and distinct trade or business, X Corporation must use a principal method under paragraph (a)(3) of this section, unless either the principal method is impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the principal method in accordance with paragraph (a)(5) of this section. Because on the date of distribution or transfer T Corporation's employment agency is not larger than X Corporation's employment agency, the principal method for the overall method of accounting is the cash receipts and disbursements method used by X Corporation's employment agency. X Corporation need not secure the Commissioner's consent to use this method of accounting. However, in accordance with paragraph (d)(1) of this section, X Corporation must change the method of accounting for the employment agency acquired from T Corporation to the cash receipts and disbursements method.</P>
            </EXAMPLE>
            <EXAMPLE>
              <HD SOURCE="HED">Example</HD>
              <P>(2).<E T="03">Principal method is the method used by the acquiring corporation</E>—(i)<E T="03">Facts</E>. The facts are the same as in<E T="03">Example</E>(1), except that the gross receipts of T Corporation's employment agency for the representative period exceed the gross receipts of X Corporation's employment agency for the period.</P>
              <P>(ii)<E T="03">Conclusion.</E>The result is the same as in<E T="03">Example</E>(1). Although the gross receipts of T Corporation's employment agency exceed the gross receipts of X Corporation's employment agency, T Corporation's employment agency is not larger than X Corporation's employment agency because the adjusted bases of the assets of T Corporation's employment agency do not exceed the adjusted bases of the assets of X Corporation's employment agency. Thus, the principal method for the overall method of accounting is the cash receipts and disbursements method of accounting used by X Corporation's employment agency immediately prior to the date of distribution or transfer. X Corporation need not secure the Commissioner's consent to use this method of accounting. However, in accordance with paragraph (d)(1) of this section, X Corporation must change the method of accounting for the employment agency business acquired from T Corporation to the cash receipts and disbursements method.</P>
            </EXAMPLE>
            <EXAMPLE>
              <HD SOURCE="HED">Example</HD>
              <P>(3).<E T="03">Principal method is the method used by the distributor or transferor corporation</E>—(i)<E T="03">Facts</E>. The facts are the same as in<E T="03">Example</E>(2), except that the adjusted bases of the assets held by T Corporation's employment agency immediately prior to the date of distribution or transfer exceed the adjusted bases of the assets held by X Corporation's employment agency.</P>
              <P>(ii)<E T="03">Conclusion</E>. The principal method for the overall method of accounting is the accrual method of accounting used by T Corporation's employment agency immediately prior to the date of distribution or transfer because on the date of distribution or transfer T Corporation's employment agency is larger than X Corporation's employment agency. The adjusted bases of the assets of T Corporation's employment agency exceed the adjusted bases of the assets of X Corporation's employment agency, and the gross receipts of T Corporation's employment agency exceed the gross receipts of X Corporation's employment agency. X Corporation need not secure the Commissioner's consent to use this method of accounting. However, in accordance with paragraph (d)(1) of this section, X Corporation must change the method of accounting for the employment agency business it operated prior to the date of distribution or transfer to the accrual method of accounting used by T Corporation's employment agency immediately prior to the date of distribution or transfer.</P>
            </EXAMPLE>
            <EXAMPLE>
              <HD SOURCE="HED">Example</HD>
              <P>(4).<E T="03">Impermissible principal method</E>—(i)<E T="03">Facts</E>. The facts are the same as in<E T="03">Example</E>(1), except that X Corporation is prohibited under section 448 from using the cash receipts and disbursements method of accounting after the date of distribution or transfer.</P>
              <P>(ii)<E T="03">Conclusion</E>. Because section 448 prohibits X Corporation from using the cash receipts and disbursements method of accounting, X Corporation is not permitted to use the principal method for the overall method of accounting as determined in<E T="03">Example</E>(1). Because after the date of distribution or transfer that method is not a permissible method, under paragraph (a)(4) of this section X Corporation must secure the Commissioner's consent to change to a permissible method in accordance with the procedures set forth in paragraph (d)(2) of this section.</P>
            </EXAMPLE>
            <EXAMPLE>
              <HD SOURCE="HED">Example</HD>
              <P>(5).<E T="03">Voluntary change not allowable</E>—(i)<E T="03">Facts</E>. The facts are the same as in<E T="03">Example</E>(4), except that T Corporation wants to discontinue using the overall accrual method of accounting for its employment agency and change to the cash receipts and disbursements method for the taxable year in which the section 381(a) transaction occurs or is expected to occur.</P>
              <P>(ii)<E T="03">Conclusion</E>. Under paragraph (a)(5) of this section, the Commissioner will grant a request to change a method of accounting for the taxable year that includes the date of distribution or transfer only if the requested method is the method that the acquiring corporation must use after the date of distribution or transfer. The Commissioner will not consent to a request by T Corporation to change to the cash receipts and disbursements method for the taxable year in which the section 381(a) transaction occurs or is expected to occur because X Corporation cannot use the cash receipts and disbursements method after the date of distribution or transfer.</P>
              <P>
                <E T="03">Example</E>(6).<E T="03">Principal methods are the acquiring corporation's methods</E>—(i)<E T="03">Facts</E>. X Corporation and T Corporation each publishes magazines. X Corporation acquires the assets of T Corporation in a transaction to which section 381(a) applies. Both X Corporation and T Corporation use an overall accrual method of accounting. X Corporation has elected to defer income from its subscription sales under section 455. T Corporation has not elected to defer income from its subscription sales under section 455 and instead has recognized the income from these sales in accordance with section 451. The adjusted bases of the assets in X Corporation's publication business immediately prior to the date of distribution or transfer exceed the adjusted bases of the assets in T Corporation's publication business, and the gross receipts in X Corporation's publication business for the representative period exceed the gross receipts in T Corporation's publication business for the representative period. After the date of distribution or transfer, X Corporation will not operate its publication business as a trade or business that is separate and distinct from T Corporation's publication business.</P>
              <P>(ii)<E T="03">Conclusion</E>. Because after the date of distribution or transfer X Corporation will not operate its publication business as a separate and distinct trade or business, X Corporation must use the principal method under paragraph (a)(3) of this section, unless either the principal method is impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the principal method in accordance with paragraph (a)(5) of this section. The adjusted bases of the assets in T Corporation's publication business do not exceed the adjusted bases of the assets in X Corporation's publication business, and the gross receipts in T Corporation's publication business do not exceed the gross receipts in X Corporation's publication business. Because on the date of distribution or transfer T Corporation's publication business is not<PRTPAGE P="45679"/>larger than X Corporation's publication business, the principal method for the overall method of accounting is the accrual method used by X Corporation's publication business immediately prior to the date of distribution or transfer. The principal method for subscription sales is the section 455 deferral method used by X Corporation immediately prior to the date of distribution or transfer. X Corporation need not secure the Commissioner's consent to use the principal method for either the overall method of accounting or the special method of accounting. However, in accordance with paragraph (d)(1) of this section, X Corporation must change both the overall method of accounting and the special method of accounting for the publication business acquired from T Corporation to the accrual method and the section 455 deferral method used by X Corporation immediately prior to the date of distribution or transfer.</P>
            </EXAMPLE>
            <EXAMPLE>
              <HD SOURCE="HED">Example</HD>
              <P>(7).<E T="03">Principal methods are the acquiring corporation's methods</E>—(i)<E T="03">Facts</E>. The facts are the same as in<E T="03">Example</E>(6), except that the adjusted bases of the assets in T Corporation's publication business immediately prior to the date of distribution or transfer exceed the adjusted bases of the assets in X Corporation's business.</P>
              <P>(ii)<E T="03">Conclusion</E>. The result is the same as in<E T="03">Example</E>(6). Because on the date of distribution or transfer T Corporation's publication business is not larger than X Corporation's publication business, the principal method for the overall method of accounting is the accrual method used by X Corporation's publication business immediately prior to the date of distribution or transfer. The principal method for subscription sales is the section 455 deferral method used by X Corporation immediately prior to the date of distribution or transfer. X Corporation need not secure the Commissioner's consent to use the principal method for either the overall method of accounting or the special method of accounting. However, in accordance with paragraph (d)(1) of this section, X Corporation must change both the overall method of accounting and the special method of accounting for the publication business acquired from T Corporation to the accrual method and the section 455 deferral method used by X Corporation immediately prior to the date of distribution or transfer.</P>
            </EXAMPLE>
            <EXAMPLE>
              <HD SOURCE="HED">Example</HD>
              <P>(8).<E T="03">Principal method determination when larger component trade or business does not have a special method of accounting</E>—(i)<E T="03">Facts</E>. X Corporation and T Corporation both install ice skating rinks. Both X Corporation and T Corporation use an overall accrual method of accounting for their respective businesses. X Corporation completes its installation contracts within the contracting year and uses an accrual method of accounting to recognize the revenue from its installation contracts. T Corporation's installation contracts are subject to section 460, and T Corporation recognizes the revenue from such contracts under the percentage-of-completion method. X Corporation acquires the assets of T Corporation in a transaction to which section 381(a) applies. The adjusted bases of the assets in X Corporation's installation business immediately prior to the date of distribution or transfer exceed the adjusted bases of the assets in T Corporation's installation business, and the gross receipts in X Corporation's installation business for the representative period exceed the gross receipts in T Corporation's installation business for the representative period. After the date of distribution or transfer, X Corporation will not operate its installation business as a trade or business that is separate and distinct from T Corporation's installation business.</P>
              <P>(ii)<E T="03">Conclusion.</E>Because after the date of distribution or transfer X Corporation will not operate its installation business as a separate and distinct trade or business, X Corporation must use a principal method under paragraph (a)(3) of this section, unless either the principal method is impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the principal method in accordance with paragraph (a)(5) of this section. The adjusted bases of the assets in T Corporation's installation business do not exceed the adjusted bases of the assets in X Corporation's installation business, and the gross receipts in T Corporation's installation business do not exceed the gross receipts in X Corporation's installation business. Because on the date of distribution or transfer T Corporation's installation business is not larger than X Corporation's installation business, the principal method for the overall method of accounting is the accrual method used by X Corporation's installation business immediately prior to the date of distribution or transfer. X Corporation need not secure the Commissioner's consent to use the principal method for the overall method of accounting. However, in accordance with paragraph (d)(1) of this section, X Corporation must change the overall method of accounting for the installation business acquired from T Corporation to the accrual method used by X Corporation. Under paragraph (c) of this section, the principal method for T Corporation's long-term contracts is the percentage-of-completion method used by T Corporation immediately prior to the date of distribution or transfer because X Corporation's installation business does not have a method of accounting for long-term contracts. There is no change in method of accounting, and X Corporation need not secure the Commissioner's consent to use T Corporation's percentage-of-completion method.</P>
            </EXAMPLE>
            <EXAMPLE>
              <HD SOURCE="HED">Example</HD>
              <P>(9).<E T="03">Principal method determination with a combined trade or business and a separate and distinct trade or business</E>—(i)<E T="03">Facts</E>. X Corporation operates a tennis academy as a trade or business that is separate and distinct from its trade or business of operating a golf academy. X Corporation uses the overall cash receipts and disbursements method of accounting for the tennis academy and an overall accrual method of accounting for the golf academy. T Corporation operates a tennis academy and uses an accrual method of accounting for the overall method. X Corporation acquires the assets of T Corporation in a transaction to which section 381(a) applies. After the date of distribution or transfer, X Corporation will not operate its tennis academy as a trade or business that is separate and distinct from T Corporation's tennis academy. X Corporation will continue to operate its golf academy as a trade or business that is separate and distinct from the operation of the tennis academy. The adjusted bases of the assets in T Corporation's tennis academy exceed the adjusted bases of the assets in X Corporation's tennis academy immediately prior to the date of distribution or transfer. The gross receipts of T Corporation's tennis academy for the representative period exceed the gross receipts of X Corporation's tennis academy for that period.</P>
              <P>(ii)<E T="03">Conclusion.</E>Because after the date of distribution or transfer X Corporation will not operate its tennis academy as a separate and distinct trade or business, X Corporation must use a principal method under paragraph (a)(3) of this section, unless either the principal method is impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the principal method in accordance with paragraph (a)(5) of this section. Because on the date of distribution or transfer the tennis academy operated by T Corporation is larger than the tennis academy operated by X Corporation, the principal method for the overall method of accounting for the combined tennis academy business is the accrual method used by T Corporation's tennis academy immediately prior to the date of distribution or transfer. X Corporation need not secure the Commissioner's consent to use the principal method for the overall method of accounting. However, in accordance with paragraph (d)(1) of this section, X Corporation must change the method of accounting for its tennis academy to the accrual method. Because X Corporation will operate the golf academy as a separate trade or business, under paragraph (a)(2) of this section X Corporation must continue to use the accrual method that it used immediately prior to the date of distribution or transfer as the carryover method for the golf academy. There is no change in method of accounting, and X Corporation need not secure the Commissioner's consent to use the carryover method.</P>
            </EXAMPLE>
            <EXAMPLE>
              <HD SOURCE="HED">Example</HD>
              <P>(10).<E T="03">Principal method determination with multiple component trades or businesses</E>—(i)<E T="03">Facts</E>. The facts are the same as in<E T="03">Example</E>(9), except that after the date of distribution or transfer X Corporation will not operate its golf academy as a trade or business that is separate and distinct from the tennis academy. In addition, X Corporation's component trades or businesses are larger than T Corporation's component trade or business: (1) the adjusted bases of the assets of X Corporation's tennis academy and golf academy businesses, in the aggregate, exceed the adjusted bases of the assets held by T Corporation's tennis academy; and (2) the gross receipts for the representative period of X Corporation's tennis academy and golf academy businesses, in the aggregate, exceed the gross receipts in T Corporation's tennis academy.</P>
              <P>(ii)<E T="03">Conclusion</E>. Because on the date of distribution or transfer T Corporation's tennis academy is not larger than X Corporation's<PRTPAGE P="45680"/>combined tennis academy and golf academy, the principal method for the overall method of accounting is the method of accounting used by the component trades or businesses of X Corporation that will be combined with T Corporation's component trade or business on that date. Because on the date of distribution or transfer X Corporation operates two component trades or businesses with different overall methods of accounting that will be integrated after the date of distribution or transfer, X Corporation may choose under paragraph (c)(2) of this section which overall method (and any special method of accounting) used by its component trades or businesses will be the principal method. X Corporation may choose to use either the accrual method used by the golf academy or the cash receipts and disbursements method used by its tennis academy as the principal method after the date of distribution or transfer, if either method is a permissible method. In accordance with paragraph (d)(1) of this section, X Corporation must change T Corporation's overall method of accounting to the principal method. Under paragraph (a)(3) of this section, X Corporation also must change either its golf academy business or its tennis academy business, depending on which principal method X Corporation selects, to the principal method.</P>
            </EXAMPLE>
            
            <P>(d)<E T="03">Procedures for changing a method of accounting</E>—(1)<E T="03">Change made to principal method under paragraph (a)(3) of this section</E>—(i)<E T="03">Section 481(a) adjustment</E>—(A)<E T="03">In general</E>. An acquiring corporation that changes its method of accounting or the distributor or transferor corporation's method of accounting under paragraph (a)(3) of this section does not need to secure the Commissioner's consent to use the principal method. To the extent the use of a principal method constitutes a change in method of accounting, the change in method is treated as a change initiated by the acquiring corporation for purposes of section 481(a)(2). Any change to a principal method, whether the change relates to a trade or business of the acquiring corporation or a trade or business of the distributor or transferor corporation, must be reflected on the acquiring corporation's federal income tax return for the taxable year that includes the date of distribution or transfer. The amount of the section 481(a) adjustment and the adjustment period, if any, necessary to implement a change to the principal method are determined under § 1.446-1(e) and the applicable administrative procedures that govern voluntary changes in methods of accounting under section 446(e). If the Internal Revenue Code, the Income Tax Regulations, or administrative procedures require that a method of accounting be implemented on a cut-off basis, the acquiring corporation must implement the change on a cut-off basis as of the date of distribution or transfer on its federal income tax return for the taxable year that includes the date of distribution or transfer. If the Internal Revenue Code, the Income Tax Regulations, or administrative procedures require a section 481(a) adjustment, the acquiring corporation must determine the section 481(a) adjustment and include the appropriate amount of the section 481(a) adjustment on its federal income tax return for the taxable year that includes the date of distribution or transfer and subsequent taxable year(s), as necessary. This adjustment is determined by the acquiring corporation as of the beginning of the day that is immediately after the date of distribution or transfer.</P>
            <P>(B)<E T="03">Example</E>. The following example illustrates the rules of this paragraph (d)(1)(i):</P>
            
            <EXAMPLE>
              <HD SOURCE="HED">Example.</HD>
              <P>X Corporation uses the overall cash receipts and disbursements method of accounting, and T Corporation uses an overall accrual method of accounting. X Corporation acquires the assets of T Corporation in a transaction to which section 381(a) applies. X Corporation determines that under the rules of paragraph (c)(1) of this section X Corporation must change the method of accounting for the business acquired from T Corporation to the cash receipts and disbursements method. X Corporation will determine the section 481(a) adjustment pertaining to the change to the cash receipts and disbursements method by consolidating the adjustments (whether the amounts thereof represent increases or decreases in items of income or deductions) arising with respect to balances in the various accounts, such as accounts receivable, as of the beginning of the day that immediately follows the day on which X Corporation acquires the assets of T Corporation. X Corporation will reflect this adjustment, or an appropriate part thereof, on its federal income tax return for the taxable year that includes the date of distribution or transfer.</P>
            </EXAMPLE>
            
            <P>(ii)<E T="03">Audit protection.</E>Notwithstanding any other provision in any other Income Tax Regulation or administrative procedure, no audit protection is provided for any change in method of accounting under paragraph (d)(1) of this section.</P>
            <P>(iii)<E T="03">Other terms and conditions.</E>Except as otherwise provided in this section, other terms and conditions provided in § 1.446-1(e) and the applicable administrative procedures for voluntary changes in method of accounting under section 446(e) apply to a change in method of accounting under this section. Thus, for example, if the administrative procedures for a particular change in method of accounting have a term and condition that provides for the acceleration of the section 481(a) adjustment period, this term and condition applies to a change made under this paragraph (d)(1). However, any scope limitation in the applicable administrative procedures will not apply for purposes of making a change under this paragraph (d)(1). For example, if the administrative procedures provide as a limitation that an identical change in method of accounting is barred for a period of years, this limitation will not bar a change to the principal method made under this section.</P>
            <P>(2)<E T="03">Change made to a method of accounting under paragraph (a)(4) or (a)(5) of this section</E>—(i)<E T="03">In general.</E>A party to a section 381(a) transaction that changes a method of accounting under either paragraph (a)(4) or paragraph (a)(5) of this section must follow the provisions of § 1.446-(1)(e) and the applicable administrative procedures, including scope limitations, for voluntary changes in method of accounting under section 446(e), except as provided in paragraphs (d)(2)(ii) and (d)(2)(iii) of this section. An application on Form 3115, “Application for Change in Accounting Method,” filed with the IRS to change a method of accounting under this paragraph (d)(2) should be labeled “Filed under section 381(c)(4)” at the top.</P>
            <P>(ii)<E T="03">Final year limitation.</E>Any scope limitation relating to the final year of a trade or business will not apply to a taxpayer that changes its method of accounting in the final year of a trade or business that is terminated as the result of a section 381(a) transaction.</P>
            <P>(iii)<E T="03">Time to file.</E>Under the authority of § 1.446-1(e)(3)(ii), for a change in method of accounting requiring advance consent, the application for a change in method of accounting (for example, Form 3115) must be filed with the IRS on or before the later of—</P>
            <P>(A) The due date for filing a Form 3115 as specified in § 1.446-1(e), for example, the last day of the taxable year in which the distribution or transfer occurred, or</P>
            <P>(B) The earlier of—</P>
            <P>(<E T="03">1</E>) The day that is 180 days after the date of distribution or transfer, or</P>
            <P>(<E T="03">2</E>) The day on which the acquiring corporation files its federal income tax return for the taxable year in which the distribution or transfer occurred.</P>
            <P>(e)<E T="03">Rules and procedures</E>—(1)<E T="03">No method of accounting.</E>If a party to a section 381(a) transaction is not using a method of accounting, does not have a method of accounting for a particular item, or came into existence as a result of the transaction, the party will not be treated as having a method of accounting different from that used by<PRTPAGE P="45681"/>another party to the section 381(a) transaction.</P>
            <P>(2)<E T="03">Elections and adoptions allowed.</E>If an election does not require the Commissioner's consent, an acquiring corporation or a distributor or transferor corporation is not precluded from making any election that is otherwise permissible for the taxable year that includes the date of distribution or transfer. For purposes of this section, a corporation shall be deemed as having made any election as of the first day of the taxable year that includes the date of distribution or transfer. Similarly, where adoption is permissible, an acquiring corporation or a distributor or transferor corporation may adopt any permissible method of accounting for the taxable year that includes the date of distribution or transfer.</P>
            <P>(3)<E T="03">Elections continue after section 381(a) transaction</E>—(i)<E T="03">General rule.</E>An acquiring corporation is not required to renew any election not otherwise requiring renewal and previously made by it or by a distributor or transferor corporation for a carryover method or a principal method if the acquiring corporation uses the method after the section 381(a) transaction. If the acquiring corporation uses a method after the date of distribution or transfer, an election made by the acquiring corporation or by a distributor or transferor corporation for that method that was in effect on the date of distribution or transfer continues after the section 381(a) transaction as though the distribution or transfer had not occurred.</P>
            <P>(ii)<E T="03">Example.</E>The following example illustrates the rules of this paragraph (e)(3):</P>
            
            <EXAMPLE>
              <HD SOURCE="HED">Example.</HD>
              <P>The acquiring corporation, X Corporation, previously elected to amortize bond premium under section 171. X Corporation acquires the assets of T Corporation in a transaction to which section 381(a) applies. X Corporation determines under the rules of paragraph (c)(1) of this section that X Corporation's method of amortizing bond premium is the principal method. After the date of distribution or transfer, X Corporation is not required to renew its bond premium amortization election and is bound by it. Additionally, X Corporation would not be required to renew its election to amortize bond premium if the method were the carryover method under paragraph (a)(2) of this section.</P>
            </EXAMPLE>
            
            <P>(4)<E T="03">Appropriate times for certain determinations</E>—(i)<E T="03">Determining the method of accounting.</E>The method of accounting used by a party to a section 381(a) transaction on the date of distribution or transfer is the method of accounting used by that party as of the end of the day that is immediately prior to the date of distribution or transfer.</P>
            <P>(ii)<E T="03">Determining whether there are separate and distinct trades or businesses after the date of distribution or transfer.</E>Whether an acquiring corporation will operate the trades or businesses of the parties to a section 381(a) transaction as separate and distinct trades or businesses after the date of distribution or transfer will be determined as of the date of distribution or transfer based upon the facts and circumstances. Intent to combine books and records of the trades or businesses may be demonstrated by contemporaneous records and documents or by other objective evidence that reflects the acquiring corporation's ultimate plan of operation, even though the actual combination of the books and records may extend beyond the end of the taxable year that includes the date of distribution or transfer.</P>
            <P>(5)<E T="03">Representative period for aggregating gross receipts.</E>The representative period for measuring gross receipts is generally the 12 consecutive months preceding the date of distribution or transfer. If a component trade or business was not in existence for the 12 consecutive months preceding the date of distribution or transfer, then all component trades or businesses of each integrated trade or business will compare their gross receipts for the period that such trade or business was in existence. For example, if the acquiring corporation's component trade or business was formed in August and the date of distribution or transfer occurred in December of the same year, the gross receipts for those five months will be compared with the gross receipts of the other component trades or businesses for the same period.</P>
            <P>(6)<E T="03">Establishing a method of accounting.</E>A method of accounting used by the distributor or transferor corporation immediately prior to the date of distribution or transfer that continues to be used by the acquiring corporation after the date of distribution or transfer is an established method of accounting for purposes of section 446(e), whether or not such method is proper or is permitted under the Internal Revenue Code or any applicable Income Tax Regulations.</P>
            <P>(7)<E T="03">Other applicable provisions.</E>This section does not preempt any other provision of the Internal Revenue Code or the Income Tax Regulations that is applicable to the acquiring corporation's circumstances. For example, income, deductions, credits, allowances, and exclusions may be allocated among the parties to a section 381(a) transaction and other taxpayers under sections 269 and 482, if appropriate. Similarly, transfers of contracts accounted for using a long-term contract method of accounting are governed by the rules provided in § 1.460-4(k). Further, if other paragraphs of section 381(c) apply for purposes of determining the methods of accounting to be used following the date of distribution or transfer, section 381(c)(4) and this § 1.381(c)(4)-1 will not apply to the tax treatment of the items. For example, this section does not apply to inventories that an acquiring corporation obtains in a transaction to which section 381(a) applies. Instead, the rules of section 381(c)(5) govern the inventory method to be used by the acquiring corporation after the distribution or transfer. Similarly, if the acquiring corporation assumes an obligation of the distributor or transferor corporation that gives rise to a liability after the date of distribution or transfer and to which § 1.381(c)(16)-1 applies, the deductibility of the item is determined under this section only after the rules of section 381(c)(16) are applied.</P>
            <P>(8)<E T="03">Character of items of income and deduction.</E>After the date of distribution or transfer, items of income and deduction have the same character in the hands of the acquiring corporation as they would have had in the hands of the distributor or transferor corporation if no distribution or transfer had occurred.</P>
            <P>(9)<E T="03">Method of accounting selected by project or job.</E>If other sections of the Internal Revenue Code, Income Tax Regulations, or other administrative guidance permit an acquiring corporation to elect a method of accounting on a project-by-project, job-by-job, or other similar basis, then for purposes of this section the method elected with respect to each project or job is the established method only for that project or job. For example, the election under section 460 to classify a contract to perform both manufacturing and construction activities as a long-term construction contract if at least 95 percent of the estimated total allocable contract costs are reasonably allocated to the construction activities is made on a contract-by-contract basis. Accordingly, the method of accounting previously elected for a project or job generally continues after the date of distribution or transfer. However, if the trades or businesses of the parties to a section 381(a) transaction are not operated as separate and distinct trades or businesses after the date of distribution or transfer, and two or more of the parties to the section 381(a) transaction previously worked on the same project or job and used different<PRTPAGE P="45682"/>methods of accounting for the project or job immediately before the distribution or transfer, then the acquiring corporation must determine the principal method for that project or job under paragraph (c) of this section and make changes, if necessary, to the principal method in accordance with paragraph (d)(1) of this section.</P>
            <P>(10)<E T="03">Impermissible method of accounting.</E>This section does not limit the Commissioner's ability under section 446(b) to determine whether a taxpayer's method of accounting is an impermissible method or otherwise fails to clearly reflect income. For example, an acquiring corporation may not use the method of accounting determined under paragraph (a)(2) of this section if the method fails to clearly reflect the acquiring corporation's income within the meaning of section 446(b).</P>
            <P>(f)<E T="03">Effective/applicability date.</E>This section applies to corporate reorganizations and tax-free liquidations described in section 381(a) that occur on or after August 31, 2011.</P>
          </SECTION>
          <AMDPAR>
            <E T="04">Par. 4.</E>Section 1.381(c)(5)-1 is revised to read as follows:</AMDPAR>
          <SECTION>
            <SECTNO>§ 1.381(c)(5)-1</SECTNO>
            <SUBJECT>Inventory method.</SUBJECT>
            <P>(a)<E T="03">Introduction</E>—(1)<E T="03">Purpose.</E>This section provides guidance regarding the inventory method an acquiring corporation must use following a distribution or transfer to which sections 381(a) and 381(c)(5) apply and how to implement any associated change in method of accounting. See § 1.381(c)(4)-1 for guidance regarding the method of accounting or combination of methods (other than inventory and depreciation methods) an acquiring corporation must use following a distribution or transfer to which sections 381(a) and 381(c)(4) apply. See § 1.381(c)(6)-1 for guidance regarding the depreciation method an acquiring corporation must use following a distribution or transfer to which sections 381(a) and 381(c)(6) apply.</P>
            <P>(2)<E T="03">Carryover method requirement for separate and distinct trades or businesses.</E>In a transaction to which section 381(a) applies, if an acquiring corporation continues to operate a trade or business of the parties to the section 381(a) transaction as a separate and distinct trade or business after the date of distribution or transfer, the acquiring corporation must use a carryover method as defined in paragraph (b)(4) of this section for each continuing trade or business, unless either the carryover method is impermissible and must be changed under paragraph (a)(4) of this section or the acquiring corporation changes the carryover method in accordance with paragraph (a)(5) of this section. The acquiring corporation need not secure the Commissioner's consent to continue a carryover method.</P>
            <P>(3)<E T="03">Principal method requirement for trades or businesses not operated as separate and distinct trades or businesses.</E>In a transaction to which section 381(a) applies, if an acquiring corporation does not operate the trades or businesses of the parties to the section 381(a) transaction as separate and distinct trades or businesses after the date of distribution or transfer, the acquiring corporation must use a principal method determined under paragraph (c) of this section, unless either the principal method is impermissible and must be changed under paragraph (a)(4) of this section or the acquiring corporation changes the principal method in accordance with paragraph (a)(5) of this section. The acquiring corporation must change to a principal method in accordance with paragraph (d)(1) of this section for each integrated trade or business and need not secure the Commissioner's consent to use a principal method.</P>
            <P>(4)<E T="03">Carryover method or principal method not a permissible method.</E>If a carryover method or principal method is not a permissible inventory method, the acquiring corporation must secure the Commissioner's consent to change to a permissible inventory method as provided in paragraph (d)(2) of this section. If the acquiring corporation must use a single inventory method for a particular type of goods after the date of distribution or transfer regardless of the number of separate and distinct trades or businesses operated on that date, the acquiring corporation must use the principal method for that type of goods as determined under paragraph (c) of this section, unless either the principal method is impermissible and must be changed under this paragraph (a)(4) or the acquiring corporation changes the principal method in accordance with paragraph (a)(5) of this section.</P>
            <P>(5)<E T="03">Voluntary change.</E>Any party to a section 381(a) transaction may request permission under section 446(e) to change an inventory method for the taxable year in which the transaction occurs or is expected to occur. For trades or businesses that will not operate as separate and distinct trades or businesses after the date of distribution or transfer, a change in method of accounting for the taxable year that includes that date will be granted only if the requested inventory method is the method that the acquiring corporation must use after the date of distribution or transfer. The time and manner of obtaining the Commissioner's consent to change to a different inventory method is described in paragraph (d)(2) of this section.</P>
            <P>(6)<E T="03">Examples.</E>The following examples illustrate the rules of this paragraph (a). Unless otherwise noted, the carryover method is a permissible inventory method.</P>
            
            <EXAMPLE>
              <HD SOURCE="HED">Example</HD>
              <P>(1).<E T="03">Carryover method for separate and distinct trades or businesses after the date of distribution or transfer</E>—(i)<E T="03">Facts.</E>X Corporation manufactures radios and television sets. X Corporation uses the first-in, first-out (FIFO) method of inventory identification, the cost method of valuing its inventories, and capitalizes inventory costs in accordance with section 263A. T Corporation manufactures washing machines and dryers. T Corporation uses the last-in, first-out (LIFO) method of inventory identification, the cost method of valuing its inventories, and capitalizes inventory costs under section 263A using methods other than those used by X Corporation. X Corporation acquires the inventory of T Corporation in a transaction to which section 381(a) applies. After the date of distribution or transfer, X Corporation operates its radio and television manufacturing business as a trade or business that is separate and distinct from its washing machines and dryers manufacturing business.</P>
              <P>(ii)<E T="03">Conclusion.</E>Because after the date of distribution or transfer X Corporation operates its manufacturing businesses as separate and distinct trades or businesses, under paragraph (a)(2) of this section X Corporation must use the carryover methods for each continuing trade or business, unless either the carryover methods are impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the carryover methods in accordance with paragraph (a)(5) of this section. As defined in paragraph (b)(4) of this section, the carryover methods for the radios and television sets manufacturing business are the FIFO method, the cost basis of valuation, and X Corporation's methods of accounting for section 263A costs immediately prior to the date of distribution or transfer. The carryover methods for the washing machines and dryers manufacturing business are the LIFO method, the cost basis of valuation, and T Corporation's methods of accounting for section 263A costs immediately prior to the date of distribution or transfer. There is no change in method of accounting, and X Corporation need not secure the Commissioner's consent to use any carryover method.</P>
            </EXAMPLE>
            <EXAMPLE>
              <HD SOURCE="HED">Example</HD>
              <P>(2).<E T="03">Carryover method not permissible</E>—(i)<E T="03">Facts.</E>X Corporation manufactures food and beverages and uses the FIFO method of inventory identification, the cost method of valuing its inventories, and capitalizes costs in accordance with section 263A. T Corporation sells sporting equipment. T Corporation uses the FIFO method of inventory identification and the cost method of valuing its inventories. T Corporation does not capitalize costs under section 263A because it meets the small reseller exception under section 263A. X<PRTPAGE P="45683"/>Corporation acquires the inventory of T Corporation in a transaction to which section 381(a) applies. After the date of distribution or transfer, X Corporation operates the food and beverages business as a trade or business that is separate and distinct from the sporting equipment business, and X Corporation does not qualify for the small reseller exception under section 263A for its sporting equipment business.</P>
              <P>(ii)<E T="03">Conclusion.</E>Because after the date of distribution or transfer X Corporation operates the food and beverages business as a separate and distinct trade or business, under paragraph (a)(2) of this section X Corporation must use the carryover methods for each continuing trade or business, unless either the carryover methods are impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the carryover methods in accordance with paragraph (a)(5) of this section. As defined in paragraph (b)(4) of this section, the carryover methods for the food and beverages business are the FIFO method, the cost basis of valuation, and X Corporation's methods of capitalizing costs under section 263A immediately prior to the date of distribution or transfer. The carryover methods for the sporting equipment business are the FIFO method and the cost basis of valuation. There is no change in method of accounting, and X Corporation need not secure the Commissioner's consent to use any carryover method. However, because X Corporation does not qualify for the small reseller exception under section 263A for its sporting equipment business, X Corporation's method of not capitalizing additional section 263A costs is an impermissible carryover method under paragraph (a)(4) of this section. X Corporation must secure the Commissioner's consent to change to a permissible method of capitalizing costs under section 263A for the sporting equipment business as provided in paragraph (d)(2) of this section.</P>
            </EXAMPLE>
            
            <P>(b)<E T="03">Definitions.</E>(1)<E T="03">Inventory method.</E>An inventory method is a method of accounting used to account for merchandise on hand (including finished goods, work in process, and raw materials) at the beginning of a year for purposes of computing taxable income for that year. The term includes not only the method for identifying inventory, for example, the FIFO inventory method or the LIFO inventory method, but also all other methods necessary to account for merchandise.</P>
            <P>(2)<E T="03">Adoption of a method of accounting.</E>Adoption of a method of accounting has the same meaning as provided in § 1.446-1(e)(1).</P>
            <P>(3)<E T="03">Change in method of accounting.</E>A change in method of accounting has the same meaning as provided in § 1.446-1(e)(2).</P>
            <P>(4)<E T="03">Carryover method.</E>A carryover method is an inventory method that each party to a section 381(a) transaction uses for each separate and distinct trade or business immediately prior to the date of distribution or transfer.</P>
            <P>(5)<E T="03">Principal method.</E>A principal method is an inventory method that is determined under paragraph (c) of this section.</P>
            <P>(6)<E T="03">Permissible method of accounting.</E>A permissible method of accounting is a method of accounting that is proper or permitted under the Internal Revenue Code or any applicable Income Tax Regulations.</P>
            <P>(7)<E T="03">Acquiring corporation.</E>An acquiring corporation has the same meaning as provided in § 1.381(a)-1(b)(2).</P>
            <P>(8)<E T="03">Distributor corporation.</E>A distributor corporation means the corporation, foreign or domestic, that distributes its assets to another corporation described in section 332(b) in a distribution to which section 332 (relating to liquidations of subsidiaries) applies.</P>
            <P>(9)<E T="03">Transferor corporation.</E>A transferor corporation means the corporation, foreign or domestic, that transfers its assets to another corporation in a transfer to which section 361 (relating to nonrecognition of gain or loss to corporations) applies, but only if—</P>
            <P>(i) The transfer is in connection with a reorganization described in section 368(a)(1)(A), (a)(1)(C), or (a)(1)(F), or</P>
            <P>(ii) The transfer is in connection with a reorganization described in section 368(a)(1)(D) or (a)(1)(G), provided the requirements of section 354(b) are met.</P>
            <P>(10)<E T="03">Parties to the section 381(a) transaction.</E>Parties to the section 381(a) transaction means the acquiring corporation and the distributor or transferor corporation that participate in a transaction to which section 381(a) applies.</P>
            <P>(11)<E T="03">Date of distribution or transfer.</E>The date of distribution or transfer has the same meaning as provided in section 381(b)(2) and § 1.381(b)-1(b).</P>
            <P>(12)<E T="03">Separate and distinct trades or businesses.</E>Separate and distinct trades or businesses has the same meaning as provided in § 1.446-1(d).</P>
            <P>(13)<E T="03">Audit protection.</E>Audit protection means, for purposes of paragraph (d)(1) of this section, that the IRS will not require an acquiring corporation that is required to change a method of accounting under paragraph (a)(3) of this section to change that method for a taxable year ending prior to the taxable year that includes the date of distribution or transfer.</P>
            <P>(14)<E T="03">Section 481(a) adjustment.</E>The section 481(a) adjustment means an adjustment that must be taken into account as required under section 481(a) to prevent amounts from being duplicated or omitted when the taxable income of an acquiring corporation is computed under a method of accounting different from the method used to compute taxable income for the preceding taxable year.</P>
            <P>(15)<E T="03">Cut-off basis.</E>A cut-off basis means a manner in which a change in method of accounting is made without a section 481(a) adjustment and under which only the items arising after the beginning of the year of change (or, in the case of a change made under paragraph (d)(1) of this section, after the date of distribution or transfer) are accounted for under the new method of accounting. When it implements the change on a cut-off basis, a taxpayer using the LIFO inventory method to identify its inventory goods that makes a change in method of accounting within the LIFO inventory method from one LIFO method or sub-method to another LIFO method or sub-method uses the new LIFO inventory method to determine its current-year cost and base-year cost of ending inventories for the year of change, but does not recompute the cost of beginning inventories for the year of change using the new LIFO inventory method.</P>
            <P>(16)<E T="03">Adjustment period.</E>The adjustment period means the number of taxable years for taking into account the section 481(a) adjustment required as a result of a change in method of accounting.</P>
            <P>(17)<E T="03">Component trade or business.</E>A component trade or business is a trade or business of a party to the section 381(a) transaction that will be combined and integrated with a trade or business of the other party to the section 381 transaction. See paragraph (e)(7)(ii) of this section for the determination of whether a trade or business is operated as a separate and distinct trade or business after the date of distribution or transfer.</P>
            <P>(c)<E T="03">Principal method</E>—(1)<E T="03">In general.</E>For each integrated trade or business, the principal method for a particular type of goods is generally the inventory method used by the component trade or business of the acquiring corporation immediately prior to the date of distribution or transfer for that type of goods. If, however, on the date of distribution or transfer the component trade or business of the distributor or transferor corporation holds more inventory of a type of goods than the component trade or business of the acquiring corporation, the principal method for such goods is the inventory method used by the component trade or business of the distributor or transferor corporation immediately prior to that date. For each integrated trade or<PRTPAGE P="45684"/>business, the component trade or business of the distributor or transferor corporation holds more inventory if, for a particular type of goods, the aggregate of the fair market value of the goods held by each component trade or business of the distributor or transferor corporation exceeds the aggregate of the fair market value of the goods held by each component trade or business of the acquiring corporation immediately prior to the date of distribution or transfer. Alternatively, as a simplifying convention, the acquiring corporation may elect to apply the preceding sentence to the aggregate fair market value of the entire inventories, held by each component trade or business of the acquiring corporation and each component trade or business of the distributor or transferor corporation, that will be integrated after the date of distribution or transfer. If the component trade or business with the larger aggregate fair market value of the entire inventories does not have an inventory method for a particular type of goods immediately prior to the date of distribution or transfer, the principal method for that type of goods is the inventory method used by the component trade or business that does have an inventory method for that type of goods.</P>
            <P>(2)<E T="03">Multiple component trades or businesses with different principal methods.</E>If a party to the section 381(a) transaction has multiple component trades or businesses and more than one principal inventory method for a particular type of goods, then the acquiring corporation may choose which of the inventory methods used by such component trades or businesses will be the principal method of the integrated trade or business. The acquiring corporation must choose a principal method that is a permissible method of accounting. In general, a change to a principal method in a transaction to which section 381(a) and paragraph (a)(3) of this section apply is made under paragraph (d)(1) of this section.</P>
            <P>(3)<E T="03">Examples.</E>The following examples illustrate the rules of this paragraph (c). Unless otherwise noted, the principal method is a permissible inventory method.</P>
            
            <EXAMPLE>
              <HD SOURCE="HED">Example</HD>
              <P>(1).<E T="03">Principal methods are the methods used by the acquiring corporation</E>—<E T="01">(i)</E>
                <E T="03">Facts.</E>X Corporation and T Corporation each manufacture tennis equipment. X Corporation's manufacturing business uses the FIFO method of inventory identification, the cost method of valuing inventories, and allocates indirect costs to the property produced using the burden rate method provided in § 1.263A-1(f)(3)(i). T Corporation's manufacturing business uses the LIFO method of inventory identification, the cost method of valuing its inventories, and allocates indirect costs to the property it produces using the standard cost method provided in § 1.263A-1(f)(3)(ii). X Corporation acquires the inventory of T Corporation in a transaction to which section 381(a) applies. The fair market value of each particular type of goods held by X Corporation's manufacturing business immediately prior to the date of distribution or transfer exceeds the fair market value of each particular type of goods held by T Corporation's manufacturing business on that date. After the date of distribution or transfer, X Corporation will not operate its manufacturing business as a trade or business that is separate and distinct from T Corporation's manufacturing business.</P>
              <P>(ii)<E T="03">Conclusion.</E>Because after the date of distribution or transfer X Corporation will not operate its manufacturing business as a separate and distinct trade or business, X Corporation must use the principal methods under paragraph (a)(3) of this section, unless either the principal methods are impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the principal methods in accordance with paragraph (a)(5) of this section. The fair market value of each particular type of goods held by T Corporation's manufacturing business immediately prior to the date of distribution or transfer does not exceed the fair market value of each particular type of goods held by X Corporation's manufacturing business on that date. Because on the date of distribution or transfer T Corporation's manufacturing business does not hold more inventory than X Corporation's manufacturing business, the principal methods are the FIFO method of inventory identification, the cost method of valuation, and X Corporation's method of allocating indirect costs under section 263A using the burden rate method. X Corporation need not secure the Commissioner's consent to use these methods. However, in accordance with paragraph (d)(1) of this section, X Corporation must change the inventory methods for the manufacturing business acquired from T Corporation to the principal methods.</P>
              <P>
                <E T="03">Example</E>(2).<E T="03">Principal methods are the methods used by the acquiring corporation</E>—(i)<E T="03">Facts.</E>The facts are the same as in<E T="03">Example</E>(1), except that the fair market value of each particular type of goods held by X Corporation's manufacturing business immediately prior to the date of distribution or transfer is identical to the fair market value of each particular type of goods held by T Corporation's manufacturing business on that date.</P>
              <P>(ii)<E T="03">Conclusion.</E>The result is the same as in<E T="03">Example</E>(1). The principal methods are the FIFO method of inventory identification, the cost method of valuation, and X Corporation's method of allocating indirect costs under section 263A using the burden rate method. X Corporation need not secure the Commissioner's consent to use the principal methods. However, in accordance with paragraph (d)(1) of this section, X Corporation must change the inventory methods for the manufacturing business acquired from T Corporation to the principal methods.</P>
              <P>
                <E T="03">Example</E>(3).<E T="03">Principal methods are the methods used by the distributor or transferor corporation—</E>(i)<E T="03">Facts.</E>The facts are the same as in<E T="03">Example</E>(1), except that the fair market value of each particular type of goods held by T Corporation's manufacturing business immediately prior to the date of distribution or transfer exceeds the fair market value of each particular type of goods held by X Corporation's manufacturing business on that date.</P>
              <P>(ii)<E T="03">Conclusion.</E>Because after the date of distribution or transfer X Corporation will not operate its manufacturing business as a separate and distinct trade or business, X Corporation must use the principal methods under paragraph (a)(3) of this section, unless either the principal methods are impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the principal methods in accordance with paragraph (a)(5) of this section. The fair market value of each particular type of goods held by T Corporation's manufacturing business immediately prior to the date of distribution or transfer exceeds the fair market value of each particular type of goods held by X Corporation's manufacturing business on that date. Because on the date of distribution or transfer T Corporation's manufacturing business holds more inventory than X Corporation's manufacturing business, the principal methods are the LIFO method of inventory identification, the cost method of valuation, and T Corporation's method of allocating indirect costs under section 263A using the standard cost method. X Corporation need not secure the Commissioner's consent to use the principal methods. However, in accordance with paragraph (d)(1) of this section, X Corporation must change the inventory methods for the manufacturing business operated by X Corporation prior to the date of distribution or transfer to the principal methods.</P>
              <P>
                <E T="03">Example</E>(4).<E T="03">Voluntary change allowable</E>—(i)<E T="03">Facts.</E>The facts are the same as in<E T="03">Example</E>(1), except that T Corporation wants to discontinue using the LIFO method for its manufacturing business and change to the FIFO method for the taxable year in which the section 381(a) transaction occurs or is expected to occur.</P>
              <P>(ii)<E T="03">Conclusion.</E>Under paragraph (a)(5) of this section, the Commissioner will grant a request to change a method of accounting for the taxable year that includes the date of distribution or transfer only if the requested method is the method that the acquiring corporation must use after the date of distribution or transfer. The Commissioner will consent to a request by T Corporation to change to the FIFO method for the taxable year in which the section 381(a) transaction occurs or is expected to occur because X Corporation will use this method after the date of distribution or transfer.</P>
              <P>
                <E T="03">Example</E>(5).<E T="03">Principal method determination when larger component trade or business does not have a method of<PRTPAGE P="45685"/>accounting for a particular type of goods</E>—(i)<E T="03">Facts.</E>The facts are the same as in<E T="03">Example</E>(1), except that T Corporation's manufacturing business has a particular type of goods that is not held by X Corporation's manufacturing business.</P>
              <P>(ii)<E T="03">Conclusion.</E>The result is similar to<E T="03">Example</E>(1). In general, the principal methods are the FIFO method of inventory identification, the cost method of valuation, and X Corporation's method of allocating indirect costs to the property produced using the burden rate method. X Corporation need not secure the Commissioner's consent to use the principal methods. However, in accordance with paragraph (d)(1) of this section, X Corporation must change the inventory methods for the manufacturing business acquired from T Corporation to the principal methods. Under paragraph (c) of this section, the principal methods for the particular type of goods held only by T Corporation's manufacturing business are the LIFO method of inventory identification, the cost method of valuation, and T Corporation's method of allocating indirect costs to the property it produces using the standard cost method. X Corporation must determine whether the principal methods for the type of goods previously held by T Corporation are permissible given that such methods are different than the principal methods that must be used by X for all other goods. If X Corporation's use of the standard cost method would be impermissible after the date of distribution or transfer, X Corporation must change to a permissible method under section 263A for those goods in accordance with paragraph (a)(4) of this section.</P>
              <P>
                <E T="03">Example</E>(6).<E T="03">Inventory convention elected—</E>(i)<E T="03">Facts.</E>X Corporation manufactures planes and T Corporation manufactures planes and communications satellites. X Corporation's manufacturing business uses the FIFO method of inventory identification and values its inventories at cost or market, whichever is lower, while T Corporation's manufacturing business uses the LIFO method of inventory identification and values its inventories at cost. X Corporation's manufacturing business and T Corporation's manufacturing business, use the same methods to capitalize costs under section 263A. X Corporation acquires the inventory of T Corporation in a transaction to which section 381(a) applies. In lieu of determining the fair market value of each particular type of goods held on the date of distribution or transfer, X Corporation elects to value the entire inventories of its manufacturing business and the entire inventories of T Corporation's manufacturing business in accordance with paragraph (c)(1) of this section. The fair market value of the inventory held by T Corporation's manufacturing business immediately prior to the date of distribution or transfer does not exceed the fair market value of the inventory held by X Corporation's manufacturing business on that date. After the date of distribution or transfer, X Corporation will not operate its manufacturing business as a trade or business that is separate and distinct from T Corporation's manufacturing business.</P>
              <P>(ii)<E T="03">Conclusion.</E>Because after the date of distribution or transfer X Corporation will not operate its manufacturing business as a separate and distinct trade or business, X Corporation must use the principal methods under paragraph (a)(3) of this section, unless either the principal methods are impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the principal methods in accordance with paragraph (a)(5) of this section. The fair market value of the entire inventory held by T Corporation's manufacturing business immediately prior to the date of distribution or transfer does not exceed the fair market value of the entire inventory of X Corporation's manufacturing business on that date. Because on the date of distribution or transfer T Corporation's manufacturing business does not hold more inventory than X Corporation's manufacturing business, the principal methods are the FIFO method, the cost or market, whichever is lower, method of valuation, and X Corporation's method of capitalizing costs under section 263A on the date of distribution or transfer. X Corporation need not secure the Commissioner's consent to use the principal methods. However, in accordance with paragraph (d)(1) of this section, X Corporation must change the inventory methods for the manufacturing business acquired from T Corporation to the principal methods.</P>
              <P>
                <E T="03">Example</E>(7).<E T="03">Principal method determination with a combined trade or business and a separate and distinct trade or business</E>—(i)<E T="03">Facts.</E>X Corporation manufactures tennis equipment in a trade or business that is separate and distinct from its trade or business of manufacturing golf equipment. X Corporation uses the FIFO method of inventory identification for its tennis equipment and the LIFO method of inventory identification for its golf equipment. X Corporation values the goods in both inventories at cost and allocates indirect costs to the property produced using the burden rate method provided in § 1.263A-1(f)(3)(i). T Corporation manufactures tennis equipment. T Corporation's manufacturing business uses the FIFO method of inventory identification, values inventories at cost, and allocates indirect costs to the property it produces using the standard cost method provided in § 1.263A-1(f)(3)(ii). X Corporation acquires the inventory of T Corporation in a transaction to which section 381(a) applies. Immediately prior to the date of distribution or transfer, the fair market value of T Corporation's inventories in the tennis equipment manufacturing business exceeds the fair market value of the inventories held by X Corporation's tennis equipment manufacturing business. After the date of distribution or transfer, X Corporation will not operate its tennis equipment manufacturing business as a trade or business that is separate and distinct from T Corporation's tennis equipment manufacturing business, but X Corporation will operate its golf equipment manufacturing business as a trade or business that is separate and distinct from the tennis equipment manufacturing business.</P>
              <P>(ii)<E T="03">Conclusion.</E>Because after the date of distribution or transfer X Corporation will not operate its tennis equipment manufacturing business as a separate and distinct trade or business, X Corporation must use the principal methods under paragraph (a)(3) of this section, unless either the principal methods are impermissible and must be changed under paragraph (a)(4) of this section or X Corporation changes the principal methods in accordance with paragraph (a)(5) of this section. Under paragraph (c)(1) of this section, X Corporation elects to compare the fair market values of the entire inventories of the component trades or businesses on the date of distribution or transfer to determine whether T Corporation holds more inventory than X Corporation. The fair market value of the inventory held by T Corporation's tennis equipment manufacturing business exceeds the fair market value of the tennis equipment held by X Corporation's tennis equipment manufacturing business. Because on the date of distribution or transfer T Corporation's tennis equipment manufacturing business holds more inventory than X Corporation's tennis equipment manufacturing business, the principal methods for the combined tennis equipment business are the FIFO method of inventory identification, the cost basis of valuation, and T Corporation's methods of allocating indirect costs under section 263A using the standard cost method provided in § 1.263A-1(f)(3)(ii). X Corporation need not secure the Commissioner's consent to use the principal methods. However, in accordance with paragraph (d)(1) of this section, X Corporation must change the methods of accounting for its tennis equipment manufacturing business to the principal methods. Under paragraph (a)(2) of this section, because X Corporation will operate the golf equipment manufacturing business as a separate trade or business, for the inventories held by the golf equipment manufacturing business X Corporation must continue to use the LIFO method of inventory identification, use the cost basis of valuation, and allocate indirect costs under section 263A using the burden rate method provided in § 1.263A-1(f)(3)(i). There are no changes in method of accounting for the golf manufacturing business, and X Corporation need not secure the Commissioner's consent to use these carryover methods.</P>
              <P>
                <E T="03">Example</E>(8).<E T="03">Principal method determination with multiple component trades or businesses</E>—(i)<E T="03">Facts.</E>The facts are the same as in<E T="03">Example</E>(7), except that after the date of distribution or transfer X Corporation will not operate the golf equipment manufacturing business as a trade or business that is separate and distinct from the tennis equipment manufacturing business. In addition, the fair market value of the inventories of X Corporation's tennis equipment manufacturing business and golf equipment manufacturing business, in the aggregate, exceed the fair market value of the inventories of T Corporation's tennis equipment manufacturing business.</P>
              <P>(ii)<E T="03">Conclusion.</E>Because on the date of distribution or transfer T Corporation's tennis equipment manufacturing business does not<PRTPAGE P="45686"/>hold more inventory than X Corporation's tennis equipment manufacturing business and golf equipment manufacturing business, in the aggregate, the principal method for identifying inventory is the method used by X Corporation's component trade or business on the date of distribution or transfer. However, because on the date of distribution or transfer X Corporation operates two separate and distinct trades or businesses with different inventory identification methods that will be combined after the date of distribution or transfer, X Corporation may choose under paragraph (c)(2) of this section which method used by its component trades or businesses will be the principal method. After the date of distribution or transfer, X Corporation may use either the FIFO method of inventory identification used by the tennis equipment manufacturing business or the LIFO method of inventory identification used by the golf equipment manufacturing business as the principal method of identification, if either method is a permissible method. For the integrated trade or business, X Corporation will use the cost method of valuation and allocate indirect costs under section 263A using the burden rate method provided in § 1.263A-1(f)(3)(i). In accordance with paragraph (d)(1) of this section, X Corporation must change the inventory methods of T Corporation's manufacturing business to the principal methods. Under paragraph (a)(3) of this section, X Corporation also must change either its golf equipment manufacturing business or its tennis equipment manufacturing business, depending on which principal method X Corporation selects, to the principal method.</P>
            </EXAMPLE>
            
            <P>(d)<E T="03">Procedures for changing a method of accounting</E>—(1)<E T="03">Change made to principal method under paragraph (a)(3) of this section</E>—(i)<E T="03">Section 481(a) adjustment</E>—(A)<E T="03">In general.</E>An acquiring corporation that changes its method of accounting or the distributor or transferor corporation's method of accounting under paragraph (a)(3) of this section does not need to secure the Commissioner's consent to use a principal method. To the extent the use of a principal method constitutes a change in method of accounting, the change in method is treated as a change initiated by the acquiring corporation for purposes of section 481(a)(2). Any change to a principal method, whether the change relates to a trade or business of the acquiring corporation or a trade or business of the distributor or transferor corporation, must be reflected on the acquiring corporation's federal income tax return for the taxable year that includes the date of distribution or transfer. The amount of the section 481(a) adjustment and the adjustment period, if any, necessary to implement a change to the principal method are determined under § 1.446-1(e) and the applicable administrative procedures that govern voluntary changes in methods of accounting under section 446(e). If the Internal Revenue Code, the Income Tax Regulations, or administrative procedures require that a method of accounting be implemented on a cut-off basis, the acquiring corporation must implement the change, on a cut-off basis as of the date of distribution or transfer, on its federal income tax return for the taxable year that includes the date of distribution or transfer. If the Internal Revenue Code, the Income Tax Regulations, or administrative procedures require a section 481(a) adjustment, the acquiring corporation must determine the section 481(a) adjustment and include the appropriate amount of the section 481(a) adjustment on its federal income tax return for the taxable year that includes the date of distribution or transfer and subsequent taxable year(s), as necessary. This adjustment is determined by the acquiring corporation as of the beginning of the day that is immediately after the date of distribution or transfer.</P>
            <P>(B)<E T="03">Example.</E>The following example illustrates the rules of this paragraph (d)(1)(i):</P>
            
            <EXTRACT>
              <P>
                <E T="03">Example.</E>X Corporation uses the FIFO method of inventory identification, and T Corporation uses the LIFO method of inventory identification. X Corporation acquires the inventory of T Corporation in a transaction to which section 381(a) applies. X Corporation determines that under the rules of paragraph (c)(1) of this section, X Corporation must change the inventory method for the business acquired from T Corporation to the FIFO method. X Corporation will determine the section 481(a) adjustment pertaining to the change to the FIFO method (whether the amounts thereof represent increases or decreases in income) as of the beginning of the day that immediately follows the day on which X Corporation acquires the inventory of T Corporation. X Corporation will reflect this adjustment, or an appropriate part thereof, on its federal income tax return for the taxable year that includes the date of distribution or transfer.</P>
            </EXTRACT>
            
            <P>(ii)<E T="03">Audit protection.</E>Notwithstanding any other provision in any other Income Tax Regulation or administrative procedure, no audit protection is provided for any change in method of accounting under paragraph (d)(1) of this section.</P>
            <P>(iii)<E T="03">Other terms and conditions.</E>Except as otherwise provided in this section, other terms and conditions provided in § 1.446-1(e) and the applicable administrative procedures for voluntary changes in method of accounting under section 446(e) apply to a change in method of accounting under this section. Thus, for example, if the administrative procedures for a particular change in method of accounting have a term and condition that provides for the acceleration of the section 481(a) adjustment period, this term and condition applies to a change made under this paragraph (d)(1). However, any scope limitation in the applicable administrative procedures will not apply for purposes of making a change under this paragraph (d)(1). For example, if the administrative procedures provide as a limitation that an identical change in method of accounting is barred for a period of years, this limitation will not bar a change to the principal method made under this section.</P>
            <P>(2)<E T="03">Change made to a method of accounting under paragraph (a)(4) or (a)(5) of this section</E>—(i)<E T="03">In general.</E>A party to a section 381(a) transaction that changes a method of accounting under either paragraph (a)(4) or paragraph (a)(5) of this section must follow the provisions of § 1.446-(1)(e) and the applicable administrative procedures, including scope limitations, for voluntary changes in method of accounting under section 446(e), except as provided in paragraphs (d)(2)(ii) and (d)(2)(iii) of this section. An application on Form 3115, “Application for Change in Accounting Method,” filed with the IRS to change a method of accounting under this paragraph (d)(2) should be labeled “Filed under section 381(c)(5)” at the top.</P>
            <P>(ii)<E T="03">Final year limitation.</E>Any scope limitation relating to the final year of a trade or business will not apply to a taxpayer that changes its method of accounting in the final year of a trade or business that is terminated as the result of a section 381(a) transaction.</P>
            <P>(iii)<E T="03">Time to file.</E>Under the authority of § 1.446-1(e)(3)(ii), for a change in method of accounting requiring advance consent, the application for a change in method of accounting (for example, Form 3115), must be filed with the IRS on or before the later of—</P>
            <P>(A) The due date for filing a Form 3115 as specified in § 1.446-1(e), for example, the last day of the taxable year in which the distribution or transfer occurred, or</P>
            <P>(B) The earlier of—</P>
            <P>(<E T="03">1</E>) The day that is 180 days after the date of distribution or transfer, or</P>
            <P>(<E T="03">2</E>) The day on which the acquiring corporation files its federal income tax return for the taxable year in which the distribution or transfer occurred.</P>
            <P>(e)<E T="03">Rules and procedures</E>—(1)<E T="03">Inventory method selected for a particular type of goods.</E>If other sections of the Internal Revenue Code or Income Tax Regulations allow a taxpayer to elect an inventory method for a particular type of goods, the<PRTPAGE P="45687"/>method elected with respect to those goods is the established inventory method only for those goods. For example, an election to use the LIFO inventory method to identify specified goods in inventory, such as certain products in finished goods, is the inventory method only for those products.</P>
            <P>(2)<E T="03">No method of accounting.</E>If a party to a section 381(a) transaction is not using an inventory method, does not have an inventory method for a particular type of goods, or came into existence as a result of the transaction, the party will not be treated as having an inventory method different from that used by another party to the section 381(a) transaction.</P>
            <P>(3)<E T="03">Elections and adoptions allowed.</E>If an election does not require the Commissioner's consent, an acquiring corporation or a distributor or transferor corporation is not precluded from making any election that is otherwise permissible for the taxable year that includes the date of distribution or transfer. For example, an acquiring corporation may elect to identify its inventory using the LIFO inventory method in the year of the distribution or transfer. For purposes of this section, a corporation shall be deemed as having made any election as of the first day of the taxable year that includes the date of distribution or transfer. Similarly, where adoption is permissible, an acquiring corporation or a distributor or transferor corporation may adopt any permissible method of accounting for the taxable year that includes the date of distribution or transfer.</P>
            <P>(4)<E T="03">Elections continue after section 381(a) transaction</E>—(i)<E T="03">General rule.</E>An acquiring corporation is not required to renew any election not requiring renewal and previously made by it or by a distributor or transferor corporation for a carryover method or a principal method if the acquiring corporation uses the method after the section 381(a) transaction. If the acquiring corporation uses a method after the date of distribution or transfer, an election made by the acquiring corporation or by a distributor or transferor corporation for that method that was in effect on the date of distribution or transfer continues after the section 381(a) transaction as though the distribution or transfer had not occurred.</P>
            <P>(ii)<E T="03">Example.</E>The following example illustrates the rules of paragraph (e)(4):</P>
            
            <EXAMPLE>
              <HD SOURCE="HED">Example.</HD>
              <P>Since its incorporation in 1982, X Corporation elected to use the LIFO inventory method under section 472 to identify its inventory of tennis balls. Since its incorporation in 2002, T Corporation elected to use the FIFO inventory method to identify its inventory of tennis balls. X Corporation acquires the assets of T Corporation in a transaction to which section 381(a) applies. Immediately prior to the date of distribution or transfer, the fair market value of X Corporation's inventory in its tennis balls exceeds the fair market value of the tennis balls inventory held by T Corporation. After the date of distribution or transfer, X Corporation will not operate its business as a trade or business that is separate and distinct from T Corporation's business. Because on the date of distribution or transfer T Corporation does not hold more inventory than X Corporation, the principal method for identifying inventory is the method used by X Corporation on the date of distribution or transfer. After the date of distribution or transfer, X Corporation need not renew its election to identify inventory using the LIFO inventory method, and X Corporation is bound by the election.</P>
            </EXAMPLE>
            
            <P>(5)<E T="03">Adopting the LIFO inventory method.</E>A party to a section 381(a) transaction will be deemed to be using the LIFO inventory method for a particular type of goods on the date of distribution or transfer if that party elects under section 472 to adopt that inventory method with respect to those goods for its taxable year within which the date of distribution or transfer occurs. See section 472 for the requirements to adopt the LIFO inventory method.</P>
            <P>(6)<E T="03">Inventory layers treatment</E>—(i)<E T="03">Adjustments required after a section 381(a) transaction.</E>An acquiring corporation that determines the principal method of taking an inventory after a section 381(a) transaction under paragraphs (a)(3) and (c) of this section after the date of distribution or transfer may need to integrate inventories and make appropriate adjustments as provided in paragraphs (e)(6)(ii) and (e)(6)(iii) of this section.</P>
            <P>(ii)<E T="03">LIFO inventory method used after the section 381(a) transaction</E>—(A)<E T="03">LIFO inventory method used by the acquiring corporation and the distributor or transferor corporation</E>—(<E T="03">1</E>)<E T="03">Principal method is the dollar-value LIFO method.</E>If, under paragraphs (a)(3) and (c) of this section, the acquiring corporation changes its inventory method or the inventory method of the distributor or transferor corporation from the specific goods LIFO method of pricing inventories to the dollar-value LIFO method of pricing inventories (dollar-value LIFO method) for a particular type of goods, the inventory accounted for under the specific goods method shall be placed on the dollar-value method as provided in § 1.472-8(f), and then the inventory shall be integrated with the inventory previously accounted for under the dollar-value LIFO method. If pools of each corporation are permitted or required to be combined, the pools must be combined as provided in § 1.472-8(g)(2). For purposes of combining pools, all base year inventories or layers of increment that occur in taxable years including the same December 31 shall be combined. A base year inventory or layer of increment occurring in any short taxable year of a distributor or transferor corporation shall be merged with and considered a layer of increment of its immediately preceding taxable year.</P>
            <P>(<E T="03">2</E>)<E T="03">Principal method is the specific goods LIFO method.</E>If, under paragraphs (a)(3) and (c) of this section, the acquiring corporation changes its inventory method or the inventory method of the distributor or transferor corporation from the dollar-value LIFO method of pricing inventories to the specific goods LIFO method of pricing inventories, the acquiring corporation shall treat the inventory being changed to the specific goods LIFO method as having the same acquisition dates and costs as such inventory had under the dollar-value LIFO method.</P>
            <P>(B)<E T="03">Change from the FIFO inventory method to either the specific goods LIFO method or the dollar-value LIFO method.</E>If, under paragraphs (a)(3) and (c) of this section, the acquiring corporation changes its inventory method or the inventory method of the distributor or transferor corporation from the FIFO inventory method to either the specific goods LIFO method or the dollar-value method of pricing LIFO inventories, the inventory accounted for under the FIFO inventory method shall be treated by the acquiring corporation as having been acquired at their average unit cost in a single transaction on the date of the distribution or transfer. Thus, if an inventory of a particular type of goods is combined in an existing dollar-value pool, the goods shall be treated as if they were purchased by the acquiring corporation at the average unit cost on the date of the distribution or transfer with respect to such pool. Alternatively, if the goods are not combined in an existing pool, the goods will be treated as if they were purchased by the acquiring corporation at the average unit cost on the date of the distribution or transfer with respect to a new pool, with the base-year being the year of the section 381(a) transaction. Adjustments resulting from a restoration to cost of any write-down to market value of the inventories shall be taken into account by the acquiring corporation ratably in each of the three taxable years beginning with the taxable year that includes the<PRTPAGE P="45688"/>date of the distribution or transfer. See section 472(d).</P>
            <P>(iii)<E T="03">FIFO inventory method used after the section 381(a) transaction</E>—(A)<E T="03">FIFO inventory method used by the acquiring corporation and the distributor or transferor corporation.</E>If, under paragraphs (a)(3) and (c) of this section, the FIFO inventory method is the principal method and the component trades or businesses of both the acquiring corporation and the distributor or transferor corporation use the FIFO method immediately prior to the distribution or transfer, the acquiring corporation must treat the inventory that must change to the principal method as having the same acquisition dates and costs as such inventory had immediately prior to the date of distribution or transfer. However, if the principal method of valuing inventories is the cost or market, whichever is lower, method, the acquiring corporation must treat the inventories that must change to the principal method as having been acquired at cost or market, whichever is lower.</P>
            <P>(B)<E T="03">Change from either the specific goods LIFO method or the dollar-value LIFO method to the FIFO inventory method.</E>If, under paragraphs (a)(3) and (c) of this section, the acquiring corporation changes its inventory method or the inventory method of the distributor or transferor corporation from either the specific goods LIFO method or the dollar-value LIFO method to the FIFO inventory method, the acquiring corporation must treat the inventory accounted for under the LIFO method as having the same acquisition dates and costs that the inventory would have had if the FIFO inventory method had been used on the date of distribution or transfer. However, if the principal method of valuing inventories is the cost or market, whichever is lower, method, the acquiring corporation must treat the inventories accounted for under the LIFO method as having been acquired at cost or market, whichever is lower.</P>
            <P>(7)<E T="03">Appropriate times for certain determinations</E>—(i)<E T="03">Determining the inventory method.</E>The inventory method used by a party to a section 381(a) transaction on the date of distribution or transfer is the method used by that party as of the end of the day that is immediately prior to the date of distribution or transfer.</P>
            <P>(ii)<E T="03">Determining whether there are separate and distinct trades or businesses after the date of distribution or transfer.</E>Whether an acquiring corporation will operate the trades or businesses of the parties to a section 381(a) transaction as separate and distinct trades or businesses after the date of distribution or transfer will be determined as of the date of distribution or transfer based upon the facts and circumstances. Intent to combine books and records of the trades or businesses may be demonstrated by contemporaneous records and documents or by other objective evidence that reflects the acquiring corporation's ultimate plan of operation, even though the actual combination of the books and records may extend beyond the end of the taxable year that includes the date of distribution or transfer.</P>
            <P>(8)<E T="03">Establishing an inventory method.</E>An inventory method used by the distributor or transferor corporation immediately prior to the date of distribution or transfer that continues to be used by the acquiring corporation after the date of distribution or transfer is an established method of accounting for purposes of section 446(e), whether or not such method is proper or is permitted under the Internal Revenue Code or any applicable Income Tax Regulations.</P>
            <P>(9)<E T="03">Other applicable provisions.</E>This section does not preempt any other provision of the Internal Revenue Code or the Income Tax Regulations that is applicable to the acquiring corporation's circumstances. Section 381(c)(5) and this § 1.381(c)(5)-1 determine only the inventory method to be used after a section 381(a) transaction. If other paragraphs of section 381(c) apply for purposes of determining the methods of accounting to be used following the date of distribution or transfer, section 381(c)(5) and this § 1.381(c)(5)-1 will not apply to the tax treatment of the items. Specifically, section 381(c)(5) and this § 1.381(c)(5)-1 do not apply to assets other than inventory that an acquiring corporation obtains in a transaction to which section 381(a) applies.</P>
            <P>(10)<E T="03">Use of the cash receipts and disbursements method of accounting.</E>If immediately prior to the date of distribution or transfer, an acquiring corporation or a distributor or transferor corporation uses the cash receipts and disbursements method of accounting within the meaning of section 446(c)(1) and § 1.446-1(c)(1)(i), or is not required to use an inventory method for its goods, section 381(c)(5) and § 1.381(c)(5)-1 do not apply. Instead, section 381(c)(4) and § 1.381(c)(4)-1 must be applied to determine the methods of accounting that continue after the transaction.</P>
            <P>(11)<E T="03">Character of items of income and deduction.</E>After the date of distribution or transfer, items of income and deduction have the same character in the hands of the acquiring corporation as they would have had in the hands of the distributor or transferor corporation if no distribution or transfer had occurred.</P>
            <P>(12)<E T="03">Impermissible inventory method.</E>This section does not limit the Commissioner's ability under section 446(b) to determine whether a taxpayer's inventory method is an impermissible method or otherwise fails to clearly reflect income. For example, an acquiring corporation may not use the method of accounting determined under paragraph (a)(2) of this section if the method fails to clearly reflect the acquiring corporation's income within the meaning of section 446(b).</P>
            <P>(f)<E T="03">Effective/applicability date.</E>This section applies to corporate reorganizations and tax-free liquidations described in section 381(a) that occur on or after August 31, 2011.</P>
          </SECTION>
        </REGTEXT>
        <REGTEXT PART="1" TITLE="26">
          <AMDPAR>
            <E T="04">Par. 5.</E>Section 1.446-1 is amended by:</AMDPAR>
          <AMDPAR>1. Revising the first sentence and adding a second new sentence in paragraph (e)(3)(i).</AMDPAR>
          <AMDPAR>2. Revising the first sentence in paragraph (e)(4)(i).</AMDPAR>
          <AMDPAR>3. Adding paragraph (e)(4)(iii).</AMDPAR>
          <P>The revisions and addition read as follows:</P>
          <SECTION>
            <SECTNO>§ 1.446-1</SECTNO>
            <SUBJECT>General rule for methods of accounting.</SUBJECT>
            <STARS/>
            <P>(e) * * *</P>
            <P>(3)(i) Except as otherwise provided under the authority of paragraph (e)(3)(ii) of this section, to secure the Commissioner's consent to a taxpayer's change in method of accounting the taxpayer generally must file an application on Form 3115, “Application for Change in Accounting Method,” with the Commissioner during the taxable year in which the taxpayer desires to make the change in method of accounting. See §§ 1.381(c)(4)-1(d)(2) and 1.381(c)(5)-1(d)(2) for rules allowing additional time, in some circumstances, for the filing of an application on Form 3115 with respect to a transaction to which section 381(a) applies. * * *</P>
            <STARS/>
            <P>(4) * * * (i) * * * Except as provided in paragraphs (e)(3)(iii), (e)(4)(ii), and (e)(4)(iii) of this section, paragraph (e) of this section applies on or after December 30, 2003. * * *</P>
            <STARS/>
            <P>(iii)<E T="03">Effective/applicability date for paragraph (e)(3)(i).</E>The rules of paragraph (e)(3)(i) of this section apply<PRTPAGE P="45689"/>to corporate reorganizations and tax-free liquidations described in section 381(a) that occur on or after August 31, 2011.</P>
          </SECTION>
        </REGTEXT>
        <SIG>
          <DATED>Approved: July 20, 2011.</DATED>
          <NAME>Steven T. Miller,</NAME>
          <TITLE>Deputy Commissioner for Services and Enforcement.</TITLE>
          <NAME>Emily S. McMahon,</NAME>
          <TITLE>Acting Assistant Secretary of the Treasury (Tax Policy).</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19256 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4830-01-P</BILCOD>
    </RULE>
    <RULE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF THE TREASURY</AGENCY>
        <SUBAGY>Financial Crimes Enforcement Network</SUBAGY>
        <CFR>31 CFR Part 1010</CFR>
        <RIN>RIN 1506-AA82</RIN>
        <SUBJECT>Financial Crimes Enforcement Network; Repeal of the Final Rule and Withdrawal of the Finding of Primary Money Laundering Concern Against VEF Banka</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Financial Crimes Enforcement Network (“FinCEN”), Treasury.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Final rule.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>This document repeals FinCEN's final rule, “Imposition of Special Measure Against VEF Banka” of July 13, 2006, and withdraws the finding of VEF Banka as a Financial Institution of Primary Money Laundering Concern of April 26, 2005, issued pursuant to 31 U.S.C. 5318A of the Bank Secrecy Act (the “BSA”).</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>
            <E T="03">Effective Date:</E>August 1, 2011.</P>
        </EFFDATE>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Regulatory Policy and Programs Division, Financial Crimes Enforcement Network, (800) 949-2732 and select Option 1.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">I. Background</HD>
        <HD SOURCE="HD2">A. Statutory Provisions</HD>
        <P>On October 26, 2001, the President signed into law the Uniting and Strengthening America by Providing Appropriate Tools Required to Intercept and Obstruct Terrorism Act of 2001, Public Law 107-56 (“USA PATRIOT Act”). Title III of the USA PATRIOT Act amends the anti-money laundering provisions of the BSA, codified at 12 U.S.C. 1829b, 12 U.S.C. 1951-1959, and 31 U.S.C. 5311-5314 and 5316-5332, to promote the prevention, detection, and prosecution of money laundering and the financing of terrorism. Regulations implementing the BSA appear at 31 CFR Chapter X.<SU>1</SU>
          <FTREF/>The authority of the Secretary of the Treasury (the “Secretary”) to administer the BSA and its implementing regulations has been delegated to the Director of the Financial Crimes Enforcement Network.<SU>2</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>1</SU>On October 26, 2010, FinCEN issued a final rule creating a new Chapter X in Title 31 of the Code of Federal Regulations for the BSA regulations. See 75 FR 65806 (October 26, 2010) (Transfer and Reorganization of Bank Secrecy Act Regulations Final Rule) (referred to herein as the “Chapter X Final Rule”). The Chapter X Final Rule became effective on March 1, 2011.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>2</SU>Therefore, references to the authority of the Secretary under section 311 of the USA PATRIOT Act apply equally to the Director of the Financial Crimes Enforcement Network.</P>
        </FTNT>
        <P>Section 311 of the USA PATRIOT Act (“section 311”) added Section 5318A to the BSA, granting the Secretary the authority, upon finding that reasonable grounds exist for concluding that a foreign jurisdiction, foreign financial institution, class of international transactions, or type of account is of “primary money laundering concern,” to require domestic financial institutions and domestic financial agencies to take certain “special measures” against the primary money laundering concern.<SU>3</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>3</SU>Available special measures include requiring: (1) Recordkeeping and reporting of certain financial transactions; (2) collection of information relating to beneficial ownership; (3) collection of information relating to certain payable-through accounts; (4) collection of information relating to certain correspondent accounts; and (5) prohibition or conditions on the opening or maintaining of correspondent or payable-through accounts. 31 U.S.C. 5318A(b)(1)-(5). For a complete discussion of the range of possible countermeasures, see 68 FR 18917 (April 17, 2003) (proposing to impose special measures against Nauru).</P>
        </FTNT>
        <P>Taken as a whole, Section 5318A provides the Secretary with a range of options that can be adapted to target specific money laundering and terrorist financing concerns most effectively. These options provide the authority to bring additional and useful pressure on those jurisdictions and institutions that pose money-laundering threats and the ability to take steps to protect the U.S. financial system. Through the imposition of various special measures, FinCEN can: gain more information about the concerned jurisdictions, financial institutions, transactions, and accounts; monitor more effectively the respective jurisdictions, financial institutions, transactions, and accounts; and, ultimately, protect U.S. financial institutions from involvement with jurisdictions, financial institutions, transactions, or accounts that pose a money laundering concern.</P>
        <HD SOURCE="HD2">B. VEF Banka</HD>
        <P>At the time of issuance of the final rule on July 13, 2006, VEF Banka was headquartered in Riga, Latvia. VEF Banka was one of the smallest of Latvia's 23 banks, and, in 2004, was reported to have approximately $80 million in assets and 87 employees. Total assets for the bank, as of June 30, 2005, were 27.3 million LATS, equivalent to approximately $47.4 million. VEF Banka had one subsidiary, Veiksmes līzings, which offered financial leasing and factoring services. In addition to its headquarters in Riga, VEF Banka had one branch in Riga and one representative office in the Czech Republic. VEF Banka offered corporate and private banking services, issued credit cards for non-Latvians, and provided currency exchange through Internet banking services (i.e., virtual currencies). In addition, according to its financial statements, VEF Banka maintained correspondent accounts in countries worldwide, but reported none in the United States at the time of the final rule.</P>
        <HD SOURCE="HD1">II. The Finding, Final Rule, and Subsequent Developments</HD>
        <HD SOURCE="HD2">A. The Finding and Final Rule</HD>
        <P>Based upon review and analysis of relevant information, consultations with relevant Federal agencies and departments, and after consideration of the factors enumerated in section 311, the Secretary, through his delegate, the Director of FinCEN, found that reasonable grounds existed for concluding that VEF Banka was a financial institution of primary money laundering concern. This finding was published on April 26, 2005,<SU>4</SU>
          <FTREF/>in a notice of proposed rulemaking which proposed prohibiting covered financial institutions from, directly or indirectly, opening or maintaining correspondent accounts in the United States for VEF Banka or any of its branches, offices, or subsidiaries, pursuant to the authority under 31 U.S.C. 5318A. The notice of proposed rulemaking outlined the various factors supporting the finding and proposed prohibition.</P>
        <FTNT>
          <P>
            <SU>4</SU>
            <E T="03">See</E>70 FR 21369 (April 26, 2005, RIN 1506-AA82).</P>
        </FTNT>
        <P>After consulting with required Federal agencies and parties, reviewing public comments received from the April 26, 2005 notice of proposed rulemaking, and considering additional relevant factors, FinCEN issued a final rule on July 13, 2006 that imposed the special measure authorized under 31 U.S.C. 5318A(b)(5) against VEF Banka.<SU>5</SU>

          <FTREF/>This final rule requires covered financial institutions to terminate any correspondent or payable-through<PRTPAGE P="45690"/>accounts for, or on behalf of, VEF Banka, and to apply due diligence reasonably designed to guard against indirect use of their correspondent or payable-through accounts by VEF Banka.</P>
        <FTNT>
          <P>
            <SU>5</SU>
            <E T="03">See</E>71 FR 39554 (July 13, 2006, RIN 1506-AA82).</P>
        </FTNT>
        <HD SOURCE="HD2">B. VEF Banka's Subsequent Developments</HD>
        <P>On May 26, 2010, VEF Banka's Latvian banking regulator, the Financial and Capital Market Commission (the “FCMC”), revoked VEF Banka's operating license on the grounds that the shareholders of the bank had not received authorization from the FCMC for the acquisition of qualifying holdings and the bank failed to ensure compliance with provisions of the Credit Institution Law.<SU>6</SU>
          <FTREF/>As a result, the shareholders had no decision-making rights and were unable to “ensure prudent bank operations.” The FCMC's decision to revoke VEF Banka's license was confirmed by the Senate of Latvia's Supreme Court on July 22, 2010 and terminated VEF Banka's ability to operate as a financial institution under Latvian law.<SU>7</SU>
          <FTREF/>On November 15, 2010, the Riga District Court issued a non-appealable order to begin liquidating the bank.<SU>8</SU>
          <FTREF/>The liquidation process is expected to be complete in one to two years and will result in the disposition of all of VEF Banka's assets, including its subsidiary, Veiksmes līzings.</P>
        <FTNT>
          <P>

            <SU>6</SU>“On Withdrawal of the JSC `VEF Banka's' Operating Licence,” Financial Capital Market Commission press release, May 26, 2010 (<E T="03">http://www.fktk.lv/en/publications/press_releases/2010-05-29_on_withdrawal_of_the_jsc/</E>)</P>
        </FTNT>
        <FTNT>
          <P>

            <SU>7</SU>“VEF Bank Loses License,” The Baltic Times, July 28, 2010 (<E T="03">http://www.baltictimes.com/news/articles/26661/</E>).</P>
        </FTNT>
        <FTNT>
          <P>

            <SU>8</SU>“Court Rule for Liquidation of VEF Banka,” The Baltic Course, November 16, 2010 (<E T="03">http://www.baltic-course.com/eng/finances/?doc=33962&amp;underline=vef+banka</E>).</P>
        </FTNT>
        <HD SOURCE="HD1">III. Withdrawal of the Finding of Primary Money Laundering Concern Against VEF Banka and Repeal of the Final Rule</HD>

        <P>For the reasons set forth above, FinCEN hereby withdraws the finding of primary money laundering concern against VEF Banka, as published in the<E T="04">Federal Register</E>on April 26, 2005 (70 FR 21369) and finalized on July 13, 2006 (71 FR 39554), as of August 1, 2011. As a result, FinCEN is also repealing the final rule, as published in the<E T="04">Federal Register</E>on July 13, 2006 (71 FR 39554) as 31 CFR 103.192 (now 31 CFR 1010.654), that was based upon the finding. FinCEN's withdrawal of the finding of primary money laundering concern against VEF Banka and the repeal of the related final rule do not acknowledge any remedial measure taken by VEF Banka, but are the result of the revocation of VEF Banka's Latvian banking license and the non-appealable decision by the Riga District Court to liquidate the bank.<SU>9</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>

            <SU>9</SU>The “Republic of Latvia” was described at length in the April 26, 2005 notice of proposed rulemaking, 70 FR 21369, and July 13, 2006 final rule, 71 FR 39554. Today's repeal of the final rule and withdrawal of the finding of primary money laundering concern against VEF Banka do not provide updates on jurisdictional developments. Further discussion of jurisdictional developments can be found at the U.S. Department of State's “2011 International Narcotics Control Strategy Report” (<E T="03">http://www.state.gov/p/inl/rls/nrcrpt/2011/vol2/156375.htm#latvia</E>).</P>
        </FTNT>
        <HD SOURCE="HD1">IV. Regulatory Matters</HD>
        <HD SOURCE="HD2">A. Executive Order 12866</HD>
        <P>It has been determined that this rulemaking is not a significant regulatory action for purposes of Executive Order 12866. Accordingly, a regulatory impact analysis is not required.</P>
        <HD SOURCE="HD2">B. Unfunded Mandates Reform Act of 1995</HD>
        <P>Section 202 of the Unfunded Mandates Reform Act of 1995 (“Unfunded Mandates Act”), Public Law 104-4 (March 22, 1995), requires that an agency prepare a budgetary impact statement before promulgating a rule that may result in expenditure by state, local, and tribal governments, in the aggregate, or by the private sector, of $100 million or more in any one year. If a budgetary impact statement is required, section 202 of the Unfunded Mandates Act also requires an agency to identify and consider a reasonable number of regulatory alternatives before promulgating a rule. FinCEN has determined that it is not required to prepare a written statement under Section 202 and has concluded that on balance the rule provides the most cost-effective and least burdensome alternative to achieve the objectives of the rule.</P>
        <HD SOURCE="HD2">C. Regulatory Flexibility Act</HD>

        <P>Pursuant to the Regulatory Flexibility Act (RFA) (5 U.S.C. 601<E T="03">et seq.</E>), FinCEN certifies that this final regulation likely will not have a significant economic impact on a substantial number of small entities. The regulatory changes in this final rule merely remove the current obligations for financial institutions under 31 CFR 103.192 (now 31 CFR 1010.654).</P>
        <HD SOURCE="HD2">D. Paperwork Reduction Act</HD>

        <P>This regulation discontinues the Office of Management and Budget Control Number 1506-0041 assigned to the final rule and, as a result, reduces the estimated average burden of one hour per affected financial institution, totaling 5,000 hours. This regulation contains no new information collection requirements subject to review and approval by the Office of Management and Budget under the Paperwork Reduction Act of 1995 (44 U.S.C. 3507(d)<E T="03">et seq</E>.).</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 31 CFR Part 1010</HD>
          <P>Administrative practice and procedure, Banks, banking, Brokers, Currency, Foreign banking, Foreign currencies, Gambling, Investigations, Penalties, Reporting and recordkeeping requirements, Securities, Terrorism.</P>
        </LSTSUB>
        <HD SOURCE="HD1">Authority and Issuance</HD>
        <P>For the reasons set forth above, 31 CFR part 1010 is amended as follows:</P>
        <REGTEXT PART="1010" TITLE="31">
          <PART>
            <HD SOURCE="HED">PART 1010—GENERAL PROVISIONS</HD>
          </PART>
          <AMDPAR>1. The authority citation for 31 CFR part 1010 continues to read as follows:</AMDPAR>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>12 U.S.C. 1829b and 1951-1959; 31 U.S.C. 5311-5314 and 5316-5332; title III, sec. 314, Pub. L. 107-56, 115 Stat. 307.</P>
          </AUTH>
        </REGTEXT>
        <REGTEXT PART="1010" TITLE="31">
          <SECTION>
            <SECTNO>§ 1010.654</SECTNO>
            <SUBJECT>[Removed]</SUBJECT>
          </SECTION>
          <AMDPAR>2. Part 1010 is amended by removing § 1010.654.</AMDPAR>
        </REGTEXT>
        <SIG>
          <DATED>Dated: July 22, 2011.</DATED>
          <NAME>James H. Freis, Jr.,</NAME>
          <TITLE>Director, Financial Crimes Enforcement Network.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19118 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4810-02-P</BILCOD>
    </RULE>
    <RULE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF HOMELAND SECURITY</AGENCY>
        <SUBAGY>Coast Guard</SUBAGY>
        <CFR>33 CFR Part 117</CFR>
        <DEPDOC>[Docket No. USCG-2010-1117]</DEPDOC>
        <RIN>RIN 1625-AA09</RIN>
        <SUBJECT>Drawbridge Operation Regulation; Raritan River, Arthur Kill and Their Tributaries, Staten Island, NY and Elizabeth, NJ</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Coast Guard, DHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Final rule.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>The Coast Guard has changed the drawbridge operation regulations that govern the operation of the Arthur Kill (AK) Railroad Bridge at mile 11.6, across Arthur Kill between Staten Island, New York and Elizabeth, New Jersey. This final rule provides relief to the bridge owner from crewing their bridge by allowing the bridge to be<PRTPAGE P="45691"/>operated from a remote location while continuing to meet the present and future needs of navigation.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>This rule is effective August 31, 2011.</P>
        </EFFDATE>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Comments and related materials received from the public, as well as documents mentioned in this preamble as being available in the docket, are part of docket USCG-2010-1117 and are available online by going to<E T="03">http://www.regulations.gov,</E>inserting USCG-2010-1117 in the “Keyword” box, and then clicking “Search.” This material is also available for inspection or copying at the Docket Management Facility (M-30), U.S. Department of Transportation, West Building Ground Floor, Room W12-140, 1200 New Jersey Avenue, SE., Washington, DC 20590, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>If you have questions on this rule, call or e-mail Mr. Joe Arca, Project Officer, First Coast Guard District Bridge Branch, 212-668-7165,<E T="03">joe.m.arca@uscg.mil.</E>If you have questions on viewing the docket, call Renee V. Wright, Program Manager, Docket Operations, telephone 202-366-9826.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">Regulatory Information</HD>

        <P>On March 25, 2011, we published a notice of proposed rulemaking (NPRM) entitled Drawbridge Operation Regulations Raritan River, Arthur Kill and their tributaries, in the<E T="04">Federal Register</E>(76 FR 16715). We received one comment in response to the proposed rule. No public meeting was requested, and none was held.</P>
        <HD SOURCE="HD1">Basis and Purpose</HD>
        <P>The Arthur Kill (AK) Railroad Bridge at mile 11.6, across Arthur Kill, has a vertical clearance of 31 feet at mean high water, and 35 feet at mean low water in the closed position. The existing drawbridge operating regulations are listed at 33 CFR 117.702.</P>
        <P>Beginning in 2009, Consolidated Rail Corporation (Conrail) conducted a year of successful remote operation tests of the AK Railroad Bridge without any objections from marine users. A draw operator was on scene at all times to ensure compliance with drawbridge operating regulations cited above. In September 2010, Conrail formally requested that the drawbridge operating regulation be revised to permit remote operation of the AK Railroad Bridge.</P>
        <P>Conrail, on October 20, 2010 and at the request of the Coast Guard, presented its proposal to remotely operate the bridge to the New York Harbor Operations Committee. Discussions between Conrail, the Coast Guard, and the New York Harbor Operations Committee ensued with no objections to the remote operation raised by the committee members.</P>
        <HD SOURCE="HD1">Discussion of Comments and Changes</HD>
        <P>The Coast Guard received one comment in response to the notice of proposed rulemaking.</P>
        <P>A comment letter was received from the Tug and Barge Committee of the Port of New York/New Jersey in opposition to operating the AK Bridge from a remote location. They stated that without bridge control and crewing on scene, the safe transport of products by the marine industry would be at risk if the remote control malfunctioned.</P>
        <P>The AK Bridge is normally maintained in the full open position except for the passage of rail traffic which occurs approximately four times each day.</P>
        <P>Should the remote operation fail a repair crew will be dispatched to the bridge within 45 minutes of the reported failure to repair the bridge.</P>
        <P>Prior to publishing the notice of proposed rulemaking, the Coast Guard had discussions with the New York Harbor Operations Committee and Conrail. No objections to the remote operation were voiced at that time.</P>
        <P>Subsequently, the remote operation was then successfully tested for a year with a draw tender present at all times. During the one year test period there were no failures or complaints received from mariners.</P>
        <P>Based on the successful testing of the remote operation system, the Coast Guard believes that operating the AK Bridge remotely should safely meet the present and future needs of navigation. Should the remote operation fail a repair crew will be dispatched to the bridge within 45 minutes of the reported failure to repair the bridge.</P>
        <P>As a result, no changes have been made to this final rule as far as the remote operation is concerned.</P>
        <P>In drafting this final rule we noted a typographical error that was made in our notice of proposed rulemaking in the Basis and Background Section. We stated that the existing regulations were listed at 33 CFR 117.72, which was in error. The existing regulations are listed at 33 CFR 117.702. We corrected that error in this final rule.</P>
        <HD SOURCE="HD1">Regulatory Analyses</HD>
        <P>We developed this rule after considering numerous statutes and executive orders related to rulemaking. Below we summarize our analyses based on 13 of these statutes or executive orders.</P>
        <HD SOURCE="HD1">Regulatory Planning and Review</HD>
        <P>This rule is not a significant regulatory action under section 3(f) of Executive Order 12866, Regulatory Planning and Review, as supplemented by Executive Order 13563, Improving Regulation and Regulatory Review, and does not require an assessment of potential costs and benefits under section 6(a)(3) of that Order. The Office of Management and Budget has not reviewed it under that Order. This conclusion is based on the fact that the bridge will continue to operate according to the existing regulations except that it will be controlled from either a remote location or locally.</P>
        <HD SOURCE="HD1">Small Entities</HD>
        <P>Under the Regulatory Flexibility Act (5 U.S.C. 601-612), we have considered whether this rule would have a significant economic impact on a substantial number of small entities. The term “small entities” comprises small businesses, not-for-profit organizations that are independently owned and operated and are not dominant in their fields, and governmental jurisdictions with populations of less than 50,000.</P>
        <P>The Coast Guard certifies under 5 U.S.C. 605(b) that this rule will not have a significant economic impact on a substantial number of small entities. This action will not have a significant economic impact on a substantial number of small entities for the following reason. The bridge will continue to operate according to existing regulations except that it will be controlled from either a remote location or locally.</P>
        <HD SOURCE="HD1">Assistance for Small Entities</HD>
        <P>Under section 213(a) of the Small Business Regulatory Enforcement Fairness Act of 1996 (Pub. L. 104-121), in the NPRM we offered to assist small entities in understanding the rule so that they could better evaluate its effects on them and participate in the rulemaking process.</P>
        <HD SOURCE="HD1">Collection of Information</HD>
        <P>This rule calls for no new collection of information under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501-3520).</P>
        <HD SOURCE="HD1">Federalism</HD>

        <P>A rule has implications for federalism under Executive Order 13132, Federalism, if it has a substantial direct effect on State or local governments and would either preempt State law or<PRTPAGE P="45692"/>impose a substantial direct cost of compliance on them. We have analyzed this rule under that Order and have determined that it does not have implications for federalism.</P>
        <HD SOURCE="HD1">Unfunded Mandates Reform Act</HD>
        <P>The Unfunded Mandates Reform Act of 1995 (2 U.S.C. 1531-1538) requires Federal agencies to assess the effects of their discretionary regulatory actions. In particular, the Act addresses actions that may result in the expenditure by a State, local, or tribal government, in the aggregate, or by the private sector of $100,000,000 (adjusted for inflation) or more in any one year. Though this rule will not result in such an expenditure, we do discuss the effects of this rule elsewhere in this preamble.</P>
        <HD SOURCE="HD1">Taking of Private Property</HD>
        <P>This rule will not cause a taking of private property or otherwise have taking implications under Executive Order 12630, Governmental Actions and Interference with Constitutionally Protected Property Rights.</P>
        <HD SOURCE="HD1">Civil Justice Reform</HD>
        <P>This rule meets applicable standards in sections 3(a) and 3(b)(2) of Executive Order 12988, Civil Justice Reform, to minimize litigation, eliminate ambiguity, and reduce burden.</P>
        <HD SOURCE="HD1">Protection of Children</HD>
        <P>We have analyzed this rule under Executive Order 13045, Protection of Children from Environmental Health Risks and Safety Risks. This rule is not an economically significant rule and would not create an environmental risk to health or risk to safety that might disproportionately affect children.</P>
        <HD SOURCE="HD1">Indian Tribal Governments</HD>
        <P>This rule does not have tribal implications under Executive Order 13175, Consultation and Coordination with Indian Tribal Governments, because it does not have a substantial direct effect on one or more Indian tribes, on the relationship between the Federal Government and Indian tribes, or on the distribution of power and responsibilities between the Federal Government and Indian tribes.</P>
        <HD SOURCE="HD1">Energy Effects</HD>
        <P>We have analyzed this rule under Executive Order 13211, Actions Concerning Regulations That Significantly Affect Energy Supply, Distribution, or Use. We have determined that it is not a “significant energy action” under that order because it is not a “significant regulatory action” under Executive Order 12866 and is not likely to have a significant adverse effect on the supply, distribution, or use of energy. The Administrator of the Office of Information and Regulatory Affairs has not designated it as a significant energy action. Therefore, it does not require a Statement of Energy Effects under Executive Order 13211.</P>
        <HD SOURCE="HD1">Technical Standards</HD>
        <P>The National Technology Transfer and Advancement Act (NTTAA) (15 U.S.C. 272 note) directs agencies to use voluntary consensus standards in their regulatory activities unless the agency provides Congress, through the Office of Management and Budget, with an explanation of why using these standards would be inconsistent with applicable law or otherwise impractical. Voluntary consensus standards are technical standards (e.g., specifications of materials, performance, design, or operation; test methods; sampling procedures; and related management systems practices) that are developed or adopted by voluntary consensus standards bodies.</P>
        <P>This rule does not use technical standards. Therefore, we did not consider the use of voluntary consensus standards.</P>
        <HD SOURCE="HD1">Environment</HD>
        <P>We have analyzed this rule under Department of Homeland Security Management Directive 023-01 and Commandant Instruction M16475.lD, which guides the Coast Guard in complying with the National Environmental Policy Act of 1969 (NEPA) (42 U.S.C. 4321-4370f), and have concluded that this action is one of a category of actions which do not individually or cumulatively have a significant effect on the human environment. This rule is related to the promulgation of operating regulations or procedures for drawbridges and therefore is categorically excluded, under figure 2-1, paragraph (32)(e), of the Instruction. Under figure 2-1, paragraph (32)(e), of the Instruction, an environmental analysis checklist and a categorical exclusion determination are not required for this rule.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 33 CFR Part 117</HD>
          <P>Bridges.</P>
        </LSTSUB>
        
        <P>For the reasons discussed in the preamble, the Coast Guard amends 33 CFR part 117 as follows:</P>
        <REGTEXT PART="117" TITLE="33">
          <PART>
            <HD SOURCE="HED">PART 117—DRAWBRIDGE OPERATION REGULATIONS</HD>
          </PART>
          <AMDPAR>1. The authority citation for part 117 continues to read as follows:</AMDPAR>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>33 U.S.C. 499; 33 CFR 1.05-1; Department of Homeland Security Delegation No. 0170.1.</P>
          </AUTH>
        </REGTEXT>
        <REGTEXT PART="117" TITLE="33">
          <AMDPAR>2. Revise § 117.702 to read as follows:</AMDPAR>
          <SECTION>
            <SECTNO>§ 117.702</SECTNO>
            <SUBJECT>Arthur Kill.</SUBJECT>
            <P>(a) The draw of the Arthur Kill (AK) Railroad Bridge shall be maintained in the full open position for navigation at all times, except during periods when it is closed for the passage of rail traffic.</P>
            <P>(b) The bridge owner/operator shall maintain a dedicated telephone hot line for vessel operators to call the bridge in advance to coordinate anticipated bridge closures. The telephone hot line number shall be posted on signs at the bridge clearly visible from both the up and downstream sides of the bridge.</P>
            <P>(c) Tide constrained deep draft vessels shall notify the bridge operator, daily, of their expected times of vessel transits through the bridge, by calling the designated telephone hot line.</P>
            <P>(d) The bridge shall not be closed for the passage of rail traffic during any predicted high tide period if a tide constrained deep draft vessel has provided the bridge operator with an advance notice of their intent to transit through the bridge. For the purposes of this regulation, the predicted high tide period shall be considered to be from two hours before each predicted high tide to a half-hour after each predicted high tide taken at the Battery, New York.</P>
            <P>(e) The bridge operator shall issue a manual broadcast notice to mariners of the intent to close the bridge for a period of up to 30 minutes for the passage of rail traffic, on VHF-FM channels 13 and 16 (minimum range of 15 miles) 90 minutes before and again at 75 minutes before each bridge closure.</P>
            <P>(f) Beginning at 60 minutes prior to each bridge closure, automated or manual broadcast notice to mariners must be repeated at 15 minute intervals and again at 10 and 5 minutes prior to each bridge closure and once again as the bridge begins to close, at which point the appropriate sound signal will be given.</P>
            <P>(g) Two 15 minute bridge closures may be provided each day for the passage of multiple rail traffic movements across the bridge. Each 15 minute bridge closure shall be separated by at least a 30 minute period when the bridge is returned to and remains in the full open position. Notification of the two 15 minute closures shall follow the same procedures outlined in paragraphs (e) and (f) above.</P>

            <P>(h) A vessel operator may request up to a 30 minute delay for any bridge closure in order to allow vessel traffic to<PRTPAGE P="45693"/>meet tide or current requirements; however, the request to delay the bridge closure must be made within 30 minutes following the initial broadcast for the bridge closure. Requests received after the initial 30 minute broadcast will not be granted.</P>
            <P>(i) In the event of a bridge operational failure, the bridge operator shall immediately notify the Coast Guard Captain of the Port New York. The bridge owner/operator must provide and dispatch a bridge repair crew to be on scene at the bridge no later than 45 minutes after the bridge fails to operate. A repair crew must remain on scene during the operational failure until the bridge has been fully restored to normal operations or until the bridge is raised and locked in the fully open position.</P>
            <P>(j) When the bridge is not tended locally it must be operated from a remote location. A sufficient number of closed circuit TV cameras, approved by the Coast Guard, shall be operated and maintained at the bridge site to enable the remotely located bridge tender to have full view of both river traffic and the bridge.</P>
            <P>(k) VHF-FM channels 13 and 16 shall be maintained and monitored to facilitate communication in both the remote and local control locations. The bridge shall also be equipped with directional microphones and horns to receive and deliver signals to vessels.</P>
            <P>(l) Whenever the remote control system equipment is disabled or fails to operate for any reason, the bridge operator shall immediately notify the Captain of the Port New York. The bridge shall be physically tended and operated by local control as soon as possible, but no more than 45 minutes after malfunction or disability of the remote system.</P>
            <P>(m)  Mechanical bypass and override capability of the remote operation system shall be provided and maintained at all times.</P>
          </SECTION>
        </REGTEXT>
        <SIG>
          <DATED>Dated: July 6, 2011.</DATED>
          <NAME>James B. McPherson,</NAME>
          <TITLE>Captain, U.S. Coast Guard,  Acting Commander, First Coast Guard District.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19322 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 9110-04-P</BILCOD>
    </RULE>
    <RULE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HOMELAND SECURITY</AGENCY>
        <SUBAGY>Coast Guard</SUBAGY>
        <CFR>33 CFR Part 165</CFR>
        <DEPDOC>[Docket No. USCG-2011-0567]</DEPDOC>
        <RIN>RIN 1625-AA00</RIN>
        <SUBJECT>Safety Zone; San Diego POPS Fireworks, San Diego, CA</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Coast Guard, DHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Temporary final rule.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Coast Guard is establishing a temporary safety zone on the navigable waters of San Diego Bay in support of the San Diego POPS Fireworks. This safety zone is necessary to provide for the safety of the participants, crew, spectators, participating vessels, and other vessels and users of the waterway during scheduled fireworks events. Persons and vessels will be prohibited from entering into, transiting through, or anchoring within this safety zone unless authorized by the Captain of the Port or his designated representative.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>
            <E T="03">Effective Date:</E>This rule is effective in the CFR from August 1, 2011 until 10 p.m., September 4, 2011. This rule is effective with actual notice for purposes of enforcement beginning 9 p.m. July 1, 2011.</P>
        </EFFDATE>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Documents indicated in this preamble as being available in the docket are part of docket USCG-2011-0567 and are available online by going to<E T="03">http://www.regulations.gov,</E>inserting USCG-2011-0567 in the “Keyword” box, and then clicking “Search.” They are also available for inspection or copying at the Docket Management Facility (M-30), U.S. Department of Transportation, West Building Ground Floor, Room W12-140, 1200 New Jersey Avenue, SE., Washington, DC 20590, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>If you have questions on this temporary rule, call or e-mail Petty Officer Shane Jackson, Waterways Management, U.S. Coast Guard Sector San Diego, CA; telephone (619) 278-7262, e-mail<E T="03">Shane.E.Jakcson@uscg.mil.</E>If you have questions on viewing the docket, call Renee V. Wright, Program Manager, Docket Operations, telephone 202-366-9826.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">Regulatory Information</HD>
        <P>The Coast Guard is issuing this temporary final rule without prior notice and opportunity to comment pursuant to authority under section 4(a) of the Administrative Procedure Act (APA) (5 U.S.C. 553(b)). This provision authorizes an agency to issue a rule without prior notice and opportunity to comment when the agency for good cause finds that those procedures are “impracticable, unnecessary, or contrary to the public interest.” Under 5 U.S.C. 553(b)(B), the Coast Guard finds that good cause exists for not publishing a notice of proposed rulemaking (NPRM) with respect to this rule because immediate action is necessary to ensure the safety of vessels, spectators, participants, and others in the vicinity of the marine event on the dates and times this rule will be in effect and delay would be impracticable.</P>
        <P>Under 5 U.S.C. 553(d)(3), the Coast Guard finds that good cause exists for making this rule effective less than 30 days after publication in the Federal Register because delaying the effective date would be impracticable, since immediate action is needed to ensure the public's safety.</P>
        <HD SOURCE="HD1">Basis and Purpose</HD>
        <P>The San Diego Symphony Orchestra and Copley Symphony Hall are sponsoring the San Diego POPS Fireworks, which will include a fireworks presentation conducted from a barge in San Diego Bay. The barge will be located near the navigational channel in the vicinity of North Embarcadero. The temporary safety zone will be a 400-foot radius around the firing barge. The sponsor will provide a chase boat to patrol the safety zone and inform vessels of the safety zone. This temporary safety zone is necessary to provide for the safety of the crew, spectators, and other vessels and users of the waterway.</P>
        <HD SOURCE="HD1">Discussion of Rule</HD>
        <P>The Coast Guard is establishing a temporary safety zone that will be enforced from 9 p.m. to 10 p.m. on the following dates: July 1-3, July 8-9, July 15-16, July 22-23, July 29-30, August 5-6, August 12-13, August 19-20, August 26-27, and September 2-4, 2011. The limits of the safety zone will be a 400-foot radius around the anchored firing barge in approximate position 32°42.13′ N, 117°10.01′ W.</P>

        <P>The temporary safety zone is necessary to provide for the safety of the crews, spectators, and other vessels and users of the waterway. Persons and vessels will be prohibited from entering into, transiting through, or anchoring within the safety zone unless authorized by the Captain of the Port, or his designated representative.<PRTPAGE P="45694"/>
        </P>
        <HD SOURCE="HD1">Regulatory Analyses</HD>
        <P>We developed this rule after considering numerous statutes and executive orders related to rulemaking. Below we summarize our analyses based on 13 of these statutes and executive orders.</P>
        <HD SOURCE="HD1">Regulatory Planning and Review</HD>
        <P>This rule is not a significant regulatory action under section 3(f) of Executive Order 12866, Regulatory Planning and Review, and does not require an assessment of potential costs and benefits under section 6(a)(3) of that Order. The Office of Management and Budget has not reviewed it under that Order.</P>
        <P>We expect the economic impact of this proposed rule to be so minimal that a full Regulatory Evaluation is unnecessary.</P>
        <P>This determination is based on the limited duration and size and location of the safety zone. Recreational vessels will not be allowed to transit through the designated safety zone during the specified times. Vessels may transit through the safety zone with permission from the Captain of the Port San Diego or designated representative.</P>
        <HD SOURCE="HD1">Small Entities</HD>
        <P>Under the Regulatory Flexibility Act (5 U.S.C. 601-612), we have considered whether this rule would have a significant economic impact on a substantial number of small entities. The term “small entities” comprises small businesses, not-for-profit organizations that are independently owned and operated and are not dominant in their fields, and governmental jurisdictions with populations of less than 50,000.</P>
        <P>The Coast Guard certifies under 5 U.S.C. 605(b) that this rule will not have a significant economic impact on a substantial number of small entities. This rule may affect the following entities, some of which may be small entities: The owners or operators of vessels intending to transit or anchor in the specified waters of San Diego Bay within the safety zone.</P>
        <P>This rule will not have a significant economic impact on a substantial number of small entities for the following reasons. Vessel traffic can pass safely around the safety zone. Before the effective period, the Coast Guard will publish a local notice to mariners (LNM) and will issue broadcast notice to mariners (BNM) alerts via marine channel 16 VHF before the safety zone is enforced.</P>
        <HD SOURCE="HD1">Assistance for Small Entities</HD>
        <P>Under section 213(a) of the Small Business Regulatory Enforcement Fairness Act of 1996 (Pub. L. 104-121), we offer to assist small entities in understanding the rule so that they can better evaluate its effects on them and participate in the rulemaking process.</P>
        <P>Small businesses may send comments on the actions of Federal employees who enforce, or otherwise determine compliance with, Federal regulations to the Small Business and Agriculture Regulatory Enforcement Ombudsman and the Regional Small Business Regulatory Fairness Boards. The Ombudsman evaluates these actions annually and rates each agency's responsiveness to small business. If you wish to comment on actions by employees of the Coast Guard, call 1-888-REG-FAIR (1-888-734-3247). The Coast Guard will not retaliate against small entities that question or complain about this rule or any policy or action of the Coast Guard.</P>
        <HD SOURCE="HD1">Collection of Information</HD>
        <P>This rule calls for no new collection of information under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501-3520).</P>
        <HD SOURCE="HD1">Federalism</HD>
        <P>A rule has implications for federalism under Executive Order 13132, Federalism, if it has a substantial direct effect on State or local governments and would either preempt State law or impose a substantial direct cost of compliance on them. We have analyzed this rule under that Order and have determined that it does not have implications for federalism.</P>
        <HD SOURCE="HD1">Unfunded Mandates Reform Act</HD>
        <P>The Unfunded Mandates Reform Act of 1995 (2 U.S.C. 1531-1538) requires Federal agencies to assess the effects of their discretionary regulatory actions. In particular, the Act addresses actions that may result in the expenditure by a State, local, or tribal government, in the aggregate, or by the private sector of $100,000,000 (adjusted for inflation) or more in any one year. Though this rule will not result in such an expenditure, we do discuss the effects of this rule elsewhere in this preamble.</P>
        <HD SOURCE="HD1">Taking of Private Property</HD>
        <P>This rule will not cause a taking of private property or otherwise have taking implications under Executive Order 12630, Governmental Actions and Interference with Constitutionally Protected Property Rights.</P>
        <HD SOURCE="HD1">Civil Justice Reform</HD>
        <P>This rule meets applicable standards in sections 3(a) and 3(b)(2) of Executive Order 12988, Civil Justice Reform, to minimize litigation, eliminate ambiguity, and reduce burden.</P>
        <HD SOURCE="HD1">Protection of Children</HD>
        <P>We have analyzed this rule under Executive Order 13045, Protection of Children from Environmental Health Risks and Safety Risks. This rule is not an economically significant rule and does not create an environmental risk to health or risk to safety that may disproportionately affect children.</P>
        <HD SOURCE="HD1">Indian Tribal Governments</HD>
        <P>This rule does not have tribal implications under Executive Order 13175, Consultation and Coordination with Indian Tribal Governments, because it does not have a substantial direct effect on one or more Indian tribes, on the relationship between the Federal Government and Indian tribes, or on the distribution of power and responsibilities between the Federal Government and Indian tribes.</P>
        <HD SOURCE="HD1">Energy Effects</HD>
        <P>We have analyzed this rule under Executive Order 13211, Actions Concerning Regulations That Significantly Affect Energy Supply, Distribution, or Use. We have determined that it is not a “significant energy action” under that order because it is not a “significant regulatory action” under Executive Order 12866 and is not likely to have a significant adverse effect on the supply, distribution, or use of energy. The Administrator of the Office of Information and Regulatory Affairs has not designated it as a significant energy action. Therefore, it does not require a Statement of Energy Effects under Executive Order 13211.</P>
        <HD SOURCE="HD1">Technical Standards</HD>

        <P>The National Technology Transfer and Advancement Act (NTTAA) (15 U.S.C. 272 note) directs agencies to use voluntary consensus standards in their regulatory activities unless the agency provides Congress, through the Office of Management and Budget, with an explanation of why using these standards would be inconsistent with applicable law or otherwise impractical. Voluntary consensus standards are technical standards (e.g., specifications of materials, performance, design, or operation; test methods; sampling procedures; and related management systems practices) that are developed or adopted by voluntary consensus standards bodies.<PRTPAGE P="45695"/>
        </P>
        <P>This rule does not use technical standards. Therefore, we did not consider the use of voluntary consensus standards.</P>
        <HD SOURCE="HD1">Environment</HD>

        <P>We have analyzed this rule under Department of Homeland Security Management Directive 023-01 and Commandant Instruction M16475.lD, which guide the Coast Guard in complying with the National Environmental Policy Act of 1969 (NEPA) (42 U.S.C. 4321-4370f), and have concluded this action is one of a category of actions that do not individually or cumulatively have a significant effect on the human environment. This rule is categorically excluded, under figure 2-1, paragraph (34)(g), of the Instruction. This rule involves the establishment of a temporary safety zone to protect the public from dangers associated with fireworks display. An environmental analysis checklist and a categorical exclusion determination are available in the docket where indicated under<E T="02">ADDRESSES</E>.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 33 CFR Part 165</HD>
          <P>Harbors, Marine safety, Navigation (water), Reporting and recordkeeping requirements, Security measures, Waterways.</P>
        </LSTSUB>
        
        <P>For the reasons discussed in the preamble, the Coast Guard amends 33 CFR part 165 as follows:</P>
        <REGTEXT PART="165" TITLE="33">
          <PART>
            <HD SOURCE="HED">PART 165—REGULATED NAVIGATION AREAS AND LIMITED ACCESS AREAS</HD>
          </PART>
          <AMDPAR>1. The authority citation for part 165 continues to read as follows:</AMDPAR>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>33 U.S.C. 1226, 1231; 46 U.S.C. Chapter 701, 3306, 3703; 50 U.S.C. 191, 195; 33 CFR 1.05-1, 6.04-1, 6.04-6, 160.5; Pub. L. 107-295, 116 Stat. 2064; Department of Homeland Security Delegation No. 0170.1.</P>
          </AUTH>
        </REGTEXT>
        
        <REGTEXT PART="165" TITLE="33">
          <AMDPAR>2. A new temporary zone § 165.T11-431 to read as follows:</AMDPAR>
          <SECTION>
            <SECTNO>§ 165.T11-431;</SECTNO>
            <SUBJECT>Safety zone; San Diego POPS Fireworks, San Diego, CA.</SUBJECT>
            <P>(a)<E T="03">Location.</E>The limits of the safety zone will be a400-foot radius around the anchored firing barge in approximate position 32°42.13′ N, 117°10.01′ W.</P>
            <P>(b)<E T="03">Enforcement Period.</E>This section will be enforced from 9 p.m. to 10 p.m. on the following dates: July 1-3, July 8-9, July 15-16, July 22-23, July 29-30, August 5-6, August 12-13, August 19-20, August 26-27, and September 2-4, 2011.</P>
            <P>(c)<E T="03">Definitions.</E>The following definition applies to this section:<E T="03">designated representative</E>means any commissioned, warrant, or petty officer of the Coast Guard on board a Coast Guard, Coast Guard Auxiliary, or local, state, or federal law enforcement vessel who has been authorized to act on the behalf of the Captain of the Port.</P>
            <P>(d)<E T="03">Regulations.</E>(1) Entry into, transit through or anchoring within this safety zone is prohibited unless authorized by the Captain of the Port of San Diego or his designated representative on scene.</P>
            <P>(2) Mariners requesting permission to transit through the safety zone may request authorization to do so from the Sector San Diego Command Center. The Command Center may be contacted on VHF-FM Channel 16.</P>
            <P>(3) All persons and vessels shall comply with the instructions of the Coast Guard Captain of the Port or his designated representative. Upon being hailed by U.S. Coast Guard patrol personnel by siren, radio, flashing light, or other means, the operator of a vessel shall proceed as directed.</P>
            <P>(4) The Coast Guard may be assisted by other federal, state, or local agencies.</P>
          </SECTION>
        </REGTEXT>
        <SIG>
          <DATED>Dated: June 27, 2011.</DATED>
          <NAME>T.H. Farris,</NAME>
          <TITLE>Captain, U.S. Coast Guard, Captain of the Port San Diego.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19321 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 9110-04-P</BILCOD>
    </RULE>
    <RULE>
      <PREAMB>
        <AGENCY TYPE="N">LIBRARY OF CONGRESS</AGENCY>
        <SUBAGY>Copyright Royalty Board</SUBAGY>
        <CFR>37 CFR Parts 370 and 382</CFR>
        <DEPDOC>[Docket No. RM 2011-5]</DEPDOC>
        <SUBJECT>Notice and Recordkeeping for Use of Sound Recordings Under Statutory License</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Copyright Royalty Board, Library of Congress.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Final rule.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Copyright Royalty Judges are amending their regulations to authorize the use of proxy reports of use to permit distribution of royalties collected for the period April 1, 2004, through December 31, 2009, for the public performance of sound recordings by means of digital audio transmissions pursuant to statutory license. Proxy reports of use will be used for those services for which no reports of use were submitted or for which the reports of use were unusable.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>
            <E T="03">Effective Date:</E>August 31, 2011.</P>
        </EFFDATE>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Richard Strasser, Senior Attorney, or Gina Giuffreda, Attorney Advisor, by telephone at (202) 707-7658 or e-mail at<E T="03">crb@loc.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">Background</HD>
        <P>Sections 112 and 114 of the Copyright Act, title 17 of the United States Code, are the statutory licenses governing the public performance of sound recordings by certain types of eligible services<SU>1</SU>

          <FTREF/>by means of a digital audio transmission. 17 U.S.C. 112(e), 114. Services operating under these licenses are required to, among other things, pay royalty fees and report to copyright owners of sound recordings on the use of their works.<E T="03">Id.</E>The Copyright Act directs the Copyright Royalty Judges (“Judges”) to determine the royalty rates to be paid, 17 U.S.C. 114(f)(1)(A), (f)(2)(A) and 17 U.S.C. 112(e)(3), and to establish regulations to give copyright owners reasonable notice of the use of their works and create and maintain records of use for delivery to copyright owners. 17 U.S.C. 114(f)(4)(A) and 17 U.S.C. 112(e)(4). The purpose of the notice and recordkeeping requirement is to ensure that the royalties collected under the statutory licenses are distributed by a central source—a Collective—or other agents designated to receive royalties from the Collective to the correct recipients. The Judges promulgated final notice and recordkeeping regulations on October 13, 2009.<SU>2</SU>
          <FTREF/>
          <E T="03">See</E>74 FR 52418.</P>
        <FTNT>
          <P>
            <SU>1</SU>The types of eligible services consist of subscription, nonsubscription, satellite digital audio radio services, and business establishment services.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>2</SU>Until that time, interim regulations were in effect. See 71 FR 59010 (October 6, 2006).</P>
        </FTNT>

        <P>On March 24, 2011, SoundExchange, Inc., the entity designated by the Judges as the Collective, petitioned the Judges to commence a rulemaking proceeding to consider adopting regulations to authorize SoundExchange “to use proxy reporting data to distribute to copyright owners and performers certain sound recording royalties for periods before 2010 that are otherwise undistributable due to licensees' failure to provide reports of use” or their provision of “reports of use that are so deficient as to be unusable.” Petition of SoundExchange, Inc., for a Rulemaking to Authorize Use of a Proxy to Distribute Certain Pre-2010 Sound Recordings at 1 and 2 (March 24, 2011). The proxy proposed by SoundExchange uses “available data for services of the same license type, for the same year.”<E T="03">Id</E>at 9. SoundExchange stated that the proxy would be used to distribute $28 million in royalties, which represents 4.5% of all the royalties collected for the relevant timeframe—April 1, 2004, through December 31, 2009.<E T="03">Id.</E>at 2. In<PRTPAGE P="45696"/>support of its request, SoundExchange noted that a proxy had been utilized once before when the lack of reports of use rendered the reasonable distribution of royalties difficult if not impossible.<E T="03">Id.</E>at 3. In that instance, reporting data did not exist for the period from when the statutory licenses first became available for services other than preexisting subscription services (October 1998) to the promulgation of interim notice and recordkeeping regulations (March 2004).<SU>3</SU>
          <FTREF/>
          <E T="03">See Notice and Recordkeeping for Use of Sound Recordings Under Statutory License, Docket No. RM 2002-1G, Final rule,</E>69 FR 58241. There the proxy data was used to distribute 100% of the royalties collected for that time period.<E T="03">Id.</E>
        </P>
        <FTNT>
          <P>
            <SU>3</SU>Prior to May 31, 2005, the statutory licenses were administered by the Copyright Office under the Copyright Arbitration Royalty Panel (“CARP”) system. The Copyright Royalty and Distribution Reform Act of 2004, Public Law 108-419, 118 Stat. 234, replaced the CARP system with the Copyright Royalty Judges.</P>
        </FTNT>

        <P>On April 19, 2011, the Judges published a notice of proposed rulemaking (“NPRM”) seeking comment on SoundExchange's proposal. 76 FR 21833. In addition to soliciting comments on the proposal, the Judges invited comment on, among other things, the reasonableness, fairness and appropriateness of the use of the proposed proxy and sought comment on possible alternatives to the proposed proxy.<E T="03">Id.</E>at 21834-35 (April 19, 2011). Comments were due May 19, 2011.</P>

        <P>The Judges received a single comment from SoundExchange in response to the NPRM. SoundExchange noted that since the filing of its petition, additional reports of use had been provided allowing a further distribution of royalties, thereby reducing the amount of undistributable royalties to $19.4 million, or about 3% of the total royalties collected for the April 1, 2004, to December 31, 2009, period. Comments of SoundExchange, Inc. at 1. In response to the questions posed in the NPRM, SoundExchange reiterated that the proposed proxy would be applied to a much smaller percentage of royalties than the one the Copyright Office approved for the October 1998 to March 2004 period.<E T="03">See e.g.,</E>
          <E T="03">id.</E>at 4, 5. SoundExchange also recounted its efforts in arriving at the proposed proxy and noted that it “has not devised any alternative that would be demonstrably more fair.”<E T="03">Id.</E>at 5.</P>
        <P>Given that the proxy will be applied to a small percentage of royalties for the relevant time period and that no viable alternatives have been provided, the Judges are adopting as final the proposed regulations as set forth in the NPRM allowing for the use of the proxy proposed by SoundExchange for the distribution of royalties for the period of April1, 2004, through December 31, 2009. Adoption of the proposed regulations, especially in the absence of opposition to the proposed proxy, will promote the expeditious distribution of the affected royalties.</P>
        <P>The Judges also are adopting as final the technical corrections to part 382 proposed by SoundExchange as set forth in the NPRM reflecting the renumbering of certain sections in part 370 resulting from the Judges' adoption of final notice and recordkeeping regulations in October 2009.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects</HD>
          <CFR>37 CFR Part 370</CFR>
          <P>Copyright, Sound recordings.</P>
          <CFR>37 CFR Part 382</CFR>
          <P>Copyright, Digital audio transmissions, Performance right, Sound recordings.</P>
        </LSTSUB>
        <HD SOURCE="HD1">Final Regulations</HD>
        <P>For the reasons set forth in the preamble, the Copyright Royalty Judges amend 37 CFR parts 370 and 382 as follows:</P>
        <REGTEXT PART="370" TITLE="37">
          <PART>
            <HD SOURCE="HED">PART 370—NOTICE AND RECORDKEEPING REQUIREMENTS FOR STATUTORY LICENSES</HD>
          </PART>
          <AMDPAR>1. The authority citation for part 370 continues to read as follows:</AMDPAR>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>17 U.S.C. 112(e)(4), 114(f)(4)(A).</P>
          </AUTH>
        </REGTEXT>
        
        <REGTEXT PART="370" TITLE="37">
          <AMDPAR>2. Section 370.3 is amended by adding new paragraph (i) to read as follows:</AMDPAR>
          <SECTION>
            <SECTNO>§ 370.3</SECTNO>
            <SUBJECT>Reports of use of sound recordings under statutory license for preexisting subscription services.</SUBJECT>
            <STARS/>
            <P>(i) In any case in which a preexisting subscription service has not provided a report of use required under this section for use of sound recordings under section 112(e) or section 114 of title 17 of the United States Code, or both, prior to January 1, 2010, reports of use for the corresponding calendar year filed by other preexisting subscription services shall serve as the reports of use for the non-reporting service, solely for purposes of distribution of any corresponding royalties by the Collective.</P>
          </SECTION>
        </REGTEXT>
        <REGTEXT PART="370" TITLE="37">
          <AMDPAR>3. Section 370.4 is amended by adding new paragraph (f) to read as follows:</AMDPAR>
          <SECTION>
            <SECTNO>§ 370.4</SECTNO>
            <SUBJECT>Reports of use of sound recordings under statutory license for nonsubscription transmission services, preexisting satellite digital audio radio services, new subscription services and business establishment services.</SUBJECT>
            <STARS/>
            <P>(f) In any case in which a nonsubscription transmission service, preexisting satellite digital audio radio service, new subscription service, or business establishment service has not provided a report of use required under this section for use of sound recordings under section 112(e) or section 114 of title 17 of the United States Code, or both, prior to January 1, 2010, reports of use for the corresponding calendar year filed by other services of the same type shall serve as the reports of use for the non-reporting service, solely for purposes of distribution of any corresponding royalties by the Collective.</P>
          </SECTION>
        </REGTEXT>
        <REGTEXT PART="382" TITLE="37">
          <PART>
            <HD SOURCE="HED">PART 382—RATES AND TERMS FOR DIGITAL TRANSMISSIONS OF SOUND RECORDINGS AND THE REPRODUCTION OF EPHEMERAL RECORDINGS BY PREEXISTING SUBSCRIPTION SERVICES AND PREEXISTING SATELLITE DIGITAL AUDIO RADIO SERVICES</HD>
          </PART>
          <AMDPAR>4. The authority citation of part 382 continues to read as follows:</AMDPAR>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>17 U.S.C. 112(e), 114, and 801(b)(1).</P>
          </AUTH>
          <SECTION>
            <SECTNO>§ 382.3</SECTNO>
            <SUBJECT>[Amended]</SUBJECT>
          </SECTION>
        </REGTEXT>
        <REGTEXT PART="382" TITLE="37">
          <AMDPAR>5. Section 382.3(c)(1) is amended by removing “§ 370.2” and adding “§ 370.3” in its place.</AMDPAR>
          <SECTION>
            <SECTNO>§ 382.13</SECTNO>
            <SUBJECT>[Amended]</SUBJECT>
          </SECTION>
        </REGTEXT>
        <REGTEXT PART="382" TITLE="37">
          <AMDPAR>6. Section 382.13(f)(1) is amended by removing “§ 370.3” and adding “§ 370.4” in its place.</AMDPAR>
        </REGTEXT>
        <SIG>
          <DATED>Dated: July 14, 2011.</DATED>
          <NAME>James Scott Sledge,</NAME>
          <TITLE>Chief U.S. Copyright Royalty Judge.</TITLE>
          <P>Approved by:</P>
          
          <NAME>James H. Billington,</NAME>
          <TITLE>Librarian of Congress.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19306 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 1410-72-P</BILCOD>
    </RULE>
    <RULE>
      <PREAMB>
        <PRTPAGE P="45697"/>
        <AGENCY TYPE="N">DEPARTMENT OF VETERANS AFFAIRS</AGENCY>
        <CFR>38 CFR Part 21</CFR>
        <RIN>RIN 2900-AO10</RIN>
        <SUBJECT>Vocational Rehabilitation and Employment Program—Changes to Subsistence Allowance</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Department of Veterans Affairs.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Interim final rule.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>This interim final rule amends Department of Veterans Affairs (VA) regulations to reflect changes made by the Post-9/11 Veterans Educational Assistance Improvements Act of 2010, effective August 1, 2011, that affect payment of vocational rehabilitation benefits for certain service-disabled veterans. Pursuant to these changes, a veteran, who is eligible for a subsistence allowance under chapter 31 of title 38, United States Code, and educational assistance under chapter 33 of title 38, United States Code, may participate in a rehabilitation program under chapter 31 and elect to receive a payment equal in amount to an applicable military housing allowance payable under title 37, United States Code, instead of the regular subsistence allowance under chapter 31. In addition, payments of subsistence allowances during periods between school terms are discontinued, and payments during periods of temporary school closings are modified. This rulemaking amends VA regulations consistent with this new authority.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>This interim final rule is effective August 1, 2011. Comments must be received on or before August 31, 2011.</P>
        </EFFDATE>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>Written comments may be submitted through<E T="03">http://www.Regulations.gov</E>; by mail or hand-delivery to Director, Regulations Management (02REG), Department of Veterans Affairs, 810 Vermont Ave., NW., Room 1068, Washington, DC 20420; or by fax to (202) 273-9026. Comments should indicate that they are submitted in response to “RIN 2900-AO10, Vocational Rehabilitation and Employment Program—Changes to Subsistence Allowance.” Copies of comments received will be available for public inspection in the Office of Regulation Policy and Management, Room 1063B, between the hours of 8:00 a.m. and 4:30 p.m., Monday through Friday (except holidays). Please call (202) 461-4902 for an appointment. (This is not a toll-free number.) In addition, during the comment period, comments are available online through the Federal Docket Management System (FDMS) at<E T="03">http://www.Regulations.gov</E>.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Alvin Bauman, Senior Policy Analyst, Vocational Rehabilitation and Employment Service (28), Veterans Benefits Administration, Department of Veterans Affairs, 810 Vermont Ave., NW, Washington, DC 20420, (202) 461-9600 (not a toll-free number).</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>Section 3108 of title 38, United States Code (U.S.C.), requires the payment of a subsistence allowance to veterans during a period of participation in a rehabilitation program under chapter 31 of title 38, United States Code. Pursuant to 38 U.S.C. 3322(a), a veteran cannot receive assistance under chapter 31 and chapter 33, Post-9/11 Educational Assistance, concurrently; he or she must elect under which chapter to receive assistance. Because the monthly housing allowance authorized under chapter 33 for eligible individuals pursuing programs of education may be considerably higher than the appropriate chapter 31 subsistence allowance, veterans with service-connected disabilities have an incentive to apply for chapter 33 educational assistance rather than enroll in VA's chapter 31 program of vocational rehabilitation and training. By doing so, they would forego certain individualized rehabilitation services, such as counseling and employment assistance, which are available under chapter 31. Congress recognized this and was “concerned that the greater benefit available under the chapter 33 program provides a disincentive for service-connected disabled veterans to enroll in the chapter 31 program, which means they would forego the important and valuable benefits, services, counseling, and employment assistance support that are available under the chapter 31 program of training and rehabilitation.” S. Rep. No. 111-346 at 23 (2010). Congress intended to remove this disincentive by allowing eligible veterans to elect a payment equal in amount to an applicable military housing allowance payable under title 37, United States Code, if they enroll in a chapter 31 rehabilitation program. Id.</P>

        <P>Accordingly, Congress amended 38 U.S.C. 3108(b), effective August 1, 2011, to authorize a veteran, eligible for both a chapter 31 subsistence allowance and a chapter 33 educational assistance to participate in a rehabilitation program under chapter 31 and elect to receive a payment in an alternate amount in lieu of the chapter 31 subsistence allowance. The Post-9/11 Veterans Educational Assistance Improvements Act of 2010, Public Law 111-377, sec. 205. The alternate amount must be equal to the “applicable monthly amount of basic allowance for housing payable under [37 U.S.C. 403] for a member with dependents in pay grade E-5 residing in the military housing area that encompasses all or the majority portion of the ZIP code area in which is located the institution providing the rehabilitation program concerned” (<E T="03">BAH</E>). Id. Under the new law, veterans may receive the individualized supportive services provided under chapter 31 and elect the alternate amount to receive a greater monthly allowance than they would otherwise receive.</P>

        <P>We are therefore amending 38 CFR 21.264 to allow a veteran to elect a subsistence allowance in an alternate amount, which we refer to as the<E T="03">Post-9/11 subsistence allowance</E>, in lieu of the amount provided for in 38 CFR 21.260(b). We are indicating that, to be eligible to elect the<E T="03">Post-9/11 subsistence allowance</E>, a veteran must be found to be eligible for training or education under chapter 31 and educational assistance under chapter 33. We specifically indicate that entitlement to all chapter 31 services and assistance remains when this election is made. For administrative purposes, we will allow a veteran who has elected to receive payment of the<E T="03">Post-9/11 subsistence allowance</E>to reelect payment of the chapter 31 subsistence allowance at the rate in § 21.260(b) only after completion of a term, quarter, semester, or defined period of instruction, unless the veteran no longer meets the eligibility criteria for the election or would be unable to continue in a rehabilitation program without immediate approval of the reelection.</P>
        <P>We are also amending 38 CFR 21.260(a) to include the<E T="03">Post-9/11 subsistence allowance</E>as a type of subsistence allowance that a veteran participating in a rehabilitation program under 38 U.S.C. chapter 31 may elect to receive. In addition, we are amending § 21.260 by adding a new paragraph (c) to provide for payment of the<E T="03">Post-9/11 subsistence allowance</E>in the event of an election, beginning August 1, 2011, based on the basic allowance for housing payable under 37 U.S.C. 403. In a footnote, we clarify that the<E T="03">Post-9/11 subsistence allowance</E>is paid in lieu of the subsistence allowance authorized in § 21.260(b) and is not adjusted for dependents. We interpret Congress' intent in basing the alternate amount a veteran may elect to receive on the basic allowance for housing payable to a member of the military with dependents in pay grade E-5 to mean that all veterans who elect to receive the<E T="03">Post-9/11 subsistence allowance</E>should<PRTPAGE P="45698"/>receive an amount adjusted for dependents. Therefore, we are not further adjusting the<E T="03">Post-9/11 subsistence allowance</E>for dependents as we do for chapter 31 subsistence allowance under § 21.260(b).</P>

        <P>The rehabilitation program under chapter 31 includes on-job training and non-paid work experience, during which an employer or agency rather than an institution provides the training or rehabilitation. Pub. L. 111-377 authorizes any veteran eligible for both a chapter 31 subsistence allowance and chapter 33 educational assistance, to participate in a rehabilitation program and elect the alternate amount of payment of subsistence allowance, but it does not specify how to calculate the alternate amount in the absence of an institution. To allow payment of the<E T="03">Post-9/11 subsistence allowance</E>for veterans who are participating in on-job training or non-paid work experience, in § 21.260(c)(1), we include in the definition of<E T="03">BAH</E>that the zip code of the institution, employer, or agency providing the training or rehabilitation may be used in determining the amount of the<E T="03">Post-9/11 subsistence allowance</E>.</P>

        <P>The applicable rates of payment of the subsistence allowance for veterans participating in a chapter 31 rehabilitation program are set forth in 38 U.S.C. 3108(b) and adjusted based on the rate of pursuit of training, whether full-time, three-quarter-time, or half-time, and increased yearly by the percentage by which the Consumer Price Index increases. Rates of payment for each type of training or rehabilitation program are also found in tables in 38 CFR 21.260(b), with current rates published yearly on the VA's Internet Web site. As stated previously, Pub. L. 111-377, sec. 205, specifies that the alternate amount that may be elected in lieu of the subsistence allowance must be equal to the applicable monthly amount of basic allowance for housing payable under 37 U.S.C. 403 for a member with dependents in pay grade E-5 residing in the military housing area that encompasses all or the majority portion of the ZIP code area in which is located the institution providing the rehabilitation program concerned. However, the new law does not specify that this alternate amount be paid regardless of whether the training is pursued full-time or part-time. There is no indication by Congress that the<E T="03">Post-9/11 subsistence allowance</E>must be paid in a manner different than the way current subsistence allowance is paid. We interpret the lack of specificity in this regard as an indication that we may continue to follow our current practice of adjusting subsistence allowance rates based on rate of pursuit of training. Furthermore, we continue to believe that veterans who pursue training on a less than full-time basis should not be paid the full amount of subsistence allowance.</P>
        <P>Accordingly, we are adjusting rates of the<E T="03">Post-9/11 subsistence allowance</E>based on rates of pursuit of training. In a table in new § 21.260(c), we specify the payments of the<E T="03">Post-9/11 subsistence allowance</E>for the rehabilitation program that currently qualifies for payment of a subsistence allowance under chapter 31. In a footnote to the table, we explain that payments for courses being taken simultaneously at more than one institution will be based on the<E T="03">BAH</E>of the zip code assigned to the parent institution. We retain the rule with respect to payment of the current subsistence allowance for on-job training that the rate paid may not exceed the difference between the monthly training wage, not including overtime, and the entrance journeyman wage for the veteran's objective. We also retain the rule with respect to payment of the current subsistence allowance for improvement of rehabilitation potential that the quarter-time rate may be paid only during a period of extended evaluation.</P>
        <P>For veterans pursuing a program of in-home training, including training with an independent instructor or training solely through distance learning, in which case the institution is in a different zip code than where the veteran is located, Public Law 111-377 does not specify how to calculate payments of the alternate subsistence allowance that may be elected under this law. With respect to payments of the monthly living stipend for veterans receiving chapter 33 educational assistance for pursuit of a program of education solely by distance learning, Public Law 111-377 does specify how to calculate payments. For veterans pursuing a program of education on more than a half-time basis, solely by distance learning, Public Law 111-377 provides for payment of the chapter 33 living stipend at the rate of up to 50 percent of the national average of basic allowance for housing payable under 37 U.S.C. 403 for a member of the military with dependents in pay grade E-5, adjusted based on the rate of pursuit. Congress provided for such rate because it believed that, although “payment of some portion of the living allowance is appropriate . . . since one of the basic purposes of the living allowance is to offset the cost of housing away from home and since most distance learning is pursued from home, the full allowance does not appear supported at this time.” S. Rep. No. 111-346 at 11 (2010). Similarly, for veterans pursuing training or rehabilitation under chapter 31 through a program of in-home training, including solely through distance learning, there is no local institution providing the rehabilitation or training and no housing costs to offset. We believe Congress' statement with regard to the monthly living stipend for veterans pursuing a program of education was intended to apply to the similarly situated veterans pursuing training or rehabilitation under chapter 31.</P>
        <P>Accordingly, we will base the rate of the<E T="03">Post-9/11 subsistence allowance</E>for veterans pursuing training or rehabilitation full-time through a program of in-home training or solely through distance learning on the national average of basic allowance for housing payable under 37 U.S.C. 403 for a member of the military with dependents in pay grade E-5 and pay the allowance at 50 percent of the national average. In § 21.260(c)(2) we define<E T="03">BAH National Average</E>as “the average (i.e., unweighted arithmetic mean) monthly amount of the basic allowance for housing payable under 37 U.S.C. 403 for a member of the military with dependents in pay grade E-5 residing in the United States”. We will continue to make payments, adjusted based on rate of pursuit, for veterans pursuing training or rehabilitation in-home or solely through distance learning. We will therefore calculate the rates of the<E T="03">Post-9/11 subsistence allowance</E>for those veterans pursuing training or rehabilitation in home or solely through distance learning at less than full-time (three-quarter time or half-time) in the same manner as we do for veterans pursuing institutional training or rehabilitation. Thus, veterans pursuing training or rehabilitation in-home or solely through distance learning at three-quarter time will receive<FR>3/4</FR>of 50 percent of the<E T="03">BAH National Average,</E>or<FR>3/8</FR>of the<E T="03">BAH National Average,</E>and veterans pursuing training or rehabilitation in-home or solely through distance learning half-time will receive<FR>1/2</FR>of 50 percent of the<E T="03">BAH National Average,</E>or<FR>1/4</FR>of the<E T="03">BAH National Average.</E>These rates of payment will be found in the table in § 21.260(c). In a footnote to the table, we clarify that payments for training consisting of both distance learning and courses at a local institution are based on the<E T="03">BAH</E>of the local institution because the veteran will incur costs away from home that the allowance is intended to offset.<PRTPAGE P="45699"/>
        </P>

        <P>In addition, for veterans pursuing training or rehabilitation under chapter 31 in foreign institutions, in which case there is no institution with a zip code on which to base the rates of payment, Public Law 111-377 does not specify how to calculate payments of the<E T="03">Post-9/11 subsistence allowance.</E>For veterans pursuing a program of education under chapter 33 in a foreign country, Public Law 111-377 does specify that payment of the living stipend be based on the national average of basic allowance for housing payable under 37 U.S.C. 403 for a member of the military with dependents in pay grade E-5 and adjusted based on the rate of pursuit. We believe it is reasonable to calculate payments of the Post-911 subsistence allowance for veterans pursuing training or rehabilitation under chapter 31 in foreign institutions in the same manner that Congress provided for similarly situated veterans pursuing a program of education under chapter 33. Therefore, we will base rates of payment of the<E T="03">Post-9/11 subsistence allowance</E>for training in foreign institutions on the<E T="03">BAH National Average</E>amount. We will continue to make payments of the<E T="03">Post-9/11 subsistence allowance</E>for training in foreign institutions adjusted based on rate of pursuit of training.</P>

        <P>Under 38 CFR 21.79, VA charges for entitlement usage to determine remaining entitlement. VA bases charges for entitlement usage on the principle that a veteran who pursues a rehabilitation program for one day should be charged one day of entitlement. When a chapter 31 participant elects to receive payment of the<E T="03">Post-9/11 subsistence allowance</E>under § 21.260(c) in lieu of a subsistence allowance under § 21.260(b), he or she will continue to receive chapter 31 benefits and services. In such cases, the entitlement usage will be deducted from the veteran's chapter 31 entitlement. No entitlement charges will be made against chapter 33 because the veteran will not be using chapter 33 benefits. We are revising § 21.79 to make clear that we will determine entitlement usage in this manner in the event of an election of the<E T="03">Post-9/11 subsistence allowance.</E>
        </P>

        <P>Section 3112 of title 38, United States Code, establishes a revolving fund for VA to use to make advances of no more than twice the amount of the full-time institutional monthly subsistence allowance for a veteran with no dependents to veterans pursuing a rehabilitation program under chapter 31. Section 21.274 of title 38, Code of Federal Regulations, specifies that the fund is to pay veterans who would otherwise be unable to begin or continue in a rehabilitation program without such assistance. Section 21.274 also specifies that the amount of the advance may not exceed the amount needed or twice the monthly subsistence allowance for a veteran without dependents in full-time institutional training. Section 3112 clearly establishes that the limit on these advances is based on the full-time institutional rate for a veteran with no dependents. The full-time institutional rate for a veteran with no dependents is specified in § 21.260(b), whereas all rates in new § 21.260(c) are based on an allowance that includes dependents. Therefore, the limit on the advances may not be based on the rates of the<E T="03">Post-9/11 subsistence allowance</E>in § 21.260(c). Accordingly, we clarify in § 21.274(d)(1)(iii) that the limit placed on the amount advanced from the revolving fund is based on the subsistence allowance in § 21.260(b).</P>
        <P>Pursuant to 38 U.S.C. 3680(a)(3)(B), subsistence allowances are authorized to be paid during periods when schools are temporarily closed under an established policy based upon an Executive Order of the President or due to an emergency situation, during periods between consecutive school terms if there is a transfer to enroll in and pursue a similar course at a different educational institution if the period between consecutive terms is 30 days or less, or, in certain circumstances, during periods between school terms, where the educational institution certifies enrollment on an individual term basis. Section 206 of Public Law 111-377 removes the authority to continue to pay allowances between consecutive school terms involving a transfer to another educational institution and between school terms where the educational institution certifies enrollment on an individual term basis. Section 206 also restricts the total number of weeks for which allowances may be paid during periods when schools are temporarily closed under an established policy based upon an Executive Order of the President or due to an emergency situation to 4 weeks in any 12-month period.</P>
        <P>Accordingly, we are amending our regulation, § 21.270, “Payment of subsistence allowance during leave and between periods of instruction”, that allows for the payment of subsistence allowance between periods of instruction. We are removing paragraph (b), “Payment for intervals between periods of instruction”, which currently directs the payment of subsistence allowances for periods between consecutive school terms involving a transfer and between school terms where the educational institution certifies enrollment on an individual term basis. We are also redesignating paragraph (c), “Payment for other periods”, as paragraph (b). The new paragraph will continue to specify that subsistence allowance will be paid for periods in which the school is closed temporarily under emergency conditions described in § 21.4138(f). In a separate rulemaking, VA is preparing a revision to § 21.4138(f) to incorporate the change in law regarding the restriction on the total number of weeks for which allowances for veterans receiving any VA education benefit, including chapter 31 benefits, may be paid during periods of temporary closure. In addition, we are adding an authority citation to the end of the section for clarification, correcting a misspelling, and revising the section heading to replace the words “between periods of instruction” with the words “other periods”.</P>
        <HD SOURCE="HD1">Administrative Procedure Act</HD>

        <P>In accordance with 5 U.S.C. 553(b)(3)(B), the Secretary of Veterans Affairs finds that there is good cause to dispense with advance public notice and opportunity to comment on this rule and good cause to publish this rule with an immediate effective date. The Secretary finds that it is impracticable and contrary to the public interest to delay this regulation for the purpose of soliciting prior public comment. Sections 205 and 206 of Public Law 111-377 require that certain changes to the rehabilitation program take effect on August 1, 2011. This interim final rule is necessary to implement by August 1, 2011, the statutory changes as they relate to chapter 31 subsistence allowances. For instance, Public Law 111-377 does not address how the alternate rate of subsistence allowance will be calculated in different situations. Allowing veterans to elect an alternate rate of subsistence allowance will ensure that such veterans receive the supportive services under chapter 31 to assist them in the transition from military to civilian careers. Because eligible veterans will begin to make the election on August 1, 2011, it is important to have procedures in place by this date to allow veterans to receive the alternate rate of subsistence allowance authorized under the law as soon as they are able. For these reasons, the Secretary of Veterans Affairs is issuing this rule as an interim final rule. The Secretary of Veterans Affairs will consider and address comments that are received within 30 days of the date this<PRTPAGE P="45700"/>interim final rule is published in the<E T="04">Federal Register</E>.</P>
        <HD SOURCE="HD1">Unfunded Mandates</HD>
        <P>The Unfunded Mandates Reform Act of 1995 requires, at 2 U.S.C. 1532, that agencies prepare an assessment of anticipated costs and benefits before issuing any rule that may result in the expenditure by State, local, and tribal governments, in the aggregate, or by the private sector, of $100 million or more (adjusted annually for inflation) in any given year. This interim final rule will have no such effect on State, local, and tribal governments, or on the private sector.</P>
        <HD SOURCE="HD1">Paperwork Reduction Act</HD>
        <P>This interim final rule does not contain any collections of information under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501-3521).</P>
        <HD SOURCE="HD1">Regulatory Flexibility Act</HD>
        <P>The Secretary hereby certifies that this regulatory action will not have a significant economic impact on a substantial number of small entities as they are defined in the Regulatory Flexibility Act, 5 U.S.C. 601-612. This regulatory action will affect individuals and will not affect any small entities. Therefore, pursuant to 5 U.S.C. 605(b), this regulatory action is exempt from the initial and final flexibility analysis requirements of sections 603 and 604.</P>
        <HD SOURCE="HD1">Congressional Review Act</HD>
        <P>Under the Congressional Review Act, 5 U.S.C. 801-08, a major rule is one that would have an annual effect on the economy of $100 million or more, cause major increases in costs or prices for consumers, or have significant adverse effects on competition or other aspects of the economy. We have determined this rulemaking to be a major rule because it will have an annual effect on the economy in excess of $100 million. However, this rulemaking falls within an exception to the requirement in 5 U.S.C. 801(a)(3) that a rule may not take effect until at least 60 days after the rule and accompanying report are submitted to Congress. VA will submit a copy of this regulatory action and VA's Regulatory Impact Analysis to the Comptroller General and to Congress, but the rule will become effective upon publication in the Federal Register. The Secretary has determined in accordance with 5 U.S.C. 808(2) that there is good cause to make this regulatory action effective immediately because advance public notice and opportunity to comment thereon are impractical and contrary to the public interest. Sections 205 and 206 of Public Law 111-377 require that the changes to the rehabilitation program take effect on August 1, 2011. VA regulations must be in effect because Public Law 111-377 does not address how the alternate rate of subsistence allowance will be calculated in different situations. Allowing veterans to elect an alternate rate of subsistence allowance will ensure that such veterans receive the supportive services under chapter 31 to assist them in the transition from military to civilian careers. Because eligible veterans will begin to make the election on August 1, 2011, it is important to have procedures in place by this date to allow veterans to receive the alternate rate of subsistence allowance authorized under the law as soon as they are able.</P>
        <HD SOURCE="HD1">Executive Orders 13563 and 12866</HD>
        <P>Executive Orders 13563 and 12866 direct agencies to assess the costs and benefits of available regulatory alternatives and, when regulation is necessary, to select regulatory approaches that maximize net benefits (including potential economic, environmental, public health and safety effects, distributive impacts, and equity). Executive Order 13563 emphasizes the importance of quantifying both costs and benefits, of reducing costs, of harmonizing rules, and of promoting flexibility. Executive Order defines a “significant regulatory action,” which requires review by the Office of Management and Budget (OMB), as any regulatory action that is likely to result in a rule that may: (1) Have an annual effect on the economy of $100 million or more or adversely affect in a material way the economy, a sector of the economy, productivity, competition, jobs, the environment, public health or safety, or State, local, or tribal governments or communities; (2) create a serious inconsistency or otherwise interfere with an action taken or planned by another agency; (3) materially alter the budgetary impact of entitlements, grants, user fees, or loan programs or the rights and obligations of recipients thereof; or (4) raise novel legal or policy issues arising out of legal mandates, the President's priorities, or the principles set forth in the Executive Order. This rule has been designated an “economically” significant regulatory action under section 3(f)(1) of Executive Order 12866. Accordingly, the rule has been reviewed by OMB.</P>
        <P>VA has examined the economic, interagency, budgetary, legal, and policy implications of this regulatory action and followed OMB Circular A-4 to the extent feasible in this Regulatory Impact Analysis. The circular first calls for a discussion of the need for the regulatory action.</P>
        <HD SOURCE="HD1">Statement of Need</HD>

        <P>This rulemaking will amend VA regulations to reflect changes made by the Post-9/11 Veterans Educational Assistance Improvements Act of 2010. We are revising § 21.264 to allow veterans eligible for a chapter 31 subsistence allowance and chapter 33 educational assistance to elect either the allowable chapter 31 subsistence allowance or an alternate amount of subsistence allowance, referred to as the<E T="03">Post-9/11 subsistence allowance.</E>In addition, we are amending § 21.260 to include the<E T="03">Post-9/11 subsistence allowance</E>rates, which are based on the military housing allowance payable under title 37, United States Code, referred to as the<E T="03">BAH</E>. The<E T="03">BAH</E>is based on the ZIP code area where the institution providing the rehabilitation program is located.</P>

        <P>We are also amending § 21.274 to clarify that the maximum amount allowable for an advance from the revolving fund will stay the same—twice the amount of full-time subsistence allowance for a veteran with no dependents in institutional training. In § 21.274, we are adding the phrase “specified in 21.260(b)” to clarify that the advance from the revolving fund is based on the chapter 31 subsistence allowance rates and not on the<E T="03">Post-9/11 subsistence allowance</E>rates specified in § 21.260(c).</P>

        <P>In addition, we are amending § 21.270 to prohibit payment of either the chapter 31 subsistence allowance or the<E T="03">Post-9/11 subsistence allowance</E>during intervals between school terms. Payments of subsistence allowance between school terms are no longer authorized and payments of subsistence allowance during temporary school closings are limited to 4 weeks in any 12-month period.</P>
        <HD SOURCE="HD1">Summary of Estimated Impact</HD>

        <P>The estimated costs associated with this regulation are $111,239,000.00 for Fiscal Year (FY) 2012 and $854,897,000.00 over a 5 year period. These are estimated costs based on the fact that there are significant costs to VA based on new provisions to § 21.264 and an offset of costs (projected savings) from the new provisions to § 21.270 of this rulemaking.<PRTPAGE P="45701"/>
        </P>
        <GPOTABLE CDEF="s25,20,20,20" COLS="4" OPTS="L2,tp0,i1">
          <TTITLE/>
          <BOXHD>
            <CHED H="1">Fiscal year</CHED>
            <CHED H="1">Estimated impact of paying increased subsistence allowance based on BAH<LI>($000)</LI>
            </CHED>
            <CHED H="1">Projected savings from no longer allowing payment of subsistence allowance during intervals between terms<LI>($000)</LI>
            </CHED>
            <CHED H="1">Estimated costs<LI>($000)</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">2012</ENT>
            <ENT>$162,579</ENT>
            <ENT>$51,340</ENT>
            <ENT>$111,239</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2013</ENT>
            <ENT>194,298</ENT>
            <ENT>53,685</ENT>
            <ENT>140,613</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2014</ENT>
            <ENT>224,957</ENT>
            <ENT>55,252</ENT>
            <ENT>169,705</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2015</ENT>
            <ENT>257,256</ENT>
            <ENT>56,865</ENT>
            <ENT>200,391</ENT>
          </ROW>
          <ROW RUL="n,s">
            <ENT I="01">2016</ENT>
            <ENT>291,533</ENT>
            <ENT>58,584</ENT>
            <ENT>232,949</ENT>
          </ROW>
          <ROW>
            <ENT I="03">5-Year Total</ENT>
            <ENT>1,130,623</ENT>
            <ENT>275,726</ENT>
            <ENT>854,897</ENT>
          </ROW>
        </GPOTABLE>
        <P>Estimated costs and projections are based on the best reasonably obtainable and available economic information. This analysis sets forth the basic assumptions, methods, and data underlying the analysis and discusses the uncertainties associated with the estimates. Assumptions and methodologies for each portion of the analysis are explained in more detail in the Estimate of Potential Program Costs below. VA invites public comments on all of these projections.</P>
        <HD SOURCE="HD1">Cost Benefit</HD>
        <P>The<E T="03">Post-9/11 subsistence allowance</E>rates are greater than the current chapter 31 subsistence allowance rates. Therefore, VA believes that chapter 31 participants who are eligible to receive the greater subsistence allowance will require less dependence on support programs and will be able to devote more attention to their chapter 31 training/rehabilitation program, thus creating better employment opportunities and a better quality of life.</P>
        <HD SOURCE="HD1">Alternatives</HD>
        <P>VA believes that there are no alternatives to the promulgation of this rulemaking. The provisions of sections 205 and 206 of Public Law 111-377 must be implemented in the Code of Federal Regulations to ensure accurate and consistent application of the law.</P>
        <HD SOURCE="HD1">Estimate of Potential Program Costs</HD>
        <HD SOURCE="HD2">Section 21.264</HD>

        <P>To project the best possible economic impact of § 21.264 in this rulemaking, VA conducted an analysis to determine the average annual difference between the chapter 31 subsistence allowance rate and the new<E T="03">Post-9/11 subsistence allowance</E>rate. Utilizing the FY 2012 President's Budget, the average annual chapter 31 subsistence allowance rate is estimated to be $4,962.12 in FY 2012, and the average annual<E T="03">Post-9/11 subsistence allowance</E>rate is estimated to be $12,444.94 in FY 2012. With the average annual<E T="03">Post-9/11 subsistence allowance</E>rate being $7,482.82 more than the average annual chapter 31 subsistence allowance rate, VA assumes that all eligible chapter 31 participants will elect to receive the<E T="03">Post-9/11 subsistence allowance</E>rate under the new provisions of § 21.264.</P>
        <P>VA also conducted an analysis on the total population of participants in the Vocational Rehabilitation and Employment's (VR&amp;E) chapter 31 program. The analysis focused on the number of participants who are currently receiving a monthly chapter 31 subsistence allowance and who also have Operations Enduring Freedom and Iraqi Freedom (OEF/OIF) military service.</P>

        <P>Data from VR&amp;E's FY 2012 Workload Projections for Trainees/Participants indicate that there will be approximately a total of 62,078 chapter 31 participants receiving chapter 31 subsistence allowance in FY 2012. Workload projections for the number of participants receiving subsistence allowance were based on FY 2010 actual number of 61,405 from the VA Benefits Delivery Network Computer Output Identification Number Target System Report 6002 with projected increases for FY 2011 and FY 2012. To align with projections from the FY 2012 President's Budget, the number of participants for FY 2012 (63,259) was then reduced by the number of participants that VA projected would transfer from chapter 31 benefits to the Post-9/11 GI Bill. Data-Matching between the Department of Defense and VA databases indicated that approximately 30% of VR&amp;E participants in FY 2011 had OEF/OIF military service that qualified them to elect the<E T="03">Post-9/11 subsistence allowance.</E>Over the next five years, VR&amp;E projects an increase of 5% per year of VR&amp;E participants who have OEF/OIF service based on the influx of more recent veterans leaving active duty and applying for benefits while veterans from previous eras complete participation in VR&amp;E.</P>

        <P>This data also identified an estimated 21,727 chapter 31 participants, or 35% of the total chapter 31 participants (62,078), who will receive a monthly subsistence allowance in FY 2012 and have OEF/OIF military service. It is estimated that all of these 21,727 participants will elect and receive the<E T="03">Post-9/11 subsistence allowance</E>based on their OEF/OIF service in FY 2012.</P>

        <P>The estimated total number of chapter 31 participants (21,727) who will be eligible to elect and receive the<E T="03">Post-9/11 subsistence allowance</E>based on their OEF/OIF service in FY 2012 was multiplied by the difference between the two subsistence allowance rates ($7,482.82), totaling approximately $163 million in FY 2012.</P>
        <P>Projected increases to participants receiving subsistence allowance, average annual payments, and the percentage of chapter 31 participants receiving subsistence allowance were applied in the out-years and shown in the table below.</P>
        <GPOTABLE CDEF="s25,14,14,14,14,14" COLS="6" OPTS="L2,i1">

          <TTITLE>Estimated Impact of Paying Increased Subsistence Allowance Based on<E T="03">BAH</E>
          </TTITLE>
          <BOXHD>
            <CHED H="1">FY</CHED>
            <CHED H="1">Total # of Chapter 31 (CH31) participants receiving Subsistence Allowance (SA)</CHED>
            <CHED H="1">Total # of CH31 participants receiving SA with OEF/OIF service</CHED>
            <CHED H="1">* Percent of CH31 participants receiving SA with OEF/OIF service</CHED>
            <CHED H="1">Average annual difference between current CH31 SA and new post-9/11 SA</CHED>
            <CHED H="1">Obligations ($000)</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">2012</ENT>
            <ENT>62,078</ENT>
            <ENT>21,727</ENT>
            <ENT>35</ENT>
            <ENT>$7,482.82</ENT>
            <ENT>$162,579</ENT>
          </ROW>
          <ROW>
            <PRTPAGE P="45702"/>
            <ENT I="01">2013</ENT>
            <ENT>63,892</ENT>
            <ENT>25,557</ENT>
            <ENT>40</ENT>
            <ENT>7,602.54</ENT>
            <ENT>194,298</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2014</ENT>
            <ENT>64,531</ENT>
            <ENT>29,038</ENT>
            <ENT>45</ENT>
            <ENT>7,746.99</ENT>
            <ENT>224,957</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2015</ENT>
            <ENT>65,176</ENT>
            <ENT>32,588</ENT>
            <ENT>50</ENT>
            <ENT>7,894.19</ENT>
            <ENT>257,256</ENT>
          </ROW>
          <ROW RUL="n,s">
            <ENT I="01">2016</ENT>
            <ENT>65,828</ENT>
            <ENT>36,206</ENT>
            <ENT>55</ENT>
            <ENT>8,052.07</ENT>
            <ENT>291,533</ENT>
          </ROW>
          <ROW>
            <ENT I="03">5-Year Total</ENT>
            <ENT/>
            <ENT/>
            <ENT/>
            <ENT/>
            <ENT>1,130,623</ENT>
          </ROW>
          <TNOTE>* VA assumes that the percentage of CH31 participants receiving SA and who have OEF/OIF military service will increase by 5% each year based on the influx of more recent veterans leaving active duty and applying for benefits while veterans from previous eras complete participation in VR&amp;E.</TNOTE>
        </GPOTABLE>
        <HD SOURCE="HD2">Section 21.270</HD>

        <P>To project the best possible economic impact of § 21.270 in this rulemaking, VA conducted an analysis to determine the associated costs and/or savings by no longer allowing payment of either chapter 31 or<E T="03">Post-9/11 subsistence allowance</E>during intervals between school terms.</P>
        <P>This amendment applies to all participants of the chapter 31 program who are currently participating in a training/rehabilitation program for which subsistence allowance is payable.</P>
        <P>Based on the FY 2012 President's Budget, the average annual subsistence allowance payment is estimated to be $4,962.12 in FY 2012. The average annual payment is based on 9 months of enrollment; therefore, an average monthly subsistence payment would be $551.35. We assumed that, on average, participants would have received one-and-a-half months of interval subsistence allowance based on enrollment in training for 9 months of the year. Therefore, the average annual interval subsistence allowance rate for this 1.5 month interval period is estimated to be $827.03 ($551.35 × 1.5) in FY 2012.</P>
        <P>Data from VR&amp;E's FY 2012 Workload Projections for Trainees/Participants indicate that there will be approximately 62,078 chapter 31 participants receiving chapter 31 subsistence allowance in FY 2012. Workload projections for the number of participants receiving subsistence allowance were based on FY 2010 actual number of 61,405 from the VA Benefits Delivery Network Computer Output Identification Number Target System Report 6002 with projected increases for FY 2011 and FY 2012. To align with projections from the FY 2012 President's Budget, the number of participants for FY 2012 (63,259) was then reduced by the number of participants that VA projected would transfer from chapter 31 benefits to the Post-9/11 GI Bill.</P>
        <P>The FY 2012 average annual interval subsistence allowance rate ($827.03) was multiplied by the FY 2012 total number of CH31 participants receiving subsistence allowance (62,078), totaling approximately $51,340,000.00 in projected savings to VA in FY 2012. Projected savings are estimated to be $51.3 million during FY 2012 and $275.7 million over a five-year period.</P>
        <P>Projected increases to participants receiving subsistence allowance and average annual payments were applied in the out-years and are shown in the table below.</P>
        <GPOTABLE CDEF="s50,14,14,14" COLS="4" OPTS="L2,i1">
          <TTITLE>Projected Savings From No Longer Allowing Payment of Subsistence Allowance During Intervals Between Terms</TTITLE>
          <BOXHD>
            <CHED H="1">FY</CHED>
            <CHED H="1">Total # of CH31<LI>participants</LI>
              <LI>receiving</LI>
              <LI>subsistence</LI>
              <LI>allowance (SA)</LI>
            </CHED>
            <CHED H="1">Average<LI>annual interval</LI>
              <LI>SA rate (1.5</LI>
              <LI>mths. of SA)</LI>
            </CHED>
            <CHED H="1">Obligations<LI>($000)</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">2012</ENT>
            <ENT>62,078</ENT>
            <ENT>$827.03</ENT>
            <ENT>$51,340</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2013</ENT>
            <ENT>63,892</ENT>
            <ENT>840.25</ENT>
            <ENT>53,685</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2014</ENT>
            <ENT>64,530</ENT>
            <ENT>856.22</ENT>
            <ENT>55,252</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2015</ENT>
            <ENT>65,176</ENT>
            <ENT>872.49</ENT>
            <ENT>56,865</ENT>
          </ROW>
          <ROW RUL="n,s">
            <ENT I="01">2016</ENT>
            <ENT>65,829</ENT>
            <ENT>889.94</ENT>
            <ENT>58,584</ENT>
          </ROW>
          <ROW>
            <ENT I="03">5-Year Total</ENT>
            <ENT/>
            <ENT/>
            <ENT>275,726</ENT>
          </ROW>
        </GPOTABLE>
        <HD SOURCE="HD1">Accounting Statement and Table</HD>

        <P>As required by OMB Circular A-4, in the table below, VA has prepared an accounting statement showing the classification of transfers, benefits and costs associated with the provisions of this rulemaking.<PRTPAGE P="45703"/>
        </P>
        <GPOTABLE CDEF="s25,xs36,7,7,7,7,7,7,7,7,7" COLS="11" OPTS="L2,tp0,i1">
          <TTITLE/>
          <BOXHD>
            <CHED H="1">Category</CHED>
            <CHED H="1">Year<LI>dollar</LI>
            </CHED>
            <CHED H="1">Transfers</CHED>
            <CHED H="2">FY2012</CHED>
            <CHED H="2">FY2013</CHED>
            <CHED H="2">FY2014</CHED>
            <CHED H="2">FY2015</CHED>
            <CHED H="2">FY2016</CHED>
            <CHED H="2">Present value</CHED>
            <CHED H="3">3%</CHED>
            <CHED H="3">7%</CHED>
            <CHED H="2">Annualized</CHED>
            <CHED H="3">3%</CHED>
            <CHED H="3">7%</CHED>
          </BOXHD>
          <ROW RUL="s">
            <ENT I="01">Federal Annualized Monetized Transfers</ENT>
            <ENT>2010</ENT>
            <ENT>$111.2</ENT>
            <ENT>$140.6</ENT>
            <ENT>$169.7</ENT>
            <ENT>$200.4</ENT>
            <ENT>$232.9</ENT>
            <ENT>$774.7</ENT>
            <ENT>$684.2</ENT>
            <ENT>$164.2</ENT>
            <ENT>$156.0</ENT>
          </ROW>
          <ROW RUL="s">
            <ENT I="22"/>
            <ENT O="xl"/>
            <ENT A="08">Benefits</ENT>
          </ROW>
          <ROW RUL="s">
            <ENT I="01">Qualitative benefits</ENT>
            <ENT O="xl"/>
            <ENT A="L08">The Post-9/11 subsistence allowance rates are greater than the current CH31 subsistence allowance rates. Therefore, VA believes that CH31 participants who are eligible to receive the greater subsistence allowance will require less dependence on support programs and will be able to devote more attention to their CH31 training/rehabilitation program, thus creating better employment opportunities and a better quality of life.</ENT>
          </ROW>
          <ROW RUL="s">
            <ENT I="22"/>
            <ENT O="xl"/>
            <ENT A="08">Costs</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Costs</ENT>
            <ENT O="xl"/>
            <ENT A="L08">None.</ENT>
          </ROW>
        </GPOTABLE>
        <HD SOURCE="HD1">Identification of Duplicative, Overlapping, or Conflicting Federal Rules</HD>
        <P>There are no duplicative, overlapping, or conflicting Federal rules identified with this regulatory action.</P>
        <HD SOURCE="HD1">Catalog of Federal Domestic Assistance</HD>
        <P>The Catalog of Federal Domestic Assistance number and title for the program that would be affected by this interim final rule is 64.116, Vocational Rehabilitation for Disabled Veterans.</P>
        <HD SOURCE="HD1">Signing Authority</HD>
        <P>The Secretary of Veterans Affairs, or designee, approved this document and authorized the undersigned to sign and submit the document to the Office of the Federal Register for publication electronically as an official document of the Department of Veterans Affairs. John R. Gingrich, Chief of Staff, Department of Veterans Affairs, approved this document on July 21, 2011, for publication.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 38 CFR Part 21</HD>
          <P>Administrative practice and procedure, Armed forces, Civil rights, Claims, Colleges and universities, Conflict of interests, Education, Employment, Grant programs—education, Grant programs—veterans, Health care, Loan programs—education, Loan programs—veterans, Manpower training programs, Reporting and recordkeeping requirements, Schools, Travel and transportation expenses, Veterans, Vocational education, Vocational rehabilitation.</P>
        </LSTSUB>
        <SIG>
          <DATED>Dated: July 21, 2011.</DATED>
          <NAME>Robert C. McFetridge,</NAME>
          <TITLE>Director, Regulation Policy and Management,Office of the General Counsel,Department of Veterans Affairs.</TITLE>
        </SIG>
        <P>For the reasons set forth in the preamble, VA amends 38 CFR part 21 (subpart A) as follows:</P>
        <REGTEXT PART="21" TITLE="38">
          <PART>
            <HD SOURCE="HED">PART 21—VOCATIONAL REHABILITATION AND EDUCATION</HD>
            <SUBPART>
              <HD SOURCE="HED">Subpart A—Vocational Rehabilitation and Employment Under 38 U.S.C. Chapter 31</HD>
            </SUBPART>
          </PART>
          <AMDPAR>1. The authority citation for part 21, subpart A continues to read as follows:</AMDPAR>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>38 U.S.C. 501(a), chs. 18, 31, and as noted in specific sections.</P>
          </AUTH>
        </REGTEXT>
        <REGTEXT PART="21" TITLE="38">
          <AMDPAR>2. Amend § 21.79 by:</AMDPAR>
          <AMDPAR>a. Redesignating paragraphs (f)(2), (f)(2)(i), (f)(2)(ii), and (f)(3) as paragraphs (f)(3), (f)(3)(i), (f)(3)(ii), and (f)(4) respectively.</AMDPAR>
          <AMDPAR>b. Adding a new paragraph (f)(2).</AMDPAR>
          <AMDPAR>c. Adding an authority citation at the end of new paragraph (f)(2).</AMDPAR>
          <P>The additions read as follows:</P>
          <SECTION>
            <SECTNO>§ 21.79</SECTNO>
            <SUBJECT>Determining entitlement usage under Chapter 31.</SUBJECT>
            <STARS/>
            <P>(f)<E T="03">Special situations.</E>* * *</P>

            <P>(2) When a chapter 31 participant elects to receive payment of the<E T="03">Post-9/11 subsistence allowance</E>under § 21.260(c) in lieu of a subsistence allowance under § 21.260(b), the entitlement usage is deducted from the veteran's chapter 31 entitlement. No entitlement charges are made against chapter 33.(Authority: 38 U.S.C. 3108(b))</P>
            <STARS/>
          </SECTION>
        </REGTEXT>
        <REGTEXT PART="21" TITLE="38">
          <AMDPAR>3. Amend § 21.260 by:</AMDPAR>
          <AMDPAR>a. Revising paragraph (a).</AMDPAR>
          <AMDPAR>b. Redesignating paragraphs (c) and (d) as paragraphs (d) and (e), respectively.</AMDPAR>
          <AMDPAR>c. Adding a new paragraph (c).</AMDPAR>
          <P>The revisions and addition read as follows:</P>
          <SECTION>
            <SECTNO>§ 21.260</SECTNO>
            <SUBJECT>Subsistence allowance.</SUBJECT>
            <P>(a)<E T="03">General.</E>A veteran participating in a rehabilitation program under 38 U.S.C. chapter 31 will receive a monthly subsistence allowance at the rates in paragraph (b) of this section, unless the veteran elects to receive an alternate payment (for the purposes of part 21, subpart A, referred to as the<E T="03">Post-9/11 subsistence allowance</E>) as specified in paragraph (c) of this section, or payment at the rate of monthly educational assistance allowance payable under 38 U.S.C. chapter 30 for the veteran's type of training.<E T="03">See</E>§ 21.264(a) for election of payment at the chapter 30 rate and § 21.264(b) for election of the<E T="03">Post-9/11 subsistence allowance. See</E>§§ 21.7136, 21.7137, and 21.7138 to determine the applicable chapter 30 rate.</P>
            <SECAUTH>(Authority: 38 U.S.C. 3108(a), 3108(b), 3108(f))</SECAUTH>
            <STARS/>
            <P>(c)<E T="03">Rate of payment of Post-9/11 subsistence allowance.</E>In lieu of the subsistence allowance payable under paragraph (b) of this section, VA pays the<E T="03">Post-9/11 subsistence allowance</E>at the rates in the table at the end of this paragraph, effective August 1, 2011, based on the basic allowance for housing payable under 37 U.S.C. 403. For purposes of the following table:</P>
            <P>(1)<E T="03">BAH</E>means “the applicable amount of basic allowance for housing payable under 37 U.S.C. 403 for a member of the military with dependents in pay grade E-5 residing in the military housing area that encompasses all or the majority portion of the ZIP code area in which is located the institution, agency,<PRTPAGE P="45704"/>or employer providing the rehabilitation program concerned”.</P>
            <P>(2)<E T="03">BAH National Average</E>means “the average (i.e., unweighted arithmetic mean) monthly amount of the basic allowance for housing payable under 37 U.S.C. 403 for a member of the military with dependents in pay grade E-5 residing in the United States”.</P>
            <GPOTABLE CDEF="s200,r100" COLS="2" OPTS="L2,i1">
              <TTITLE>Payment of Post-9/11 Subsistence Allowance in Accordance With Public Law 111-377</TTITLE>
              <TDESC>[Effective August 1, 2011]<SU>1</SU>
              </TDESC>
              <BOXHD>
                <CHED H="1">Type of program</CHED>
                <CHED H="1">Payment</CHED>
              </BOXHD>
              <ROW>
                <ENT I="22">Institutional:<SU>2</SU>
                </ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="03">Full-time</ENT>
                <ENT>Entire<E T="03">BAH</E>of institution ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">
                  <FR>3/4</FR>time</ENT>
                <ENT>
                  <FR>3/4</FR>
                  <E T="03">BAH</E>of institution ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">
                  <FR>1/2</FR>time</ENT>
                <ENT>
                  <FR>1/2</FR>
                  <E T="03">BAH</E>of institution ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="22">Nonpay or nominal pay on-job training in a Federal, State, local, or federally recognized Indian tribe agency; vocational course in a rehabilitation facility or sheltered workshop; institutional non-farm cooperative:</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="03">Full-time only</ENT>
                <ENT>Entire<E T="03">BAH</E>of agency or institution ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="01" O="xl">Nonpay or nominal pay work experience in a Federal, State, local, or federally recognized Indian tribe agency:</ENT>
              </ROW>
              <ROW>
                <ENT I="03">Full-time</ENT>
                <ENT>Entire<E T="03">BAH</E>of agency ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">
                  <FR>3/4</FR>time</ENT>
                <ENT>
                  <FR>3/4</FR>
                  <E T="03">BAH</E>of agency ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">
                  <FR>1/2</FR>time</ENT>
                <ENT>
                  <FR>1/2</FR>
                  <E T="03">BAH</E>of agency ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="22">Farm cooperative, apprenticeship, or other on-job training (OJT):<SU>3</SU>
                </ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="03">Full-time only</ENT>
                <ENT>Entire<E T="03">BAH</E>of employer ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="22">Combination of institutional and OJT (Full-time only):</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="03">Institutional greater than<FR>1/2</FR>time</ENT>
                <ENT>Entire<E T="03">BAH</E>of institution ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">OJT greater than<FR>1/2</FR>time<SU>3</SU>
                </ENT>
                <ENT>Entire<E T="03">BAH</E>of employer ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="22">Non-farm cooperative (Full-time only):</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="03">Institutional</ENT>
                <ENT>Entire<E T="03">BAH</E>of institution ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">On-job<SU>3</SU>
                </ENT>
                <ENT>Entire<E T="03">BAH</E>of employer ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="22">Improvement of rehabilitation potential:</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="03">Full-time</ENT>
                <ENT>Entire<E T="03">BAH</E>of institution ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">
                  <FR>3/4</FR>time</ENT>
                <ENT>
                  <FR>3/4</FR>
                  <E T="03">BAH</E>of institution ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">
                  <FR>1/2</FR>time</ENT>
                <ENT>
                  <FR>1/2</FR>
                  <E T="03">BAH</E>of institution ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">
                  <FR>1/4</FR>time<SU>4</SU>
                </ENT>
                <ENT>
                  <FR>1/4</FR>
                  <E T="03">BAH</E>of institution ZIP code.</ENT>
              </ROW>
              <ROW>
                <ENT I="22">Training consisting of solely distance learning:<SU>5</SU>
                </ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="03">Full-time</ENT>
                <ENT>
                  <FR>1/2</FR>
                  <E T="03">BAH National Average</E>.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">
                  <FR>3/4</FR>time</ENT>
                <ENT>
                  <FR>3/8</FR>
                  <E T="03">BAH National Average</E>.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">
                  <FR>1/2</FR>time</ENT>
                <ENT>
                  <FR>1/4</FR>
                  <E T="03">BAH National Average</E>.</ENT>
              </ROW>
              <ROW>
                <ENT I="22">Training in the home, including independent instructor:</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="03">Full-time only</ENT>
                <ENT>
                  <FR>1/2</FR>
                  <E T="03">BAH National Average</E>.</ENT>
              </ROW>
              <ROW>
                <ENT I="22">Training in an institution not assigned a ZIP code, including foreigninstitutions:</ENT>
              </ROW>
              <ROW>
                <ENT I="03">Full-time</ENT>
                <ENT>Entire<E T="03">BAH National Average</E>.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">
                  <FR>3/4</FR>time</ENT>
                <ENT>
                  <FR>3/4</FR>
                  <E T="03">BAH National Average</E>.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">
                  <FR>1/2</FR>time</ENT>
                <ENT>
                  <FR>1/2</FR>
                  <E T="03">BAH National Average</E>.</ENT>
              </ROW>
              <TNOTE>
                <SU>1</SU>Effective August 1, 2011, the<E T="03">Post-9/11 subsistence allowance</E>may be paid in lieu of subsistence allowance authorized in § 21.260(b), and is not adjusted to include dependents.</TNOTE>
              <TNOTE>

                <SU>2</SU>For measurement of rate of pursuit, see §§ 21.4270 and 21.4272 through 21.4275. Payments for courses being taken simultaneously at more than one institution are based on the<E T="03">BAH</E>of the ZIP code assigned to the parent institution.</TNOTE>
              <TNOTE>
                <SU>3</SU>For on-job training, payment of the<E T="03">Post-9/11 subsistence allowance</E>may not exceed the difference between the monthly training wage, not including overtime, and the entrance journeyman wage for the veteran's objective.</TNOTE>
              <TNOTE>
                <SU>4</SU>The quarter-time rate may be paid only during extended evaluation.</TNOTE>
              <TNOTE>

                <SU>5</SU>Payment for training consisting of both distance learning and courses taken at a local institution is based on the<E T="03">BAH</E>of the ZIP code assigned to the local institution.</TNOTE>
            </GPOTABLE>
            <SECAUTH>(Authority: 38 U.S.C. 3108, 3115(a)(1))</SECAUTH>
            <STARS/>
          </SECTION>
        </REGTEXT>
        <REGTEXT PART="21" TITLE="38">
          <AMDPAR>4. Amend § 21.264 by:</AMDPAR>
          <AMDPAR>a. Revising the section heading.</AMDPAR>
          <AMDPAR>b. Redesignating paragraphs (a) introductory text, (a)(1), (a)(2), and (a)(3) as paragraphs (a)(1), (a)(1)(i), (a)(1)(ii), and (a)(1)(iii) respectively.</AMDPAR>
          <AMDPAR>c. Adding a new heading to paragraph (a).</AMDPAR>
          <AMDPAR>d. Redesignating paragraphs (b) introductory text, (b)(1), and (b)(2) as paragraphs (a)(2), (a)(2)(i), and (a)(2)(ii), respectively.</AMDPAR>
          <AMDPAR>e. Redesignating paragraphs (c) introductory text, (c)(1), (c)(2), and (c)(3) as paragraph (a)(3), (a)(3)(i), (a)(3)(ii), and (a)(3)(iii), respectively.</AMDPAR>
          <AMDPAR>f. Further redesignating paragraphs (c)(3)(i), (c)(3)(ii), and (c)(3)(iii) as paragraphs (a)(3)(iii)(A), (a)(3)(iii)(B), and (a)(3)(iii)(C), respectively.</AMDPAR>
          <AMDPAR>g. Redesignating paragraph (d) as paragraph (a)(4).</AMDPAR>
          <AMDPAR>h. Adding a new paragraph (b).</AMDPAR>
          <AMDPAR>i. Revising the authority citation at the end of the section.</AMDPAR>
          <P>The revisions and additions read as follows:</P>
          <SECTION>
            <SECTNO>§ 21.264</SECTNO>
            <SUBJECT>Election of payment at the 38 U.S.C. chapter 30 educational assistance rate or election of payment of Post-9/11 subsistence allowance.</SUBJECT>
            <P>(a)<E T="03">Election of chapter 30 educational assistance rate.</E>* * *</P>
            <P>(b)<E T="03">Election of payment of Post-9/11 subsistence allowance.</E>
            </P>
            <P>(1)<E T="03">Eligibility.</E>Effective August 1, 2011, a veteran who applies and is eligible for training or education under chapter 31 may elect to receive payment of the<E T="03">Post-9/11 subsistence allowance</E>under § 21.260(c) in lieu of a subsistence allowance under § 21.260(b), provided the veteran has remaining eligibility for, and<PRTPAGE P="45705"/>entitlement to, educational assistance under chapter 33, Post-9/11 GI Bill.</P>
            <P>(2)<E T="03">Reelection of subsistence allowance under § 21.260(b).</E>Reelection of payment of benefits at the chapter 31 subsistence allowance rate under § 21.260(b) may be made only after completion of a term, quarter, semester, or other period of instruction unless:</P>
            <P>(i) Chapter 33 eligibility or entitlement ends earlier; or</P>
            <P>(ii) Failure to approve immediate reelection would prevent the veteran from continuing in the rehabilitation program.</P>
            <P>(3)<E T="03">Services under chapter 31.</E>A veteran who elects payment of the<E T="03">Post-9/11 subsistence allowance</E>remains entitled to all other services and assistance under chapter 31.</P>
            <SECAUTH>(Authority: 38 U.S.C. 3108(b))</SECAUTH>
          </SECTION>
        </REGTEXT>
        <REGTEXT PART="21" TITLE="38">
          <AMDPAR>5. Amend § 21.270 by:</AMDPAR>
          <AMDPAR>a. Revising the section heading.</AMDPAR>
          <AMDPAR>b. Removing paragraph (b).</AMDPAR>
          <AMDPAR>c. Redesignating paragraph (c) as paragraph (b).</AMDPAR>
          <AMDPAR>d. In newly redesignated paragraph (b), removing “Weeekend” and adding, in its place, “Weekend”.</AMDPAR>
          <AMDPAR>e. Adding an authority citation at the end of the section.</AMDPAR>
          <P>The revision and addition read as follows:</P>
          <SECTION>
            <SECTNO>§ 21.270</SECTNO>
            <SUBJECT>Payment of subsistence allowance during leave and other periods.</SUBJECT>
            <STARS/>
            <SECAUTH>(Authority: 38 U.S.C. 3680(a))</SECAUTH>
          </SECTION>
        </REGTEXT>
        <REGTEXT PART="21" TITLE="38">
          <AMDPAR>6. Revise § 21.274 (d)(1)(iii) to read as follows:</AMDPAR>
          <SECTION>
            <SECTNO>§ 21.274</SECTNO>
            <SUBJECT>Revolving fund loan.</SUBJECT>
            <STARS/>
            <P>(d) * * *</P>
            <P>(1) * * *</P>
            <P>(iii) The advance does not exceed either the amount needed, or twice the monthly subsistence allowance for a veteran without dependents in full-time institutional training specified in § 21.260(b); and</P>
            <STARS/>
          </SECTION>
        </REGTEXT>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19473 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 8320-01-P</BILCOD>
    </RULE>
    <RULE>
      <PREAMB>
        <AGENCY TYPE="N">ENVIRONMENTAL PROTECTION AGENCY</AGENCY>
        <CFR>40 CFR Part 52</CFR>
        <DEPDOC>[EPA-R03-OAR-2011-0471; FRL-9445-9]</DEPDOC>
        <SUBJECT>Approval and Promulgation of Air Quality Implementation Plans;Pennsylvania; Diesel-Powered Motor Vehicle Idling Act</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Environmental Protection Agency (EPA).</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Direct final rule.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>EPA is taking direct final action to approve a revision to the Pennsylvania State Implementation Plan (SIP). The revision consists of the Commonwealth's Diesel-Powered Motor Vehicle Idling Act (hereafter referred to as the Diesel-Powered Motor Vehicle Idling Act or as Act 124 of 2008, or simply Act 124). Act 124, passed by the Pennsylvania General Assembly and signed into state law by Governor Rendell in October 2008 (and effective at the state level in February 2009), reduces the allowable time that heavy-duty, commercial highway diesel vehicles of over 10,000 pounds gross vehicle weight can idle their main propulsion engines. The law restricts idling of these commercial diesel vehicles (mostly heavy trucks and buses) to a period of 5 minutes per continuous 60 minute period (with certain allowable exemptions and exclusions). Act 124 applies statewide in the Commonwealth, and is estimated by Pennsylvania to significantly reduce emissions of nitrogen oxides, volatile organic compounds, and fine particulate matter. While idle time emissions limits are not mandatory under the Clean Air Act (CAA), incorporation of Act 124 into the SIP does strengthen the SIP, makes the state law federally enforceable by EPA, and allows the Commonwealth to take credit for emissions benefits from the rule as part of future Pennsylvania SIP revisions to demonstrate compliance with CAA National Ambient Air Quality Standards (NAAQS). EPA is approving this revision governing idling time limits on commercial heavy duty vehicles into the Pennsylvania SIP. This action is not a federal mandate required by the CAA, but provides emission reductions that aid Pennsylvania in complying with CAA NAAQS. EPA's approval of this SIP revision is being done in accordance with the requirements of the CAA.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>

          <P>This rule is effective on September 30, 2011 without further notice, unless EPA receives adverse written comment by August 31, 2011. If EPA receives such comments, it will publish a timely withdrawal of the direct final rule in the<E T="04">Federal Register</E>and inform the public that the rule will not take effect.</P>
        </EFFDATE>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>Submit your comments, identified by Docket ID Number EPA-R03-OAR-2011-0471 by one of the following methods:</P>
          <P>A.<E T="03">http://www.regulations.gov.</E>Follow the on-line instructions for submitting comments.</P>
          <P>B.<E T="03">E-mail: fernandez.cristina@epa.gov</E>
          </P>
          <P>C.<E T="03">Mail:</E>EPA-R03-OAR-2011-0471, Cristina Fernandez, Associate Director, Office of Air Program Planning, Mailcode 3AP30, U.S. Environmental Protection Agency, Region III, 1650 Arch Street, Philadelphia, Pennsylvania 19103.</P>
          <P>D.<E T="03">Hand Delivery:</E>At the previously-listed EPA Region III address. Such deliveries are only accepted during the Docket's normal hours of operation, and special arrangements should be made for deliveries of boxed information.</P>
          <P>
            <E T="03">Instructions:</E>Direct your comments to Docket ID Number EPA-R03-OAR-2011-0471. EPA's policy is that all comments received will be included in the public docket without change, and may be made available online at<E T="03">http://www.regulations.gov,</E>including any personal information provided, unless the comment includes information claimed to be Confidential Business Information (CBI) or other information whose disclosure is restricted by statute. Do not submit information that you consider to be CBI or otherwise protected through<E T="03">http://www.regulations.gov</E>or e-mail. The<E T="03">http://www.regulations.gov</E>Web site is an “anonymous access” system, which means EPA will not know your identity or contact information unless you provide it in the body of your comment. If you send an e-mail comment directly to EPA without going through<E T="03">http://www.regulations.gov,</E>your e-mail address will be automatically captured and included as part of the comment that is placed in the public docket and made available on the Internet. If you submit an electronic comment, EPA recommends that you include your name and other contact information in the body of your comment and with any disk or CD-ROM you submit. If EPA cannot read your comment due to technical difficulties and cannot contact you for clarification, EPA may not be able to consider your comment. Electronic files should avoid the use of special characters, any form of encryption, and be free of any defects or viruses.</P>
          <P>
            <E T="03">Docket:</E>All documents in the electronic docket are listed in the<E T="03">http://www.regulations.gov</E>index. Although listed in the index, some information is not publicly available,<E T="03">i.e.,</E>CBI or other information whose disclosure is restricted by statute. Certain other material, such as copyrighted material, is not placed on the Internet and will be publicly available only in hard copy form. Publicly available docket materials are available either electronically in<E T="03">http://www.regulations.gov</E>or in hard copy during normal business hours at the Air<PRTPAGE P="45706"/>Protection Division, U.S. Environmental Protection Agency, Region III, 1650 Arch Street, Philadelphia, Pennsylvania 19103. Copies of the State submittal are available at the Pennsylvania Department of Environmental Protection, Bureau of Air Quality Control, P.O. Box 8468, 400 Market Street, Harrisburg, Pennsylvania 17105.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Brian Rehn, (215) 814-2176, or by e-mail at<E T="03">rehn.brian@epa.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>Throughout this rulemaking action, whenever “we,” “us,” or “our” is used, we are referring to EPA. The following outline is provided to aid in locating information in this preamble.</P>
        <EXTRACT>
          
          <FP SOURCE="FP-2">I. Summary of the SIP Revision</FP>
          <FP SOURCE="FP1-2">A. Applicability</FP>
          <FP SOURCE="FP1-2">B. Penalties for Violations</FP>
          <FP SOURCE="FP1-2">C. Idle Restriction Signage Requirements</FP>
          <FP SOURCE="FP1-2">D. Preemption of Local Ordinances and Rules</FP>
          <FP SOURCE="FP-2">II. What action is EPA taking?</FP>
          <FP SOURCE="FP-2">III. Why is EPA approving Pennsylvania's SIP revision?</FP>
          <FP SOURCE="FP-2">IV. Final Action</FP>
          <FP SOURCE="FP-2">V. Statutory and Executive Order Reviews</FP>
        </EXTRACT>
        
        <HD SOURCE="HD1">I. Summary of the SIP Revision</HD>
        <P>On January 21, 2010, Pennsylvania submitted a SIP revision to incorporate its Diesel-Powered Motor Vehicle Idling Act. Act 124, as this statute became known, was effective at the state level on February 6, 2009, and is codified in Title 35, Chapter 23B of the Pennsylvania Statute. Act 124 restricts unnecessary idling of the main propulsion engine of in-use diesel-powered commercial, heavy duty motor vehicles of over 10,000 pounds gross vehicle weight rating. With certain exceptions and exemptions, idling of subject trucks and buses is restricted to 5 minutes in any continuous 60-minute period. The purpose of Act 124 is to reduce emissions of air pollutants, including nitrogen oxides and volatile organic compounds, both of which are precursors to the formation of ground level ozone, and which are governed by a NAAQS under authority of the CAA. Act 124 also addresses fine particulate matter, another group of pollutants which is regulated by a NAAQS under the Clean Air Act.</P>
        <HD SOURCE="HD2">A. Applicability</HD>

        <P>Act 124 restricts extended idling of diesel-powered highway vehicles that are used for commercial purposes and have a gross vehicle weight rating (GVWR) of over 10,000 pounds while operating in the Commonwealth of Pennsylvania. The regulation sets a time limit of five minutes of idling (<E T="03">i.e.,</E>defined as operation of vehicle's main propulsion engine while the vehicle is stationary) per continuous 60 minute period. Section 3 of Pennsylvania's Act 124 specifically excludes certain types of highway vehicles from these idling restrictions, including motor homes, implements of husbandry, and farm vehicles and equipment.</P>
        <P>These idling restrictions do not apply to a diesel-powered motor vehicle with a label from the California Air Resources Board showing that the vehicle's engine meets California's optional idling emission standard for nitrogen oxide emissions (per applicable California law as it relates to 1985 and newer heavy-duty vehicles and engines (13 CCR 1956.8(a)(6)(C)).</P>
        <P>For vehicles that are subject to Pennsylvania's Act 124, exemptions that allow idling beyond the five-minute per hour time limit are specified therein, including:</P>
        <P>(1) Idling caused by traffic conditions, traffic control devices or signals, or law enforcement officials;</P>
        <P>(2) idling necessary to operate defrosters, heaters, air conditioners, or cargo refrigeration equipment, or idling necessary to install equipment, or idling related to a safety or health emergency (not for purposes of a rest period), or to comply with manufacturers' operating requirements or operating specifications or warranties in accordance with federal or state motor carrier safety regulations;</P>
        <P>(3) idling of a police, fire, ambulance, public safety, military, utility service, or other law enforcement vehicle or vehicle being used in an emergency capacity and not for the convenience of the driver;</P>
        <P>(4) idling of the main propulsion engine for maintenance, particulate matter trap regeneration, servicing, or repair of the vehicle or for vehicle diagnostic purposes, if idling is required for that activity;</P>
        <P>(5) idling performed as part of a state inspection to verify the equipment is in good working order, if necessary as part of the inspection;</P>
        <P>(6) idling of a primary propulsion engine to power work-related mechanical, safety, or electrical operations other than propulsion (not done for cabin comfort or to operation nonessential onboard equipment);</P>
        <P>(7) idling of a primary propulsion engine necessary as part of a security inspection, such as entering or exiting a facility;</P>
        <P>(8) idling of an armored vehicle when a person remains inside to guard the contents or during loading or unloading;</P>
        <P>(9) idling due to mechanical difficulties in which the driver has no control (if the owner submits repair documentation to the Pennsylvania Department of Environmental Protection within 30 days) verifying that the mechanical problem has been remedied;</P>
        <P>(10) idling of a bus, school bus, or school vehicle to provide heat or air conditioning when non-driver passengers are onboard (up to a maximum of 15 minutes per continuous 60 minute period);</P>
        <P>(11) idling necessary for sampling, weighing, active loading or unloading for an attended motor vehicle waiting for sampling, weighing, loading, or unloading (up to 15 minutes per continuous 60 minute period);</P>
        <P>(12) idling by a school bus or school vehicle off school property during queuing for the sequential discharge or pickup of students where the physical configuration of the school or surrounding location does not allow for stopping;</P>
        <P>(13) idling where necessary for maintaining safe operating conditions while waiting for a police escort when transporting a load requiring issuance of a special permit for excessive size and weight;</P>
        <P>(14) idling when actively engaged in solid waste collection or the collection of source-separated recyclable materials (not to apply when a vehicle is not actively engaged in solid waste or source separated recyclables collection);</P>
        <HD SOURCE="HD2">B. Penalties for Violations</HD>
        <P>Pennsylvania Act 124 lists penalties that may result from violations of the idling limits in Section 5 of Act 124. Violations constitute a summary offense, punishable by a fine of not less than $150 and not more than $300 and court costs. In addition, the Commonwealth may issue enforcement orders and civil penalties to aid in the enforcement of Act 124.</P>
        <HD SOURCE="HD2">C. Idling Restriction Signage Requirements</HD>
        <P>Pennsylvania Act 124 requires that an owner or operator of a location where vehicles subject to the act load or unload that provide 15 or more parking spaces for vehicles subject to Act 124 shall erect and maintain permanent signs that inform drivers that idling of heavy, commercial diesel-powered vehicles is restricted in Pennsylvania.</P>
        <HD SOURCE="HD2">D. Preemption of Local Ordinances or Rules</HD>

        <P>Section 9 of Act 124 preempts and supersedes local ordinance or rules concerning idling restrictions on vehicles subject to Act 124, except where the local rule is more restrictive than the provisions of Act 124 (if the local ordinance or rule was in effect prior to January 1, 2007).<PRTPAGE P="45707"/>
        </P>
        <HD SOURCE="HD1">II. What rulemaking action is EPA taking?</HD>
        <P>EPA is approving a formal revision to the Pennsylvania SIP submitted by the Commonwealth on January 21, 2010. This SIP revision consists of the Diesel-Powered Motor Vehicle Idling Act of 2008 (codified in the Pennsylvania Statute, Title 35, chapter 23B 4601-4610), which was signed into law by Governor Rendell on October 9, 2008 and became effective as state law on February 6, 2009. EPA is taking direct final rulemaking action to approve this SIP revision, and is acting to incorporate by reference Pennsylvania Act 124 of 2008 entitled, “The Diesel Powered Motor Vehicle Idling Act” (codified at Title 35, chapter 23B, 4601-4610 of the Pennsylvania Statute).</P>
        <HD SOURCE="HD1">III. Why is EPA approving Pennsylvania's SIP revision?</HD>
        <P>Pennsylvania's Diesel-Powered Motor Vehicle Idling Act SIP results in reduced emissions of pollutants that contribute to nonattainment of NAAQS for ozone and fine particulate matter. Specifically, Pennsylvania Act 124 leads to elimination of such pollutants resulting from unnecessary extended idling of heavy-duty, diesel-powered commercial vehicles. The reduction in vehicle idling resulting from this statute decreases emissions of volatile organic compounds and nitrogen oxides, both of which are ground level ozone pollution precursors. Pennsylvania's Act 124 also reduces emissions of fine particulate matter, in addition to carbon monoxide and carbon dioxide.</P>
        <P>The approval of Pennsylvania's Act 124 will strengthen the Pennsylvania SIP and will assist the Commonwealth in complying with federal ambient air quality standards, including the NAAQS for ground level ozone and fine particulate matter. Act 124 is consistent with EPA's “Model State Idling Law” (EPA420-S-06-001, April 2006). This model rule was developed with input from the states and affected industry to address extended idling issues in a consistent manner from state to state and to aid those being regulated in compliance with compliance with idling limits.</P>
        <HD SOURCE="HD1">IV. Final Action</HD>
        <P>EPA is approving Pennsylvania's Diesel-Powered Motor Vehicle Idling SIP and incorporating Pennsylvania Act 124 of 2008 into the Pennsylvania SIP. Act 124 is intended to reduce emissions caused by unnecessary idling of heavy-duty, diesel-powered, commercial motor vehicles within the boundaries of the Commonwealth of Pennsylvania.</P>
        <P>EPA is publishing this rule without prior proposal because we view this as a noncontroversial amendment and we anticipate we will receive no adverse comment. Act 124 has been in effect at the state level in Pennsylvania since February 6, 2009. Therefore, the regulated community should be accustomed to the idling restrictions imposed by this state statute.</P>

        <P>Similar provisions for reduced idling have been adopted in many other states, including the neighboring states of Delaware, Maryland, New York, New Jersey, Ohio, and West Virginia. We anticipate the regulated parties will understand Pennsylvania's requirements as they relate to other nearby states and localities with similar vehicle idling restrictions. Pennsylvania Act 124 complies with EPA's idling guidance and model rule. For these reasons, EPA anticipates that this direct final action to approve Pennsylvania's Diesel-Powered Vehicle Idling Act SIP revision will not be controversial. However, in the “Proposed Rules” section of today's<E T="04">Federal Register</E>, EPA is publishing a separate document that will serve as the proposal to approve the SIP revision if adverse comments are filed. This rule will be effective on September 30, 2011 without further notice unless EPA receives adverse comment by August 31, 2011. If EPA receives adverse comment, EPA will publish a timely withdrawal in the<E T="04">Federal Register</E>informing the public that the rule will not take effect. EPA will address all public comments in a subsequent final rule based on the proposed rule. EPA will not institute a second comment period on this action. Any parties interested in commenting must do so at this time.</P>
        <HD SOURCE="HD1">V. Statutory and Executive Order Reviews</HD>
        <HD SOURCE="HD2">A. General Requirements</HD>
        <P>Under the CAA, the Administrator is required to approve a SIP submission that complies with the provisions of the CAA and applicable Federal regulations. 42 U.S.C. 7410(k); 40 CFR 52.02(a). Thus, in reviewing SIP submissions, EPA's role is to approve state choices, provided that they meet the criteria of the CAA. Accordingly, this action merely approves state law as meeting Federal requirements and does not impose additional requirements beyond those imposed by state law. For that reason, this action:</P>
        <P>• Is not a “significant regulatory action” subject to review by the Office of Management and Budget under Executive Order 12866 (58 FR 51735, October 4, 1993);</P>

        <P>• Does not impose an information collection burden under the provisions of the Paperwork Reduction Act (44 U.S.C. 3501<E T="03">et seq.</E>);</P>

        <P>• Is certified as not having a significant economic impact on a substantial number of small entities under the Regulatory Flexibility Act (5 U.S.C. 601<E T="03">et seq.</E>);</P>
        <P>• Does not contain any unfunded mandate or significantly or uniquely affect small governments, as described in the Unfunded Mandates Reform Act of 1995 (Pub. L. 104-4);</P>
        <P>• Does not have Federalism implications as specified in Executive Order 13132 (64 FR 43255, August 10, 1999);</P>
        <P>• Is not an economically significant regulatory action based on health or safety risks subject to Executive Order 13045 (62 FR 19885, April 23, 1997);</P>
        <P>• Is not a significant regulatory action subject to Executive Order 13211 (66 FR 28355, May 22, 2001);</P>
        <P>• Is not subject to requirements of Section 12(d) of the National Technology Transfer and Advancement Act of 1995 (15 U.S.C. 272 note) because application of those requirements would be inconsistent with the CAA; and</P>
        <P>• Does not provide EPA with the discretionary authority to address, as appropriate, disproportionate human health or environmental effects, using practicable and legally permissible methods, under Executive Order 12898 (59 FR 7629, February 16, 1994).</P>
        <P>In addition, this rule does not have tribal implications as specified by Executive Order 13175 (65 FR 67249, November 9, 2000), because the SIP is not approved to apply in Indian country located in the state, and EPA notes that it will not impose substantial direct costs on tribal governments or preempt tribal law.</P>
        <HD SOURCE="HD2">B. Submission to Congress and the Comptroller General</HD>
        <P>The Congressional Review Act, 5 U.S.C. 801<E T="03">et seq.,</E>as added by the Small Business Regulatory Enforcement Fairness Act of 1996, generally provides that before a rule may take effect, the agency promulgating the rule must submit a rule report, which includes a copy of the rule, to each House of the Congress and to the Comptroller General of the United States. EPA will submit a report containing this action and other required information to the U.S. Senate, the U.S. House of Representatives, and the Comptroller General of the United States prior to publication of the rule in the<E T="04">Federal Register</E>. A major rule cannot take effect until 60 days after it is published in the<E T="04">Federal Register</E>.<PRTPAGE P="45708"/>This action is not a “major rule” as defined by 5 U.S.C. 804(2).</P>
        <HD SOURCE="HD2">C. Petitions for Judicial Review</HD>

        <P>Under section 307(b)(1) of the CAA, petitions for judicial review of this action must be filed in the United States Court of Appeals for the appropriate circuit by September 30, 2011. Filing a petition for reconsideration by the Administrator of this final rule does not affect the finality of this action for the purposes of judicial review nor does it extend the time within which a petition for judicial review may be filed, and shall not postpone the effectiveness of such rule or action. Parties with objections to this direct final rule are encouraged to file a comment in response to the parallel notice of proposed rulemaking for this action published in the proposed rules section of today's<E T="04">Federal Register</E>, rather than file an immediate petition for judicial review of this direct final rule, so that EPA can withdraw this direct final rule and address the comment in the proposed rulemaking.</P>
        <P>This action to approve the Pennsylvania Diesel-Powered Vehicle Idling Act SIP revision may not be challenged later in proceedings to enforce its requirements. (See section 307(b)(2).)</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 40 CFR Part 52</HD>
          <P>Environmental protection, Air pollution control, Carbon monoxide, Incorporation by reference, Nitrogen dioxide, Ozone, Particulate matter, Reporting and recordkeeping requirements, Volatile organic compounds.</P>
        </LSTSUB>
        <SIG>
          <DATED>Dated: July 18, 2011.</DATED>
          <NAME>W.C. Early,</NAME>
          <TITLE>Acting Regional Administrator, Region III.</TITLE>
        </SIG>
        
        <P>40 CFR part 52 is amended as follows:</P>
        <REGTEXT PART="52" TITLE="40">
          <PART>
            <HD SOURCE="HED">PART 52—[AMENDED]</HD>
          </PART>
          <AMDPAR>1. The authority citation for part 52 continues to read as follows:</AMDPAR>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>42 U.S.C. 7401<E T="03">et seq.</E>
            </P>
          </AUTH>
        </REGTEXT>
        
        <REGTEXT PART="52" TITLE="40">
          <SUBPART>
            <HD SOURCE="HED">Subpart NN—Pennsylvania</HD>
          </SUBPART>
          <AMDPAR>2. In § 52.2020, the table in paragraph (c)(1) is amended by revising the paragraph title and adding Title 35 Pennsylvania Statute, Chapter 23B, Sections 4601 to 4610, at the end of the table to read as follows:</AMDPAR>
          <SECTION>
            <SECTNO>§ 52.2020</SECTNO>
            <SUBJECT>Identification of plan.</SUBJECT>
            <STARS/>
            <P>(c) * * *</P>
            <GPOTABLE CDEF="s50,r50,12,xs96,xs96" COLS="5" OPTS="L1,i1">
              <TTITLE>(1) EPA-Approved Pennsylvania Regulations and Statutes</TTITLE>
              <BOXHD>
                <CHED H="1">State citation</CHED>
                <CHED H="1">Title/subject</CHED>
                <CHED H="1">State effective date</CHED>
                <CHED H="1">EPA approval date</CHED>
                <CHED H="1">Additional explanation/§ 52.2063 citation</CHED>
              </BOXHD>
              <ROW>
                <ENT I="22"/>
              </ROW>
              <ROW RUL="s">
                <ENT I="28">*******</ENT>
              </ROW>
              <ROW EXPSTB="04">
                <ENT I="21">
                  <E T="02">Title 35 Pennsylvania Statute—Health and Safety</E>
                </ENT>
              </ROW>
              <ROW RUL="s">
                <ENT I="21">
                  <E T="02">Chapter 23B—Diesel-Powered Motor Vehicle Idling Act</E>
                </ENT>
              </ROW>
              <ROW EXPSTB="00">
                <ENT I="01">Section 4601</ENT>
                <ENT>Short title</ENT>
                <ENT>2/6/09</ENT>
                <ENT>8/1/11<E T="03">[Insert page number where the document begins</E>]</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="01">Section 4602</ENT>
                <ENT>Definitions</ENT>
                <ENT>2/6/09</ENT>
                <ENT>8/1/11<E T="03">[Insert page number where the document begins</E>]</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="01">Section 4603</ENT>
                <ENT>Restrictions on idling</ENT>
                <ENT>2/6/09</ENT>
                <ENT>8/1/11<E T="03">[Insert]</E>
                </ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="01">Section 4604</ENT>
                <ENT>Increase of weight limit</ENT>
                <ENT>2/6/09</ENT>
                <ENT>8/1/11<E T="03">[Insert page number where the document begins</E>]</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="01">Section 4605</ENT>
                <ENT>Penalties</ENT>
                <ENT>2/6/09</ENT>
                <ENT>8/1/11<E T="03">[Insert page number where the document begins</E>]</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="01">Section 4606</ENT>
                <ENT>Disposition of fines</ENT>
                <ENT>2/6/09</ENT>
                <ENT>8/1/11<E T="03">[Insert page number where the document begins</E>]</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="01">Section 4607</ENT>
                <ENT>Enforcement</ENT>
                <ENT>2/6/09</ENT>
                <ENT>8/1/11<E T="03">[Insert page number where the document begins</E>]</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="01">Section 4608</ENT>
                <ENT>Permanent idling restriction signs</ENT>
                <ENT>2/6/09</ENT>
                <ENT>8/1/11<E T="03">[Insert page number where the document begins</E>]</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="01">Section 4609</ENT>
                <ENT>Preemption</ENT>
                <ENT>2/6/09</ENT>
                <ENT>8/1/11<E T="03">[Insert page number where the document begins</E>]</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="01">Section 4610</ENT>
                <ENT>Applicability</ENT>
                <ENT>2/6/09</ENT>
                <ENT>8/1/11<E T="03">[Insert page number where the document begins</E>]</ENT>
                <ENT/>
              </ROW>
            </GPOTABLE>
            <PRTPAGE P="45709"/>
            <STARS/>
          </SECTION>
        </REGTEXT>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19276 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6560-50-P</BILCOD>
    </RULE>
    <RULE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>National Oceanic and Atmospheric Administration</SUBAGY>
        <CFR>50 CFR Part 679</CFR>
        <DEPDOC>[Docket No. 101126522-0640-02]</DEPDOC>
        <AGENCY TYPE="O">DEPARTMENT OF ENERGY</AGENCY>
        <RIN>RIN 0648-XA610</RIN>
        <SUBJECT>Fisheries of the Exclusive Economic Zone Off Alaska; Pacific Ocean Perch in the West Yakutat District of the Gulf of Alaska</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>National Marine Fisheries Service (NMFS), National Oceanic and Atmospheric Administration (NOAA), Commerce.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Temporary rule; closure.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>NMFS is prohibiting directed fishing for Pacific ocean perch in the West Yakutat District of the Gulf of Alaska (GOA). This action is necessary to prevent exceeding the 2011 total allowable catch (TAC) of Pacific ocean perch in the West Yakutat District of the GOA.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>Effective 1200 hrs, Alaska local time (A.l.t.), July 27, 2011, through 2400 hrs, A.l.t., December 31, 2011.</P>
        </EFFDATE>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Steve Whitney, 907-586-7269.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>NMFS manages the groundfish fishery in the GOA exclusive economic zone according to the Fishery Management Plan for Groundfish of the Gulf of Alaska (FMP) prepared by the North Pacific Fishery Management Council under authority of the Magnuson-Stevens Fishery Conservation and Management Act. Regulations governing fishing by U.S. vessels in accordance with the FMP appear at subpart H of 50 CFR part 600 and 50 CFR part 679.</P>
        <P>The 2011 TAC of Pacific ocean perch in the West Yakutat District of the GOA is 1,937 metric tons (mt) as established by the final 2011 and 2012 harvest specifications for groundfish of the GOA (76 FR 11111, March 1, 2011).</P>
        <P>In accordance with § 679.20(d)(1)(i), the Administrator, Alaska Region, NMFS (Regional Administrator), has determined that the 2011 TAC of Pacific ocean perch in the West Yakutat District of the GOA will soon be reached. Therefore, the Regional Administrator is establishing a directed fishing allowance of 1,837 mt, and is setting aside the remaining 100 mt as bycatch to support other anticipated groundfish fisheries. In accordance with § 679.20(d)(1)(iii), the Regional Administrator finds that this directed fishing allowance has been reached. Consequently, NMFS is prohibiting directed fishing for Pacific ocean perch in the West Yakutat District of the GOA.</P>
        <P>After the effective date of this closure the maximum retainable amounts at§ 679.20(e) and (f) apply at any time during a trip.</P>
        <HD SOURCE="HD1">Classification</HD>
        <P>This action responds to the best available information recently obtained from the fishery. The Assistant Administrator for Fisheries, NOAA (AA), finds good cause to waive the requirement to provide prior notice and opportunity for public comment pursuant to the authority set forth at 5 U.S.C. 553(b)(B) as such requirement is impracticable and contrary to the public interest. This requirement is impracticable and contrary to the public interest as it would prevent NMFS from responding to the most recent fisheries data in a timely fashion and would delay the closure of Pacific ocean perch in the West Yakutat District of the GOA. NMFS was unable to publish a notice providing time for public comment because the most recent, relevant data only became available as of July 26, 2011.</P>
        <P>The AA also finds good cause to waive the 30-day delay in the effective date of this action under 5 U.S.C. 553(d)(3). This finding is based upon the reasons provided above for waiver of prior notice and opportunity for public comment.</P>
        <P>This action is required by § 679.20 and is exempt from review under Executive Order 12866.</P>
        <AUTH>
          <HD SOURCE="HED">Authority:</HD>
          <P>16 U.S.C. 1801<E T="03">et seq.</E>
          </P>
        </AUTH>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>Margo Schulze-Haugen,</NAME>
          <TITLE>Acting Director, Office of Sustainable Fisheries, National Marine Fisheries Service.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19394 Filed 7-27-11; 4:15 pm]</FRDOC>
      <BILCOD>BILLING CODE 3510-22-P</BILCOD>
    </RULE>
  </RULES>
  <VOL>76</VOL>
  <NO>147</NO>
  <DATE>Monday, August 1, 2011</DATE>
  <UNITNAME>Proposed Rules</UNITNAME>
  <PRORULES>
    <PRORULE>
      <PREAMB>
        <PRTPAGE P="45710"/>
        <AGENCY TYPE="F">OFFICE OF PERSONNEL MANAGEMENT</AGENCY>
        <CFR>5 CFR Parts 530, 531, and 536</CFR>
        <RIN>RIN 3206-AM43</RIN>
        <SUBJECT>Pay in Nonforeign Areas</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>U.S. Office of Personnel Management.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Proposed rule with request for comments.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The U.S. Office of Personnel Management (OPM) proposes to revise certain pay administration rules dealing with employees in nonforeign areas outside the 48 contiguous States. The proposed regulations would allow consideration of locality pay and nonforeign area cost-of-living allowances (COLAs) in evaluating the need for special rates, special rate supplements to be computed using an alternate method in nonforeign areas, locality rates to be considered basic pay for the purpose of computing nonforeign area COLAs and post differentials, a retained rate established based on a special rate payable in a nonforeign area that is in excess of the applicable limitation on special rates on January 1, 2012, to exceed the rate payable for level IV of the Executive Schedule, and temporary and term employees in nonforeign areas to be eligible for a retained rate in certain circumstances.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments must be received on or before September 15, 2011.</P>
        </EFFDATE>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may submit comments, identified by RIN number “3206-,” using either of the following methods:</P>
          <P>
            <E T="03">Federal eRulemaking Portal: http://www.regulations.gov.</E>Follow the instructions for submitting comments.</P>
          <P>
            <E T="03">Mail:</E>Jerome D. Mikowicz, Deputy Associate Director, Pay and Leave, Employee Services, U.S. Office of Personnel Management, Room 7H31, 1900 E Street, NW., Washington, DC 20415-8200.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Carey Jones by telephone at (202) 606-2858; by fax at (202) 606-0824; or by e-mail at<E T="03">pay-leave-policy@opm.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>The U.S. Office of Personnel Management (OPM) is issuing proposed regulations to revise certain pay administration rules for employees in “nonforeign areas,” which include Alaska, Hawaii, Guam, Puerto Rico, the Virgin Islands, and certain other areas listed in 5 CFR 591.205. Some of the proposed revisions are necessary to address the effects of implementing the Non-Foreign Area Retirement Equity Assurance Act of 2009 (NAREAA), as contained in subtitle B of title XIX of the National Defense Authorization Act for Fiscal Year 2010 (Pub. L. 111-84, October 28, 2009).</P>
        <HD SOURCE="HD1">NAREAA Provisions Affecting Locality Rates, Special Rates, and Retained Rates</HD>
        <P>NAREAA provided for entitlement to locality pay in the nonforeign areas while phasing out nonforeign area cost-of-living allowances (COLAs) authorized under 5 U.S.C. 5941(a)(1). Under section 1914 of Public Law 111-84, locality pay is phased in during a transition period beginning on the first day of the first pay period in January 2010 and ending on the first day of the first pay period in January 2012, hereafter referred to as the “transition period.” As locality pay increases, payable COLA rates must be reduced as specified in section 1912(b) of NAREAA. (See also 5 U.S.C. 5941(c), as amended by section 1912(b).) NAREAA also amended 5 U.S.C. 5941 to provide that a nonforeign area COLA must be paid as a percentage of basic pay, including any applicable locality-based comparability payment. (See 5 U.S.C. 5941(c)(4), as amended by NAREAA.)</P>
        <P>Under section 1915(b)(1) of NAREAA, when locality pay for a nonforeign area is increased during the transition period, the increase in the minimum rate (step 1) of any grade of a special rate schedule under 5 U.S.C. 5305 must be increased by no less than the dollar increase in the locality payment for a non-special rate employee at the same grade and step and in the same location. Corresponding increases must be provided for all special rates at higher steps in the pay range for the given grade.</P>

        <P>OPM determined a methodology for increasing special rates for General Schedule (GS) employees in nonforeign areas in conjunction with locality pay increases during the transition period that complies with the minimum requirements in section 1915(b)(1). OPM explained this methodology in a memorandum (CPM 2009-27) issued on December 30, 2009. (See<E T="03">http://www.opm.gov/oca/compmemo/INDEX.asp.</E>) OPM calculates the dollar value of any locality pay increase for a non-special rate employee at each step rate and adds that dollar amount—referred to as an “additional adjustment”—to the corresponding special rate that would apply but for this additional adjustment. This additional adjustment is equal to a constant percentage of the employee's GS base rate based on the applicable locality payment. For example, in 2010, when locality pay in all the nonforeign areas was set at 4.72 percent (one-third of the full 2010 “Rest of U.S.” locality rate of 14.16 percent), the special rate “additional adjustment” in all nonforeign areas equaled 4.72 percent of the applicable GS base rate.</P>
        <P>As provided in section 1913(c) of NAREAA, OPM has temporarily raised the limitations on the amount of special rates to a higher level during the transition period ending on the first day of the first pay period beginning on or after January 1, 2012. In other words, during the transition period, an additional adjustment made under section 1915(b) would not be limited by the normally applicable Executive Schedule level IV (EX-IV) cap on special rates ($155,500 in 2011), as established under 5 U.S.C. 5305(a)(1). However, NAREAA section 1913(c) required that any special rate in excess of the EX-IV cap at the end of the transition period must be converted to a retained rate under 5 U.S.C. 5363. Such a converted retained rate would be in excess of the current EX-IV cap on retained rates found in 5 CFR 536.304(b)(3) and 536.306(a).</P>

        <P>Some employees in nonforeign areas were entitled to retained rates during the transition period for reasons unrelated to NAREAA. On December 27, 2010, OPM issued a memorandum (CPM 2010-23) that provided special rules for adjusting retained rates under 5 U.S.C. 5363 for employees in nonforeign areas receiving COLAs during the transition period. These special rules were<PRTPAGE P="45711"/>authorized by NAREAA section 1918(a)(2).</P>
        <HD SOURCE="HD1">Proposed Changes in Special Rate and Locality Rate Regulations</HD>
        <P>Normally, OPM computes a special rate supplement by adding a fixed-dollar amount or fixed percentage of the applicable GS base rate to all GS base rates within a rate range for a category of employees. However, adding an additional adjustment in nonforeign areas (as a result of NAREAA section 1915(b)(1)) provides a third way to compute special rate supplements by allowing a combination of a fixed-dollar supplement and a percentage-based additional adjustment. OPM proposes revising 5 CFR 530.304(c) to recognize the possibility of an alternate method for computing special rate supplements in nonforeign areas for special rate schedules established before January 1, 2012.</P>
        <P>The regulations in 5 CFR 530.304(b) provide the circumstances OPM considers in evaluating the need for special rates. OPM proposes adding locality pay for the area involved and a nonforeign area COLA for the area involved as other circumstances for OPM to consider. OPM currently has the ability to consider “any other circumstances OPM considers appropriate” under 5 CFR 530.304(b)(4). However, specifically listing locality pay and nonforeign area COLA will make it explicit that these additional circumstances are appropriate for OPM to consider in evaluating the need for special rates. For similar reasons, we are proposing to amend 5 CFR 530.306(a) to add locality pay and COLA as factors that may be considered in evaluating a special rate proposal and in determining the level of special rates, as provided under 5 CFR 530.306(b)(1).</P>
        <P>The regulations in 5 CFR 530.304 govern the establishment of a special rate schedule covering a category of employees in one or more areas or locations, grades or levels, occupational groups, series, classes, or subdivisions thereof. Certain provisions in NAREAA required increases in special rate schedules to levels beyond what may be justified to prevent significant recruitment or retention difficulties. Accordingly, OPM may consider reducing special rate schedules in nonforeign areas. Under these circumstances, and in light of the special regulatory authority provided in NAREAA section 1918(a)(1), we are proposing to add a new paragraph (e) in § 530.304, which would authorize OPM to establish a separate special rate schedule that temporarily maintains the higher special rates for current employees in a covered category—i.e., those covered by the given special rate schedule before the effective date of the schedule reduction. Employees in that same category who become employed in a nonforeign area after the effective date would be covered by the reduced special rate schedule. In other words, future hires would be covered by a lower special rate schedule established consistent with labor market conditions and other provisions of 5 U.S.C. 5305, while current employees would have “grandfather” coverage under a higher special rate schedule that would provide pay protection, but would be phased out over time.</P>
        <P>The regulations in 5 CFR 530.308 list the purposes for which a special rate is considered a rate of basic pay. Section 530.308 specifically states that special rates are considered basic pay for the purpose of computing nonforeign area COLAs and post differentials. Section 530.308 also states that special rates are considered basic pay for the same purposes that locality pay is considered basic pay, as provided in 5 CFR 531.610. Currently, § 531.610 is silent regarding the treatment of locality pay as part of basic pay in computing nonforeign area COLAs, since, at the time the regulation was issued, locality pay was not payable in nonforeign areas or to any employee receiving a COLA. Section 531.610(g) does provide that a locality rate is considered a rate of basic pay for computing nonforeign area post differentials, but mentions only the scenario in which an employee is temporarily working in a nonforeign area when the employee's official worksite is located in a locality pay area because, at the time the regulation was issued, this was the only scenario in which locality pay was payable to an employee receiving a nonforeign area post differential. However, locality pay now applies to employees whose official worksites are located in a nonforeign area, and NAREAA specifically provided that nonforeign area COLA must be paid as a percentage of basic pay, including any applicable locality-based comparability payment. (See 5 U.S.C. 5941(c)(4) as amended by NAREAA.) Based on that law change, OPM is proposing to revise § 531.610 to reflect the fact that a locality rate must be used in computing nonforeign area COLAs. In addition, based on the original intent of the § 531.610(g) regulation and in light of the change in law to provide locality pay in nonforeign areas, OPM is proposing to revise § 531.610 to clarify that a locality rate is considered a rate of basic pay for the purpose of computing nonforeign area post differentials without any qualification. OPM is also proposing to make conforming changes in § 530.308. Using locality rates to compute nonforeign area post differentials is consistent with using locality rates to compute nonforeign area COLAs, which is required by law. It is also consistent with use of special rates in computing nonforeign area post differentials, and consistency in treatment of locality rates and special rates is a key objective underlying a number of OPM pay administration regulations.</P>
        <HD SOURCE="HD1">Proposed Changes in Pay Retention Regulations</HD>
        <P>Under current pay retention regulations—specifically, 5 CFR 536.304(b)(3) and 536.306(a)—a retained rate is capped at EX-IV. However, as explained above, NAREAA allows for a special rate above EX-IV to be converted to an equal retained rate at the end of the transition period. Also, under NAREAA section 1918(a)(3), the Director of OPM is authorized to prescribe rules governing the establishment and adjustment of retained rates for any employee whose rate of pay exceeds applicable pay limitations beginning on the first day of the first pay period in January 2012. Accordingly, OPM is proposing to revise its pay retention regulations to allow a retained rate established based on a special rate payable in a nonforeign area that was in excess of the applicable limitation on special rates on January 1, 2012, to exceed the EX-IV limitation until the retained rate becomes equal to or falls below the EX-IV limitation.</P>

        <P>Under current pay retention law and regulations, an employee is not eligible for pay retention if he or she was employed on a temporary or term basis immediately before the action causing a reduction in pay. (See 5 U.S.C. 5361(1) and 5 CFR 536.102(b)(2).) OPM is proposing to revise its pay retention regulations to allow an exception to this bar on eligibility in the case of a temporary or term employee in a nonforeign area who is receiving a special rate in excess of EX-IV at the end of the transition period. This proposal is consistent with NARREA section 1913(c), which requires that “any special rate” in excess of the applicable pay limitation be converted to a retained rate. Furthermore, NAREAA section 1918(a)(3) allows OPM to prescribe rules governing the establishment of retained rates for “any employee” whose rate of pay exceeds applicable pay limitations at the end of the transition period. In addition, OPM is authorized to extend pay retention<PRTPAGE P="45712"/>provisions to individuals not otherwise eligible under 5 U.S.C. 5365(b)(2).</P>
        <P>OPM is also proposing to revise its pay retention regulations to include an additional exception allowing pay retention for a temporary or term employee who is receiving a special rate incorporating an “additional adjustment” under NAREAA section 1915(b)(1) in the event the employee's special rate schedule is reduced or terminated in the future. NAREAA section 1918(a)(1) authorizes OPM to prescribe rules for special rate employees described in NAREAA section 1913. Also, as already noted above, OPM is authorized to extend pay retention provisions to individuals not otherwise eligible under 5 U.S.C. 5365(b)(2).</P>
        <P>The above-described changes in the pay retention regulations will be made in a proposed new § 536.310. That section will be removed once all affected employees have a retained rate at or below EX-IV or have lost entitlement to pay retention under 5 CFR 536.308.</P>
        <P>OPM is not proposing to continue special retained rate adjustment rules described in CPM 2010-23 after the transition period. Those special adjustment rules were needed while locality pay was being increased by significant amounts (1/3rd phase-in in January 2010, 2/3rd phase-in in January 2011, and full phase-in in January 2012), resulting in corresponding large reductions in COLA payments. OPM believes a continuing exception to the statutory retained rate adjustment rule would not be appropriate. The NAREAA section 1918(a)(2) authority under which OPM established the special retained rate adjustment rules applies only during the transition period. After the transition period, agencies must use the retained rate adjustment rules in 5 U.S.C. 5363(b)(2)(B) and 5 CFR 536.305 to adjust an employee's retained rate, including a retained rate that is above EX-IV, when a pay schedule is adjusted.</P>
        <HD SOURCE="HD1">Waiver of 60-Day Comment Period for Proposed Rulemaking</HD>
        <P>Pursuant to 5 U.S.C. 553(b)(3)(B), I find that good cause exists to waive the 60-day comment period for general notice of proposed rulemaking. Limiting the comment period for the proposed regulations to 45 days will enable OPM to issue final regulations by the time the transition period under NAREAA ends, which will ensure appropriate treatment of nonforeign area employees following the transition period and avoid administrative difficulties. Because of the reduced period for public comment, OPM will ensure that agency human resources officials, management groups, employee organizations representing Federal workers in the nonforeign areas, and congressional offices, are notified promptly once these regulations are published for public comment.</P>
        <P>Issuance of final regulations before the end of the NAREAA transition period is necessary to ensure that certain employees will not experience reductions in pay when the transition period ends on January 1, 2012. For example, employees in nonforeign areas who are receiving special rates above level IV of the Executive Schedule (EX-IV) prior to January 1, 2012, must be converted to a retained rate under 5 U.S.C. 5363 on January 1, 2012, under NAREAA section 1913(c). Under current regulations implementing section 5363, retained rates are capped at EX-IV. However, NAREAA section 1918(a)(3) allows OPM to issue regulations under which normal retained rate limitations could be exceeded, and that is what these proposed regulations would do—thus, preventing a possible loss in pay. Similarly, regulation changes are necessary to allow certain temporary or time-limited appointees in nonforeign areas to receive a retained rate and avoid a reduction in pay.</P>
        <HD SOURCE="HD1">Executive Order 13563 and Executive Order 12866</HD>
        <P>The Office of Management and Budget has reviewed this rule in accordance with E.O. 13563 and E.O. 12866.</P>
        <HD SOURCE="HD1">Regulatory Flexibility Act</HD>
        <P>I certify that these regulations will not have a significant economic impact on a substantial number of small entities because they will apply only to Federal agencies and employees.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 5 CFR Parts 530, 531 and 536</HD>
          <P>Administrative practice and procedure, Freedom of information, Government employees, Law enforcement officers, Reporting and recordkeeping requirements, Wages.</P>
        </LSTSUB>
        <SIG>
          <FP>U.S. Office of Personnel Management.</FP>
          <NAME>John Berry,</NAME>
          <TITLE>Director.</TITLE>
        </SIG>
        
        <P>Accordingly, OPM is proposing to amend 5 CFR parts 530, 531, and 536 as follows:</P>
        <PART>
          <HD SOURCE="HED">PART 530—PAY RATES AND SYSTEMS (GENERAL)</HD>
          <P>1. Revise the authority citation for part 530 to read as follows:</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>5 U.S.C. 5305 and 5307; subpart C also issued under 5 U.S.C. 5338, sec. 4 of the Performance Management and Recognition System Termination Act of 1993 (Pub. L. 103-89), 107 Stat. 981, and sec. 1918 of Public Law 111-84, 123 Stat. 2619.</P>
          </AUTH>
          <SUBPART>
            <HD SOURCE="HED">Subpart C—Special Rate Schedules for Recruitment and Retention</HD>
          </SUBPART>
          <P>2. In § 530.304—</P>
          <P>a. Remove “or” at the end of paragraph (b)(3);</P>
          <P>b. Redesignate paragraph (b)(4) as (b)(6);</P>
          <P>c. Add new paragraphs (b)(4) and (b)(5);</P>
          <P>d. Revise paragraph (c); and</P>
          <P>e. Add a new paragraph (e).</P>
          <P>The revisions and additions read as follows:</P>
          <SECTION>
            <SECTNO>§ 530.304</SECTNO>
            <SUBJECT>Establishing or increasing special rates.</SUBJECT>
            <STARS/>
            <P>(b) * * *</P>
            <P>(4) Locality pay authorized under 5 U.S.C. 5304 for the area involved;</P>
            <P>(5) A nonforeign area cost-of-living allowance authorized under 5 U.S.C. 5941(a)(1) for the area involved; or</P>
            <STARS/>
            <P>(c) In setting the level of special rates within a rate range for a category of employees, OPM will compute the special rate supplement by adding a fixed dollar amount or a fixed percentage to all GS rates within that range, except that an alternate method may be used—</P>
            <P>(1) For grades GS-1 and GS-2, where within-grade increases vary throughout the range; and</P>
            <P>(2) In the nonforeign areas listed in 5 CFR 591.205 for special rate schedules established before January 1, 2012.</P>
            <STARS/>

            <P>(e) Using its authority in section 1918(a)(1) of the Non-Foreign Area Retirement Equity Assurance Act of 2009 in combination with its authority under 5 U.S.C. 5305, OPM may establish a separate special rate schedule for a category of employees who are in GS positions covered by a nonforeign area special rate schedule in effect on January 1, 2012, and who are employed in a nonforeign area before an OPM-specified effective date. Such a separate schedule may be established if the existing special rate schedule is being reduced. An employee's coverage under the separate special rate schedule is contingent on the employee being continuously employed in a covered GS position in the nonforeign area after the OPM-specified effective date. Such a separate special rate schedule must be designed to provide temporary pay protection and be phased out over time until all affected employees are covered under the pay schedule that would otherwise apply to the category of employees in question.<PRTPAGE P="45713"/>
            </P>
            <P>3. In § 530.306—</P>
            <P>a. Remove “and” at the end of paragraph (a)(8);</P>
            <P>b. Remove the period at the end of paragraph (a)(9) and add “; or” in its place; and</P>
            <P>c. Add a new paragraph (a)(10) to read as follows:</P>
          </SECTION>
          <SECTION>
            <SECTNO>§ 530.306</SECTNO>
            <SUBJECT>Evaluating agency requests for new or increased special rates.</SUBJECT>
            <P>(a) * * *</P>
            <P>(10) The level of any locality pay authorized under 5 U.S.C. 5304 and any nonforeign area cost-of-living allowance authorized under 5 U.S.C. 5941(a)(1) for the area involved.</P>
            <STARS/>
            <P>4. In § 530.308—</P>
            <P>a. Revise paragraph (a);</P>
            <P>b. Remove paragraph (b); and</P>
            <P>c. Redesignate paragraphs (c) and (d) as (b) and (c), respectively.</P>
            <P>The revision reads as follows:</P>
          </SECTION>
          <SECTION>
            <SECTNO>§ 530.308</SECTNO>
            <SUBJECT>Treatment of special rate as basic pay.</SUBJECT>
            <STARS/>
            <P>(a) The purposes for which a locality rate is considered to be a rate of basic pay in computing other payments or benefits to the extent provided by 5 CFR 531.610, except as otherwise provided in paragraphs (b) and (c) of this section;</P>
            <STARS/>
          </SECTION>
        </PART>
        <PART>
          <HD SOURCE="HED">PART 531—PAY UNDER THE GENERAL SCHEDULE</HD>
          <P>5. Revise the authority citation for part 531 to read as follows:</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>5 U.S.C. 5115, 5307, and 5338; sec. 4 of Public Law 103-89, 107 Stat. 981; and E.O. 12748, 56 FR 4521, 3 CFR, 1991 Comp., p. 316; Subpart B also issued under 5 U.S.C. 5303(g), 5305, 5333, 5334(a) and (b), and 7701(b)(2); Subpart D also issued under 5 U.S.C. 5335 and 7701(b)(2); Subpart E also issued under 5 U.S.C. 5336; Subpart F also issued under 5 U.S.C. 5304, 5305, and 5941(a); E.O. 12883, 58 FR 63281, 3 CFR, 1993 Comp., p. 682; and E.O. 13106, 63 FR 68151, 3 CFR, 1998 Comp., p. 224.</P>
          </AUTH>
          <SUBPART>
            <HD SOURCE="HED">Subpart F—Locality-Based Comparability Payment</HD>
          </SUBPART>
          <P>6. In § 531.610, revise paragraph (g) to read as follows:</P>
          <SECTION>
            <SECTNO>§ 531.610</SECTNO>
            <SUBJECT>Treatment of locality rate as basic pay.</SUBJECT>
            <STARS/>
            <P>(g) Nonforeign area cost-of-living allowances and post differentials under 5 U.S.C. 5941 and 5 CFR part 591, subpart B;</P>
            <STARS/>
          </SECTION>
        </PART>
        <PART>
          <HD SOURCE="HED">PART 536—GRADE AND PAY RETENTION</HD>
          <P>7. Revise the authority citation for part 536 to read as follows:</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>5 U.S.C. 5361-5366; sec. 4 of the Performance Management and Recognition System Termination Act of 1993 (Pub. L. 103-89), 107 Stat. 981; § 536.301(b) also issued under 5 U.S.C. 5334(b); § 536.308 also issued under sec. 301(d)(2) of the Federal Workforce Flexibility Act of 2004 (Pub. L. 108-411), 118 Stat. 2305; § 536.310 also issued under sections 1913 and 1918 of the Non-Foreign Area Retirement Equity Assurance Act of 2009 (subtitle B of title XIX of Pub. L. 111-84), 123 Stat. 2619; § 536.405 also issued under 5 U.S.C. 552, Freedom of Information Act, Public Law 92-502.</P>
          </AUTH>
          <SUBPART>
            <HD SOURCE="HED">Subpart C—Pay Retention</HD>
          </SUBPART>
          <P>8. Add a new § 536.310 to read as follows:</P>
          <SECTION>
            <SECTNO>§ 536.310</SECTNO>
            <SUBJECT>Exceptions for certain employees in nonforeign areas.</SUBJECT>
            <P>(a) Notwithstanding §§ 536.304(b)(3) and 536.306(a), an employee may receive a retained rate higher than Executive Schedule level IV if such employee is receiving a special rate in excess of Executive Schedule level IV on January 1, 2012, that is converted to a retained rate, consistent with section 1913 of the Non-Foreign Retirement Equity Assurance Act of 2009 (subtitle B of title XIX of Pub. L. 111-84). This paragraph ceases to apply when the retained rate becomes equal to or falls below Executive Schedule level IV or when the employee ceases to be entitled to pay retention under § 536.308.</P>
            <P>(b) Notwithstanding 5 U.S.C. 5361(1) and § 536.102(b)(2), an employee who is employed on a temporary or term basis is not barred from receiving a retained rate if such employee—</P>
            <P>(1) Is receiving a special rate above Executive Schedule level IV on January 1, 2012, and is covered by paragraph (a) of this section; or</P>
            <P>(2) Is receiving a special rate incorporating an additional adjustment under section 1915(b)(1) of the Non-Foreign Retirement Equity Assurance Act (subtitle B of title XIX of Pub. L. 111-84) at the time the employee's special rate schedule is reduced or terminated.</P>
            
          </SECTION>
        </PART>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19361 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6325-39-P</BILCOD>
    </PRORULE>
    <PRORULE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF TRANSPORTATION</AGENCY>
        <SUBAGY>Federal Aviation Administration</SUBAGY>
        <CFR>14 CFR Part 39</CFR>
        <DEPDOC>[Docket No. FAA-2011-0720; Directorate Identifier 2010-NM-252-AD]</DEPDOC>
        <RIN>RIN 2120-AA64</RIN>
        <SUBJECT>Airworthiness Directives; Bombardier Inc. Model DHC-8-400 Series Airplanes</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Federal Aviation Administration (FAA), DOT.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of proposed rulemaking (NPRM).</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>We propose to adopt a new airworthiness directive (AD) for the products listed above. This proposed AD results from mandatory continuing airworthiness information (MCAI) originated by an aviation authority of another country to identify and correct an unsafe condition on an aviation product. The MCAI describes the unsafe condition as:</P>
          
          <EXTRACT>
            <P>There has been one reported incident where the main landing gear (MLG) failed to extend during testing of the MLG alternate release system. Investigation revealed that the door release lever bushing was worn, causing an increase in the lateral movement of the release cable system. An increase in free-play within the release cable system would cause additional wear to the door release lever bushing and may lead to the turnbuckle fouling against the nacelle frame. The bushing wear at the door release lever and turnbuckle fouling could cause a failure in the alternate release system, preventing the landing gear from extending in the case of a failure of the normal MLG extension/retraction system.</P>
            <STARS/>
          </EXTRACT>
        </SUM>
        <FP>The unsafe condition is loss of control during landing. The proposed AD would require actions that are intended to address the unsafe condition described in the MCAI.</FP>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>We must receive comments on this proposed AD by September 15, 2011.</P>
        </EFFDATE>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may send comments by any of the following methods:</P>
          <P>•<E T="03">Federal eRulemaking Portal:</E>Go to<E T="03">http://www.regulations.gov.</E>Follow the instructions for submitting comments.</P>
          <P>•<E T="03">Fax:</E>(202) 493-2251.</P>
          <P>•<E T="03">Mail:</E>U.S. Department of Transportation, Docket Operations, M-30, West Building Ground Floor, Room W12-140, 1200 New Jersey Avenue, SE., Washington, DC 20590.</P>
          <P>•<E T="03">Hand Delivery:</E>U.S. Department of Transportation, Docket Operations, M-30, West Building Ground Floor, Room W12-40, 1200 New Jersey<PRTPAGE P="45714"/>Avenue, SE., Washington, DC, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays.</P>

          <P>For service information identified in this proposed AD, contact Bombardier Inc., Q-Series Technical Help Desk, 123 Garratt Boulevard, Toronto, Ontario M3K 1Y5, Canada; telephone 416-375-4000; fax 416-375-4539; e-mail<E T="03">thd.qseries@aero.bombardier.com;</E>Internet<E T="03">http://www.bombardier.com.</E>You may review copies of the referenced service information at the FAA, Transport Airplane Directorate, 1601 Lind Avenue, SW., Renton, Washington. For information on the availability of this material at the FAA, call 425-227-1221.</P>
        </ADD>
        <HD SOURCE="HD1">Examining the AD Docket</HD>
        <P>You may examine the AD docket on the Internet at<E T="03">http://www.regulations.gov;</E>or in person at the Docket Operations office between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays. The AD docket contains this proposed AD, the regulatory evaluation, any comments received, and other information. The street address for the Docket Operations office (telephone (800) 647-5527) is in the<E T="02">ADDRESSES</E>section. Comments will be available in the AD docket shortly after receipt.</P>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Fabio Buttitta, Aerospace Engineer, Airframe and Mechanical Systems Branch, ANE-171, FAA, New York Aircraft Certification Office, 1600 Stewart Avenue, Suite 410, Westbury, New York 11590; telephone (516) 228-7303; fax (516) 794-5531.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">Comments Invited</HD>

        <P>We invite you to send any written relevant data, views, or arguments about this proposed AD. Send your comments to an address listed under the<E T="02">ADDRESSES</E>section. Include “Docket No. FAA-2011-0720; Directorate Identifier 2010-NM-252-AD” at the beginning of your comments. We specifically invite comments on the overall regulatory, economic, environmental, and energy aspects of this proposed AD. We will consider all comments received by the closing date and may amend this proposed AD based on those comments.</P>
        <P>We will post all comments we receive, without change, to<E T="03">http://www.regulations.gov,</E>including any personal information you provide. We will also post a report summarizing each substantive verbal contact we receive about this proposed AD.</P>
        <HD SOURCE="HD1">Discussion</HD>
        <P>Transport Canada Civil Aviation (TCCA), which is the aviation authority for Canada, has issued Canadian Airworthiness Directive CF-2010-26, dated August 17, 2010 (referred to after this as “the MCAI”), to correct an unsafe condition for the specified products. The MCAI states:</P>
        
        <EXTRACT>
          <P>There has been one reported incident where the main landing gear (MLG) failed to extend during testing of the MLG alternate release system. Investigation revealed that the door release lever bushing was worn, causing an increase in the lateral movement of the release cable system. An increase in free-play within the release cable system would cause additional wear to the door release lever bushing and may lead to the turnbuckle fouling against the nacelle frame. The bushing wear at the door release lever and turnbuckle fouling could cause a failure in the alternate release system, preventing the landing gear from extending in the case of a failure of the normal MLG extension/retraction system.</P>
          <P>This directive is to mandate the incorporation of a new maintenance task to prevent excessive free-play of the turnbuckle and cable within the alternate release system.</P>
        </EXTRACT>
        
        <FP>The unsafe condition is loss of control during landing. You may obtain further information by examining the MCAI in the AD docket.</FP>
        <HD SOURCE="HD1">Relevant Service Information</HD>
        <P>Bombardier has issued Temporary Revision (TR) MRB-46, dated February 4, 2010, to Section 1-32, Systems/Powerplant Maintenance Program, of the Maintenance Review Board (MRB) Report Part 1, of the Bombardier Q400 Dash 8 Maintenance Requirements Manual, PSM 1-84-7. The actions described in this service information are intended to correct the unsafe condition identified in the MCAI.</P>
        <HD SOURCE="HD1">FAA's Determination and Requirements of This Proposed AD</HD>
        <P>This product has been approved by the aviation authority of another country, and is approved for operation in the United States. Pursuant to our bilateral agreement with the State of Design Authority, we have been notified of the unsafe condition described in the MCAI and service information referenced above. We are proposing this AD because we evaluated all pertinent information and determined an unsafe condition exists and is likely to exist or develop on other products of the same type design.</P>
        <HD SOURCE="HD1">Differences Between This AD and the MCAI or Service Information</HD>
        <P>We have reviewed the MCAI and related service information and, in general, agree with their substance. But we might have found it necessary to use different words from those in the MCAI to ensure the AD is clear for U.S. operators and is enforceable. In making these changes, we do not intend to differ substantively from the information provided in the MCAI and related service information.</P>
        <P>We might also have proposed different actions in this AD from those in the MCAI in order to follow FAA policies. Any such differences are highlighted in a NOTE within the proposed AD.</P>
        <HD SOURCE="HD1">Costs of Compliance</HD>
        <P>Based on the service information, we estimate that this proposed AD would affect about 65 products of U.S. registry. We also estimate that it would take about 1 work-hour per product to comply with the basic requirements of this proposed AD. The average labor rate is $85 per work-hour. Based on these figures, we estimate the cost of the proposed AD on U.S. operators to be $5,525, or $85 per product.</P>
        <HD SOURCE="HD1">Authority for This Rulemaking</HD>
        <P>Title 49 of the United States Code specifies the FAA's authority to issue rules on aviation safety. Subtitle I, section 106, describes the authority of the FAA Administrator. “Subtitle VII: Aviation Programs,” describes in more detail the scope of the Agency's authority.</P>
        <P>We are issuing this rulemaking under the authority described in “Subtitle VII, Part A, Subpart III, Section 44701: General requirements.” Under that section, Congress charges the FAA with promoting safe flight of civil aircraft in air commerce by prescribing regulations for practices, methods, and procedures the Administrator finds necessary for safety in air commerce. This regulation is within the scope of that authority because it addresses an unsafe condition that is likely to exist or develop on products identified in this rulemaking action.</P>
        <HD SOURCE="HD1">Regulatory Findings</HD>
        <P>We determined that this proposed AD would not have federalism implications under Executive Order 13132. This proposed AD would not have a substantial direct effect on the States, on the relationship between the national Government and the States, or on the distribution of power and responsibilities among the various levels of government.</P>
        <P>For the reasons discussed above, I certify this proposed regulation:</P>

        <P>1. Is not a “significant regulatory action” under Executive Order 12866;<PRTPAGE P="45715"/>
        </P>
        <P>2. Is not a “significant rule” under the DOT Regulatory Policies and Procedures (44 FR 11034, February 26, 1979); and</P>
        <P>3. Will not have a significant economic impact, positive or negative, on a substantial number of small entities under the criteria of the Regulatory Flexibility Act.</P>
        <P>We prepared a regulatory evaluation of the estimated costs to comply with this proposed AD and placed it in the AD docket.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 14 CFR Part 39</HD>
          <P>Air transportation, Aircraft, Aviation safety, Incorporation by reference, Safety.</P>
        </LSTSUB>
        <HD SOURCE="HD1">The Proposed Amendment</HD>
        <P>Accordingly, under the authority delegated to me by the Administrator, the FAA proposes to amend 14 CFR Part 39 as follows:</P>
        <PART>
          <HD SOURCE="HED">PART 39—AIRWORTHINESS DIRECTIVES</HD>
          <P>1. The authority citation for part 39 continues to read as follows:</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>49 U.S.C. 106(g), 40113, 44701.</P>
          </AUTH>
          <SECTION>
            <SECTNO>§ 39.13</SECTNO>
            <SUBJECT>[Amended]</SUBJECT>
            <P>2. The FAA amends § 39.13 by adding the following new AD:</P>
            
            <EXTRACT>
              <FP SOURCE="FP-2">
                <E T="04">Bombardier Inc.:</E>Docket No. FAA-2011-0720;Directorate Identifier 2010-NM-252-AD.</FP>
              <HD SOURCE="HD1">Comments Due Date</HD>
              <P>(a) We must receive comments by September 15, 2011.</P>
              <HD SOURCE="HD1">Affected ADs</HD>
              <P>(b) None.</P>
              <HD SOURCE="HD1">Applicability</HD>
              <P>(c) This AD applies to Bombardier Inc. Model DHC-8-400, -401, and -402 airplanes, certificated in any category, having serial numbers 4001 and subsequent.</P>
              <HD SOURCE="HD1">Subject</HD>
              <P>(d) Air Transport Association (ATA) of America Code 32: Landing Gear.</P>
              <HD SOURCE="HD1">Reason</HD>
              <P>(e) The mandatory continuing airworthiness information (MCAI) states:</P>
              <P>There has been one reported incident where the main landing gear(MLG) failed to extend during testing of the MLG alternate releasesystem. Investigation revealed that the door release lever bushing wasworn, causing an increase in the lateral movement of the release cablesystem. An increase in free-play within the release cable system wouldcause additional wear to the door release lever bushing and may lead tothe turnbuckle fouling against the nacelle frame. The bushing wear at thedoor release lever and turnbuckle fouling could cause a failure in thealternate release system, preventing the landing gear from extending inthe case of a failure of the normal MLG extension/retraction system.</P>
              <STARS/>
              <FP>The unsafe condition is loss of control during landing.</FP>
              <HD SOURCE="HD1">Compliance</HD>
              <P>(f) You are responsible for having the actions required by this AD performed within the compliance times specified, unless the actions have already been done.</P>
              <HD SOURCE="HD1">Actions</HD>
              <P>(g) Within 30 days after the effective date of this AD, revise the maintenance program by incorporating Task 323400-203 specified in Bombardier Temporary Revision (TR) MRB-46, dated February 4, 2010, to Section 1-32, Systems/Powerplant Maintenance Program, of the Maintenance Review Board (MRB) Report Part 1, of the Bombardier Q400 Dash 8 Maintenance Requirements Manual, PSM 1-84-7. The initial compliance time for the actions specified in Bombardier TR MRB-46, dated February 4, 2010, is within 6,000 flight hours after the effective date of this AD. Thereafter, operate the airplane according to the procedures and compliance times in Bombardier TRMRB-46, dated February 4, 2010.</P>
              <HD SOURCE="HD1">No Alternative Actions, Intervals, and/or Critical Design Configuration Control Limitations (CDCCLs)</HD>

              <P>(h) After accomplishing the revision required by paragraph (g) of this AD, no alternative actions (<E T="03">e.g.,</E>inspections), intervals, and/or CDCCLs may be used unless the actions, intervals, and/or CDCCLs are approved as an alternative method of compliance (AMOC) in accordance with the procedures specified in paragraph (i) of this AD.</P>
              <HD SOURCE="HD1">FAA AD Differences</HD>
              <NOTE>
                <HD SOURCE="HED">Note 1:</HD>
                <P>This AD differs from the MCAI and/or service information as follows: No differences.</P>
              </NOTE>
              <HD SOURCE="HD1">Other FAA AD Provisions</HD>
              <P>(i) The following provisions also apply to this AD:</P>
              <P>(1)<E T="03">Alternative Methods of Compliance (AMOCs):</E>The Manager, New York Aircraft Certification Office (ACO), ANE-170, FAA, has the authority to approve AMOCs for this AD, if requested using the procedures found in 14 CFR 39.19. In accordance with 14 CFR 39.19, send your request to your principal inspector or local Flight Standards District Office, as appropriate. If sending information directly to the New York ACO, Send it to ATTN: Program Manager, Continuing Operational Safety, 1600 Stewart Avenue, Suite 410, Westbury, NY 11590; telephone 516-228-7300; fax 516-794-5531. Before using any approved AMOC, notify your appropriate principal inspector, or lacking a principal inspector, the manager of the local flight standards district office/certificate holding district office. The AMOC approval letter must specifically reference this AD.</P>
              <P>(2)<E T="03">Airworthy Product:</E>For any requirement in this AD to obtain corrective actions from a manufacturer or other source, use these actions if they are FAA-approved. Corrective actions are considered FAA-approved if they are approved by the State of Design Authority (or their delegated agent). You are required to assure the product is airworthy before it is returned to service.</P>
              <HD SOURCE="HD1">Related Information</HD>
              <P>(j) Refer to MCAI Canadian Airworthiness Directive CF-2010-26, datedAugust 17, 2010; and Bombardier Temporary Revision MRB-46, dated February 4, 2010, to Section 1-32, Systems/Powerplant Maintenance Program, of the Maintenance Review Board Report Part 1, of the Bombardier Q400 Dash 8 Maintenance Requirements Manual, PSM 1-84-7; for related information.</P>
            </EXTRACT>
          </SECTION>
          <SIG>
            <DATED>Issued in Renton, Washington, on July 22, 2011.</DATED>
            <NAME>Ali Bahrami,</NAME>
            <TITLE>Manager,Transport Airplane Directorate,Aircraft Certification Service.</TITLE>
          </SIG>
        </PART>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19330 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4910-13-P</BILCOD>
    </PRORULE>
    <PRORULE>
      <PREAMB>
        <AGENCY TYPE="N">FEDERAL TRADE COMMISSION</AGENCY>
        <CFR>16 CFR Part 305</CFR>
        <RIN>[RIN 3084-AB03]</RIN>
        <SUBJECT>Appliance Labeling Rule</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Federal Trade Commission (FTC or Commission).</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Proposed rule.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Commission proposes to expand coverage of the Lighting Facts label to include all screw-based and GU-10 and GU-24 pin-based light bulbs. Under this proposal, manufacturers would have 2<FR>1/2</FR>years to conform their products and packaging to the labeling requirements. The Commission also proposes to require a specific test procedure (LM-79) for measuring light output for all light emitting diode (LED) bulbs covered by the Rule. Finally, the Commission is not proposing amendments for several other issues such as watt-equivalent standards, directional light disclosures, and lead content disclosures.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Written comments must be received on or before September 22, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Interested parties may file a comment online or on paper, by following the instructions in the Request for Comment part of the<E T="02">SUPPLEMENTARY INFORMATION</E>section below. Write “Notice of Proposed Rulemaking on Expanded Bulb Coverage for the Lighting Facts Label (16 CFR part 305) (Project No. P084206)” on your comment, and file your comment online at<E T="03">https://ftcpublic.commentworks.com/ftc/lampcoveragenprm,</E>by following the<PRTPAGE P="45716"/>instructions on the web-based form. If you prefer to file your comment on paper, mail or deliver your comment to the following address: Federal Trade Commission, Office of the Secretary, Room H-113 (Annex Y), 600 Pennsylvania Avenue, NW., Washington, DC 20580.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Hampton Newsome, Attorney, Division of Enforcement, Bureau of Consumer Protection, Federal Trade Commission, 600 Pennsylvania Avenue, NW., Washington, DC 20580, (202) 326-2889.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">I. Background</HD>
        <P>On July 19, 2010 (75 FR 41696), the Commission published new light bulb<SU>1</SU>
          <FTREF/>labeling requirements and sought comments on several unresolved issues related to those requirements.<SU>2</SU>
          <FTREF/>The new requirements, which amend the Appliance Labeling Rule, 16 CFR part 305 (“Rule”), feature a “Lighting Facts” label that discloses information about the bulb's brightness, annual energy cost, life, color appearance, and energy use.<SU>3</SU>
          <FTREF/>The Commission also sought additional comment on the following unresolved issues: the label's product coverage, light-emitting diode (LED) test procedures, watt-equivalence claims, beam spread and directional light disclosures, lead content disclosures, bilingual labels, fossil fuel lamp labels, and power factor disclosures. The Commission sought comment on these issues in response to the Congressional directive to consider reopening the labeling rulemaking in 2011 if the Commission determines that further labeling changes are necessary.<SU>4</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>1</SU>This document uses the terms lamp, light bulb, and bulb interchangeably.</P>
        </FTNT>
        <FTNT>
          <P>

            <SU>2</SU>The Energy Independence and Security Act of 2007 (EISA) directed the Commission to examine existing light bulb labeling requirements. Public Law 110-140. EISA amended the Energy Policy and Conservation Act (EPCA) (42 U.S.C. 6291<E T="03">et seq.</E>).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>3</SU>The requirements also direct manufacturers to print lumen information and, where appropriate, a mercury disclosure on the products themselves.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>4</SU>42 U.S.C. 6294(a)(2)(D)(iii)(II)(bb).</P>
        </FTNT>
        <HD SOURCE="HD1">II. Proposed Amendments</HD>
        <P>Consistent with Congress' directive, the Commission is now reopening the light bulb labeling rulemaking to seek comments on proposed amendments to the Rule. Specifically, the Commission proposes to expand label coverage to additional styles of bulbs and to require a specific test procedure requirement for LED bulb labels. The comments received in response to the July 2010 Notice suggest that these changes will help consumers with their purchasing decisions.<SU>5</SU>
          <FTREF/>As discussed in section III, the Commission is not proposing amendments related to any other issues raised in the July 2010 Notice.</P>
        <FTNT>
          <P>
            <SU>5</SU>See<E T="03">http://www.ftc.gov/os/comments/lamplabelingfinal/index.shtm.</E>Unless otherwise stated, comments discussed in this document refer to the following: Anderson (# 549189-00015); Alliance to Save Energy (including American Council for an Energy-Efficient Economy, Appliance Standards Awareness Project, Consumer Federation of America, Midwest Energy Efficiency Alliance, Northeast Energy Efficiency Partnerships, Northwest Power and Conservation Council, and Southeast Energy Efficiency Alliance) (# 549189-00018); Bell (# 549189-00003); CEE (# 549189-00019); Cree, Inc. (# 549189-00022); Fountain (# 549189-00016); Fritz (# 549189-00008); Grosslight (# 549189-00011); Krause (# 549189-00010); Meirowsky (# 549189-00004) (# 549189-00005); Moratti (# 549189-00009); Naim (# 549189-00014); Natural Resources Defense Council (# 549189-00013) (# 549189-00020); National Electrical Manufacturers Association (# 549189-00021); OSRAM SYLVANIA (# 549189-00017); Puckett (# 549189-00002); and St. Peter (# 549189-00012).</P>
        </FTNT>
        <HD SOURCE="HD2">A. Expanded Light Bulb Label Coverage</HD>
        <P>The Commission proposes to expand label coverage beyond medium screw-based products<SU>6</SU>
          <FTREF/>to include all screw-based bulbs and GU-10 and GU-24 pin-based bulbs because expanded coverage will provide consumers uniform information, such as energy cost, brightness, and bulb life, to help them with their lighting decisions.<SU>7</SU>

          <FTREF/>In imposing these requirements, the Commission plans to give manufacturers at least two and a half years to change their packaging to incorporate the new labels. As explained below, the Commission also seeks comment on the Rule's existing exclusions for specialty bulbs (<E T="03">e.g.,</E>bug, marine, and mine service lamps) and requiring the Lighting Facts labels for general service fluorescent lamp packages.</P>
        <FTNT>
          <P>
            <SU>6</SU>Currently, the new label covers all general service lamps (i.e., medium screw-based incandescent, compact fluorescent [CFL], and LED products).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>7</SU>The Commission proposes this expanded coverage pursuant to 42 U.S.C. 6294(a)(6) of EPCA, which gives the Commission authority to require disclosures for consumer products “not specified” under existing labeling requirements if the Commission “determines that labeling for the product is likely to assist consumers in making purchasing decisions.” EPCA defines “consumer product” as any article (other than an automobile) which “in operation consumes, or is designed to consume energy” and “which, to any significant extent is distributed in commerce for personal use or consumption by an individual.” 42 U.S.C. 6291(1). The Commission recently relied on this authority in requiring labels for LED bulbs, reflector lamps, and three-way lamps. 75 FR 41696, 41698 (Jul. 19, 2010).</P>
        </FTNT>
        <P>In response to the July 2010 Notice, several energy efficiency groups recommended, while industry members opposed, expanding coverage to include all screw-based models, including intermediate and candelabra based models, and GU-10 and GU-24 pin-based models. The energy efficiency groups argued that such expanded label coverage would help consumers choose among bulbs with varying light output, energy efficiency, and other factors.</P>

        <P>Specifically, the Natural Resources Defense Council (NRDC) argued that the new label should appear on packages for all screw-based models to ensure that the same information, in the form of the new label, appears on most light bulbs. In its view, the label's consistent disclosures for energy cost, brightness, life, color temperature, and watts will help consumers choose products with the characteristics they seek. According to the NRDC, consumers need the same basic light bulb information regardless of the product's shape (<E T="03">e.g.,</E>pear, globe, flame, or spiral), base (<E T="03">e.g.,</E>small, medium, or large diameter), or technology (<E T="03">e.g.,</E>incandescent, halogen, LED, CFL,<E T="03">etc.</E>).<SU>8</SU>
          <FTREF/>Although medium screw bases are the most common type of consumer lamp, NRDC identified a wide variety of lamps which use candelabra and intermediate bases. During informal visits to retail stores, NRDC observed that these bulbs can range from 2 watts to 100 watts, fit many different applications including chandeliers, night lights, ceiling fans, and halogen fixtures, and use traditional incandescent, halogen, CFL, or LED technology.<SU>9</SU>
          <FTREF/>NRDC also identified wide differences in the light output among these products, arguing that labeling them would ensure a level playing field for industry. Finally, NRDC noted that packages for these products generally have room for the new FTC label.</P>
        <FTNT>
          <P>
            <SU>8</SU>The Alliance to Save Energy also argued that no reason exists to exclude some screw-based bulbs from the label and not others. In its view, such inconsistency adds to consumer confusion when purchasing lighting products.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>9</SU>NRDC included several examples of night lights, candelabra bulbs, and chandelier bulbs. In one instance, it observed two nearly-identical 60W flame shaped lamps being sold next to each, one with a conventional medium screw base, the other with a smaller, candelabra base.</P>
        </FTNT>

        <P>The Consortium for Energy Efficiency (CEE) also urged labeling for candelabra-based bulbs but added a recommendation for pin-based (GU-24 and GU-10) lamps. In its view, expanding labeling coverage to additional styles of bulbs will better inform consumers about relative product performance and avoid confusion that could be caused by requiring the Lighting Facts label for some products but not others. CEE explained that, because these products can vary significantly in light output, energy use, and other characteristics, the label will be helpful to consumers. For example, current incandescent<PRTPAGE P="45717"/>candelabra-based bulbs generally draw 25-60 watts per lamp and thus have a broad range of energy costs. These products also occupy a significant market share, according to CEE estimates, with candelabra-based products comprising roughly 9% of bulbs sold. Similarly, pin-based CFLs, which also appear in various wattages, comprise roughly 8% of the CFLs in the U.S. in 2008 (approximately 28.3 million lamps) according to CEE estimates.<SU>10</SU>
          <FTREF/>CEE observed that candelabra and pin-based lamps appear in varied light outputs, lifetimes, and color temperatures, suggesting such label information will help consumer purchasing decisions.<SU>11</SU>
          <FTREF/>Finally, CEE recommended that the FTC minimize the burden of expanded label coverage by providing manufacturers with more time to incorporate changes into their normal production and design schedules.<SU>12</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>10</SU>The Commission recently declined to require the new label for 75-watt incandescent bulbs, which represent about<FR>1/5</FR>of the incandescent market. 76 FR 20233 (Apr. 12, 2011). However, unlike pin-based CFLs, 75-watt incandescent bulbs will be phased out by 2013 efficiency standards.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>11</SU>For example, according to CEE, ENERGY STAR-qualified GU-24 products demonstrate light output ranges from 547-2703 lumens, power draw from 9-42 watts, lifetime from 8,000-12,000 hours, and color temperature from 2700-6500 Kelvin.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>12</SU>CEE's suggestion is consistent with concerns recently raised by industry members about the effective date for labels on medium screw base bulbs. See 75 FR 81943 (Dec. 29, 2010) (NEMA petition to extend effective date for implementation of the Lighting Facts label).</P>
        </FTNT>
        <P>In contrast, the National Electrical Manufacturers Association (NEMA) opposed expanded label coverage. NEMA explained that because intermediate and candelabra-based bulbs use less energy than medium screw base bulbs on a daily basis and appear only in a few household locations such as bathrooms, dining rooms, and some outdoor lighting decorative fixtures, they do not warrant labeling.<SU>13</SU>

          <FTREF/>NEMA also argued that intermediate and candelabra based bulbs produced using differing technologies (<E T="03">e.g.,</E>incandescent, CFL, and LED) do not necessarily have the same functionality, and thus are not always direct substitutes for each other, presumably decreasing the comparative benefits of the FTC label. For example, most CFL replacements do not dim and may not provide the same “sparkle” sought by consumers. NEMA also asserted that consumers are likely to purchase intermediate and candelabra bulbs based on aesthetic shape, fit, and maximum wattage of their existing sockets, not on the information provided by the new labels. Finally, NEMA argued that packages for intermediate and candelabra bulbs (often cardboard sheets with plastic bulb covers) have little or no room for the new label.</P>
        <FTNT>
          <P>
            <SU>13</SU>NEMA explained that EISA already limits the wattage of these bulbs to 40W for intermediate-based and 60W for candelabra-based bulbs, implying that labeling is not necessary for these products because of their limited wattages and corresponding energy costs. NEMA acknowledges that a few bulb types do consume more energy (e.g., 500w DE bulb) but states that these type bulbs do not have any energy efficient alternatives for consumers to choose from.</P>
        </FTNT>
        <P>After considering the comments, the Commission finds the energy efficiency group recommendations for expanding coverage more persuasive than NEMA's arguments opposing them.<SU>14</SU>
          <FTREF/>Contrary to NEMA's assertions, expanded labeling is likely to help consumers compare the variations in energy use, technology, and performance of these products. Specifically, these products can use significant amounts of energy compared to other lighting products. For example, as detailed by the comments, candelabra and intermediate-based incandescent bulbs are likely to draw significantly more watts than their CFL and LED counterparts. These bulbs also may draw more watts than larger, medium-based CFLs and LEDs. In addition, while competing technologies may not be available for some of these bulbs, that is not always the case,<SU>15</SU>

          <FTREF/>and the development of additional competing technologies is likely in the future. Also, given the relatively high wattage and light output variation among these products, consumers are likely to consider the label's light output, energy cost, life, and other disclosures even if, as NEMA states, they also are concerned with other factors such as shape, fit, and maximum wattage. In fact, as indicated by other comments, performance characteristics for these bulbs vary significantly, strongly suggesting that the FTC label, which highlights such variations, will be relevant to many consumers. And, although typical usage patterns (<E T="03">e.g.,</E>hours per day of operation) may vary for these products, the standard usage assumption on the Lighting Facts label (<E T="03">i.e.,</E>three hours per day) will provide consumers a consistent method to compare performance. Finally, though NEMA raised concerns about package size, the Rule already addresses space limitation issues by allowing an alternative text-only label for packages with less than 24 inches of printable space.<SU>16</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>14</SU>Consistent with existing requirements, the expanded bulb coverage would also apply to disclosures for bulbs sold through websites and paper catalogs. See 16 CFR 305.20.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>15</SU>For instance, as suggested by NRDC, chandelier bulbs are commonly sold in CFL and incandescent versions.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>16</SU>In calculating such space, manufacturers should exclude the package area occupied by the bulbs themselves and the plastic necessary to cover them.</P>
        </FTNT>
        <P>To expand the label's coverage to additional styles of bulbs, the Commission proposes to amend the definition of “general service lamp” to cover all screw-based incandescent, CFL, and LED lamps, eliminate existing exclusions for specific bulb shapes generally available to consumers, and make other minor, conforming changes consistent with this proposal.<SU>17</SU>
          <FTREF/>Currently, the definition excludes G shape lamps (as defined in ANSI C78.20-2003 and C79.1-2002) with a diameter of 5 inches or more; T shape lamps (as defined in ANSI C78.20-2003 and C79.1-2002) that use not more than 40 watts or have a length of more than 10 inches; and B, BA, CA, F, G16-1/2, G-25, G30, S, or M-14 lamps (as defined in ANSI C79.1-2002 and ANSI C78.20-2003) of 40 watts or less.</P>
        <FTNT>
          <P>
            <SU>17</SU>The amendment to the definition of “general service lamp” also clarifies that the Lighting Facts label applies to lamps that are “consumer products” as defined by EPCA (42 U.S.C. 6291(1)).</P>
        </FTNT>
        <P>The Commission seeks comment on this proposal, particularly whether the Rule should retain existing exclusions for the particular shapes described above.<SU>18</SU>

          <FTREF/>Please also provide detailed reasons for all comments. In preparing responses, commenters should review carefully the proposed revisions to the definition of “general service lamp” at the end of this notice. In addition, the Commission requests that comments address whether the Commission should retain existing exclusions for special-use bulbs including appliance lamps as defined at 42 U.S.C. 6291(30); black light lamps; bug lamps; colored lamps as defined at 42 U.S.C. 6291(30); infrared lamps; left-hand thread lamps; marine lamps; marine signal service lamp; mine service lamp; plant light lamps; rough service lamps as defined at 42 U.S.C. 6291(30); shatter-resistant lamps (including shatter-proof lamps and a shatterprotected lamps); sign service lamps; silver bowl lamps; showcase lamps; traffic signal lamps; and vibration service lamps as defined at 42 U.S.C. 6291(30). In addressing label coverage for these specialty bulbs or for any particular bulb shape, comments should indicate whether such bulbs are distributed, to any significant<PRTPAGE P="45718"/>extent, for personal use or consumption by consumers.</P>
        <FTNT>
          <P>

            <SU>18</SU>Comments should also address whether these products will have space available for the disclosures required on the products themselves (<E T="03">e.g.,</E>lumens and mercury disclosure). In addition, comments should address whether test procedures are available for measuring light output, energy use, life, and color temperature for these products.</P>
        </FTNT>
        <P>Finally, commenters should address whether the Lighting Facts label should appear on the package of general service fluorescent lamps.<SU>19</SU>

          <FTREF/>Currently, the Rule requires an encircled “E” on the package of these lamps to denote compliance with federal efficiency standards. When it issued this requirement in 1994, the Commission declined to require more detailed disclosures (<E T="03">e.g.,</E>lumens, life,<E T="03">etc.</E>) because of similarities in the characteristics of competing general service fluorescent lamps.<SU>20</SU>
          <FTREF/>The Commmission asks now whether it should reconsider this decision and, if so, why. In particular, comments should address the extent to which these products are sold to consumers in the residential market, the amount of energy such products use, the variability in energy use between comparable products, the burdens associated with such label changes, and the likelihood the new label information would help consumers in their purchasing decisions for these products.</P>
        <FTNT>
          <P>
            <SU>19</SU>One commenter, Meirowsky, suggested that the Commission label these products but did not provide details.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>20</SU>59 FR 25176, 25197 (May 13, 1994).</P>
        </FTNT>
        <HD SOURCE="HD2">B. LED Test Procedure</HD>
        <P>Based on unchallenged support in the comments, the Commission proposes to require a specific test procedure, IES-LM-79-2008 (LM-79), for measuring LED light output and color characteristics to help ensure consistent label content. The July 2010 Notice identified this procedure as a “safe harbor,” allowing manufacturers to use LM-79 as a reasonable basis for LED light output claims. Now, the Commission proposes to make the procedure mandatory and provide manufacturers one year to begin using the procedure as the basis for their label information for LED bulbs. The Commission seeks comment on this proposal.</P>
        <P>Comments provided convincing support for the adoption of LM-79.<SU>21</SU>
          <FTREF/>CEE argued that an FTC requirement for LM-79 would create more consistency in the market. It explained that the procedure offers the only test available to measure LED products, given their unique properties. CEE also noted that representatives of industry, research institutions, and test laboratories contributed to its development and that the ENERGY STAR program has incorporated LM-79 into its specifications. Cree, Inc., also explained that most manufacturers know the LM-79 procedures, test labs conduct these measurements, and, in the commercial market at least, consumers are looking for this test data when they purchase LED bulbs.</P>
        <FTNT>
          <P>
            <SU>21</SU>See NEMA, CEE, and Cree, Inc.</P>
        </FTNT>
        <HD SOURCE="HD1">III. Issues Not Included in Proposed Amendments</HD>
        <P>After reviewing the comments submitted in response to the July 2010 Notice, the Commission is not proposing any new requirements for watt-equivalence standards, beam spread disclosures, directional light disclosures, lead content disclosures, bilingual labels, fossil fuel lamp labels, and power factor at this time.<SU>22</SU>
          <FTREF/>Unless stated otherwise, the Commission is not seeking additional comments on these issues.</P>
        <FTNT>
          <P>

            <SU>22</SU>The Commission also received comments on issues already addressed by the Final Rule notice (<E T="03">e.g.</E>, bulb life disclosures, mercury disclosures, color rendering index, and dimmers) and issues not identified for comment in that notice (<E T="03">e.g.</E>, operating temperature disclosures). This Notice does not address those issues because the Commission has already considered them earlier or because they are not relevant to the issues currently under consideration.</P>
        </FTNT>
        <HD SOURCE="HD2">A. Watt-Equivalence Claims</HD>
        <P>The Commission is not proposing standards for watt-equivalence claims because such requirements may inhibit helpful, truthful representations, and thus may not necessarily help consumers in their bulb purchasing decisions. Nevertheless, manufacturers should heed the Commission's earlier recommendation to use ENERGY STAR equivalence benchmarks for general guidance in developing their watt-equivalence claims.<SU>23</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>23</SU>75 FR at 41701.</P>
        </FTNT>

        <P>Watt-equivalence claims often appear on CFL packages and generally contain conspicuous comparisons of the CFL's light output to equivalent incandescent lamps (<E T="03">e.g.,</E>“this bulb is a ‘60-watt’ equivalent” or “13W=60W”). In the June 2010 Notice, the Commission sought comment on establishing mandatory, watt-equivalence requirements for these claims.<SU>24</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>24</SU>
            <E T="03">Id.</E>
          </P>
        </FTNT>
        <P>The comments offered conflicting views. NRDC suggested the Commission set standards to mandate consistency in watt-equivalence claims on light bulb packages. In particular, NRDC, which provided several examples of problematic watt-equivalence claims, urged the Commission to use the ENERGY STAR watt-equivalence benchmarks in that program's CFL specifications. It also noted that the European Union has already adopted such standards. Additionally, NRDC urged standards for reflector lamps separate from those for conventional incandescent bulbs. NEMA also supported standards but, as an alternative, recommended the Commission impose a blanket prohibition on all watt-equivalence claims. Such a prohibition, in NEMA's view, would shift consumers away from using older, nearly obsolete technology as the basis for their bulb comparisons.</P>
        <P>Conversely, Cree, Inc. argued that strict standards may actually encourage watt-equivalence claims and cause continued consumer reliance on power as a shorthand for light output. Cree, Inc. also argued that watt-equivalence comparisons should take into account factors other than light output such as light quality and distribution. According to Cree, Inc., products with identical light outputs and color temperature may actually appear to be substantially different to consumers because of factors such as color rendition index, light distribution, and color point location.</P>
        <P>After considering these comments, the Commission is not proposing watt-equivalence standards at this time. As discussed by the Commission in the July 2010 Notice, the ENERGY STAR benchmarks provide important guidance, but they may not be applicable in every case.<SU>25</SU>

          <FTREF/>Variables such as color appearance and other factors discussed in the comments make it difficult to apply a “one-size-fits-all” approach. Indeed, rigid equivalence standards could inhibit truthful claims. For example, while typical 60-watt incandescent bulbs have an 800-lumen rating, some 60-watt bulbs that have a cooler light appearance, could have lower lumen ratings (<E T="03">e.g.,</E>675 lumens). A strict legal standard requiring at least 800 lumens for all 60-watt comparisons would prohibit such claims for those cooler, dimmer (<E T="03">e.g.,</E>675 lumens) bulbs even though they are truthful.<SU>26</SU>
          <FTREF/>The<PRTPAGE P="45719"/>comments did not address these concerns in any detail.</P>
        <FTNT>
          <P>
            <SU>25</SU>
            <E T="03">Id.</E>
          </P>
        </FTNT>
        <FTNT>
          <P>
            <SU>26</SU>EPCA authorizes the Commission to consider “alternative labeling approaches that will help consumers to understand new high-efficiency lamp products and to base the purchase decisions of the consumers on the most appropriate source that meets the requirements of the consumers for lighting level, light quality, lamp lifetime, and total lifecycle cost.” 42 U.S.C. 6294(a)(2)(D)(iii). Although EPCA gives the FTC authority to require affirmative energy disclosures on packages and products, the statute does not indicate that the FTC has authority to prohibit what are otherwise truthful, substantiated claims. Under § 5 of the FTC Act, the Commission has authority to prohibit deceptive and unfair claims. 15 U.S.C. 45(a)(1). There is no evidence that the watt-equivalence claims discussed here are categorically deceptive or unfair. In fact, as the Commission has acknowledged previously (74 FR 57950, 57955 (Nov. 10, 2009)), watt-equivalence claims may be useful to consumers as they transition toward using<PRTPAGE/>lumens as the primary indicator of brightness. The Commission generally does not set environmental or performance standards, particularly if such standards will prohibit truthful, non-deceptive claims. See 75 FR 63552, 63596 (Oct. 15, 2010) (proposed FTC Green Guides revisions).</P>
        </FTNT>

        <P>However, even in the absence of rigid watt-equivalence standards, manufacturers must ensure they can substantiate their watt-equivalence claims. The comments highlight the need for manufacturers to ensure their watt-equivalence claims are not deceptive. In particular, manufacturers must take into account the brightness of the bulbs they are comparing, as well as other material factors such as light appearance (<E T="03">i.e.,</E>color temperature). To help manufacturers with these claims, the ENERGY STAR program has issued watt-equivalence standards that provide general benchmarks for comparing the light output of traditional incandescents to CFLs. In the short run, the Commission recommends that manufacturers adhere to the benchmarks in the ENERGY STAR watt-equivalence guidelines (see Table 1 below) unless they have a reasonable basis for a different equivalence standard. Simply put, if a manufacturer's claim is inconsistent with the ENERGY STAR benchmarks, it must possess another competent and reliable basis to substantiate its claims and should consider clearly qualifying its claims to avoid deception. Deceptive watt-equivalence comparisons are subject to FTC law enforcement actions under § 5 of the FTC Act.</P>
        <GPOTABLE CDEF="s25,14" COLS="2" OPTS="L2,i1">
          <TTITLE>Table 1—ENERGY STAR Watt-Equivalence Benchmarks</TTITLE>
          <BOXHD>
            <CHED H="1">A-shaped incandescent bulb</CHED>
            <CHED H="1">Typical luminous flux (lumens)</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">25</ENT>
            <ENT>250</ENT>
          </ROW>
          <ROW>
            <ENT I="01">40</ENT>
            <ENT>450</ENT>
          </ROW>
          <ROW>
            <ENT I="01">60</ENT>
            <ENT>800</ENT>
          </ROW>
          <ROW>
            <ENT I="01">75</ENT>
            <ENT>1,100</ENT>
          </ROW>
          <ROW>
            <ENT I="01">100</ENT>
            <ENT>1,600</ENT>
          </ROW>
          <ROW>
            <ENT I="01">125</ENT>
            <ENT>2,000</ENT>
          </ROW>
          <ROW>
            <ENT I="01">150</ENT>
            <ENT>2,600</ENT>
          </ROW>
          <ROW>
            <ENT I="01">30-70-100</ENT>
            <ENT>1,200</ENT>
          </ROW>
          <ROW>
            <ENT I="01">50-100-150</ENT>
            <ENT>2,150</ENT>
          </ROW>
          <TNOTE>Note: Does not apply to globes, reflectors, or decorative CFLs. Lumens for 3-way lamps correspond to maximum equivalence shown.</TNOTE>
        </GPOTABLE>
        <P>In the long run, as more high-efficiency products appear and older incandescent technology leaves the market, watt-equivalence comparisons will have decreasing relevance to consumers. As equivalence claims recede, lumens will continue to provide a clear, consistent measurement for light output. However, consumer transition from watts to lumens will take time. The Commission encourages manufacturers to focus their communication efforts on lumens to help consumers with their lighting decisions. Eventually, consumer education, coupled with the phase-out of old incandescent bulbs, will help consumers look to lumens, not to obsolete watt-equivalence claims to evaluate bulb brightness.</P>
        <HD SOURCE="HD2">B. Beam Spread and Directional Light Disclosure</HD>
        <P>The Commission is not proposing requirements for beam spread or directional light disclosures because the need for such mandatory disclosures to help consumers is unclear. In particular, no consistent definition exists for beam spread across different bulb types and the need for mandatory directional light disclosures is uncertain.</P>

        <P>NEMA's comments opposed a beam spread disclosure because definitions of beam spread vary among different bulb types (<E T="03">e.g.,</E>reflector and PAR [parabolic aluminized reflector] products). In addition, NEMA asserted that most residential consumers do not understand beam spread terminology. NEMA also indicated that commercial consumers and lighting designers generally obtain beam spread information from manufacturer catalogs, not from packages, thus suggesting that beam spread information on label packages would not be particularly helpful. No other commenter specifically addressed this issue. The Commission does not plan to pursue it further at this time.</P>

        <P>NEMA and Cree, Inc. supported a directional light disclosure, arguing it would be useful to consumers and use little space on the package. In particular, NEMA recommended Center Beam Candlepower (CBCP) (<E T="03">i.e.,</E>brightness at the center of the beam) for the directional disclosure on packaging for reflector lamps, including PARs. Cree, Inc. added that the label should disclose beam angle (either a specific angle or a category such as spot, flood, etc.).</P>
        <P>Despite support in the comments, the Commission is not proposing to require CBCP disclosures at this time because nothing on the record suggests such information is familiar to typical consumers. Given this, CBCP or directional disclosure information may detract from information already on the label. If manufacturers believe such disclosures are important, nothing in the Rule prohibits them from providing it somewhere on the package (other than on the Lighting Facts label), as long as the information is truthful and substantiated.</P>
        <HD SOURCE="HD2">C. Lead Content Disclosure</HD>
        <P>The Commission is not proposing a lead disclosure on the Lighting Facts label at this time because there is no clear basis in the comments demonstrating that this additional requirement would assist consumers in their purchasing decisions. According to NEMA, manufacturers have removed most of the lead from regulated products and any remaining lead is not available to human touch.</P>
        <HD SOURCE="HD2">D. Bilingual Label Requirements</HD>
        <P>The current Rule allows, but does not require, bilingual labels. In light of the substantial marketing directed at non-English speakers, the July 2010 Notice sought comment on whether, when manufacturers make claims in a foreign language on a light bulb package, they should be required to include the Lighting Facts label in both that language and English. NEMA, the only organization to comment on this issue, opposed such a bilingual labeling requirement, citing space limitations on packages and the confusion multiple languages may cause. The Commission heard from no organizations or persons with expertise in issues affecting non-English speaking consumers.</P>
        <P>The Commission believes this issue warrants further consideration. For nearly 40 years, Commission rules, guides, and cease-and-desist orders that mandate the clear and conspicuous disclosure of information in advertisements and sales material have required that such information be displayed in the language of the target audience (ordinarily, the language principally used in the advertisement or sales material in question).<SU>27</SU>
          <FTREF/>Before adopting an alternative approach in the context of light bulb packaging, the Commission will continue to consider this issue and seeks additional information from a wider group of stakeholders. As part of that process, the Commission requests further comment on whether non-English claims on light bulb packages should trigger mandatory bilingual labels or other disclosures, and specifically asks commenters to address the following questions:</P>
        <FTNT>
          <P>
            <SU>27</SU>16 CFR 14.9 (<E T="03">see</E>38 FR 21494 (Aug. 4, 1973));<E T="03">see also</E>16 CFR 610.4(a)(3)(ii) (mandatory disclosures about free credit reports must be made in same language as that principally used in the advertisement); 16 CFR 308.3(a)(1) (mandatory disclosures about pay-per-call services must be made in same language as that principally used in advertisement); 16 CFR 455.5 (where used car sale conducted in Spanish, mandatory disclosures must be made in Spanish); 16 CFR 429.1(a) (in door-to-door sales, failure to furnish completed receipt or contract in same language as oral sales presentation is an unfair and deceptive act or practice).</P>
        </FTNT>
        <PRTPAGE P="45720"/>
        <P>1. How prevalent today are non-English claims on light bulb packages? What are the languages being used? What types of information is typically conveyed through such non-English claims?</P>
        <P>2. Do any light bulb packages currently include non-English information without displaying a bilingual version of the required FTC label? If so, please address whether, in such circumstances, the English label sufficiently conveys lighting information to non-English speaking consumers given the label's emphasis on numerical information. If so, why? If not, why not?</P>
        <P>3. Would a bilingual label requirement triggered by non-English claims on packages discourage manufacturers from including non-English information on their packages? If so why, and what could be done to ameliorate that effect? If not, why not?</P>
        <P>4. Could a bilingual label fit on all light bulb packages? If so, why? If not, why not? If the bilingual label could fit some but not all package sizes, how big would the package have to be to reasonably carry a bilingual label? Should a triggered disclosure depend on the size of the label?</P>
        <P>5. Finally, the Commission seeks input on any other measures it should consider to help non-English speaking consumers obtain the information provided on the Lighting Facts Label concerning estimated annual energy cost, brightness, light appearance, life energy use, and the presence of mercury.</P>
        <HD SOURCE="HD2">E. Fossil Fuel Lamps</HD>

        <P>The Commission is not proposing to require fossil fuel lamp labels (<E T="03">e.g.,</E>natural gas lights, propane lights, and kerosene lamps) at this time because there is no clear basis in the record to indicate the Lighting Facts label would be appropriate for these products and thus help consumers in their purchasing decisions. In earlier comments, the Edison Electric Institute urged labeling for fossil fuel lamps noting their high energy costs.<SU>28</SU>
          <FTREF/>However, fossil fuel lamps are significantly different from electric lamps in factors such as fuel type and use. For example, the usage and cost assumptions applicable to electric light bulbs may not apply to fossil fuel lamps. NEMA, which provided the only comments on this issue, noted that consumers use fossil fuel lamps for different applications than other lamps. NEMA also stated that consumers do not expect fossil fuel lamps to be energy efficient.</P>
        <FTNT>
          <P>
            <SU>28</SU>See 75 FR at 41698, n.16.</P>
        </FTNT>
        <HD SOURCE="HD2">F. Power Factor</HD>
        <P>The Commission is not proposing to include power factor on the Lighting Facts label because, according to the comments, power factor does not affect a consumer's energy costs and few consumers are likely to understand the term.<SU>29</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>29</SU>See NEMA, Cree, Inc., and CEE. Power factor, which is expressed as a number between 0 and 1, is a measure of the efficiency with which a device uses the power made available to it from the electric grid.</P>
        </FTNT>
        <HD SOURCE="HD1">IV. Minor, Clarifying Changes</HD>

        <P>The Commission also proposes to clarify the Rule language for labeling bulbs that operate at multiple, separate light levels (<E T="03">e.g.,</E>“3-way” bulbs) to clarify that such language applies to all covered bulb technologies. Currently, the Rule's language addressing such bulbs applies only to incandescent bulbs.</P>
        <HD SOURCE="HD1">V. Request for Comment</HD>
        <P>The Commission invites interested persons to submit written comments on any issue of fact, law, or policy that may bear upon the proposals under consideration. Please include explanations for any answers provided, as well as supporting evidence where appropriate. After examining the comments, the Commission will determine whether to issue specific amendments.</P>

        <P>You can file a comment online or on paper. For the Commission to consider your comment, we must receive it on or before September 22, 2011. Write “Notice of Proposed Rulemaking on Expanded Bulb Coverage for the Lighting Facts Label (16 CFR part 305) (Project No. P084206)” on your comment. Your comment—including your name and your state—will be placed on the public record of this proceeding, including, to the extent practicable, on the public Commission Web site, at<E T="03">http://www.ftc.gov/os/publiccomments.shtm.</E>As a matter of discretion, the Commission tries to remove individuals' home contact information from comments before placing them on the Commission Website.</P>
        <P>Because your comment will be made public, you are solely responsible for making sure that your comment does not include any sensitive personal information, like anyone's Social Security number, date of birth, driver's license number or other state identification number or foreign country equivalent, passport number, financial account number, or credit or debit card number. You are also solely responsible for making sure that your comment does not include any sensitive health information, like medical records or other individually identifiable health information. In addition, do not include any “[t]rade secret or any commercial or financial information which is obtained from any person and which is privileged or confidential,” as provided in Section 6(f) of the FTC Act, 15 U.S.C. 46(f), and FTC Rule 4.10(a)(2), 16 CFR 4.10(a)(2). If you want the Commission to give your comment confidential treatment, you must file it in paper form, with a request for confidential treatment, and you have to follow the procedure explained in FTC Rule 4.9(c), 16 CFR 4.9(c).<SU>30</SU>
          <FTREF/>Your comment will be kept confidential only if the FTC General Counsel, in his or her sole discretion, grants your request in accordance with the law and the public interest.</P>
        <FTNT>
          <P>
            <SU>30</SU>In particular, the written request for confidential treatment that accompanies the comment must include the factual and legal basis for the request, and must identify the specific portions of the comment to be withheld from the public record. See FTC Rule 4.9(c), 16 CFR 4.9(c).</P>
        </FTNT>

        <P>Postal mail addressed to the Commission is subject to delay due to heightened security screening. As a result, we encourage you to submit your comments online, or to send them to the Commission by courier or overnight service. To make sure that the Commission considers your online comment, you must file it at<E T="03">https://ftcpublic.commentworks.com/ftc/lampcoveragenprm,</E>by following the instructions on the web-based form. If this Notice appears at<E T="03">http://www.regulations.gov/#!home,</E>you also may file a comment through that website.</P>
        <P>If you file your comment on paper, write “Notice of Proposed Rulemaking on Expanded Bulb Coverage for the Lighting Facts Label (16 CFR part 305) (Project No. P084206)” on your comment and on the envelope, and mail or deliver it to the following address: Federal Trade Commission, Office of the Secretary, Room H-113 (Annex Y), 600 Pennsylvania Avenue, NW., Washington, DC 20580. If possible, submit your paper comment to the Commission by courier or overnight service.</P>
        <P>Visit the Commission Web site at<E T="03">http://www.ftc.gov</E>to read this Notice and the news release describing it. The FTC Act and other laws that the Commission administers permit the collection of public comments to consider and use in this proceeding as appropriate. The Commission will consider all timely and responsive<PRTPAGE P="45721"/>public comments that it receives on or before September 22, 2011. You can find more information, including routine uses permitted by the Privacy Act, in the Commission's privacy policy, at<E T="03">http://www.ftc.gov/ftc/privacy.htm.</E>
        </P>

        <P>Because written comments appear adequate to present the views of all interested parties, the Commission has not scheduled an oral hearing regarding these proposed amendments. Interested parties may request an opportunity to present views orally. If such a request is made, the Commission will publish a document in the<E T="04">Federal Register</E>stating the time and place for such oral presentation(s) and describing the procedures that will be followed. Interested parties who wish to present oral views must submit a hearing request, on or before September 22, 2011, in the form of a written comment that describes the issues on which the party wishes to speak. If there is no oral hearing, the Commission will base its decision on the written rulemaking record.</P>
        <HD SOURCE="HD1">VI. Paperwork Reduction Act</HD>
        <P>The current Rule contains recordkeeping, disclosure, and testing requirements that constitute a “collection of information” as defined by 5 CFR 1320.3(c), the definitions provision within OMB regulations that implement the Paperwork Reduction Act (PRA).<SU>31</SU>
          <FTREF/>OMB has approved the Rule's existing information collection requirements through January 31, 2014 (OMB Control No. 3084-0069). The amendments make changes in the Rule's labeling requirements. Accordingly, the Commission has submitted this notice of proposed rulemaking and associated Supporting Statement to OMB for review under the PRA.<SU>32</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>31</SU>44 U.S.C. 3501-3521.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>32</SU>The PRA analysis for this rulemaking focuses strictly on the information collection requirements created by and/or otherwise affected by the amendments. Unaffected information collection provisions, specifically those regarding recordkeeping and reporting requirements, have previously been accounted for in past FTC analyses under the Rule and are covered by the current PRA clearance from OMB.</P>
        </FTNT>
        <P>
          <E T="03">Package and Product Labeling:</E>The proposed amendments require manufacturers to label several new bulb types. Accordingly, manufacturers will have to amend their package and product labeling to include new disclosures. The new requirements impose a one-time adjustment for manufacturers. The Commission estimates that there are 50 manufacturers making approximately 3,000 of these newly covered products. This adjustment will require an estimated 600 hours per manufacturer on average.<SU>33</SU>
          <FTREF/>Annualized for a single year reflective of a prospective 3-year PRA clearance, this averages to 200 hours per year. Thus, the label design change will result in cumulative burden of 10,000 hours (50 manufacturers × 200 hours). In estimating the associated labor cost, the Commission assumes that the label design change will be implemented by graphic designers at an hourly wage rate of $23.44 per hour based on Bureau of Labor Statistics information.<SU>34</SU>
          <FTREF/>Thus, the Commission estimates annual labor cost for this adjustment will total $234,400 (10,000 hours × $23.44 per hour).</P>
        <FTNT>
          <P>
            <SU>33</SU>The Commission has increased its estimate of the hours required to make this change from earlier estimates given recent concerns raised about the burden of implementing label changes. See 75 FR 81943 (Dec. 29, 2010).</P>
        </FTNT>
        <FTNT>
          <P>

            <SU>34</SU>See U.S. Department of Labor, National Compensation Survey: Occupational Earnings in the United States 2009 (June 2010), Bulletin 2738, Table 3 (“Full-time civilian workers,” mean and median hourly wages),<E T="03">http://www.bls.gov/ncs/ncswage2009.htm, at 3-12.</E>
          </P>
        </FTNT>
        <P>The Commission estimates that the annualized capital cost of expanding the light bulb label coverage is $1,535,000. This estimate is based on the assumptions that manufacturers will have to change 3,000 model packages over a three-year period to meet the new requirements<SU>35</SU>
          <FTREF/>and that package label changes for each product will cost $1,335.<SU>36</SU>
          <FTREF/>Manufacturers place information on products in the normal course of business. Annualized in the context of a 3-year PRA clearance, these non-labor costs would average $1,335,000 (3,000 model packages × $1,335 each ÷ 3 years). As for product labeling, the Commission assumes that the one-time labeling change will cost $200 per model for an annualized estimated total of $200,000 (3,000 models × $200 ÷ 3 years). Annualized in the context of a 3-year PRA clearance, these non-labor costs would average $1,535,000.</P>
        <FTNT>
          <P>
            <SU>35</SU>This assumes that manufacturers will change packages for one third of their products in the normal course of business over the compliance period (i.e., 2<FR>1/2</FR>). The two and a half year compliance period and the notice provided by this proceeding should minimize the likelihood that manufacturers will have to discard package inventory. In addition, manufacturers may use stickers in lieu of discarding inventory.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>36</SU>See 75 FR at 41712 n. 149 and accompanying text.</P>
        </FTNT>
        <P>
          <E T="03">Catalog Sellers:</E>The proposed amendments will also require catalog sellers (<E T="03">e.g.,</E>website and print catalog sellers) to make required disclosures for these products pursuant to 16 CFR 305.20. The Commission estimates that there are approximately 150 entities subject to the amended requirements. The Commission estimates that these sellers each require approximately 17 hours per year to incorporate the data into their catalogs. This estimate is based on the assumption that entry of the required information takes on average one minute per covered product and an assumption that the average online catalog contains approximately 1,000 covered products. Given that there is great variety among sellers in the volume of products that they offer online, it is very difficult to estimate such numbers with precision. In addition, this analysis assumes that information for all 1,000 products is entered into the catalog each year. This is a conservative assumption because the number of incremental additions to the catalog from year to year is likely to be much lower after initial start-up efforts have been completed. Thus, the total annual disclosure burden for all catalog sellers of light bulbs covered by the proposed Rule is 2,550 hours (150 sellers × 17 hours annually). In estimating the associated labor cost, the Commission assumes that the label design change will be implemented by graphic designers at an hourly wage rate of $23.44 per hour.<SU>37</SU>
          <FTREF/>Thus, estimated labor cost for this adjustment is $59,772 (2,550 hours × $23.44 per hour).</P>
        <FTNT>
          <P>
            <SU>37</SU>See<E T="03">supra</E>note 34.</P>
        </FTNT>
        <P>
          <E T="03">Testing:</E>The Commission assumes conservatively that manufacturers will have to test 3,000 basic models at 14 hours for each model for a total of 42,000 hours.<SU>38</SU>
          <FTREF/>In calculating the associated labor cost estimate, the Commission assumes that this work will be implemented by electrical engineers at an hourly wage rate of $39.72 per hour.<SU>39</SU>
          <FTREF/>Thus, the Commission estimates that the new label design change will result in associated labor costs of approximately $1,668,240 (42,000 hours × $39.72 per hour). The Commission does not expect that the final amendments will create any capital or other non-labor costs for such testing.</P>
        <FTNT>
          <P>
            <SU>38</SU>The Commission also assumes conservatively that manufacturers will conduct new testing for 3,000 out of the 6,000 estimated covered products. The Commission does not expect the specific LED testing requirements will increase burden because existing burden estimates account for testing of products already covered by the Rule. See 75 FR 81943 (Dec. 29, 2010).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>39</SU>
            <E T="03">Supra</E>note 34.</P>
        </FTNT>

        <P>Accordingly, the revised estimated total hour burden of the amendments is 54,550 hours (10,000 hours for packaging and labeling + 2,550 hours for catalog compliance + 42,000 hours for additional testing for correlated color temperature) with associated labor costs of $1,962,412 and annualized capital or other non-labor costs totaling $1,535,000.<PRTPAGE P="45722"/>
        </P>
        <P>Comments on any proposed labeling requirements subject to review under the Paperwork Reduction Act should additionally be submitted to OMB. If sent by U.S. mail, they should be addressed to Office of Information and Regulatory Affairs, Office of Management and Budget, Attention: Desk Officer for the Federal Trade Commission, New Executive Office Building, Docket Library, Room 10102, 725 17th Street, NW., Washington, DC 20503. Comments sent to OMB by U.S. postal mail, however, are subject to delays due to heightened security precautions. Thus, comments instead should be sent by facsimile to (202) 395-5167.</P>
        <HD SOURCE="HD1">VII. Regulatory Flexibility Act</HD>
        <P>The Regulatory Flexibility Act (RFA), 5 U.S.C. 601-612, requires that the Commission provide an Initial Regulatory Flexibility Analysis (IRFA) with a proposed rule and a Final Regulatory Flexibility Analysis (FRFA), if any, with the final rule, unless the Commission certifies that the rule will not have a significant economic impact on a substantial number of small entities. See 5 U.S.C. 603-605.</P>
        <P>The Commission does not anticipate that the proposed rule will have a significant economic impact on a substantial number of small entities. The Commission recognizes that some of the affected manufacturers may qualify as small businesses under the relevant thresholds. However, the Commission does not expect that the economic impact of the proposed amendments will be significant.</P>
        <P>In its July 19, 2010 Notice (75 FR 41711), the Commission estimated that the new labeling requirements will apply to about 50 product manufacturers and an additional 150 online and paper catalog sellers of covered products. The Commission expects that approximately 150 qualify as small businesses.</P>
        <P>Accordingly, this document serves as notice to the Small Business Administration of the FTC's certification of no effect. To ensure the accuracy of this certification, however, the Commission requests comment on whether the proposed rule will have a significant impact on a substantial number of small entities, including specific information on the number of entities that would be covered by the proposed rule, the number of these companies that are “small entities,” and the average annual burden for each entity. Although the Commission certifies under the RFA that the rule proposed in this notice would not, if promulgated, have a significant impact on a substantial number of small entities, the Commission has determined, nonetheless, that it is appropriate to publish an IRFA in order to inquire into the impact of the proposed rule on small entities. Therefore, the Commission has prepared the following analysis:</P>
        <HD SOURCE="HD2">A. Description of the Reasons That Action by the Agency Is Being Taken</HD>
        <P>Section 321(b) of the Energy Independence and Security Act of 2007 (Pub. L. 110-140) requires the Commission to consider reopening light bulb labeling requirements in 2011. The Commission is proposing expanded product coverage and additional testing requirements to help consumers in their purchasing decisions for high efficiency products.</P>
        <HD SOURCE="HD2">B. Statement of the Objectives of, and Legal Basis for, the Proposed Rule</HD>
        <P>The objective of the rule is to improve the effectiveness of the current lamp labeling program. Section 321(b) of the Energy Independence and Security Act of 2007 (Pub. L. 110-140) requires the Commission consider reopening light bulb labeling requirements in 2011 to consider whether alternative labeling approaches would help consumers better understand new high-efficiency lamp products and help them choose lamps that meet their needs.</P>
        <HD SOURCE="HD2">C. Small Entities to Which the Proposed Rule Will Apply</HD>
        <P>Under the Small Business Size Standards issued by the Small Business Administration, lamp manufacturers qualify as small businesses if they have fewer than 1,000 employees (for other household appliances the figure is 500 employees). Lamp catalog sellers qualify as small businesses if their sales are less than $8.0 million annually. The Commission estimates that there are approximately 150 entities subject to the proposed rule's requirements that qualify as small businesses.<SU>40</SU>
          <FTREF/>The Commission seeks comment and information with regard to the estimated number or nature of small business entities for which the proposed rule would have a significant economic impact.</P>
        <FTNT>
          <P>
            <SU>40</SU>See 75 FR at 41712.</P>
        </FTNT>
        <HD SOURCE="HD2">D. Projected Reporting, Recordkeeping and Other Compliance Requirements</HD>
        <P>The changes under consideration would not increase any reporting or recordkeeping requirements associated with the Commission's labeling rules (75 FR 41696). The amendments will increase compliance burdens by extending the labeling requirements to new types of light bulbs. The Commission assumes that the label design change will be implemented by graphic designers.</P>
        <HD SOURCE="HD2">E. Duplicative, Overlapping, or Conflicting Federal Rules</HD>
        <P>The Commission has not identified any other federal statutes, rules, or policies that would duplicate, overlap, or conflict with the proposed rule. The Commission invites comment and information on this issue.</P>
        <HD SOURCE="HD2">F. Significant Alternatives to the Proposed Rule</HD>
        <P>The Commission seeks comment and information on the need, if any, for alternative compliance methods that, consistent with the statutory requirements, would reduce the economic impact of the rule on small entities. For example, in proposing to extend the bulb coverage, the Commission is currently unaware of the need to adopt any special provision for small entities to be able to take advantage of the proposed extension or exemption, where applicable. However, if such issues are identified, the Commission could consider alternative approaches such as extending the effective date of these amendments for catalog sellers to allow them additional time to comply beyond the labeling deadline set for manufacturers. Nonetheless, if the comments filed in response to this notice identify small entities that are affected by the rule, as well as alternative methods of compliance that would reduce the economic impact of the rule on such entities, the Commission will consider the feasibility of such alternatives and determine whether they should be incorporated into the final rule.</P>
        <HD SOURCE="HD1">VIII. Communications by Outside Parties to the Commissioners or Their Advisors</HD>
        <P>Written communications and summaries or transcripts of oral communications respecting the merits of this proceeding, from any outside party to any Commissioner or Commissioner's advisor, will be placed on the public record. See 16 CFR 1.26(b)(5).</P>
        <HD SOURCE="HD1">IX. Proposed Rule</HD>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 16 CFR Part 305</HD>
          <P>Advertising, Energy conservation, Household appliances, Labeling, Reporting and recordkeeping requirements.</P>
        </LSTSUB>
        

        <P>For the reasons discussed above, the Commission proposes to amend part<PRTPAGE P="45723"/>305 of title 16, Code of Federal Regulations, as follows:</P>
        <PART>
          <HD SOURCE="HED">PART 305—RULE CONCERNING DISCLOSURES REGARDING ENERGY CONSUMPTION AND WATER USE OF CERTAIN HOME APPLIANCES AND OTHER PRODUCTS REQUIRED UNDER THE ENERGY POLICY AND CONSERVATION ACT (“APPLIANCE LABELING RULE”)</HD>
          <P>1. The authority citation for part 305 continues to read as follows:</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>42 U.S.C. 6294.</P>
          </AUTH>
          
          <P>2. In § 305.3, revise paragraphs (l), (m), (n), (o), (p) and (q) to read as follows:</P>
          <SECTION>
            <SECTNO>§ 305.3</SECTNO>
            <SUBJECT>Description of covered products.</SUBJECT>
            <STARS/>
            <P>(l)<E T="03">General service lamp</E>means:</P>
            <P>(1) A lamp that is a consumer product and is:</P>
            <P>(i) A compact fluorescent lamp;</P>
            <P>(ii) A general service incandescent lamp;</P>
            <P>(iii) A general service light-emitting diode (LED or OLED) lamp; or</P>
            <P>(iv) Any other lamp that the Secretary of Energy determines is used to satisfy lighting applications traditionally served by general service incandescent lamps.</P>
            <P>(2) Exclusions. The term general service lamp does not include—</P>
            <P>(i) Any lighting application or bulb shape described in paragraphs (n)(2)(ii)(A) through (Q) of this section; and</P>
            <P>(ii) Any general service fluorescent lamp.</P>
            <P>(m)<E T="03">Compact fluorescent lamp</E>means an integrally ballasted fluorescent lamp with a screw, GU-10 pin, or GU-24 pin base, and a rated input voltage range of 115 to 130 volts; however, the term does not include any lamp that is specifically designed to be used for special purpose applications described in paragraphs (n)(2)(ii)(A) through (Q) of this section.</P>
            <P>(n)<E T="03">Incandescent lamp:</E>
            </P>
            <P>(1) Means a lamp in which light is produced by a filament heated to incandescence by an electric current, including only the following:</P>
            <P>(i) Any lamp (commonly referred to as lower wattage nonreflector general service lamps, including any tungsten-halogen lamp) that has a rated wattage up to 199 watts, has an screw base, has a rated voltage or voltage range that lies at least partially within 115 and 130 volts, and is not a reflector lamp;</P>
            <P>(ii) Any lamp (commonly referred to as a reflector lamp) which is not colored or designed for rough or vibration service applications, that contains an inner reflective coating on the outer bulb to direct the light, an R, PAR, ER, BR, BPAR, or similar bulb shapes with screw bases and a rated voltage or voltage range that lies at least partially within 115 and 130 volts;</P>
            <P>(iii) Any general service incandescent lamp (commonly referred to as a high or higher-wattage lamp) that has a rated wattage above 199 watts (above 205 watts for a high wattage reflector lamp);</P>
            <P>(2) General service incandescent lamp means</P>
            <P>(i) In general, a standard incandescent, halogen, or reflector type lamp that—</P>
            <P>(A) Is intended for general service applications;</P>
            <P>(B) Has a screw base;</P>
            <P>(C) Has a lumen range of not more than 2,600 lumens; and</P>
            <P>(D) Is capable of being operated at a voltage range at least partially within 110 and 130 volts.</P>
            <P>(ii) Exclusions. The term “general service incandescent lamp” does not include the following incandescent lamps:</P>
            <P>(A) An appliance lamp as defined at 42 U.S.C. 6291(30);</P>
            <P>(B) A black light lamp;</P>
            <P>(C) A bug lamp;</P>
            <P>(D) A colored lamp as defined at 42 U.S.C. 6291(30);</P>
            <P>(E) An infrared lamp;</P>
            <P>(F) A left-hand thread lamp;</P>
            <P>(G) A marine lamp;</P>
            <P>(H) A marine signal service lamp;</P>
            <P>(I) A mine service lamp;</P>
            <P>(J) A plant light lamp;</P>
            <P>(K) A rough service lamp as defined at 42 U.S.C. 6291(30);</P>
            <P>(L) A shatter-resistant lamp (including a shatter-proof lamp and a shatterprotected lamp);</P>
            <P>(M) A sign service lamp;</P>
            <P>(N) A silver bowl lamp;</P>
            <P>(O) A showcase lamp;</P>
            <P>(P) A traffic signal lamp; or</P>
            <P>(Q) A vibration service lamp as defined at 42 U.S.C. 6291(30);</P>
            <P>(3) Incandescent reflector lamp means a lamp described in paragraph (n)(1)(ii) of this section; and</P>
            <P>(4) Tungsten-halogen lamp means a gas-filled tungsten filament incandescent lamp containing a certain proportion of halogens in an inert gas.</P>
            <P>(o) Light-emitting diode (LED) means a p-n junction solid state device the radiated output of which is a function of the physical construction, material used, and exciting current of the device.</P>
            <P>The output of a light-emitting diode may be in—</P>
            <P>(1) The infrared region;</P>
            <P>(2) The visible region; or</P>
            <P>(3) The ultraviolet region.</P>
            <P>(p) Organic light-emitting diode (OLED) means a thin-film light-emitting device that typically consists of a series of organic layers between 2 electrical contacts (electrodes).</P>
            <P>(q) General service light-emitting diode (LED or OLED) lamp means any light-emitting diode (LED or OLED) lamp that:</P>
            <P>(1) Is intended for general service applications;</P>
            <P>(2) Has a screw base;</P>
            <P>(3) Has a lumen range of not more than 2,600 lumens; and</P>
            <P>(4) Is capable of being operated at a voltage range at least partially within 110 and 130 volts.</P>
            <STARS/>
            <P>3. In § 305.5, paragraphs (b), (c), and (d) are redesignated as paragraphs (c), (d), and (e), add a new paragraph (b), and revise the newly designated paragraph (c) to read as follows:</P>
          </SECTION>
          <SECTION>
            <SECTNO>§ 305.5</SECTNO>
            <SUBJECT>Determinations of estimated annual energy consumption, estimated annual operating cost, and energy efficiency rating, and of water use rate.</SUBJECT>
            <STARS/>

            <P>(b) Manufacturers and private labelers of any covered product that is a general service light- emitting diode lamp must determine the product's light output and correlated color temperature using “IES LM-79-08, Electrical and Photometric Measurements of Solid-State Lighting Products.” This procedure is incorporated by reference into this section. The Director of the Federal Register approved these incorporations by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies of the test procedure may be inspected or obtained at the Federal Trade Commission, Consumer Response Center, Room 130, 600 Pennsylvania Avenue, N.W., Washington, DC 20580; at the National Archives and Records Administration (NARA) by calling (202) 741-6030 or going to<E T="03">http://www.archives.gov/federal_register/code_of_federal_regulations/ibr_locations.html;</E>or from the Illuminating Engineering Society at<E T="03">www.iesna.org.</E>
            </P>

            <P>(c) Unless otherwise provided in paragraph (a) or (b) of this section or § 305.8, manufacturers and private labelers of any covered product that is a general service fluorescent lamp, general service lamp, or metal halide lamp fixture, must, for any representation required by this Part including but not limited to of the design voltage, wattage, energy cost, light output, life, correlated color temperature, or color rendering index of such lamp or for any representation made by the encircled “E” that such a lamp is in compliance with an<PRTPAGE P="45724"/>applicable standard established by section 325 of the Act, possess and rely upon a reasonable basis consisting of competent and reliable scientific tests substantiating the representation. For representations of the light output and life ratings of any covered product that is a general service lamp, unless otherwise provided by paragraph (a), the Commission will accept as a reasonable basis scientific tests conducted according to the following applicable IES test protocols that substantiate the representations:</P>
            <GPOTABLE CDEF="s150,xs50" COLS="2" OPTS="L2,tp0,i1">
              <TTITLE/>
              <BOXHD>
                <CHED H="1">For measuring light output (in lumens):</CHED>
                <CHED H="1"/>
              </BOXHD>
              <ROW>
                <ENT I="01">General Service Fluorescent</ENT>
                <ENT>IES LM 9.</ENT>
              </ROW>
              <ROW>
                <ENT I="01">Compact Fluorescent</ENT>
                <ENT>IES LM 66.</ENT>
              </ROW>
              <ROW>
                <ENT I="01">General Service Incandescent (Other than Reflector Lamps)</ENT>
                <ENT>IES LM 45.</ENT>
              </ROW>
              <ROW>
                <ENT I="01">General Service Incandescent (Reflector Lamps)</ENT>
                <ENT>IES LM 20.</ENT>
              </ROW>
              <ROW>
                <ENT I="22">For measuring laboratory life (in hours):</ENT>
                <ENT/>
              </ROW>
              <ROW>
                <ENT I="03">General Service Fluorescent</ENT>
                <ENT>IES LM 40.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">Compact Fluorescent</ENT>
                <ENT>IES LM 65.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">General Service Incandescent (Other than Reflector Lamps)</ENT>
                <ENT>IES LM 49.</ENT>
              </ROW>
              <ROW>
                <ENT I="03">General Service Incandescent (Reflector Lamps)</ENT>
                <ENT>IES LM 49.</ENT>
              </ROW>
            </GPOTABLE>
            <P>4. In § 305.15(d)(4) is revised to read as follows:</P>
          </SECTION>
          <SECTION>
            <SECTNO>§ 305.15</SECTNO>
            <SUBJECT>Labeling for lighting products.</SUBJECT>
            <STARS/>
            <P>(d) * * *</P>

            <P>(4) For any covered product that is a general service lamp and operates at discrete, multiple light levels (<E T="03">e.g.,</E>800, 1600, and 2500 lumens), the light output, energy cost, and wattage disclosures required by this section must be provided at each of the lamp's levels of light output and the lamp's life provided on the basis of the shortest lived operating mode. The multiple numbers shall be separated by a “/” (<E T="03">e.g.,</E>800/1600/2500 lumens) if they appear on the same line on the label.</P>
            <STARS/>
          </SECTION>
          <SIG>
            <P>By direction of the Commission.</P>
            <NAME>Donald S. Clark,</NAME>
            <TITLE>Secretary.</TITLE>
          </SIG>
        </PART>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19041 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6750-01-P</BILCOD>
    </PRORULE>
    <PRORULE>
      <PREAMB>
        <AGENCY TYPE="N">COMMODITY FUTURES TRADING COMMISSION</AGENCY>
        <CFR>17 CFR Parts 1 and 23</CFR>
        <RIN>RIN 3038-AD51</RIN>
        <SUBJECT>Clearing Member Risk Management</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Commodity Futures Trading Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of proposed rulemaking.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Commodity Futures Trading Commission (Commission or CFTC) is proposing rules to implement new statutory provisions enacted by Title VII of the Dodd-Frank Wall Street Reform and Consumer Protection Act. These proposed rules address risk management for cleared trades by futures commission merchants, swap dealers, and major swap participants that are clearing members.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Submit comments on or before September 30, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may submit comments, identified by RIN number 3038-AD51, by any of the following methods:</P>
          <P>•<E T="03">Agency Web site, via its Comments Online process: http://comments.cftc.gov.</E>Follow the instructions for submitting comments through the Web site.</P>
          <P>•<E T="03">Federal eRulemaking Portal: http://www.regulations.gov.</E>Follow the instructions for submitting comments.</P>
          <P>•<E T="03">Mail:</E>David A. Stawick, Secretary of the Commission, Commodity Futures Trading Commission, Three Lafayette Centre, 1155 21st Street, NW., Washington, DC 20581.</P>
          <P>•<E T="03">Courier:</E>Same as mail above.</P>

          <P>Please submit your comments using only one method. RIN number, 3038-AD51, must be in the subject field of responses submitted via e-mail, and clearly indicated on written submissions. All comments must be submitted in English, or if not, accompanied by an English translation. Comments will be posted as received to<E T="03">http://www.cftc.gov.</E>You should submit only information that you wish to make available publicly. If you wish the CFTC to consider information that you believe is exempt from disclosure under the Freedom of Information Act, a petition for confidential treatment of the exempt information may be submitted according to the procedures established in § 145.9 of the CFTC's regulations.<SU>1</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>1</SU>17 CFR 145.9.</P>
          </FTNT>

          <P>The CFTC reserves the right, but shall have no obligation, to review, pre-screen, filter, redact, refuse or remove any or all of your submission from<E T="03">http://www.cftc.gov</E>that it may deem to be inappropriate for publication, such as obscene language. All submissions that have been redacted or removed that contain comments on the merits of this action will be retained in the public comment file and will be considered as required under the Administrative Procedure Act and other applicable laws, and may be accessible under the Freedom of Information Act.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>John C. Lawton, Deputy Director and Chief Counsel, 202-418-5480,<E T="03">jlawton@cftc.gov,</E>or Christopher A. Hower, Attorney-Advisor, 202-418-6703,<E T="03">chower@cftc.gov,</E>Division of Clearing and Intermediary Oversight, Commodity Futures Trading Commission, Three Lafayette Centre, 1155 21st Street, NW., Washington, DC 20581.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">I. Background</HD>
        <P>On July 21, 2010, President Obama signed the Dodd-Frank Wall Street Reform and Consumer Protection Act (Dodd-Frank Act).<SU>2</SU>
          <FTREF/>Title VII of the Dodd-Frank Act amended the Commodity Exchange Act (CEA or Act)<SU>3</SU>

          <FTREF/>to establish a comprehensive new regulatory framework for swaps. The legislation was enacted to reduce risk, increase transparency, and promote market integrity within the financial system by, among other things: (1) Providing for the registration and comprehensive regulation of swap dealers and major swap participants; (2) imposing clearing and trade execution requirements on standardized derivative products; (3) creating rigorous recordkeeping and real-time reporting regimes; and (4) enhancing the Commission's rulemaking and enforcement authorities with respect to, among others, all registered entities and intermediaries subject to the Commission's oversight. Title VII also includes amendments to the federal securities laws to establish a similar<PRTPAGE P="45725"/>regulatory framework for security-based swaps under the authority of the Securities and Exchange Commission (SEC).</P>
        <FTNT>
          <P>
            <SU>2</SU>
            <E T="03">See</E>Dodd-Frank Wall Street Reform and Consumer Protection Act, Pub. L. 111-203, 124 Stat. 1376 (2010).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>3</SU>7 U.S.C. 1<E T="03">et seq.</E>
          </P>
        </FTNT>
        <HD SOURCE="HD1">II. Proposed Regulations</HD>
        <HD SOURCE="HD2">A. Introduction</HD>
        <P>A fundamental premise of the Dodd-Frank Act is that the use of properly regulated central clearing can reduce systemic risk. The Commission has proposed extensive regulations addressing open access and risk management at the derivatives clearing organization (DCO) level.<SU>4</SU>
          <FTREF/>The Commission also has proposed regulations addressing risk management for swap dealers (SDs) and major swap participants (MSPs).<SU>5</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>4</SU>
            <E T="03">See, e.g.,</E>76 FR 3698 (Jan. 20, 2011) (Risk Management Requirements for Derivatives Clearing Organizations). These proposed regulations include a requirement that a DCO adopt rules addressing each clearing member's risk management policies and procedures.<E T="03">See</E>proposed § 39.13(h)(5).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>5</SU>
            <E T="03">See, e.g.,</E>75 FR 91397 (Nov. 23, 2010) (Regulations Establishing Duties of Swap Dealers and Major Swap Participants).</P>
        </FTNT>
        <P>Clearing members provide the portals through which market participants gain access to DCOs as well as the first line of risk management. Accordingly, the Commission is proposing regulations to facilitate customer access to clearing and to bolster risk management at the clearing member level. The proposal addresses risk management for cleared trades by FCMs and SDs and MSPs that are clearing members.</P>
        <HD SOURCE="HD2">B. Clearing Member Risk Management</HD>
        <P>Section 3(b) provides that one of the purposes of the Act is to ensure the financial integrity of all transactions subject to the Act and to avoid systemic risk. Section 8a(5) authorizes the Commission to promulgate such regulations that it believes are reasonably necessary to effectuate any of the provisions or to accomplish any of the purposes of the Act. Risk management systems are critical to the avoidance of systemic risks.</P>
        <P>Section 4s(j)(2) requires each SD and MSP to have risk management systems adequate for managing its business. Section 4s(j)(4) requires each SD and MSP to have internal systems and procedures to perform any of the functions set forth in Section 4s.</P>
        <P>Section 4d requires FCMs to register with the Commission. It further requires FCMs to segregate customer funds. Section 4f requires FCMs to maintain certain levels of capital. Section 4g establishes reporting and recordkeeping requirements for FCMs.</P>
        <P>These provisions of law and Commission regulations promulgated pursuant to these provisions create a web of obligations designed to secure the financial integrity of the markets and the clearing system, to avoid systemic risk, and to protect customer funds. Effective risk management by FCMs is essential to achieving these goals. For example, a poorly managed position in the customer account can cause an FCM to become undersegregated. A poorly managed position in the proprietary account can cause an FCM to fall out of compliance with capital requirements.</P>
        <P>Even more significantly, a failure of risk management can cause an FCM to become insolvent and default to a DCO. This can disrupt the markets and the clearing system and harm customers. Such failures have been predominately attributable to failures in risk management.<SU>6</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>6</SU>
            <E T="03">See, e.g.,</E>the failure of Volume Investors Corporation in 1986, the failure of Griffin Trading Company in 1998, and the failure of Klein &amp; Company Futures, Inc. in 2000.</P>
        </FTNT>
        <P>As noted previously, the Dodd-Frank Act requires the increased use of central clearing. In particular, Section 2(h) establishes procedures for the mandatory clearing of certain swaps. As stated in the Senate Committee report: “Increasing the use of central clearinghouses * * * will provide safeguards for American taxpayers and the financial system as a whole.<SU>7</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>7</SU>S. Rep. No. 111-176, at 32 (2010) (report of the Senate Committee on Banking, Housing, and Urban Affairs).</P>
        </FTNT>
        <P>The Commission has proposed extensive risk management standards at the DCO level. Given the increased importance of clearing and the expected entrance of new products and new participants into the clearing system, the Commission believes that enhancing the safeguards at the clearing member level is necessary as well.</P>
        <P>Bringing swaps into clearing will increase the magnitude of the risks faced by clearing members. In many cases, it will change the nature of those risks as well. Many types of swaps have their own unique set of risk characteristics. The Commission believes that the increased concentration of risk in the clearing system combined with the changing configuration of the risk warrant additional vigilance not only by DCOs but by clearing members as well.</P>
        <P>FCMs generally have extensive experience managing the risk of futures. They generally have less experience managing the risks of swaps. The Commission believes that it is a reasonable precaution to require that certain safeguards be in place. It would ensure that FCMs, who clear on behalf of customers, are subject to standards at least as stringent as those applicable to SDs and MSPs, who clear only for themselves. Failure to require SDs, MSPs, and FCMs that are clearing members to maintain such safeguards would frustrate the regulatory regime established in the CEA, as amended by the Dodd-Frank Act. Accordingly, the Commission believes that applying the risk-management requirements in the proposed rules to SDs, MSPs, and FCMs that are clearing members are reasonably necessary to effectuate the provisions and to accomplish the purposes of the CEA.</P>
        <P>Proposed § 1.73 would apply to clearing members that are FCMs; proposed § 23.609 would apply to clearing members that are SDs or MSPs. These provisions would require these clearing members to have procedures to limit the financial risks they incur as a result of clearing trades and liquid resources to meet the obligations that arise. The proposal would require clearing members to:</P>
        <P>(1) Establish credit and market risk-based limits based on position size, order size, margin requirements, or similar factors;</P>
        <P>(2) Use automated means to screen orders for compliance with the risk-based limits;</P>
        <P>(3) Monitor for adherence to the risk-based limits intra-day and overnight;</P>
        <P>(4) Conduct stress tests of all positions in the proprietary account and all positions in any customer account that could pose material risk to the futures commission merchant at least once per week;</P>
        <P>(5) Evaluate its ability to meet initial margin requirements at least once per week;</P>
        <P>(6) Evaluate its ability to meet variation margin requirements in cash at least once per week;</P>
        <P>(7) Evaluate its ability to liquidate the positions it clears in an orderly manner, and estimate the cost of the liquidation at least once per month; and</P>
        <P>(8) Test all lines of credit at least once per quarter.</P>
        <P>Each of these items has been observed by Commission staff as an element of an existing sound risk management program at a DCO or an FCM.</P>

        <P>The Commission does not intend to prescribe the particular means of fulfilling these obligations. As is the case with DCOs, clearing members will have flexibility in developing procedures that meet their needs. For example, items (1) and (2) could be addressed through simple numerical limits on order or position size or through more complex margin-based limits. Further examples could include<PRTPAGE P="45726"/>price limits to reject orders that are too far away from the market, or limits on the number of orders that could be placed in a short time.</P>
        <P>The following are examples of tools that could be used to monitor for risk and to mitigate it:</P>
        
        <FP SOURCE="FP-1">—The ability to see all working and filled orders for intraday risk management;</FP>
        <FP SOURCE="FP-1">—A “kill button” that cancels all open orders for an account and disconnects electronic access.</FP>
        <P>The Commission believes that these proposals are consistent with international standards. In August 2010, the International Organization of Securities Commissions issued a report entitled “Direct Electronic Access to Markets.”<SU>8</SU>
          <FTREF/>The report set out a number of principles to guide markets, regulators, and intermediaries. Principle 6 states that:</P>
        <FTNT>
          <P>
            <SU>8</SU>The report can be found at<E T="03">http://www.iosco.org.</E>
          </P>
        </FTNT>
        <EXTRACT>
          
          <P>A market should not permit DEA [direct electronic access] unless there are in place effective systems and controls reasonably designed to enable the management of risk with regard to fair and orderly trading including, in particular, automated pre-trade controls that enable intermediaries to implement appropriate trading limits.</P>
        </EXTRACT>
        
        <P>Principle 7 states that:</P>
        
        <EXTRACT>
          <P>Intermediaries (including, as appropriate, clearing firms) should use controls, including automated pre-trade controls, which can limit or prevent a DEA Customer from placing an order that exceeds a relevant intermediary's existing position or credit limits.</P>
        </EXTRACT>
        
        <P>Stress tests are an essential risk management tool. The purpose in conducting stress tests is to determine the potential for significant losses in the event of extreme market events and the ability of traders and clearing members to absorb the losses. As was the case with the DCO risk management proposal, the Commission does not intend to prescribe the manner in which clearing members conduct stress tests. Rather, the Commission would monitor to determine whether clearing members were routinely conducting stress tests reasonably designed for the types of risk the clearing members and their customers face.</P>
        <P>The proposal also would require clearing members to evaluate their ability to meet calls for initial and variation margin. This includes testing for liquidity of financial resources available to cover exposures due to market events. Routine testing of this sort diminishes the chance of a default based on liquidity problems.</P>
        <P>Each clearing member also would be required to evaluate periodically its ability to liquidate, in an orderly manner, the positions in the proprietary and customer accounts and estimate the cost of the liquidation. In recent years, Commission staff has observed instances where a trader was unable to meet its financial obligations and the FCM had to assume responsibility for the trader's portfolio. Under these conditions, an FCM would normally liquidate the portfolio promptly. In some instances, however, where the portfolio contained large and complex options positions, the FCM found that it was not easy to liquidate. The Commission believes that clearing members should periodically review portfolios to ensure that they have the ability to liquidate them and to estimate the cost of such liquidation. The exercise should also address the ability of the FCM to put on appropriate hedges to mitigate risk pending liquidation. Such an exercise would take into account the size of the positions, the concentration of the positions in particular markets, and the liquidity of the markets.</P>
        <P>Finally, the proposal would require each clearing member to establish written procedures to comply with this regulation and to keep records documenting its compliance. The Commission believes that these are important elements of a good risk management program.</P>
        <P>The Commission requests comments on all aspects of the risk management proposal. In particular the Commission requests comment on:</P>
        <P>• The extent to which each DCO already (i) Requires clearing member FCMs, SDs, and MSPs to have each component, and (ii) audits compliance with such requirement;</P>
        <P>• The extent to which each component has otherwise been incorporated into exsisting risk management systems of clearing member FCMs, SDs, and MSPs; and</P>
        <P>• The potential costs and benefits of each component.</P>
        <HD SOURCE="HD1">III. Related Matters</HD>
        <HD SOURCE="HD2">A. Regulatory Flexibility Act</HD>
        <P>The Regulatory Flexibility Act (RFA) requires that agencies consider whether the regulations they propose will have a significant economic impact on a substantial number of small entities.<SU>9</SU>
          <FTREF/>The Commission previously has established certain definitions of “small entities” to be used in evaluating the impact of its regulations on small entities in accordance with the RFA.<SU>10</SU>
          <FTREF/>The proposed regulations would affect FCMs, DCOs, SDs, and MSPs.</P>
        <FTNT>
          <P>
            <SU>9</SU>5 U.S.C. 601<E T="03">et seq.</E>
          </P>
        </FTNT>
        <FTNT>
          <P>
            <SU>10</SU>47 FR 18618, Apr. 30, 1982.</P>
        </FTNT>
        <P>The Commission previously has determined, however, that FCMs should not be considered to be small entities for purposes of the RFA.<SU>11</SU>
          <FTREF/>The Commission's determination was based, in part, upon the obligation of FCMs to meet the minimum financial requirements established by the Commission to enhance the protection of customers' segregated funds and protect the financial condition of FCMs generally.<SU>12</SU>
          <FTREF/>The Commission also has previously determined that DCOs are not small entities for the purpose of the RFA.<SU>13</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>11</SU>
            <E T="03">Id.</E>at 18619.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>12</SU>
            <E T="03">Id.</E>
          </P>
        </FTNT>
        <FTNT>
          <P>
            <SU>13</SU>
            <E T="03">See</E>66 FR 45605, 45609, Aug. 29, 2001.</P>
        </FTNT>
        <P>SDs and MSPs are new categories of registrants. Accordingly, the Commission has not previously addressed the question of whether such persons are, in fact, small entities for purposes of the RFA. Like FCMs, SDs will be subject to minimum capital and margin requirements and are expected to comprise the largest global financial firms. The Commission is required to exempt from SD registration any entities that engage in a de minimis level of swap dealing in connection with transactions with or on behalf of customers. The Commission anticipates that this exemption would tend to exclude small entities from registration. Accordingly, for purposes of the RFA for this rulemaking, the Commission is hereby proposing that SDs not be considered “small entities” for essentially the same reasons that FCMs have previously been determined not to be small entities and in light of the exemption from the definition of SD for those engaging in a de minimis level of swap dealing.</P>
        <P>The Commission also has previously determined that large traders are not “small entities” for RFA purposes.<SU>14</SU>

          <FTREF/>In that determination, the Commission considered that a large trading position was indicative of the size of the business. MSPs, by statutory definition, maintain substantial positions in swaps or maintain outstanding swap positions that create substantial counterparty exposure that could have serious adverse effects on the financial stability of the United States banking system or financial markets. Accordingly, for purposes of the RFA for this rulemaking, the Commission is hereby proposing that MSPs not be considered “small entities” for essentially the same reasons that large traders have<PRTPAGE P="45727"/>previously been determined not to be small entities.</P>
        <FTNT>
          <P>
            <SU>14</SU>
            <E T="03">Id.</E>at 18620.</P>
        </FTNT>
        <P>Accordingly, the Chairman, on behalf of the Commission, hereby certifies pursuant to 5 U.S.C. 605(b) that the proposed regulations will not have a significant economic impact on a substantial number of small entities. The Commission invites the public to comment on whether SDs and MSPs should be considered small entities for purposes of the RFA.</P>
        <HD SOURCE="HD2">B. Paperwork Reduction Act</HD>
        <P>The Paperwork Reduction Act (PRA)<SU>15</SU>
          <FTREF/>imposes certain requirements on Federal agencies (including the Commission) in connection with their conducting or sponsoring any collection of information as defined by the PRA. This proposed rulemaking would result in new collection of information requirements within the meaning of the PRA. The Commission therefore is submitting this proposal to the Office of Management and Budget (OMB) for review in accordance with 44 U.S.C. 3507(d) and 5 CFR 1320.11. The title for this collection of information is “Clearing Member Position Risk Management.” An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid control number. The OMB has not yet assigned this collection a control number.</P>
        <FTNT>
          <P>
            <SU>15</SU>44 U.S.C. 3501<E T="03">et seq.</E>
          </P>
        </FTNT>
        <P>The collection of information under these proposed regulations is necessary to implement certain provisions of the CEA, as amended by the Dodd-Frank Act. Specifically, it is essential both for effective risk management and for the efficient operation of trading venues among swap dealers, major swap participants, and futures commission merchants. The position risk management requirement established by the proposed rules diminishes the chance for a default, thus ensuring the financial integrity of markets as well as customer protection.</P>
        <P>If the proposed regulations are adopted, responses to this collection of information would be mandatory. The Commission will protect proprietary information according to the Freedom of Information Act and 17 CFR part 145, “Commission Records and Information.” In addition, section 8(a)(1) of the CEA strictly prohibits the Commission, unless specifically authorized by the CEA, from making public “data and information that would separately disclose the business transactions or market positions of any person and trade secrets or names of customers.” The Commission is also required to protect certain information contained in a government system of records according to the Privacy Act of 1974, 5 U.S.C. 552a.</P>
        <HD SOURCE="HD3">1. Information Provided by Reporting Entities/Persons</HD>
        <P>Swap dealers, major swap participants, and futures commission merchants would be required to develop and monitor procedures for position risk management in accordance with proposed rules 1.73 and 23.609.</P>
        <P>The annual burden associated with these proposed regulations is estimated to be 524 hours, at an annual cost of $52,400 for each futures commission merchant, swap dealer, and major swap participant. Burden means the total time, effort, or financial resources expended by persons to generate, maintain, retain, disclose, or provide information to or for a federal agency. The Commission has characterized the annual costs as initial costs because the Commission anticipates that the cost burdens will be reduced dramatically over time as the documentation and procedures required by the proposed regulations become increasingly standardized within the industry.</P>
        <P>This hourly burden primarily results from the position risk management obligations that would be imposed by proposed regulations 1.73 and 23.609. Proposed 1.73 and 23.609 would require each futures commission merchant, swap dealer, and major swap participant to establish and enforce procedures to establish risk-based limits, conduct stress testing, evaluate the ability to meet initial and variation margin, test lines of credit, and evaluate the ability to liquidate, in an orderly manner, the positions in the proprietary and customer accounts and estimate the cost of the liquidation. The Commission believes that each of these items is currently an element of existing risk management programs at a DCO or an FCM. Accordingly, any additional expenditure related to §§ 1.73 and 23.609 likely would be limited to the time initially required to review and, as needed, amend, existing risk management procedures to ensure that they encompass all of the required elements and to develop a system for performing these functions as often as required.</P>
        <P>In addition, proposed §§ 1.73 and 23.609 would require each futures commission merchant, swap dealer, and major swap participant to establish written procedures to comply, and maintain records documenting compliance. Maintenance of compliance procedures and records of compliance is prudent business practice and the Commission anticipates that swap dealers and major swap participants already maintain some form of this documentation.</P>
        <P>With respect to the required position risk management, the Commission estimates that futures commission merchants, swap dealers, and major swap participants will spend an average of 2 hours per trading day, or 504 hours per year, performing the required tests. The Commission notes that the specific information required for these tests is of the type that would be performed in a prudent market participant's ordinary course of business.</P>
        <P>In addition to the above, the Commission anticipates that futures commission merchants, swap dealers, and major swap participants will spend an average of 16 hours per year drafting and, as needed, updating the written policies and procedures to ensure compliance required by proposed §§ 1.73 and 23.609, and 4 hours per year maintaining records of the compliance.</P>
        <P>The hour burden calculations below are based upon a number of variables such as the number of futures commission merchants, swap dealers, and major swap participants in the marketplace and the average hourly wage of the employees of these registrants that would be responsible for satisfying the obligations established by the proposed regulation.</P>
        <P>There are currently 134 futures commission merchants based on industry data. Swap dealers and major swap participants are new categories of registrants. Accordingly, it is not currently known how many swap dealers and major swap participants will become subject to these rules, and this will not be known to the Commission until the registration requirements for these entities become effective after July 16, 2011, the date on which the Dodd-Frank Act becomes effective. While the Commission believes there will be approximately 200 swap dealers and 50 major swap participants, it has taken a conservative approach, for PRA purposes, in estimating that there will be a combined number of 300 swap dealers and major swap participants who will be required to comply with the recordkeeping requirements of the proposed rules. The Commission estimated the number of affected entities based on industry data.</P>

        <P>According to recent Bureau of Labor Statistics, the mean hourly wage of an employee under occupation code 11-3031, “Financial Managers,” (which includes operations managers) that is employed by the “Securities and Commodity Contracts Intermediation<PRTPAGE P="45728"/>and Brokerage” industry is $74.41.<SU>16</SU>
          <FTREF/>Because swap dealers, major swap participants, and futures commission merchants include large financial institutions whose operations management employees' salaries may exceed the mean wage, the Commission has estimated the cost burden of these proposed regulations based upon an average salary of $100 per hour.</P>
        <FTNT>
          <P>
            <SU>16</SU>
            <E T="03">http://www.bls.gov/oes/current/oes113031.htm.</E>
          </P>
        </FTNT>

        <P>Accordingly, the estimated hour burden was calculated as follows:<E T="03">Developing and Conducting Position Risk Management Procedures for Swap Dealers and Major Swap Participants.</E>This hourly burden arises from the proposed requirement that swap dealers and major swap participants establish and perform testing of clearing member risk management procedures.</P>
        <P>
          <E T="03">Number of registrants:</E>300.</P>
        <P>
          <E T="03">Frequency of collection:</E>Daily.</P>
        <P>
          <E T="03">Estimated number of responses per registrant:</E>252 [252 trading days].</P>
        <P>
          <E T="03">Estimated aggregate number of responses:</E>75,600 [300 registrants × 252 trading days].</P>
        <P>
          <E T="03">Estimated annual burden per registrant:</E>504 hours [252 trading days × 2 hours per record].</P>
        <P>
          <E T="03">Estimated aggregate annual hour burden:</E>151,200 hours [300 registrants × 252 trading days × 2 hours per record].</P>
        <P>
          <E T="03">Developing Written Procedures for Compliance, and Maintaining Records Documenting Compliance for Swap Dealers and Major Swap Participants.</E>This hourly burden arises from the proposed requirement that swap dealers and major swap participants make and maintain records documenting compliance related to clearing member risk management.</P>
        <P>
          <E T="03">Number of registrants:</E>300.</P>
        <P>
          <E T="03">Frequency of collection:</E>As needed.</P>
        <P>
          <E T="03">Estimated number of annual responses per registrant:</E>1.</P>
        <P>
          <E T="03">Estimated aggregate number of annual responses:</E>300.</P>
        <P>
          <E T="03">Estimated annual hour burden per registrant:</E>20 hours.</P>
        <P>
          <E T="03">Estimated aggregate annual hour burden:</E>6,000 burden hours [300 registrants × 20 hours per registrant].</P>
        <P>
          <E T="03">Developing and Conducting Position Risk Management Procedures for Futures Commission Merchants:</E>This hourly burden arises from the proposed requirement that futures commission merchants establish and perform testing of clearing member risk management procedures.</P>
        <P>
          <E T="03">Number of registrants:</E>134.</P>
        <P>
          <E T="03">Frequency of collection:</E>Daily.</P>
        <P>
          <E T="03">Estimated number of responses per registrant:</E>252 [252 trading days].</P>
        <P>
          <E T="03">Estimated aggregate number of responses:</E>33,768 [134 registrants × 252 trading days].</P>
        <P>
          <E T="03">Estimated annual burden per registrant:</E>504 hours [252 trading days × 2 hours per record].</P>
        <P>
          <E T="03">Estimated aggregate annual hour burden:</E>67,536 hours [134 registrants × 252 trading days × 2 hours per record].</P>
        <P>
          <E T="03">Developing Written Procedures for Compliance, and Maintaining Records Documenting Compliance for Futures Commission Merchants.</E>This hourly burden arises from the proposed requirement that futures commission merchants make and maintain records documenting compliance related to clearing member risk management.</P>
        <P>
          <E T="03">Number of registrants:</E>134.</P>
        <P>
          <E T="03">Frequency of collection:</E>As needed.</P>
        <P>
          <E T="03">Estimated number of annual responses per registrant:</E>1.</P>
        <P>
          <E T="03">Estimated aggregate number of annual responses:</E>134.</P>
        <P>
          <E T="03">Estimated annual hour burden per registrant:</E>20 hours.</P>
        <P>
          <E T="03">Estimated aggregate annual hour burden:</E>2,680 burden hours [134 registrants × 20 hours per registrant].</P>
        <P>Based upon the above, the aggregate hour burden cost for all registrants is 227,416 burden hours and $22,741,600 [227,416 × $100 per hour].</P>
        <P>In addition to the per hour burden discussed above, the Commission anticipates that swap dealers, major swap participants, and futures commission merchants may incur certain start-up costs in connection with the proposed recordkeeping obligations. Such costs would include the expenditures related to re-programming or updating existing recordkeeping technology and systems to enable the swap dealer, major swap participant, or futures commission merchant to collect, capture, process, maintain, and re-produce any newly required records. The Commission believes that swap dealers, major swap participants, and futures commission merchants generally could adapt their current infrastructure to accommodate the new or amended technology and thus no significant infrastructure expenditures would be needed. The Commission estimates the programming burden hours associated with technology improvements to be 60 hours.</P>
        <P>According to recent Bureau of Labor Statistics, the mean hourly wages of computer programmers under occupation code 15-1021 and computer software engineers under program codes 15-1031 and 1032 are between $34.10 and $44.94.<SU>17</SU>
          <FTREF/>Because swap dealers, major swap participants, and futures commission merchants generally will be large entities that may engage employees with wages above the mean, the Commission has conservatively chosen to use a mean hourly programming wage of $60 per hour. Accordingly, the start-up burden associated with the required technological improvements would be $3,600 [$60 × 60 hours] per affected registrant or $1,562,400 [$3,600 × 434 registrants] in the aggregate.</P>
        <FTNT>
          <P>
            <SU>17</SU>
            <E T="03">http://www.bls.gov/oes/current/oes113031.htm.</E>
          </P>
        </FTNT>
        <HD SOURCE="HD3">2. Information Collection Comments</HD>
        <P>The Commission invites the public and other federal agencies to comment on any aspect of the recordkeeping burdens discussed above. Pursuant to 44 U.S.C. 3506(c)(2)(B), the Commission solicits comments in order to: (i) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the Commission, including whether the information will have practical utility; (ii) evaluate the accuracy of the Commission's estimate of the burden of the proposed collection of information; (iii) determine whether there are ways to enhance the quality, utility, and clarity of the information to be collected; and (iv) minimize the burden of the collection of information on those who are to respond, including through the use of automated collection techniques or other forms of information technology.</P>

        <P>Comments may be submitted directly to the Office of Information and Regulatory Affairs, by fax at (202) 395-6566 or by e-mail at<E T="03">OIRAsubmissions@omb.eop.gov.</E>Please provide the Commission with a copy of submitted comments so that all comments can be summarized and addressed in the final rule preamble. Refer to the<E T="02">Addresses</E>section of this notice of proposed rulemaking for comment submission instructions to the Commission. A copy of the supporting statements for the collection of information discussed above may be obtained by visiting<E T="03">http://www.RegInfo.gov.</E>OMB is required to make a decision concerning the collection of information between 30 and 60 days after publication of this document in the<E T="04">Federal Register</E>. Therefore, a comment is best assured of having its full effect if OMB receives it within 30 days of publication.</P>
        <HD SOURCE="HD2">C. Consideration of Costs and Benefits Under Section 15(a) of the CEA</HD>

        <P>Section 15(a) of the CEA requires the Commission to consider the costs and benefits of its action before promulgating a regulation under the CEA. Section 15(a) of the CEA specifies<PRTPAGE P="45729"/>that costs and benefits shall be evaluated in light of five broad areas of market and public concern: (1) Protection of market participants and the public; (2) efficiency, competitiveness, and financial integrity of futures markets; (3) price discovery; (4) sound risk management practices; and (5) other public interest considerations. The Commission may in its discretion give greater weight to any one of the five enumerated areas and could in its discretion determine that, notwithstanding its costs, a particular order is necessary or appropriate to protect the public interest or to effectuate any of the provisions or to accomplish any of the purposes of the CEA.</P>
        <P>The proposed rules involve risk management for cleared trades by futures commission merchants, swap dealers, and major swap participants that Are clearing members. The discussion below will consider the proposed rule in light of each section 15(a) concerns.</P>
        <HD SOURCE="HD1">Position Risk Management for Cleared Trades by Futures Commission Merchants, Swap Dealers, and Major Swap Participants That Are Clearing Members</HD>
        <P>The Commission is proposing regulations that would require FCMs, SDs, and MSPs to put into place certain risk management procedures.</P>
        <HD SOURCE="HD2">1. Protection of Market Participants</HD>
        <P>Good risk management practices among FCMs, SDs, and MSPs help insulate DCOs from financial distress. Moreover, while the rule calls for standard risk mitigation measures, it allows FCMs, SDs, and MSPs to use diverse techniques to implement those measures. This makes it less likely that multiple FCMs, SDs, and MSPs would be exposed to identical blind spots during unexpected market developments.</P>
        <P>As far as costs are concerned, regular testing of various systems and financial positions requires significant personnel hours and potentially the services of external vendors. The requirement that records be created and maintained may impose costs on FCMs, SDs, and MSPs. The Commission believes that some costs might only be incremental because it believes that well-managed firms would generally already create and maintain records of this type.</P>
        <HD SOURCE="HD2">2. Efficiency, Competitiveness, and Financial Integrity of Futures Markets</HD>

        <P>The integrity of the markets is enhanced with the certainty that the customer's counterparties (<E T="03">i.e.,</E>FCMs, SDs, and MSPs, as well as DCOs) are more likely to remain solvent during strenuous financial conditions.</P>
        <P>As for the costs related to this rule, rigorous stress tests may encourage conservative margin requirements that reduce customers' ability to leverage their positions. Also, higher costs associated with maintaining more stringent risk management practices will ultimately be passed along to customers, likely in the form of larger spreads, which may reduce the liquidity and efficiency of the market. However, more conservative margin requirements and stringent risk management practices will also help reduce systemic risk thereby protecting the integrity of the financial system as a whole.</P>
        <HD SOURCE="HD2">3. Sound Risk Management Practices</HD>
        <P>The rule extends the range of parties responsible for rigorous risk management practices which promotes further stability of the entire financial system. However, as mentioned previously, risk management systems can be costly to implement. The Commission does not know at this time, and requests comment on, how many parties will need to upgrade their systems, if any. Additionally, the Commission requests comment from the public as to what the costs might be to upgrade existing systems or install new systems to comply with the proposed regulation.</P>
        <HD SOURCE="HD2">4. Other Public Interest Considerations</HD>
        <P>Requiring a significant investment in risk mitigation structures and procedures by all FCMs, SDs, and MSPs increases the number of entities committing time and resources to development of new techniques that have the potential to advance the practice across the entire industry. Such measures contribute to the overall stability of our global financial system.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects</HD>
          <CFR>17 CFR Part 1</CFR>
          <P>Conflicts of interest, Futures commission merchants, Major swap participants, Swap dealers.</P>
          <CFR>17 CFR Part 23</CFR>
          <P>Conflicts of interests, Futures commission merchants, Major swap participants, Swap dealers.</P>
        </LSTSUB>
        
        <P>In light of the foregoing, the Commission hereby proposes to amend Part 1, and Part 23, as proposed to be added at 75 FR 71390, November 23, 2010, and further amended at 75 FR 81530, December 28, 2010, of Title 17 of the Code of Federal Regulations as follows:</P>
        <PART>
          <HD SOURCE="HED">PART 1—GENERAL REGULATIONS UNDER THE COMMODITY EXCHANGE ACT</HD>
          <P>1. The authority citation for part 1 is revised to read as follows:</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>7 U.S.C. 1a, 2, 2a, 5, 6, 6a, 6b, 6c, 6d, 6e, 6f, 6g, 6h, 6i, 6k, 6l, 6m, 6n, 6o, 6p, 6r, 6s, 7, 7a-1, 7a-2, 7b, 7b-3, 8, 9, 10a, 12, 12a, 12c, 13a, 13a-1, 16, 16a, 19, 21, 23, and 24, as amended by Title VII of the Dodd-Frank Wall Street Reform and Consumer Protection Act, Pub. L. 111-203, 124 Stat. 1376 (2010).</P>
          </AUTH>
          
          <P>2. Add § 1.73 to part 1 to read as follows:</P>
          <SECTION>
            <SECTNO>§ 1.73</SECTNO>
            <SUBJECT>Clearing futures commission merchant risk management.</SUBJECT>
            <P>(a) Each futures commission merchant that is a clearing member of a derivatives clearing organization shall:</P>
            <P>(1) Establish risk-based limits in the proprietary account and in each customer account based on position size, order size, margin requirements, or similar factors;</P>
            <P>(2) Use automated means to screen orders for compliance with the risk-based limits;</P>
            <P>(3) Monitor for adherence to the risk-based limits intra-day and overnight;</P>
            <P>(4) Conduct stress tests of all positions in the proprietary account and in each customer account that could pose material risk to the futures commission merchant at least once per week;</P>
            <P>(5) Evaluate its ability to meet initial margin requirements at least once per week;</P>
            <P>(6) Evaluate its ability to meet variation margin requirements in cash at least once per week;</P>
            <P>(7) Evaluate its ability to liquidate, in an orderly manner, the positions in the proprietary and customer accounts and estimate the cost of the liquidation at least once per month; and</P>
            <P>(8) Test all lines of credit at least once per quarter.</P>
            <P>(b) Each futures commission merchant that is a clearing member of a derivatives clearing organization shall:</P>
            <P>(1) Establish written procedures to comply with this regulation; and</P>
            <P>(2) Keep full, complete, and systematic records documenting its compliance with this regulation.</P>
          </SECTION>
        </PART>
        <PART>
          <HD SOURCE="HED">PART 23—SWAP DEALERS AND MAJOR SWAP PARTICIPANTS</HD>
          <P>3. The authority citation for part 23 is revised to read as follows:</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>7 U.S.C. 1a, 2, 6, 6a, 6b, 6b-1, 6c, 6p, 6r, 6s, 6t, 9, 9a, 12, 12a, 13b, 13c, 16a, 18, 19, 21.</P>
          </AUTH>
          
          <P>4. Add § 23.609 to part 23, subpart J, to read as follows:</P>
          <SECTION>
            <PRTPAGE P="45730"/>
            <SECTNO>§ 23.609</SECTNO>
            <SUBJECT>Clearing member risk management.</SUBJECT>
            <P>(a) With respect to clearing activities in futures, security futures products, swaps, agreements, contracts, or transactions described in section 2(c)(2)(C)(i) or section 2(c)(2)(D)(i) of the Act, commodity options authorized under section 4c of the Act, or leveraged transactions authorized under section 19 of the Act, each swap dealer or major swap participant that is a clearing member of a derivatives clearing organization shall:</P>
            <P>(1) Establish risk-based limits based on position size, order size, margin requirements, or similar factors;</P>
            <P>(2) Use automated means to screen orders for compliance with the risk-based limits;</P>
            <P>(3) Monitor for adherence to the risk-based limits intra-day and overnight;</P>
            <P>(4) Conduct stress tests of all positions at least once per week;</P>
            <P>(5) Evaluate its ability to meet initial margin requirements at least once per week;</P>
            <P>(6) Evaluate its ability to meet variation margin requirements in cash at least once per week;</P>
            <P>(7) Test all lines of credit at least once per quarter; and</P>
            <P>(8) Evaluate its ability to liquidate the positions it clears in an orderly manner, and estimate the cost of the liquidation.</P>
            <P>(b) Each swap dealer or major swap participant that is a clearing member of a derivatives clearing organization shall:</P>
            <P>(1) Establish written procedures to comply with this regulation; and</P>
            <P>(2) Keep full, complete, and systematic records documenting its compliance with this regulation.</P>
          </SECTION>
          <SIG>
            <DATED>Issued in Washington, DC, on July 19, 2011, by the Commission.</DATED>
            <NAME>David A. Stawick,</NAME>
            <TITLE>Secretary of the Commission.</TITLE>
          </SIG>
          <HD SOURCE="HD1">Appendices to Clearing Member Risk Management—Commission Voting Summary and Statements of Commissioners</HD>
          <NOTE>
            <HD SOURCE="HED">Note:</HD>
            <P>The following appendices will not appear in the Code of Federal Regulations.</P>
          </NOTE>
          <HD SOURCE="HD1">Appendix 1—Commission Voting Summary</HD>
          <EXTRACT>
            <P>On this matter, Chairman Gensler and Commissioners Dunn and Chilton voted in the affirmative; Commissioners O'Malia and Sommers voted in the negative.</P>
          </EXTRACT>
          <HD SOURCE="HD1">Appendix 2—Statement of Chairman Gary Gensler</HD>
          <EXTRACT>
            <P>I support the proposed rulemaking for enhanced risk management for clearing members. One of the primary goals of the Dodd-Frank Wall Street Reform and Consumer Protection Act was to reduce the risk that swaps pose to the economy. The proposed rule would require clearing members, including swap dealers, major swap participants and futures commission merchants to establish risk-based limits on their house and customer accounts. The proposed rule also would require clearing members to establish procedures to, amongst other provisions, evaluate their ability to meet margin requirements, as well as liquidate positions as needed. These risk filters and procedures would help secure the financial integrity of the markets and the clearing system and protect customer funds.</P>
          </EXTRACT>
          
        </PART>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19362 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6351-01-P</BILCOD>
    </PRORULE>
    <PRORULE>
      <PREAMB>
        <AGENCY TYPE="S">COMMODITY FUTURES TRADING COMMISSION</AGENCY>
        <CFR>17 CFR Parts 1, 23, and 39</CFR>
        <RIN>RIN 3038-AD51</RIN>
        <SUBJECT>Customer Clearing Documentation and Timing of Acceptance for Clearing</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Commodity Futures Trading Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of proposed rulemaking.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Commodity Futures Trading Commission (Commission or CFTC) is proposing rules to implement new statutory provisions enacted by Title VII of the Dodd-Frank Wall Street Reform and Consumer Protection Act. These proposed rules address: The documentation between a customer and a futures commission merchant that clears on behalf of the customer, and the timing of acceptance or rejection of trades for clearing by derivatives clearing organizations and clearing members.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>Submit comments on or before September 30, 2011.</P>
        </EFFDATE>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may submit comments, identified by RIN number 3038-AD51, by any of the following methods:</P>
          <P>•<E T="03">Agency Web site, via its Comments Online process: http://comments.cftc.gov.</E>Follow the instructions for submitting comments through the Web site.</P>
          <P>•<E T="03">Federal eRulemaking Portal: http://www.regulations.gov.</E>Follow the instructions for submitting comments.</P>
          <P>•<E T="03">Mail:</E>David A. Stawick, Secretary of the Commission, Commodity Futures Trading Commission, Three Lafayette Centre, 1155 21st Street, NW., Washington, DC 20581.</P>
          <P>•<E T="03">Courier:</E>Same as mail above.</P>
          

          <P>Please submit your comments using only one method. RIN number, 3038-AD51, must be in the subject field of responses submitted via e-mail, and clearly indicated on written submissions. All comments must be submitted in English, or if not, accompanied by an English translation. Comments will be posted as received to<E T="03">http://www.cftc.gov.</E>You should submit only information that you wish to make available publicly. If you wish the CFTC to consider information that you believe is exempt from disclosure under the Freedom of Information Act, a petition for confidential treatment of the exempt information may be submitted according to the procedures established in § 145.9 of the CFTC's regulations.<SU>1</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>1</SU>17 CFR 145.9.</P>
          </FTNT>

          <P>The CFTC reserves the right, but shall have no obligation, to review, pre-screen, filter, redact, refuse or remove any or all of your submission from<E T="03">http://www.cftc.gov</E>that it may deem to be inappropriate for publication, such as obscene language. All submissions that have been redacted or removed that contain comments on the merits of this action will be retained in the public comment file and will be considered as required under the Administrative Procedure Act and other applicable laws, and may be accessible under the Freedom of Information Act.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>John C. Lawton, Deputy Director and Chief Counsel, 202-418-5480,<E T="03">jlawton@cftc.gov,</E>or Christopher A. Hower, Attorney-Advisor, 202-418-6703,<E T="03">chower@cftc.gov,</E>Division of Clearing and Intermediary Oversight, Commodity Futures Trading Commission, Three Lafayette Centre, 1155 21st Street, NW., Washington, DC 20581.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">I. Background</HD>
        <P>On July 21, 2010, President Obama signed the Dodd-Frank Wall Street Reform and Consumer Protection Act (Dodd-Frank Act).<SU>2</SU>
          <FTREF/>Title VII of the Dodd-Frank Act amended the Commodity Exchange Act (CEA or Act)<SU>3</SU>

          <FTREF/>to establish a comprehensive new regulatory framework for swaps. The legislation was enacted to reduce risk, increase transparency, and promote market integrity within the financial system by, among other things: (1) Providing for the registration and comprehensive regulation of swap dealers and major swap participants; (2) imposing clearing and trade execution requirements on standardized derivative products; (3) creating rigorous recordkeeping and real-time reporting<PRTPAGE P="45731"/>regimes; and (4) enhancing the Commission's rulemaking and enforcement authorities with respect to, among others, all registered entities and intermediaries subject to the Commission's oversight. Title VII also includes amendments to the federal securities laws to establish a similar regulatory framework for security-based swaps under the authority of the Securities and Exchange Commission (SEC).</P>
        <FTNT>
          <P>
            <SU>2</SU>
            <E T="03">See</E>Dodd-Frank Wall Street Reform and Consumer Protection Act, Public Law 111-203, 124 Stat. 1376 (2010).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>3</SU>7 U.S.C. 1<E T="03">et seq.</E>
          </P>
        </FTNT>
        <HD SOURCE="HD1">II. Proposed Regulations</HD>
        <HD SOURCE="HD2">A.<E T="03">Introduction</E>
        </HD>
        <P>A fundamental premise of the Dodd-Frank Act is that the use of properly regulated central clearing can reduce systemic risk. Another tenet of the Dodd-Frank Act is that open access to clearing by market participants will increase market transparency and promote market efficiency by enabling market participants to reduce counterparty risk and by facilitating offset of open positions. The Commission has proposed extensive regulations addressing open access at the derivatives clearing organization (DCO) level.<SU>4</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>4</SU>
            <E T="03">See, e.g.,</E>76 FR 3698 (Jan. 20, 2011) (Risk Management Requirements for Derivatives Clearing Organizations).</P>
        </FTNT>
        <P>Clearing members provide the portals through which market participants gain access to DCOs as well as the first line of risk management. Accordingly, the Commission is proposing regulations to facilitate customer access to clearing and to bolster risk management through timely processing. The proposals address: (i) The documentation between a customer and a futures commission merchant (FCM) that clears on behalf of the customer; and (ii) the timing of acceptance or rejection of trades for clearing by DCOs and clearing members.</P>
        <HD SOURCE="HD2">B. Customer Clearing Documentation</HD>
        <P>Section 4d(c) of the CEA, as amended by the Dodd-Frank Act, directs the Commission to require FCMs to implement conflict of interest procedures that address such issues the Commission determines to be appropriate. Similarly, section 4s(j)(5), as added by the Dodd-Frank Act, requires SDs and MSPs to implement conflict of interest procedures that address such issues the Commission determines to be appropriate. Section 4s(j)(5) also requires SDs and MSPs to ensure that any persons providing clearing activities or making determinations as to accepting clearing customers are separated by appropriate informational partitions from persons whose involvement in pricing, trading, or clearing activities might bias their judgment or contravene the core principle of open access.</P>
        <P>Pursuant to these provisions, the Commission has proposed § 1.71(d)(1) relating to FCMs and § 23.605(d)(1) relating to SDs and MSPs.<SU>5</SU>
          <FTREF/>These regulations would prohibit SDs and MSPs from interfering or attempting to influence the decisions of affiliated FCMs with regard to the provision of clearing services and activities and would prohibit FCMs from permitting them to do so.</P>
        <FTNT>
          <P>
            <SU>5</SU>75 FR 70152 (Nov. 17, 2010) (Implementation of Conflicts of Interest Policies and Procedures by Futures Commission Merchants and Introducing Brokers); 75 FR 71391 (Nov. 23, 2010) (Implementation of Conflicts of Interest Policies and Procedures by Swap Dealers and Major Swap Participants).</P>
        </FTNT>
        <P>Section 4s(j)(6) of the CEA prohibits an SD or MSP from adopting any process or taking any action that results in any unreasonable restraint on trade or imposes any material anticompetitive burden on trading or clearing, unless necessary or appropriate to achieve the purposes of the Act. The Commission has proposed § 23.607 to implement this provision.<SU>6</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>6</SU>75 FR 91397 (Nov. 23, 2010) (Regulations Establishing Duties of Swap Dealers and Major Swap Participants).</P>
        </FTNT>
        <P>Section 2(h)(1)(B)(ii) of the CEA requires that DCO rules provide for the non-discriminatory clearing of swaps executed bilaterally or through an unaffiliated designated contract market (DCM) or swap execution facility (SEF). The Commission has proposed § 39.12(b)(2) to implement this provision.<SU>7</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>7</SU>76 FR 3698 (Jan. 20, 2011) (Risk Management Requirements for Derivatives Clearing Organizations); 76 FR 13101 (March 10, 2011) (Requirements for Processing, Clearing, and Transfer of Customer Positions).</P>
        </FTNT>
        <P>On June 16, 2011, the Futures Industry Association (FIA) and the International Swap and Derivatives Association (ISDA), published an FIA-ISDA Cleared Derivatives Execution Agreement (Agreement) as a template for use by swap market participants in negotiating execution-related agreements with counterparties to swaps that are intended to be cleared.<SU>8</SU>
          <FTREF/>The Agreement was developed with the assistance of a committee comprised of representatives of certain FIA and ISDA member firms which included both swap dealers and buy-side firms. More than 60 organizations provided input during the development of the document.<SU>9</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>8</SU>
            <E T="03">See</E>press release, “FIA and ISDA Publish Documentation for Cleared Swaps” (June 16, 2011) at<E T="03">http://www.futuresindustry.org.</E>
          </P>
        </FTNT>
        <FTNT>
          <P>
            <SU>9</SU>
            <E T="03">Id.</E>
          </P>
        </FTNT>
        <P>FIA and ISDA emphasized that the use of the agreement is voluntary and may not be necessary and appropriate under all circumstances.<SU>10</SU>
          <FTREF/>FIA and ISDA recognized that many of the provisions in the Agreement will be superseded by new regulatory requirements and the rules of swap execution venues and clearing organizations.<SU>11</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>10</SU>
            <E T="03">Id.</E>
          </P>
        </FTNT>
        <FTNT>
          <P>
            <SU>11</SU>
            <E T="03">Id.</E>
          </P>
        </FTNT>
        <P>The Agreement includes optional annexes that make the clearing member to one or both of the executing parties a party to the Agreement (the Tri-party annexes). Some of the participants in the process, as well as some market participants that were not included, have expressed concern to the Commission that aspects of the Tri-party annexes may be inconsistent with certain principles of the Dodd-Frank Act.<SU>12</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>12</SU>
            <E T="03">See, e.g.,</E>letter dated April 11, 2011 from Stuart J. Kaswell, Executive Vice President, Managing Director, and General Counsel, Managed Funds Association; letter dated April 19, 2011 from James Cawley, Swaps &amp; Derivatives Market Association. These letters can be found in the Commission's comment file for 76 FR 13101.</P>
        </FTNT>
        <P>Specifically, concerns arise in connection with certain provisions that would permit a customer's FCM, in consultation with the SD, to establish specific credit limits for the customer's swap transactions with the SD, and to declare that with regard to trades with that SD, the FCM will only accept for clearing those transactions that fall within these specific limits.<SU>13</SU>
          <FTREF/>The limits set for trades with the SD might be less than the overall limits set for the customer for all trades cleared through the FCM. The result would be to create a “sublimit” for the customer for trades with that SD. Some market participants have stated that the setting of such “sublimits” would result in restrictions of customer counterparties because, without such “sublimits,” the customer may enter into transactions with whomever it chooses, up to its overall limit with the FCM.<SU>14</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>13</SU>
            <E T="03">See</E>Kaswell letter at 9.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>14</SU>
            <E T="03">Id.</E>at 10.</P>
        </FTNT>

        <P>Generally, in cleared markets, an FCM does not know the identity of its customer's executing counterparty. Another effect of such sublimits would be to disclose the identity of the customer's counterparty to the FCM. In many instances, the FCM and the customer's counterparty—the SD—might be affiliated entities. Some market participants have stated that such disclosure may lead to “greater information exchange” between the FCM and the affiliated SD, which would<PRTPAGE P="45732"/>“force the customer to execute with the clearing member's trading desk affiliate.”<SU>15</SU>
          <FTREF/>A third effect of such sublimits could be to delay acceptance of the trades into clearing while the FCM verifies compliance with the sublimits.</P>
        <FTNT>
          <P>
            <SU>15</SU>
            <E T="03">Id.</E>
          </P>
        </FTNT>
        <P>Arrangements with these effects potentially conflict with the concepts of open access to clearing and execution of customer transactions on a DCM or SEF on terms that have a reasonable relationship to the best terms available. More specifically, they potentially conflict with proposed §§ 1.71(d)(1), 23.605(d)(1), 23.608, and 39.12. As certain market participants have stated, tri-party agreements of the type described above could lead to undue influence by FCMs on a customer's choice of counterparties (or, conversely, undue influence by SDs on a customer's choice of clearing member). Therefore, they could constrain a customer's opportunity to obtain execution of the trade on the terms that have a reasonable relationship to the best terms available by limiting the number of potential counterparties.<SU>16</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>16</SU>The Commission previously proposed § 155.7, an execution standard that would apply to swaps available for trading on a DCM or SEF to ensure fair dealing and protect against fraud and other abusive practices. 75 FR 80638, 80648 (Dec. 22, 2010). The proposed rule would require Commission registrants to execute swaps available for trading on a DCM or SEF on terms that have a reasonable relationship to the best terms available.</P>
        </FTNT>
        <P>To address these concerns and to provide further clarity in this area, the Commission is now proposing § 1.72 relating to FCMs, § 23.608 relating to SDs and MSPs, and § 39.12(a)(1)(vi) relating to DCOs. These new regulations would prohibit arrangements involving FCMs, SDs, MSPs, or DCOs that would (a) disclose to an FCM, SD, or MSP the identity of a customer's original executing counterparty; (b) limit the number of counterparties with whom a customer may enter into a trade; (c) restrict the size of the position a customer may take with any individual counterparty, apart from an overall credit limit for all positions held by the customer at the FCM; (d) impair a customer's access to execution of a trade on terms that have a reasonable relationship to the best terms available; or (e) prevent compliance with specified time frames for acceptance of trades into clearing.</P>
        <P>The Commission believes that implementation of the proposal would reduce risk and foster open access to clearing, as well as execution of customer trades on terms that have a reasonable relationship to the best terms available. Restrictions of the sort prohibited by the proposed rules could increase risk by delaying or blocking access to clearing. They could increase costs and reduce market efficiency by limiting the number of counterparties available for trading. They could restrict access to clearing by limiting the potential clearing members with which a customer could deal.</P>
        <P>The Commission is not proposing to dictate here what happens to a trade that is rejected for clearing by an FCM or a DCO. Three outcomes are possible: (i) The parties could try to clear the trade through another DCO or FCM; (ii) the trade could revert to a bilateral transaction; or (iii) the parties could break the trade. The parties should agree in advance, subject to applicable law, which alternative will apply and how to measure and apportion any resulting losses. The Commission believes that the proposals herein will decrease the likelihood that trades will be rejected and diminish the potential for loss in cases where rejection does occur.</P>
        <P>The Commission requests comment on whether the proposals will achieve the intended goals and on the costs and benefits of the proposed means of achieving those goals. In particular, the Commission requests comment on:</P>
        <P>• Whether the proposal would increase open access to clearing and execution of customer transactions on a DCM or SEF on terms that have a reasonable relationship to the best terms available;</P>
        <P>• Whether the proposal could decrease open access to clearing in any way; and</P>
        <P>• Whether the proposals would increase risk to DCOs, FCMs, SDs, or MSPs in any way.</P>
        <HD SOURCE="HD2">C.<E T="03">Time Frames for Acceptance Into Clearing</E>
        </HD>
        <P>As noted above, a goal of the Dodd-Frank Act is to reduce risk by increasing the use of central clearing. Minimizing the time between trade execution and acceptance into clearing is an important risk mitigant. The Commission recently proposed § 39.12(b)(7) regarding time frames for clearing.<SU>17</SU>
          <FTREF/>Upon review of the comments received, the Commission is now proposing a revised version of that provision.<SU>18</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>17</SU>76 FR 13101 (March 10, 2011) (Requirements for Processing, Clearing, and Transfer of Customer Positions).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>18</SU>The Commission continues to review comments on other aspects of the March 10 proposal and they will be addressed separately.</P>
        </FTNT>

        <P>As previously proposed, § 39.12(b)(7)(i) required DCOs to coordinate with designated contract markets (DCMs) and swap execution facilities (SEFs) to facilitate prompt and efficient processing of trades. In response to a comment, the Commission now proposes to require prompt, efficient,<E T="03">and accurate</E>processing of trades.<SU>19</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>19</SU>
            <E T="03">See</E>letter from Robert Pickel, Executive Vice Chairman, International Swaps and Derivatives Association, dated April 8, 2011.</P>
        </FTNT>
        <P>Recognizing the key role clearing members play in trade processing and submission of trades to central clearing, the Commission is also now proposing parallel provisions for coordination among DCOs and clearing members. Proposed § 39.12(b)(7)(i)(B) would require DCOs to coordinate with clearing members to establish systems for prompt processing of trades. Proposed §§ 1.74(a) and 23.610(a) would require reciprocal coordination with DCOs by FCMs, SDs, and MSPs that are clearing members.</P>
        <P>As previously proposed, § 39.12(b)(7)(ii) required DCOs to accept immediately upon execution all transactions executed on a DCM or SEF. A number of DCOs and other commenters expressed concern that this requirement could expose DCOs to unwarranted risk because DCOs need to be able to screen trades for compliance with applicable clearinghouse rules related to product and credit filters.<SU>20</SU>
          <FTREF/>The Commission recognizes that while immediate acceptance for clearing upon execution currently occurs in some futures markets, it might not be feasible for all cleared markets at this time. For example, where the same cleared product is traded on multiple execution venues, a DCO needs to be able to aggregate the risk of trades coming in to ensure that a clearing member or customer has not exceeded its credit limits. Accordingly, the Commission is proposing to modify § 39.12(b)(7)(ii) to permit DCOs to screen trades against applicable product and credit criteria before accepting or rejecting them. Consistent with principles of open access, the proposal would require that such criteria be non-discriminatory with respect to trading venues and clearing participants.</P>
        <FTNT>
          <P>
            <SU>20</SU>
            <E T="03">See</E>letter from Craig S. Donohue, Chief Executive Officer, CME Group, dated April 11, 2011; letter from R. Trabue Bland, Vice President and Assistant General Counsel, ICE, dated April 11, 2011; letter from Iona J. Levine, Group General Counsel and Managing Director, LCH.Clearnet, dated April 11, 2011; letter from William H. Navin, Executive Vice President and General Counsel, Options Clearing Corporation, dated April 11, 2011; letter from John M. Damgard, President, Futures Industry Association, dated April 14, 2011.</P>
        </FTNT>

        <P>The Commission continues to believe that acceptance or rejection for clearing in close to real time is crucial both for effective risk management and for the<PRTPAGE P="45733"/>efficient operation of trading venues.<SU>21</SU>
          <FTREF/>Rather than prescribe a specific length of time, the Commission is proposing as a standard that action be taken “as quickly as would be technologically practicable if fully automated systems were used.” The Commission anticipates that this standard would require action in a matter of milliseconds or seconds or, at most, a few minutes, not hours or days.<SU>22</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>21</SU>
            <E T="03">See</E>letter from James Cawley, Swaps and Derivatives Market Association, dated April 19, 2011.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>22</SU>The Commission notes that processing times may vary by market or product.</P>
        </FTNT>
        <P>This is intended to be a performance standard, not the prescription of a particular method of trade processing. The Commission expects that fully automated systems will be in place at some DCOs, FCMs, SDs, and MSPs. Others might have systems with some manual steps. This would be permitted so long as the process could operate within the same time frame as the automated systems.</P>
        <P>The Commission recognizes that some trades on a DCM or SEF are executed non-competitively. Examples include block trades and exchanges of futures for physicals (EFPs). A DCO may not be notified immediately upon execution of these trades. Accordingly, as discussed below, they will be treated in the same manner as trades that are not executed on a DCM or SEF.</P>
        <P>As previously proposed, §§ 39.12(b)(7)(iii) and 39.12(b)(7)(iv) distinguished between swaps subject to mandatory clearing and swaps not subject to mandatory clearing. Upon review of the comments, the Commission believes that this distinction is unnecessary with regard to processing time frames. If a DCO lists a product for clearing, it should be able to process it regardless of whether clearing is mandatory or voluntary. Therefore, newly proposed § 39.12(b)(7)(iii) would cover all trades not executed on a DCM or SEF. It would require acceptance or rejection by the DCO as quickly after submission as would be technologically practicable if fully automated systems were used.</P>
        <P>Proposed § 1.74(b) would set up a parallel requirement for clearing FCMs; proposed § 23.610(b) would set up a parallel requirement for SDs and MSPs that are clearing members. These rules, again, would apply a performance standard, not a prescribed method for achieving it.</P>
        <P>The Commission notes that from both a timing perspective and a risk perspective, the most efficient method would be to screen all orders using predetermined criteria established by the rules of the DCO and the provisions of the clearing documentation between the customer and its clearing member. In such a case all trades would be accepted for clearing upon execution because the clearing member and DCO would have already applied their credit and product filters.</P>
        <P>A less efficient means would be for the clearing member to authorize the DCO to screen trades on its behalf and to accept or reject according to criteria set by the clearing member. The least efficient would be for the DCO to send a message to the clearing member for each trade requesting acceptance or rejection.</P>
        <P>The Commission requests comment on the costs and benefits of the proposal. In particular, the Commission requests comment on whether the performance standard is appropriate and workable.</P>
        <HD SOURCE="HD1">III. Related Matters</HD>
        <HD SOURCE="HD2">A. Regulatory Flexibility Act</HD>
        <P>The Regulatory Flexibility Act (RFA) requires that agencies consider whether the regulations they propose will have a significant economic impact on a substantial number of small entities.<SU>23</SU>
          <FTREF/>The Commission previously has established certain definitions of “small entities” to be used in evaluating the impact of its regulations on small entities in accordance with the RFA.<SU>24</SU>
          <FTREF/>The proposed regulations would affect FCMs, DCOs, SDs, and MSPs.</P>
        <FTNT>
          <P>
            <SU>23</SU>5 U.S.C. 601<E T="03">et seq.</E>
          </P>
        </FTNT>
        <FTNT>
          <P>
            <SU>24</SU>47 FR 18618, Apr. 30, 1982.</P>
        </FTNT>
        <P>The Commission previously has determined, however, that FCMs should not be considered to be small entities for purposes of the RFA.<SU>25</SU>
          <FTREF/>The Commission's determination was based, in part, upon the obligation of FCMs to meet the minimum financial requirements established by the Commission to enhance the protection of customers' segregated funds and protect the financial condition of FCMs generally.<SU>26</SU>
          <FTREF/>The Commission also has previously determined that DCOs are not small entities for the purpose of the RFA.<SU>27</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>25</SU>
            <E T="03">Id.</E>at 18619.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>26</SU>
            <E T="03">Id.</E>
          </P>
        </FTNT>
        <FTNT>
          <P>
            <SU>27</SU>
            <E T="03">See</E>66 FR 45605, 45609, Aug. 29, 2001.</P>
        </FTNT>
        <P>SDs and MSPs are new categories of registrants. Accordingly, the Commission has not previously addressed the question of whether such persons are, in fact, small entities for purposes of the RFA. Like FCMs, SDs will be subject to minimum capital and margin requirements and are expected to comprise the largest global financial firms. The Commission is required to exempt from SD registration any entities that engage in a de minimis level of swap dealing in connection with transactions with or on behalf of customers. The Commission anticipates that this exemption would tend to exclude small entities from registration. Accordingly, for purposes of the RFA for this rulemaking, the Commission is hereby proposing that SDs not be considered “small entities” for essentially the same reasons that FCMs have previously been determined not to be small entities and in light of the exemption from the definition of SD for those engaging in a de minimis level of swap dealing.</P>
        <P>The Commission also has previously determined that large traders are not “small entities” for RFA purposes.<SU>28</SU>
          <FTREF/>In that determination, the Commission considered that a large trading position was indicative of the size of the business. MSPs, by statutory definition, maintain substantial positions in swaps or maintain outstanding swap positions that create substantial counterparty exposure that could have serious adverse effects on the financial stability of the United States banking system or financial markets. Accordingly, for purposes of the RFA for this rulemaking, the Commission is hereby proposing that MSPs not be considered “small entities” for essentially the same reasons that large traders have previously been determined not to be small entities.</P>
        <FTNT>
          <P>
            <SU>28</SU>
            <E T="03">Id.</E>at 18620.</P>
        </FTNT>
        <P>Accordingly, the Chairman, on behalf of the Commission, hereby certifies pursuant to 5 U.S.C. 605(b) that the proposed regulations will not have a significant economic impact on a substantial number of small entities. The Commission invites the public to comment on whether SDs and MSPs should be considered small entities for purposes of the RFA.</P>
        <HD SOURCE="HD2">B. Paperwork Reduction Act</HD>
        <P>The Paperwork Reduction Act (PRA)<SU>29</SU>

          <FTREF/>imposes certain requirements on Federal agencies (including the Commission) in connection with their conducting or sponsoring any collection of information as defined by the PRA. This proposed rulemaking would result in new collection of information requirements within the meaning of the PRA. The Commission therefore is submitting this proposal to the Office of Management and Budget (OMB) for review in accordance with 44 U.S.C. 3507(d) and 5 CFR 1320.11. The title for this collection of information is<PRTPAGE P="45734"/>“Customer Clearing Documentation and Timing of Acceptance for Clearing.” An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid control number. The OMB has not yet assigned this collection a control number.</P>
        <FTNT>
          <P>
            <SU>29</SU>44 U.S.C. 3501<E T="03">et seq.</E>
          </P>
        </FTNT>
        <P>The collection of information under these proposed regulations is necessary to implement certain provisions of the CEA, as amended by the Dodd-Frank Act. Specifically, it is essential to reducing risk and fostering open access to clearing and execution of customer transactions on a DCM or SEF on terms that have a reasonable relationship to the best terms available by prohibiting restrictions in customer clearing documentation of SDs, MSPs, FCMs, or DCOs that could delay or block access to clearing, increase costs, and reduce market efficiency by limiting the number of counterparties available for trading. The proposed regulations are also crucial both for effective risk management and for the efficient operation of trading venues among SDs, MSPs, FCMs, and DCOs.</P>
        <P>If the proposed regulations are adopted, responses to this collection of information would be mandatory. The Commission will protect proprietary information according to the Freedom of Information Act and 17 CFR part 145, “Commission Records and Information.” In addition, section 8(a)(1) of the CEA strictly prohibits the Commission, unless specifically authorized by the CEA, from making public “data and information that would separately disclose the business transactions or market positions of any person and trade secrets or names of customers.” The Commission is also required to protect certain information contained in a government system of records according to the Privacy Act of 1974, 5 U.S.C. 552a.</P>
        <HD SOURCE="HD3">1. Information Provided by Reporting Entities/Persons</HD>
        <P>SDs, MSPs, FCMs, and DCOs would be required to develop and maintain written customer clearing documentation in compliance with proposed regulations 1.72, 23.608, and 39.12. Proposed regulation 39.12(b)(7)(i)(B) would require DCOs to coordinate with clearing members to establish systems for prompt processing of trades. Proposed regulations 1.74(a) and 23.610(a) require reciprocal coordination with DCOs by FCMs, SDs, and MSPs that are clearing members.</P>
        <P>The annual burden associated with these proposed regulations is estimated to be 16 hours, at an annual cost of $1,600 for each FCM, SD, and MSP. Burden means the total time, effort, or financial resources expended by persons to generate, maintain, retain, disclose, or provide information to or for a federal agency. The Commission has characterized the annual costs as initial costs because the Commission anticipates that the cost burdens will be reduced dramatically over time as the documentation and procedures required by the proposed regulations become increasingly standardized within the industry.</P>
        <P>Proposed §§ 1.72 and 23.608 would require each FCM, SD, and MSP to ensure compliance with the proposed regulations. Maintenance of contracts is prudent business practice and the Commission anticipates that SDs and MSPs already maintain some form of this documentation. Additionally, the Commission believes that much of the existing customer clearing documentation already complies with the proposed rules, and therefore that compliance will require a minimal burden.</P>
        <P>In addition to the above, the Commission anticipates that FCMs, SDs, and MSPs will spend an average of 16 hours per year drafting and, as needed, updating customer clearing documentation to ensure compliance required by proposed §§ 1.72 and 23.608.</P>
        <P>For each DCO, the annual burden associated with these proposed regulations is estimated to be 40 hours, at an annual cost of $4,000. Burden means the total time, effort, or financial resources expended by persons to generate, maintain, retain, disclose, or provide information to or for a federal agency. The Commission has characterized the annual costs as initial costs as the Commission anticipates that the cost burdens will be reduced dramatically over time as once the documentation and procedures required by the proposed regulations are implemented, any additional expenditure related to § 39.12 likely would be limited to the time required to review and, as needed, amend, existing documentation and procedures.</P>
        <P>Proposed 39.12(b)(7) would require each DCO to coordinate with clearing members to establish systems for prompt processing of trades. The Commission believes that this is currently a practice of DCOs. Accordingly, any additional expenditure related to § 39.12(b)(7) likely would be limited to the time initially required to review and, as needed, amend, existing trade processing procedures to ensure that they conform to all of the required elements and to coordinate with FCMs, SDs, and MSPs to establish reciprocal procedures.</P>
        <P>The Commission anticipates that DCOs will spend an average of 20 hours per year drafting and, as needed, updating the written policies and procedures to ensure compliance required by proposed § 39.12, and 20 hours per year coordinating with FCMs, SDs, and MSPs on reciprocal procedures.</P>
        <P>The hour burden calculations below are based upon a number of variables such as the number of FCMs, SDs, MSPs, and DCOs in the marketplace and the average hourly wage of the employees of these registrants that would be responsible for satisfying the obligations established by the proposed regulation.</P>
        <P>There are currently 134 FCMs and 14 DCOs based on industry data. SDs and MSPs are new categories of registrants. Accordingly, it is not currently known how many SD and MSPs will become subject to these rules, and this will not be known to the Commission until the registration requirements for these entities become effective after July 16, 2011, the date on which the Dodd-Frank Act becomes effective. While the Commission believes there will be approximately 200 SD and 50 MSPs, it has taken a conservative approach, for PRA purposes, in estimating that there will be a combined number of 300 SDs and MSPs who will be required to comply with the recordkeeping requirements of the proposed rules. The Commission estimated the number of affected entities based on industry data.</P>
        <P>According to recent Bureau of Labor Statistics, the mean hourly wage of an employee under occupation code 11-3031, “Financial Managers,” (which includes operations managers) that is employed by the “Securities and Commodity Contracts Intermediation and Brokerage” industry is $74.41.<SU>30</SU>
          <FTREF/>Because SDs, MSPs, FCMs, and DCOs include large financial institutions whose operations management employees' salaries may exceed the mean wage, the Commission has estimated the cost burden of these proposed regulations based upon an average salary of $100 per hour.</P>
        <FTNT>
          <P>
            <SU>30</SU>
            <E T="03">http://www.bls.gov/oes/current/oes113031.htm.</E>
          </P>
        </FTNT>
        <P>Accordingly, the estimated hour burden was calculated as follows:</P>
        <P>
          <E T="03">Developing Written Procedures for Compliance, and Maintaining Records Documenting Compliance for SDs and MSPs.</E>This hourly burden arises from the proposed requirement that SDs and MSPs make and maintain records documenting compliance related to client clearing documentation.<PRTPAGE P="45735"/>
        </P>
        <P>
          <E T="03">Number of registrants:</E>300.</P>
        <P>
          <E T="03">Frequency of collection:</E>as needed.</P>
        <P>
          <E T="03">Estimated number of annual responses per registrant:</E>1.</P>
        <P>
          <E T="03">Estimated aggregate number of annual responses:</E>300.</P>
        <P>
          <E T="03">Estimated annual hour burden per registrant:</E>16 hours.</P>
        <P>
          <E T="03">Estimated aggregate annual hour burden:</E>4,800 burden hours [300 registrants × 16 hours per registrant].</P>
        <P>
          <E T="03">Developing Written Procedures for Compliance, and Maintaining Records Documenting Compliance for FCMs.</E>This hourly burden arises from the proposed requirement that FCMs make and maintain records documenting compliance related to client clearing documentation.</P>
        <P>
          <E T="03">Number of registrants:</E>134.</P>
        <P>
          <E T="03">Frequency of collection:</E>as needed.</P>
        <P>
          <E T="03">Estimated number of annual responses per registrant:</E>1.</P>
        <P>
          <E T="03">Estimated aggregate number of annual responses:</E>134.</P>
        <P>
          <E T="03">Estimated annual hour burden per registrant:</E>16 hours.</P>
        <P>
          <E T="03">Estimated aggregate annual hour burden:</E>2,144 burden hours [134 registrants × 16 hours per registrant].</P>
        <P>
          <E T="03">Drafting and Updating Trade Processing Procedures for DCOs.</E>This hour burden arises from the time necessary to develop and periodically update the trade processing procedures required by the proposed regulations.</P>
        <P>
          <E T="03">Number of registrants:</E>14.</P>
        <P>
          <E T="03">Frequency of collection:</E>Initial drafting, updating as needed.</P>
        <P>
          <E T="03">Estimated number of annual responses per registrant:</E>1.</P>
        <P>
          <E T="03">Estimated aggregate number of annual responses:</E>14.</P>
        <P>
          <E T="03">Estimated annual hour burden per registrant:</E>40 hours.</P>
        <P>
          <E T="03">Estimated aggregate annual hour burden:</E>560 burden hours [14 registrants × 40 hours per registrant].</P>
        <P>Based upon the above, the aggregate hour burden cost for all registrants is 7,504 burden hours and $750,400 [7,504 × $100 per hour].</P>
        <HD SOURCE="HD3">2. Information Collection Comments</HD>
        <P>The Commission invites the public and other federal agencies to comment on any aspect of the recordkeeping burdens discussed above. Pursuant to 44 U.S.C. 3506(c)(2)(B), the Commission solicits comments in order to: (i) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the Commission, including whether the information will have practical utility; (ii) evaluate the accuracy of the Commission's estimate of the burden of the proposed collection of information; (iii) determine whether there are ways to enhance the quality, utility, and clarity of the information to be collected; and (iv) minimize the burden of the collection of information on those who are to respond, including through the use of automated collection techniques or other forms of information technology.</P>

        <P>Comments may be submitted directly to the Office of Information and Regulatory Affairs, by fax at (202) 395-6566 or by e-mail at<E T="03">OIRAsubmissions@omb.eop.gov.</E>Please provide the Commission with a copy of submitted comments so that all comments can be summarized and addressed in the final rule preamble. Refer to the Addresses section of this notice of proposed rulemaking for comment submission instructions to the Commission. A copy of the supporting statements for the collections of information discussed above may be obtained by visiting<E T="03">RegInfo.gov.</E>OMB is required to make a decision concerning the collection of information between 30 and 60 days after publication of this document in the<E T="04">Federal Register.</E>Therefore, a comment is best assured of having its full effect if OMB receives it within 30 days of publication.</P>
        <HD SOURCE="HD2">C.<E T="03">Consideration of Costs and Benefits Under Section 15(a) of the CEA</E>
        </HD>
        <P>Section 15(a) of the CEA requires the Commission to consider the costs and benefits of its action before promulgating a regulation under the CEA. Section 15(a) of the CEA specifies that costs and benefits shall be evaluated in light of five broad areas of market and public concern: (1) Protection of market participants and the public; (2) efficiency, competitiveness, and financial integrity of futures markets; (3) price discovery; (4) sound risk management practices; and (5) other public interest considerations. The Commission may in its discretion give greater weight to any one of the five enumerated areas and could in its discretion determine that, notwithstanding its costs, a particular order is necessary or appropriate to protect the public interest or to effectuate any of the provisions or to accomplish any of the purposes of the CEA.</P>
        <P>The proposed rules have two major components: (i) The documentation between a customer and a futures commission merchant that clears on behalf of the customer; and (ii) the timing of acceptance or rejection of trades for clearing by derivatives clearing organizations and clearing members. The discussion below will consider each component in light of the section 15(a) concerns.</P>
        <HD SOURCE="HD2">A.<E T="03">Documentation Between a Customer and Futures Commission Merchant That Clears on Behalf of the Customer</E>
        </HD>
        <P>The Commission is proposing regulations that would prohibit arrangements involving FCMs, SDs, MSPs, or DCOs that would (a) disclose to an FCM, SD, or MSP the identity of a customer's counterparty; (b) limit the number of counterparties with whom a customer may enter into swaps; (c) restrict the size of the position a customer may take with any individual counterparty, apart from an overall limit for all positions held by the customer at the FCM; (d) impair a customer's access to execution of trades on a DCM or SEF on terms that have a reasonable relationship to the best terms available; or (e) prevent compliance with specified time frames for acceptance of trades into clearing.</P>
        <HD SOURCE="HD3">1. Protection of Market Participants and the Public</HD>
        <P>This measure protects the customer from any discriminatory behavior by potential clearing members or counterparties and helps ensure that customers have open access to the markets and an opportunity to obtain execution on competitive terms. The proposal would also promote financial integrity by removing potential obstacles such as more documentation requirements imposed by dealers or unnecessary restrictions on trading by a third-party, and by accelerating the timeframe for acceptance or rejection of a trade for clearing thereby reducing risk of delay or uncertainty as to whether a swap will be accepted or rejected for clearing. For example, by contrast, under a tri-party agreement, an FCM might have to evaluate each customer transaction not only against the customer's overall credit limit but also against a sub-limit for each counterparty which can delay acceptance.</P>

        <P>As far as costs are concerned, the possibility of “breakage” remains for SDs and other counterparties. However, this concern is mitigated by the timelines required in the second section of this rule, which reduce the likelihood that a SD would have time to enter into other transactions before the one in view is accepted or rejected for clearing. Similarly, if a SD has to enter into a replacement trade, the costs will be mitigated by the tight timeline, because the SD would know quickly whether the trade was accepted or rejected for clearing. As noted above, the process of evaluating individual transactions against counterparty sub-limits could<PRTPAGE P="45736"/>delay notification of acceptance or rejection for clearing. In the absence of this rule, the cost to trade will have to account for these factors and additional market risk during that time.</P>
        <HD SOURCE="HD3">2. Efficiency, Competitiveness, and Financial Integrity of Futures Markets</HD>
        <P>This rule helps prevent the disclosure, to the FCM, of the identity of the counterparty of its customer. Such lack of disclosure promotes integrity in the market by ensuring that all participants who meet certain qualifying criteria for trading have open access to all available counterparties because intermediaries will be unable to set sub-limits by counterparty. Moreover, in the absence of this rule, tri-party agreements or other similar arrangements among FCMs, SDs or MSPs and customers could result in matching processes that have the potential to be time intensive. Preventing these agreements will promote faster matching which may increase liquidity through lower transaction costs.</P>
        <P>This rule also prevents customers from being penalized (or having distorted commercial incentives) in their choice of FCM due to previous transactions with a given FCM or SD. As a consequence, this rule also has the potential to promote competition among FCMs to deliver services efficiently. Lastly, this rule would reduce duplicative risk management because DCOs and their members already have access to information necessary to perform credit analysis on individual customers and counterparties. SDs would be unnecessarily duplicating work that has already been done.</P>
        <HD SOURCE="HD3">3. Price Discovery</HD>
        <P>By not forcing a customer to transact with counterparties who may be offering less attractive terms, this rule may improve pricing. In addition, adhering to time frames specified for acceptance of trades into clearing helps to prevent stale prices.</P>
        <HD SOURCE="HD3">4. Sound Risk Management Practices</HD>
        <P>The rule does not affect the risk management structure of FCMs. Moreover, by preventing customers from learning their counterparty's identity, the responsibility for risk management remains clear. The FCM must be responsible for evaluating each customer's credit risk. It cannot rely on a counterparty to conduct due diligence. Moreover, preserving anonymity in the market increases the number of available counterparties, which leads to a more liquid market, thereby reducing risk.</P>
        <P>As mentioned before, to the extent that the SD experiences “breakage,” it exposes a SD to counterparty risk which is a potential cost. However, by facilitating quicker acceptance or rejection into clearing, the proposal would mitigate such costs by compressing the time within which the counterparty exposure would exist.</P>
        <HD SOURCE="HD2">B. Timing of Acceptance or Rejection of Trades for Clearing by Derivatives Clearing Organizations and Clearing Members</HD>
        <P>The Commission is proposing regulations that would require prompt, efficient, and accurate processing of trades, and require DCOs to coordinate with clearing members to establish systems for prompt processing of trades.</P>
        <HD SOURCE="HD3">1. Protection of Market Participants</HD>
        <P>Rapid processing protects market participants from acting on bad information by making additional trades under the presumption that an initial trade has gone through if that trade may, in fact, not clear. As mentioned, compressing the time for acceptance or rejection for clearing also reduces the time within exposures can accumulate if a trade is rejected.</P>
        <P>As far as costs are concerned, coordination among the DCOs, FCMs, SDs and MSPs in order to design and implement a system to clear transactions “as quickly as would be technologically practicable if fully automated systems were used” will likely require capital investment and personnel hours in some instances. The Commission believes, however, that DCOs and clearing members may already be using procedures that comply with the standard. To the extent that participants do not currently have automated systems, they made need to install or upgrade existing systems to comply.</P>
        <HD SOURCE="HD3">2. Efficiency, Competitiveness, and Financial Integrity of Futures Markets</HD>
        <P>Rapid clearing helps ensure that eligible counterparties will not be tied up in transactions that do not clear. They will be available to other eligible customers. This increases both competitiveness and efficiency of the market. In addition, extensive coordination among the DCOs, FCMs, SDs, and MSPs has the potential to standardize processes and technologies to support this rule. That reduces switching costs for customers and increases competitiveness.</P>
        <P>Costs will be incurred in developing systems and procedures for those products and participants where the proposed standards are not currently being met. The Commission anticipates, however, that eventually such costs would be compensated for by increased efficiency and market integrity. The Commission does not know at this time, and requests comment on, how many parties will need to upgrade their systems, if any. Additionally, the Commission requests comment from the public as to what the costs might be to upgrade existing systems or install new systems to comply with the proposed regulation.</P>
        <HD SOURCE="HD3">3. Price Discovery</HD>
        <P>Requiring rapid clearing encourages screening for credit worthiness of customers. That helps ensure that only bids and offers of qualified parties are contained in the limit order book which helps protect its informational value. Moreover, pricing feedback from cleared transactions will reach the market more quickly.</P>
        <HD SOURCE="HD3">4. Sound Risk Management Practices</HD>
        <P>Timely clearing allows each party to the transaction to act more quickly if they need to implement a hedge or other transactions related to the swap. This reduces the risk associated with potential adverse movements of the market while waiting for clearing to occur. However, if some of the processes are manual, the mandate for greater speed increases the possibility of errors.</P>
        <HD SOURCE="HD3">5. Other Public Interest Considerations</HD>
        <P>Rapid clearing makes U.S. based DCOs, FCMs, SDs, and MSPs more attractive as service providers for global swap business. Furthermore, the proposal would facilitate achievement of the overarching Dodd-Frank Act mandate to promote clearing.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects</HD>
          <CFR>17 CFR Part 1</CFR>
          <P>Conflicts of interest, Futures commission merchants, Major swap participants, Swap dealers.</P>
          <CFR>17 CFR Part 23</CFR>
          <P>Conflicts of interests, Futures commission merchants, Major swap participants, Swap dealers.</P>
          <CFR>17 CFR Part 39</CFR>
          <P>Derivatives clearing organizations, Risk management, Swaps.</P>
        </LSTSUB>
        
        <P>In light of the foregoing, the Commission hereby proposes to amend part 1; part 23, as proposed to be added at 75 FR 71390, November 23, 2010, and further amended at 75 FR 81530, December 28, 2010; and part 39, as proposed to be amended at 76 FR 13101, March 10, 2011, of Title 17 of the Code of Federal Regulations as follows:</P>
        <PART>
          <PRTPAGE P="45737"/>
          <HD SOURCE="HED">PART 1—GENERAL REGULATIONS UNDER THE COMMODITY EXCHANGE ACT</HD>
          <P>1. The authority citation for part 1 is revised to read as follows:</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>7 U.S.C. 1a, 2, 2a, 5, 6, 6a, 6b, 6c, 6d, 6e, 6f, 6g, 6h, 6i, 6k, 6l, 6m, 6n, 6o, 6p, 6r, 6s, 7, 7a-1, 7a-2, 7b, 7b-3, 8, 9, 10a, 12, 12a, 12c, 13a, 13a-1, 16, 16a, 19, 21, 23, and 24, as amended by Title VII of the Dodd-Frank Wall Street Reform and Consumer Protection Act, Pub. L. 111-203, 124 Stat. 1376 (2010).</P>
          </AUTH>
          
          <P>2. Add § 1.72 to part 1 to read as follows:</P>
          <SECTION>
            <SECTNO>§ 1.72</SECTNO>
            <SUBJECT>Restrictions on customer clearing arrangements.</SUBJECT>
            <P>No futures commission merchant providing clearing services to customers shall enter into an arrangement that:</P>
            <P>(a) Discloses to the futures commission merchant or any swap dealer or major swap participant the identity of a customer's original executing counterparty;</P>
            <P>(b) Limits the number of counterparties with whom a customer may enter into a trade;</P>
            <P>(c) Restricts the size of the position a customer may take with any individual counterparty, apart from an overall limit for all positions held by the customer at the futures commission merchant;</P>
            <P>(d) Impairs a customer's access to execution of a trade on terms that have a reasonable relationship to the best terms available; or</P>
            <P>(e) Prevents compliance with the time frames set forth in § 1.73(a)(9)(ii), § 23.609(a)(9)(ii), or § 39.12(b)(7) of this chapter.</P>
            <P>3. Add § 1.74 to part 1 to read as follows:</P>
          </SECTION>
          <SECTION>
            <SECTNO>§ 1.74</SECTNO>
            <SUBJECT>Futures commission merchant acceptance for clearing.</SUBJECT>
            <P>(a) Each futures commission merchant that is a clearing member of a derivatives clearing organization shall coordinate with each derivatives clearing organization on which it clears to establish systems that enable the futures commission merchant, or the derivatives clearing organization acting on its behalf, to accept or reject each trade submitted to the derivatives clearing organization for clearing by or for the futures commission merchant or a customer of the futures commission merchant as quickly as would be technologically practicable if fully automated systems were used; and</P>
            <P>(b) Each futures commission merchant that is a clearing member of a derivatives clearing organization shall accept or reject each trade submitted by or for it or its customers as quickly as would be technologically practicable if fully automated systems were used; a clearing futures commission merchant may meet this requirement by:</P>
            <P>(1) Establishing systems to pre-screen orders for compliance with criteria specified by the clearing futures commission merchant;</P>
            <P>(2) Establishing systems that authorize a derivatives clearing organization to accept or reject on its behalf trades that meet, or fail to meet, criteria specified by the clearing futures commission merchant; or</P>
            <P>(3) Establishing systems that enable the clearing futures commission merchant to communicate to the derivatives clearing organization acceptance or rejection of each trade as quickly as would be technologically practicable if fully automated systems were used.</P>
          </SECTION>
        </PART>
        <PART>
          <HD SOURCE="HED">PART 23—SWAP DEALERS AND MAJOR SWAP PARTICIPANTS</HD>
          <P>4. The authority citation for part 23 is revised to read as follows:</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>7 U.S.C. 1a, 2, 6, 6a, 6b, 6b-1, 6c, 6p, 6r, 6s, 6t, 9, 9a, 12, 12a, 13b, 13c, 16a, 18, 19, 21.</P>
          </AUTH>
          
          <P>5. Add § 23.608 to part 23, subpart J, to read as follows:</P>
          <SECTION>
            <SECTNO>§ 23.608</SECTNO>
            <SUBJECT>Restrictions on counterparty clearing relationships.</SUBJECT>
            <P>No swap dealer or major swap participant entering into a cleared swap with a counterparty that is a customer of a futures commission merchant shall enter into an arrangement that:</P>
            <P>(a) Discloses to the futures commission merchant or any swap dealer or major swap participant the identity of a customer's original executing counterparty;</P>
            <P>(b) Limits the number of counterparties with whom a customer may enter into a trade;</P>
            <P>(c) Restricts the size of the position a customer may take with any individual counterparty, apart from an overall limit for all positions held by the customer at the futures commission merchant;</P>
            <P>(d) Impairs a customer's access to execution of a trade on terms that have a reasonable relationship to the best terms available; or</P>
            <P>(e) Prevents compliance with the time frames set forth in § 1.73(a)(9)(ii), § 23.609(a)(9)(ii), or § 39.12(b)(7) of this chapter.</P>
            <P>6. Add § 23.610 to part 23, subpart J, to read as follows:</P>
          </SECTION>
          <SECTION>
            <SECTNO>§ 23.610</SECTNO>
            <SUBJECT>Clearing member acceptance for clearing.</SUBJECT>
            <P>(a) Each swap dealer or major swap participant that is a clearing member of a derivatives clearing organization shall coordinate with each derivatives clearing organization on which it clears to establish systems that enable the clearing member, or the derivatives clearing organization acting on its behalf, to accept or reject each trade submitted to the derivatives clearing organization for clearing by or for the clearing member as quickly as would be technologically practicable if fully automated systems were used; and</P>
            <P>(b) Each swap dealer or major swap participant that is a clearing member of a derivatives clearing organization shall accept or reject each trade submitted by or for it as quickly as would be technologically practicable if fully automated systems were used; a clearing member may meet this requirement by:</P>
            <P>(1) Establishing systems to pre-screen orders for compliance with criteria specified by the clearing member;</P>
            <P>(2) Establishing systems that authorize a derivatives clearing organization to accept or reject on its behalf trades that meet, or fail to meet, criteria specified by the clearing member; or</P>
            <P>(3) Establishing systems that enable the clearing member to communicate to the derivatives clearing organization acceptance or rejection of each trade as quickly as would be technologically practicable if fully automated systems were used.</P>
          </SECTION>
        </PART>
        <PART>
          <HD SOURCE="HED">PART 39—DERIVATIVES CLEARING ORGANIZATIONS</HD>
          <P>7. Revise the authority citation for part 39 to read as follows:</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>7 U.S.C. 1a, 2, 5, 6, 6d, 7a-1, 7a-2, and 7b as amended by the Dodd-Frank Wall Street Reform and Consumer Protection Act, Pub. L. 111-203, 124 Stat. 1376.</P>
          </AUTH>
          <SUBPART>
            <HD SOURCE="HED">Subpart B—Compliance With Core Principles</HD>
          </SUBPART>
          <P>8. In § 39.12, add paragraph (a)(1)(vi) to read as follows:</P>
          <P>(a) * * *</P>
          <P>(1) * * *</P>
          <P>(vi) No derivatives clearing organization shall require as a condition of accepting a swap for clearing that a futures commission merchant enter into an arrangement with a customer that:</P>
          <P>(A) Discloses to the futures commission merchant or any swap dealer or major swap participant the identity of a customer's original executing counterparty;</P>
          <P>(B) Limits the number of counterparties with whom a customer may enter into trades;</P>

          <P>(C) Restricts the size of the position a customer may take with any individual counterparty, apart from an overall limit for all positions held by the customer at the futures commission merchant;<PRTPAGE P="45738"/>
          </P>
          <P>(D) Impairs a customer's access to execution of a trade on terms that have a reasonable relationship to the best terms available; or</P>
          <P>(E) Prevents compliance with the time frames set forth in § 1.73(a)(9)(ii), § 23.609(a)(9)(ii), or § 39.12(b)(7) of this chapter.</P>
          <P>9. Amend § 39.12 by:</P>
          <P>a. Redesignating paragraph (b)(7)(v) as paragraph (b)(8); and</P>
          <P>b. Revising § 39.12(b)(7) to read as follows:</P>
          <P>(i)<E T="03">Coordination with markets and clearing members</E>
          </P>
          <P>(A) Each derivatives clearing organization shall coordinate with each designated contract market and swap execution facility that lists for trading a product that is cleared by the derivatives clearing organization in developing rules and procedures to facilitate prompt, efficient, and accurate processing of all transactions submitted to the derivatives clearing organization for clearing.</P>
          <P>(B) Each derivatives clearing organization shall coordinate with each clearing member that is a futures commission merchant, swap dealer, or major swap participant to establish systems that enable the clearing member, or the derivatives clearing organization acting on its behalf, to accept or reject each trade submitted to the derivatives clearing organization for clearing by or for the clearing member or a customer of the clearing member as quickly as would be technologically practicable if fully automated systems were used.</P>
          <P>(ii)<E T="03">Transactions executed competitively on or subject to the rules of a designated contract market or swap execution facility.</E>A derivatives clearing organization shall have rules that provide that the derivatives clearing organization will accept or reject for clearing as quickly after execution as would be technologically practicable if fully automated systems were used, all contracts that are listed for clearing by the derivatives clearing organization and are executed competitively on a designated contract market or a swap execution facility. The derivatives clearing organization shall accept all trades:</P>
          <P>(A) For which the executing parties have clearing arrangements in place with clearing members of the derivatives clearing organization;</P>
          <P>(B) For which the executing parties identify the derivatives clearing organization as the intended clearinghouse; and</P>
          <P>(C) That satisfy the criteria of the derivatives clearing organization, including but not limited to applicable risk filters; provided that such criteria are non-discriminatory across trading venues and are applied as quickly as would be technologically practicable if fully automated systems were used.</P>
          <P>(iii)<E T="03">Swaps not executed on or subject to the rules of a designated contract market or a swap execution facility or executed non-competitively on or subject to the rules of a designated contract market or a swap execution facility.</E>A derivatives clearing organization shall have rules that provide that the derivatives clearing organization will accept or reject for clearing as quickly after submission to the derivatives clearing organization as would be technologically practicable if fully automated systems were used, all swaps that are listed for clearing by the derivatives clearing organization and are not executed on a designated contract market or a swap execution facility. The derivatives clearing organization shall accept all trades:</P>
          <P>(A) That are submitted by the parties to the derivatives clearing organization, in accordance with § 23.506 of this chapter;</P>
          <P>(B) For which the executing parties have clearing arrangements in place with clearing members of the derivatives clearing organization;</P>
          <P>(C) For which the executing parties identify the derivatives clearing organization as the intended clearinghouse; and</P>
          <P>(D) That satisfy the criteria of the derivatives clearing organization, including but not limited to applicable risk filters; provided that such criteria are non-discriminatory across trading venues and are applied as quickly as would be technologically practicable if fully automated systems were used.</P>
          <SIG>
            <DATED>Issued in Washington, DC, on July 19, 2011, by the Commission.</DATED>
            <NAME>David A. Stawick,</NAME>
            <TITLE>Secretary of the Commission.</TITLE>
          </SIG>
          <HD SOURCE="HD1">Appendices to Customer Clearing Documentation and Timing of Acceptance for Clearing—Commission Voting Summary and Statements of Commissioners</HD>
          <NOTE>
            <HD SOURCE="HED">Note:</HD>
            <P>The following appendices will not appear in the Code of Federal Regulations</P>
          </NOTE>
          <HD SOURCE="HD1">Appendix 1—Commission Voting Summary</HD>
          <EXTRACT>
            <P>On this matter, Chairman Gensler and Commissioners Dunn and Chilton voted in the affirmative; Commissioners O'Malia and Sommers voted in the negative.</P>
          </EXTRACT>
          <APPENDIX>
            <HD SOURCE="HED">Appendix 2—Statement of Chairman Gary Gensler</HD>
            <P>I support the proposed rulemaking for customer clearing documentation and timing of acceptance for clearing. The proposed rule promotes market participants' access to central clearing, increases market transparency and supports market efficiency. This proposal will foster bilateral clearing arrangements between customers and their futures commission merchants. This proposal also re-proposes certain time-frame provisions of the Commission's proposed rule in February related to straight-through processing.</P>
            
          </APPENDIX>
        </PART>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19365 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE P</BILCOD>
    </PRORULE>
    <PRORULE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF HOMELAND SECURITY</AGENCY>
        <SUBAGY>Coast Guard</SUBAGY>
        <CFR>33 CFR Part 165</CFR>
        <DEPDOC>[Docket No. USCG-2010-1145]</DEPDOC>
        <RIN>RIN 1625-AA11</RIN>
        <SUBJECT>Regulated Navigation Area; Pacific Sound Resources and Lockheed Shipyard EPA Superfund Cleanup Sites, Elliott Bay, Seattle, WA</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Coast Guard, DHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of proposed rulemaking.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Coast Guard proposes to establish a permanent regulated navigation area (RNA) on a portion of Elliott Bay in Seattle, Washington. The RNA would protect the seabed in portions of the bay that are subject to the U.S. Environmental Protection Agency (EPA)'s Pacific Sound Resources (PSR) and Lockheed Shipyard superfund cleanup remediation efforts. This RNA would prohibit activities that would disturb the seabed, such as anchoring, dragging, trawling, spudding or other activities that involve disrupting the integrity of the sediment caps that cover the superfund sites. It will not affect transit or navigation of the area.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments and related material must be received by the Coast Guard on or before October 31, 2011. Requests for public meetings must be received by the Coast Guard on or before September 15, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may submit comments identified by docket number USCG-2010-1145 using any one of the following methods:</P>
          <P>(1)<E T="03">Federal eRulemaking Portal: http://www.regulations.gov.</E>
          </P>
          <P>(2)<E T="03">Fax:</E>202-493-2251.</P>
          <P>(3)<E T="03">Mail:</E>Docket Management Facility (M-30), U.S. Department of<PRTPAGE P="45739"/>Transportation, West Building Ground Floor, Room W12-140, 1200 New Jersey Avenue, SE., Washington, DC 20590-0001.</P>
          <P>(4)<E T="03">Hand delivery:</E>Same as mail address above, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays. The telephone number is 202-366-9329.</P>

          <P>To avoid duplication, please use only one of these four methods. See the “Public Participation and Request for Comments” portion of the<E T="02">SUPPLEMENTARY INFORMATION</E>section below for instructions on submitting comments.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>If you have questions on this proposed rule, call or e-mail LTJG Ian Hanna, Waterways Management Division, Sector Puget Sound, Coast Guard; telephone 206-217-6045, e-mail<E T="03">SectorSeattleWWM@uscg.mil.</E>If you have questions on viewing or submitting material to the docket, call Renee V. Wright, Program Manager, Docket Operations, telephone 202-366-9826.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">Public Participation and Request for Comments</HD>

        <P>We encourage you to participate in this rulemaking by submitting comments and related materials. All comments received will be posted without change to<E T="03">http://www.regulations.gov</E>and will include any personal information you have provided.</P>
        <HD SOURCE="HD2">Submitting Comments</HD>

        <P>If you submit a comment, please include the docket number for this rulemaking (USCG-2010-1145), indicate the specific section of this document to which each comment applies, and provide a reason for each suggestion or recommendation. You may submit your comments and material online (via<E T="03">http://www.regulations.gov</E>) or by fax, mail, or hand delivery, but please use only one of these means. If you submit a comment online via<E T="03">http://www.regulations.gov</E>, it will be considered received by the Coast Guard when you successfully transmit the comment. If you fax, hand deliver, or mail your comment, it will be considered as having been received by the Coast Guard when it is received at the Docket Management Facility. We recommend that you include your name and a mailing address, an e-mail address, or a telephone number in the body of your document so that we can contact you if we have questions regarding your submission.</P>
        <P>To submit your comment online, go to<E T="03">http://www.regulations.gov</E>, click on the “submit a comment” box, which will then become highlighted in blue. In the “Document Type” drop down menu select “Proposed Rule” and insert “USCG-2010-1145” in the “Keyword” box. Click “Search” then click on the balloon shape in the “Actions” column. If you submit your comments by mail or hand delivery, submit them in an unbound format, no larger than 8<FR>1/2</FR>; by 11 inches, suitable for copying and electronic filing. If you submit comments by mail and would like to know that they reached the Facility, please enclose a stamped, self-addressed postcard or envelope. We will consider all comments and material received during the comment period and may change the rule based on your comments.</P>
        <HD SOURCE="HD2">Viewing Comments and Documents</HD>

        <P>To view comments, as well as documents mentioned in this preamble as being available in the docket, go to<E T="03">http://www.regulations.gov</E>, click on the “read comments” box, which will then become highlighted in blue. In the “Keyword” box insert “USCG-2010-1145” and click “Search.” Click the “Open Docket Folder” in the “Actions” column. You may also visit the Docket Management Facility in Room W12-140 on the ground floor of the Department of Transportation West Building, 1200 New Jersey Avenue, SE., Washington, DC 20590, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays. We have an agreement with the Department of Transportation to use the Docket Management Facility.</P>
        <HD SOURCE="HD2">Privacy Act</HD>

        <P>Anyone can search the electronic form of comments received into any of our dockets by the name of the individual submitting the comment (or signing the comment, if submitted on behalf of an association, business, labor union, etc.). You may review a Privacy Act notice regarding our public dockets in the January 17, 2008, issue of the<E T="04">Federal Register</E>(73 FR 3316).</P>
        <HD SOURCE="HD2">Public Meeting</HD>

        <P>We do not now plan to hold a public meeting. But you may submit a request for one on or before September 15, 2011 using one of the four methods specified under<E T="02">ADDRESSES</E>. Please explain why you believe a public meeting would be beneficial. If we determine that one would aid this rulemaking, we will hold one at a time and place announced by a later notice in the<E T="04">Federal Register</E>.</P>
        <HD SOURCE="HD1">Background and Purpose</HD>
        <P>The PSR superfund site, which is located on the north shore of West Seattle within Elliott Bay, and northwest of the mouth of the Duwamish river, was created by the EPA to cover the remains of the Wyckoff West Seattle Wood Treating Facility. The wood treating facility, which was in operation between 1909 and 1994, was mostly located on a pile-supported facility extending into Elliott Bay. The area was added to the federal Superfund National Priorities List in May 1994. Later that year the entire wood treatment facility was demolished and approximately 4000 cubic yards of highly contaminated soil and process sludge were removed from the site. Construction of a subsurface physical containment barrier was started in 1996 and completed in 1999. The final sediment cap, completed in 2004, is approximately 58-acres which includes approximately 1500 linear feet of shoreline, and intertidal and subtidal areas to depth of about 300 feet.</P>
        <P>The Lockheed Shipyard Sediment Operable Unit consists of contaminated near shore sediments within and adjacent to the Lockheed Shipyard on Harbor Island. Harbor Island is located approximately one mile southwest of the Central Business District of Seattle, in King County, Washington, and lies at the mouth of the Duwamish Waterway on the southern edge of Elliott Bay. The Lockheed Shipyard sediments are located on the west side of Harbor Island and face the West Waterway of the Duwamish Waterway. The final site does not protrude a significant distance into the West Duwamish waterway. Lockheed Shipyards acquired established shipbuilding operations in 1959 and the facility until 1986. In April 1997, Lockheed sold the upland property and its legal rights to the submerged portions of the site to the Port of Seattle. The remedy for the contaminated sediments included demolition of 3 piers, three shipways and one finger pier. The piers and shipways primarily consist of timber superstructures supported by approximately 6000 piles. Contaminants found in sediments which were either dredged or capped are arsenic, copper, lead, mercury, zinc, PAHs and PCBs. The metal contaminants were associated with sand blast grit and paint clips.</P>

        <P>Remedial actions for both of these sites as established by the EPA include preventing use of large anchors on the cap. This rulemaking is necessary to assist the EPA in that remedial action.<PRTPAGE P="45740"/>
        </P>
        <HD SOURCE="HD1">Discussion of Proposed Rule</HD>
        <P>This rule is necessary to prevent disturbance of the PSR and Lockheed Shipyard sediment caps. It does so by restricting anchoring, dragging, trawling, spudding or other activities that involve disrupting the integrity of the cap in an RNA around the sediment caps. This RNA is similar to RNAs which protect other caps in the area. Enforcement of this RNA will be managed by Coast Guard Sector Puget Sound assets including Vessel Traffic Service Puget Sound through radar and closed circuit television sensors. The Captain of the Port Puget Sound may also be assisted by other government agencies in the enforcement of this zone.</P>
        <HD SOURCE="HD1">Regulatory Analyses</HD>
        <P>We developed this proposed rule after considering numerous statutes and executive orders related to rulemaking. Below we summarize our analyses based on 13 of these statutes or executive orders.</P>
        <HD SOURCE="HD2">Regulatory Planning and Review</HD>
        <P>This proposed rule is not a significant regulatory action under section 3(f) of Executive Order 12866, Regulatory Planning and Review, and does not require an assessment of potential costs and benefits under section 6(a)(3) of that Order. The Office of Management and Budget has not reviewed it under that Order. This expectation is based on the fact that the RNA established by the rule would encompass a small area that should not impact commercial or recreational traffic, and prohibited activities are not routine for the designated areas.</P>
        <HD SOURCE="HD2">Small Entities</HD>
        <P>Under the Regulatory Flexibility Act (5 U.S.C. 601-612), we have considered whether this proposed rule would have a significant economic impact on a substantial number of small entities. The term “small entities” comprises small businesses, not-for-profit organizations that are independently owned and operated and are not dominant in their fields, and governmental jurisdictions with populations of less than 50,000.</P>
        <P>The Coast Guard certifies under 5 U.S.C. 605(b) that this proposed rule would not have a significant economic impact on a substantial number of small entities. This rule would affect the following entities, some of which may be small entities: The owners or operators of vessels intending to anchor, dredge, spud, lay cable or disturb the seabed in any fashion when this rule is in effect. The RNA would not have a significant economic impact on small entities due to its minimal restrictive area and the opportunity for a waiver to be granted for any legitimate use of the seabed.</P>

        <P>If you think that your business, organization, or governmental jurisdiction qualifies as a small entity and that this rule would have a significant economic impact on it, please submit a comment (see<E T="02">ADDRESSES</E>) explaining why you think it qualifies and how and to what degree this rule would economically affect it.</P>
        <HD SOURCE="HD2">Assistance for Small Entities</HD>

        <P>Under section 213(a) of the Small Business Regulatory Enforcement Fairness Act of 1996 (Pub. L. 104-121), we want to assist small entities in understanding this proposed rule so that they can better evaluate its effects on them and participate in the rulemaking. If the rule would affect your small business, organization, or governmental jurisdiction and you have questions concerning its provisions or options for compliance, please contact LTJG Ian Hanna, Waterways Management, Sector Puget Sound, Coast Guard; telephone 206-217-6045, e-mail<E T="03">SectorSeattleWWM@uscg.mil.</E>The Coast Guard will not retaliate against small entities that question or complain about this proposed rule or any policy or action of the Coast Guard.</P>
        <HD SOURCE="HD2">Collection of Information</HD>
        <P>This proposed rule would call for no new collection of information under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501-3520).</P>
        <HD SOURCE="HD2">Federalism</HD>
        <P>A rule has implications for federalism under Executive Order 13132, Federalism, if it has a substantial direct effect on State or local governments and would either preempt State law or impose a substantial direct cost of compliance on them. We have analyzed this proposed rule under that Order and have determined that it does not have implications for federalism.</P>
        <HD SOURCE="HD2">Unfunded Mandates Reform Act</HD>
        <P>The Unfunded Mandates Reform Act of 1995 (2 U.S.C. 1531-1538) requires Federal agencies to assess the effects of their discretionary regulatory actions. In particular, the Act addresses actions that may result in the expenditure by a State, local, or tribal government, in the aggregate, or by the private sector of $100,000,000 (adjusted for inflation) or more in any one year. Though this proposed rule would not result in such an expenditure, we do discuss the effects of this rule elsewhere in this preamble.</P>
        <HD SOURCE="HD2">Taking of Private Property</HD>
        <P>This proposed rule would not cause a taking of private property or otherwise have taking implications under Executive Order 12630, Governmental Actions and Interference with Constitutionally Protected Property Rights.</P>
        <HD SOURCE="HD2">Civil Justice Reform</HD>
        <P>This proposed rule meets applicable standards in sections 3(a) and 3(b)(2) of Executive Order 12988, Civil Justice Reform, to minimize litigation, eliminate ambiguity, and reduce burden.</P>
        <HD SOURCE="HD2">Protection of Children</HD>
        <P>We have analyzed this proposed rule under Executive Order 13045, Protection of Children from Environmental Health Risks and Safety Risks. This rule is not an economically significant rule and would not create an environmental risk to health or risk to safety that might disproportionately affect children.</P>
        <HD SOURCE="HD2">Indian Tribal Governments</HD>
        <P>In preparation for this rulemaking, on October 8, 2010, Sector Puget Sound conducted a tribal consultation with representatives from the Suquamish and Muckleshoot tribes in accordance with Executive Order 13175, Consultation and Coordination with Indian Tribal Governments. The group noted that the sediment caps were in the usual and accustomed (U&amp;A) fishing grounds of both tribes. Their main concern was that this RNA would prohibit them from exercising their U&amp;A fishing. The Coast Guard and EPA clarified that nothing in this rulemaking is intended to conflict with these tribes' treaty fishing rights and they are not restricted from any type of fishing in the described areas. As a result of the consultation the Coast Guard added paragraph b.(3) to the regulation.</P>
        <HD SOURCE="HD2">Energy Effects</HD>

        <P>We have analyzed this proposed rule under Executive Order 13211, Actions Concerning Regulations That Significantly Affect Energy Supply, Distribution, or Use. We have determined that it is not a “significant energy action” under that order because it is not a “significant regulatory action” under Executive Order 12866 and is not likely to have a significant adverse effect on the supply, distribution, or use of energy. The Administrator of the Office of Information and Regulatory Affairs has not designated it as a significant<PRTPAGE P="45741"/>energy action. Therefore, it does not require a Statement of Energy Effects under Executive Order 13211.</P>
        <HD SOURCE="HD2">Technical Standards</HD>
        <P>The National Technology Transfer and Advancement Act (NTTAA) (15 U.S.C. 272 note) directs agencies to use voluntary consensus standards in their regulatory activities unless the agency provides Congress, through the Office of Management and Budget, with an explanation of why using these standards would be inconsistent with applicable law or otherwise impractical. Voluntary consensus standards are technical standards (e.g., specifications of materials, performance, design, or operation; test methods; sampling procedures; and related management systems practices) that are developed or adopted by voluntary consensus standards bodies.</P>
        <P>This proposed rule does not use technical standards. Therefore, we did not consider the use of voluntary consensus standards.</P>
        <HD SOURCE="HD2">Environment</HD>

        <P>We have analyzed this proposed rule under Department of Homeland Security Management Directive 023-01 and Commandant Instruction M16475.lD, which guide the Coast Guard in complying with the National Environmental Policy Act of 1969 (NEPA) (42 U.S.C. 4321-4370f), and have made a preliminary determination that this action is one of a category of actions that do not individually or cumulatively have a significant effect on the human environment. A preliminary environmental analysis checklist supporting this determination is available in the docket where indicated under<E T="02">ADDRESSES</E>.</P>
        <P>This proposed rule involves no factors in this case that would limit the use of a categorical exclusion under section 2.B.2 of the Instruction. Therefore, we believe that this rule should be categorically excluded, under figure 2-1, paragraph (34)(g), of the Instruction, from further environmental documentation. As a proposal to establish a regulated navigation area, this rule meets the criteria outlined in paragraph (34)(g). We seek any comments or information that may lead to the discovery of a significant environmental impact from this proposed rule.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 33 CFR Part 165</HD>
          <P>Harbors, Marine safety, Navigation (water), Reporting and recordkeeping requirements, Security measures, Waterways.</P>
        </LSTSUB>
        
        <P>For the reasons discussed in the preamble, the Coast Guard proposes to amend 33 CFR part 165 as follows:</P>
        <PART>
          <HD SOURCE="HED">PART 165—REGULATED NAVIGATION AREAS AND LIMITED ACCESS AREAS</HD>
          <P>1. The authority citation for part 165 continues to read as follows:</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>33 U.S.C. 1231; 46 U.S.C. Chapter 701, 3306, 3703; 50 U.S.C. 191, 195; 33 CFR 1.05-1, 6.04-1, 6.04-6, and 160.5; Pub. L. 107-295, 116 Stat. 2064; Department of Homeland Security Delegation No. 0170.1.</P>
          </AUTH>
          
          <P>2. Add § 165.1336 to read as follows:</P>
          <SECTION>
            <SECTNO>§ 165.1336</SECTNO>
            <SUBJECT>Regulated Navigation Area; Pacific Sound Resources and Lockheed Shipyard Superfund Sites, Elliott Bay, Seattle, WA.</SUBJECT>
            <P>(a)<E T="03">Regulated Areas.</E>The following areas are regulated navigation areas:</P>
            <P>(1) All waters inside an area beginning at a point on the shore at 47°35′02.7″ N 122°22′23.00″ W; thence north to 47°35′26.00″ N 122°22′23.00″ W; thence east to 47°35′26.00″ N 122°21′52.50″ W; thence south to 47°35′10.80″ N 122°21′52.50″ W; thence southwest to a point on the shoreline at 47°35′05.9″ N 122°21′58.00″ W. [Datum: NAD 1983].</P>
            <P>(2) All waters inside an area beginning at 47°34′52.16″ N 122°21′27.11″ W; thence to 47°34′53.46″ N 122°21′30.42″ W; thence to 47°34′37.92″ N 122°21′30.51″ W; thence to 47°34′37.92″ N 122°21′27.65″ W. [Datum: NAD 1983].</P>
            <P>(b)<E T="03">Regulations.</E>
            </P>
            <P>(1) All vessels and persons are prohibited from activities that would disturb the seabed, such as anchoring, dragging, trawling, spudding, or other activities that involve disrupting the integrity of the sediment caps installed in the designated regulated navigation area, pursuant to the remediation efforts of the U.S. Environmental Protection Agency (EPA) and others in the Pacific Sound Resources and Lockheed Shipyard EPA superfund sites. Vessels may otherwise transit or navigate within this area without reservation.</P>
            <P>(2) The prohibition described in paragraph (b)(1) of this section does not apply to vessels or persons engaged in activities associated with remediation efforts in the superfund sites, provided that the Captain of the Port, Puget Sound (COTP), is given advance notice of those activities by the EPA.</P>
            <P>(3) Nothing in this rulemaking is intended to conflict with treaty fishing rights of the Muckleshoot and Suquamish tribes, and they are not restricted from any type of fishing in the described area.</P>
            <P>(c)<E T="03">Waivers.</E>
            </P>
            <P>(1) Upon written request stating the need and proposed conditions of the waiver, and any proposed precautionary measures, the COTP may authorize a waiver from this section if they determine that the activity for which the waiver is sought can take place without undue risk to the remediation efforts described in paragraph (b)(1) of this section. The COTP will consult with EPA in making this determination when necessary and practicable.</P>
          </SECTION>
          <SIG>
            <DATED>Dated: July 6, 2011.</DATED>
            <NAME>G.T. Blore,</NAME>
            <TITLE>Rear Admiral, U.S. Coast Guard, Commander, Thirteenth Coast Guard District.</TITLE>
          </SIG>
        </PART>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19320 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 9110-04-P</BILCOD>
    </PRORULE>
    <PRORULE>
      <PREAMB>
        <AGENCY TYPE="N">ENVIRONMENTAL PROTECTION AGENCY</AGENCY>
        <CFR>40 CFR Part 52</CFR>
        <DEPDOC>[EPA-R03-OAR-2011-0471; FRL-9446-1]</DEPDOC>
        <SUBJECT>Approval and Promulgation of Air Quality Implementation Plans; Pennsylvania; Diesel-Powered Motor Vehicle Idling Act</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Environmental Protection Agency (EPA).</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Proposed rule.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>EPA proposes to approve the State Implementation Plan (SIP) revision submitted by the Commonwealth of Pennsylvania for the purpose of incorporating the Commonwealth's Diesel-Powered Motor Vehicle Idling Act (Act 124 of 2008, or simply Act 124) into the Pennsylvania SIP. Act 124, passed by the Pennsylvania General Assembly and signed into state law by Governor Rendell in October 2008 (and effective at the state level in February 2009), reduces the allowable time that heavy-duty, commercial highway diesel vehicles of over 10,000 pounds gross vehicle weight can idle their main propulsion engines. The law restricts idling of these commercial diesel vehicles (mostly heavy trucks and buses) to a period of 5 minutes per continuous 60 minute period (with certain allowable exemptions and exclusions). Act 124 applies statewide in the Commonwealth, and is estimated by Pennsylvania to significantly reduce emissions of nitrogen oxides (NO<E T="52">X</E>), volatile organic compounds (VOCs), and fine particulate matter (PM). While idle time emissions limits are not mandatory under the Clean Air Act (CAA), incorporation of Act 124 into the SIP does strengthen the SIP, makes the state<PRTPAGE P="45742"/>law federally enforceable by EPA, and allows the Commonwealth to take credit for emissions benefits from the rule as part of future Pennsylvania SIP revisions to demonstrate compliance with CAA National Ambient Air Quality Standards (NAAQS). This action is being taken under the CAA.</P>
          <P>In the Final Rules section of this<E T="04">Federal Register</E>, EPA is approving the Commonwealth's SIP submittal as a direct final rule without prior proposal because EPA views this as a noncontroversial submittal and anticipates no adverse comments. A detailed rationale for the approval is set forth in the direct final rule. If no adverse comments are received in response to this action, no further activity is contemplated. If EPA receives adverse comments, the direct final rule will be withdrawn and all public comments received will be addressed in a subsequent final rule based on this proposed rule. EPA will not institute a second comment period. Any parties interested in commenting on this action should do so at this time.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments must be received in writing by August 31, 2011.</P>
        </EFFDATE>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>Submit your comments, identified by Docket ID Number EPA-R03-OAR-2011-0471 by one of the following methods:</P>
          <P>A.<E T="03">http://www.regulations.gov.</E>Follow the on-line instructions for submitting comments.</P>
          <P>B.<E T="03">E-mail: fernandez.cristina@epa.gov</E>
          </P>
          <P>C.<E T="03">Mail:</E>EPA-R03-OAR-2011-0471, Cristina Fernandez, Associate Director, Office of Air Program Planning, Mailcode 3AP30, U.S. Environmental Protection Agency, Region III, 1650 Arch Street, Philadelphia, Pennsylvania 19103.</P>
          <P>D.<E T="03">Hand Delivery:</E>At the previously-listed EPA Region III address. Such deliveries are only accepted during the Docket's normal hours of operation, and special arrangements should be made for deliveries of boxed information.</P>
          <P>
            <E T="03">Instructions:</E>Direct your comments to Docket ID No. EPA-R03-OAR-2011-0471. EPA's policy is that all comments received will be included in the public docket without change, and may be made available online at<E T="03">http://www.regulations.gov,</E>including any personal information provided, unless the comment includes information claimed to be Confidential Business Information (CBI) or other information whose disclosure is restricted by statute. Do not submit information that you consider to be CBI or otherwise protected through<E T="03">http://www.regulations.gov</E>or e-mail. The<E T="03">http://www.regulations.gov</E>Web site is an “anonymous access” system, which means EPA will not know your identity or contact information unless you provide it in the body of your comment. If you send an e-mail comment directly to EPA without going through<E T="03">http://www.regulations.gov,</E>your e-mail address will be automatically captured and included as part of the comment that is placed in the public docket and made available on the Internet. If you submit an electronic comment, EPA recommends that you include your name and other contact information in the body of your comment and with any disk or CD-ROM you submit. If EPA cannot read your comment due to technical difficulties and cannot contact you for clarification, EPA may not be able to consider your comment. Electronic files should avoid the use of special characters, any form of encryption, and be free of any defects or viruses.</P>
          <P>
            <E T="03">Docket:</E>All documents in the electronic docket are listed in the<E T="03">http://www.regulations.gov</E>index. Although listed in the index, some information is not publicly available, i.e., CBI or other information whose disclosure is restricted by statute. Certain other material, such as copyrighted material, is not placed on the Internet and will be publicly available only in hard copy form.</P>

          <P>Publicly available docket materials are available either electronically in<E T="03">http://www.regulations.gov</E>or in hard copy during normal business hours at the Air Protection Division, U.S. Environmental Protection Agency, Region III, 1650 Arch Street, Philadelphia, Pennsylvania 19103. Copies of the State submittal are available at the Pennsylvania Department of Environmental Protection, Bureau of Air Quality Control, P.O. Box 8468, 400 Market Street, Harrisburg, Pennsylvania 17105.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Brian Rehn, (215) 814-2176, or by e-mail at<E T="03">rehn.brian@epa.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>

        <P>For further information, please see the information provided in the direct final action, with the same title, that is located in the “Rules and Regulations” section of this<E T="04">Federal Register</E>publication.</P>
        <SIG>
          <DATED>Dated: July 18, 2011.</DATED>
          <NAME>W.C. Early,</NAME>
          <TITLE>Acting Regional Administrator, Region III.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19275 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6560-50-P</BILCOD>
    </PRORULE>
    <PRORULE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>National Oceanic and Atmospheric Administration</SUBAGY>
        <CFR>50 CFR Part 648</CFR>
        <DEPDOC>[Docket No. 0808041037-81092-02]</DEPDOC>
        <RIN>RIN 0648-AX05</RIN>
        <SUBJECT>Fisheries of the Northeastern United States; Atlantic Mackerel, Squid, and Butterfish Fisheries; Amendment 11</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>National Marine Fisheries Service (NMFS), National Oceanic and Atmospheric Administration (NOAA), Commerce.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Proposed rule, request for comments.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>NMFS proposes regulations to implement measures in Amendment 11 to the Atlantic Mackerel, Squid, and Butterfish (MSB) Fishery Management Plan (FMP). Amendment 11 was developed by the Mid-Atlantic Fishery Management Council (Council) to establish a tiered limited access program for the Atlantic mackerel (mackerel) fishery, and to make other changes to the management of the MSB fisheries. The Amendment 11 management measures include: A limited access program for mackerel; an open access incidental catch permit for mackerel; an update to essential fish habitat (EFH) designations for all life stages of mackerel,<E T="03">Loligo</E>squid,<E T="03">Illex</E>squid, and butterfish; and the establishment of a recreational allocation for mackerel. This rule also proposes minor, technical corrections to the existing regulations pertaining to the MSB fisheries.</P>
        </SUM>
        <EFFDATE>
          <HD SOURCE="HED">DATES:</HD>
          <P>Public comments must be received no later than 5 p.m., eastern standard time, on September 15, 2011.</P>
        </EFFDATE>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Copies of supporting documents used by the Mid-Atlantic Fishery Management Council (Council), including the Environmental Assessment (EA) and Regulatory Impact Review (RIR)/Initial Regulatory Flexibility Analysis (IRFA), are available from: Dr. Christopher M. Moore, Executive Director, Mid-Atlantic Fishery Management Council, Room 2115, Federal Building, 300 South New Street, Dover, DE 19904-6790. The EA/RIR/IRFA is accessible via the Internet at<E T="03">http://www.nero.noaa.gov.</E>
          </P>
          <P>You may submit comments, identified by 0648-AX05, by any one of the following methods:</P>
          <P>•<E T="03">Electronic Submissions:</E>Submit all electronic public comments via the Federal e-Rulemaking Portal<E T="03">http://www.regulations.gov;</E>
            <PRTPAGE P="45743"/>
          </P>
          <P>•<E T="03">Fax:</E>(978) 281-9135, Attn: Aja Szumylo;</P>
          <P>• Mail to NMFS, Northeast Regional Office, 55 Great Republic Dr., Gloucester, MA 01930. Mark the outside of the envelope “Comments on MSB Amendment 11.”</P>
          <P>
            <E T="03">Instructions:</E>All comments received are a part of the public record and will generally be posted to<E T="03">http://www.regulations.gov</E>without change. All Personal Identifying Information (for example, name, address, etc.) voluntarily submitted by the commenter may be publicly accessible. Do not submit Confidential Business Information or otherwise sensitive or protected information.</P>
          <P>NMFS will accept anonymous comments (enter N/A in the required fields, if you wish to remain anonymous). You may submit attachments to electronic comments in Microsoft Word, Excel, WordPerfect, or Adobe PDF file formats only.</P>

          <P>Written comments regarding the burden-hour estimates or other aspects of the collection-of-information requirements contained in this proposed rule may be submitted to NMFS, Northeast Regional Office and by e-mail to<E T="03">OIRA_Submission@omb.eop.gov,</E>or fax to 202-395-7285.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Aja Szumylo, Fishery Policy Analyst, 978-281-9195, fax 978-281-9135.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P/>
        <HD SOURCE="HD1">Background</HD>
        <P>The Council has considered a limited access program for the mackerel fishery on multiple occasions since 1992, with the most recent control date set as July 5, 2002 (67 FR 44792, later reaffirmed on June 9, 2005, 70 FR 33728). The Council initially notified the public of its intent to consider the impacts of alternatives for limiting access to the mackerel fishery in a Notice of Intent to Prepare a Supplemental Environmental Impact Statement (SEIS) for Amendment 9 to the MSB FMP (Amendment 9) on March 4, 2005 (70 FR 10605). The Council subsequently conducted scoping meetings in March 2005 on the development of a limited access program through Amendment 9. However, due to unforeseen delays in the development of Amendment 9, the Council notified the public on December 19, 2005 (70 FR 75114), that the mackerel limited access program would instead be analyzed in Amendment 11. The Council notified the public on February 27, 2007 (75 FR 8693), that it would begin the development of Amendment 11 in an SEIS, and finally notified the public on August 11, 2008 (73 FR 46590), that it would be necessary to prepare a full environmental impact statement (EIS) for Amendment 11. During further development of Amendment 11, the Council determined that the additional issues, namely updates to EFH designations and recreational allocations for the mackerel fishery, would also be considered.</P>
        <P>The Council conducted public hearings in February 2010 and was originally scheduled to take final action on Amendment 11 in April of 2010, but decided to revise certain alternatives after reviewing public comment. The revisions were deemed to require a Supplement to the Draft Environmental Impact Statement (SDEIS) and an additional comment period through October 12, 2010.</P>
        <P>This action proposes management measures that were recommended by the Council in Amendment 11. If implemented, these management measures would:</P>
        <P>• Implement a three-tiered limited access system, with vessels grouped based on the following landings thresholds, with all qualifiers required to have possessed a valid permit on March 21, 2007. A vessel must have landed at least 400,000 lb (181.44 mt) in any one year 1997-2005 to qualify for a Tier 1 permit; at least 100,000 lb (45.36 mt) in any one year March 1, 1994—December 31, 2005, to qualify for a Tier 2 permit; or at least 1,000 lb (0.45 mt) in any one year March 1, 1994—December 31, 2005, to qualify for a Tier 3 permit, with Tier 3 allocated up to 7 percent of the commercial quota, through the specifications process;</P>
        <P>• Establish an open access permit for all other vessels;</P>
        <P>• Establish trip limits for all tiers annually through the specifications process, with possession limits initially set as unlimited for Tier 1; 135,000 lb (61.23 mt) for Tier 2; 100,000 lb (45.36 mt) for Tier 3; and 20,000 lb (9.07 mt) for open access;</P>
        <P>• Establish permit application, permit appeal, vessel baseline, and vessel upgrade, replacement, and confirmation of permit history provisions similar to established for other Northeast region limited access fisheries;</P>
        <P>• Establish a 10-percent maximum volumetric fish hold upgrade for Tier 1 and Tier 2 vessels;</P>
        <P>• Allow vessel owners to retain mackerel fishing history in a purchase and sale agreement and use the history to qualify a different vessel for a mackerel permit (permit splitting);</P>
        <P>• Require Tier 3 vessels to submit VTRs on a weekly basis;</P>

        <P>• Designate as EFH the area associated with 90 percent of survey catch for each life stage of non-overfished species and the area associated with 95 percent of survey catch for each life stage of overfished or status unknown species (i.e., butterfish, mackerel,<E T="03">Loligo</E>squid, and<E T="03">Illex</E>squid); and</P>
        <P>• Establish an annual recreational mackerel allocation equaling 6.2 percent of the mackerel allowable biological catch.</P>

        <P>The Council took final action on October 13, 2010, and submitted Amendment 11 for NMFS review on May 12, 2011. A Notice of Availability (NOA) for Amendment 11, as submitted by the Council for review by the Secretary of Commerce, was published in the<E T="04">Federal Register</E>on July 6, 2011 (76 FR 39374). The comment period on Amendment 11 ends on September 6, 2011. In addition to the implementing measures proposed in this rule, Amendment 11 contains changes in the EFH designations for MSB species that are not reflected in the regulations.</P>
        <HD SOURCE="HD1">Proposed Measures</HD>
        <P>The proposed regulations are based on the measures in Amendment 11. NMFS has noted several instances where it has interpreted the language in Amendment 11 to account for any missing details in the Council's description of the proposed measures. In addition, some of the proposed regulations in Amendment 11 are associated with the Council's Omnibus Annual Catch Limit and Accountability Measures (ACL/AM) Amendment, for a proposed rule which published on June 17, 2011 (76 FR 35578). Several sections of regulatory text are affected by both actions. The proposed regulations for both actions will present adjustments to the existing regulatory text. In the likely event that the Omnibus ACL/AM Amendment is finalized prior to Amendment 11, the finalized regulations for Amendment 11 will be presented as modifications to the regulations that will be implemented in the Omnibus ACL/AM Amendment, and will thus differ in structure, but not content, from the regulations presented in this proposed rule. The adjustments will be similar to those in this proposed rule. NMFS seeks comments on all of the measures in Amendment 11.</P>
        <HD SOURCE="HD2">1. Limited Access Mackerel Permits and Trip Limits</HD>

        <P>Amendment 11 would implement a three-tiered limited access permit system for the mackerel fishery. Vessels that do not qualify for a limited access mackerel permit would still be able to<PRTPAGE P="45744"/>receive the open access mackerel permit described below. The initial trip limits proposed for each permit category below would be adjustable through the specifications process.</P>
        <P>In order to be eligible for a limited access mackerel permit, applicants would have to meet both a permit history requirement and a landings requirement. The permit history requirement and landings requirement must be derived from the same vessel (i.e., it is not possible to combine the permit criteria from Vessel A with the landings criteria from Vessel B to create a mackerel eligibility).</P>
        <P>To qualify for a Tier 1 Limited Access Mackerel permit, a vessel must have been issued a Federal mackerel permit that was valid on March 21, 2007, and must have landed at least 400,000 lb (181.44 mt) of mackerel in any one year between January 1, 1997, and December 31, 2005, as verified by NMFS records or documented through dealer receipts submitted by the applicant. The Tier 1 Limited Access Mackerel permit would allow such vessels to possess and land unlimited amounts of mackerel.</P>
        <P>To qualify for a Tier 2 Limited Access Mackerel permit, a vessel must have been issued a Federal mackerel permit that was valid on March 21, 2007, and must have landed at least 100,000 lb (45.36 mt) of mackerel in any one year between March 1, 1994, and December 31, 2005, as verified by NMFS records or documented through dealer receipts submitted by the applicant. The Tier 2 Limited Access Mackerel permit would allow such vessels to possess and land 135,000 lb (61.23 mt) of mackerel per trip.</P>
        <P>To qualify for a Tier 3 Limited Access Mackerel permit, a vessel must have been issued a Federal mackerel permit that was valid on March 21, 2007, and must have landed at least 1,000 lb (0.45 mt) of mackerel in any one year between March 1, 1994, and December 31, 2005, as verified by NMFS records or documented through dealer receipts submitted by the applicant. The Tier 3 Limited Access Mackerel permit would allow such vessels to possess and land 100,000 lb (45.36 mt) of mackerel per trip.</P>
        <P>The current regulations state that during a closure of the directed mackerel fishery that occurs prior to June 1, vessels issued a mackerel permit may not fish for, possess, or land more than 20,000 lb (9.08 mt) of mackerel per trip, and that during any closure that occurs after June 1, vessels may not fish for, possess, or land more than 50,000 lb (22.7 mt) of mackerel per trip. This provision would be maintained for limited access mackerel permit holders.</P>
        <HD SOURCE="HD2">2. Limited Access Vessel Permit Provisions</HD>
        <P>Amendment 11 would establish measures to govern future transactions related to limited access vessels, such as purchases, sales, or reconstruction. These measures would apply to all limited access mackerel vessels. Except as noted, the provisions proposed in this amendment are consistent with those that govern most of the other Northeast region limited access fisheries; there are some differences in the limited access program for American lobster.</P>
        <HD SOURCE="HD3">Initial Eligibility and Application</HD>
        <P>Initial eligibility for a mackerel limited access permit would have to be established during the first year after the implementation of Amendment 11. A vessel owner would required to submit an application for a mackerel limited access permit within 12 months of the effective date of the final regulations. In order to expedite the transition to the limited access mackerel program, NMFS would require applicants wishing to fish for mackerel with a limited access permit after January 1, 2012, to submit an application at least 30 days prior to the start of the 2012 fishing year (November 30, 2011). After January 1, 2012, current mackerel permit holders who have not yet submitted an application for a limited access mackerel permit, and individuals who have submitted incomplete or unsuccessful applications for a limited access mackerel permit, would automatically be re-designated as open access permit holders under the new mackerel permit system, and would be subject to the open access possession limit described in this proposed rule. All applicants would have until December 31, 2012, to submit an initial application.</P>
        <HD SOURCE="HD1">Initial Confirmation of Permit History (CPH) Application</HD>
        <P>A person who does not currently own a fishing vessel, but who has owned a qualifying vessel that has sunk, been destroyed, or transferred to another person, and the applicant has lawfully retained the valid mackerel permit and fishing history, would be required to apply for and receive a CPH. To be eligible to obtain a CPH, the applicant would have to show that the qualifying vessel meets the eligibility requirements for the limited access mackerel permit in question, and that all other permit restrictions described below are satisfied. If the vessel sank, was destroyed, or was transferred before March 21, 2007, the permit issuance criteria may be satisfied if the vessel was issued a valid Federal mackerel permit at any time between March 21, 2006, and March 21, 2007.</P>
        <P>Issuance of a valid CPH would preserve the eligibility of the applicant to apply for a limited access permit for a replacement vessel based on the qualifying vessel's fishing and permit history at a subsequent time. A CPH would have to be applied for in order for the applicant to preserve the limited access eligibility of the qualifying vessel. Vessel owners who were issued a CPH could obtain a vessel permit for a replacement vessel, consistent with the vessel size upgrade restrictions, based upon the vessel length, tonnage, and horsepower of the vessel on which the CPH issuance is based.</P>
        <P>The Amendment 11 document is unclear regarding application deadline for vessels applying to receive a CPH during the application period. The document states that applications for CPH would have to be submitted no later than 30 days prior to the end of the first full permit year in which a vessel permit cannot be issued. This would mean that, if the limited access program is effective on January 1, 2012, applicants applying directly into CPH would only have until March 31, 2012 (30 days before the end of the permit year) to apply for a CPH, while applicants applying for an active mackerel permit would have until December 31, 2012, to apply. NMFS clarifies that applicants wishing to place their limited access mackerel permit directly into CPH will be given the same initial application deadline as applicants applying for an active limited access mackerel permit, namely from January 1, 2012, to December 31, 2012.</P>
        <HD SOURCE="HD1">Landings History</HD>
        <P>NMFS will use dealer data in NMFS's database to determine eligibility. If NMFS data do not demonstrate that a vessel made landings of mackerel that satisfy the eligibility criteria for a limited access permit, applicants would have to submit dealer receipts that verify landings, or use other sources of information (e.g., joint venture receipts) to demonstrate that there is incorrect or missing information in the Federal dealer records via the appeals process described below.</P>

        <P>Amendment 11 does not specify a method for dividing qualifying landings between vessels that fished cooperatively for mackerel in pair trawl operations that wish to each use a subset of shared landings history to qualify individual vessels. NMFS proposes that owners of pair trawl vessels may divide the catch history<PRTPAGE P="45745"/>between the two vessels in the pair through third party verification and supplemental information, such as previously submitted VTRs, or dealer reporting. The two owners must apply for a limited access mackerel permit jointly and must submit proof that they have agreed to the division of landings. This approach was used to qualify pair trawl vessels in Amendment 1 to the Atlantic Herring FMP.</P>
        <HD SOURCE="HD1">Permit Transfers</HD>
        <P>An Atlantic mackerel limited access permit and fishing history would be presumed to transfer with a vessel at the time it is bought, sold, or otherwise transferred from one owner to another, unless it is retained through a written agreement signed by both parties in the vessel sale or transfer.</P>
        <HD SOURCE="HD1">Multiple Vessels With One Owner</HD>
        <P>The Council proposed a provision specific to multiple vessel ownership, qualification, and replacement. The provision states that, if an individual owns more than one vessel, but only one of those vessels has the permit and landings history required to be eligible for a limited access mackerel permit, the individual can replace the vessel that it determined to be eligible with one of his/her other vessels, provided that the replacement vessel complies with the upgrade restrictions detailed below. The proposed rule does not contain a regulation specific to the Council's proposed measure. Rather, the individual regulations pertaining to qualification, baselines, upgrades, and vessel replacements separately address the Council's proposed measure.</P>
        <P>This provision would not exempt owners of multiple vessels from the permit splitting provision, described below. For example, if a vessel owner has a limited access multispecies permit on the same vessel that created the mackerel eligibility, the entire suite of permits would need to be replaced onto the owner's other vessel in order to move the mackerel eligibility. In addition, if an individual owns two vessels, a 50-ft (15.2 m) vessel with a mackerel eligibility, and a 65-ft (19.8 m) vessel, he would not be able to move the mackerel eligibility onto the larger vessel, because it is outside of the vessel upgrade restrictions.</P>
        <HD SOURCE="HD1">Permit Splitting</HD>
        <P>Amendment 11 adopts the permit splitting provision currently in effect for other limited access fisheries in the region. Therefore, a limited access mackerel permit may not be issued to a vessel if the vessel's permit history was used to qualify another vessel for any other limited access permit. This means all limited access permits, including limited access mackerel permits, must be transferred as a package when a vessel is replaced or sold.</P>
        <P>However, Amendment 11 explicitly states that the permit-splitting provision would not apply to the retention of an open access mackerel permit and fishing history that occurred prior to April 3, 2009, if any limited access permits were issued to the subject vessel. Thus, vessel owners who sold a vessel with limited access permits and retained the open access mackerel permit and landings history prior to April 3, 2009, with the intention of qualifying a different vessel for a limited access mackerel permit, would be allowed to do so under Amendment 11. This differs from the current permit splitting provisions of other limited access fishery regulations, specifically the Atlantic herring limited access permit splitting provision implemented under Amendment 1 to the Atlantic Herring FMP. It is consistent with permit splitting provisions implemented for the scallop limited access general category permit program.</P>
        <HD SOURCE="HD1">Qualification Restriction</HD>
        <P>Consistent with previous limited access programs, no more than one vessel would be able to qualify, at any one time, for a limited access permit or CPH based on that or another vessel's fishing and permit history, unless more than one owner has independently established fishing and permit history on the vessel during the qualification period and has either retained the fishing and permit history, as specified above, or owns the vessel at the time of initial application under Amendment 11. If more than one vessel owner claimed eligibility for a limited access permit or CPH, based on a vessel's single fishing and permit history, the NMFS Regional Administrator would determine who is entitled to qualify for the permit or CPH based on information submitted and in compliance with the applicable permit provisions.</P>
        <HD SOURCE="HD1">Appeal of Permit Denial</HD>
        <P>Amendment 11 specifies an appeals process for applicants who have been denied a limited access Atlantic mackerel permit. Applicants would have two opportunities to appeal the denial of a limited access mackerel permit. The review of initial application denial appeals would be conducted under the authority of the Regional Administrator at NMFS's Northeast Regional Office. The review of second denial appeals would be conducted by a hearing officer appointed by the Regional Administrator, or through a National Appeals program, which is under development by NMFS and may be utilized for mackerel appeals.</P>
        <P>An appeal of the denial of an initial permit application (first level of appeal) must be made in writing to the NMFS Northeast Regional Administrator. Under this amendment, appeals would be based on the grounds that the information used by the Regional Administrator in denying the permit was incorrect. The only items subject to appeal under this limited access program would be the accuracy of the amount of landings, and the correct assignment of landings to a vessel and/or permit holder. Amendment 11 would require appeals to be submitted to the Regional Administrator, postmarked no later than 30 days after the denial of an initial limited access mackerel permit application. The appeal must be in writing, must state the specific grounds for the appeal, the limited access mackerel permit category for which the applicant believes he should qualify, and information to support the appeal. The appeal shall set forth the basis for the applicant's belief that the Regional Administrator's decision was made in error. The appeal would not be reviewed without submission of information in support of the appeal. The Regional Administrator would appoint a designee to make the initial decision on the appeal.</P>
        <P>Should the appeal be denied, the applicant would be allowed to request a review of the Regional Administrator's appeal decision (second level of appeal). Such a request must be in writing postmarked no later than 30 days after the appeal decision, must state the specific grounds for the appeal, and must include information to support the appeal. A hearing would not be conducted without submission of information in support of the appeal. If the request for review of the appeal decision is not made within 30 days, the appeal decision is the final administrative action of the Department of Commerce. If the National Appeals process is not fully established, the Regional Administrator will appoint a hearing officer. The hearing officer would make findings and a recommendation to the Regional Administrator, which would be advisory only. The Regional Administrator's decision is the final administrative action of the Department of Commerce.</P>

        <P>The owner of a vessel denied a limited access mackerel permit could fish for mackerel, provided that the denial has been appealed, the appeal was pending, and the vessel had on<PRTPAGE P="45746"/>board a letter from the Regional Administrator authorizing the vessel to fish under the limited access category for which the applicant has submitted the appeal. The Regional Administrator would issue such a letter for the pendency of any appeal. If the appeal is ultimately denied, the Regional Administrator would send a notice of final denial to the vessel owner; and the authorizing letter would become invalid 5 days after the receipt of the notice of denial.</P>
        <HD SOURCE="HD1">Establishing Vessel Baselines</HD>
        <P>A vessel's baseline refers to those specifications (length overall, gross registered tonnage (GRT), net tonnage (NT), and horsepower (HP)) from which any future vessel size change is measured. The vessel baseline specifications for vessels issued a limited access mackerel permits would be the specifications of the vessel that was initially issued the limited access permit as of the date that the vessel qualifies for such a permit. If a vessel owner is initially issued a CPH instead of a mackerel permit, the attributes of the vessel that is the basis of the CPH would establish the size baseline against which future vessel limitations would be evaluated. If the vessel that established the CPH is less than 20 ft (6.09 m) in length, then the baseline specifications associated with other limited access permits in the CPH suite will be used to establish the mackerel baseline specifications. If the vessel that established the CPH is less than 20 ft (6.09 m) in length, the limited access mackerel eligibility was established on another vessel, and there are no other limited access permits in the CPH suite, then the applicant must submit valid documentation of the baseline specifications of the vessel that established the eligibility. If a vessel owner applying for a CPH has a contract to purchase a vessel to replace the vessel for which CPH was issued prior to the submission of the mackerel limited access permit application (for the CPH), then the contracted vessel would form the baseline specifications for that vessel, provided an initial application for the contract vessel to replace the vessel for which the CPH was issued is received by December 31, 2012 (1 full year after the end of the proposed initial application period).</P>
        <HD SOURCE="HD1">Vessel Upgrades</HD>
        <P>A vessel could be upgraded in size, whether through retrofitting or replacement, and be eligible to retain or renew a limited access permit, only if the upgrade complies with the limitations in Amendment 11. The vessel's HP could be increased only once, whether through refitting or vessel replacement. Such an increase could not exceed 20 percent of the vessel's baseline specifications. The vessel's length, GRT, and NT could be increased only once, whether through refitting or vessel replacement. Any increase in any of these three specifications of vessel size could not exceed 10 percent of the vessel's baseline specifications. If any of these three specifications is increased, any increase in the other two must be performed at the same time. This type of upgrade could be done separately from an engine HP upgrade. Amendment 11 maintains the existing specification of maximum length, size and HP for vessels engaged in the Atlantic mackerel fishery (165 ft (50.02 m), 75 GRT (680.3 mt), and 3,000 HP). Tier 1 and Tier 2 vessels must also comply with the upgrade restrictions relevant to the vessel hold volume certification described below.</P>
        <HD SOURCE="HD1">Vessel Hold Capacity Certification</HD>
        <P>In addition to the standard baseline specifications, Tier 1 and Tier 2 vessels would be required to obtain a fish hold capacity measurement from a certified marine surveyor. The hold capacity measurement submitted at the time of application for a Tier 1 or Tier 2 limited access mackerel permit would serve as an additional permit baseline for these permit categories. The hold volume for at Tier 1 or Tier 2 permit could only be increased once, whether through refitting or vessel replacement. Any increase could not exceed 10 percent of the vessel's baseline hold measurement. This type of upgrade could be done separately from the size and HP upgrades.</P>
        <P>Amendment 11 does not specify how a hold capacity baseline should be established for vessels whose permits go directly into CPH. In cases where the qualifying vessel has sunk or been destroyed, it will not be feasible for the applicant to obtain a hold capacity certification. NMFS proposes that the hold capacity baseline for such vessels will be the hold capacity of the first replacement vessel after the permits are removed from CPH.</P>
        <HD SOURCE="HD1">Vessel Replacements</HD>
        <P>The term “vessel replacement,” in general, refers to replacing an existing limited access vessel with another vessel. In addition to addressing increases in vessel size, hold capacity, and HP, Amendment 11 would establish a restriction that requires that the same entity must own both the limited access vessel (permit and fishing history) that is being replaced, and the replacement vessel.</P>
        <HD SOURCE="HD1">Voluntary Relinquishment of Eligibility</HD>
        <P>Amendment 11 includes a provision to allow a vessel owner to voluntarily exit a limited access fishery. Such relinquishment would be permanent. In some circumstances, it could allow vessel owners to choose between different permits with different restrictions without being bound by the more restrictive requirement (e.g., lobster permits holders may choose to relinquish their other Northeast Region limited access permits to avoid being subject to the reporting requirements associated with those other permits). If a vessel's limited access permit history for the mackerel fishery is voluntarily relinquished to the Regional Administrator, no limited access permit for that fishery may be reissued or renewed based on that vessel's history.</P>
        <HD SOURCE="HD1">Permit Renewals and CPH Issuance</HD>
        <P>Amendment 11 specifies that a vessel owner must maintain the limited access permit status for an eligible vessel by renewing the permits on an annual basis or applying for the issuance of a CPH. A CPH is issued to a person who does not currently own a particular fishing vessel, but who has legally retained the fishing and permit history of the vessel for the purposes of transferring it to a replacement vessel at a future date. The CPH provides a benefit to a vessel owner by securing limited access eligibility through a registration system when the individual does not currently own a vessel.</P>
        <P>A vessel's limited access permit history would be cancelled due to the failure to renew, in which case, no limited access permit could ever be reissued or renewed based on the vessel's history or to any other vessel relying on that vessel's history. All limited access permits must be issued on an annual basis by the last day of the fishing year for which the permit is required, unless a CPH has been issued. A complete application for such permits must be received no later than 30 days before the last day of the permit year.</P>
        <HD SOURCE="HD2">3. Tier 3 Allocation and Additional Reporting Requirements</HD>

        <P>Amendment 11 proposes an allocation for participants in the limited access mackerel fishery that hold a Tier 3 permit. Tier 3 would be allocated a maximum catch of up to 7 percent of the commercial mackerel quota (the remainder of the commercial mackerel quota would be available to Tier 1 or Tier 2 vessels). The Tier 3 allocation would be set annually during the<PRTPAGE P="45747"/>specifications process. NMFS presumes that, during a closure of the Tier 3 mackerel fishery that occurs prior to June 1, vessels issued a mackerel permit may not fish for, possess, or land more than 20,000 lb (9.08 mt) of mackerel per trip, and that during a closure that occurs after June 1, vessels may not fish for, possess, or land more than 50,000 lb (22.7 mt) of mackerel per trip. In order to monitor Tier 3 landings, Amendment 11 would require vessels that hold a Tier 3 limited access mackerel permit to submit vessel trip reports (VTRs) on a weekly basis.</P>
        <HD SOURCE="HD2">4. Open Access Permit and Possession Limit</HD>
        <P>Any vessel could be issued an open access mackerel permit that would authorize the possession and landing of up to 20,000 lb (9.07 mt) of mackerel per trip. The open access possession limit would stay the same during a closure of the directed mackerel fishery.</P>
        <HD SOURCE="HD2">5. Updates to EFH Definitions</HD>

        <P>Section 600.815(a)(9) of the final rule to revise the regulations implementing the EFH provisions of the Magnuson-Stevens Act requires a complete review of EFH information at least once every 5 years. With the exception of the establishment of<E T="03">Loligo</E>egg EFH in Amendment 9 to the MSB FMP in 2008, the EFH information for MSB fisheries has not been updated since the original analysis and designations were done for Amendment 8 to the MSB FMP (Amendment 8) in 1998. Amendment 11 would revise the EFH text descriptions for all MSB species based on updated data from the Northeast Fishery Science Center (NEFSC) trawl survey, the Marine Resources Monitoring Assessment and Prediction Program (MARMAP), state bottom trawl surveys, NOAA's Estuarine Living Marine Resources (ELMR) program, and scientific literature on habitat requirements. Amendment 11 would designate as EFH the area associated with 90 percent of the cumulative geometric mean catches for non-overfished species, and the area associated with 95 percent of the cumulative geometric mean catches for unknown or overfished species. All MSB species currently fall in the latter category. Text descriptions and maps for the new proposed EFH designation can be found in Amendment 11.</P>
        <HD SOURCE="HD2">6. Recreational Mackerel Allocation</HD>
        <P>Amendment 11 proposes an allocation to the recreational fishery in order to incorporate recreational mackerel ACLs/AMs into the framework for the Council's Omnibus ACL/AM Amendment. The recreational allocation would be set equal to 6.2 percent of the domestic mackerel allowable biological catch (ABC). This allocation corresponds to the proportion of total U.S. mackerel landings that was accounted for by the recreational fishery from 1997-2007 times 1.5. The Council would be able to take action via specifications, a framework adjustment, or amendment to adjust any disconnect between the recreational allocation and future recreational harvests.</P>
        <HD SOURCE="HD1">Classification</HD>
        <P>Pursuant to section 304(b)(1)(A) of the Magnuson-Stevens Act, the NMFS Assistant Administrator has determined that this proposed rule is consistent with the MSB FMP, other provisions of the Magnuson-Stevens Act, and other applicable law, subject to further consideration after public comment.</P>
        <P>This proposed rule has been determined to be not significant for purposes of Executive Order 12866.</P>
        <P>This proposed rule contains collection-of-information requirements subject to review and approval by the Office of Management and Budget (OMB) under the Paperwork Reduction Act (PRA). Several of these requirements have been submitted to OMB for approval under the MSB Amendment 10 Family of Forms (OMB Control No. 0648-0601). Under the proposed limited access program, vessel owners would be required to submit to NMFS application materials to demonstrate their eligibility for a limited access permit. The public burden for the application requirement pertaining to the limited access program is estimated to average 45 min per application, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing the collection information.</P>
        <P>Only 410 vessels are expected to qualify and consequently renew their limited access mackerel permits via the renewal application each year. The renewal application is estimated to take 30 min on average to complete. Up to 30 applicants are expected to appeal the denial of their permit application. The appeals process is estimated to take an average of 2 hr to complete. Vessels that qualify for a Tier 1 or Tier 2 mackerel permit would be required to submit documentation of hold volume size. The Council estimated that 74 vessels would qualify for either a Tier 1 or Tier 2 limited access mackerel permit. Tier 1 and 2 vessel owners will experience a time burden due to this requirement in the form of travel time to/from a certified marine surveyor. It is not possible to estimate a time burden associated with obtaining a hold volume measurement, as vessels would have to travel varying distances to visit certified marine surveyors. Travel time to a marine surveyor is not an information collection burden, so is not considered a response.</P>
        <P>Completion of a replacement or upgrade application requires an estimated 3 hr per response. It is estimated that no more than 40 of 410 vessels possessing these permits will request a vessel replacement or upgrade annually. Completion of a CPH application requires an estimated 30 min per response. It is estimated that no more than 30 of the 410 vessels possessing these limited access permits will request a CPH annually.</P>
        <P>The proposed rule also modifies the VTR requirement for Tier 3 mackerel vessel. All mackerel vessels are currently required to submit VTRs on a monthly basis; this requirement is currently approved under the Northeast Region Logbook Family of Forms (OMB Control No. 0648-0212). This proposed rule would require vessels issued a Tier 3 mackerel permit to submit VTRs on a weekly basis. A change request for this requirement has been submitted to OMB for approval. The public burden for the revised VTR requirement is expected to average 5 min for each additional VTR submission.</P>

        <P>Public comment is sought regarding: Whether this proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; the accuracy of the burden estimate; ways to enhance the quality, utility, and clarity of the information to be collected; and ways to minimize the burden of the collection of information, including through the use of automated collection techniques or other forms of information technology. Send comments on these or any other aspects of the collection of information to the Regional Administrator (see<E T="02">ADDRESSES</E>), and email to<E T="03">OIRA_Submission@omb.eop.gov</E>or fax to 202-395-7285.</P>
        <P>Notwithstanding any other provision of the law, no person is required to respond to, and no person shall be subject to penalty for failure to comply with, a collection of information subject to the requirements of the PRA, unless that collection of information displays a currently valid OMB Control Number.</P>

        <P>The Council prepared an IRFA, as required by section 603 of the Regulatory Flexibility Act (RFA). The IRFA describes the economic impact this proposed rule, if adopted, would<PRTPAGE P="45748"/>have on small entities. A description of the action, why it is being considered, and the legal basis for this action are contained at the beginning of this section in the preamble and in the<E T="02">SUMMARY</E>. A summary of the analysis follows. A copy of this analysis is available from the Council or NMFS (see<E T="02">ADDRESSES</E>) or via the Internet at<E T="03">http://www.nero.noaa.gov.</E>
        </P>
        <HD SOURCE="HD2">Description and Estimate of Number of Small Entities to Which the Rule Will Apply</HD>
        <P>The proposed measures in Amendment 11 would primarily affect participants in the mackerel fishery. All of the potentially affected businesses are considered small entities under the standards described in NMFS guidelines, because they have gross receipts that do not exceed $4 million annually. There were 2,331 vessels issued open access mackerel permits in 2010. The Small Business Administration (SBA) size standard for commercial fishing (NAICS code 114111) is $4 million in sales. Available data indicate that no single fishing entity earned more than $4 million annually. Although there are likely to be entities that, based on rules of affiliation, would qualify as large business entities, due to lack of reliable ownership affiliation data NMFS cannot apply the business size standard at this time. Data are currently being compiled on vessel ownership that should permit a more refined assessment and determination of the number of large and small entities in the mackerel fishery for future actions. For this action, since available data are not adequate to identify affiliated vessels, each operating unit is considered a small entity for purposes of the RFA, and, therefore, there is no differential impact between small and large entities. Therefore, there are no disproportionate economic impacts on small entities. Section 6.5 in Amendment 11 describes the vessels, key ports, and revenue information for the mackerel fishery, therefore, that information is not repeated here.</P>
        <HD SOURCE="HD2">Description of Projected Reporting, Recordkeeping, and Other Compliance Requirements Minimizing Significant Economic Impacts on Small Entities</HD>
        <P>There will be an estimated 820 applications for a limited access mackerel permit. With an average processing time of 45 min, the total time burden for this application is 615 hr. Only 410 vessels are expected to qualify and consequently renew their permit via the renewal application each year. The renewal application is estimated to take 30 min on average to process, for a burden of 205 hr. Up to 30 applicants are expected to appeal the denial of their permit application (other FMPs estimated between 5-7 percent of applications would move on to the appeal stage). The appeals process is estimated to take 2 hr to complete, on average, with a total burden of 60 hr. The 3-yr average total public cost burden for permit applications, appeals, and renewals is $261, which includes postage and copy fees for submissions.</P>
        <P>Each hold volume measurement done by a certified marine surveyor is estimated to cost $4,000. An estimated 74 vessels would qualify for either a Tier 1 or Tier 2 limited access mackerel permit, and would be required to submit a hold volume measurement at the time of permit issuance. Roughly 40 vessels are expected to upgrade or replace vessels each year, and would be required to submit a hold volume measurement for the upgraded or replacement vessel. Therefore, annual average cost over a 3-yr period is estimated to be $258,667 ($98,667 for annualized initial hold volume certifications, plus $160,000 for replacement hold volume certifications), not including travel expenses.</P>
        <P>New limited access mackerel vessels would be subject to the same replacement, upgrade, and permit history restrictions as other limited access vessels. Completion of a replacement or upgrade application requires an estimated 3 hr per response. It is estimated that no more than 40 of the 410 vessels possessing these limited access permits will request a vessel replacement or upgrade annually. This resultant burden would be up to 120 hr. Completion of a CPH application requires an estimated 30 min per response. It is estimated that owners of no more than 30 of the 410 vessels possessing a limited access mackerel permit will request a CPH annually. The resultant burden would be up to 15 hr. The total public cost burden for replacement, upgrade, and CPH applications is $140 for postage and copy fees.</P>
        <P>An estimated 329 Tier 3 limited access mackerel vessels would be required to submit VTRs on a weekly basis. Completion of a VTR is estimated to take 5 min per submission. The resultant burden would be 1,151.5 hr. The total public cost burden for VTR submission is $5,790.40 for postage.</P>
        <HD SOURCE="HD2">Economic Impacts of the Proposed Action Compared to Significant Non-Selected Alternatives</HD>
        <HD SOURCE="HD3">Tiered Limited Access Program</HD>
        <P>The FEIS estimates the numbers of vessel that would qualify for limited access permits under the different alternatives. In addition to the no action alternative and preferred alternative, six additional alternatives for tiered limited access programs, and two alternatives that would qualify participants in the Atlantic herring fishery for limited access mackerel permits. Information from the dealer weighout database was used to estimate how many vessels would qualify under each of the proposed limited access alternatives. The economic impacts of these alternatives on both individual vessels and the overall capacity of mackerel fleet is described in sections 5.1.4 and 7.5 of the FEIS and are summarized below.</P>
        <P>The composition of the qualifying group that results under each of the tiered limited access programs described in this segment changes based on each alternative. In most instances, the quota allocation and trip limit alternatives described below are averages or percentages based on the composition of the qualifying group. Accordingly, the Tier allocation and trip limit alternative sets described below are different for each of the tiered limited access program alternatives.</P>
        <P>Under the preferred alternative, 29 vessels would qualify for a Tier 1 permit, 45 vessels would qualify for a Tier 2 permit, and 329 vessels would qualify for a Tier 3 permit, resulting in a total of 403 vessels that would qualify for the various limited access mackerel permits. The preferred alternative would cap Tier 3 with a maximum allocation of up to 7 percent of the commercial mackerel quota, with no other additional allocations for any other Tiers. The economic impacts of the Tier allocations will be discussed separately from the structure of the limited access program.</P>

        <P>The eligibility criteria for a Tier 1 permit in Alternative 1B would have required a vessel to possess a mackerel permit and have landed at least 1,000,000 lb (453.6 mt) in any one year between January 1, 1997, and December 31, 2007. To qualify for a Tier 2 permit, a vessel would have been required to possess a permit and have landed at least 100,000 lb (45.36 mt) between January 1, 1988, and December 31, 2007. To qualify for a Tier 3 permit, a vessel would have been required to possess a permit and have landed at least 25,000 lb (11.34 mt) between January 1, 1988,<PRTPAGE P="45749"/>and December 31, 2007. Under Alternative 1B, 26 vessels would qualify for a Tier 1 permit, 64 vessels would qualify for a Tier 2 permit, and 56 vessels would qualify for a Tier 3 permit, resulting in a total of 146 vessels that would qualify for the various limited access mackerel permits.</P>
        <P>The eligibility criteria for a Tier 1 permit in Alternative 1C would have required a vessel to possess a mackerel permit and have landed at least 1,000,000 lb (453.6 mt) in any one year between January 1, 1997, and December 31, 2007. To qualify for a Tier 2 permit, a vessel would have been required to possess a permit and have landed at least 100,000 lb (45.36 mt) between January 1, 1997, and December 31, 2007. To qualify for a Tier 3 permit, a vessel would have been required to possess a permit and have landed at least 1,000 lb (.45 mt) between January 1, 1997, and December 31, 2007. As with the preferred alternative, 1C would have capped Tier 3 with a maximum allocation of up to 7 percent of the commercial mackerel quota, with no other additional allocations for any other Tiers. Under Alternative 1C, 26 vessels would qualify for a Tier 1 permit, 36 vessels would qualify for a Tier 2 permit, and 309 vessels would qualify for a Tier 3 permit, resulting in a total of 371 vessels that would qualify for the various limited access mackerel permits.</P>
        <P>The eligibility criteria for a Tier 1 permit in Alternative 1E would have required a vessel to possess a mackerel permit and have landed at least 400,000 lb (181.44 mt) of mackerel in any one year between January 1, 1997, and December 31, 2005. To qualify for a Tier 2 permit, a vessel would have been required to possess a permit and have landed at least 100,000 lb (45.36 mt) of mackerel in any one year between January 1, 1997, and December 31, 2005. To qualify for a Tier 3 permit, a vessel would have been required to possess a permit and have landed at least 25,000 lb (11.34 mt) of mackerel in any one year between January 1, 1997, and December 31, 2007. Under Alternative 1E, 29 vessels would qualify for a Tier 1 permit, 25 vessels would qualify for a Tier 2 permit, and 50 vessels would qualify for a Tier 3 permit, resulting in a total of 104 vessels that would qualify for the various limited access mackerel permits.</P>
        <P>The eligibility criteria for a Tier 1 permit in Alternative 1F would have required a vessel to possess a mackerel permit and have landed at least 1,000,000 lb (453.6 mt) in any one year between January 1, 1997, and December 31, 2007. To qualify for a Tier 2 permit, a vessel would have been required to possess a permit and have landed at least 100,000 lb (45.36 mt) between January 1, 1988, and December 31, 2007. To qualify for a Tier 3 permit, a vessel would have been required to possess a permit and have landed at least 10,000 lb (4.5 mt) between January 1, 1988, and December 31, 2007. Under Alternative 1F, 26 vessels would qualify for a Tier 1 permit, 64 vessels would qualify for a Tier 2 permit, and 121 vessels would qualify for a Tier 3 permit, resulting in a total of 211 vessels that would qualify for the various limited access mackerel permits.</P>
        <P>Alternative 1G would implement a single-tiered limited access program for which 26 vessels would qualify. The eligibility criteria for a limited access permit would have required a vessel to possess a mackerel permit and have landed at least 1,000,000 lb (453.6 mt) in any one year between January 1, 1997, and December 31, 2007.</P>
        <P>The eligibility criteria for a Tier 1 permit in Alternative 1J would have required a vessel to possess a mackerel permit and have landed at least 1,000,000 lb (453.6 mt) of mackerel in any one year between January 1, 1997, and December 31, 2007. To qualify for a Tier 2 permit, a vessel would have been required to possess a permit and have landed at least 100,000 lb (45.36 mt) of mackerel in any one year between March 1, 1994, and December 31, 2007. To qualify for a Tier 3 permit, a vessel would have been required to possess a permit and have landed at least 25,000 lb (11.34 mt) of mackerel in any one year between March 1, 1994, and December 31, 2007. Under Alternative 1J, 26 vessels would qualify for a Tier 1 permit, 55 vessels would qualify for a Tier 2 permit, and 49 vessels would qualify for a Tier 3 permit, resulting in a total of 130 vessels that would qualify for the various limited access mackerel permits.</P>
        <P>The number of individual qualifiers resulting from these management alternatives primarily varies based on the start date and end date of the qualifying landings period, and the required landings threshold for each Tier. A comparison of Alternatives 1B and 1C illustrates the effects of different start dates on numbers of qualifiers. Alternative 1C, which has a 1997 start date, results in 42 fewer qualifying vessels (29 fewer vessels in Tier 2, 13 fewer in Tier 3) than Alternative 1B, which has a 1988 start date. While the later start dates result in fewer qualifiers in Tiers 2 and 3, the economic impacts on these individual vessels should not be significant when compared to their recent level of participation in the fishery. Vessels are still placed in a Tier based on their participation in the fishery since 1997, and analysis in Amendment 11 shows that lower Tiers generally derive a small percentage of their revenue (less than 2 percent for all alternatives) from mackerel.</P>
        <P>Vessels that had sizable landings in 2006 or 2007 would be most impacted by the use of a 2005 qualifying landings period end date; this can be illustrated by comparing Alternative 1C (2007) and 1E (2005). With the 2007 end date in 1C, there would be 26 Tier 1 vessels and 35 Tier 2 vessels. If the end date is switched to 2005, as in 1E, three Tier 1 vessels and six Tier 2 vessels fall into lower Tiers. These vessels fell into lower Tiers because their best years of participation were more recent. Depending on the trip limits selected for the lower Tiers, these vessels may be negatively impacted by the earlier end date because they would be constrained compared to their recent participation in the mackerel fishery.</P>
        <P>The FEIS presents an estimate of the maximum feasible annual capacity for the Tier 1 and Tier 2 vessels projected to qualify in each of proposed alternatives; this estimate indicates the maximum amount of mackerel the fleet could land under the various management alternatives in a single year. Only Tier 1 and Tier 2 were included in the analysis because, with the exception of Alternative 1G, the other tiers in the presented alternatives will be constrained by trip limits or tier allocations. The highest capacity estimates are associated with the no action alternative and Alternative 1G (202,111 mt). The capacity for the open access vessels is included in the estimate for Alternative 1G because of the relatively high open access trip limit alternatives associated with 1G (20,000-121,000 mt). Alternative 1E restricts capacity the most, and results in a 49-percent reduction in capacity compared to the no action alternative. The least restrictive alternatives (1B and 1F) result in a 35-percent capacity reduction. The preferred alternative (1D) is the second most restrictive, and results in a 47-percent capacity reduction compared to no action. Alternatives with lower capacity, such as the preferred alternative, could provide greater long-term economic benefits to the qualifying fleet if reduced capacity contributes to the continued health of the mackerel resource.</P>

        <P>Alternative 1H and 1I would grant Tier 3 permits to limited access Atlantic herring vessels that would not otherwise qualify for a limited access mackerel permit. Alternative 1H would award a Tier 3 permit to vessels with Category<PRTPAGE P="45750"/>A or B herring permits, and Alternative 1I would award Tier 3 permits to vessels with Category A, B, or C herring permits. Individual vessels are known to target both mackerel and Atlantic herring on the same trip. This provision would prevent forced regulatory discards of incidentally captured mackerel on trips primarily targeting Atlantic herring, and would be expected to result in positive economic benefits for the Atlantic herring fleet. The Council ultimately did not select this alternative because it concluded that the preferred open access mackerel possession limit (20,000 lb (9.07 mt) per trip) would be sufficient to prevent regulatory discards. This alternative was not expected to have a large economic impact on the overall mackerel fishery, as this small number of vessels would be granted access to Tier 3, which would be limited by low trip limits or a Tier allocation.</P>
        <HD SOURCE="HD3">Quota Allocation for Limited Access Tiers</HD>
        <P>The FEIS describes four alternatives for allocating the commercial mackerel quota between the limited access Tiers. These alternatives were proposed as another mechanism to ensure that each Tier in the limited access program maintained their historical level of participation in the mackerel fishery in the future. The action alternatives would create a shared allocation for Tier 1, Tier 3, and the open access vessels, but allocate Tier 2 the percentage of total landings that Tier 2 landed from 1997-2007 (2B), double the Tier 2 percentage from 1997-2007 (2C), or triple the Tier 2 percentage from 1997-2007 (2D). Alternatives 2C and 2D feature a provision that, if less than half of Tier 2's allocation has been harvested on April 1, would transfer half of the remaining allocation to the Tier 1/Tier 3/open access allocation.</P>
        <P>Based on public comment after the Draft Environmental Impact Statement (DEIS) was published, the Council modified alternatives 1C and 1D (preferred) to provide accommodations for smaller, historical participants in the mackerel fishery. These alternatives would result in more Tier 3 qualifiers, and would initially award Tier 3 a fairly high trip limit in order to allow the qualifiers occasional sizeable landings of mackerel. However, these alternatives would also cap Tier 3 at a maximum of 7 percent of the commercial quota, with no additional allocations for any other Tiers. Given the selection of Alternative 1D as preferred, the Council ultimately recommended the no action alternative regarding allocations for Tier 2.</P>
        <P>All three action alternatives base the Tier 2 quota on a minimum of 100 percent of their collective landings from 1997-2007. When combined with the tiered limited access alternatives described above, the resulting Tier 2 allocations would range from 3.5 to 3.8 percent of the annual commercial mackerel quota for Alternative 2B; 7.0 to 7.7 percent of the quota for 2C; and 10.5 to 11.5 percent of the quota for 2D. Given the lower 2011 mackerel quotas, these allocations may constrain landings for all Tiers. The quota transfer provisions in 2C and 2D could benefit Tier 1 in that they would help avoid a situation where Tier 1 is closed, but Tier 2 is left open with a significant portion of its allocation unused.</P>
        <P>The no action alternative (preferred), which also includes a cap on Tier 3 under preferred Alternative 1D, should not have substantial economic impact on most fishery participants. While Tier 3 would include an estimated 329 vessels with a relatively high trip limit, the Tier would be capped at a maximum of 7 percent of the commercial fishery allocation, so it should not affect the directed fishery. The economic impact of the Tier 2 allocations depends on Tier activity. If fishing opportunities expand for Tier 2, the no action alternative could allow Tier 2 participants to increase their activity, which could negatively impact other Tiers also attempting to access quota. On the other hand, the no action alternative could have negative impacts on Tier 2 if Tier 1 is very active in a given year and accesses a significant amount of the quota before Tier 2 vessels are able to given Tier 1's higher capacity.</P>
        <HD SOURCE="HD3">Limited Access Trip Limits</HD>
        <P>Amendment 11 includes five trip limit alternatives in addition to the no action and preferred alternative. The trip limits analyzed in the FEIS are intended to restrict vessels to a range of landings that are characteristic of trips by vessels within a Tier. Under all alternatives, Tier 1 is not constrained by a trip limit, and all other trip limits would be established annually through specifications. The preferred alternative (3F) would initially set the trip limits at 135,000 lb (61.24 mt) for Tier 2; 100,000 lb (45.36 mt) for Tier 3; and 20,000 lb (9.07 mt) for open access. Alternatives 3B, 3C, and 3D would initially set the trip limits for Tier 2, Tier 3, and open access vessels such that 99 percent, 98 percent, and 95 percent of the trips in each would not have been affected, respectively. This would result in initial trip limits ranging from 39,000-553,000 lb (14.6-206.4 mt) for Tier 2; 4,000-100,000 lb (1.5-37.3 mt) for Tier 3; and 1,000-20,000 lb (0.4-7.5 mt) for open access, depending on the selected limited access program. Alternative 3E initially exempts Tier 2 from a trip limit, and sets all other trip limits in the range described in Alternatives 3B-3D. Alternative 3G was designed to be selected with Alternative 1G (single-tiered alternative), and would initially set the open access trip limit in range calculated for Tier 2 with Alternatives 3B-3D under Alternative 1B (61,000-121,000 lb; 22.8-45.2 mt).</P>
        <P>The alternatives analyzed in the FEIS where designed to establish a trip limits that would be higher than historical landings for a majority of the fleet. Accordingly, none of the proposed trip limits are expected to have a negative economic impact on most of the mackerel fleet. In addition, the Tiers with trip limits typically derive a small percentage of their revenue from mackerel (less than 2 percent), so the trip limits are not expected to limit the contribution of mackerel to these vessels' annual revenue. In the event that mackerel availability increases in the future, the trip limits will benefit all mackerel fishery participants in that they will keep vessels in one Tier from significantly expanding effort to the point that their activity is characteristic of a higher Tier; put another way, trip limits could reduce additional capitalization, which could have long-term economic benefits if lower fishery capacity helps sustain the mackerel resource.</P>
        <HD SOURCE="HD3">Limited Access Permit Provisions</HD>

        <P>Amendment 11 includes most of the provisions adopted in other limited access fisheries in the Northeast Region to govern the initial qualification process, future ownership changes, and vessel replacements. For the most part, there is no direct economic impact. The nature of a limited access program requires rules for governing the transfer of limited access fishing permits. The procedures have been relatively standard for previous limited access programs, which makes it easier for a vessel owner issued permits for several limited access fisheries to undertake vessel transactions. The standard provisions adopted in Amendment 11 are those governing change in ownership; replacement vessels; CPH; abandonment or voluntary relinquishment of permits; and appeal and denial of permits. This action would also allow a vessel owner to retain an open access mackerel fishing history prior to the implementation of Amendment 11 to be eligible for issuance of a mackerel permit based on the eligibility of the vessel that was<PRTPAGE P="45751"/>sold, even if the vessel was sold with other limited access permits.</P>
        <P>The economic impacts of the limited access permit provisions are analyzed in section 7.5.4 of the Amendment 11 document. The preferred alternative that requires hold volume measurements for Tier 1 and Tier 2 vessels would cost qualifiers for these permits an estimated $4,000 per vessel, not including travel expenses, and would prevent such vessels from increasing hold volume by more than 10 percent through refitting or replacement. This provision, and other provisions that restrict vessel upgrades, may constrain future business opportunities for vessels with immediate plans for vessel refitting or replacement. However, these restrictions may have long-term benefits to fishery participants by limiting capitalization in the mackerel fishery. The proposed regulations regarding qualification with retained vessel histories may have positive economic impacts for participants that sold their vessel but retained their mackerel fishing history. However, this provision could result in more vessels qualifying for mackerel permits, which may result in increased fishery capitalization. This could have a negative impact on the mackerel fleet if any additional capitalization impacts the sustained health of the mackerel resource. The preferred alternative requiring weekly VTR submissions from Tier 3 vessels is expected to cost qualifiers an additional $5,790.40 annually for postage.</P>
        <HD SOURCE="HD3">EFH Updates</HD>
        <P>EFH designations identify the geographic domain within which fishery management measures that would minimize the adverse impacts of fishing and non-fishing activities could be implemented. The no action alternative would maintain the current text and map designations for EFH for all MSB species and life stages. The preferred alternative would designate as EFH the area associated with 90 percent of the cumulative geometric mean catches for non-overfished species, and the area associated with 95 percent of the cumulative geometric mean catches for unknown or overfished species. The three non-preferred alternatives vary slightly from the preferred, and include: (1) 75 percent area for non-overfished species, 90 percent for unknown or overfished species; (2) 95 percent area for non-overfished species, 100 percent for unknown or overfished species; and (3) 100 percent for all species.</P>
        <P>With the exception of egg life stage for<E T="03">Loligo,</E>all of the MSB species are pelagic and have life stages that inhabit the water column. Because the fishing gears that have the potential to adversely impact EFH are bottom-tending, the EFH for MSB species is not vulnerable to fishing impacts. None of the EFH alternatives analyzed in Amendment 11 would result in regulations affecting fishing activity. Accordingly, none of analyzed alternatives are expected to have negative economic impact on the fishing industry. Overall, the preferred alternative would allow for more effective consultations on oversight of EFH when compared to current EFH definitions, which could have positive impacts on the MSB resource.</P>
        <HD SOURCE="HD3">Recreational Mackerel Allocation</HD>
        <P>The commercial fishery currently closes when it reaches 90 percent of the total mackerel quota (commercial plus recreational). It is assumed that recreational fishery will harvest 15,000 mt of the commercial quota each year, regardless of the total commercial quota, but there is no hard allocation for the recreational fishery. The no action alternative would maintain the assumption that the recreational mackerel fishery could harvest 15,000 mt of the commercial quota. If the mackerel fishery is closed at 90 percent of the commercial quota, and the recreational fishery was actually able to harvest the assumed 15,000 mt, the mackerel quota would be exceeded. For example, the commercial mackerel quota for the 2011 fishing year is 46,779 mt. If the commercial mackerel fishery is closed when 90 percent of this quota is attained (42,101 mt), and the recreational mackerel fishery has harvested the assumed 15,000 mt, then the mackerel quota would be exceeded by 22 percent (42,101 mt + 15,000 mt = 57,101 mt). Mackerel quota overages can compromise the sustainability of the resource, resulting in negative long-term economic impacts on the fishery.</P>
        <P>The preferred alternative would designate an allocation for the recreational mackerel fishery that corresponds to the proportion of total U.S. landings that were accounted for by the recreational fishery from 1997-2007 times 1.5 (6.2 percent of total U.S. mackerel landings). Other alternatives include an allocation equal to the proportion of U.S. landings accounted for by the recreational mackerel fishery during this period (4.1 percent), and two times the proportion from this period (8.2 percent).</P>
        <P>The proposed allocation is unlikely to constrain the current operations of the recreational mackerel fishery. Recreational landings from 2000-2009 ranged from 530-1,633 mt, with average recreational landings of 774 mt from 2007-2009. Under the preferred alternative, the recreational sector would have received an allocation of 2,900 mt in 2011 (6.2 percent of 46,779 mt). Given recent reduced mackerel quotas, the proposed recreational mackerel allocation could constrain the commercial mackerel fishery compared to the no action alternative. However, the constraint on the commercial fishery is more related to the overall quota than to any of the potential recreational allocations considered in Amendment 11.</P>
        <HD SOURCE="HD3">At-Sea Processing</HD>
        <P>Finally, Amendment 11 considered the establishment of a cap for at-sea processing via transfers for the mackerel fishery. The action alternatives included caps on at-sea processing initially set equal to 7 percent, 14 percent, 21 percent, 50 percent, or 75 percent of the mackerel initial optimum yield (IOY), with the cap set annually through specifications. Though there has not been at-sea processing for mackerel by mother ship-type processors since the foreign fishery ended in the early 1990s, the Council developed this set of alternatives in response to public comment about the potential impacts if large-scale at-sea processing of mackerel were to commence in the future. In particular, commenters noted that, if there were significant amounts of at-sea mackerel processing, the disruption of the supply of mackerel to land-based processors could have negative economic impacts on fishing communities.</P>
        <P>There is little information available about the possible impacts of at-sea processing in the mackerel fishery. Under the proposed no action alternative, if at-sea processing were to become significant for mackerel, an unlimited portion of the mackerel market share could be transferred to at-sea processors. Land-based mackerel processors, and the shoreside communities in which they reside, would be impacted to the extent that mackerel processing shifts to the at-sea operations. Limiting at-sea processing (action alternatives) could have economic benefits by ensuring a portion of the mackerel supply would still be available to land-based mackerel processors.</P>
        <LSTSUB>
          <HD SOURCE="HED">List of Subjects in 50 CFR Part 648</HD>
          <P>Fisheries, Fishing, Recordkeeping and reporting requirements.</P>
        </LSTSUB>
        <SIG>
          <PRTPAGE P="45752"/>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>John Oliver,</NAME>
          <TITLE>Deputy Assistant Administrator for Operations, National Marine Fisheries Service.</TITLE>
        </SIG>
        
        <P>For the reasons set out in the preamble, 50 CFR part 648 is proposed to be amended as follows:</P>
        <PART>
          <HD SOURCE="HED">PART 648—FISHERIES OF THE NORTHEASTERN UNITED STATES</HD>
          <P>1. The authority citation for part 648 continues to read as follows:</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>16 U.S.C. 1801<E T="03">et seq.</E>
            </P>
          </AUTH>
          
          <P>2. In § 648.4, paragraph (a)(5)(iii) is revised, and paragraph (c)(2)(vii) is added to read as follows:</P>
          <SECTION>
            <SECTNO>§ 648.4</SECTNO>
            <SUBJECT>Vessel permits.</SUBJECT>
            <P>(a) * * *</P>
            <P>(5) * * *</P>
            <P>(iii)<E T="03">Limited access Atlantic mackerel permits.</E>(A)<E T="03">Vessel size restriction.</E>A vessel of the United States is eligible for and may be issued an Atlantic mackerel permit to fish for, possess, or land Atlantic mackerel in or from the EEZ, except for any vessel that is greater than or equal to 165 ft (50.3 m) in length overall (LOA), or greater than 750 gross registered tons (680.4 mt), or the vessel's total main propulsion machinery is greater than 3,000 horsepower. Vessels that exceed the size or horsepower restrictions may seek to obtain an at-sea processing permit specified in § 648.6(a)(2)(i).</P>
            <P>(B)<E T="03">Limited access mackerel permits.</E>A vessel of the United States that fishes for, possesses, or lands more than 20,000 lb (7.46 mt) of mackerel per trip, except vessels that fish exclusively in state waters for mackerel, must have been issued and carry on board one of the limited access mackerel permits described in paragraphs (a)(5)(iii)(B)(<E T="03">1</E>) through (<E T="03">3</E>) of this section, including both vessels engaged in pair trawl operations.</P>
            <P>(<E T="03">1</E>)<E T="03">Tier 1 Limited Access Mackerel Permit.</E>A vessel may fish for, possess, and land unlimited amounts of mackerel, provided the vessel qualifies for and has been issued this permit, subject to all other regulations of this part.</P>
            <P>(<E T="03">2</E>)<E T="03">Tier 2 Limited Access Mackerel Permit.</E>A vessel may fish for, possess, and land up to 135,000 lb (50 mt) of mackerel per trip, provided the vessel qualifies for and has been issued this permit, subject to all other regulations of this part.</P>
            <P>(<E T="03">3</E>)<E T="03">Tier 3 Limited Access Mackerel Permit.</E>A vessel may fish for, possess, and land up to 100,000 lb (37.3 mt) of mackerel per trip, provided the vessel qualifies for and has been issued this permit, subject to all other regulations of this part.</P>
            <P>(C)<E T="03">Eligibility criteria for mackerel permits.</E>A vessel is eligible for and may be issued a Tier 1, Tier 2, or Tier 3 Limited Access Mackerel Permit if it meets the permit history criteria in paragraph (a)(5)(iii)(C)(<E T="03">1</E>) of this section and the relevant landings requirements specified in paragraphs (a)(5)(iii)(C)(<E T="03">2</E>) through (<E T="03">4</E>) of this section. The permit criteria and landings requirement must either be derived from the same vessel, or joined on a vessel through replacement prior to March 21, 2007.</P>
            <P>(<E T="03">1</E>)<E T="03">Permit history criteria for Limited Access Mackerel Permits.</E>(<E T="03">i</E>) The vessel must have been issued a Federal mackerel permit that was valid as of March 21, 2007. The term “as of” means that the vessel must have had a valid mackerel permit on March 21, 2007.</P>
            <P>(<E T="03">ii</E>) The vessel is replacing a vessel that was issued a Federal mackerel permit that was valid as of March 21, 2007. To qualify as a replacement vessel, the replacement vessel and the vessel being replaced must both be owned by the same vessel owner; or if the vessel being replaced was sunk or destroyed, the vessel owner must have owned the vessel being replaced at the time it sunk or was destroyed; or, if the vessel being replaced was sold to another person, the vessel owner must provide a copy of a written agreement between the buyer of the vessel being replaced and the owner/seller of the vessel, documenting that the vessel owner/seller retained the mackerel permit and all mackerel landings history.</P>
            <P>(<E T="03">2</E>)<E T="03">Landings criteria for Limited Access Mackerel Permits.</E>(<E T="03">i</E>)<E T="03">Tier 1.</E>The vessel must have landed at least 400,000 lb (149.3 mt) of mackerel in any one calendar year between January 1, 1997, and December 31, 2005, as verified by dealer reports submitted to NMFS or documented through valid dealer receipts, if dealer reports were not required by NMFS. The owners of vessels that fished in pair trawl operations may provide landings information as specified in paragraph (a)(5)(iii)(C)(<E T="03">2</E>)(<E T="03">iv</E>) of this section. Landings made by a vessel that is being replaced may be used to qualify a replacement vessel consistent with the requirements specified in paragraph (a)(5)(iii)(C)(<E T="03">1</E>)(<E T="03">ii</E>) of this section.</P>
            <P>(<E T="03">ii</E>)<E T="03">Tier 2.</E>The vessel must have landed at least 100,000 lb (37.3 mt) of mackerel in any one calendar year between March 1, 1994, and December 31, 2005, as verified by dealer reports submitted to NMFS or documented through valid dealer receipts, if dealer reports were not required by NMFS. The owners of vessels that fished in pair trawl operations may provide landings information as specified in paragraph (a)(5)(iii)(C)(<E T="03">2</E>)(<E T="03">iv</E>) of this section. Landings made by a vessel that is being replaced may be used to qualify a replacement vessel consistent with the requirements specified in paragraph (a)(5)(iii)(C)(<E T="03">1</E>)(<E T="03">ii</E>) of this section.</P>
            <P>(<E T="03">iii</E>)<E T="03">Tier 3.</E>The vessel must have landed at least 1,000 lb (0.4 mt) of mackerel in any one calendar year between March 1, 1994, and December 31, 2005, as verified by dealer reports submitted to NMFS or documented through valid dealer receipts, if dealer reports were not required by NMFS. The owners of vessels that fished in pair trawl operations may provide landings information as specified in paragraph (a)(5)(iii)(C)(<E T="03">2</E>)(<E T="03">iv</E>) of this section. Landings made by a vessel that is being replaced may be used to qualify a replacement vessel consistent with the requirements specified in paragraph (a)(5)(iii)(C)(<E T="03">1</E>)(<E T="03">ii</E>) of this section.</P>
            <P>(<E T="03">iv</E>)<E T="03">Landings criteria for vessels using landings from pair trawl operations.</E>To qualify for a limited access permit using landings from pair trawl operations, the owners of the vessels engaged in that operation must agree on how to divide such landings between the two vessels and apply for the permit jointly, as supported by the required NMFS dealer reports or signed dealer receipts.</P>
            <P>(<E T="03">3</E>)<E T="03">CPH.</E>A person who does not currently own a fishing vessel, but owned a vessel that satisfies the permit eligibility requirement in paragraph (a)(5)(iii)(B)(<E T="03">1</E>) and (<E T="03">2</E>) of this section that has sunk, been destroyed, or transferred to another person without its fishing and permit history, and that has not been replaced, may apply for and receive a CPH. A CPH allows for a replacement vessel to obtain the relevant limited access mackerel permit if the fishing and permit history of such vessel has been retained lawfully by the applicant as specified in paragraph (a)(5)(iii)(C)(<E T="03">1</E>)(<E T="03">ii</E>) of this section. If the vessel sank, was destroyed, or was transferred before March 21, 2007, the permit issuance criteria may be satisfied if the vessel was issued a valid Federal mackerel permit at any time between March 21, 2006, and March 21, 2007.</P>
            <P>(D)<E T="03">Application/renewal restrictions.</E>See paragraph (a)(1)(i)(B) of this section. Applications for a limited access mackerel permit described in paragraph (a)(5)(iii) of this section must be postmarked no later than December 31, 2012. Applications for limited access mackerel permits that are not postmarked before December 31, 2012, will not be processed because of this regulatory restriction, and returned to<PRTPAGE P="45753"/>the sender with a letter explaining the denial. Such denials may not be appealed and shall be the final decision of the Department of Commerce.</P>
            <P>(E)<E T="03">Qualification restrictions.</E>(<E T="03">1</E>) See paragraph (a)(1)(i)(C) of this section. The following restrictions in paragraphs (a)(5)(iii)(E)(<E T="03">2</E>) and (<E T="03">3</E>) of this section are applicable to limited access mackerel permits.</P>
            <P>(<E T="03">2</E>) Mackerel landings history generated by separate owners of a single vessel at different times during the qualification period for limited access mackerel permits may be used to qualify more than one vessel, provided that each owner applying for a limited access mackerel permit demonstrates that he/she created distinct fishing histories, that such histories have been retained, and if the vessel was sold, that each applicant's eligibility and fishing history is distinct. In such a case, each applicant would still need to have been issued a valid mackerel permit as of March 21, 2007, in order to create a full eligibility, as detailed in paragraph (a)(5)(iii)(C) of this section.</P>
            <P>(<E T="03">3</E>) A vessel owner applying for a limited access mackerel permit who sold or transferred a vessel with non-mackerel limited access permits, as specified in paragraph (a)(1)(i)(D) of this section, and retained only the mackerel permit and landings history of such vessel as specified in paragraph (a)(1)(i)(D) of this section, before April 3, 2009, may use the mackerel history to qualify a different vessel for the initial limited access mackerel permit, regardless of whether the history from the sold or transferred vessel was used to qualify for any other limited access permit. Such eligibility may be used if the vessel for which the initial limited access mackerel permit has been submitted meets the upgrade restrictions described at paragraph (a)(5)(iii)(H) of this section. Applicants must be able to provide baseline documentation for both vessels in order to be eligible to use this provision.</P>
            <P>(F)<E T="03">Change of ownership.</E>See paragraph (a)(1)(i)(D) of this section.</P>
            <P>(G)<E T="03">Replacement vessels.</E>See paragraph (a)(1)(i)(E) of this section.</P>
            <P>(H)<E T="03">Vessel baseline specification.</E>(<E T="03">1</E>) In addition to the baseline specifications specified in paragraph (a)(1)(i)(H) of this section, the volumetric fish hold capacity of a vessel at the time it was initially issued a Tier 1 or Tier 2 limited access mackerel permit will be considered a baseline specification. The fish hold capacity measurement must be obtained from an individual credentialed as a Certified Marine Surveyor with a fishing specialty by the National Association of Marine Surveyors (NAMS) or from an individual credentialed as an Accredited Marine Surveyor with a fishing specialty by the Society of Accredited Marine Surveyors (SAMS). Vessels that are sealed by the Maine State Sealer of Weights and Measures will also be deemed to meet this requirement. Vessels that qualify for a Tier 1 or Tier 2 mackerel permit must submit a fish hold capacity measurement to NMFS with the annual permit renewal application for the 2013 fishing year, as specified in paragraph (c)(2)(viii) of this section, or with the first vessel replacement application after a vessel qualifies for a Tier 1 or Tier 2 mackerel permit, whichever is sooner.</P>
            <P>(<E T="03">2</E>) If a mackerel CPH is initially issued, the vessel that provided the CPH eligibility establishes the size baseline against which future vessel size limitations shall be evaluated, unless the applicant has a vessel under contract prior to the submission of the mackerel limited access application. The replacement application to move permits onto the contracted vessel must be received by December 31, 2013. If the vessel that established the CPH is less than 20 ft (6.09 m) in length, then the baseline specifications associated with other limited access permits in the CPH suite will be used to establish the mackerel baseline specifications. If the vessel that established the CPH is less than 20 ft (6.09 m) in length, the limited access mackerel eligibility was established on another vessel, and there are no other limited access permits in the CPH suite, then the applicant must submit valid documentation of the baseline specifications of the vessel that established the eligibility. The hold capacity baseline for such vessels will be the hold capacity of the first replacement vessel after the permits are removed from CPH.</P>
            <P>(I)<E T="03">Upgraded vessel.</E>See paragraph (a)(1)(i)(F) of this section. In addition, for Tier 1 and Tier 2 limited access mackerel permits, the replacement vessel's volumetric fish hold capacity may not exceed by more than 10 percent the volumetric fish hold capacity of the vessel's baseline specifications. The modified fish hold, or the fish hold of the replacement vessel, must be resurveyed by a surveyor (accredited as in paragraph (a)(5)(iii)(H) of this section) unless the replacement vessel already had an appropriate certification, and the documentation would have to be submitted to NMFS.</P>
            <P>(J)<E T="03">Consolidation restriction.</E>See paragraph (a)(1)(i)(G) of this section.</P>
            <P>(K)<E T="03">Confirmation of permit history.</E>See paragraph (a)(1)(i)(J) of this section.</P>
            <P>(L)<E T="03">Abandonment or voluntary relinquishment of permits.</E>See paragraph (a)(1)(i)(K) of this section.</P>
            <P>(M)<E T="03">Appeal of denial of permit.</E>(<E T="03">1</E>)<E T="03">Eligibility.</E>Any applicant eligible to apply for a limited access mackerel permit who is denied such permit may appeal the denial to the Regional Administrator within 30 days of the notice of denial. The only ground for appeal is that the Regional Administrator erred in concluding that the vessel did not meet the criteria in this section. The appeal must set forth the basis for the applicant's belief that the decision of the Regional Administrator was made in error.</P>
            <P>(<E T="03">2</E>)<E T="03">Appeal review.</E>Applicants have two opportunities to appeal the denial of a limited access mackerel permit. The review of initial appeals will be conducted under the authority of the Regional Administrator at NMFS's Northeast Regional Office. The Regional Administrator shall appoint a hearing officer for review of second denial appeals.</P>
            <P>(<E T="03">i</E>) An appeal of the denial of an initial permit application (first level of appeal) must be made in writing to NMFS Northeast Regional Administrator. Appeals must be based on the grounds that the information used by the Regional Administrator in denying the permit was incorrect. The only items subject to appeal are the accuracy of the amount of landings, and the correct assignment of landings to a vessel and/or permit holder. Appeals must be submitted to the Regional Administrator, postmarked no later than 30 days after the denial of an initial limited access mackerel permit application. The appeal shall set forth the basis for the applicant's belief that the Regional Administrator's decision was made in error. The appeal must be in writing, must state the specific grounds for the appeal, the limited access mackerel permit category for which the applicant believes he should qualify, and must include information to support the appeal. The appellant may also request an LOA, as described in paragraph (a)(5)(iii)(M)(<E T="03">3</E>) of this section. The appeal will not be reviewed without submission of information in support of the appeal. The Regional Administrator would appoint a designee to make the initial decision on the appeal.</P>
            <P>(<E T="03">ii</E>) Should the appeal be denied, the applicant may request a hearing to review the Regional Administrator's appeal decision (second level of appeal). Such a request must be in writing, postmarked no later than 30 days after the appeal decision, must state the specific grounds for the hearing request,<PRTPAGE P="45754"/>and must include information to support the hearing request. If the request for a hearing to review of the appeal decision is not made within 30 days, the appeal decision is the final administrative action of the Department of Commerce. The appeal will not be reviewed in a hearing without submission of information in support of the hearing request. The Regional Administrator will appoint a hearing officer; the hearing process may take place within the National Appeals program. The hearing officer shall make findings and a recommendation to the Regional Administrator, which shall be advisory only. The Regional Administrator's decision is the final administrative action of the Department of Commerce.</P>
            <P>(<E T="03">3</E>) A vessel denied a limited access mackerel permit may fish for mackerel, provided that the denial has been appealed, the appeal is pending, and the vessel has on board a letter from the Regional Administrator authorizing the vessel to fish under the limited access category for which the applicant has submitted an appeal. A request for a letter of authorization (LOA) must be made at the time of appeal. The Regional Administrator will issue such a letter for the pending period of any appeal. The LOA must be carried on board the vessel. If the appeal is finally denied, the Regional Administrator shall send a notice of final denial to the vessel owner; the authorizing letter becomes invalid 5 days after the receipt of the notice of denial, but no later than 10 days from the date of the letter of denial.</P>
            <P>(iv)<E T="03">Atlantic mackerel incidental catch permits.</E>Any vessel of the United States may obtain a permit to fish for or retain up to 20,000 lb (7.46 mt) of Atlantic mackerel as an incidental catch in another directed fishery, provided that the vessel does not exceed the size restrictions specified in paragraph (a)(5)(iii)(A) of this section. The incidental catch allowance may be revised by the Regional Administrator based upon a recommendation by the Council following the procedure set forth in § 648.21.</P>
            <P>(v)<E T="03">Party and charter boat permits.</E>The owner of any party or charter boat must obtain a permit to fish for, possess, or retain in or from the EEZ mackerel, squid, or butterfish while carrying passengers for hire.</P>
            <STARS/>
            <P>(c) * * *</P>
            <P>(2) * * *</P>
            <P>(vii) The owner of a vessel that has been issued a Tier 1 or Tier 2 limited access mackerel must submit a volumetric fish hold certification measurement, as described in paragraph (a)(5)(iii)(H) of this section, with the permit renewal application for the 2013 fishing year.</P>
            <STARS/>
            <P>3. In § 648.7, paragraph (f)(2)(i) is revised to read as follows:</P>
          </SECTION>
          <SECTION>
            <SECTNO>§ 648.7</SECTNO>
            <SUBJECT>Recordkeeping and reporting requirements.</SUBJECT>
            <STARS/>
            <P>(f) * * *</P>
            <P>(2) * * *</P>
            <P>(i) For any vessel not issued a NE multispecies permit or a Tier 3 Limited Access mackerel permit, fishing vessel log reports, required by paragraph (b)(1)(i) of this section, must be postmarked or received by NMFS within 15 days after the end of the reporting month. If no fishing trip is made during a particular month for such a vessel, a report stating so must be submitted, as instructed by the Regional Administrator. For any vessel issued a NE multispecies permit or a Tier 3 Limited Access mackerel permit, fishing vessel log reports must be postmarked or received by midnight of the first Tuesday following the end of the reporting week. If no fishing trip is made during a reporting week for such a vessel, a report stating so must be submitted and received by NMFS by midnight of the first Tuesday following the end of the reporting week, as instructed by the Regional Administrator. For the purposes of this paragraph (f)(2)(i), the date when fish are offloaded will establish the reporting week or month that the VTR must be submitted to NMFS, as appropriate. Any fishing activity during a particular reporting week (i.e., starting a trip, landing, or offloading catch) will constitute fishing during that reporting week and will eliminate the need to submit a negative fishing report to NMFS for that reporting week. For example, if a vessel issued a NE multispecies permit or Tier 3 Limited Access Mackerel Vessel begins a fishing trip on Wednesday, but returns to port and offloads its catch on the following Thursday (i.e., after a trip lasting 8 days), the VTR for the fishing trip would need to be submitted by midnight Tuesday of the third week, but a negative report (i.e., a “did not fish” report) would not be required for either week.</P>
            <STARS/>
            <P>4. In § 648.14, paragraph (g)(1)(iii) is removed; paragraphs (g)(2)(ii)(C), (g)(2)(ii)(D) and (g)(2)(ii)(E) are revised, and paragraphs (g)(2)(ii)(F), (g)(2)(iii)(D) and (g)(2)(iv) are added to read as follows:</P>
          </SECTION>
          <SECTION>
            <SECTNO>§ 648.14</SECTNO>
            <SUBJECT>Prohibitions.</SUBJECT>
            <STARS/>
            <P>(g) * * *</P>
            <P>(2) * * *</P>
            <P>(ii) * * *</P>
            <P>(C) Possess more than the incidental catch allowance of mackerel, unless issued a Limited Access mackerel permit.</P>
            <P>(D) Take, retain, possess, or land mackerel, squid, or butterfish in excess of a possession allowance specified in § 648.25.</P>
            <P>(E) Possess 5,000 lb (2.27 mt) or more of butterfish, unless the vessel meets the minimum mesh requirements specified in § 648.23(a).</P>
            <P>(F) Take, retain, possess, or land mackerel, squid, or butterfish after a total closure specified under § 648.22.</P>
            <STARS/>
            <P>(iii) * * *</P>
            <P>(D) If fishing with midwater trawl or purse seine gear, fail to comply with the requirements of § 648.80(d) and (e).</P>
            <STARS/>
            <P>(iv)<E T="03">Observer requirements for Loligo fishery.</E>Fail to comply with any of the provisions specified in § 648.26.</P>
            <STARS/>
            <P>6. In § 648.21, paragraphs (a)(3), (b)(2)(iii) introductory text, (c)(3), (c)(6), and (c)(9) are revised to read as follows:</P>
          </SECTION>
          <SECTION>
            <SECTNO>§ 648.21</SECTNO>
            <SUBJECT>Procedures for determining initial annual amounts.</SUBJECT>
            <P>(a) * * *</P>
            <P>(3) IOY, including RQ, DAH, Tier 3 allocation (up to 7 percent of the DAH), DAP, recreational allocation, joint venture processing (JVP), if any, and TALFF, if any, for mackerel, which, subject to annual review, may be specified for a period of up to 3 years. The Monitoring Committee may also recommend that certain ratios of TALFF, if any, for mackerel to purchases of domestic harvested fish and/or domestic processed fish be established in relation to the initial annual amounts.</P>
            <STARS/>
            <P>(b) * * *</P>
            <P>(2) * * *</P>

            <P>(iii) IOY is composed of RQ, DAH, Tier 3 allocation (up to 7 percent of DAH), recreational allocation, and TALFF. Recreational allocation shall be equal to 6.2 percent of the mackerel ABC. RQ shall be based on request for research quota as described in paragraph (g) of this section. DAH, Tier 3 allocation (up to 7 of the DAH), recreational allocation, DAP, and JVP shall be set after deduction for RQ, if applicable, and must be projected by reviewing data from sources specified in paragraph (b) of this section and other<PRTPAGE P="45755"/>relevant data, including past domestic landings, projected amounts of mackerel, necessary for domestic processing and for joint ventures during the fishing year, and other data pertinent for such projection. The JVP component of DAH is the portion of DAH that domestic processors either cannot or will not use. In addition, IOY shall be based on the criteria set forth in the Magnuson-Stevens Act, specifically section 201(e), and on the following economic factors:</P>
            <STARS/>
            <P>(c) * * *</P>
            <P>(3) The amount of<E T="03">Loligo, Illex,</E>and butterfish that may be retained and landed by vessels issued the incidental catch permit specified in § 648.4(1)(5)(ii), and the amount of mackerel that may be retained, possessed and landed by any of the limited access mackerel permits described at § 648.4(1)(5)(iii) and the incidental mackerel permit at § 648.4(1)(5)(iv).</P>
            <STARS/>
            <P>(6) Commercial seasonal quotas/closures for<E T="03">Loligo</E>and<E T="03">Illex,</E>and allocation for the Limited Access Mackerel Tier 3.</P>
            <STARS/>
            <P>(9) Recreational allocation for mackerel.</P>
            <STARS/>
            <P>7. In § 648.22, paragraph (a)(1) is revised to read as follows:</P>
          </SECTION>
          <SECTION>
            <SECTNO>§ 648.22</SECTNO>
            <SUBJECT>Closure of the fishery.</SUBJECT>
            <P>(a) * * *</P>
            <P>(1)<E T="03">Mackerel closures.</E>(i) NMFS shall close the commercial mackerel fishery in the EEZ when the Regional Administrator projects that 90 percent of the mackerel DAH is harvested, if such a closure is necessary to prevent the DAH from being exceeded. The closure of the directed fishery shall be in effect for the remainder of that fishing period, with incidental catches allowed as specified in § 648.25(a)(2)(i). When the Regional Administrator projects that the DAH for mackerel shall be landed, NMFS shall close the mackerel fishery in the EEZ and the incidental catches specified for mackerel at § 648.25(a)(2)(i) will be prohibited.</P>
            <P>(ii) NMFS shall close the Tier 3 commercial mackerel fishery in the EEZ when the Regional Administrator projects that 90 percent of the Tier 3 mackerel allocation is harvested, if such a closure is necessary to prevent the DAH from being exceeded. The closure of the Tier 3 commercial mackerel fishery shall be in effect for the remainder of that fishing period, with incidental catches allowed as specified in § 648.25(a)(2)(ii).</P>
            <STARS/>
            <P>8. In § 648.24, paragraph (a)(1) is revised to read as follows:</P>
          </SECTION>
          <SECTION>
            <SECTNO>§ 648.24</SECTNO>
            <SUBJECT>Framework adjustments to management measures.</SUBJECT>
            <P>(a) * * *</P>
            <P>(1)<E T="03">Adjustment process.</E>The Council shall develop and analyze appropriate management actions over the span of at least two Council meetings. The Council must provide the public with advance notice of the availability of the recommendation(s), appropriate justification(s) and economic and biological analyses, and the opportunity to comment on the proposed adjustment(s) at the first meeting and prior to and at the second Council meeting. The Council's recommendations on adjustments or additions to management measures must come from one or more of the following categories: Minimum fish size, maximum fish size, gear restrictions, gear requirements or prohibitions, permitting restrictions, recreational allocation, recreational possession limit, recreational seasons, closed areas, commercial seasons, commercial trip limits, commercial quota system including commercial quota allocation procedure and possible quota set asides to mitigate bycatch, recreational harvest limit, annual specification quota setting process, FMP Monitoring Committee composition and process, description and identification of EFH (and fishing gear management measures that impact EFH), description and identification of habitat areas of particular concern, overfishing definition and related thresholds and targets, regional gear restrictions, regional season restrictions (including option to split seasons), restrictions on vessel size (LOA and GRT) or shaft horsepower, changes to the Northeast Region SBRM (including the CV-based performance standard, the means by which discard data are collected/obtained, fishery stratification, reports, and/or industry-funded observers or observer set-aside programs), any other management measures currently included in the FMP, set aside quota for scientific research, regional management, and process for inseason adjustment to the annual specification.</P>
            <STARS/>
            <P>9. In § 648.25, paragraph (a) is revised to read as follows:</P>
          </SECTION>
          <SECTION>
            <SECTNO>§ 648.25</SECTNO>
            <SUBJECT>Possession restrictions.</SUBJECT>
            <P>(a)<E T="03">Atlantic mackerel.</E>(1) A vessel must be issued a valid limited access mackerel permit to fish for, possess, or land more than 20,000 lb (9.08 mt) of Atlantic mackerel from or in the EEZ per trip, provided that the fishery has not been closed because 90 percent of the DAH has been harvested, as specified in § 648.22(a)(1)(i).</P>
            <P>(i) A vessel issued a Tier 1 Limited Access Mackerel Permit is authorized to fish for, possess, or land Atlantic mackerel with no possession restriction in the EEZ per trip, and may only land Atlantic mackerel once on any calendar day, which is defined as the 24-hr period beginning at 0001 hours and ending at 2,400 hours, provided that the fishery has not been closed because 90 percent of the DAH has been harvested, as specified in § 648.22(a)(1)(i).</P>
            <P>(ii) A vessel issued a Tier 2 Limited Access Mackerel Permit is authorized to fish for, possess, or land up to 135,000 lb (61.23 mt) of Atlantic mackerel in the EEZ per trip, and may only land Atlantic mackerel once on any calendar day, which is defined as the 24-hr period beginning at 0001 hours and ending at 2400 hours, provided that the fishery has not been closed because 90 percent of the DAH has been harvested, as specified in § 648.22(a)(1)(i).</P>
            <P>(iii) A vessel issued a Tier 3 Limited Access Mackerel Permit is authorized to fish for, possess, or land up to 100,000 lb (45.36 mt) of Atlantic mackerel in the EEZ per trip, and may only land Atlantic mackerel once on any calendar day, which is defined as the 24-hr period beginning at 0001 hours and ending at 2400 hours, provided that the fishery has not been closed because 90 percent of the Tier 3 allocation has been harvested, or 90 percent of the DAH has been harvested, as specified in § 648.22(a)(1)(i) and (ii).</P>
            <P>(iv) A vessel issued an open access mackerel permit may fish for, possess, or land up to 20,000 lb (9.08 mt) of Atlantic mackerel in the EEZ per trip, and may only land Atlantic mackerel once on any calendar day, which is defined as the 24-hr period beginning at 0001 hours and ending at 2400 hours.</P>
            <P>(v) Both vessels involved in a pair trawl operation must be issued a valid mackerel permits to fish for, possess, or land Atlantic mackerel in the EEZ. Both vessels must be issued the mackerel permit appropriate for the amount of mackerel jointly possessed by both of the vessels participating in the pair trawl operation.</P>
            <P>(2)<E T="03">Mackerel closure possession restrictions.</E>(i)<E T="03">Commercial mackerel fishery.</E>During a closure of the commercial Atlantic mackerel fishery, including closure of the Tier 3 fishery, vessels issued a Limited Access Mackerel Permit may not fish for, possess, or land more than 20,000 lb<PRTPAGE P="45756"/>(9.08 mt) of Atlantic mackerel per trip at any time, and may only land Atlantic mackerel once on any calendar day, which is defined as the 24-hr period beginning at 0001 hours and ending at 2,400 hours.</P>
            <P>(ii) [Reserved]</P>
            <STARS/>
          </SECTION>
        </PART>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19415 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3510-22-P</BILCOD>
    </PRORULE>
  </PRORULES>
  <VOL>76</VOL>
  <NO>147</NO>
  <DATE>Monday, August 1, 2011</DATE>
  <UNITNAME>Notices</UNITNAME>
  <NOTICES>
    <NOTICE>
      <PREAMB>
        <PRTPAGE P="45757"/>
        <AGENCY TYPE="F">BUREAU OF CONSUMER FINANCIAL PROTECTION</AGENCY>
        <SUBJECT>Privacy Act of 1974, as Amended</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Bureau of Consumer Financial Protection.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of Proposed Privacy Act System of Records.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>In accordance with the Privacy Act of 1974, as amended, the Bureau of Consumer Financial Protection, hereinto referred to as the Consumer Financial Protection Bureau (“CFPB”) gives notice of the establishment of a Privacy Act System of Records.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments must be received no later than August 31, 2011. The new system of records will be effective September 12, 2011 unless the comments received result in a contrary determination.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may submit comments, identified by Docket No. CFPB-2011-0013, by any of the following methods:</P>
          <P>•<E T="03">Electronic: http://www.regulations.gov.</E>Follow the instructions for submitting comments.</P>
          <P>•<E T="03">Mail or Hand Delivery/Courier in Lieu of Mail:</E>Claire Stapleton, Chief Privacy Officer, Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036.</P>

          <P>All submissions must include the agency name and docket number or Regulatory Information Number (RIN) for this notice. In general all comments received will be posted without change to<E T="03">http://www.regulations.gov.</E>In addition, comments will be available for public inspection and copying at 1801 L St., NW., Washington, DC 20036, on official business days between the hours of 10 a.m. and 5 p.m. Eastern Time. You can make an appointment to inspect comments by telephoning (202) 435-7220. All comments, including attachments and other supporting materials, will become part of the public record and subject to public disclosure. You should submit only information that you wish to make available publicly.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Claire Stapleton, Chief Privacy Officer, Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036, (202) 435-7220.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>The Dodd-Frank Wall Street Reform and Consumer Protection Act (“Act”), Public Law 111-203, Title X, established the CFPB to administer and enforce federal consumer financial protection law. The CFPB will maintain the records covered by this notice.</P>
        <P>The new systems of records described in this notice, CFPB.004—Enforcement Database, will enable the CFPB to carry out its responsibilities with respect to the enforcement of federal consumer financial protection law. A description of the new system of records follows this Notice.</P>
        <P>The report of a new system of records has been submitted to the Committee on Oversight and Government Reform of the House of Representatives, the Committee on Homeland Security and Governmental Affairs of the Senate, and the Office of Management and Budget, pursuant to Appendix I to OMB Circular A-130, “Federal Agency Responsibilities for Maintaining Records About Individuals,” dated November 30, 2000, and the Privacy Act, 5 U.S.C. 552a(r).</P>
        <P>The system of records entitled, “CFPB.004—Enforcement Database” is published in its entirety below.</P>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>Claire Stapleton,</NAME>
          <TITLE>Chief Privacy Officer.</TITLE>
        </SIG>
        <PRIACT>
          <HD SOURCE="HD1">CFPB.004</HD>
          <HD SOURCE="HD2">System Name:</HD>
          <P>CFPB Enforcement Database.</P>
          <HD SOURCE="HD2">System Location:</HD>
          <P>Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Categories of individuals covered by the system:</HD>
          <P>Covered individuals include:</P>
          <P>(1) Individuals who are current or former directors, officers, employees, shareholders, agents, and independent contractors of covered persons or service providers, who are or have been the subjects of or otherwise associated with an investigation or enforcement action by the CFPB, or have been named in connection with suspicious activity reports or administrative enforcement orders or agreement. Covered persons and service providers include banks, savings associations, credit unions, thrifts, non-depository institutions, or other persons, offering, providing, or assisting with the provision of consumer financial products or services.</P>
          <P>(2) Current, former, and prospective consumers who are or have been customers or prospective customers of, solicited by, or serviced by covered persons or service providers if such individuals have provided information, including complaints about covered persons or service providers, or are or have been witnesses in or otherwise associated with an enforcement action by the CFPB.</P>
          <P>(3) Applicants, current and former directors, officers, employees, shareholders, agents, and independent contractors of persons and entities that have business relationships with covered persons or service providers who are or have been the subject of an enforcement action by the CFPB.</P>
          <P>(4) Current, former, and prospective customers of persons and entities that have business relationships with covered persons or service providers that are or have been the subject of an enforcement action by the CFPB, and the customers are complainants against covered persons or service providers, or witnesses in or otherwise associated with an enforcement action.</P>
          <P>(5) Other individuals who have inquired about or may have information relevant to an investigation or proceeding concerning a possible violation of federal consumer financial law. Information collected regarding consumer financial products and services is subject to the Privacy Act only to the extent that it concerns individuals; information pertaining to corporations and other business entities and aggregate, non-identifiable information is not subject to the Privacy Act.</P>
          <HD SOURCE="HD2">Categories of records in the system:</HD>

          <P>Records maintained in the system may contain: Identifiable information about individuals such as name, address, e-mail address, phone number, social security number, employment status, age, date of birth, financial<PRTPAGE P="45758"/>information, credit information, and personal history. Records in this system are collected and generated during the investigation of potential violations and enforcement of laws and regulations under the jurisdiction of the CFPB and may include (1) Records provided to the CFPB about potential or pending investigations, administrative proceedings, and civil litigation; (2) evidentiary materials gathered or prepared by the CFPB or obtained for use in investigations, proceedings, or litigation, and work product derived from or related thereto; (3) staff working papers, memoranda, analyses, databases, and other records and work product relating to possible or actual investigations, proceedings, or litigation; (4) databases, correspondence, and reports tracking the initiation, status, and closing of investigations, proceedings, and litigation; (5) correspondence and materials used by the CFPB to refer criminal and other matters to the appropriate agency or authority, and records reflecting the status of any outstanding referrals; (6) correspondence and materials shared between the CFPB and other federal and state agencies; (7) consumer complaints made or referred to the CFPB.</P>
          <HD SOURCE="HD2">Authority for maintenance of the system:</HD>
          <P>Public Law 111-203, Title X, Sections 1011, 1012, 1021, codified at 12 U.S.C. 5491, 5492, 5511.<SU>1</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>1</SU>Section 1066 of the Act grants the Secretary of the Treasury interim authority to perform certain functions of the CFPB. Pursuant to that authority, Treasury published rules on the Disclosure of Records and Information within 12 CFR Chapter X. This SORN is published pursuant to those rules and the Privacy Act.</P>
          </FTNT>
          <HD SOURCE="HD2">Purpose(s):</HD>
          <P>The information in the system is being collected to enable the CFPB to carry out its responsibilities with respect to enforcement of Title X of the Dodd-Frank Wall Street Reform and Consumer Protection Act and other federal consumer financial law, including: (1) The investigation of potential violations of federal consumer financial law; (2) the pursuit of administrative or civil enforcement actions; and (3) the referral of matters, as appropriate, to the Department of Justice or other federal or state agencies.</P>
          <HD SOURCE="HD2">Routine uses of records maintained in the system, including categories of users and the purposes of such uses:</HD>
          <P>These records may be disclosed, consistent with the CFPB Disclosure of Records and Information Rules promulgated in the title of the CFR to:</P>
          <P>(1) Appropriate agencies, entities, and persons when: (a) The CFPB suspects or has confirmed that the security or confidentiality of information in the system of records has been compromised; (b) the CFPB has determined that as a result of the suspected or confirmed compromise there is a risk of harm to economic or property interests, identity theft or fraud, or harm to the security or integrity of this system or other systems or programs (whether maintained by the CFPB or another agency or entity) that rely upon the compromised information; and (c) the disclosure made to such agencies, entities, and persons is reasonably necessary to assist in connection with the CFPB's efforts to respond to the suspected or confirmed compromise and prevent, minimize, or remedy such harm;</P>
          <P>(2) Another federal or state agency to: (a) Permit a decision as to access, amendment or correction of records to be made in consultation with or by that agency; or (b) verify the identity of an individual or the accuracy of information submitted by an individual who has requested access to, or amendment or correction of records;</P>
          <P>(3) To the Office of the President in response to an inquiry from that office made at the request of the subject of a record or a third party on that person's behalf;</P>
          <P>(4) Congressional offices in response to an inquiry made at the request of the individual to whom the record pertains;</P>
          <P>(5) Contractors, agents, or other authorized individuals performing work on a contract, service, cooperative agreement, job or other activity on behalf of the CFPB or Federal Government and who have a need to access information in the performance of their duties or activities;</P>
          <P>(6) Any authorized agency or component of the Department of Treasury, the Department of Justice, the Federal Reserve System, the Federal Deposit Insurance Corporation or other law enforcement authorities including disclosure by such authorities:</P>
          <P>(a) To the extent relevant and necessary in connection with litigation in proceedings before a court or other adjudicative body, where (i) the United States is a party to or has an interest in the litigation, including where the agency, or an agency component, or an agency official or employee in his or her official capacity, or an individual agency official or employee whom the Department of Justice or the Bureau has agreed to represent, is or may likely become a party, and (ii) the litigation is likely to affect the agency or any component thereof; or</P>
          <P>(b) To outside experts or consultants when considered appropriate by CFPB staff to assist in the conduct of agency matters;</P>
          <P>(7) The U.S. Department of Justice (“DOJ”) for its use in providing legal advice to the CFPB or in representing the CFPB in a proceeding before a court, adjudicative body, or other administrative body, where the use of such information by the DOJ is deemed by the CFPB to be relevant and necessary to the advice or proceeding, and in the case of a proceeding, such proceeding names as a party in interest:</P>
          <P>(a) The CFPB;</P>
          <P>(b) Any employee of the CFPB in his or her official capacity;</P>
          <P>(c) Any employee of the CFPB in his or her individual capacity where DOJ or the CFPB has agreed to represent the employee; or</P>
          <P>(d) The United States, where the CFPB determines that litigation is likely to affect the CFPB or any of its components;</P>
          <P>(8) A grand jury pursuant either to a federal or state grand jury subpoena, or to a prosecution request that such record be released for the purpose of its introduction to a grand jury, where the subpoena or request has been specifically approved by a court. In those cases where the Federal Government is not a party to the proceeding, records may be disclosed if a subpoena has been signed by a judge;</P>
          <P>(9) A court, magistrate, or administrative tribunal in the course of an administrative proceeding or judicial proceeding, including disclosures to opposing counsel or witnesses (including expert witnesses) in the course of discovery or other pre-hearing exchanges of information, litigation, or settlement negotiations, where relevant or potentially relevant to a proceeding, or in connection with criminal law proceedings;</P>
          <P>(10) Appropriate agencies, entities, and persons, including but not limited to potential expert witnesses or witnesses in the course of investigations, to the extent necessary to secure information relevant to the investigation;</P>
          <P>(11) Appropriate federal, state, local, foreign, tribal, or self-regulatory organizations or agencies responsible for investigating, prosecuting, enforcing, implementing, issuing, or carrying out a statute, rule, regulation, order, policy, or license if the information may be relevant to a potential violation of civil or criminal law, rule, regulation, order, policy or license; and</P>

          <P>(12) An entity or person that is the subject of supervision or enforcement activities including examinations,<PRTPAGE P="45759"/>investigations, administrative proceedings, and litigation, and the attorney or non-attorney representative for that entity or person.</P>
          <HD SOURCE="HD2">Policies and practices for storing, retrieving, accessing, retaining, and dispensing of records in the system:</HD>
          <HD SOURCE="HD2">Storage:</HD>
          <P>Paper and electronic records.</P>
          <HD SOURCE="HD2">Retrievability:</HD>
          <P>Records are retrievable by a variety of fields including without limitation the individual's name, address, account number, social security number, transaction number, phone number, date of birth, or by some combination thereof.</P>
          <HD SOURCE="HD2">Safeguards:</HD>
          <P>Access to electronic records is restricted to authorized personnel who have been issued non-transferrable access codes and passwords. Other records are maintained in locked file cabinets or rooms with access limited to those personnel whose official duties require access.</P>
          <HD SOURCE="HD2">Retention and disposal:</HD>
          <P>The CFPB will maintain computer and paper records indefinitely until the National Archives and Record Administration approves the CFPB's records disposition schedule.</P>
          <HD SOURCE="HD2">System manager(s) and address:</HD>
          <P>The Consumer Financial Protection Bureau, Assistant Director for Enforcement, 1801 L Street, NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Notification procedure:</HD>
          <P>Individuals seeking notification and access to any record contained in this system of records, or seeking to contest its content, may inquire in writing in accordance with instructions appearing in Title 12, Chapter 10 of the CFR, “Disclosure of Records and Information.” Address such requests to: Chief Privacy Officer, Bureau of Consumer Financial Protection, 1801 L St., NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Record access procedures:</HD>
          <P>See “Notification Procedures” above.</P>
          <HD SOURCE="HD2">Contesting record procedures:</HD>
          <P>See “Notification Procedures” above.</P>
          <HD SOURCE="HD2">Record source categories:</HD>
          <P>Information in this system is obtained from banks, savings associations, credit unions, or non-depository institutions or other persons offering or providing consumer financial products or services, current, former, and prospective consumers who are or have been customers or prospective employees and agents of such persons, and current, former, and prospective customers of such entities and persons, and others with information relevant to the enforcement of federal consumer financial laws.</P>
          <HD SOURCE="HD2">Exemptions claimed for the system:</HD>
          <P>Portions of the records in this system are complied for law enforcement purposes and are exempt from disclosure under CFPB's Privacy Act regulations and 5 U.S.C. 552a(k)(2). Federal criminal law enforcement investigatory reports maintained as part of this system may be the subject of exemptions imposed by the originating agency pursuant to 5 U.S.C. 552a(j)(2).</P>
        </PRIACT>
        
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19424 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4810-25-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">BUREAU OF CONSUMER FINANCIAL PROTECTION</AGENCY>
        <SUBJECT>Privacy Act of 1974, as Amended</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Bureau of Consumer Financial Protection.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of Proposed Privacy Act System of Records.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>In accordance with the Privacy Act of 1974, as amended, the Bureau of Consumer Financial Protection, hereinto referred to as the Consumer Financial Protection Bureau (“CFPB”) gives notice of the establishment of a Privacy Act System of Records.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments must be received no later than August 31, 2011. The new system of records will be effective September 12, 2011 unless the comments received result in a contrary determination.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may submit comments, identified by Docket No. CFPB-2011-0014, by any of the following methods:</P>
          <P>•<E T="03">Electronic: http://www.regulations.gov.</E>Follow the instructions for submitting comments.</P>
          <P>•<E T="03">Mail or Hand Delivery/Courier in Lieu of Mail:</E>Claire Stapleton, Chief Privacy Officer, Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036.</P>

          <P>All submissions must include the agency name and docket number or Regulatory Information Number (RIN) for this notice. In general all comments received will be posted without change to<E T="03">http://www.regulations.gov.</E>In addition, comments will be available for public inspection and copying at 1801 L St., NW., Washington, DC 20036, on official business days between the hours of 10 a.m. and 5 p.m. Eastern Time. You can make an appointment to inspect comments by telephoning (202) 435-7220. All comments, including attachments and other supporting materials, will become part of the public record and subject to public disclosure. You should submit only information that you wish to make available publicly.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Claire Stapleton, Chief Privacy Officer, Consumer Financial Protection Bureau, 1801 L. Street, NW., Washington, DC 20036, (202) 435-7220.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>The Dodd-Frank Wall Street Reform and Consumer Protection Act (“Act”), Public Law 111-203, Title X, established the CFPB to administer and enforce federal consumer financial protection law. The CFPB will maintain the records covered by this notice.</P>
        <P>The new systems of records described in this notice, CFPB.006—Social Networks and Citizen Engagement System, will assist the CFPB by providing effective, social media-based ways to share information and interact with the public. A description of the new system of records follows this Notice.</P>
        <P>The report of a new system of records has been submitted to the Committee on Oversight and Government Reform of the House of Representatives, the Committee on Homeland Security and Governmental Affairs of the Senate, and the Office of Management and Budget, pursuant to Appendix I to OMB Circular A-130, “Federal Agency Responsibilities for Maintaining Records About Individuals,” dated November 30, 2000, and the Privacy Act, 5 U.S.C. 552a(r).</P>
        <P>The system of records entitled, “CFPB.006—Social Networks and Citizen Engagement System” is published in its entirety below.</P>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>Claire Stapleton,</NAME>
          <TITLE>Chief Privacy Officer.</TITLE>
        </SIG>
        <PRIACT>
          <HD SOURCE="HD1">CFPB.006</HD>
          <HD SOURCE="HD2">System Name:</HD>
          <P>CFPB Social Networks and Citizen Engagement System.</P>
          <HD SOURCE="HD2">System Location:</HD>
          <P>Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Categories of individuals covered by the system:</HD>

          <P>Users of social media who interact with the CFPB through various social media outlets, including but not limited to third-party sites and services such as<PRTPAGE P="45760"/>Facebook, Twitter, YouTube, and Flickr. Other covered individuals may include those who sign on to various parts of the CFPB web site with a user identity provided by a third-party, such as Disqus. These may be members of the public, employees, or contractors.</P>
          <HD SOURCE="HD2">Categories of records in the system:</HD>
          <P>Records maintained in the system may contain information that an individual shares with the CFPB through various social media sites and services. They may also contain information that is stored to ensure that an individual can access web sites where a login is required. This may include without limitation: name, username, email address, birth date, security questions, IP addresses, location, passwords, authentication, business affiliation, demographic information, videos, photos, and other general information.</P>
          <HD SOURCE="HD2">Authority for maintenance of the system:</HD>
          <P>Public Law 111-203, Title X, Sections 1011, 1012, 1021, codified at 12 U.S.C. 5491, 5492, 5511. OMB Open Government Directive, M-10-06, Dec. 8, 2009. Presidential Memorandum to the Heads of Executive Departments and Agencies on Transparency and Open Government, January 21, 2009. OMB Guidance for Online Use of Web Measurement and Customization Technologies, M-10-22, June 25, 2010. OMB Guidance for Agency Use of Third-Party Websites and Applications, M-10-23, June 25, 2010. Executive Order 13571, Streamlining Service Delivery and Improving Customer Service, April 27, 2011.<SU>1</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>1</SU>Section 1066 of the Act grants the Secretary of the Treasury interim authority to perform certain functions of the CFPB. Pursuant to that authority, Treasury published rules on the Disclosure of Records and Information within 12 CFR Chapter X. This SORN is published pursuant to those rules and the Privacy Act.</P>
          </FTNT>
          <HD SOURCE="HD2">Purpose(s):</HD>
          <P>The information in the system is being collected to facilitate internal and external interactions concerning the CFPB and CFPB programs. The use of social media platforms will increase collaboration and transparency with the public, as well as employees and contractors. The use of social media will enable the CFPB to interact with the public in effective and meaningful ways, encourage the wide sharing of consumer financial information and the strengthening of an online community of consumers, and ensure that critical information about the agency and key consumer finance issues is distributed.</P>
          <HD SOURCE="HD2">Routine uses of records maintained in the system, including categories of users and the purposes of such uses:</HD>
          <P>These records may be disclosed, consistent with the CFPB Disclosure of Records and Information Rules promulgated in the title of the CFR to:</P>
          <P>(1) Appropriate agencies, entities, and persons when (a) the CFPB suspects or has confirmed that the security or confidentiality of information in the system of records has been compromised; (b) the CFPB has determined that as a result of the suspected or confirmed compromise there is a risk of harm to economic or property interests, identity theft or fraud, or harm to the security or integrity of this system or other systems or programs (whether maintained by the CFPB or another agency or entity) that rely upon the compromised information; and (c) the disclosure made to such agencies, entities, and persons is reasonably necessary to assist in connection with the CFPB's efforts to respond to the suspected or confirmed compromise and prevent, minimize, or remedy such harm;</P>
          <P>(2) Another federal or state agency to: (a) permit a decision as to access, amendment or correction of records to be made in consultation with or by that agency; or (b) verify the identity of an individual or the accuracy of information submitted by an individual who has requested access to or amendment or correction of records;</P>
          <P>(3) To the Office of the President in response to an inquiry from that office made at the request of the subject of a record or a third party on that person's behalf;</P>
          <P>(4) Congressional offices in response to an inquiry made at the request of the individual to whom the record pertains;</P>
          <P>(5) Contractors, agents, or other authorized individuals performing work on a contract, service, cooperative agreement, job or other activity on behalf of the CFPB or Federal Government and who have a need to access information in the performance of their duties or activities;</P>
          <P>(6) Any authorized agency or component of the Department of Treasury, the Department of Justice, the Federal Reserve System, the Federal Deposit Insurance Corporation or other law enforcement authorities including disclosure by such authorities:</P>
          <P>(a) To the extent relevant and necessary in connection with litigation in proceedings before a court or other adjudicative body, where (i) the United States is a party to or has an interest in the litigation, including where the agency, or an agency component, or an agency official or employee in his or her official capacity, or an individual agency official or employee whom the Department of Justice or the Bureau has agreed to represent, is or may likely become a party, and (ii) the litigation is likely to affect the agency or any component thereof; or</P>
          <P>(b) To outside experts or consultants when considered appropriate by CFPB staff to assist in the conduct of agency matters;</P>
          <P>(7) The U.S. Department of Justice (“DOJ”) for its use in providing legal advice to the CFPB or in representing the CFPB in a proceeding before a court, adjudicative body, or other administrative body, where the use of such information by the DOJ is deemed by the CFPB to be relevant and necessary to the advice or proceeding, and in the case of a proceeding, such proceeding names as a party in interest:</P>
          <P>(a) The CFPB;</P>
          <P>(b) Any employee of the CFPB in his or her official capacity;</P>
          <P>(c) Any employee of the CFPB in his or her individual capacity where DOJ or the CFPB has agreed to represent the employee; or</P>
          <P>(d) The United States, where the CFPB determines that litigation is likely to affect the CFPB or any of its components;</P>
          <P>(8) A court, magistrate, or administrative tribunal in the course of an administrative proceeding or judicial proceeding, including disclosures to opposing counsel or witnesses (including expert witnesses) in the course of discovery or other pre-hearing exchanges of information, litigation, or settlement negotiations, where relevant or potentially relevant to a proceeding, or in connection with criminal law proceedings; and</P>
          <P>(9) Appropriate federal, state, local, foreign, tribal, or self-regulatory organizations or agencies responsible for investigating, prosecuting, enforcing, implementing, issuing, or carrying out a statute, rule, regulation, order, policy, or license if the information may be relevant to a potential violation of civil or criminal law, rule, regulation, order, policy or license.</P>
          <HD SOURCE="HD2">Policies and practices for storing, retrieving, accessing, retaining, and dispensing of records in the system:</HD>
          <HD SOURCE="HD2">Storage:</HD>
          <P>Paper and electronic records.</P>
          <HD SOURCE="HD2">Retrievability:</HD>

          <P>Records are retrievable by full-text search. Records may also be retrieved by personal identifiers which may include without limitation: name, username, e-mail address, IP addresses, geographic information, and demographic information.<PRTPAGE P="45761"/>
          </P>
          <HD SOURCE="HD2">Safeguards:</HD>
          <P>Access to electronic records that are not otherwise available to the general public by virtue of their presence on social media sites is restricted to authorized personnel who have been issued non-transferrable access codes and passwords. Other records are maintained in locked file cabinets or rooms with access limited to those personnel whose official duties require access.</P>
          <HD SOURCE="HD2">Retention and disposal:</HD>
          <P>The CFPB will maintain computer and paper records indefinitely until the National Archives and Records Administration approves the CFPB's records deposition schedule.</P>
          <HD SOURCE="HD2">System manager(s) and address:</HD>
          <P>Consumer Financial Protection Bureau, Chief Technology Officer, 1801 L Street, NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Notification procedure:</HD>
          <P>Individuals seeking notification and access to any record contained in this system of records, or seeking to contest its content, may inquire in writing in accordance with instructions appearing in Title 12, Chapter 10 of the CFR, “Disclosure of Records and Information.” Address such requests to: Chief Privacy Officer, Bureau of Consumer Financial Protection, 1801 L St., NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Record access procedures:</HD>
          <P>See “Notification Procedures” above.</P>
          <HD SOURCE="HD2">Contesting record procedures:</HD>
          <P>See “Notification Procedures” above.</P>
          <HD SOURCE="HD2">Record source categories:</HD>
          <P>Information in this system is obtained from individuals who interact with the CFPB through social media networks or as a result of public outreach.</P>
          <HD SOURCE="HD2">Exemptions claimed for the system:</HD>
          <P>None.</P>
        </PRIACT>
        
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19426 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4810-25-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">BUREAU OF CONSUMER FINANCIAL PROTECTION</AGENCY>
        <SUBJECT>Privacy Act of 1974, as Amended</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Bureau of Consumer Financial Protection.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of Proposed Privacy Act System of Records.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>In accordance with the Privacy Act of 1974, as amended, the Bureau of Consumer Financial Protection, hereinto referred to as the Consumer Financial Protection Bureau (“CFPB”) or the “Bureau” gives notice of the establishment of a Privacy Act System of Records.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments must be received no later than August 31, 2011. The new system of records will be effective September 12, 2011 unless the comments received result in a contrary determination.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may submit comments, identified by Docket No. CFPB-2011-0012, by any of the following methods:</P>
          <P>•<E T="03">Electronic: http://www.regulations.gov.</E>Follow the instructions for submitting comments.</P>
          <P>•<E T="03">Mail or Hand Delivery/Courier in Lieu of Mail:</E>Claire Stapleton, Chief Privacy Officer, Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036.</P>

          <P>All submissions must include the agency name and docket number or Regulatory Information Number (RIN) for this notice. In general all comments received will be posted without change to<E T="03">http://www.regulations.gov.</E>In addition, comments will be available for public inspection and copying at 1801 L St., NW., Washington, DC 20036, on official business days between the hours of 10 a.m. and 5 p.m. Eastern Time. You can make an appointment to inspect comments by telephoning (202) 435-7220. All comments, including attachments and other supporting materials, will become part of the public record and subject to public disclosure. You should submit only information that you wish to make available publicly.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Claire Stapleton, Chief Privacy Officer, Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036, (202) 435-7220.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>The Dodd-Frank Wall Street Reform and Consumer Protection Act (“Act”), Public Law 111-203, Title X, established the CFPB to administer and enforce federal consumer financial protection law. The CFPB will maintain the records covered by this notice.</P>
        <P>The new systems of records described in this notice, CFPB.003—Non-depository Supervision Database will be used to enable the CFPB to carry out its responsibilities with respect to individuals related to non-depository covered persons subject to the authority of the CFPB, including the internal coordination of examinations, supervision evaluations and analyses, and enforcement actions. This system will also allow the CFPB to coordinate with other financial regulatory agencies. A description of the new system of records follows this Notice.</P>
        <P>The report of a new system of records has been submitted to the Committee on Oversight and Government Reform of the House of Representatives, the Committee on Homeland Security and Governmental Affairs of the Senate, and the Office of Management and Budget, pursuant to Appendix I to OMB Circular A-130, “Federal Agency Responsibilities for Maintaining Records About Individuals,” dated November 30, 2000, and the Privacy Act, 5 U.S.C. 552a(r).</P>
        <P>The system of records entitled, “CFPB.003—Non-depository Supervision Database” is published in its entirety below.</P>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>Claire Stapleton,</NAME>
          <TITLE>Chief Privacy Officer.</TITLE>
        </SIG>
        <PRIACT>
          <HD SOURCE="HD1">CFPB.003</HD>
          <HD SOURCE="HD2">System Name:</HD>
          <P>CFPB Non-depository Supervision Database.</P>
          <HD SOURCE="HD2">System Location:</HD>
          <P>Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Categories of individuals covered by the system:</HD>
          <P>Individuals covered by this system are: (1) Individuals who themselves are current and former directors, officers, employees, agents, shareholders, and independent contractors of non-depository covered persons subject to the supervision of the CFPB; (2) Current and former consumers who are or have been in the past serviced by non-depository covered persons subject to the supervision of the CFPB; and (3) CFPB employees assigned to supervise non-depository covered persons. Information collected regarding consumer products and services is subject to the Privacy Act only to the extent that it concerns individuals; information pertaining to corporations and other organizations is not subject to the Privacy Act.</P>
          <HD SOURCE="HD2">Categories of records in the system:</HD>

          <P>Records in the system may contain information provided by a covered person, by individuals who are or have been serviced by a covered person, or other governmental authorities, to the CFPB in the exercise of the CFPB's responsibilities and used to assess a covered person's compliance with various statutory and regulatory obligations. This may include: (1) Personally identifiable information from customers of non-depository covered persons, including without limitation,<PRTPAGE P="45762"/>name, social security number, account numbers, address, phone number, email address, and date of birth; (2) contact information for officials of non-depository covered persons such as members of the Board of Directors, Audit Committee Chair, Chief Executive Officer, Chief Compliance Officer, Internal Auditor, and Independent Auditor including, without limitation, name, address, phone number and email address; (3) information about CFPB employees assigned supervision tasks for non-depository covered persons; and (4) confidential supervision information or personal information, including information relating to individuals that is derived from such information or from consumer complaints. This information may include, without limitation, reports of examinations and associated documentation regarding compliance with consumer financial law; documents assessing the current and past safety and soundness/risk management of a covered person or service provider; reports of consumer complaints; and correspondence relating to any category of information discussed above and actions taken to remedy deficiencies in these areas.</P>
          <P>Information contained in the Non-depository Supervision Database is collected from a variety of sources, including, without limitation: (1) The individuals who own, control, or work for covered persons or service providers; (2) existing databases maintained by other federal and state regulatory associations, law enforcement agencies, and related entities; (3) third-parties with relevant information about covered persons or service providers; and (4) information generated by CFPB employees. Whenever practicable, the CFPB will collect information about an individual directly from that individual.</P>
          <HD SOURCE="HD2">Authority for maintenance of the system:</HD>
          <P>Public Law 111-203, Title X, Section 1011, 1012, 1021, 1024, codified at 12 U.S.C. 5491, 5492, 5511, 5514.<SU>1</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>1</SU>Section 1066 of the Act grants the Secretary of the Treasury interim authority to perform certain functions of the CFPB. Pursuant to that authority, Treasury published rules on the Disclosure of Records and Information within 12 CFR Chapter X. This SORN is published pursuant to those rules and the Privacy Act.</P>
          </FTNT>
          <HD SOURCE="HD2">Purpose(s):</HD>
          <P>The information in the system is being collected to enable the CFPB to carry out its responsibilities with respect to non-depository covered persons and service providers, including the coordination and conduct of examinations, supervisory evaluations and analyses, enforcement actions, actions in federal court, and coordination with other financial regulatory agencies. The information collected in this system will also support the conduct of investigations or could be used as evidence by the CFPB or other supervisory or law enforcement agencies. This may result in criminal referrals, referral to the Federal Reserve Office of the Inspector General, or the initiation of administrative or federal court actions. This system will track and store examination and inspection documents created during the performance of the CFPB's statutory duties. This system also will enable the CFPB to monitor and coordinate regular examinations and required reports, supervisory evaluations and analyses, and enforcement actions internally and with other federal and state regulators.</P>
          <HD SOURCE="HD2">Routine uses of records maintained in the system, including categories of users and the purposes of such uses:</HD>
          <P>These records may be disclosed, consistent with the CFPB Disclosure of Records and Information Rules promulgated in the title of the CFR to:</P>
          <P>(1) Appropriate agencies, entities, and persons when: (a) the CFPB suspects or has confirmed that the security or confidentiality of information in the system of records has been compromised; (b) the CFPB has determined that, as a result of the suspected or confirmed compromise, there is a risk of harm to economic or property interests, identity theft or fraud, or harm to the security or integrity of this system or other systems or programs (whether maintained by the CFPB or another agency or entity) that rely upon the compromised information; and (c) the disclosure made to such agencies, entities, and persons is reasonably necessary to assist in connection with the CFPB's efforts to respond to the suspected or confirmed compromise and prevent, minimize, or remedy such harm;</P>
          <P>(2) Another federal or state agency to: (a) permit a decision as to access, amendment or correction of records to be made in consultation with or by that agency; or (b) verify the identity of an individual or the accuracy of information submitted by an individual who has requested access to or amendment or correction of records;</P>
          <P>(3) The Office of the President in response to an inquiry from that office made at the request of the subject of a record or a third party on that person's behalf;</P>
          <P>(4) Congressional offices in response to an inquiry made at the request of the individual to whom the record pertains;</P>
          <P>(5) Contractors, agents, or other authorized individuals performing work on a contract, service, cooperative agreement, job, or other activity on behalf of the CFPB or Federal Government and who have a need to access the information in the performance of their duties or activities;</P>
          <P>(6) Any authorized agency or component of the Department of Treasury, the Department of Justice, the Federal Reserve System, the Federal Deposit Insurance Corporation or other law enforcement authorities including disclosure by such authorities:</P>
          <P>(a) To the extent relevant and necessary in connection with litigation in proceedings before a court or other adjudicative body, where (i) the United States is a party to or has an interest in the litigation, including where the agency, or an agency component, or an agency official or employee in his or her official capacity, or an individual agency official or employee whom the Department of Justice or the Bureau has agreed to represent, is or may likely become a party, and (ii) the litigation is likely to affect the agency or any component thereof; or</P>
          <P>(b) To outside experts or consultants when considered appropriate by CFPB staff to assist in the conduct of agency matters;</P>
          <P>(7) The U.S. Department of Justice (“DOJ”) for its use in providing legal advice to the CFPB or in representing the CFPB in a proceeding before a court, adjudicative body, or other administrative body, where the use of such information by the DOJ is deemed by the CFPB to be relevant and necessary to the advice or proceeding, and in the case of a proceeding, such proceeding names as a party in interest:</P>
          <P>(a) The CFPB;</P>
          <P>(b) Any employee of the CFPB in his or her official capacity;</P>
          <P>(c) Any employee of the CFPB in his or her individual capacity where DOJ or the CFPB has agreed to represent the employee; or</P>
          <P>(d) The United States, where the CFPB determines that litigation is likely to affect the CFPB or any of its components;</P>
          <P>(8) A grand jury pursuant either to a federal or state grand jury subpoena, or to a prosecution request that such record be released for the purpose of its introduction to a grand jury, where the subpoena or request has been specifically approved by a court. In those cases where the Federal Government is not a party to the proceeding, records may be disclosed if a subpoena has been signed by a judge;</P>

          <P>(9) A court, magistrate, or administrative tribunal in the course of<PRTPAGE P="45763"/>an administrative proceeding or judicial proceeding, including disclosures to opposing counsel or witnesses (including expert witnesses) in the course of discovery or other pre-hearing exchanges of information, litigation, or settlement negotiations, where relevant or potentially relevant to a proceeding, or in connection with criminal law proceedings;</P>
          <P>(10) Appropriate agencies, entities, and persons, including but not limited to potential expert witnesses or witnesses in the course of investigations, to the extent necessary to secure information relevant to the investigation;</P>
          <P>(11) Appropriate federal, state, local, foreign, tribal, or self-regulatory organizations or agencies responsible for investigating, prosecuting, enforcing, implementing, issuing, or carrying out a statute, rule, regulation, order, policy, or license if the information may be relevant to a potential violation of civil or criminal law, rule, regulation, order, policy or license; and</P>
          <P>(12) An entity or person that is the subject of supervision or enforcement activities including examinations, investigations, administrative proceedings, and litigation, and the attorney or non-attorney representative for that entity or person.</P>
          <HD SOURCE="HD2">Policies and practices for storing, retrieving, accessing, retaining, and dispensing of records in the system:</HD>
          <HD SOURCE="HD2">Storage:</HD>
          <P>Paper and electronic records.</P>
          <HD SOURCE="HD2">Retrievability:</HD>
          <P>Records are retrievable by a variety of fields including, but not limited to, the individual's name, complaint/inquiry case number, address, account number, transaction number, phone number, date of birth, or by some combination thereof.</P>
          <HD SOURCE="HD2">Safeguards:</HD>
          <P>Access to electronic records is restricted to authorized personnel who have been issued non-transferable access codes and passwords. Other records are maintained in locked file cabinets or rooms with access limited to those personnel whose official duties require access.</P>
          <HD SOURCE="HD2">Retention and disposal:</HD>
          <P>The CFPB will maintain computer and paper records indefinitely until the National Archives and Records Administration approves the CFPB's records disposition schedule.</P>
          <HD SOURCE="HD2">System manager(s) and address:</HD>
          <P>Consumer Financial Protection Bureau, Assistant Director of Nonbank Supervision,1801 L Street, NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Notification procedure:</HD>
          <P>Individuals seeking notification and access to any record contained in this system of records, or seeking to contest its content, may inquire in writing in accordance with instructions appearing in Title 12, Chapter 10 of the CFR, “Disclosure of Records and Information.” Address such requests to: Chief Privacy Officer, Bureau of Consumer Financial Protection, 1801 L St., NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Record access procedures:</HD>
          <P>See “Notification Procedures” above.</P>
          <HD SOURCE="HD2">Contesting record procedures:</HD>
          <P>See “Notification Procedures” above.</P>
          <HD SOURCE="HD2">Record source categories:</HD>
          <P>Information in this system is obtained from covered persons subject to the CFPB's authority, and current, former, and prospective consumers who are or have been customers or prospective customers of covered persons, and others with information relevant to the enforcement of federal consumer financial laws.</P>
          <HD SOURCE="HD2">Exemptions claimed for the system:</HD>
          <P>Portions of the records in this system are complied for law enforcement purposes and are exempt from disclosure under the CFPB's Privacy Act regulations and 5 U.S.C. 552a(k)(2). Federal criminal law enforcement investigatory reports maintained as part of this system may be the subject of exemptions imposed by the originating agency pursuant to 5 U.S.C. 552a(j)(2).</P>
        </PRIACT>
        
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19427 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4810-25-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">BUREAU OF CONSUMER FINANCIAL PROTECTION</AGENCY>
        <SUBJECT>Privacy Act of 1974, as Amended</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Bureau of Consumer Financial Protection.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of Proposed Privacy Act System of Records.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>In accordance with the Privacy Act of 1974, as amended, the Bureau of Consumer Financial Protection, hereinto referred to as the Consumer Financial Protection Bureau (“CFPB”) or the “Bureau” gives notice of the establishment of a Privacy Act System of Records.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments must be received no later than August 31, 2011. The new system of records will be effective September 12, 2011 unless the comments received result in a contrary determination.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may submit comments, identified by Docket No. CFPB-2011-0015, by any of the following methods:</P>
          <P>•<E T="03">Electronic: http://www.regulations.gov.</E>Follow the instructions for submitting comments.</P>
          <P>•<E T="03">Mail or Hand Delivery/Courier in Lieu of Mail:</E>Claire Stapleton, Chief Privacy Officer, Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036.</P>

          <P>All submissions must include the agency name and docket number or Regulatory Information Number (RIN) for this notice. In general all comments received will be posted without change to<E T="03">http://www.regulations.gov.</E>In addition, comments will be available for public inspection and copying at 1801 L St., NW., Washington, DC 20036, on official business days between the hours of 10 a.m. and 5 p.m. Eastern Time. You can make an appointment to inspect comments by telephoning (202) 435-7220. All comments, including attachments and other supporting materials, will become part of the public record and subject to public disclosure. You should submit only information that you wish to make available publicly.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Claire Stapleton, Chief Privacy Officer Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036, (202) 435-7220.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>The Dodd-Frank Wall Street Reform and Consumer Protection Act (“Act”), Public Law No. 111-203, Title X, established the CFPB to administer and enforce Federal consumer financial protection law. The CFPB will maintain the records covered by this notice.</P>
        <P>The new system of records described in this notice, CFPB.007—Directory Database, will provide the CFPB with a single, agency-wide repository of identifying and registration information concerning entities offering or providing, or materially assisting in the offering or provision of, consumer financial products or services. By ensuring the use of consistent information across the agency, the Directory Database will enable the CFPB to carry out its supervisory, enforcement, and regulatory authorities in an efficient and effective manner. A description of the new system of records follows this Notice.</P>

        <P>The report of a new system of records has been submitted to the Committee on Oversight and Government Reform of the House of Representatives, the Committee on Homeland Security and<PRTPAGE P="45764"/>Governmental Affairs of the Senate, and the Office of Management and Budget, pursuant to Appendix I to OMB Circular A-130, “Federal Agency Responsibilities for Maintaining Records About Individuals,” dated November 30, 2000, and the Privacy Act, 5 U.S.C. 552a(r).</P>
        <P>The system of records entitled, “CFPB.007—Directory Database” is published in its entirety below.</P>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>Claire Stapleton,</NAME>
          <TITLE>Chief Privacy Officer.</TITLE>
        </SIG>
        <PRIACT>
          <HD SOURCE="HD1">CFPB.007</HD>
          <HD SOURCE="HD2">System Name:</HD>
          <P>CFPB Directory Database.</P>
          <HD SOURCE="HD2">System Location:</HD>
          <P>Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Categories of individuals covered by the system:</HD>
          <P>Individuals covered by this system are: (1) Individuals who directly, indirectly, or acting through or concert with one or more other individuals, own or control an entity offering or providing, or materially assisting in the offering or provision of, consumer financial products or services (collectively, “covered persons” and “service providers”); (2) current and former directors, officers, employees, shareholders, agents, and independent contractors of such entities; (3) other related persons, as necessary, including without limitation, persons who have personal financial arrangements with covered persons, representatives or counsel of covered persons or related persons; and (4) individuals who provide information on covered persons or entities such as employees of state attorneys general offices. Information contained in the Directory Database is subject to the Privacy Act only to the extent that it concerns individuals; information pertaining to corporations and other business entities and aggregate, non-identifiable information is not subject to the Privacy Act.</P>
          <HD SOURCE="HD2">Categories of records in the system:</HD>
          <P>Records maintained in this system may contain, without limitation, the following types of personally identifiable information: name, address, e-mail address, phone number, social security number, alien registration number, passport number, driver's license or state identification number, or other unique number used to establish identity of the owner or controlling person, employment status, age, gender, ethnicity, and date of birth. Additionally, records may contain information relating to the business activities and transactions of covered persons and entities and their associated persons. Other information may include without limitation: name, location, charter number, charter type, and date of last examination of each entity and the types of financial products offered by each organization.</P>
          <P>Information contained in the Directory Database will be collected from a variety of sources, including, without limitation: (1) The individuals who own, control, or work for covered persons or service providers; (2) existing databases maintained by other Federal and state regulatory associations, agencies, and related entities; (3) third-parties with relevant information about covered persons or services providers; and (4) information generated by CFPB employees. Whenever practicable, the CFPB will collect information about an individual directly from that individual.</P>
          <HD SOURCE="HD2">Authority for maintenance of the system:</HD>
          <P>Pub. L. No. 111-203, Title X, Sections 1011, 1012, 1021, codified at 12 U.S.C. 5491, 5492, 5511.<SU>1</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>1</SU>Section 1066 of the Act grants the Secretary of the Treasury interim authority to perform certain functions of the CFPB. Pursuant to that authority, Treasury published rules on the Disclosure of Records and Information within 12 CFR Chapter X. This SORN is published pursuant to those rules and the Privacy Act.</P>
          </FTNT>
          <HD SOURCE="HD2">Purpose(s):</HD>
          <P>The information in the system is being collected to create an agency-wide repository of identifying and registration information concerning entities and their affiliates offering or providing, or materially assisting in the offering or provision of, consumer financial products or services. By ensuring the use of consistent information across the agency, the Directory Database will enable the CFPB to carry out its supervisory, enforcement, and regulatory authorities in an efficient and effective manner.</P>
          <HD SOURCE="HD2">Routine uses of records maintained in the system, including categories of users and the purposes of such uses:</HD>
          <P>These records may be disclosed, consistent with the CFPB Disclosure of Records and Information Rules promulgated in the title of the CFR to:</P>
          <P>(1) Appropriate agencies, entities, and persons when: (a) The CFPB suspects or has confirmed that the security or confidentiality of information in the system of records has been compromised; (b) the CFPB has determined that, as a result of the suspected or confirmed compromise, there is a risk of harm to economic or property interests, identity theft or fraud, or harm to the security or integrity of this system or other systems or programs (whether maintained by the CFPB or another agency or entity) that rely upon the compromised information; and (c) the disclosure made to such agencies, entities, and persons is reasonably necessary to assist in connection with the CFPB's efforts to respond to the suspected or confirmed compromise and prevent, minimize, or remedy such harm;</P>
          <P>(2) Another Federal or state agency to: (a) Permit a decision as to access, amendment or correction of records to be made in consultation with or by that agency; or (b) verify the identity of an individual or the accuracy of information submitted by an individual who has requested access to, or amendment or correction of records;</P>
          <P>(3) The Office of the President in response to an inquiry from that office made at the request of the subject of a record or a third party on that person's behalf;</P>
          <P>(4) Congressional offices in response to an inquiry made at the request of the individual to whom the record pertains;</P>
          <P>(5) Contractors, agents, or other authorized individuals performing work on a contract, service, cooperative agreement, job, or other activity on behalf of the CFPB or Federal Government and who have a need to access the information in the performance of their duties or activities;</P>
          <P>(6) Any authorized agency or component of the Department of Treasury, the Department of Justice, the Federal Reserve System, the Federal Deposit Insurance Corporation or other law enforcement authorities including disclosure by such authorities:</P>
          <P>(a) To the extent relevant and necessary in connection with litigation in proceedings before a court or other adjudicative body, where (i) the United States is a party to or has an interest in the litigation, including where the agency, or an agency component, or an agency official or employee in his or her official capacity, or an individual agency official or employee whom the Department of Justice or the Bureau has agreed to represent, is or may likely become a party, and (ii) the litigation is likely to affect the agency or any component thereof; or</P>
          <P>(b) To outside experts or consultants when considered appropriate by CFPB staff to assist in the conduct of agency matters;</P>

          <P>(7) The U.S. Department of Justice (“DOJ”) for its use in providing legal advice to the CFPB or in representing the CFPB in a proceeding before a court,<PRTPAGE P="45765"/>adjudicative body, or other administrative body, where the use of such information by the DOJ is deemed by the CFPB to be relevant and necessary to the advice or proceeding, and in the case of a proceeding, such proceeding names as a party in interest:</P>
          <P>(a) The CFPB;</P>
          <P>(b) Any employee of the CFPB in his or her official capacity;</P>
          <P>(c) Any employee of the CFPB in his or her individual capacity where DOJ or the CFPB has agreed to represent the employee; or</P>
          <P>(d) The United States, where the CFPB determines that litigation is likely to affect the CFPB or any of its components;</P>
          <P>(8) A court, magistrate, or administrative tribunal in the course of an administrative proceeding or judicial proceeding, including disclosures to opposing counsel or witnesses (including expert witnesses) in the course of discovery or other pre-hearing exchanges of information, litigation, or settlement negotiations, where relevant or potentially relevant to a proceeding, or in connection with criminal law proceedings;</P>
          <P>(9) Appropriate agencies, entities, and persons, including but not limited to potential expert witnesses or witnesses in the course of investigations, to the extent necessary to secure information relevant to the investigation; and</P>
          <P>(10) Appropriate Federal, state, local, foreign, tribal, or self-regulatory organizations or agencies responsible for investigating, prosecuting, enforcing, implementing, issuing, or carrying out a statute, rule, regulation, order, policy, or license if the information may be relevant to a potential violation of civil or criminal law, rule, regulation, order, policy or license.</P>
          <HD SOURCE="HD2">Policies and practices for storing, retrieving, accessing, retaining, and dispensing of records in the system:</HD>
          <HD SOURCE="HD2">Storage:</HD>
          <P>Paper and electronic records.</P>
          <HD SOURCE="HD2">Retrievability:</HD>
          <P>Records are retrievable by a variety of fields including without limitation the individual's name, social security number, passport number, driver's license or state identification number, or other unique number used to establish identity of the owner or controlling person, address, account number, phone number, or by some combination thereof.</P>
          <HD SOURCE="HD2">Safeguards:</HD>
          <P>Access to electronic records is restricted to authorized personnel who have been issued non-transferrable access codes and passwords. Other records are maintained in locked file cabinets or rooms with access limited to those personnel whose official duties require access.</P>
          <HD SOURCE="HD2">Retention and disposal:</HD>
          <P>The CFPB will maintain computer and paper records indefinitely until the National Archives and Records Administration approves the CFPB's records disposition schedule.</P>
          <HD SOURCE="HD2">System manager(s) and address:</HD>
          <P>Consumer Financial Protection Bureau, Chief Technology Officer, 1801 L Street, NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Notification procedure:</HD>
          <P>Individuals seeking notification and access to any record contained in this system of records, or seeking to contest its content, may inquire in writing in accordance with instructions appearing in Title 12, Chapter 10 of the CFR, “Disclosure of Records and Information.” Address such requests to: Chief Privacy Officer, Bureau of Consumer Financial Protection, 1801 L St., NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Record access procedures:</HD>
          <P>See “Notification Procedures” above.</P>
          <HD SOURCE="HD2">Contesting record procedures:</HD>
          <P>See “Notification Procedures” above.</P>
          <HD SOURCE="HD2">Record source categories:</HD>
          <P>Information in this system is obtained from entities offering or providing consumer financial products or services.</P>
          <HD SOURCE="HD2">Exemptions claimed for the system:</HD>
          <P>None.</P>
          
        </PRIACT>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19425 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4810-25-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">BUREAU OF CONSUMER FINANCIAL PROTECTION</AGENCY>
        <SUBJECT>Privacy Act of 1974, as Amended</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Bureau of Consumer Financial Protection.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of Proposed Privacy Act System of Records.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>In accordance with the Privacy Act of 1974, as amended, the Bureau of Consumer Financial Protection, hereinto referred to as the Consumer Financial Protection Bureau (“CFPB”) or the “Bureau” gives notice of the establishment of a Privacy Act System of Records.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments must be received no later than August 31, 2011. The new system of records will be effective September 12, 2011 unless the comments received result in a contrary determination.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may submit comments, identified by Docket No. CFPB-2011-0011, by any of the following methods:</P>
          <P>•<E T="03">Electronic:</E>
            <E T="03">http://www.regulations.gov</E>. Follow the instructions for submitting comments.</P>
          <P>•<E T="03">Mail or Hand Delivery/Courier in Lieu of Mail:</E>Claire Stapleton, Chief Privacy Officer, Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036. All submissions must include the agency name and docket number or Regulatory Information Number (RIN) for this notice. In general all comments received will be posted without change to<E T="03">http://www.regulations.gov.</E>In addition, comments will be available for public inspection and copying at 1801 L St., NW., Washington, DC 20036, on official business days between the hours of 10 a.m. and 5 p.m. Eastern Time. You can make an appointment to inspect comments by telephoning (202) 435-7220. All comments, including attachments and other supporting materials, will become part of the public record and subject to public disclosure. You should submit only information that you wish to make available publicly.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Claire Stapleton, Chief Privacy Officer, Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036, (202) 435-7220.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>The Dodd-Frank Wall Street Reform and Consumer Protection Act (“Act”), Public Law No. 111-203, Title X, established the CFPB to administer and enforce Federal consumer financial protection law. The CFPB will maintain the records covered by this notice.</P>
        <P>The new system of records described in this notice, CFPB.002—Depository Institution Supervision Database, will be used to enable the CFPB to carry out its responsibilities with respect to certain banks, savings associations, credit unions, and their affiliates and service providers, including the coordination and conduct of examinations, supervisory evaluations and analyses, and enforcement actions. The system will also allow the CFPB to coordinate with other financial regulatory agencies. A description of the new system of records follows this Notice.</P>

        <P>The report of a new system of records has been submitted to the Committee on Oversight and Government Reform of the House of Representatives, the Committee on Homeland Security and Governmental Affairs of the Senate, and<PRTPAGE P="45766"/>the Office of Management and Budget, pursuant to Appendix I to OMB Circular A-130, “Federal Agency Responsibilities for Maintaining Records About Individuals,” dated November 30, 2000, and the Privacy Act, 5 U.S.C. 552a(r).</P>
        <P>The system of records entitled, “CFPB.002—Depository Institution Supervision Database” is published in its entirety below.</P>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>Claire Stapleton,</NAME>
          <TITLE>Chief Privacy Officer.</TITLE>
        </SIG>
        <PRIACT>
          <HD SOURCE="HD1">CFPB.002</HD>
          <HD SOURCE="HD2">System Name:</HD>
          <P>CFPB Depository Institution Supervision Database.</P>
          <HD SOURCE="HD2">System Location:</HD>
          <P>Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Categories of individuals covered by the system:</HD>
          <P>Individuals covered by this system are: (1) Individuals who themselves are, and current and former directors, officers, employees, agents, shareholders, and independent contractors of banks, savings associations, or credit unions; (2) Current and former consumers who are or have been in the past serviced by banks, savings associations, or credit unions subject to the supervision of the CFPB; and (3) CFPB employees assigned to supervise banks, savings associations, or credit unions. Information collected regarding consumer products and services is subject to the Privacy Act only to the extent that it concerns individuals; information pertaining to corporations and other business entities is not subject to the Privacy Act.</P>
          <HD SOURCE="HD2">Categories of records in the system:</HD>
          <P>Records in the system may contain information provided by a supervised institution, by individuals who are or have been serviced by a supervised institution, or other government authorities, to the CFPB in the exercise of CFPB's responsibilities and used to assess an institution's compliance with various statutory and regulatory obligations. This may include: (1) Personally identifiable information from customers of banks, savings associations, or credit unions, including without limitation, name, account numbers, address, phone number, e-mail address, and date of birth; (2) contact information of officials of institutions such as members of the Board of Directors, Audit Committee Chair, Chief Executive Officer, Chief Compliance Officer, Internal Auditor, and Independent Auditor including, without limitation, name, address, phone number and e-mail address; (3) information about CFPB employees assigned to depository institution supervision tasks, including, without limitation, name, phone number, e-mail address, address, and other employment information; and (4) Confidential Supervision Information or Personal Information, including information relating to individuals that is derived from Confidential Supervisory Information or from consumer complaints. This information may include, without limitation, reports of examinations and associated documentation regarding compliance with consumer financial protection laws; documents assessing the current and past safety and soundness/risk management of a covered person or service provider; reports of consumer complaints; and correspondence relating to any category of information discussed above and actions taken to remedy deficiencies in these areas.</P>
          <P>Information contained in the Depository Institution Supervision Database is collected from a variety of sources, including, without limitation: (1) The individuals who own, control, or work for covered persons or service providers; (2) existing databases maintained by other Federal and state regulatory associations, law enforcement agencies, and related entities; (3) third parties with relevant information about covered persons or services providers; and (4) information generated by CFPB employees or about CFPB employees assigned supervisory tasks. Whenever practicable, the CFPB will collect information about an individual directly from that individual.</P>
          <HD SOURCE="HD2">Authority for maintenance of the system:</HD>
          <P>Public Law 111-203, Title X, Section 1011, 1012, 1021, 1025, codified at 12 U.S.C. 5491, 5492, 5511, 5515.<SU>1</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>1</SU>Section 1066 of the Act grants the Secretary of the Treasury interim authority to perform certain functions of the CFPB. Pursuant to that authority, Treasury published rules on the Disclosure of Records and Information within 12 CFR Chapter X. This SORN is published pursuant to those rules and the Privacy Act.</P>
          </FTNT>
          <HD SOURCE="HD2">Purpose(s):</HD>
          <P>The information in the system is being collected to enable the CFPB to carry out its responsibilities with respect to banks, savings associations, credit unions, and their affiliates and service providers, including the coordination and conduct of examinations, supervisory evaluations and analyses, enforcement actions, actions in Federal court, and coordination with other financial regulatory agencies. The information collected in this system will also support the conduct of investigations or be used as evidence by the CFPB or other supervisory or law enforcement agencies. This may result in criminal referrals, referral to the Federal Reserve Office of Inspector General, or the initiation of administrative or Federal court actions. This system will track and store examination and inspection documents created during the performance of the CFPB's statutory duties. This system also will enable the CFPB to monitor and coordinate regular examinations and required reports, supervisory evaluations and analyses, and enforcement actions internally and with other Federal and state regulators.</P>
          <HD SOURCE="HD2">Routine uses of records maintained in the system, including categories of users and the purposes of such uses:</HD>
          <P>These records may be disclosed, consistent with the CFPB Disclosure of Records and Information Rules promulgated in the title of the CFR to:</P>
          <P>(1) Appropriate agencies, entities, and persons when: (a) The CFPB suspects or has confirmed that the security or confidentiality of information in the system of records has been compromised; (b) the CFPB has determined that, as a result of the suspected or confirmed compromise, there is a risk of harm to economic or property interests, identity theft or fraud, or harm to the security or integrity of this system or other systems or programs (whether maintained by the CFPB or another agency or entity) that rely upon the compromised information; and (c) the disclosure made to such agencies, entities, and persons is reasonably necessary to assist in connection with the CFPB's efforts to respond to the suspected or confirmed compromise and prevent, minimize, or remedy such harm;</P>
          <P>(2) Another Federal or state agency to: (a) Permit a decision as to access, amendment or correction of records to be made in consultation with or by that agency; or (b) verify the identity of an individual or the accuracy of information submitted by an individual who has requested access to, or amendment or correction of records;</P>
          <P>(3) The Office of the President in response to an inquiry from that office made at the request of the subject of a record or a third party on that person's behalf;</P>

          <P>(4) Congressional offices in response to an inquiry made at the request of the individual to whom the record pertains;<PRTPAGE P="45767"/>
          </P>
          <P>(5) Contractors, agents, or other authorized individuals performing work on a contract, service, cooperative agreement, job, or other activity on behalf of the CFPB or Federal Government and who have a need to access the information in the performance of their duties or activities;</P>
          <P>(6) Any authorized agency or component of the Department of Treasury, the Department of Justice, the Federal Reserve System, the Federal Deposit Insurance Corporation or other law enforcement authorities including disclosure by such authorities:</P>
          <P>(a) To the extent relevant and necessary in connection with litigation in proceedings before a court or other adjudicative body, where (i) The United States is a party to or has an interest in the litigation, including where the agency, or an agency component, or an agency official or employee in his or her official capacity, or an individual agency official or employee whom the Department of Justice or the Bureau has agreed to represent, is or may likely become a party, and (ii) the litigation is likely to affect the agency or any component thereof; or</P>
          <P>(b) To outside experts or consultants when considered appropriate by CFPB staff to assist in the conduct of agency matters;</P>
          <P>(7) The U.S. Department of Justice (“DOJ”) for its use in providing legal advice to the CFPB or in representing the CFPB in a proceeding before a court, adjudicative body, or other administrative body, where the use of such information by the DOJ is deemed by the CFPB to be relevant and necessary to the advice or proceeding, and in the case of a proceeding, such proceeding names as a party in interest:</P>
          <P>(a) The CFPB;</P>
          <P>(b) Any employee of the CFPB in his or her official capacity;</P>
          <P>(c) Any employee of the CFPB in his or her individual capacity where DOJ or the CFPB has agreed to represent the employee; or</P>
          <P>(d) The United States, where the CFPB determines that litigation is likely to affect the CFPB or any of its components;</P>
          <P>(8) A grand jury pursuant either to a Federal or state grand jury subpoena, or to a prosecution request that such record be released for the purpose of its introduction to a grand jury, where the subpoena or request has been specifically approved by a court. In those cases where the Federal Government is not a party to the proceeding, records may be disclosed if a subpoena has been signed by a judge;</P>
          <P>(9) A court, magistrate, or administrative tribunal in the course of an administrative proceeding or judicial proceeding, including disclosures to opposing counsel or witnesses (including expert witnesses) in the course of discovery or other pre-hearing exchanges of information, litigation, or settlement negotiations, where relevant or potentially relevant to a proceeding, or in connection with criminal law proceedings;</P>
          <P>(10) Appropriate agencies, entities, and persons, including but not limited to potential expert witnesses or witnesses in the course of investigations, to the extent necessary to secure information relevant to the investigation;</P>
          <P>(11) Appropriate Federal, state, local, foreign, tribal, or self-regulatory organizations or agencies responsible for investigating, prosecuting, enforcing, implementing, issuing, or carrying out a statute, rule, regulation, order, policy, or license if the information may be relevant to a potential violation of civil or criminal law, rule, regulation, order, policy or license; and</P>
          <P>(12) An entity or person that is the subject of supervision or enforcement activities including examinations, investigations, administrative proceedings, and litigation, and the attorney or non-attorney representative for that entity or person.</P>
          <HD SOURCE="HD2">Policies and practices for storing, retrieving, accessing, retaining, and dispensing of records in the system:</HD>
          <HD SOURCE="HD2">Storage:</HD>
          <P>Paper and electronic records.</P>
          <HD SOURCE="HD2">Retrievability:</HD>
          <P>Records are retrievable by a variety of fields including without limitation the individual's name, complaint/inquiry case number, address, account number, transaction number, phone number, date of birth, or by some combination thereof.</P>
          <HD SOURCE="HD2">Safeguards:</HD>
          <P>Access to electronic records is restricted to authorized personnel who have been issued non-transferrable access codes and passwords. Other records are maintained in locked file cabinets or rooms with access limited to those personnel whose official duties require access.</P>
          <HD SOURCE="HD2">Retention and disposal:</HD>
          <P>The CFPB will maintain computer and paper records indefinitely until the National Archives and Records Administration approves the CFPB's records disposition schedule.</P>
          <HD SOURCE="HD2">System manager(s) and address:</HD>
          <P>Consumer Financial Protection Bureau, Assistant Director of Large Bank Supervision, 1801 L Street, NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Notification procedure:</HD>
          <P>Individuals seeking notification and access to any record contained in this system of records, or seeking to contest its content, may inquire in writing in accordance with instructions appearing in Title 12, Chapter 10 of the CFR, “Disclosure of Records and Information.” Address such requests to: Chief Privacy Officer, Bureau of Consumer Financial Protection, 1801 L St., NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Record access procedures:</HD>
          <P>See “Notification Procedures” above.</P>
          <HD SOURCE="HD2">Contesting record procedures:</HD>
          <P>See “Notification Procedures” above.</P>
          <HD SOURCE="HD2">Record source categories:</HD>
          <P>Information in this system is obtained from banks, savings associations, credit unions, and their affiliates and service providers, persons subject to the CFPB's authority, and current, former, and prospective consumers who are or have been customers or prospective customers of covered persons, and others with information relevant to the enforcement of Federal consumer financial laws.</P>
          <HD SOURCE="HD2">Exemptions claimed for the system:</HD>
          <P>Portions of the records in this system are complied for law enforcement purposes and are exempt from disclosure under CFPB's Privacy Act regulations and 5 U.S.C. 552a(k)(2). Federal criminal law enforcement investigatory reports maintained as part of this system may be the subject of exemptions imposed by the originating agency pursuant to 5 U.S.C. 552a(j)(2).</P>
        </PRIACT>
        
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19428 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4810-25-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">BUREAU OF CONSUMER FINANCIAL PROTECTION</AGENCY>
        <SUBJECT>Privacy Act of 1974, as Amended</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Bureau of Consumer Financial Protection.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of Proposed Privacy Act System of Records.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>In accordance with the Privacy Act of 1974, as amended, the Bureau of Consumer Financial Protection, hereinto referred to as the Consumer Financial Protection Bureau (“CFPB”) gives notice of the establishment of a Privacy Act System of Records.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>

          <P>Comments must be received no later than August 31, 2011. The new<PRTPAGE P="45768"/>database will be effective September 12, 2011, unless the comments received result in a contrary determination.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may submit comments, identified by Docket No. CFPB-2011-0010, by any of the following methods:</P>
          <P>•<E T="03">Electronic: http://www.regulations.gov.</E>Follow the instructions for submitting comments.</P>
          <P>•<E T="03">Mail or Hand Delivery/Courier in Lieu of Mail:</E>Claire Stapleton, Chief Privacy Officer, Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036.</P>

          <P>All submissions must include the agency name and docket number or Regulatory Information Number (RIN) for this notice. In general all comments received will be posted without change to<E T="03">http://www.regulations.gov.</E>In addition, comments will be available for public inspection and copying at 1801 L St., NW., Washington, DC 20036, on official business days between the hours of 10 a.m. and 5 p.m. Eastern Time. You can make an appointment to inspect comments by telephoning (202) 435-7220. All comments, including attachments and other supporting materials, will become part of the public record and subject to public disclosure. You should submit only information that you wish to make available publicly.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Claire Stapleton, Chief Privacy Officer, Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036, (202) 435-7220.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>The Dodd-Frank Wall Street Reform and Consumer Protection Act (“Act”), Public Law No. 111-203, Title X, established the CFPB to administer and enforce Federal consumer financial protection law. The CFPB will maintain the records covered by this notice.</P>
        <P>The new system of records described in this notice, CFPB.001—Freedom of Information Act (“FOIA”)/Privacy Act (“PA”) System will be used by the CFPB to collect, process, log, track, and respond to all FOIA and/or PA related requests. It will be used to appropriately document information about the requestors' and/or entities' requests and the CFPB staff assigned to process, consider, and respond to the requests. The system will serve as the central repository for submitted requests for access to, correction of, and/or amendment to CFPB records. It will document the accounting of disclosures of records under FOIA and/or PA to include the status of requested records; responses to the requests; process responsive records; process FOIA-related calculations and fees; and proactively address frequently-requested records publicly available under the CFPB rules of practice and FOIA/PA requirements. It will also be used to maintain records, document the consideration and disposition of these requests for annual reporting, statistical analysis, fee management, and recordkeeping purposes. A description of the new system of records follows this Notice.</P>
        <P>The report of the new system of records has been submitted to the Committee on Oversight and Government Reform of the House of Representatives, the Committee on Homeland Security and Governmental Affairs of the Senate, and the Office of Management and Budget, pursuant to Appendix I to OMB Circular A-130, “Federal Agency Responsibilities for Maintaining Records About Individuals,” dated November 30, 2000, and the Privacy Act, 5 U.S.C. 552a(r).</P>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>Claire Stapleton,</NAME>
          <TITLE>Chief Privacy Officer.</TITLE>
        </SIG>
        <PRIACT>
          <HD SOURCE="HD1">CFPB.001</HD>
          <HD SOURCE="HD2">System Name:</HD>
          <P>CFPB Freedom of Information Act/Privacy Act System.</P>
          <HD SOURCE="HD2">System Location:</HD>
          <P>Consumer Financial Protection Bureau, 1801 L Street, NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Categories of individuals covered by the system:</HD>
          <P>Individuals covered by this system are persons who cite the Freedom of Information Act or Privacy Act to request access to records or whose information requests are treated as FOIA requests. Other individuals covered include CFPB staff assigned to process such requests, and employees who may have responsive records or are mentioned in such records. FOIA requests are subject to the PA only to the extent that they concern individuals; information pertaining to corporations and other business entities and organizations are not subject to the PA.</P>
          <HD SOURCE="HD2">Categories of records in the system:</HD>
          <P>Records in the system may contain: (1) Correspondence with the requester including initial requests and appeals; (2) documents generated or compiled during the search and processing of the request; (3) fee schedules, cost calculations, and accessed cost for disclosed FOIA records; (4) documents and memoranda supporting the decision made in response to the request, referrals, and copies of records provided or withheld; (5) CFPB staff assigned to process, consider, and respond to requests and, where a request has been referred to another agency with equities in a responsive document, information about the individual handling the request on behalf of that agency; (6) information identifying the entity that is subject to the requests or appeals; (7) requester information, including name, address, phone number, email address; FOIA tracking number, phone number, fax number, or some combination thereof; and (8) for access requests under the Privacy Act, identifying information regarding both the party who is making the written request or appeal, and the individual on whose behalf such written requests or appeals are made, including name, social security number (SSNs may be submitted with documentation or as proof of identification), address, phone number, email address, FOIA number, phone number, fax number, or some combination thereof.</P>
          <HD SOURCE="HD2">Authority for maintenance of the system:</HD>
          <P>Pub. L. 111-203, Title X, Sections 1011, 1012, 1021, codified at 12 U.S.C. 5491, 5492, 5511; The Freedom of Information Act of 1996, as amended 5 U.S.C. 552; Privacy Act of 1974, as amended 5 U.S.C. 552a.<SU>1</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>1</SU>Section 1066 of the Act grants the Secretary of the Treasury interim authority to perform certain functions of the CFPB. Pursuant to that authority, Treasury published rules on the Disclosure of Records and Information within 12 CFR Chapter X. This SORN is published pursuant to those rules and the Privacy Act.</P>
          </FTNT>
          <HD SOURCE="HD2">Purpose:</HD>
          <P>The information in the system is being collected to enable the CFPB to carry out its responsibilities under the FOIA and the PA, including enabling staff to receive, track, and respond to requests. This requires maintaining documentation gathered during the consideration and disposition process, administering annual reporting requirements, managing FOIA-related fees and calculations, and delivering responsive records.</P>
          <HD SOURCE="HD2">Routine uses of records maintained in the system, including categories of users and the purposes of such uses:</HD>
          <P>These records may be disclosed, consistent with the CFPB Disclosure of Records and Information Rules promulgated in the title of the CFR to:</P>

          <P>(1) Appropriate agencies, entities, and persons when: (a) The CFPB suspects or has confirmed that the security or confidentiality of information in the system of records has been compromised; (b) the CFPB has determined that, as a result of the<PRTPAGE P="45769"/>suspected or confirmed compromise, there is a risk of harm to economic or property interests, identity theft or fraud, or harm to the security or integrity of this system or other systems or programs (whether maintained by the CFPB or another agency or entity) that rely upon the compromised information; and (c) the disclosure made to such agencies, entities, and persons is reasonably necessary to assist in connection with the CFPB's efforts to respond to the suspected or confirmed compromise and prevent, minimize, or remedy such harm;</P>
          <P>(2) Another Federal or state agency to: (a) Permit a decision as to access, amendment, or correction of records to be made in consultation with or by that agency; or (b) verify the identity of an individual or the accuracy of information submitted by an individual who has requested access to or amendment or correction of records;</P>
          <P>(3) To the Office of the President in response to an inquiry from that office made at the request of the subject of a record or a third party on that person's behalf;</P>
          <P>(4) Congressional offices in response to an inquiry made at the request of the individual to whom the record pertains;</P>
          <P>(5) Contractors, agents, or other authorized individuals performing work on a contract, service, cooperative agreement, job, or other activity on behalf of the CFPB or Federal Government and who have a need to access the information in the performance of their duties or activities;</P>
          <P>(6) Any authorized agency or component of the Department of Treasury, the Department of Justice, the Federal Reserve System, the Federal Deposit Insurance Corporation or other law enforcement authorities including disclosure by such authorities:</P>
          <P>(a) To the extent relevant and necessary in connection with litigation in proceedings before a court or other adjudicative body, where (i) The United States is a party to or has an interest in the litigation, including where the agency, or an agency component, or an agency official or employee in his or her official capacity, or an individual agency official or employee whom the Department of Justice or the Bureau has agreed to represent, is or may likely become a party, and (ii) the litigation is likely to affect the agency or any component thereof; or</P>
          <P>(b) To outside experts or consultants when considered appropriate by CFPB staff to assist in the conduct of agency matters;</P>
          <P>(7) The U.S. Department of Justice (“DOJ”) for its use in providing legal advice to the CFPB or in representing the CFPB in a proceeding before a court, adjudicative body, or other administrative body, where the use of such information by the DOJ is deemed by the CFPB to be relevant and necessary to the advice or proceeding, and in the case of a proceeding, such proceeding names as a party in interest:</P>
          <P>(a) The CFPB;</P>
          <P>(b) Any employee of the CFPB in his or her official capacity;</P>
          <P>(c) Any employee of the CFPB in his or her individual capacity where DOJ or the CFPB has agreed to represent the employee; or</P>
          <P>(d) The United States, where the CFPB determines that litigation is likely to affect the CFPB or any of its components;</P>
          <P>(8) A court, magistrate, or administrative tribunal in the course of an administrative proceeding or judicial proceeding, including disclosures to opposing counsel or witnesses (including expert witnesses) in the course of discovery or other pre-hearing exchanges of information, litigation, or settlement negotiations, where relevant or potentially relevant to a proceeding, or in connection with criminal law proceedings; and</P>
          <P>(9) Appropriate agencies, entities, and persons, including but not limited to potential expert witnesses or witnesses in the course of investigations, to the extent necessary to secure information relevant to the investigation.</P>
          <HD SOURCE="HD2">Policies and practices for storing, retrieving, accessing, retaining, and dispensing of records in the system:</HD>
          <HD SOURCE="HD2">Storage:</HD>
          <P>Paper and electronic records.</P>
          <HD SOURCE="HD2">Retrievability:</HD>
          <P>Records are retrievable by a variety of fields including, but not limited to, the requester's name, the subject matter of request, requestor's organization, FOIA tracking number, and staff member assigned to process the request. Records may also be searched by the address, phone number, fax number, e-mail address of the requesting party, and subject matter of the request, or by some combination thereof.</P>
          <HD SOURCE="HD2">Safeguards:</HD>
          <P>Access to electronic records is restricted to authorized personnel who have been issued non-transferrable access codes and passwords. Other records are maintained in locked file cabinets or rooms with access limited to those personnel whose official duties require access.</P>
          <HD SOURCE="HD2">Retention and disposal:</HD>
          <P>Computer and paper records will be maintained in accordance with published National Archives and Records Administration Disposition Schedule, Transmittal No. 22, General Records Schedule 14, Information Service Records.</P>
          <HD SOURCE="HD2">System manager(s) and address:</HD>
          <P>Consumer Financial Protection Bureau, Chief FOIA Officer, 1801 L Street, NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Notification procedure:</HD>
          <P>Individuals seeking notification and access to any record contained in this system of records, or seeking to contest its content, may inquire in writing in accordance with instructions appearing in Title 12, Chapter 10 of the CFR, “Disclosure of Records and Information.” Address such requests to: Chief Privacy Officer, Bureau of Consumer Financial Protection, 1801 L St., NW., Washington, DC 20036.</P>
          <HD SOURCE="HD2">Record access procedures:</HD>
          <P>See “Notification Procedure” above.</P>
          <HD SOURCE="HD2">Contesting record procedures:</HD>
          <P>See “Notification Procedure” above.</P>
          <HD SOURCE="HD2">Record source categories:</HD>
          <P>Information in this system covers individuals about whom records are maintained; agency staff assigned to help process, consider, and respond to the request, including any appeals; entities filing requests or appeals on behalf of the requestor; other governmental authorities; and entities that are the subjects of the request or appeals.</P>
          <HD SOURCE="HD2">Exemptions claimed for the system:</HD>
          <P>None.</P>
        </PRIACT>
        
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19429 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4810-25-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF AGRICULTURE</AGENCY>
        <SUBAGY>Animal and Plant Health Inspection Service</SUBAGY>
        <DEPDOC>[Docket No. APHIS-2011-0069]</DEPDOC>
        <SUBJECT>Notice of Request for Extension of Approval of an Information Collection; Pork and Poultry Products From Mexico Transiting the United States</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Animal and Plant Health Inspection Service, USDA.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Extension of approval of an information collection; comment request.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>In accordance with the Paperwork Reduction Act of 1995, this notice announces the Animal and Plant Health Inspection Service's intention to request an extension of approval of an<PRTPAGE P="45770"/>information collection associated with regulations for pork and poultry products from Mexico transiting the United States.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>We will consider all comments that we receive on or before September 30, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may submit comments by either of the following methods:</P>
          <P>•<E T="03">Federal eRulemaking Portal:</E>Go to<E T="03">http://www.regulations.gov/#!documentDetail;D=APHIS-2011-0069-0001.</E>
          </P>
          <P>•<E T="03">Postal Mail/Commercial Delivery:</E>Send your comment to Docket No. APHIS-2011-0069, Regulatory Analysis and Development, PPD, APHIS, Station 3A-03.8, 4700 River Road Unit 118, Riverdale, MD 20737-1238.</P>

          <P>Supporting documents and any comments we receive on this docket may be viewed at<E T="03">http://www.regulations.gov/#!docketDetail;D=APHIS-20110069</E>or in our reading room, which is located in room 1141 of the USDA South Building, 14th Street and Independence Avenue, SW., Washington, DC. Normal reading room hours are 8 a.m. to 4:30 p.m., Monday through Friday, except holidays. To be sure someone is there to help you, please call (202) 690-2817 before coming.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>For information on pork and poultry products from Mexico transiting the United States, contact Dr. Lynette Williams-McDuffie, Staff Veterinarian, Technical Trade Services—Products, National Center for Import and Export, VS, APHIS, 4700 River Road Unit 40, Riverdale, MD 20737; (301) 734-0677. For copies of more detailed information on the information collection, contact Mrs. Celeste Sickles, APHIS' Information Collection Coordinator, at (301) 851-2908.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>
          <E T="03">Title</E>: Pork and Poultry Products From Mexico Transiting the United States.</P>
        <P>
          <E T="03">OMB Number</E>: 0579-0145.</P>
        <P>
          <E T="03">Type of Request</E>: Extension of approval of an information collection.</P>
        <P>
          <E T="03">Abstract</E>: Under the Animal Health Protection Act (7 U.S.C. 8301<E T="03">et seq</E>.), the Animal and Plant Health Inspection Service (APHIS) of the United States Department of Agriculture is authorized, among other things, to prohibit the importation and interstate movement of animals and animal products to prevent the introduction into and dissemination within the United States of animal diseases and pests. To fulfill this mission, APHIS regulates the importation of animals and animal products into the United States. The regulations are contained in title 9, chapter 1, subchapter D, parts 91 through 99, of the Code of Federal Regulations.</P>
        <P>The regulations in 9 CFR 94.15 allow fresh (chilled or frozen) pork and pork products and poultry carcasses, parts, and products (except eggs and egg products) that are not eligible to enter into the United States to transit the United States from specified States in Mexico, via land ports, for export to another country.</P>
        <P>The regulations set out conditions for the transit movements that protect against the introduction of classical swine fever or exotic Newcastle disease into the United States. These conditions involve the use of information collection activities, including the completion of an import permit application, the placement of serially numbered seals on product containers, and the forwarding of a pre-arrival notification to U.S. port personnel.</P>
        <P>We are asking the Office of Management and Budget (OMB) to approve our use of these information collection activities for an additional 3 years.</P>
        <P>The purpose of this notice is to solicit comments from the public (as well as affected agencies) concerning our information collection. These comments will help us:</P>
        <P>(1) Evaluate whether the collection of information is necessary for the proper performance of the functions of the Agency, including whether the information will have practical utility;</P>
        <P>(2) Evaluate the accuracy of our estimate of the burden of the collection of information, including the validity of the methodology and assumptions used;</P>
        <P>(3) Enhance the quality, utility, and clarity of the information to be collected; and</P>
        <P>(4) Minimize the burden of the collection of information on those who are to respond, through use, as appropriate, of automated, electronic, mechanical, and other collection technologies; e.g., permitting electronic submission of responses.</P>
        <P>
          <E T="03">Estimate of burden</E>: The public reporting burden for this collection of information is estimated to average 0.91667 hours per response.</P>
        <P>
          <E T="03">Respondents</E>: U.S. importers of pork and poultry products from Mexico to the United States and Federal animal health authorities in Mexico.</P>
        <P>
          <E T="03">Estimated annual number of respondents</E>: 29.</P>
        <P>
          <E T="03">Estimated annual number of responses per respondent</E>: 1.2413793.</P>
        <P>
          <E T="03">Estimated annual number of responses</E>: 36.</P>
        <P>
          <E T="03">Estimated total annual burden on respondents</E>: 33 hours. (Due to averaging, the total annual burden hours may not equal the product of the annual number of responses multiplied by the reporting burden per response.)</P>
        <P>All responses to this notice will be summarized and included in the request for OMB approval. All comments will also become a matter of public record.</P>
        <SIG>
          <DATED>Done in Washington, DC, this 26th day of July 2011.</DATED>
          <NAME>Kevin Shea,</NAME>
          <TITLE>Acting Administrator, Animal and Plant Health Inspection Service.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19363 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3410-34-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF AGRICULTURE</AGENCY>
        <SUBAGY>Forest Service</SUBAGY>
        <SUBJECT>Tehama County Resource Advisory Committee</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Forest Service, USDA.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of meeting.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Tehama County Resource Advisory Committee (RAC) will meet in Red Bluff, California. The committee is authorized under the Secure Rural Schools and Community Self-Determination Act (Pub. L. 110-343) (the Act) and operates in compliance with the Federal Advisory Committee Act. The purpose of the committee is to improve collaborative relationships and to provide advice and recommendations to the Forest Service concerning projects and funding consistent with the title II of the Act. The meeting is open to the public. The purpose of the meeting is to discuss the future of the committee and to closeout business for 2011.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>The meeting will be held on August 25, 2011 from 9 a.m. and end at approximately 12 noon.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>The meeting will be held at the Lincoln Street School, Pine Room, 1135 Lincoln Street, Red Bluff, CA. Written comments may be submitted as described under<E T="02">SUPPLEMENTARY INFORMATION</E>.</P>
          <P>All comments, including names and addresses when provided, are placed in the record and are available for public inspection and copying. The public may inspect comments received at 825 N. Humboldt Ave., Willows, CA 95988. Please call ahead to (530) 934-1269 to facilitate entry into the building to view comments.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Randy Jero, Committee Coordinator, USDA, Mendocino National Forest, Grindstone Ranger District, 825 N. Humboldt Ave., Willows, CA 95988. (530) 934-1269; e-mail<E T="03">rjero@fs.fed.us.</E>
            <PRTPAGE P="45771"/>
          </P>

          <P>Individuals who use telecommunication devices for the deaf (TDD) may call the Federal Information Relay Service (FIRS) at 1-800-877-8339 between 8 a.m. and 8 p.m., Eastern Standard Time, Monday through Friday. Requests for reasonable accomodation for access to the facility or procedings may be made by contacting the person listed<E T="02">FOR FURTHER INFORMATION</E>.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>

        <P>The meeting is open to the public. Agenda items to be covered include: (1) Introductions, (2) Approval of Minutes, (3) Public Comment, (4) RAC Administrative Updates, (5) General Discussion, (6) Next Agenda. Anyone who would like to bring related matters to the attention of the committee may file written statements with the committee staff before or after the meeting. The agenda will include time for people to make oral statements of three minutes or less. Individuals wishing to make an oral statement should request in writing by August 22, 2011 to be scheduled on the agenda. Written comments and requests for time for oral comments must be sent to Randy Jero, Committee Coordinator, USDA, Mendocino National Forest, Grindstone Ranger District, 825 N. Humboldt Ave., Willows, CA 95988 or by e-mail to<E T="03">rjero@fs.fed.us</E>or via facsimile to 530-934-1212.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Eduardo Olmedo,</NAME>
          <TITLE>District Ranger.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19366 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3410-11-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF AGRICULTURE</AGENCY>
        <SUBAGY>Forest Service</SUBAGY>
        <SUBJECT>Glenn/Colusa County Resource Advisory Committee</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Forest Service, USDA.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of meeting.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Glenn/Colusa County Resource Advisory Committee (RAC) will meet in Willows, California. The committee is authorized under the Secure Rural Schools and Community Self-Determination Act (Pub. L 110-343) (the Act) and operates in compliance with the Federal Advisory Committee Act. The purpose of the committee is to improve collaborative relationships and to provide advice and recommendations to the Forest Service concerning projects and funding consistent with the title II of the Act. The meeting is open to the public. The purpose of the meeting is to present projects and vote on projects.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>The meeting will be held on August 22, 2011 from 1:30 p.m. and end at approximately 4:30 p.m.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>The meeting will be held in the field during the monitoring trip beginning at the Mendocino NF Supervisor's Office, 825 North Humboldt Ave., Willows, CA. Written comments may be submitted as described under Supplementary Information.</P>
          <P>All comments, including names and addresses when provided, are placed in the record and are available for public inspection and copying. The public may inspect comments received at 825 N. Humboldt Ave., Willows, CA 95988. Please call ahead to (530) 934-1269 to facilitate entry into the building to view comments.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Randy Jero, Committee Coordinator, USDA, Mendocino National Forest, Grindstone Ranger District, 825 N. Humboldt Ave, Willows, CA 95988. (530) 934-1269; e-mail<E T="03">rjero@fs.fed.us.</E>
          </P>

          <P>Individuals who use telecommunication devices for the deaf (TDD) may call the Federal Information Relay Service (FIRS) at 1-800-877-8339 between 8 a.m. and 8 p.m., Eastern Standard Time, Monday through Friday. Requests for reasonable accomodation for access to the facility or procedings may be made by contacting the person listed<E T="02">FOR FURTHER INFORMATION</E>.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>

        <P>The meeting is open to the public. Agenda items to be covered include: (1) Introductions, (2) Approval of Minutes, (3) RAC Administrative Updates, (4) Public Comment, (5) Project Presentations, (6) Vote on New Project Proposals, (7) General Discussion, (8) Adjourn. Anyone who would like to bring related matters to the attention of the committee may file written statements with the committee staff before or after the meeting. The agenda will include time for people to make oral statements of three minutes or less. Individuals wishing to make an oral statement should request in writing by August 15, 2011 to be scheduled on the agenda. Written comments and requests for time for oral comments must be sent to Randy Jero, Committee Coordinator, USDA, Mendocino National Forest, Grindstone Ranger District, 825 N. Humboldt Ave, Willows, CA 95988 or by e-mail to<E T="03">rjero@fs.fed.us</E>or via facsimile to 530-934-1212.</P>
        <SIG>
          <DATED>Dated: July 25, 2011.</DATED>
          <NAME>Eduardo Olmedo,</NAME>
          <TITLE>District Ranger.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19368 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3410-11-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF AGRICULTURE</AGENCY>
        <SUBAGY>Forest Service</SUBAGY>
        <SUBJECT>Plumas County Resource Advisory Committee (RAC)</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Forest Service, USDA.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of Meeting.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Plumas County Resource Advisory Committee (RAC) will hold a meeting on August 19, 2011 in Quincy, CA. This meeting was rescheduled from July 8, 2011. The purpose of the meeting is to review applications for Cycle 11 funding and select projects to be recommended to the Plumas National Forest Supervisor for calendar year 2012 funding consideration. The funding is made available under Title II provisions of the Secure Rural Schools and Community Self-Determination Act of 2000.</P>
          <P>
            <E T="03">Date &amp; Address:</E>The meeting will take place from 9-1:30 at the Mineral Building-Plumas/Sierra County Fairgrounds, 208 Fairgrounds Road, Quincy, CA.</P>
        </SUM>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>(or for special needs): Lee Anne Schramel Taylor, Forest Coordinator, USDA, Plumas National Forest, P.O. Box 11500/159 Lawrence Street, Quincy, CA 95971; (530) 283-7850; or by E-MAIL<E T="03">eataylor@fs.fed.us.</E>Other RAC information may be obtained at<E T="03">http://www.fs.fed.us/srs</E>.</P>
          <SIG>
            <DATED>Dated: July 25, 2011.</DATED>
            <NAME>Laurence Crabtree,</NAME>
            <TITLE>Deputy Forest Supervisor.</TITLE>
          </SIG>
        </FURINF>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19354 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>Foreign-Trade Zones Board</SUBAGY>
        <DEPDOC>[Docket 50-2011]</DEPDOC>
        <SUBJECT>Foreign-Trade Zone 26—Atlanta, GA; Application for Manufacturing Authority; Makita Corporation of America (Hand-Held Power Tool and Gasoline/Electric-Powered Garden Product Manufacturing); Buford, GA</SUBJECT>

        <P>An application has been submitted to the Foreign-Trade Zones Board (the Board) by Georgia Foreign-Trade Zone, Inc., grantee of FTZ 26, requesting manufacturing authority on behalf of Makita Corporation of America (Makita), located in Buford, Georgia. The application was submitted pursuant to the provisions of the Foreign-Trade Zones Act, as amended (19 U.S.C. 81a-81u), and the regulations of the Board<PRTPAGE P="45772"/>(15 CFR part 400). It was formally filed on July 26, 2011.</P>
        <P>The Makita facility (300 employees, 75 acres, up to 3 million units per year capacity) is located within Site 20 of FTZ 26. The facility is used for the manufacture of hand-held power tools and gasoline/electric-powered garden products. Components and materials sourced from abroad (representing 64% of the value of the finished product) include: batteries; armatures; tool bags; driver, hammer and angle drills; chargers; flashlights; gears, housings, clutches and gear shafts; radios; grips, thumb screws, knobs and handles; wrenches; switch units; power cords; flanges; screws; nuts and bolts; rubber rings, sleeves, grommets and plates; screws; ball bearings; battery covers and lenses; grease, lubricants and additives; felt rings; lock springs; lead wire assemblies; needle cages; drill bits; socket wrenches; styrene polymers; polyamides; resins; caulk; glues and adhesives; vinyl cases; vinyl tubes; labels; plastic bags; water tanks; plastic grips; rubber knobs and handles; plastic cases; dust bag assemblies; tool belts; grinding wheels; tapping screws; lock lever connectors; cotters and cotter pins; lock and spring pins; cup washers; set plates; safety wires; pipe clamps; copper nozzles; aluminum miter scales; caps, switch covers, throttle levers and pipe ends; safety guard assemblies; bearing boxes; steel balls; bearing housings and bushings; pulleys; joints; DC motors; heat sinks and spacers; coils; electrical outlets; electrical switches; switch levers; safety goggles; lighting assemblies; and ribbon (duty rate ranges from duty free to 20%). The application also requests authority to include a broad range of inputs and finished hand-held power tools and gasoline/electric-powered garden products that Makita may produce under FTZ procedures in the future. New major activity involving these inputs/products would require review by the FTZ Board.</P>
        <P>FTZ procedures could exempt Makita from customs duty payments on the foreign components used in export production. The company anticipates that some 47 percent of the plant's shipments will be exported. On its domestic sales, Makita would be able to choose for the foreign inputs noted above the duty rates during customs entry procedures that apply to: Engine blowers; pneumatic compressors; pneumatic tools; table, slide and compound miter saws; drills and drill kits; drill and saw kits; drill, grinder, hammer, sander, planer, router and screw driver kits; gasoline/electric-powered brush cutters; and hedge trimmers (duty free—4.5%). FTZ designation would further allow Makita to realize logistical benefits through the use of weekly customs entry procedures. Customs duties also could possibly be deferred or reduced on foreign status production equipment. The request indicates that the savings from FTZ procedures would help improve the plant's international competitiveness.</P>
        <P>In accordance with the Board's regulations, Christopher Kemp of the FTZ Staff is designated examiner to evaluate and analyze the facts and information presented in the application and case record and to report findings and recommendations to the Board.</P>
        <P>Public comment is invited from interested parties. Submissions (original and 3 copies) shall be addressed to the Board's Executive Secretary at the address below. The closing period for their receipt is September 30, 2011. Rebuttal comments in response to material submitted during the foregoing period may be submitted during the subsequent 15-day period to October 17, 2011.</P>

        <P>A copy of the application will be available for public inspection at the Office of the Executive Secretary, Foreign-Trade Zones Board, Room 2111, U.S. Department of Commerce, 1401 Constitution Avenue, NW., Washington, DC 20230-0002, and in the “Reading Room” section of the Board's Web site, which is accessible via<E T="03">http://www.trade.gov/ftz.</E>
        </P>
        <P>For further information, contact Christopher Kemp at<E T="03">Christopher.Kemp@trade.gov</E>or (202) 482-0862.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Andrew McGilvray,</NAME>
          <TITLE>Executive Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19405 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3510-DS-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>Foreign-Trade Zones Board</SUBAGY>
        <DEPDOC>[Docket 49-2011]</DEPDOC>
        <SUBJECT>Proposed Foreign-Trade Zone—Brunswick, ME; Application</SUBJECT>
        <P>An application has been submitted to the Foreign-Trade Zones Board (the Board) by the Midcoast Regional Redevelopment Authority to establish a general-purpose foreign-trade zone at a site in Brunswick, Maine, adjacent to the Portland CBP port of entry. The application was submitted pursuant to the provisions of the Foreign-Trade Zones Act, as amended (19 U.S.C. 81a-81u), and the regulations of the Board (15 CFR part 400). It was formally filed on July 26, 2011. The applicant is authorized to make the proposal under Maine Statute Title 5, Section 13083-Q.</P>
        <P>The proposed zone would be the second general-purpose zone for the Portland CBP port of entry. The existing zone is as follows: FTZ 263, Auburn, Maine (Grantee: Lewiston-Auburn Economic Growth Council, Board Order 1354, 10/01/04).</P>
        <P>The proposed zone would consist of one site in Brunswick, Maine: Proposed Site 1 (394 acres)—within the 3,200-acre Brunswick Landing's Airport complex located at the intersection of Bath Road and Fitch Avenue. The site is owned by the Midcoast Regional Redevelopment Authority.</P>
        <P>The application indicates a need for zone services in the Brunswick, Maine area. Several firms have indicated an interest in using zone procedures for warehousing/distribution activities for a variety of products. Specific manufacturing approvals are not being sought at this time. Such requests would be made to the Board on a case-by-case basis.</P>
        <P>In accordance with the Board's regulations, Kathleen Boyce of the FTZ Staff is designated examiner to evaluate and analyze the facts and information presented in the application and case record and to report findings and recommendations to the Board.</P>
        <P>Public comment is invited from interested parties. Submissions (original and 3 copies) shall be addressed to the Board's Executive Secretary at the address below. The closing period for their receipt is September 30, 2011. Rebuttal comments in response to material submitted during the foregoing period may be submitted during the subsequent 15-day period to October 17, 2011.</P>

        <P>A copy of the application will be available for public inspection at the Office of the Executive Secretary, Foreign-Trade Zones Board, Room 2111, U.S. Department of Commerce, 1401 Constitution Avenue, NW., Washington, DC 20230-0002, and in the “Reading Room” section of the Board's Web site, which is accessible via<E T="03">http://www.trade.gov/ftz.</E>
        </P>
        <P>For further information, contact Kathleen Boyce at<E T="03">Kathleen.Boyce@trade.gov</E>or (202) 482-1346.</P>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>Andrew McGilvray,</NAME>
          <TITLE>Executive Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19404 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <PRTPAGE P="45773"/>
        <AGENCY TYPE="S">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>International Trade Administration</SUBAGY>
        <SUBJECT>Antidumping or Countervailing Duty Order, Finding, or Suspended Investigation; Opportunity To Request Administrative Review</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Import Administration, International Trade Administration, Department of Commerce.</P>
        </AGY>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Sheila E. Forbes, Office of AD/CVD Operations, Customs Unit, Import Administration, International Trade Administration, U.S. Department of Commerce, 14th Street and Constitution Avenue, NW., Washington, DC 20230, telephone: (202) 482-4697.</P>
          <HD SOURCE="HD1">Background</HD>
          <P>Each year during the anniversary month of the publication of an antidumping or countervailing duty order, finding, or suspension of investigation, an interested party, as defined in section 771(9) of the Tariff Act of 1930, as amended (“the Act”), may request, in accordance with section 351.213 of the Department of Commerce (“the Department”) regulations, that the Department conduct an administrative review of that antidumping or countervailing duty order, finding, or suspended investigation.</P>
          <P>All deadlines for the submission of comments or actions by the Department discussed below refer to the number of calendar days from the applicable starting date.</P>
          <HD SOURCE="HD1">Respondent Selection</HD>

          <P>In the event the Department limits the number of respondents for individual examination for administrative reviews initiated pursuant to requests made for the orders identified below, the Department intends to select respondents based on U.S. Customs and Border Protection (“CBP”) data for U.S. imports during the period of review. We intend to release the CBP data under Administrative Protective Order (“APO”) to all parties having an APO within five days of publication of the initiation notice and to make our decision regarding respondent selection within 21 days of publication of the initiation<E T="04">Federal Register</E>notice. Therefore, we encourage all parties interested in commenting on respondent selection to submit their APO application on the date of publication of the initiation notice, or as soon thereafter as possible. The Department invites comments regarding the CBP data and respondent selection within five days of placement of the CBP data on the record of the review.</P>
          <P>In the event the Department decides it is necessary to limit individual examination of respondents and conduct respondent selection under section 777A(c)(2) of the Act:</P>

          <P>In general, the Department has found that determinations concerning whether particular companies should be “collapsed” (<E T="03">i.e.,</E>treated as a single entity for purposes of calculating antidumping duty rates) require a substantial amount of detailed information and analysis, which often require follow-up questions and analysis. Accordingly, the Department will not conduct collapsing analyses at the respondent selection phase of this review and will not collapse companies at the respondent selection phase unless there has been a determination to collapse certain companies in a previous segment of this antidumping proceeding (<E T="03">i.e.,</E>investigation, administrative review, new shipper review or changed circumstances review). For any company subject to this review, if the Department determined, or continued to treat, that company as collapsed with others, the Department will assume that such companies continue to operate in the same manner and will collapse them for respondent selection purposes. Otherwise, the Department will not-collapse companies for purposes of respondent selection. Parties are requested to (a) identify which companies subject to review previously were collapsed, and (b) provide a citation to the proceeding in which they were collapsed. Further, if companies are requested to complete the Quantity and Value Questionnaire for purposes of respondent selection, in general each company must report volume and value data separately for itself. Parties should not include data for any other party, even if they believe they should be treated as a single entity with that other party. If a company was collapsed with another company or companies in the most recently completed segment of this proceeding where the Department considered collapsing that entity, complete quantity and value data for that collapsed entity must be submitted.</P>
          <HD SOURCE="HD1">Deadline for Withdrawal of Request for Administrative Review</HD>
          <P>Pursuant to section 351.213(d)(1) of the Department's regulations, a party that has requested a review may withdraw that request within 90 days of the date of publication of the notice of initiation of the requested review. The regulation provides that the Department may extend this time if it is reasonable to do so. In order to provide parties additional certainty with respect to when the Department will exercise its discretion to extend this 90-day deadline, interested parties are advised that, with regard to reviews requested on the basis of anniversary months on or after August 2011, the Department will not consider extending the 90-day deadline unless the requestor demonstrates that an extraordinary circumstance has prevented it from submitting a timely withdrawal request. Determinations by the Department to extend the 90-day deadline will be made on a case-by-case basis.</P>
          <P>The Department is providing this notice on its Web site, as well as in its “Opportunity to Request Administrative Review” notices, so that interested parties will be aware of the manner in which the Department intends to exercise its discretion in the future.</P>
          <P>
            <E T="03">Opportunity to Request a Review:</E>Not later than the last day of August 2011,<SU>1</SU>
            <FTREF/>interested parties may request administrative review of the following orders, findings, or suspended investigations, with anniversary dates in August for the following periods:</P>
          <FTNT>
            <P>
              <SU>1</SU>Or the next business day, if the deadline falls on a weekend, federal holiday or any other day when the Department is closed.</P>
          </FTNT>
          <GPOTABLE CDEF="s100,15" COLS="2" OPTS="L2,tp0,i1">
            <TTITLE/>
            <BOXHD>
              <CHED H="1"/>
              <CHED H="1">Period of review</CHED>
            </BOXHD>
            <ROW>
              <ENT I="21">
                <E T="02">Antidumping Duty Proceedings</E>
              </ENT>
            </ROW>
            
            <ROW>
              <ENT I="22">Germany:</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Corrosion-Resistant Carbon Steel Flat Products, A-428-815</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Certain Small Diameter Seamless Carbon and Alloy Steel Standard, Line and Pressure Pipe, A-428-820</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Sodium Nitrite, A-428-841</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="01">Italy: Granular Polytetrafluoroethylene Resin, A-475-703</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="22">Japan:</ENT>
            </ROW>
            <ROW>
              <PRTPAGE P="45774"/>
              <ENT I="03">Brass Sheet &amp; Strip, A-588-704</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Granular Polytetrafluoroethylene Resin, A-588-707</ENT>
              <ENT>8/1/10-12/21/10</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Tin Mill Products, A-588-854</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="01">Malaysia: Polyethylene Retail Carrier Bags, A-557-813</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="01">Mexico: Light-Walled Rectangular Pipe and Tube, A-201-836</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="01">Romania: Carbon and Alloy Seamless Standard, Line, and Pressure Pipe (Under 4<FR>1/2</FR>Inches), A-485-805</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="22">South Korea:</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Corrosion-Resistant Carbon Steel Flat Products, A-580-816</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Light-Walled Rectangular Pipe and Tube, A-580-859</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="01">Thailand: Polyethylene Retail Carrier Bags, A-549-821</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="22">The People's Republic of China:</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Certain Tow-Behind Lawn Groomers and Certain Parts Thereof, A-570-939</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Certain Woven Electric Blankets, A-570-951</ENT>
              <ENT>2/3/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Floor Standing Metal-Top Ironing Tables and Parts Thereof, A-570-888</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Laminated Woven Sacks, A-570-916</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Light-Walled Rectangular Pipe and Tube, A-570-914</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Petroleum Wax Candles, A-570-504</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Polyethylene Retail Carrier Bags, A-570-886</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Sodium Nitrite, A-570-925</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Steel Nails, A-570-909</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Sulfanilic Acid, A-570-815</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Tetrahydrofurfuryl Alcohol, A-570-887</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            <ROW>
              <ENT I="01">Vietnam: Frozen Fish Fillets, A-552-801</ENT>
              <ENT>8/1/10-7/31/11</ENT>
            </ROW>
            
            <ROW>
              <ENT I="21">
                <E T="02">Countervailing Duty Proceedings</E>
              </ENT>
            </ROW>
            
            <ROW>
              <ENT I="22">South Korea:</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Corrosion-Resistant Carbon Steel Flat Products, C-580-818</ENT>
              <ENT>1/1/10-12/31/10</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Stainless Steel Sheet and Strip in Coils, C-580-835</ENT>
              <ENT>1/1/10-12/31/10</ENT>
            </ROW>
            <ROW>
              <ENT I="22">The People's Republic of China:</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Certain Tow-Behind Lawn Groomers and Certain Parts Thereof, C-570-940</ENT>
              <ENT>1/1/10-12/31/10</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Laminated Woven Sacks, C-570-917</ENT>
              <ENT>1/1/10-12/31/10</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Light-Walled Rectangular Pipe and Tube, C-570-915</ENT>
              <ENT>1/1/10-12/31/10</ENT>
            </ROW>
            <ROW>
              <ENT I="03">Sodium Nitrite, C-570-926</ENT>
              <ENT>1/1/10-12/31/10</ENT>
            </ROW>
          </GPOTABLE>
          <HD SOURCE="HD1">Suspension Agreements</HD>
          <P>None.</P>
          <P>In accordance with section 351.213(b), an interested party as defined by section 771(9) of the Act may request in writing that the Secretary conduct an administrative review. For both antidumping and countervailing duty reviews, the interested party must specify the individual producers or exporters covered by an antidumping finding or an antidumping or countervailing duty order or suspension agreement for which it is requesting a review. In addition, a domestic interested party or an interested party described in section 771(9)(B) of the Act must state why it desires the Secretary to review those particular producers or exporters.<SU>2</SU>
            <FTREF/>If the interested party intends for the Secretary to review sales of merchandise by an exporter (or a producer if that producer also exports merchandise from other suppliers) which were produced in more than one country of origin and each country of origin is subject to a separate order, then the interested party must state specifically, on an order-by-order basis, which exporter(s) the request is intended to cover.</P>
          <FTNT>
            <P>
              <SU>2</SU>If the review request involves a non-market economy and the parties subject to the review request do not qualify for separate rates, all other exporters of subject merchandise from the non-market economy country who do not have a separate rate will be covered by the review as part of the single entity of which the named firms are a part.</P>
          </FTNT>
          <P>Please note that, for any party the Department was unable to locate in prior segments, the Department will not accept a request for an administrative review of that party absent new information as to the party's location. Moreover, if the interested party who files a request for review is unable to locate the producer or exporter for which it requested the review, the interested party must provide an explanation of the attempts it made to locate the producer or exporter at the same time it files its request for review, in order for the Secretary to determine if the interested party's attempts were reasonable, pursuant to section 351.303(f)(3)(ii) of the Department's regulations.</P>
          <P>As explained in<E T="03">Antidumping and Countervailing Duty Proceedings: Assessment of Antidumping Duties,</E>68 FR 23954 (May 6, 2003), the Department has clarified its practice with respect to the collection of final antidumping duties on imports of merchandise where intermediate firms are involved. The public should be aware of this clarification in determining whether to request an administrative review of merchandise subject to antidumping findings and orders.<E T="03">See also</E>the Import Administration Web site at<E T="03">http://ia.ita.doc.gov.</E>
          </P>

          <P>If the request is filed prior to August 5, 2011, six copies of the request should be submitted to the Assistant Secretary for Import Administration, International Trade Administration, Room 1870, U.S. Department of Commerce, 14th Street and Constitution Avenue, NW., Washington, DC 20230. For requests filed on or after August 5, 2011, the request must be filed electronically in Import Administration's Antidumping and Countervailing Duty Centralized Electronic Service System (“IA ACCESS”) on the IA ACCESS Web site at<E T="03">http://iaaccess.trade.gov. See</E>
            <E T="03">Antidumping and Countervailing Duty Proceedings: Electronic Filing Procedures; Administrative Protective Order Procedures,</E>76 FR 39263 (July 6, 2011). Further, in accordance with section 351.303(f)(l)(i) of the regulations, a copy of each request must be served on the petitioner and each exporter or producer specified in the request.</P>
          <P>The Department will publish in the<E T="04">Federal Register</E>a notice of “Initiation of Administrative Review of Antidumping or Countervailing Duty Order, Finding, or Suspended Investigation” for requests received by the last day of August 2011. If the<PRTPAGE P="45775"/>Department does not receive, by the last day of August 2011, a request for review of entries covered by an order, finding, or suspended investigation listed in this notice and for the period identified above, the Department will instruct CBP to assess antidumping or countervailing duties on those entries at a rate equal to the cash deposit of (or bond for) estimated antidumping or countervailing duties required on those entries at the time of entry, or withdrawal from warehouse, for consumption and to continue to collect the cash deposit previously ordered.</P>
          <P>For the first administrative review of any order, there will be no assessment of antidumping or countervailing duties on entries of subject merchandise entered, or withdrawn from warehouse, for consumption during the relevant provisional-measures “gap” period, of the order, if such a gap period is applicable to the period of review.</P>
          <P>This notice is not required by statute but is published as a service to the international trading community.</P>
          <SIG>
            <DATED>Dated: July 27, 2011.</DATED>
            <NAME>Christian Marsh,</NAME>
            <TITLE>Deputy Assistant Secretary for Antidumping and Countervailing Duty Operations.</TITLE>
          </SIG>
        </FURINF>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19411 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3510-DS-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>International Trade Administration</SUBAGY>
        <SUBJECT>Antidumping or Countervailing Duty Order, Finding, or Suspended Investigation; Advance Notification of Sunset Reviews</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Import Administration, International Trade Administration, Department of Commerce.</P>
        </AGY>
        <HD SOURCE="HD1">Background</HD>
        <P>Every five years, pursuant to section 751(c) of the Tariff Act of 1930, as amended (“the Act”), the Department of Commerce (“the Department”) and the International Trade Commission automatically initiate and conduct a review to determine whether revocation of a countervailing or antidumping duty order or termination of an investigation suspended under section 704 or 734 of the Act would be likely to lead to continuation or recurrence of dumping or a countervailable subsidy (as the case may be) and of material injury.</P>
        <HD SOURCE="HD1">Upcoming Sunset Reviews for September 2011</HD>
        <P>The following Sunset Reviews are scheduled for initiation in September 2011 and will appear in that month's Notice of Initiation of Five-Year Sunset Reviews.</P>
        <GPOTABLE CDEF="s150,r40" COLS="2" OPTS="L2,tp0,i1">
          <TTITLE/>
          <BOXHD>
            <CHED H="1">Antidumping duty proceedings</CHED>
            <CHED H="1">Department contact</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Furfuryl Alcohol from the People's Republic of China (A-570-835) (3rd Review)</ENT>
            <ENT>Julia Hancock,  (202) 482-1394.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Fresh Garlic from the People's Republic of China (A-570-831) (3rd Review)</ENT>
            <ENT>Dana Mermelstein, (202) 482-1391.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Ferrovanadium and Nitrided Vanadium from Russia (A-821-807) (3rd Review)</ENT>
            <ENT>David Goldberger, (202) 482-4136.</ENT>
          </ROW>
        </GPOTABLE>
        <HD SOURCE="HD1">Countervailing Duty Proceedings</HD>
        <P>No Sunset Review of countervailing duty orders is scheduled from initiation in September 2011.</P>
        <HD SOURCE="HD1">Suspended Investigations</HD>
        <P>No Sunset Review of suspended investigations is scheduled from initiation in September 2011.</P>

        <P>The Department's procedures for the conduct of Sunset Reviews are set forth in 19 CFR 351.218. Guidance on methodological or analytical issues relevant to the Department's conduct of Sunset Reviews is set forth in the Department's Policy Bulletin 98.3—<E T="03">Policies Regarding the Conduct of Five-year (“Sunset”) Reviews of Antidumping and Countervailing Duty Orders; Policy Bulletin,</E>63 FR 18871 (April 16, 1998). The Notice of Initiation of Five-Year (“Sunset”) Reviews provides further information regarding what is required of all parties to participate in Sunset Reviews.</P>
        <P>Pursuant to 19 CFR 351.103(c), the Department will maintain and make available a service list for these proceedings. To facilitate the timely preparation of the service list(s), it is requested that those seeking recognition as interested parties to a proceeding contact the Department in writing within 10 days of the publication of the Notice of Initiation.</P>
        <P>Please note that if the Department receives a Notice of Intent to Participate from a member of the domestic industry within 15 days of the date of initiation, the review will continue. Thereafter, any interested party wishing to participate in the Sunset Review must provide substantive comments in response to the notice of initiation no later than 30 days after the date of initiation.</P>
        <P>This notice is not required by statute but is published as a service to the international trading community.</P>
        <SIG>
          <DATED>Dated: July 19, 2011.</DATED>
          <NAME>Christian Marsh,</NAME>
          <TITLE>Deputy Assistant Secretary for Antidumping and Countervailing Duty Operations.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19413 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3510-DS-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>International Trade Administration</SUBAGY>
        <DEPDOC>[A-552-802]</DEPDOC>
        <SUBJECT>Fourth New Shipper Review of Certain Frozen Warmwater Shrimp From the Socialist Republic of Vietnam: Final Results of Antidumping Duty New Shipper Review</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Import Administration, International Trade Administration, Department of Commerce.</P>
        </AGY>
        
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>On April 13, 2011, the Department of Commerce (the “Department”) published the preliminary results of the fourth new shipper review (“NSR”) on certain frozen warmwater shrimp (“shrimp”) from the Socialist Republic of Vietnam (“Vietnam”), covering the period of review (“POR”) of February 1, 2010-July 31, 2010.<SU>1</SU>
            <FTREF/>The Department received no comments on its<E T="03">Preliminary Results.</E>
          </P>
          <FTNT>
            <P>
              <SU>1</SU>
              <E T="03">See</E>
              <E T="03">Certain Frozen Warmwater Shrimp from the Socialist Republic of Vietnam: Preliminary Results of Antidumping Duty New Shipper Review,</E>76 FR 20627 (April 13, 2011) (“<E T="03">Preliminary Results</E>”).</P>
          </FTNT>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>
            <E T="03">Effective Date:</E>August 1, 2011.</P>
        </DATES>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Paul Walker, AD/CVD Operations, Import Administration, International Trade Administration, U.S. Department of<PRTPAGE P="45776"/>Commerce, 14th Street and Constitution Avenue, NW., Washington, DC 20230; telephone: (202) 482-0413.</P>
          <HD SOURCE="HD1">Case History</HD>

          <P>The Department invited interested parties to comment on the<E T="03">Preliminary Results.</E>On May 13, 2011, Quoc Viet Seaproducts Processing Trading and Import-Export Co., Ltd. (“Quoc Viet”) submitted a case brief.<SU>2</SU>
            <FTREF/>No other interested party submitted a case brief. On May 16, 2011 Quoc Viet withdrew its case brief.<SU>3</SU>
            <FTREF/>On June 23, 2011 the Department released a letter concerning labor wage rates.<SU>4</SU>
            <FTREF/>On July 7, 2011 Quoc Viet submitted comments on labor wage rates. On July 11, 2011 Quoc Viet withdrew its labor wage rate comments.<SU>5</SU>

            <FTREF/>As a consequence, there are no case briefs, comments or hearing requests since the<E T="03">Preliminary Results</E>on the record of this NSR.</P>
          <FTNT>
            <P>
              <SU>2</SU>
              <E T="03">See</E>Quoc Viet's May 13, 2011 submission.</P>
          </FTNT>
          <FTNT>
            <P>

              <SU>3</SU>According to Quoc Viet, because no other party submitted comments on the final results, and because the issues raised by Quoc Viet in its case brief would have no impact on the<E T="03">Preliminary Determination,</E>which has already established that Quoc Viet is not dumping, Quoc Viet withdrew its case brief.<E T="03">See</E>Quoc Viet's May 16, 2011 submission.</P>
          </FTNT>
          <FTNT>
            <P>
              <SU>4</SU>
              <E T="03">See</E>the Department's letter dated June 23, 2011.</P>
          </FTNT>
          <FTNT>
            <P>

              <SU>5</SU>Quoc Viet reiterated its statements made in its May 16, 2011, submission, that that its comments would have no impact on the<E T="03">Preliminary Results,</E>and thus, withdrew its comments.<E T="03">See</E>Quoc Viet's July 11, 2011 submission.</P>
          </FTNT>
          <HD SOURCE="HD1">Scope of Order</HD>
          <P>The scope of the order includes certain warmwater shrimp and prawns, whether frozen, wild-caught (ocean harvested) or farm-raised (produced by aquaculture), head-on or head-off, shell-on or peeled, tail-on or tail-off,<SU>6</SU>
            <FTREF/>deveined or not deveined, cooked or raw, or otherwise processed in frozen form.</P>
          <FTNT>
            <P>
              <SU>6</SU>“Tails” in this context means the tail fan, which includes the telson and the uropods.</P>
          </FTNT>
          <P>The frozen warmwater shrimp and prawn products included in the scope of this order, regardless of definitions in the Harmonized Tariff Schedule of the United States (“HTS”), are products which are processed from warmwater shrimp and prawns through freezing and which are sold in any count size.</P>

          <P>The products described above may be processed from any species of warmwater shrimp and prawns. Warmwater shrimp and prawns are generally classified in, but are not limited to, the<E T="03">Penaeidae</E>family. Some examples of the farmed and wild-caught warmwater species include, but are not limited to, whiteleg shrimp (<E T="03">Penaeus vannemei</E>), banana prawn (<E T="03">Penaeus merguiensis</E>), fleshy prawn (<E T="03">Penaeus chinensis</E>), giant river prawn (<E T="03">Macrobrachium rosenbergii</E>), giant tiger prawn (<E T="03">Penaeus monodon</E>), redspotted shrimp (<E T="03">Penaeus brasiliensis</E>), southern brown shrimp (<E T="03">Penaeus subtilis</E>), southern pink shrimp (<E T="03">Penaeus notialis</E>), southern rough shrimp (<E T="03">Trachypenaeus curvirostris</E>), southern white shrimp (<E T="03">Penaeus schmitti</E>), blue shrimp (<E T="03">Penaeus stylirostris</E>), western white shrimp (<E T="03">Penaeus occidentalis</E>) and Indian white prawn (<E T="03">Penaeus indicus</E>).</P>
          <P>Frozen shrimp and prawns that are packed with marinade, spices or sauce are included in the scope of this order. In addition, food preparations (including dusted shrimp), which are not “prepared meals,” that contain more than 20 percent by weight of shrimp or prawn are also included in the scope of this order.</P>

          <P>Excluded from the scope are: (1) Breaded shrimp and prawns (HTS subheading 1605.20.1020); (2) shrimp and prawns generally classified in the<E T="03">Pandalidae</E>family and commonly referred to as coldwater shrimp, in any state of processing; (3) fresh shrimp and prawns whether shell-on or peeled (HTS subheadings 0306.23.0020 and 0306.23.0040); (4) shrimp and prawns in prepared meals (HTS subheading 1605.20.0510); (5) dried shrimp and prawns; (6) canned warmwater shrimp and prawns (HTS subheading 1605.20.1040); and (7) certain battered shrimp. Battered shrimp is a shrimp-based product: (1) That is produced from fresh (or thawed-from-frozen) and peeled shrimp; (2) to which a “dusting” layer of rice or wheat flour of at least 95 percent purity has been applied; (3) with the entire surface of the shrimp flesh thoroughly and evenly coated with the flour; (4) with the non-shrimp content of the end product constituting between four and 10 percent of the product's total weight after being dusted, but prior to being frozen; and (5) that is subjected to individually quick frozen (“IQF”) freezing immediately after application of the dusting layer. When dusted in accordance with the definition of dusting above, the battered shrimp product is also coated with a wet viscous layer containing egg and/or milk, and par-fried.</P>
          <P>The products covered by this order are currently classified under the following HTS subheadings: 0306.13.0003, 0306.13.0006, 0306.13.0009, 0306.13.0012, 0306.13.0015, 0306.13.0018, 0306.13.0021, 0306.13.0024, 0306.13.0027, 0306.13.0040, 1605.20.1010 and 1605.20.1030. These HTS subheadings are provided for convenience and for customs purposes only and are not dispositive, but rather the written description of the scope of this order is dispositive.</P>
          <HD SOURCE="HD1">Labor Wage Rate</HD>
          <P>Section 733(c) of the Tariff Act of 1930, as amended (the “Act”), provides that the Department will value the factors of production (“FOP”) in NME cases using the best available information regarding the value of such factors in a market economy (“ME”) country or countries considered to be appropriate by the administering authority. The Act requires that when valuing FOP, the Department utilize, to the extent possible, the prices or costs of factors of production in one or more ME countries that are (1) At a comparable level of economic development and (2) significant producers of comparable merchandise.<SU>7</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>7</SU>
              <E T="03">See</E>section 773(c)(4) of the Act.</P>
          </FTNT>

          <P>Previously, the Department used regression-based wages that captured the worldwide relationship between<E T="03">per capita</E>Gross National Income (“GNI”) and hourly manufacturing wages, pursuant to section 351.408(c)(3) of the Department's regulations, to value the respondent's cost of labor. However, on May 14, 2010 the Court of Appeals for the Federal Circuit (“CAFC”), in<E T="03">Dorbest Ltd.</E>v.<E T="03">United States,</E>604 F.3d 1363, 1372 (Fed. Cir. 2010) (“<E T="03">Dorbest”</E>), invalidated section 351.408(c)(3) of the Department's regulations. As a consequence of the CAFC's ruling in<E T="03">Dorbest,</E>the Department no longer relies on the regression-based wage rate methodology described in its regulations. On February 18, 2011 the Department published a request for public comment on the interim methodology, and the data sources.<SU>8</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>8</SU>
              <E T="03">See Antidumping Methodologies in Proceedings Involving Non-Market Economies: Valuing the Factor of Production: Labor, Request for Comment,</E>76 FR 9544 (Feb. 18, 2011).</P>
          </FTNT>
          <P>On June 21, 2011 the Department revised its methodology for valuing the labor input in NME antidumping proceedings.<SU>9</SU>
            <FTREF/>In<E T="03">Labor Methodologies,</E>the Department determined that the best methodology to value the labor input is to use industry-specific labor rates from the primary surrogate country. Additionally, the Department determined that the best data source for industry-specific labor rates is Chapter 6A: Labor Cost in Manufacturing, from the International Labor Organization (“ILO”)<E T="03">Yearbook of Labor Statistics</E>(“<E T="03">Yearbook”</E>).</P>
          <FTNT>
            <P>
              <SU>9</SU>
              <E T="03">See Antidumping Methodologies in Proceedings Involving Non-Market Economies: Valuing the Factor of Production: Labor,</E>76 FR 36092 (June 21, 2011) (“<E T="03">Labor Methodologies”</E>).</P>
          </FTNT>

          <P>As Bangladesh does not report labor data to the ILO, we are unable to use<PRTPAGE P="45777"/>Chapter 6 data to value Quoc Viet's labor wage rate for these final results. However, the record does contain a labor value for shrimp processing in Bangladesh, published by the Bangladesh Bureau of Statistics. The Department finds this labor value to be the best available information on the record because it is specific to the industry being examined, and is therefore derived from industries that produce comparable merchandise. Because this value is not contemporaneous to the POR, we inflated it using the Consumer Price Index (“CPI”) rate for Bangladesh, as published in the<E T="03">International Financial Statistics</E>of the International Monetary Fund. Thus, for the final results we valued labor using an industry-specific labor rate from the primary surrogate country. The calculated industry-specific wage rate is 16.71 Bangladeshi takas per hour. A more detailed description of the wage rate calculation methodology is provided in the Memorandum to the File, through Scot T. Fullerton, Program Manager, from Paul Walker, Case Analyst, “Fourth New Shipper Review of Certain Frozen Warmwater Shrimp from the Socialist Republic of Vietnam: Surrogate Values for the Final Results,” dated concurrently with this memorandum.</P>

          <P>As stated above, the Department valued Quoc Viet's labor using Bangladeshi government data. Because there is no record evidence as to whether this data contains all costs related to labor, including wages, benefits, housing, training, etc., we have made no adjustments to the surrogate financial ratios for the itemized detail of indirect labor costs, as noted in<E T="03">Labor Methodologies.</E>
          </P>
          <HD SOURCE="HD1">Final Results of Review</HD>
          <P>The Department finds that the following margin exists for Quoc Viet for the period February 1, 2010-July 31, 2010:</P>
          <GPOTABLE CDEF="s50,r50" COLS="2" OPTS="L2,i1">
            <TTITLE>Certain Frozen Warmwater Shrimp From Vietnam</TTITLE>
            <BOXHD>
              <CHED H="1">Manufacturer/Exporter</CHED>
              <CHED H="1">Margin percent</CHED>
            </BOXHD>
            <ROW>
              <ENT I="01">Quoc Viet</ENT>
              <ENT>0.00 (<E T="03">de minimis.</E>)</ENT>
            </ROW>
          </GPOTABLE>
          <HD SOURCE="HD1">Assessment of Antidumping Duties</HD>

          <P>Upon issuance of the final results, the Department will determine, and U.S. Customs and Border Protection (“CBP”) shall assess, antidumping duties on all appropriate entries. The Department intends to issue assessment instructions to CBP 15 days after the date of publication of the final results of review. Pursuant to section 351.212(b)(1) of the Department's regulations, we will calculate importer-specific (or customer-specific)<E T="03">ad valorem</E>duty assessment rates based on the ratio of the total amount of the dumping margins calculated for the examined sales to the total entered value of those same sales. In accordance with section 351.106(c)(2) of the Department's regulations, we will instruct CBP to liquidate, without regard to antidumping duties, all entries of subject merchandise during the POR for which the importer-specific assessment rate is zero or<E T="03">de minimis.</E>
          </P>
          <HD SOURCE="HD1">Cash Deposit Requirements</HD>
          <P>The following cash deposit requirements will be effective upon publication of the final results of this new shipper review for all shipments of subject merchandise by Quoc Viet, entered, or withdrawn from warehouse, for consumption on or after the publication date, as provided by section 751(a)(2)(C) of the Tariff Act of 1930, as amended (the “Act”): (1) For subject merchandise produced and exported by Quoc Viet, the cash deposit rate will be zero; (2) for subject merchandise exported by Quoc Viet, but not manufactured by Quoc Viet, the cash deposit rate will continue to be the Vietnam-wide rate of 25.76 percent; and (3) for subject merchandise manufactured by Quoc Viet, but exported by any party other than Quoc Viet, the cash deposit rate will be the rate applicable to the exporter. These cash deposit requirements will remain in effect until further notice.</P>
          <HD SOURCE="HD1">Notification to Importers</HD>
          <P>This notice serves as a final reminder to importers of their responsibility under section 351.402(f)(2) of the Department's regulations to file a certificate regarding the reimbursement of antidumping duties prior to liquidation of the relevant entries during the POR. Failure to comply with this requirement could result in the Department's presumption that reimbursement of antidumping duties has occurred and the subsequent assessment of doubled antidumping duties.</P>
          <HD SOURCE="HD1">Administrative Protective Orders</HD>
          <P>This notice also serves as a final reminder to parties subject to the administrative protective order (“APO”) of their responsibility concerning the return or destruction of proprietary information disclosed under the APO, in accordance with section 351.305 of the Department's regulations, which continues to govern business proprietary information in this segment of the proceeding. Timely written notification of the return or destruction of APO materials or conversion to judicial protective order is hereby requested. Failure to comply with the regulations and the terms of an APO is a sanctionable violation.</P>
          <P>We are issuing and publishing this NSR notice in accordance with sections 751(a)(2)(b) and 777(i) of the Act.</P>
          <SIG>
            <DATED>Dated: July 25, 2011.</DATED>
            <NAME>Ronald K. Lorentzen,</NAME>
            <TITLE>Deputy Assistant Secretary for Import Administration.</TITLE>
          </SIG>
        </FURINF>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19388 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3510-DS-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>International Trade Administration</SUBAGY>
        <DEPDOC>[A-570-601]</DEPDOC>
        <SUBJECT>Tapered Roller Bearings and Parts Thereof, Finished and Unfinished From the People's Republic of China: Initiation of Antidumping Duty New Shipper Review</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Import Administration, International Trade Administration, Department of Commerce.</P>
        </AGY>
        
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>
            <E T="03">Effective Date:</E>August 1, 2011.</P>
        </DATES>
        
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Department of Commerce (“Department”) has determined that a request for a new shipper review (“NSR”) of the antidumping duty order on tapered roller bearings (“TRBs”) from the People's Republic of China (“PRC”) meets the statutory and regulatory requirements for initiation. The period of review (“POR”) for this NSR is June 1, 2010, through May 31, 2011.</P>
        </SUM>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Demitri Kalogeropoulos, AD/CVD Operations, Office 8, Import Administration, International Trade Administration, U.S. Department of Commerce, 14th Street and Constitution Avenue, NW., Washington, DC 20230; telephone: 202-482-2623.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">Background</HD>

        <P>The notice announcing the antidumping duty order on TRBs from the PRC was published in the<E T="04">Federal Register</E>on June 15, 1987.<E T="03">See Antidumping Duty Order; Tapered Roller Bearings and Parts Thereof, Finished or Unfinished, From the People's Republic of China,</E>52 FR 22667 (June 15, 1987) (“<E T="03">Order”</E>). On June 30, 2011, pursuant to section 751(a)(2)(B)(i) of the Tariff Act of 1930, as amended (“Act”), and 19 CFR 351.214(b), the<PRTPAGE P="45778"/>Department received a NSR request from GGB Bearing Technology (Suzhou) Co., Ltd. (“GGB”). GGB's request was made in June 2011, which is the anniversary month of the<E T="03">Order. See</E>19 CFR 351.214(d).</P>
        <P>In its submission, GGB certified that it is the exporter and producer of the subject merchandise upon which the request was based. Pursuant to section 751(a)(2)(B)(i)(I) of the Act and 19 CFR 351.214(b)(2)(i), GGB certified that it did not export TRBs to the United States during the period of investigation (“POI”). In addition, pursuant to section 751(a)(2)(B)(i)(II) of the Act and 19 CFR 351.214(b)(2)(iii)(A), GGB certified that, since the initiation of the investigation, it has not been affiliated with a PRC exporter or producer who exported TRBs to the United States during the POI, including those not individually examined during the investigation. As required by 19 CFR 351.214(b)(2)(iii)(B), GGB also certified that its export activities were not controlled by the central government of the PRC.</P>
        <P>In addition to the certifications described above, pursuant to 19 CFR 351.214(b)(2)(iv), GGB submitted documentation establishing the following: (1) The date on which GGB first shipped TRBs for export to the United States and the date on which the TRBs were first entered, or withdrawn from warehouse, for consumption; (2) the volume of its first shipment; and (3) the date of its first sale to an unaffiliated customer in the United States.</P>
        <P>The Department conducted U.S. Customs and Border Protection (“CBP”) database queries in an attempt to confirm that GGB's shipments of subject merchandise had entered the United States for consumption and that liquidation of such entries had been properly suspended for antidumping duties. The Department also examined whether the CBP data confirmed that such entries were made during the NSR POR.<SU>1</SU>
          <FTREF/>The information which the Department examined was consistent with that provided by GGB in its request. See Memorandum to the File titled “Initiation of Antidumping New Shipper Review: Tapered Roller Bearings and Parts Thereof, Finished and Unfinished, from the People's Republic of China, A-570-601,” (“Initiation Checklist”) dated concurrently with this notice.</P>
        <FTNT>
          <P>
            <SU>1</SU>
            <E T="03">See</E>July 14, 2011, memorandum to the file, regarding “U.S. Customs and Border Protection Data.”</P>
        </FTNT>
        <HD SOURCE="HD1">Period of Review</HD>
        <P>In accordance with 19 CFR 351.214(g)(1)(i)(A), the POR for a NSR initiated in the month immediately following the anniversary month will be the twelve-month period immediately preceding the anniversary month. Therefore, the POR for this NSR is June 1, 2010, through May 31, 2011. The sales and entries into the United States of subject merchandise produced and exported by GGB occurred during this twelve-month POR.</P>
        <HD SOURCE="HD1">Initiation of New Shipper Review</HD>

        <P>Pursuant to section 751(a)(2)(B) of the Act and 19 CFR 351.214(b), the Department finds that the request submitted by GGB meets the threshold requirements for initiation of a NSR for the shipment of TRBs from the PRC produced and exported by GGB.<E T="03">See</E>Initiation Checklist. However, if the information supplied by GGB is later found to be incorrect or insufficient during the course of this proceeding, the Department may rescind the review or apply adverse facts available pursuant to section 776 of the Act, depending upon the facts on record. The Department intends to issue the preliminary results of this NSR no later than 180 days from the date of initiation, and the final results no later than 90 days from the issuance of the preliminary results. See section 751(a)(2)(B)(iv) of the Act.</P>

        <P>It is the Department's usual practice, in cases involving non-market economies, to require that a company seeking to establish eligibility for an antidumping duty rate separate from the country-wide rate provide evidence of<E T="03">de jure</E>and<E T="03">de facto</E>absence of government control over the company's export activities. Accordingly, the Department will issue a questionnaire to GGB which will include a section requesting information with regard to GGB's export activities for separate rates purposes. The review will proceed if the response provides sufficient indication that GGB is not subject to either<E T="03">de jure</E>or<E T="03">de facto</E>government control with respect to its export of subject merchandise.</P>
        <P>The Department will instruct CBP to allow, at the option of the importer, the posting, until the completion of the review, of a bond or security in lieu of a cash deposit for each entry of the subject merchandise from GGB in accordance with section 751(a)(2)(B)(iii) of the Act and 19 CFR 351.214(e). Because GGB certified that it produced and exported the subject merchandise, the Department will apply the bonding privilege to GGB for all subject merchandise produced and exported by GGB.</P>
        <P>To assist in its analysis of the<E T="03">bona fides</E>of GGB's sales, upon initiation of this new shipper review, the Department will require GGB to submit on an ongoing basis complete transaction information concerning any sales of subject merchandise to the United States that were made subsequent to the POR.</P>
        <P>Interested parties requiring access to proprietary information in this NSR should submit applications for disclosure under administrative protective order in accordance with 19 CFR 351.305 and 19 CFR 351.306. This initiation and notice are in accordance with section 751(a)(2)(B) of the Act and 19 CFR 351.214 and 19 CFR 351.221(c)(1)(i).</P>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>Christian Marsh,</NAME>
          <TITLE>Deputy Assistant Secretary for Antidumping and Countervailing Duty Operations.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19407 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3510-DS-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>International Trade Administration</SUBAGY>
        <SUBJECT>Initiation of Five-Year (“Sunset”) Review</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Import Administration, International Trade Administration, Department of Commerce.</P>
        </AGY>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>In accordance with section 751(c) of the Tariff Act of 1930, as amended (“the Act”), the Department of Commerce (“the Department”) is automatically initiating a five-year review (“Sunset Review”) of the antidumping and countervailing duty orders listed below. The International Trade Commission (“the Commission”) is publishing concurrently with this notice its notice of<E T="03">Institution of Five-Year Review</E>which covers the same orders.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>
            <E T="03">Effective Date:</E>August 1, 2011.</P>
        </DATES>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>The Department official identified in the<E T="03">Initiation of Review</E>section below at AD/CVD Operations, Import Administration, International Trade Administration, U.S. Department of Commerce, 14th Street and Constitution Avenue, NW., Washington, DC 20230. For information from the Commission contact Mary Messer, Office of Investigations, U.S. International Trade Commission at (202) 205-3193.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">Background</HD>

        <P>The Department's procedures for the conduct of Sunset Reviews are set forth in its<E T="03">Procedures for Conducting Five-Year (“Sunset”) Reviews of<PRTPAGE P="45779"/>Antidumping and Countervailing Duty Orders,</E>63 FR 13516 (March 20, 1998) and 70 FR 62061 (October 28, 2005). Guidance onmethodological or analytical issues relevant to the Department's conduct of Sunset Reviews is set forth in the Department's Policy Bulletin 98.3—<E T="03">Policies Regarding the Conduct of Five-Year (“Sunset”) Reviews of Antidumping and Countervailing Duty Orders: Policy Bulletin,</E>63 FR 18871 (April 16, 1998).</P>
        <HD SOURCE="HD1">Initiation of Review</HD>
        <P>In accordance with 19 CFR 351.218(c), we are initiating the Sunset Review of the following antidumping and countervailing duty orders:</P>
        <GPOTABLE CDEF="s25,13,r25,r75,r50" COLS="5" OPTS="L2,tp0,i1">
          <TTITLE/>
          <BOXHD>
            <CHED H="1">DOC  Case No.</CHED>
            <CHED H="1">ITC Case No.</CHED>
            <CHED H="1">Country</CHED>
            <CHED H="1">Product</CHED>
            <CHED H="1">Department Contact</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">A-570-601</ENT>
            <ENT>731-TA-344</ENT>
            <ENT>PRC</ENT>
            <ENT>Tapered Roller Bearings and Parts Thereof, Finished and Unfinished (3rd Review)</ENT>
            <ENT>Julia Hancock, (202) 482-1394.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">A-570-828</ENT>
            <ENT>731-TA-672</ENT>
            <ENT>PRC</ENT>
            <ENT>Silicomanganese (3rd Review)</ENT>
            <ENT>Julia Hancock, (202) 482-1394.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">A-351-824</ENT>
            <ENT>731-TA-671</ENT>
            <ENT>Brazil</ENT>
            <ENT>Silicomanganese (3rd Review)</ENT>
            <ENT>Dana Mermelstein, (202) 482-1391.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">A-823-805</ENT>
            <ENT>731-TA-673</ENT>
            <ENT>Ukraine</ENT>
            <ENT>Silicomanganese (3rd Review)</ENT>
            <ENT>Dana Mermelstein, (202) 482-1391.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">A-427-801</ENT>
            <ENT>731-TA-392-A</ENT>
            <ENT>France</ENT>
            <ENT>Ball Bearings and Parts Thereof (3rd Review)</ENT>
            <ENT>Dana Mermelstein,  (202) 482-1391.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">A-428-801</ENT>
            <ENT>731-TA-391-A</ENT>
            <ENT>Germany</ENT>
            <ENT>Ball Bearings and Parts Thereof (3rd Review)</ENT>
            <ENT>Dana Mermelstein, (202) 482-1391.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">A-475-801</ENT>
            <ENT>731-TA-393-A</ENT>
            <ENT>Italy</ENT>
            <ENT>Ball Bearings and Parts Thereof (3rd Review)</ENT>
            <ENT>Dana Mermelstein,  (202) 482-1391.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">A-588-804</ENT>
            <ENT>731-TA-394-A</ENT>
            <ENT>Japan</ENT>
            <ENT>Ball Bearings and Parts Thereof (3rd Review)</ENT>
            <ENT>Dana Mermelstein,  (202) 482-1391.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">A-412-801</ENT>
            <ENT>731-TA-399-A</ENT>
            <ENT>United Kingdom</ENT>
            <ENT>Ball Bearings and Parts Thereof (3rd Review)</ENT>
            <ENT>Dana Mermelstein,  (202) 482-1391.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">A-570-901</ENT>
            <ENT>731-TA-1095</ENT>
            <ENT>PRC</ENT>
            <ENT>Lined Paper Products (a.k.a. Lined Paper School Supplies)</ENT>
            <ENT>David Goldberger,  (202) 482-4136.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">A-533-843</ENT>
            <ENT>731-TA-1096</ENT>
            <ENT>India</ENT>
            <ENT>Lined Paper Products (a.k.a. Lined Paper School Supplies)</ENT>
            <ENT>David Goldberger,  (202) 482-4136.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">A-560-818</ENT>
            <ENT>731-TA-1097</ENT>
            <ENT>Indonesia</ENT>
            <ENT>Lined Paper Products (a.k.a. Lined Paper School Supplies)</ENT>
            <ENT>David Goldberger,  (202) 482-4136.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">C-533-844</ENT>
            <ENT>731-TA-442</ENT>
            <ENT>India</ENT>
            <ENT>Lined Paper Products (a.k.a. Lined Paper School Supplies)</ENT>
            <ENT>David Goldberger,  (202) 482-4136.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">C-560-819</ENT>
            <ENT>731-TA-443</ENT>
            <ENT>Indonesia</ENT>
            <ENT>Lined Paper Products (a.k.a. Lined Paper School Supplies)</ENT>
            <ENT>David Goldberger,  (202) 482-4136.</ENT>
          </ROW>
        </GPOTABLE>
        <HD SOURCE="HD1">Filing Information</HD>

        <P>As a courtesy, we are making information related to Sunset proceedings, including copies of the pertinent statute and Department's regulations, the Department schedule for Sunset Reviews, a listing of past revocations and continuations, and current service lists, available to the public on the Department's Internet Web site at the following address:<E T="03">http://ia.ita.doc.gov/sunset/.</E>All submissions in these Sunset Reviews must be filed in accordance with the Department's regulations regarding format, translation, and service of documents. These rules can be found at 19 CFR 351.303.</P>

        <P>This notice serves as a reminder that any party submitting factual information in an AD/CVD proceeding must certify to the accuracy and completeness of that information.<E T="03">See</E>section 782(b) of the Act. Parties are hereby reminded that revised certification requirements are in effect for company/government officials as well as their representatives in all AD/CVD investigations or proceedings initiated on or after March 14, 2011.<E T="03">See Certification of Factual Information to Import Administration During Antidumping and Countervailing Duty Proceedings: Interim Final Rule,</E>76 FR 7491 (February 10, 2011) (“<E T="03">Interim Final Rule</E>”) amending 19 CFR 351.303(g)(1) and (2). The formats for the revised certifications are provided at the end of the<E T="03">Interim Final Rule.</E>The Department intends to reject factual submissions in investigations/proceedings initiated on or after March 14, 2011 if the submitting party does not comply with the revised certification requirements.</P>
        <P>Pursuant to 19 CFR 351.103(d), the Department will maintain and make available a service list for these proceedings. To facilitate the timely preparation of the service list(s), it is requested that those seeking recognition as interested parties to a proceeding contact the Department in writing within 10 days of the publication of the Notice of Initiation.</P>

        <P>Because deadlines in Sunset Reviews can be very short, we urge interested parties to apply for access to proprietary information under administrative protective order (“APO”) immediately following publication in the<E T="04">Federal Register</E>of this notice of initiation by filing a notice of intent to participate. The Department's regulations on submission of proprietary information and eligibility to receive access to business proprietary information under APO can be found at 19 CFR 351.304-351.306.</P>
        <HD SOURCE="HD1">Information Required From Interested Parties</HD>

        <P>Domestic interested parties defined in section 771(9)(C), (D), (E), (F), and (G) of the Act and 19 CFR 351.102(b) wishing to participate in a Sunset Review must respond not later than 15 days after the date of publication in the<E T="04">Federal Register</E>of this notice of initiation by filing a notice of intent to participate. The required contents of the notice of intent to participateare set forth at 19 CFR 351.218(d)(1)(ii). In accordance with the Department's regulations, if we do not receive a notice of intent to participate from at least one domestic interested party by the 15-day deadline, the Department will automatically revoke the order without further review.<E T="03">See</E>19 CFR 351.218(d)(1)(iii).</P>

        <P>If we receive an order-specific notice of intent to participate from a domestic interested party, the Department's regulations provide that<E T="03">all parties</E>wishing to participate in the Sunset Review must file complete substantive responses not later than 30 days after the date of publication in the<E T="04">Federal Register</E>of this notice of initiation. The required contents of a substantive<PRTPAGE P="45780"/>response, on an order-specific basis, are set forth at 19 CFR 351.218(d)(3). Note that certain information requirements differ for respondent and domestic parties. Also, note that the Department's information requirements are distinct from the Commission's information requirements. Please consult the Department's regulations for information regarding the Department's conduct of Sunset Reviews.<SU>1</SU>
          <FTREF/>Please consult the Department's regulations at 19 CFR part 351 for definitions of terms and for other general information concerning antidumping and countervailing duty proceedings at the Department.</P>
        <FTNT>
          <P>
            <SU>1</SU>In comments made on the interim final sunset regulations, a number of parties stated that the proposed five-day period for rebuttals to substantive responses to a notice of initiation was insufficient. This requirement was retained in the final sunset regulations at 19 CFR 351.218(d)(4). As provided in 19 CFR 351.302(b), however, the Department will consider individual requests to extend that five-day deadline based upon a showing of good cause.</P>
        </FTNT>
        <P>This notice of initiation is being published in accordance with section 751(c) of the Act and 19 CFR 351.218 (c).</P>
        <SIG>
          <DATED>Dated: July 21, 2011.</DATED>
          <NAME>Christian Marsh,</NAME>
          <TITLE>Deputy Assistant Secretary for Antidumping and Countervailing Duty Operations.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19402 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3510-DS-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>National Oceanic and Atmospheric Administration</SUBAGY>
        <RIN>RIN 0648-XA600</RIN>
        <SUBJECT>Notice of Availability for a Finding of No Significant Impact and Environmental Assessment for Emergency Restoration of Seagrass Impacts From the Deepwater Horizon Oil Spill Response</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>National Marine Fisheries Service (NMFS), National Oceanic and Atmospheric Administration (NOAA), Commerce.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of availability; request for comments.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>Officials of the National Oceanic and Atmospheric Administration of the U.S. Department of Commerce (NOAA); U.S. Department of Interior; and the five states of Florida, Alabama, Mississippi, Louisiana and Texas are all designated, pursuant to section 1006(b) of the Oil Pollution Act of 1990 (OPA), as trustees (Trustees) for natural resources harmed by this Incident. NOAA is serving as the Lead Administrative Trustee (LAT) for this emergency seagrass restoration. Under the National Environmental Policy Act, an Environmental Assessment for Emergency Restoration of Seagrass Impacts from the Deepwater Horizon Oil Spill Response (EA) was completed by NOAA, and a Finding of No Significant Impact (FONSI) was signed on July 8, 2011.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments on this EA and FONSI must be received by August 16, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Submit comments to: Kay McGraw, NOAA Restoration Center, Rm 15862, 1315 East West Highway, Silver Spring, MD 20910; or electronically to<E T="03">Kay.McGraw@noaa.gov.</E>
          </P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Patricia A. Montanio, 301-427-8600.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>The purpose of this project is to address injuries to seagrass beds that resulted from Deepwater Horizon (DWH) oil spill response activities. The injuries were caused by motorized boats, and included propeller scars, blowholes from response vessels, and scouring from boom curtains and anchor tethers. The proposed action will restore damaged seagrass beds and decrease risk of secondary injury to nearby seagrass communities. The environmental review process led NOAA to conclude that this action will not have a significant effect on the human environment, therefore an environmental impact statement will not be prepared.</P>

        <P>Section 990.26(d) of OPA requires the Trustees to provide notice to the public, to the extent practicable, of any planned emergency restoration actions. Trustees must also provide public notice of the justification for, nature and extent of, and results of emergency restoration actions within a reasonable time frame. NOAA is expediting regulatory clearance of this action due to the emergency nature of it. The Trustees believe the best method to address this requirement is to post a copy of the FONSI and EA on NOAA's Deepwater Horizon Web site at<E T="03">http://www.gulfspillrestoration.noaa.gov/.</E>The documents will be available there on August 1, 2011.</P>
        <P>NOAA believes it is important to undertake the restoration immediately in order to minimize the possibility of further adverse sea grass impacts that may occur in the absence of immediate action, such as secondary damage that may result from storms or other events. NOAA will accept public comments on this EA and FONSI until August 16, 2011. All comments will be fully considered and included in the administrative record for this action.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Brian Pawlak,</NAME>
          <TITLE>Acting Director, Office of Habitat Conservation, National Marine Fisheries Service.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19403 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3510-22-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>National Oceanic and Atmospheric Administration</SUBAGY>
        <RIN>RIN 0648-XA609</RIN>
        <SUBJECT>South Atlantic Fishery Management Council; Public Hearings</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Commerce, National Oceanic and Atmospheric Administration, National Marine Fisheries Service (NMFS).</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of Public Hearing Series.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>The South Atlantic Fishery Management Council (Council) will hold a series of public hearings regarding Amendment 24 to the Snapper Grouper Fishery Management Plan (FMP) for the South Atlantic Region. See<E T="02">SUPPLEMENTARY INFORMATION</E>for the public hearings schedule.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>

          <P>The series of four public hearings will be held August 22, 2011 through August 25, 2011. The hearings will be held from 5 p.m. until 7 p.m. Council staff will present an overview of the amendment and will be available for informal discussions and to answer questions. Members of the public will have an opportunity to go on record at any time during the meeting hours to record their comments on the public hearing topics for consideration by the Council. Local Council representatives will attend the meetings and take public comment. Written comments will be accepted from August 12, 2011 until 5 p.m. on September 1, 2011. See<E T="02">SUPPLEMENTARY INFORMATION</E>.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Written comments should be sent to Bob Mahood, Executive Director, South Atlantic Fishery Management Council, 4055 Faber Place Drive, Suite 201, North Charleston, SC 29405, or via e-mail to:<E T="03">SGAmend24PHcomment@safmc.net</E>for Amendment 24 to the Snapper Grouper FMP. Written comments will be received from August 12, 2011 until 5 p.m. on September 1, 2011.</P>

          <P>Copies of the public hearing documents are available by contacting Kim Iverson, Public Information Officer,<PRTPAGE P="45781"/>South Atlantic Fishery Management Council, 4055 Faber Place Drive, Suite 201, North Charleston, SC 29405; telephone: (843) 571-4366 or toll free at (866) SAFMC-10. Copies will also be available online at<E T="03">http://www.safmc.net</E>as they become available.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Kim Iverson, South Atlantic Fishery Management Council, 4055 Faber Place Drive, Suite 201, North Charleston, SC 29405;<E T="03">telephone:</E>(843) 571-4366;<E T="03">fax:</E>(843) 769-4520;<E T="03">e-mail address: kim.iverson@safmc.net.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>Amendment 24 to the Snapper Grouper FMP would implement a rebuilding plan for red grouper in the South Atlantic as required by the Magnuson-Stevens Fishery Conservation and Management Act (Magnuson-Stevens Act) for species determined to be overfished and undergoing overfishing. The intent of the rebuilding plan is to end overfishing immediately and increase biomass of overfished stocks to a sustainable level within a specified period of time. The amendment would also specify Maximum Sustainable Yield (MSY), the Maximum Fishing Mortality Threshold (MSST), and Optimum Yield (OY) for the red grouper fishery. In addition, Annual Catch Limits (ACLs) and Accountability Measures (AMs) would be established for both recreational and commercial sectors of the red grouper fishery.</P>
        <P>
          <E T="03">Public Hearing Schedule:</E>
        </P>

        <P>(1) August 22, 2011—Hilton Wilmington Riverside, 301 North Water Street, Wilmington, NC 28401;<E T="03">Phone:</E>(910) 763-5900;</P>

        <P>(2) August 23, 2011—Hilton Garden Inn, 5265 International Boulevard, North Charleston, SC 29418;<E T="03">Phone:</E>(843) 308-9330;</P>

        <P>(3) August 24, 2011—Jacksonville Marriott, 4670 Salisbury Road, Jacksonville, FL 32256;<E T="03">Phone:</E>(904) 296-2222;</P>

        <P>(4) August 25, 2011—Radisson Resort at the Port, 8701 Astronaut Boulevard, Cape Canaveral, FL 32920;<E T="03">Phone:</E>(321) 784-0000.</P>
        <HD SOURCE="HD1">Special Accommodations</HD>

        <P>These meetings are physically accessible to people with disabilities. Requests for sign language interpretation or other auxiliary aids should be directed to the Council office (see<E T="02">ADDRESSES</E>) three days prior to the start of each meeting.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Tracey L. Thompson,</NAME>
          <TITLE>Acting Director, Office of Sustainable Fisheries, National Marine Fisheries Service.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19309 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3510-22-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>National Oceanic and Atmospheric Administration</SUBAGY>
        <RIN>RIN 0648-XA573</RIN>
        <SUBJECT>Atlantic Highly Migratory Species; Meeting of the Atlantic Highly Migratory Species Advisory Panel</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>National Marine Fisheries Service (NMFS), National Oceanic and Atmospheric Administration (NOAA), Commerce.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of public meeting.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>NMFS will hold a 3-day Atlantic Highly Migratory Species (HMS) Advisory Panel (AP) meeting in September 2011. The intent of the meeting is to consider options for the conservation and management of Atlantic HMS. The meeting is open to the public.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>The AP meeting will be held Sept. 20, 2011, through Sept. 22, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>The meeting will be held in Silver Spring, MD 20910.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Brian Parker or Margo Schulze-Haugen at (301) 427-8503.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>

        <P>The Magnuson-Stevens Fishery Conservation and Management Act, 16 U.S.C. 1801<E T="03">et seq.,</E>as amended by the Sustainable Fisheries Act, Public Law 104-297, provided for the establishment of an AP to assist in the collection and evaluation of information relevant to the development of any Fishery Management Plan (FMP) or FMP amendment for Atlantic HMS. NMFS consults with and considers the comments and views of AP members when preparing and implementing FMPs or FMP amendments for Atlantic tunas, swordfish, billfish, and sharks.</P>
        <P>The AP has previously consulted with NMFS on: Amendment 1 to the Billfish FMP (April 1999); the HMS FMP (April 1999); Amendment 1 to the HMS FMP (December 2003); the Consolidated HMS FMP (October 2006); Amendments 1, 2, and 3 to the Consolidated HMS FMP (April and October 2008, February and September 2009, and May 2010); an Advanced Notice of the Proposed Rule (ANPR) for the future management of the shark fishery (September 2010) and the ANPR for Atlantic HMS published June 2009 (September 2010); and a proposed rule to allow retention of swordfish caught by squid trawl vessels (April 2011), among other things.</P>
        <P>At the September 2011 AP meeting, NMFS plans to discuss Atlantic bluefin tuna management, revitalizing the swordfish fishery, the Future of the Shark Fishery, other shark fishery management issues, and items contained in the Advanced Notice of Proposed Rulemaking that published June 1, 2009 (74 FR 26174). The meeting may also continue discussions on the implementation of 2010 International Commission for the Conservation of Atlantic Tunas measures, an update on the recreational action plan for Atlantic HMS, permitting and management options for swordfish and smoothhound sharks in trawl fisheries, electronic dealer reporting, vessel monitoring systems, and monitoring methods for HMS fisheries. NMFS also plans to hold a shark catch share workshop for interested fishermen after the AP meeting. Information on the venue and agenda will be provided at a later date.</P>
        <HD SOURCE="HD1">Special Accommodations</HD>
        <P>This meeting is physically accessible to people with disabilities. Requests for sign language interpretation or other auxiliary aids should be directed to Brian Parker at (301) 427-8503 at least 7 days prior to the meeting.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Margo Schulze-Haugen,</NAME>
          <TITLE>Acting Director, Office of Sustainable Fisheries, National Marine Fisheries Service.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19401 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3510-22-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF COMMERCE</AGENCY>
        <SUBAGY>National Oceanic and Atmospheric Administration</SUBAGY>
        <RIN>RIN 0648-XA601</RIN>
        <SUBJECT>Endangered Species; File No. 15552</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>National Marine Fisheries Service (NMFS), National Oceanic and Atmospheric Administration (NOAA), Commerce.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Issuance of permit.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>Notice is hereby given that the National Marine Fisheries Service Southeast Fisheries Science Center (SEFSC) [Dr. Bonnie Ponwith, Responsible Party] has been issued a permit to take green (<E T="03">Chelonia mydas</E>), hawksbill (<E T="03">Eretmochelys imbricata</E>), loggerhead (<E T="03">Caretta caretta</E>), Kemp's ridley (<E T="03">Lepidochelys kempii</E>), olive ridley (<E T="03">Lepidochelys olivacea</E>), leatherback (<E T="03">Dermochelys coriacea</E>), and<PRTPAGE P="45782"/>unidentified hardshell sea turtles for the purposes of scientific research.</P>
        </SUM>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>The permit and related documents are available for review upon written request or by appointment in the following offices:</P>
          <P>Permits, Conservation and Education Division, Office of Protected Resources, NMFS, 1315 East-West Highway, Room 13705, Silver Spring, MD 20910; phone (301) 427-8401; fax (301) 713-0376; and</P>
          <P>Southeast Region, NMFS, 263 13th Ave. South, St. Petersburg, FL 33701; phone (727) 824-5312; fax (727) 824-5309.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Colette Cairns or Amy Hapeman, (301) 427-8401.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>On January 26, 2011, notice was published in the<E T="04">Federal Register</E>(76 FR 4636) that a request for a scientific research permit to take green, loggerhead, hawksbill, leatherback, Kemp's ridley, olive ridley, and unidentified hardshell sea turtles had been submitted by the above-named organization. The requested permit has been issued under the authority of the Endangered Species Act of 1973, as amended (ESA; 16 U.S.C. 1531<E T="03">et seq.</E>) and the regulations governing the taking, importing, and exporting of endangered and threatened species (50 CFR parts 222-226).</P>
        <P>The five-year permit authorizes the SEFSC to monitor the take of green, loggerhead, hawksbill, leatherback, Kemp's ridley, olive ridley, and unidentified hardshell sea turtles by observed commercial fisheries and collect data to estimate bycatch and its effects on sea turtle sub-populations. SEFSC-certified observers are authorized to handle, photograph, measure, weigh, flipper and passive integrated transponder tag, tissue sample, carapace mark and salvage specimens taken during commercial fishing activities. The research will take place in the Atlantic Ocean, the Gulf of Mexico, the Caribbean Sea, and their tributaries. These efforts would aid in the development and refinement of management efforts to recover these species.</P>
        <P>Issuance of this permit, as required by the ESA, was based on a finding that such permit (1) was applied for in good faith, (2) will not operate to the disadvantage of such endangered or threatened species, and (3) is consistent with the purposes and policies set forth in section 2 of the ESA.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>P. Michael Payne,</NAME>
          <TITLE>Chief, Permits, Conservation and Education Division, Office of Protected Resources, National Marine Fisheries Service.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19399 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3510-22-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">COMMITTEE FOR PURCHASE FROM PEOPLE WHO ARE  BLIND OR SEVERELY DISABLED</AGENCY>
        <SUBJECT>Information Collection Submitted to the Office of Management and Budget (OMB) for Approval Under the Paperwork Reduction Act; Nonprofit Agency Recordkeeping Requirements</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Committee for Purchase From People Who Are Blind or Severely Disabled.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice; request for comments.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Committee for Purchase From People Who Are Blind or Severely Disabled (The Committee) is submitting the collection of information listed below to OMB for approval under the provisions of the Paperwork Reduction Act. This notice solicits comments on that collection of information.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>The Office of Management and Budget (OMB) has up to 60 days to approve or disapprove information collection but may respond after 30 days. Therefore, to ensure maximum consideration, your comments should be received by OMB by August 28, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Written comments should be addressed to the Office of Information and Regulatory Affairs, Attention: Desk Officer for the Committee for Purchase from People Who Are Blind or Severely Disabled, Office of Management and Budget, 725 17th Street, NW., Room 10222, Washington, DC 20503. Commenters are encouraged to submit responses electronically by e-mail to<E T="03">oira_submission@omb.eop.gov</E>or via fax to (202) 395-6974. Commenters should include the following subject line in their response: “Comment: 3037-0005 Nonprofit Agency Responsibilities.” Persons submitting comments electronically should not submit paper copies.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Louis Bartalot, Director of Compliance, Committee for Purchase From People Who Are Blind or Severely Disabled, 1421 Jefferson Davis Highway, Jefferson Plaza 2, Suite 10800, Arlington, VA 22202-3259; phone (703) 603-2124; fax (703) 603-0655; or e-mail<E T="03">rulescomment@abilityone.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>

        <P>The Office of Management and Budget (OMB) Regulations at 5 CFR part 1320, which implement provisions of the Paperwork Reduction Act of 1995 (44 U.S.C. 3501<E T="03">et seq.</E>), require that interested members of the public and affected agencies have an opportunity to comment on information collection and recordkeeping activities (see 5 CFR 1320.8(d)). The Committee plans to submit a request to OMB to renew its approval of the collection of information for nonprofit agency responsibilities related to recordkeeping. The Committee is requesting a 3-year term of approval for this information collection activity.</P>
        <P>Federal agencies may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. The OMB control number for this collection of information is 3037-0005.</P>
        <P>The Javits-Wagner-O'Day (JWOD) Act of 1971 (41 U.S.C. 46-48c) is the authorizing legislation for the AbilityOne Program. The AbilityOne Program creates jobs and training opportunities for people who are blind or who have other severe disabilities. Its primary means of doing so is by requiring Government agencies to purchase selected products and services from nonprofit agencies employing such individuals. The AbilityOne Program is administered by the Committee. Two national, independent organizations, National Industries for the Blind (NIB) and NISH, help state and private nonprofit agencies participate in the AbilityOne Program.</P>
        <P>The implementing regulations for the JWOD Act, which are located at 41 CFR Chapter 51, detail the recordkeeping requirements imposed on nonprofit agencies participating in the AbilityOne Program. Section 51-2.4 of the regulations describes the criteria that the Committee must consider when adding a product or service to its Procurement List. One of these criteria is that a proposed addition must demonstrate a potential to generate employment for people who are blind or severely disabled. The Committee decided that evidence that employment will be generated for those individuals consists of recordkeeping that tracks direct labor and revenues for products or services sold through an AbilityOne Program contract. This recordkeeping can be done on each individual AbilityOne project or by product or service family.</P>

        <P>In addition, Section 51-4.3 of the regulations requires that nonprofit agencies keep records on direct labor<PRTPAGE P="45783"/>hours performed by each worker and keep an individual record or file for each individual who is blind or severely disabled, documenting that individual's disability and capabilities for competitive employment. The records that nonprofit agencies must keep in accordance with Section 51-4.3 of the regulations constitute the bulk of the hour burden associated with this OMB control number.</P>
        <P>This information collection renewal request seeks approval for the Committee to continue to ensure compliance with recordkeeping requirements established by the authority of the JWOD Act and set forth in the Act's implementing regulations and to ensure that the Committee has the ability to confirm the suitability of products and services on its Procurement List. The recordkeeping requirements described in this document are the same as those currently imposed on nonprofit agencies participating in the AbilityOne Program.</P>
        <P>
          <E T="03">Title:</E>Nonprofit Agency Responsibilities, 41 CFR 51-2.4 and 51-4.3.</P>
        <P>
          <E T="03">OMB Control Number:</E>3037-0005.</P>
        <P>
          <E T="03">Description of Collection:</E>Recordkeeping.</P>
        <P>
          <E T="03">Description of Respondents:</E>Nonprofit agencies participating in the AbilityOne Program.</P>
        <P>
          <E T="03">Annual Number of Respondents:</E>About 625 nonprofit agencies will annually participate in recordkeeping.</P>
        <P>
          <E T="03">Total Annual Burden Hours:</E>The recordkeeping burden is estimated to average 567 hours per respondent. Total annual burden is 354,375 hours.</P>
        <P>On May 17, 2011, we published in the<E T="04">Federal Register</E>(Volume 76 Number 95, Pages 28424-28425) a notice requesting public comment on these recordkeeping requirements for 60 days, ending July 17, 2011. By that date we had received no comments.</P>
        <SIG>
          <NAME>Patricia Briscoe,</NAME>
          <TITLE>Deputy Director, Business Operations (Pricing and Information Management).</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19379 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6353-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF DEFENSE</AGENCY>
        <SUBAGY>Office of the Secretary</SUBAGY>
        <SUBJECT>Missile Defense Advisory Committee; Notice of Closed Meeting</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Department of Defense; Missile Defense Agency (MDA).</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of closed meeting.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>Under the provisions of the Federal Advisory Committee Act of 1972 (5 U.S.C., Appendix, as amended) and the Government in the Sunshine Act of 1976 (5 U.S.C. 552b, as amended) and 41 CFR 102-3.150, the Department of Defense announces that the following Federal advisory committee meeting of the Missile Defense Advisory Committee will take place.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Tuesday, August 16, 2011 through Thursday, August 18, 2011 from 8 a.m. to 5:30 p.m. each day. Security clearance and visit requests are required for access.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>5700 18th Street, Building 245, Fort Belvoir, Virginia 22060-5573.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Mr. David Bagnati, Designated Federal Officer at<E T="03">MDAC@mda.mil,</E>phone/voice mail 571-231-8113, or mail at 5700 18th Street, Building 245, Fort Belvoir, Virginia 22060-5573.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P/>
        <P SOURCE="NPAR">
          <E T="03">Purpose of the Meeting:</E>At this meeting, the Committee will receive classified information on Directed Energy.</P>
        <P>
          <E T="03">Agenda:</E>Topics tentatively scheduled for classified discussion include, but are not limited to briefings on Ballistic Missile Defense System Architecture and Laser Systems Concepts; United States European Phased Adaptive Approach; Ballistic Missile Defense Strategic Issues; Annual Ethics Training; Annual Security Refresher; Missile Defense Advisory Committee Executive Session; and Missile Defense Advisory Committee preliminary outbrief to the Director, Missile Defense Agency.</P>
        <P>
          <E T="03">Meeting Accessibility:</E>Pursuant to 5 U.S.C. 552b, as amended, and 41 CFR 102-3.155 the Missile Defense Agency has determined that the meeting shall be closed to the public. The Director, Missile Defense Agency, in consultation with the Missile Defense Agency Office of General Counsel, has determined in writing that the public interest requires that all sessions of the committee's meeting will be closed to the public because they will be concerned with classified information and matters covered by 5 U.S.C. 552b(c)(1).</P>
        <P>
          <E T="03">Committee's Designated Federal Officer:</E>Mr. David Bagnati,<E T="03">MDAC@mda.mil,</E>phone/voice mail 571-231-8113, or mail at 5700 18th Street, Building 245, Fort Belvoir, Virginia 22060-5573. Pursuant to 41 CFR 102-3.105(j) and 102-3.140, and section 10(a)(3) of the Federal Advisory Committee Act of 1972, the public or interested organizations may submit written statements to the membership of the Missile Defense Advisory Committee about its mission and functions. Written statements may be submitted at any time or in response to the stated agenda of a planned meeting of the Missile Defense Advisory Committee.</P>

        <P>All written statements shall be submitted to the Designated Federal Officer for the Missile Defense Advisory Committee, in the following formats: One hard copy with original signature and one electronic copy via e-mail (acceptable file formats: Adobe Acrobat PDF, MS Word or MS PowerPoint), and this individual will ensure that the written statements are provided to the membership for their consideration. Contact information for the Designated Federal Officer is as stated above and can also be obtained from the GSA's Federal Advisory Committee Act Database—<E T="03">https://www.fido.gov/facadatabase/public.asp.</E>
        </P>
        <P>Statements being submitted in response to the agenda mentioned in this notice must be received by the Designated Federal Officer at the address listed at least five calendar days prior to the meeting which is the subject of this notice. Written statements received after this date may not be provided to or considered by the Missile Defense Advisory Committee until its next meeting. The Designated Federal Officer will review all timely submissions with the Missile Defense Advisory Committee Chairperson and ensure they are provided to all members of the Missile Defense Advisory Committee before the meeting that is the subject of this notice.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Aaron Siegel,</NAME>
          <TITLE>Alternate OSD Federal Register Liaison Officer, Department of Defense.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19395 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 5001-06-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF DEFENSE</AGENCY>
        <SUBAGY>Department of the Army</SUBAGY>
        <DEPDOC>[Docket ID USA-2011-0018]</DEPDOC>
        <SUBJECT>Privacy Act of 1974; System of Records</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Department of the Army, DoD.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice to amend a system of records.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Department of the Army is proposing to amend a system of records notice in its existing inventory of records systems subject to the Privacy Act of 1974, (5 U.S.C. 552a), as amended.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>The changes will be effective on August 31, 2011 unless comments are received that would result in a contrary determination.</P>
        </DATES>
        <ADD>
          <PRTPAGE P="45784"/>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>You may submit comments, identified by docket number and title, by any of the following methods:</P>
          <P>*<E T="03">Federal Rulemaking Portal: http://www.regulations.gov</E>. Follow the instructions for submitting comments.</P>
          <P>*<E T="03">Mail</E>: Federal Docket Management System Office, 1160 Defense Pentagon, Washington, DC 20301-1160.</P>
          <P>
            <E T="03">Instructions:</E>All submissions received must include the agency name and docket number for this Federal Register document. The general policy for comments and other submissions from members of the public is to make these submissions available for public viewing on the Internet at<E T="03">http://www.regulations.gov</E>as they are received without change, including any personal identifiers or contact information.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Mr. Leroy Jones, Department of the Army, Privacy Office, U.S. Army Records Management and Declassification Agency, 7701 Telegraph Road, Casey Building, Suite 144, Alexandria, VA 22325-3905, or by phone at (703) 428-6185.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>

        <P>The Department of the Army systems of records notices subject to the Privacy Act of 1974, (5 U.S.C. 552a), as amended, have been published in the<E T="04">Federal Register</E>and are available from the address in<E T="02">FOR FURTHER INFORMATION CONTACT</E>.</P>
        <P>The specific changes to the records systems being amended are set forth below followed by the notices, as amended, published in their entirety. The proposed amendments are not within the purview of subsection (r) of the Privacy Act of 1974, (5 U.S.C. 552a), as amended, which requires the submission of a new or altered system report.</P>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>Aaron Siegel,</NAME>
          <TITLE>Alternate OSD Federal Register Liaison Officer, Department of Defense.</TITLE>
        </SIG>
        <PRIACT>
          <HD SOURCE="HD1">A0195-2b USACIDC</HD>
          <HD SOURCE="HD2">System name:</HD>
          <P>Criminal Investigation and Crime Laboratory Files (August 5, 2002, 67 FR 50653).</P>
          <STARS/>
          <HD SOURCE="HD2">System location:</HD>
          <P>Delete entry and replace with “Headquarters, U.S. Army Criminal Investigation Command, 27130 Telegraph Road, Quantico, VA 22134-2253.</P>
          <P>Segments exist at subordinate U.S. Army Criminal Investigation Command elements. Addresses may be obtained from the Commander, U.S. Army Criminal Investigation Command, 27130 Telegraph Road, Quantico, VA 22134-2253.</P>
          <P>An automated index of cases is maintained at the U.S. Army Crime Records Center, U.S. Army Criminal Investigation Command, 27130 Telegraph Road, Quantico, VA 22134-2253.”</P>
          <STARS/>
          <HD SOURCE="HD2">System manager(s) and address:</HD>
          <P>Delete entry and replace with “Commander, Headquarters, U.S. Army Criminal Investigation Command, 27130 Telegraph Road, Quantico, VA 22134-2253.”</P>
          <HD SOURCE="HD2">Notification procedure:</HD>
          <P>Delete entry and replace with “Individuals seeking to determine whether information about themselves is contained in this system should address written inquiries to the Director, U.S. Army Crime Records Center, U.S. Army Criminal Investigation Command, ATTN: CICR-FP, 27130 Telegraph Road, Quantico, VA 22134-2253.</P>
          <P>For verification purposes, individual should provide the full name, date and place of birth, current address, telephone numbers, and signature.”</P>
          <HD SOURCE="HD2">Record access procedures:</HD>
          <P>Delete entry and replace with “Individual seeking access to information about themselves contained in this system should address written inquiries to the Director, U.S. Army Crime Records Center, U.S. Army Criminal Investigation Command, ATTN: CICR-FP, 27130 Telegraph Road, Quantico, VA 22134-2253.</P>
          <P>For verification purposes, individual should provide the full name, date and place of birth, current address, telephone numbers, and signature.”</P>
          <STARS/>
          <HD SOURCE="HD1">A0195-2b USACIDC</HD>
          <HD SOURCE="HD2">System name:</HD>
          <P>Criminal Investigation and Crime Laboratory Files.</P>
          <HD SOURCE="HD2">System location:</HD>
          <P>Headquarters, U.S. Army Criminal Investigation Command, 27130 Telegraph Road, Quantico, VA 22134-2253.</P>
          <P>Segments exist at subordinate U.S. Army Criminal Investigation Command elements. Addresses may be obtained from the Commander, U.S. Army Criminal Investigation Command, 27130 Telegraph Road, Quantico, VA 22134-2253.</P>
          <P>An automated index of cases is maintained at the U.S. Army Crime Records Center, U.S. Army Criminal Investigation Command, 27130 Telegraph Road, Quantico, VA 22134-2253.</P>
          <HD SOURCE="HD2">Categories of individuals covered by the system:</HD>
          <P>Any individual, civilian or military, involved in, witnessing or suspected of being involved in or reporting possible criminal activity affecting the interests, property, and/or personnel of the U.S. Army.</P>
          <HD SOURCE="HD2">Categories of records in the system:</HD>
          <P>Name, Social Security Number, rank, date and place of birth, chronology of events; reports of investigation and criminal intelligence reports containing statements of witnesses, suspects, subject and agents; laboratory reports, polygraph reports, documentary evidence, physical evidence, summary and administrative data pertaining to preparation and distribution of the report; basis for allegations; Serious or Sensitive Incident Reports, modus operandi and other investigative information from Federal, State, and local investigative and intelligence agencies and departments; similar relevant documents. Indices contain codes for the type of crime, location of investigation, year and date of offense, names and personal identifiers of persons who have been subjects of electronic surveillance, suspects, subjects and victims of crimes, report number which allows access to records noted above; agencies, firms, Army and Defense Department organizations which were the subjects or victims of criminal investigations; and disposition and suspense of offenders listed in criminal investigative case files, witness identification data.</P>
          <HD SOURCE="HD2">Authority for maintenance of the system:</HD>
          <P>10 U.S.C. 3013, Secretary of the Army; Army Regulation 195-2, Criminal Investigation Activities; 42 U.S.C. 10606 et seq.; DoD Directive 1030.1, Victim and Witness Assistance; and E.O. 9397 (SSN), as amended.</P>
          <HD SOURCE="HD2">Purpose(s):</HD>

          <P>To conduct criminal investigations, crime prevention and criminal intelligence activities; to accomplish management studies involving the analysis, compilation of statistics, quality control, etc., to ensure that completed investigations are legally sufficient and result in overall improvement in techniques, training and professionalism. Includes personnel security, internal security, criminal, and other law enforcement matters, all of<PRTPAGE P="45785"/>which are essential to the effective operation of the Department of the Army.</P>
          <P>The records in this system are used for the following purposes: Suitability for access or continued access to classified information; suitability for promotion, employment, or assignment; suitability for access to military installations or industrial firms engaged in government projects/contracts; suitability for awards or similar benefits; use in current law enforcement investigation or program of any type including applicants; use in judicial or adjudicative proceedings including litigation or in accordance with a court order; advising higher authorities and Army commands of the important developments impacting on security, good order or discipline; reporting of statistical data to Army commands and higher authority; input into the Defense Security Service managed Defense Clearance and Investigations Index (DCII) database under system notice V5-02.</P>
          <HD SOURCE="HD2">Routine uses of records maintained in the system, including categories of users and the purposes of such uses:</HD>
          <P>In addition to those disclosures generally permitted under 5 U.S.C. 552a(b) of the Privacy Act of 1974, these records contained therein may specifically be disclosed outside the DoD as a routine use pursuant to 5 U.S.C. 552a(b)(3) as follows:</P>
          <P>Information concerning criminal or possible criminal activity is disclosed to Federal, State, local and/or foreign law enforcement agencies in accomplishing and enforcing criminal laws; analyzing modus operandi, detecting organized criminal activity, or criminal justice employment. Information may also be disclosed to foreign countries under the provisions of the Status of Forces Agreements, or Treaties.</P>
          <P>To the Department of Veterans Affairs to verify veterans claims. Criminal investigative files may be used to adjudicate veteran claims for disability benefits, post dramatic stress disorder, and other veteran entitlements.</P>
          <P>To Federal, state, and local agencies to comply with the Victim and Witness Assistance Program and the Victims' Rights and Restitution Act of 1990, when the agency is requesting information on behalf of the individual.</P>

          <P>To Federal, state, and local law enforcement agencies and private sector entities for the purposes of complying with mandatory background checks, i.e., Brady Handgun Violence Prevention Act (18 U.S.C. 922) and the National Child Protection Act of 1993 (42 U.S.C. 5119<E T="03">et seq</E>.).</P>
          <P>To Federal, state, and local child protection services or family support agencies for the purpose of providing assistance to the individual.</P>
          <P>To victims and witnesses of a crime for purposes of providing information, consistent with the requirements of the Victim and Witness Assistance Program, regarding the investigation and disposition of an offense.</P>
          <P>To the Immigration and Naturalization Service, Department of Justice, for use in alien admission and naturalization inquiries conducted under Section 105 of the Immigration and Naturalization Act of 1952, as amended.</P>
          <P>The DoD `Blanket Routine Uses' set forth at the beginning of the Army's compilation of systems of records notices also apply to this system.</P>
          <HD SOURCE="HD2">Policies and practices for storing, retrieving, accessing, retaining, and disposing of records in the system:</HD>
          <HD SOURCE="HD2">Storage:</HD>
          <P>Paper records in file folders and on electronic media.</P>
          <HD SOURCE="HD2">Retrievability:</HD>
          <P>By name or other identifier of individual.</P>
          <HD SOURCE="HD2">Safeguards:</HD>
          <P>Access is limited to designated authorized individuals having official need for the information in the performance of their duties. Buildings housing records are protected by security guards.</P>
          <HD SOURCE="HD2">Retention and disposal:</HD>
          <P>Reports of Investigation: At Headquarters, U.S. Army Criminal Investigation Command (USACIDC), criminal investigative case files are retained for 40 years after final action, except that at USACIDC subordinate elements, such files are retained from 1 to 5 years depending on the level of such unit and the data involved.</P>
          <P>Laboratory Reports: Laboratory reports at the USACIDC laboratory are destroyed after 5 years.</P>
          <P>Criminal Intelligence Reports: At Headquarters, USACIDC Intelligence Division criminal intelligence reports are destroyed when no longer needed. Except reports containing information of current operation value may be kept and reviewed yearly for continued retention, not to exceed 20 years. Group headquarters destroy after 5 years. District and field office elements destroy after 3 years or when no longer needed.</P>
          <HD SOURCE="HD2">System manager(s) and address:</HD>
          <P>Commander, Headquarters, U.S. Army Criminal Investigation Command, 27130 Telegraph Road, Quantico, VA 22134-2253.</P>
          <HD SOURCE="HD2">Notification procedure:</HD>
          <P>Individuals seeking to determine whether information about themselves is contained in this system should address written inquiries to the Director, U.S. Army Crime Records Center, U.S. Army Criminal Investigation Command, ATTN: CICR-FP, 27130 Telegraph Road, Quantico, VA 22134-2253.</P>
          <P>For verification purposes, individual should provide the full name, date and place of birth, current address, telephone numbers, and signature.</P>
          <HD SOURCE="HD2">Record access procedures:</HD>
          <P>Individual seeking access to information about themselves contained in this system should address written inquiries to the Director, U.S. Army Crime Records Center, U.S. Army Criminal Investigation Command, ATTN: CICR-FP, 27130 Telegraph Road, Quantico, VA 22134-2253.</P>
          <P>For verification purposes, individual should provide the full name, date and place of birth, current address, telephone numbers, and signature.</P>
          <HD SOURCE="HD2">Contesting record procedures:</HD>
          <P>The Army's rules for accessing records, and for contesting contents and appealing initial agency determinations are contained in Army Regulation 340-21; 32 CFR part 505; or may be obtained from the system manager.</P>
          <HD SOURCE="HD2">Record source categories:</HD>
          <P>Suspects, witnesses, victims, USACIDC special agents and other personnel, informants; various Department of Defense, federal, state, and local investigative agencies; departments or agencies of foreign governments; and any other individual or organization which may supply pertinent information.</P>
          <HD SOURCE="HD2">Exemptions claimed for the system:</HD>
          <P>Parts of this system may be exempt pursuant to 5 U.S.C. 552a(j)(2) if the information is compiled and maintained by a component of the agency which performs as its principle function any activity pertaining to the enforcement of criminal laws.</P>
          <P>An exemption rule for this system has been promulgated in accordance with requirements of 5 U.S.C. 553(b)(1), (2), and (3), (c) and (e) and published in 32 CFR part 505. For additional information contact the system manager.</P>
        </PRIACT>
        
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19364 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 5001-06-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <PRTPAGE P="45786"/>
        <AGENCY TYPE="N">DEPARTMENT OF ENERGY</AGENCY>
        <SUBJECT>Advanced Scientific Computing Advisory Committee; Meeting</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Office of Science, Department of Energy.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of open meeting.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>This notice announces a meeting of the Advanced Scientific Computing Advisory Committee (ASCAC). Federal Advisory Committee Act (Pub. L. 92-463, 86 Stat. 770) requires that public notice of these meetings be announced in the<E T="04">Federal Register</E>
          </P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Tuesday, August 23, 2011, 9 a.m.-5 p.m.</P>
          <P>Wednesday, August 24, 2011, 9 a.m.-12 p.m.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>Hilton Washington DC/Rockville Hotel &amp; Executive Meeting Center, 1750 Rockville Pike, Rockville, Maryland 20852.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Melea Baker, Office of Advanced Scientific Computing Research; SC-21/Germantown Building; U.S. Department of Energy; 1000 Independence Avenue, SW.; Washington, DC 20585-1290; Telephone (301) 903-7486.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P/>
        <P SOURCE="NPAR">
          <E T="03">Purpose of the Meeting:</E>The purpose of this meeting is to provide advice and guidance to the Department of Energy on scientific priorities within the field of advanced scientific computing research.</P>
        <HD SOURCE="HD1">Tentative Agenda Topics</HD>
        <P>• ASCR program updates.</P>
        <P>• EU Data Initiative.</P>
        <P>• HPC &amp; EERE Wind Program.</P>
        <P>• Early Career Research on Energy Efficient Interconnect for Exascale Computing.</P>
        <P>• Separating Algorithm and Implentation.</P>
        <P>• Update on ASCR exascale planning &amp; workshops.</P>
        <P>• Update on ASCAC COV.</P>
        <P>• Update on CSGF Review.</P>
        <P>• Public Comment (10-minute rule).</P>
        <P>
          <E T="03">Public Participation:</E>The meeting is open to the public. A webcast of this meeting may be available. Please check the Web site below for updates and information on how to view the meeting. If you would like to file a written statement with the Committee, you may do so either before or after the meeting. If you would like to make oral statements regarding any of the items on the agenda, you should contact Melea Baker by telephone at (301) 903-7486 or by e-mail at<E T="03">Melea.Baker@science.doe.gov.</E>You must make your request for an oral statement at least five business days prior to the meeting. Reasonable provision will be made to include the scheduled oral statements on the agenda. The Chairperson of the Committee is empowered to conduct the meeting in a manner that will facilitate the orderly conduct of business. Public comment will follow the 10-minute rule.</P>
        <P>
          <E T="03">Minutes:</E>The minutes of this meeting will be available on the U.S. Department of Energy's Office of Advanced Scientific Computing Web site for viewing at<E T="03">http://www.sc.doe.gov/ascr.</E>
        </P>
        <SIG>
          <DATED>Issued at Washington, DC on July 26, 2011.</DATED>
          <NAME>LaTanya Butler,</NAME>
          <TITLE>Acting Deputy Committee Management Officer.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19439 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6450-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF ENERGY</AGENCY>
        <SUBAGY>Office of Energy Efficiency and Renewable Energy</SUBAGY>
        <DEPDOC>[Docket Number EERE-2011-BT-NOA-0039]</DEPDOC>
        <SUBJECT>Proposed Agency Information Collection</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Office of Energy Efficiency and Renewable Energy, U.S. Department of Energy.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice and request for comments.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Department of Energy (DOE) invites public comment on a proposed collection of information that DOE is developing for submission to the Office of Management and Budget (OMB) pursuant to the Paperwork Reduction Act of 1995. Comments are invited on: (a) whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency's estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (c) ways to enhance the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>

          <P>Comments regarding this proposed information collection must be received on or before September 30, 2011. If you anticipate difficulty in submitting comments within that period, contact the person listed in<E T="02">ADDRESSES</E>as soon as possible.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Written comments may be sent to Mr. Alan Schroeder, U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, Building Technologies Program, EE-2J, 1000 Independence Avenue, SW., Washington, DC 20585-0121, or by fax at 202-287-1830, or by e-mail at<E T="03">TechID-RFI-2011-NOA-0039@ee.doe.gov.</E>
          </P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Requests for additional information or copies of the information collection instrument and instructions should be directed to Mr. Alan Schroeder, U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, Building Technologies Program, EE-2J, 1000 Independence Avenue SW., Washington, DC 20585-0121,<E T="03">Alan.Schroeder@ee.doe.gov, http://apps1.eere.energy.gov/buildings/alliances/cfm/tech_nomination_form.html.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>This information collection request contains: (1)<E T="03">OMB No.</E>New; (2)<E T="03">Information Collection Request Title:</E>Commercial Buildings Technology Evaluation Process Data Collection; (3)<E T="03">Type of Request:</E>New; (4)<E T="03">Purpose:</E>The collected information is needed to perform energy use evaluations of emerging and underutilized energy efficient commercial building technologies. The results of these evaluations will promote the market adoption of more energy efficient technologies in commercial building applications and will potentially prevent the duplication of technology evaluation efforts among stakeholders. (5)<E T="03">Annual Estimated Number of Respondents:</E>100; (6)<E T="03">Annual Estimated Number of Total Responses:</E>100; (7)<E T="03">Annual Estimated Number of Burden Hours:</E>25; (8)<E T="03">Annual Estimated Reporting and Recordkeeping Cost Burden:</E>$1000.</P>
        <AUTH>
          <HD SOURCE="HED">Statutory Authority:</HD>
          <P>Section 421(c) of the Energy Independence and Security Act, codified at 42 U.S.C. 17081(c).</P>
        </AUTH>
        <SIG>
          <DATED>Issued in Washington, DC, on July 26, 2011.</DATED>
          <NAME>Kathleen B. Hogan,</NAME>
          <TITLE>Deputy Assistant Secretary for Energy Efficiency, Office of Technology Development, Energy Efficiency and Renewable Energy.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19437 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6450-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <PRTPAGE P="45787"/>
        <AGENCY TYPE="S">DEPARTMENT OF ENERGY</AGENCY>
        <SUBAGY>Federal Energy Regulatory Commission</SUBAGY>
        <SUBJECT>Combined Notice of Filings #1</SUBJECT>
        <P>Take notice that the Commission received the following electric corporate filings:</P>
        
        <P>
          <E T="03">Docket Numbers:</E>EC11-97-000.</P>
        <P>
          <E T="03">Applicants:</E>J.P. Morgan Ventures Energy Corporation, Morgan Stanley Capitol Group Inc.</P>
        <P>
          <E T="03">Description:</E>Joint Section 203 Application of J.P. Morgan Ventures Energy Corporation and Morgan Stanley Capital Group.</P>
        <P>
          <E T="03">Filed Date:</E>07/22/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110722-5173.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Friday, August 12, 2011.</P>
        
        <P>
          <E T="03">Take notice that the</E>Commission received the following electric rate filings:</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER10-2042-001; ER10-1942-001; ER10-1941-001; ER10-1938-001; ER10-1888-001; ER10-1885-001; ER10-1884-001; ER10-1883-001; ER10-1878-001; ER10-1876-001; ER10-1875-001; ER10-1873-001; ER10-1947-001; ER10-1864-001; ER10-1862-001; ER10-1865-001.</P>
        <P>
          <E T="03">Applicants:</E>Calpine Energy Services, L.P., South Point Energy Center, LLC, Delta Energy Center, LLC, Geysers Power Company, LLC, Otay Mesa Energy Center, LLC, Calpine Power America—CA, LLC, Pastoria Energy Center, LLC, Metcalf Energy Center, LLC, Los Medanos Energy Center LLC, Los Esteros Critical Energy Facility LLC, Goose Haven Energy Center, LLC, Gilroy Energy Center, LLC, Creed Energy Center, LLC, Calpine Gilroy Cogen, L.P., Power Contract Financing, L.L.C., Calpine Construction Finance Co., L.P.</P>
        <P>
          <E T="03">Description:</E>Fourth Supplement to updated Market Power Analysis of Calpine Energy Services, L.P., et al.</P>
        <P>
          <E T="03">Filed Date:</E>07/22/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110722-5179.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Friday, August 12, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER10-2074-001; ER10-2097-003.</P>
        <P>
          <E T="03">Applicants:</E>Kansas City Power &amp; Light Company, KCP&amp;L Greater Missouri Operations Company.</P>
        <P>
          <E T="03">Description:</E>Supplemental Information of Kansas City Power &amp; Light Company, et al.</P>
        <P>
          <E T="03">Filed Date:</E>07/15/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110715-5153.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Friday, August 05, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER10-2758-001.</P>
        <P>
          <E T="03">Applicants:</E>EnergyConnect, Inc.</P>
        <P>
          <E T="03">Description:</E>EnergyConnect, Inc. Notice of Non-Material Change in Status.</P>
        <P>
          <E T="03">Filed Date:</E>07/22/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110722-5148.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Friday, August 12, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-3912-001.</P>
        <P>
          <E T="03">Applicants:</E>Arizona Public Service Company.</P>
        <P>
          <E T="03">Description:</E>Arizona Public Service Company submits tariff filing per 35.17(b): Amendment to APS Service Agreement No. 311 to be effective 8/29/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/22/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110722-5029.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Friday, August 12, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-3963-001.</P>
        <P>
          <E T="03">Applicants:</E>Bruce Power Inc.</P>
        <P>
          <E T="03">Description:</E>Bruce Power Inc. submits tariff filing per 35: Bruce Power Inc. Substitute First Revised Tariff submitted on 7/22/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/22/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110722-5055.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Friday, August 12, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4102-000.</P>
        <P>
          <E T="03">Applicants:</E>Public Service Company of New Mexico.</P>
        <P>
          <E T="03">Description:</E>Public Service Company of New Mexico submits tariff filing per 35: OATT Changes for Intra-Hour Scheduling to be effective 9/21/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/22/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110722-5136.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Friday, August 12, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4103-000.</P>
        <P>
          <E T="03">Applicants:</E>Arizona Public Service Company.</P>
        <P>
          <E T="03">Description:</E>Arizona Public Service Company submits tariff filing per 35.13(a)(2)(iii: FERC Electric Rate Schedule No. 253, Construction Agreement between WAPA and APS to be effective 9/9/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/22/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110722-5151.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Friday, August 12, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4104-000.</P>
        <P>
          <E T="03">Applicants:</E>Southern California Edison Company.</P>
        <P>
          <E T="03">Description:</E>Southern California Edison Company submits tariff filing per 35.13(a)(2)(iii: Letter Agreement for Three 230kV Lines Eldorado Substation with NV Energy to be effective 7/14/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/22/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110722-5154.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Friday, August 12, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4105-000.</P>
        <P>
          <E T="03">Applicants:</E>Southwest Power Pool, Inc.</P>
        <P>
          <E T="03">Description:</E>Southwest Power Pool, Inc. submits tariff filing per 35: Order No. 745 Compliance Filing to be effective N/A.</P>
        <P>
          <E T="03">Filed Date:</E>07/22/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110722-5159.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Friday, August 12, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4106-000.</P>
        <P>
          <E T="03">Applicants:</E>PJM Interconnection, L.L.C.</P>
        <P>
          <E T="03">Description:</E>PJM Interconnection, L.L.C. submits tariff filing per 35: Compliance Filing per Order 745 to be effective 12/31/9998.</P>
        <P>
          <E T="03">Filed Date:</E>07/22/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110722-5160.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Friday, August 12, 2011.</P>
        
        <P>Any person desiring to intervene or to protest in any of the above proceedings must file in accordance with Rules 211 and 214 of the Commission's Rules of Practice and Procedure (18 CFR 385.211 and 385.214) on or before 5 p.m. Eastern time on the specified comment date. It is not necessary to separately intervene again in a subdocket related to a compliance filing if you have previously intervened in the same docket. Protests will be considered by the Commission in determining the appropriate action to be taken, but will not serve to make protestants parties to the proceeding. Anyone filing a motion to intervene or protest must serve a copy of that document on the Applicant. In reference to filings initiating a new proceeding, interventions or protests submitted on or before the comment deadline need not be served on persons other than the Applicant.</P>
        <P>As it relates to any qualifying facility filings, the notices of self-certification [or self-recertification] listed above, do not institute a proceeding regarding qualifying facility status. A notice of self-certification [or self-recertification] simply provides notification that the entity making the filing has determined the facility named in the notice meets the applicable criteria to be a qualifying facility. Intervention and/or protest do not lie in dockets that are qualifying facility self-certifications or self-recertifications. Any person seeking to challenge such qualifying facility status may do so by filing a motion pursuant to 18 CFR 292.207(d)(iii). Intervention and protests may be filed in response to notices of qualifying facility dockets other than self-certifications and self-recertifications.</P>

        <P>The Commission encourages electronic submission of protests and interventions in lieu of paper, using the<PRTPAGE P="45788"/>FERC Online links at<E T="03">http://www.ferc.gov.</E>To facilitate electronic service, persons with Internet access who will eFile a document and/or be listed as a contact for an intervenor must create and validate an eRegistration account using the eRegistration link. Select the eFiling link to log on and submit the intervention or protests.</P>
        <P>Persons unable to file electronically should submit an original and 14 copies of the intervention or protest to the Federal Energy Regulatory Commission, 888 First St., NE., Washington, DC 20426.</P>

        <P>The filings in the above proceedings are accessible in the Commission's eLibrary system by clicking on the appropriate link in the above list. They are also available for review in the Commission's Public Reference Room in Washington, DC. There is an eSubscription link on the Web site that enables subscribers to receive e-mail notification when a document is added to a subscribed docket(s). For assistance with any FERC  Online service, please e-mail<E T="03">FERCOnlineSupport@ferc.gov.</E>or call (866) 208-3676 (toll free). For TTY, call (202) 502-8659.</P>
        <SIG>
          <DATED>Dated: July 25, 2011.</DATED>
          <NAME>Nathaniel J. Davis, Sr.,</NAME>
          <TITLE>Deputy Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19347 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6717-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF ENERGY</AGENCY>
        <SUBAGY>Federal Energy Regulatory Commission</SUBAGY>
        <SUBJECT>Combined Notice of Filings</SUBJECT>
        <DATE>July 15, 2011.</DATE>
        <P>Take notice that the Commission has received the following Natural Gas Pipeline Rate and Refund Report filings:</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2266-000.</P>
        <P>
          <E T="03">Applicants:</E>Dominion Transmission, Inc.</P>
        <P>
          <E T="03">Description:</E>Dominion Transmission, Inc. submits tariff filing per 154.204: DTI—July 12, 2011 Negotiated Rate Agreement to be effective 7/13/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/12/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110712-5128.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, July 25, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2267-000.</P>
        <P>
          <E T="03">Applicants:</E>Questar Pipeline Company.</P>
        <P>
          <E T="03">Description:</E>Questar Pipeline Company submits tariff filing per 154.204: ISS Cashout Provision Addition to be effective 8/15/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/13/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110713-5001.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, July 25, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2268-000.</P>
        <P>
          <E T="03">Applicants:</E>Kinder Morgan Interstate Gas Transmission LLC.</P>
        <P>
          <E T="03">Description:</E>Kinder Morgan Interstate Gas Transmission LLC submits tariff filing per 154.204: Negotiated Rate 2011-07-13 Mieco A&amp;R to be effective 7/14/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/13/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110713-5076.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, July 25, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2269-000.</P>
        <P>
          <E T="03">Applicants:</E>Big Sandy Pipeline, LLC.</P>
        <P>
          <E T="03">Description:</E>Big Sandy Pipeline, LLC submits tariff filing per 154.202: Big Sandy LINK Implementation to be effective 9/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5033.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Tuesday, July 26, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2270-000.</P>
        <P>
          <E T="03">Applicants:</E>Big Sandy Pipeline, LLC.</P>
        <P>
          <E T="03">Description:</E>Big Sandy Pipeline, LLC submits tariff filing per 154.602: Cancellation of Original Volume No. 1 to be effective 9/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5053.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Tuesday, July 26, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2271-000.</P>
        <P>
          <E T="03">Applicants:</E>Algonquin Gas Transmission, LLC.</P>
        <P>
          <E T="03">Description:</E>Algonquin Gas Transmission, LLC submits tariff filing per 154.204: AGT Modifications for Big Sandy LINK Implementation to be effective 9/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5064.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Tuesday, July 26, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2272-000.</P>
        <P>
          <E T="03">Applicants:</E>Bobcat Gas Storage.</P>
        <P>
          <E T="03">Description:</E>Bobcat Gas Storage submits tariff filing per 154.204: Bobcat Modifications for Big Sandy LINK Implementation to be effective 9/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5074.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Tuesday, July 26, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2273-000.</P>
        <P>
          <E T="03">Applicants:</E>Egan Hub Storage, LLC.</P>
        <P>
          <E T="03">Description:</E>Egan Hub Storage, LLC submits tariff filing per 154.204: Egan Modifications for Big Sandy LINK Implementation to be effective 9/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5076.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Tuesday, July 26, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2274-000.</P>
        <P>
          <E T="03">Applicants:</E>East Tennessee Natural Gas, LLC.</P>
        <P>
          <E T="03">Description:</E>East Tennessee Natural Gas, LLC submits tariff filing per 154.204: ETNG Modifications for Big Sandy LINK Implementation to be effective 9/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5077.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Tuesday, July 26, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2275-000.</P>
        <P>
          <E T="03">Applicants:</E>Ozark Gas Transmission, LLC.</P>
        <P>
          <E T="03">Description:</E>Ozark Gas Transmission, LLC submits tariff filing per 154.204: OGT Modifications for Big Sandy LINK Implementation to be effective 9/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5078.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Tuesday, July 26, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2276-000.</P>
        <P>
          <E T="03">Applicants:</E>Saltville Gas Storage Company LLC.</P>
        <P>
          <E T="03">Description:</E>Saltville Gas Storage Company LLC submits tariff filing per 154.204: Saltville Modifications for Big Sandy LINK Implementation to be effective 9/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5083.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Tuesday, July 26, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2277-000.</P>
        <P>
          <E T="03">Applicants:</E>Texas Eastern Transmission, LP.</P>
        <P>
          <E T="03">Description:</E>Texas Eastern Transmission, LP submits tariff filing per 154.204: TETLP Modifications for Big Sandy LINK Implementation to be effective 9/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5084.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Tuesday, July 26, 2011.</P>
        

        <P>Any person desiring to intervene or to protest in any of the above proceedings must file in accordance with Rules 211 and 214 of the Commission's Rules of Practice and Procedure (18 CFR 385.211 and 385.214) on or before 5 p.m. Eastern time on the specified comment date. It is not necessary to separately intervene again in a subdocket related to a compliance filing if you have previously intervened in the same docket. Protests will be considered by the Commission in determining the appropriate action to be taken, but will not serve to make protestants parties to the proceeding. Anyone filing a motion to intervene or protest must serve a copy of that document on the Applicant. In reference to filings initiating a new proceeding, interventions or protests submitted on or before the comment deadline need<PRTPAGE P="45789"/>not be served on persons other than the Applicant.</P>

        <P>The Commission encourages electronic submission of protests and interventions in lieu of paper, using the FERC Online links at<E T="03">http://www.ferc.gov.</E>To facilitate electronic service, persons with Internet access who will eFile a document and/or be listed as a contact for an intervenor must create and validate an eRegistration account using the eRegistration link. Select the eFiling link to log on and submit the intervention or protests.</P>
        <P>Persons unable to file electronically should submit an original and 14 copies of the intervention or protest to the Federal Energy Regulatory Commission, 888 First St., NE., Washington, DC 20426.</P>

        <P>The filings in the above proceedings are accessible in the Commission's eLibrary system by clicking on the appropriate link in the above list. They are also available for review in the Commission's Public Reference Room in Washington, DC. There is an eSubscription link on the Web site that enables subscribers to receive e-mail notification when a document is added to a subscribed docket(s). For assistance with any FERC Online service, please e-mail<E T="03">FERCOnlineSupport@ferc.gov</E>or call (866) 208-3676 (toll free). For TTY, call (202) 502-8659.</P>
        <SIG>
          <DATED>Dated: July 15, 2011.</DATED>
          <NAME>Nathaniel J. Davis, Sr.,</NAME>
          <TITLE>Deputy Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19350 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6717-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF ENERGY</AGENCY>
        <SUBAGY>Federal Energy Regulatory Commission</SUBAGY>
        <SUBJECT>Combined Notice of Filings #2</SUBJECT>
        <P>Take notice that the Commission received the following exempt wholesale generator filings:</P>
        
        <P>
          <E T="03">Docket Numbers:</E>EG11-109-000.</P>
        <P>
          <E T="03">Applicants:</E>Double “C” Limited.</P>
        <P>
          <E T="03">Description:</E>Notice of Self-Certification of Exempt Wholesale Generator for Double “C” Limited.</P>
        <P>
          <E T="03">Filed Date:</E>07/25/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110725-5065.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 15, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>EG11-110-000.</P>
        <P>
          <E T="03">Applicants:</E>High Sierra Limited.</P>
        <P>
          <E T="03">Description:</E>Notice of Self-Certification of Exempt Wholesale Generator for High Sierra Limited.</P>
        <P>
          <E T="03">Filed Date:</E>07/25/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110725-5067.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 15, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>EG11-111-000.</P>
        <P>
          <E T="03">Applicants:</E>Kern Front Limited.</P>
        <P>
          <E T="03">Description:</E>Notice of Self-Certific<E T="03">ation of Exempt Wholesale Generator for Kern Front Limited.</E>
        </P>
        <P>
          <E T="03">Filed Date:</E>07/25/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110725-5068.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 15, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>EG11-112-000.</P>
        <P>
          <E T="03">Applicants:</E>Cogentrix of Alamosa, LLC.</P>
        <P>
          <E T="03">Description:</E>Cogentrix of Alamosa, LLC, Notice of Self-certification of Exempt Wholesale Generator.</P>
        <P>
          <E T="03">Filed Date:</E>07/25/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110725-5070.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 15, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>EG11-113-000.</P>
        <P>
          <E T="03">Applicants:</E>Hudson Ranch Power I LLC.</P>
        <P>
          <E T="03">Description:</E>Self-Certification Notice of Exempt Wholesale Generator of Hudson Ranch Power I LLC.</P>
        <P>
          <E T="03">Filed Date:</E>07/25/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110725-5116.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 15, 2011.</P>
        <P>Take notice that the Commission received the following electric rate filings:</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-3551-002.</P>
        <P>
          <E T="03">Applicants:</E>Glacial Energy of New York.</P>
        <P>
          <E T="03">Description:</E>Glacial Energy of New York submits tariff filing per 35.17(b): Deficiency NY to be effective 7/25/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/25/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110725-5104.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 08, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-3554-002.</P>
        <P>
          <E T="03">Applicants:</E>Glacial Energy of California, Inc.</P>
        <P>
          <E T="03">Description:</E>Glacial Energy of California, Inc. submits tariff filing per 35.17(b): Deficiency Filing-CA to be effective 7/25/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/25/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110725-5109.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 08, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4065-001.</P>
        <P>
          <E T="03">Applicants:</E>PJM Interconnection, L.L.C.</P>
        <P>
          <E T="03">Description:</E>PJM Interconnection, L.L.C. submits tariff filing per 35.17(b): Errata to PJM No. V4-054; Service Agreement No. 2967—Docket No. ER11-4065-000 to be effective 6/17/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/25/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110725-5049.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 15, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4107-000.</P>
        <P>
          <E T="03">Applicants:</E>PJM Interconnection, L.L.C.</P>
        <P>
          <E T="03">Description:</E>PJM Interconnection, L.L.C. submits tariff filing per 35.13(a)(2)(iii: Queue No. W4-058; Original Service Agreement No. 2973 to be effective 6/24/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/25/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110725-5048.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 15, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4108-000.</P>
        <P>
          <E T="03">Applicants:</E>Southern California Edison Company.</P>
        <P>
          <E T="03">Description:</E>Southern California Edison Company submits tariff filing per 35.13(a)(2)(iii: LGIA Alta Visa SunTower Generating Station Project NRG Solar to be effective 7/26/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/25/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110725-5069.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 15, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4109-000.</P>
        <P>
          <E T="03">Applicants:</E>Florida Power Corporation.</P>
        <P>
          <E T="03">Description:</E>Florida Power Corporation submits tariff filing per 35.13(a)(2)(iii: Revised Service Agreement No. 143 under Florida Power Corp. OATT to be effective 5<E T="03">/18/2011</E>.</P>
        <P>
          <E T="03">Filed Date:</E>07/25/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110725-5071.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 15, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4110-000.</P>
        <P>
          <E T="03">Applicants:</E>Northern States Power Company, a Minnesota corporation, Northern States Power Company, a Wisconsin corporation, Midwest Independent Transmission System Operator, Inc.</P>
        <P>
          <E T="03">Description:</E>Northern States Power Company, a Minnesota corporation submits tariff filing per 35.13(a)(2)(iii: 07-25-11_NSP Attachment GG to be effective 8/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/25/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110725-5079.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 15, 2011.</P>
        

        <P>Any person desiring to intervene or to protest in any of the above proceedings must file in accordance with Rules 211 and 214 of the Commission's Rules of Practice and Procedure (18 CFR 385.211 and 385.214) on or before 5 p.m. Eastern time on the specified comment date. It is not necessary to separately intervene again in a subdocket related to a compliance filing if you have previously intervened in the same docket. Protests will be considered by the Commission in determining the appropriate action to be taken, but will not serve to make protestants parties to the proceeding. Anyone filing a motion to intervene or<PRTPAGE P="45790"/>protest must serve a copy of that document on the Applicant. In reference to filings initiating a new proceeding, interventions or protests submitted on or before the comment deadline need not be served on persons other than the Applicant.</P>
        <P>As it relates to any qualifying facility filings, the notices of self-certification [or self-recertification] listed above, do not institute a proceeding regarding qualifying facility status. A notice of self-certification [or self-recertification] simply provides notification that the entity making the filing has determined the facility named in the notice meets the applicable criteria to be a qualifying facility. Intervention and/or protest do not lie in dockets that are qualifying facility self-certifications or self-recertifications. Any person seeking to challenge such qualifying facility status may do so by filing a motion pursuant to 18 CFR 292.207(d)(iii). Intervention and protests may be filed in response to notices of qualifying facility dockets other than self-certifications and self-recertifications.</P>

        <P>The Commission encourages electronic submission of protests and interventions in lieu of paper, using the FERC Online links at<E T="03">http://www.ferc.gov.</E>To facilitate electronic service, persons with Internet access who will eFile a document and/or be listed as a contact for an intervenor must create and validate an eRegistration account using the eRegistration link. Select the eFiling link to log on and submit the intervention or protests.</P>
        <P>Persons unable to file electronically should submit an original and 14 copies of the intervention or protest to the Federal Energy Regulatory Commission, 888 First St., NE., Washington, DC 20426.</P>

        <P>The filings in the above proceedings are accessible in the Commission's eLibrary system by clicking on the appropriate link in the above list. They are also available for review in the Commission's Public Reference Room in Washington, DC. There is an eSubscription link on the Web site that enables subscribers to receive e-mail notification when a document is added to a subscribed docket(s). For assistance with any FERC Online service, please email<E T="03">FERCOnlineSupport@ferc.gov.</E>or call (866) 208-3676 (toll free). For TTY, call (202) 502-8659.</P>
        <SIG>
          <DATED>Dated: July 25, 2011.</DATED>
          <NAME>Nathaniel J. Davis, Sr.,</NAME>
          <TITLE>Deputy Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19352 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6717-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF ENERGY</AGENCY>
        <SUBAGY>Federal Energy Regulatory Commission</SUBAGY>
        <SUBJECT>Combined Notice of Filings #1</SUBJECT>
        <P>Take notice that the Commission received the following electric corporate filings:</P>
        
        <P>
          <E T="03">Docket Numbers:</E>EC11-95-000.</P>
        <P>
          <E T="03">Applicants:</E>El Dorado Energy, LLC, Copper Mountain Solar 1, LLC.</P>
        <P>
          <E T="03">Description:</E>El Dorardo Energy, LLC and Copper Mountain Solar 1, LLC Application pursuant to Section 203 of the FPA for Authorization of Intracorporate Transfer of Jurisdictional Assets.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5110.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Thursday, August 4, 2011.</P>
        
        <P>Take notice that the Commission received the following electric rate filings:</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4044-001.</P>
        <P>
          <E T="03">Applicants:</E>Gratiot County Wind LLC.</P>
        <P>
          <E T="03">Description:</E>Gratiot County Wind LLC submits tariff filing per 35.17(b): Supplement to Market-Based Rate Application to be effective 9/12/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5023.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Thursday, August 4, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4046-001.</P>
        <P>
          <E T="03">Applicants:</E>Gratiot County Wind II LLC.</P>
        <P>
          <E T="03">Description:</E>Gratiot County Wind II LLC submits tariff filing per 35.17(b): Supplement to Market-Based Rate Application to be effective 9/12/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5024.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Thursday, August 4, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4052-000.</P>
        <P>
          <E T="03">Applicants:</E>Alpha Gas and Electric LLC.</P>
        <P>
          <E T="03">Description:</E>Alpha Gas and Electric LLC submits tariff filing per: Marked Tariff Attachment to be effective N/A.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5093.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Thursday, August 4, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4053-000.</P>
        <P>
          <E T="03">Applicants:</E>Southwest Power Pool, Inc.</P>
        <P>
          <E T="03">Description:</E>Southwest Power Pool, Inc. submits tariff filing per 35.13(a)(2)(iii): Submission of Revisions to SPS Pricing Zone Rate to be effective 5/15/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5085.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Thursday, August 4, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4054-000.</P>
        <P>
          <E T="03">Applicants:</E>FirstEnergy Solutions Corp.</P>
        <P>
          <E T="03">Description:</E>FirstEnergy Solutions Corp. submits tariff filing per 35: Revised Market-Based Rate Power Sales Tariff to be effective 6/29/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5087.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Thursday, August 4, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>ER11-4055-000.</P>
        <P>
          <E T="03">Applicants:</E>Copper Mountain Solar 1, LLC.</P>
        <P>
          <E T="03">Description:</E>Copper Mountain Solar 1, LLC submits tariff filing per 35.12: Copper Mountain Solar 1 LLC FERC Electric Tariff No. 1 Market-Based Rates Tariff to be effective 7/14/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/14/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110714-5095.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Thursday, August 4, 2011.</P>
        
        <P>Any person desiring to intervene or to protest in any of the above proceedings must file in accordance with Rules 211 and 214 of the Commission's Rules of Practice and Procedure (18 CFR 385.211 and 385.214) on or before 5 p.m. Eastern time on the specified comment date. It is not necessary to separately intervene again in a subdocket related to a compliance filing if you have previously intervened in the same docket. Protests will be considered by the Commission in determining the appropriate action to be taken, but will not serve to make protestants parties to the proceeding. Anyone filing a motion to intervene or protest must serve a copy of that document on the Applicant. In reference to filings initiating a new proceeding, interventions or protests submitted on or before the comment deadline need not be served on persons other than the Applicant.</P>
        <P>As it relates to any qualifying facility filings, the notices of self-certification [or self-recertification] listed above, do not institute a proceeding regarding qualifying facility status. A notice of self-certification [or self-recertification] simply provides notification that the entity making the filing has determined the facility named in the notice meets the applicable criteria to be a qualifying facility. Intervention and/or protest do not lie in dockets that are qualifying facility self-certifications or self-recertifications. Any person seeking to challenge such qualifying facility status may do so by filing a motion pursuant to 18 CFR 292.207(d)(iii). Intervention and protests may be filed in response to notices of qualifying facility dockets other than self-certifications and self-recertifications.</P>

        <P>The Commission encourages electronic submission of protests and<PRTPAGE P="45791"/>interventions in lieu of paper, using the FERC Online links at<E T="03">http://www.ferc.gov.</E>To facilitate electronic service, persons with Internet access who will eFile a document and/or be listed as a contact for an intervenor must create and validate an eRegistration account using the eRegistration link. Select the eFiling link to log on and submit the intervention or protests.</P>
        <P>Persons unable to file electronically should submit an original and 14 copies of the intervention or protest to the Federal Energy Regulatory Commission, 888 First St., NE., Washington, DC 20426.</P>

        <P>The filings in the above proceedings are accessible in the Commission's eLibrary system by clicking on the appropriate link in the above list. They are also available for review in the Commission's Public Reference Room in Washington, DC. There is an eSubscription link on the Web site that enables subscribers to receive e-mail notification when a document is added to a subscribed docket(s). For assistance with any FERC Online service, please e-mail<E T="03">FERCOnlineSupport@ferc.gov</E>or call (866) 208-3676 (toll free). For TTY, call (202) 502-8659.</P>
        <SIG>
          <DATED>Dated: July 15, 2011.</DATED>
          <NAME>Nathaniel J. Davis, Sr.,</NAME>
          <TITLE>Deputy Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19351 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6717-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF ENERGY</AGENCY>
        <SUBAGY>Federal Energy Regulatory Commission</SUBAGY>
        <SUBJECT>Combined Notice of Filings No. 1</SUBJECT>
        <P>Take notice that the Commission has received the following Natural Gas Pipeline Rate and Refund Report filings:</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2278-000.</P>
        <P>
          <E T="03">Applicants:</E>Southern LNG Company, LLC.</P>
        <P>
          <E T="03">Description:</E>Southern LNG Company, LLC submits tariff filing per 154.204: BG Negotiated Rate to be effective 8/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/15/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110715-5055.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Wednesday, July 27, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2279-000.</P>
        <P>
          <E T="03">Applicants:</E>Gulf South Pipeline Company, LP.</P>
        <P>
          <E T="03">Description:</E>Gulf South Pipeline Company, LP submits tariff filing per 154.204: Devon K34694-33 Amendment to Negotiated Rate Agreement Filing to be effective 7/15/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/18/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110718-5042.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 01, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2280-000.</P>
        <P>
          <E T="03">Applicants:</E>Texas Gas Transmission, LLC.</P>
        <P>
          <E T="03">Description:</E>Texas Gas Transmission, LLC submits tariff filing per 154.204: Filing to incorporate approved changes to be effective 7/13/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/18/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110718-5063.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 01, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2281-000.</P>
        <P>
          <E T="03">Applicants:</E>Iroquois Gas Transmission System, L.P.</P>
        <P>
          <E T="03">Description:</E>Iroquois Gas Transmission System, L.P. submits tariff filing per 154.204: 07/18/11 Negotiated Rates—JP Morgan Ventures Energy Corporation to be effective 7/19/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/18/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110718-5101.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 01, 2011.</P>
        
        <P>Any person desiring to intervene or to protest in any of the above proceedings must file in accordance with Rules 211 and 214 of the Commission's Rules of Practice and Procedure (18 CFR 385.211 and 385.214) on or before 5 p.m. Eastern time on the specified comment date. It is not necessary to separately intervene again in a subdocket related to a compliance filing if you have previously intervened in the same docket. Protests will be considered by the Commission in determining the appropriate action to be taken, but will not serve to make protestants parties to the proceeding. Anyone filing a motion to intervene or protest must serve a copy of that document on the Applicant. In reference to filings initiating a new proceeding, interventions or protests submitted on or before the comment deadline need not be served on persons other than the Applicant.</P>

        <P>The Commission encourages electronic submission of protests and interventions in lieu of paper, using the FERC Online links at<E T="03">http://www.ferc.gov.</E>To facilitate electronic service, persons with Internet access who will eFile a document and/or be listed as a contact for an intervenor must create and validate an eRegistration account using the eRegistration link. Select the eFiling link to log on and submit the intervention or protests.</P>
        <P>Persons unable to file electronically should submit an original and 14 copies of the intervention or protest to the Federal Energy Regulatory Commission, 888 First St., NE., Washington, DC 20426.</P>

        <P>The filings in the above proceedings are accessible in the Commission's eLibrary system by clicking on the appropriate link in the above list. They are also available for review in the Commission's Public Reference Room in Washington, DC. There is an eSubscription link on the Web site that enables subscribers to receive e-mail notification when a document is added to a subscribed docket(s). For assistance with any FERC Online service, please e-mail<E T="03">FERCOnlineSupport@ferc.gov.</E>or call (866) 208-3676 (toll free). For TTY, call (202) 502-8659.</P>
        <SIG>
          <DATED>Dated: July 19, 2011.</DATED>
          <NAME>Nathaniel J. Davis, Sr.,</NAME>
          <TITLE>Deputy Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19349 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6717-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF ENERGY</AGENCY>
        <SUBAGY>Federal Energy Regulatory Commission</SUBAGY>
        <SUBJECT>Combined Notice of Filings No. 2</SUBJECT>
        <P>Take notice that the Commission has received the following Natural Gas Pipeline Rate and Refund Report filings:</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-1566-005.</P>
        <P>
          <E T="03">Applicants:</E>Tennessee Gas Pipeline Company.</P>
        <P>
          <E T="03">Description:</E>Tennessee Gas Pipeline Company submits tariff filing per 154.203: Tariff Cleanup FT-BH Min Commodity to be effective 6/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/13/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110713-5157.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, July 25, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-59-002.</P>
        <P>
          <E T="03">Applicants:</E>Northwest Pipeline GP.</P>
        <P>
          <E T="03">Description:</E>Northwest Pipeline GP submits tariff filing per 154.203: NWP RP11-59-002 Compliance Filing to be effective 11/13/2010.</P>
        <P>
          <E T="03">Filed Date:</E>07/15/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110715-5079.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Wednesday, July 27, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-1566-004.</P>
        <P>
          <E T="03">Applicants:</E>Tennessee Gas Pipeline Company.</P>
        <P>
          <E T="03">Description:</E>Tennessee Gas Pipeline Company submits tariff filing per: Correct June 1 to July 1 to be effective N/A.</P>
        <P>
          <E T="03">Filed Date:</E>07/18/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110718-5000.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 01, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2258-001.</P>
        <P>
          <E T="03">Applicants:</E>PetroLogistics Natural Gas Storage, LLC.</P>
        <P>
          <E T="03">Description:</E>PetroLogistics Natural Gas Storage, LLC submits tariff filing per 154.205(b): Amendment Filing to be effective 8/5/2011.<PRTPAGE P="45792"/>
        </P>
        <P>
          <E T="03">Filed Date:</E>07/18/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110718-5168.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 01, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2278-001.</P>
        <P>
          <E T="03">Applicants:</E>Southern LNG Company, LLC.</P>
        <P>
          <E T="03">Description:</E>Southern LNG Company, LLC submits tariff filing per 154.205(b): BG Negotiated Rate—Errata to be effective 8/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/18/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110718-5180.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 01, 2011.</P>
        
        <P>
          <E T="03">Docket Numbers:</E>RP11-2231-001.</P>
        <P>
          <E T="03">Applicants:</E>Gulf Crossing Pipeline Company LLC.</P>
        <P>
          <E T="03">Description:</E>Gulf Crossing Pipeline Company LLC submits tariff filing per 154.205(b): Amendment Filing in RP11-2231 to be effective 7/1/2011.</P>
        <P>
          <E T="03">Filed Date:</E>07/19/2011.</P>
        <P>
          <E T="03">Accession Number:</E>20110719-5046.</P>
        <P>
          <E T="03">Comment Date:</E>5 p.m. Eastern Time on Monday, August 01, 2011.</P>
        
        <P>Any person desiring to protest this filing must file in accordance with Rule 211 of the Commission's Rules of Practice and Procedure (18 CFR 385.211). Protests to this filing will be considered by the Commission in determining the appropriate action to be taken, but will not serve to make protestants parties to the proceeding. Such protests must be filed on or before 5 p.m. Eastern time on the specified comment date. Anyone filing a protest must serve a copy of that document on all the parties to the proceeding.</P>

        <P>The Commission encourages electronic submission of protests in lieu of paper using the “eFiling” link at<E T="03">http://www.ferc.gov.</E>Persons unable to file electronically should submit an original and 14 copies of the protest to the Federal Energy Regulatory Commission, 888 First Street, NE., Washington, DC 20426.</P>
        <P>This filing is accessible on-line at<E T="03">http://www.ferc.gov,</E>using the “eLibrary” link and is available for review in the Commission's Public Reference Room in Washington, DC. There is an “eSubscription” link on the Web site that enables subscribers to receive e-mail notification when a document is added to a subscribed docket(s). For assistance with any FERC Online service, please e-mail<E T="03">FERCOnlineSupport@ferc.gov,</E>or call (866) 208-3676 (toll free). For TTY, call (202) 502-8659.</P>
        <SIG>
          <DATED>Dated: July 19, 2011.</DATED>
          <NAME>Nathaniel J. Davis, Sr.,</NAME>
          <TITLE>Deputy Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19348 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6717-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">ENVIRONMENTAL PROTECTION AGENCY</AGENCY>
        <DEPDOC>[FRL-9445-4; Permit No. AKG-33-000]</DEPDOC>
        <SUBJECT>Proposed Reissuance of a General NPDES Permit for Facilities Related to Oil and Gas Extraction</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Environmental Protection Agency.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Proposed reissuance of a general permit.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>On January 2, 2009, the general permit (GP) regulating activities related to the extraction of oil and gas on the North Slope of the Brooks Range in the state of Alaska expired. This proposed reissuance of a general permit, AKG-33-0000, is intended to regulate activities related to the extraction of oil and gas on the North Slope of the Brooks Range in the state of Alaska plus the proposed area expansion described in the Fact Sheet including activities along the Trans Alaskan Pipeline corridor previously covered by Alyeska Pipeline Services, Inc.'s NPDES permit, AK-005056-3. The draft general permit would cover the same discharges as the previous general permit except for domestic wastewater discharges. The covered discharges include gravel pit dewatering, construction dewatering, hydrostatic test water, mobile spill response, and storm water from industrial activities. The proposed reissuance also includes a new outfall designation for the discharge of secondary containment water. When issued, the proposed permit will establish effluent limitations, standards, prohibitions and other conditions on discharges from covered facilities. These conditions are based on existing national effluent guidelines, the state of Alaska's Water Quality Standards and material contained in the administrative record. A description of the basis for the conditions and requirements of the draft general permit is given in the Fact Sheet. This is also notice of the Clean Water Act § 401 draft Certification provided by the state of Alaska and the termination of administrative extensions as described in the Fact Sheet.</P>
          <P>The reissuance of this general permit was previously public noticed on July 2, 2009. EPA has changed some permit conditions in this proposal based on the comments received in 2009.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Interested persons may submit comments on the proposed reissuance of the general permit to EPA, Region 10 at the address below. Comments must be postmarked by September 15, 2011. EPA received many comments on the previous proposal and attempted to address some of these in the re-proposal so please submit new comments on this action.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Comments on the proposed general permit reissuance should be sent to the attention of the Director, Office of Water &amp; Watersheds, EPA—Region 10, 1200 Sixth Avenue, Suite 900 OWW-130, Seattle, WA 98101. Comments may also be submitted electronically to<E T="03">godsey.cindi@epa.gov.</E>
          </P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Copies of the proposed general permit and Fact Sheet are available upon request. Requests may be made to Audrey Washington at (206) 553-0523 or to Cindi Godsey at (907) 271-6561. Requests may also be electronically mailed to:<E T="03">washington.audrey@epa.gov</E>or<E T="03">godsey.cindi@epa.gov.</E>
          </P>

          <P>These documents may also be found on the EPA Region 10 Web site at<E T="03">http://yosemite.epa.gov/r10/WATER.NSF/NPDES+Permits/DraftPermitsAK.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P SOURCE="NPAR">
          <E T="03">Executive Order 12866:</E>The Office of Management and Budget has exempted this action from the review requirements of Executive Order 12866 pursuant to Section 6 of that order.</P>
        <P>
          <E T="03">Regulatory Flexibility Act:</E>Under the Regulatory Flexibility Act (RFA), 5 U.S.C. 601<E T="03">et seq.,</E>a Federal agency must prepare an initial regulatory flexibility analysis “for any proposed rule” for which the agency “is required by section 553 of the Administrative Procedure Act (APA), or any other law, to publish general notice of proposed rulemaking.” The RFA exempts from this requirement any rule that the issuing agency certifies “will not, if promulgated, have a significant economic impact on a substantial number of small entities.” EPA has concluded that NPDES general permits are permits, not rulemakings, under the APA and thus not subject to APA rulemaking requirements or the RFA. Notwithstanding that general permits are not subject to the RFA, EPA has determined that this GP, as issued, will not have a significant economic impact on a substantial number of small entities.</P>
        <SIG>
          <DATED>Dated: July 21, 2011.</DATED>
          <NAME>Christine Psyk,</NAME>
          <TITLE>Associate Director, Office of Water &amp; Watersheds, Region 10, U.S. Environmental Protection Agency.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19127 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6560-50-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <PRTPAGE P="45793"/>
        <AGENCY TYPE="S">ENVIRONMENTAL PROTECTION AGENCY</AGENCY>
        <DEPDOC>[FRL-9446-8]</DEPDOC>
        <SUBJECT>Proposed Settlement Agreement, Clean Air Act Citizen Suit</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Environmental Protection Agency (EPA).</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of Proposed Settlement Agreement; Request for Public Comment.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>In accordance with section 113(g) of the Clean Air Act, as amended (“CAA” or the “Act”), 42 U.S.C. 7413(g), notice is hereby given of a proposed settlement agreement to address a lawsuit filed by Concerned Citizens Around Murphy in the United States District Court for the Eastern District of Louisiana:<E T="03">Concerned Citizens Around Murphy</E>v.<E T="03">Jackson,</E>No. 10-cv-04444 (E.D. La.). Plaintiff filed a deadline suit to compel the Administrator to respond to an administrative petition seeking EPA's objection to a CAA Title V operating permit issued by the Louisiana Department of Environmental Quality to Murphy Oil USA for the Meraux Refinery in St. Bernard Parish, Louisiana. Under the terms of the proposed settlement agreement, EPA has agreed to respond to the petition by September 22, 2011.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>

          <P>Written comments on the proposed settlement agreement must be received by<E T="03">August 31, 2011.</E>
          </P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Submit your comments, identified by Docket ID number EPA-HQ-OGC-2011-0635, online at<E T="03">http://www.regulations.gov</E>(EPA's preferred method); by e-mail to<E T="03">oei.docket@epa.gov;</E>by mail to EPA Docket Center, Environmental Protection Agency, Mailcode: 2822T, 1200 Pennsylvania Ave., NW., Washington, DC 20460-0001; or by hand delivery or courier to EPA Docket Center, EPA West, Room 3334, 1301 Constitution Ave., NW., Washington, DC, between 8:30 a.m. and 4:30 p.m. Monday through Friday, excluding legal holidays. Comments on a disk or CD-ROM should be formatted in Word or ASCII file, avoiding the use of special characters and any form of encryption, and may be mailed to the mailing address above.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Melina Williams, Air and Radiation Law Office (2344A), Office of General Counsel, U.S. Environmental Protection Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460; telephone: (202) 564-3406; fax number (202) 564-5603; e-mail address:<E T="03">williams.melina@epa.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">I. Additional Information About the Proposed Settlement Agreement</HD>
        <P>This proposed settlement agreement would resolve a lawsuit alleging that the Administrator failed to perform a nondiscretionary duty to grant or deny, within 60 days of submission, an administrative petition to object to a CAA Title V permit issued by the Louisiana Department of Environmental Quality to Murphy Oil USA for the Meraux Refinery. Under the terms of the proposed settlement agreement, EPA has agreed to sign a response to the petition by September 22, 2011. The proposed settlement agreement further states that EPA shall expeditiously provide written notice of such action to Concerned Citizens Around Murphy through its counsel in this matter, and that Concerned Citizens Around Murphy shall file a motion for voluntary dismissal of the Complaint with prejudice within 15 days of the date when EPA provides such notice. In addition, the proposed settlement agreement sets the attorneys' fees and costs in this matter at $3,000.00.</P>
        <P>For a period of thirty (30) days following the date of publication of this notice, the Agency will accept written comments relating to the proposed settlement agreement from persons who were not named as parties or intervenors to the litigation in question. EPA or the Department of Justice may withdraw or withhold consent to the proposed settlement agreement if the comments disclose facts or considerations that indicate that such consent is inappropriate, improper, inadequate, or inconsistent with the requirements of the Act. Unless EPA or the Department of Justice determines that consent to this settlement agreement should be withdrawn, the terms of the agreement will be affirmed.</P>
        <HD SOURCE="HD1">II. Additional Information About Commenting on the Proposed Settlement Agreement</HD>
        <HD SOURCE="HD2">A. How can I get a copy of the settlement agreement?</HD>
        <P>The official public docket for this action (identified by Docket ID No. EPA-HQ-OGC-2011-0635) contains a copy of the proposed settlement agreement. The official public docket is available for public viewing at the Office of Environmental Information (OEI) Docket in the EPA Docket Center, EPA West, Room 3334, 1301 Constitution Ave., NW., Washington, DC. The EPA Docket Center Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding legal holidays. The telephone number for the Public Reading Room is (202) 566-1744, and the telephone number for the OEI Docket is (202) 566-1752.</P>

        <P>An electronic version of the public docket is available through<E T="03">http://www.regulations.gov.</E>You may use the<E T="03">http://www.regulations.gov</E>to submit or view public comments, access the index listing of the contents of the official public docket, and to access those documents in the public docket that are available electronically. Once in the system, key in the appropriate docket identification number then select “search”.</P>

        <P>It is important to note that EPA's policy is that public comments, whether submitted electronically or in paper, will be made available for public viewing online at<E T="03">http://www.regulations.gov</E>without change, unless the comment contains copyrighted material, CBI, or other information whose disclosure is restricted by statute. Information claimed as CBI and other information whose disclosure is restricted by statute is not included in the official public docket or in the electronic public docket. EPA's policy is that copyrighted material, including copyrighted material contained in a public comment, will not be placed in EPA's electronic public docket but will be available only in printed, paper form in the official public docket. Although not all docket materials may be available electronically, you may still access any of the publicly available docket materials through the EPA Docket Center.</P>
        <HD SOURCE="HD2">B. How and to whom do I submit comments?</HD>
        <P>You may submit comments as provided in the<E T="02">ADDRESSES</E>section. Please ensure that your comments are submitted within the specified comment period. Comments received after the close of the comment period will be marked “late.” EPA is not required to consider these late comments.</P>

        <P>If you submit an electronic comment, EPA recommends that you include your name, mailing address, and an e-mail address or other contact information in the body of your comment and with any disk or CD ROM you submit. This ensures that you can be identified as the submitter of the comment and allows EPA to contact you in case EPA cannot read your comment due to technical difficulties or needs further information on the substance of your comment. Any identifying or contact information<PRTPAGE P="45794"/>provided in the body of a comment will be included as part of the comment that is placed in the official public docket, and made available in EPA's electronic public docket. If EPA cannot read your comment due to technical difficulties and cannot contact you for clarification, EPA may not be able to consider your comment.</P>
        <P>Use of the<E T="03">http://www.regulations.gov</E>Web site to submit comments to EPA electronically is EPA's preferred method for receiving comments. The electronic public docket system is an “anonymous access” system, which means EPA will not know your identity, e-mail address, or other contact information unless you provide it in the body of your comment. In contrast to EPA's electronic public docket, EPA's electronic mail (e-mail) system is not an “anonymous access” system. If you send an e-mail comment directly to the Docket without going through<E T="03">http://www.regulations.gov,</E>your e-mail address is automatically captured and included as part of the comment that is placed in the official public docket, and made available in EPA's electronic public docket.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Richard B. Ossias,</NAME>
          <TITLE>Associate General Counsel.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19397 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6560-50-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">ENVIRONMENTAL PROTECTION AGENCY</AGENCY>
        <DEPDOC>[FRL-9446-5]</DEPDOC>
        <SUBJECT>Public Water System Supervision Program Revision for the State of Louisiana</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>United States Environmental Protection Agency (EPA).</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of proposed approval.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>Notice is hereby given that the State of Louisiana is revising its approved Public Water System Supervision Program, by adopting new regulations for the Public Notification Rule, Filter Backwash Recycling Rule, Long Term 1 Enhanced Surface Water Treatment Rule, Radionuclides Rule, and the Revised Drinking Water Standard for Arsenic Rule, promulgated and published in the<E T="04">Federal Register</E>at 72 FR 57782 on October 10, 2007. Louisiana has adopted the Public Notification Rule, Filter Backwash Recycling Rule, Long Term 1 Enhanced Surface Water Treatment Rule, Radionuclides Rule, and the Revised Drinking Water Standard for Arsenic Rule, to strengthen the protection of public health. EPA has determined that the proposed program revisions submitted by Louisiana for these revisions are no less stringent than the corresponding federal regulations. Therefore, EPA proposes to approve these program revisions.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>All interested parties may request a public hearing. A request for a public hearing must be submitted by August 31, 2011 to the Regional Administrator at the EPA Region 6 address shown below. Frivolous or insubstantial requests for a hearing may be denied by the Regional Administrator. However, if a substantial request for a public hearing is made by August 31, 2011, a public hearing will be held. If no timely and appropriate request for a hearing is received and the Regional Administrator does not elect to hold a hearing on his own motion, this determination shall become final and effective on August 31, 2011. Any request for a public hearing shall include the following information: The name, address, and telephone number of the individual, organization, or other entity requesting a hearing; a brief statement of the requesting person's interest in the Regional Administrator's determination and a brief statement of the information that the requesting person intends to submit at such hearing; and the signature of the individual making the request or, if the request is made on behalf of an organization or other entity, the signature of a responsible official of the organization or other entity.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>All documents relating to this determination are available for inspection between the hours of 8 a.m. and 4:30 p.m., Monday through Friday, at the following offices: DHH-OPH-CEHS Engineering Services, 628 N. Fourth Street, P.O. Box 4489, Baton Rouge, LA 70821; and the EPA Region 6, Drinking Water Section (6WQ-SD), 1445 Ross Avenue, Suite 1200, Dallas, Texas 75202.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Andy Waite, EPA Region 6, Drinking Water Section at the Dallas address given above or at telephone (214) 665-7332, or<E T="03">waite.andrew@epa.gov.</E>
          </P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>Section 1413 of the Safe Drinking Water Act, as amended (1996), and 40 CFR part 141 and 142 of the National Primary Drinking Water Regulations.</P>
          </AUTH>
          <SIG>
            <DATED>Dated: July 20, 2011</DATED>
            <NAME>Al Armendariz,</NAME>
            <TITLE>Regional Administrator, Region 6.</TITLE>
          </SIG>
        </FURINF>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19396 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6560-50-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">FEDERAL COMMUNICATIONS COMMISSION</AGENCY>
        <SUBJECT>Notice of Public Information Collection(s) Being Reviewed by the Federal Communications Commission, Comments Requested</SUBJECT>
        <DATE>July 21, 2011.</DATE>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Federal Communications Commission, as part of its continuing effort to reduce paperwork burden invites the general public and other Federal agencies to take this opportunity to comment on the following information collection(s), as required by the Paperwork Reduction Act (PRA) of 1995, 44 U.S.C. 3501-3520. Comments are requested concerning: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the Commission, including whether the information shall have practical utility; (b) the accuracy of the Commission's burden estimate; (c) ways to enhance the quality, utility, and clarity of the information collected; (d) ways to minimize the burden of the collection of information on the respondents, including the use of automated collection techniques or other forms of information technology; and (e) ways to further reduce the information collection burden on small business concerns with fewer than 25 employees.</P>
          <P>The FCC may not conduct or sponsor a collection of information unless it displays a currently valid control number. No person shall be subject to any penalty for failing to comply with a collection of information subject to the Paperwork Reduction Act (PRA) that does not display a currently valid OMB control number.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Written Paperwork Reduction Act (PRA) comments should be submitted on or before September 30, 2011. If you anticipate that you will be submitting PRA comments, but find it difficult to do so within the period of time allowed by this notice, you should advise the FCC contact listed below as soon as possible.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Direct all PRA comments to Nicholas A. Fraser, Office of Management and Budget, via fax at 202-395-5167 or via the Internet at<E T="03">Nicholas_A._Fraser@omb.eop.gov</E>and to the Federal Communications Commission via e-mail to<E T="03">PRA@fcc.gov.</E>
          </P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Leslie F. Smith, Office of Managing Director, (202) 418-0217. For additional information, contact Leslie F. Smith at<E T="03">Leslie.Smith@fcc.gov</E>or call 202-418-0217.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>
          <PRTPAGE P="45795"/>
        </P>
        <P>
          <E T="03">OMB Control Number:</E>3060-0430.</P>
        <P>
          <E T="03">Title:</E>Section 1.1206, Permit-but-Disclose Proceedings.</P>
        <P>
          <E T="03">Form Number:</E>N/A.</P>
        <P>
          <E T="03">Type of Review:</E>Revision of a currently approved collection.</P>
        <P>
          <E T="03">Respondents:</E>Individuals or households; Business or other for-profit; Not-for-profit institutions; Federal Government; and State, local, or tribal governments.</P>
        <P>
          <E T="03">Number of Respondents and Responses:</E>11,500 respondents; 11,500 responses.</P>
        <P>
          <E T="03">Estimated Time per Response:</E>45 minutes (0.75 hours).</P>
        <P>
          <E T="03">Frequency of Response:</E>On occasion reporting requirements.</P>
        <P>
          <E T="03">Obligation to Respond:</E>Required to obtain or retain benefits. Statutory authority for this information collection is contained in sections 4(i) and (j), 303(r), and 409 of the Communications Act of 1934, as amended, 47 U.S.C. 154(i) and (j), 303(r), and 409.</P>
        <P>
          <E T="03">Total Annual Burden:</E>25,875 hours.</P>
        <P>
          <E T="03">Total Annual Cost:</E>$0.00.</P>
        <P>
          <E T="03">Privacy Act Impact Assessment:</E>No impact(s).</P>
        <P>
          <E T="03">Nature and Extent of Confidentiality:</E>Consistent with the Commission's rules on confidential treatment of submissions, under 47 CFR 0.459, a presenter may request confidential treatment of<E T="03">ex parte</E>presentations. In addition, the Commission will permit parties to remove metadata containing confidential or privileged information, and the Commission will also not require parties to file electronically<E T="03">ex parte</E>notices that contain confidential information. The Commission will, however, require a redacted version to be filed electronically at the same time the paper filing is submitted, and that the redacted version must be machine-readable whenever technically possible.</P>
        <P>
          <E T="03">Needs and Uses:</E>The Commission's rules, under 47 CFR 1.1206, require that a public record be made of<E T="03">ex parte</E>presentations (<E T="03">i.e.,</E>written presentations not served on all parties to the proceeding or oral presentations as to which all parties have not been given notice and an opportunity to be present) to decision-making personnel in “permit-but-disclose” proceedings, such as notice-and-comment rulemakings and declaratory ruling proceedings.</P>
        <P>On February 2, 2011, the FCC released a<E T="03">Report and Order and Further Notice of Proposed Rulemaking,</E>GC Docket Number 10-43, FCC 11-11, which amended and reformed the Commission's rules on<E T="03">ex parte</E>presentations (47 CFR 1.1206(b)(2)) made in the course of Commission rulemakings and other permit-but-disclose proceedings. The modifications to the existing rules adopted in this Report and Order require that parties file more descriptive summaries of their<E T="03">ex parte</E>contacts, by ensuring that other parties and the public have an adequate opportunity to review and respond to information submitted<E T="03">ex parte,</E>and by improving the FCC's oversight and enforcement of the<E T="03">ex parte</E>rules. The modified<E T="03">ex parte</E>rules provide as follows: (1)<E T="03">Ex parte</E>notices will be required for all oral<E T="03">ex parte</E>presentations in permit-but-disclose proceedings, not just for those presentations that involve new information or arguments not already in the record; (2) If an oral<E T="03">ex parte</E>presentation is limited to material already in the written record, the notice must contain either a succinct summary of the matters discussed or a citation to the page or paragraph number in the party's written submission(s) where the matters discussed can be found; (3) Notices for all<E T="03">ex parte</E>presentations must include the name of the person(s) who made the<E T="03">ex parte</E>presentation as well as a list of all persons attending or otherwise participating in the meeting at which the presentation was made; (4) Notices of<E T="03">ex parte</E>presentations made outside the Sunshine period must be filed within two business days of the presentation; (5) The Sunshine period will begin on the day (including business days, weekends, and holidays) after issuance of the Sunshine notice, rather than when the Sunshine Agenda is issued (as the current rules provide); (6) If an<E T="03">ex parte</E>presentation is made on the day the Sunshine notice is released, an<E T="03">ex parte</E>notice must be submitted by the next business day, and any reply would be due by the following business day. If a permissible<E T="03">ex parte</E>presentation is made during the Sunshine period (under an exception to the Sunshine period prohibition), the<E T="03">ex parte</E>notice is due by the end of the same day on which the presentation was made, and any reply would need to be filed by the next business day. Any reply must be in writing and limited to the issues raised in the<E T="03">ex parte</E>notice to which the reply is directed; (7) Commissioners and agency staff may continue to request<E T="03">ex parte</E>presentations during the Sunshine period, but these presentations should be limited to the specific information required by the Commission; (8)<E T="03">Ex parte</E>notices must be submitted electronically in machine-readable format. PDF images created by scanning a paper document may not be submitted, except in cases in which a word-processing version of the document is not available. Confidential information may continue to be submitted by paper filing, but a redacted version must be filed electronically at the same time the paper filing is submitted. An exception to the electronic filing requirement will be made in cases in which the filing party claims hardship. The basis for the hardship claim must be substantiated in the<E T="03">ex parte</E>filing; (9) To facilitate stricter enforcement of the<E T="03">ex parte</E>rules, the Enforcement Bureau is authorized to levy forfeitures for<E T="03">ex parte</E>rule violations; (10) Copies of electronically filed<E T="03">ex parte</E>notices must also be sent electronically to all staff and Commissioners present at the<E T="03">ex parte</E>meeting so as to enable them to review the notices for accuracy and completeness. Filers may be asked to submit corrections or further information as necessary for compliance with the rules; and (11) Minor conforming and clarifying rule changes proposed in the Notice are adopted. The only changes entailing increased information collection are the requirement that parties making permissible<E T="03">ex parte</E>presentations in restricted proceedings file an<E T="03">ex parte</E>notice, and that<E T="03">ex parte</E>notices contain either a summary of the presentation or a reference to where the information can be found in the written record, and that<E T="03">ex parte</E>notices list all persons attending the presentation.</P>

        <P>The information is used by parties to permit-but-disclose proceedings, including interested members of the public, to respond to the arguments made and data offered in the presentations. The responses may then be used by the Commission in its decision-making. The availability of the<E T="03">ex parte</E>materials ensures that the Commission's decisional processes are fair, impartial, and comport with the concept of due process in that all interested parties can know of and respond to the arguments made to the decision-making officials.</P>
        <P>On May 10, 2011, the Commission published a notice in the<E T="04">Federal Register</E>(76 FR 27048) announcing that it had sought OMB approval under the emergency processing provisions of the PRA for this information collection. OMB approved this collection as an emergency on May 16, 2011. With this 60-day notice, the Commission is beginning the regular PRA process seeking OMB approval for this collection for three years.</P>
        <SIG>
          <PRTPAGE P="45796"/>
          <FP>Federal Communications Commission.</FP>
          <NAME>Marlene H. Dortch,</NAME>
          <TITLE>Secretary, Office of the Secretary, Office of Managing Director.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19408 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6712-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">FEDERAL COMMUNICATIONS COMMISSION</AGENCY>
        <SUBJECT>Information Collection Being Submitted to the Office of Management and Budget for Review and Approval</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Federal Communications Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice and request for comments.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Federal Communications Commission (FCC), as part of its continuing effort to reduce paperwork burdens, invites the general public and other Federal agencies to take this opportunity to comment on the following information collection, as required by the Paperwork Reduction Act (PRA) of 1995. Comments are requested concerning (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the Commission, including whether the information shall have practical utility; (b) the accuracy of the Commission's burden estimate; (c) ways to enhance the quality, utility, and clarity of the information collected; (d) ways to minimize the burden of the collection of information on the respondents, including the use of automated collection techniques or other forms of information technology; and (e) ways to further reduce the information collection burden on small business concerns with fewer than 25 employees.</P>
          <P>The FCC may not conduct or sponsor a collection of information unless it displays a currently valid control number. No person shall be subject to any penalty for failing to comply with a collection of information subject to the PRA that does not display a valid Office of Management and Budget (OMB) control number.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Written comments should be submitted on or before August 31, 2011. If you anticipate that you will be submitting comments, but find it difficult to do so within the period of time allowed by this notice, you should advise the contacts below as soon as possible.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Direct all PRA comments to Nicholas A. Fraser, OMB, via fax 202-395-5167, or via e-mail<E T="03">Nicholas_A._Fraser@omb.eop.gov;</E>and to Cathy Williams, FCC, via e-mail<E T="03">PRA@fcc.gov</E>and to<E T="03">Cathy.Williams@fcc.gov.</E>Include in the comments the OMB control number as shown in the “Supplementary Information” section below.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>For additional information or copies of the information collection, contact Cathy Williams at (202) 418-2918. To view a copy of this information collection request (ICR) submitted to OMB: (1) Go to the Web page<E T="03">http://www.reginfo.gov/public/do/PRAMain,</E>(2) look for the section of the Web page called “Currently Under Review,” (3) click on the downward-pointing arrow in the “Select Agency” box below the “Currently Under Review” heading, (4) select “Federal Communications Commission” from the list of agencies presented in the “Select Agency” box, (5) click the “Submit” button to the right of the “Select Agency” box, (6) when the list of FCC ICRs currently under review appears, look for the OMB control number of this ICR and then click on the ICR Reference Number. A copy of the FCC submission to OMB will be displayed.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P/>
        <P>
          <E T="03">OMB Control Number:</E>3060-1145.</P>
        <P>
          <E T="03">Title:</E>Structure and Practices of the Video Relay Service Program, CG Docket No. 10-51.</P>
        <P>
          <E T="03">Form Number:</E>N/A.</P>
        <P>
          <E T="03">Type of Review:</E>Revision of a currently approved collection.</P>
        <P>
          <E T="03">Respondents:</E>Business or other for-profit.</P>
        <P>
          <E T="03">Number of Respondents and Responses:</E>20 respondents; 1,423 responses.</P>
        <P>
          <E T="03">Estimated Time per Response:</E>.5 hours (30 minutes) to 50 hours.</P>
        <P>
          <E T="03">Frequency of Response:</E>Annual, monthly, on occasion, one-time, and semi-annually reporting requirements; recordkeeping and third party disclosure requirements.</P>
        <P>
          <E T="03">Obligation to Respond:</E>Required to obtain or retain benefit. The statutory authority for the information collection requirements is found at Section 225 of the Communications Act, 47 U.S.C. 225. The law was enacted on July 26, 1990, as Title IV of the ADA, Pub. L. 101-336, 104 Stat. 327, 366-69.</P>
        <P>
          <E T="03">Total Annual Burden:</E>4,632 hours.</P>
        <P>
          <E T="03">Total Annual Cost:</E>$35,600.</P>
        <P>
          <E T="03">Nature and Extent of Confidentiality:</E>An assurance of confidentiality is not offered because this information collection does not require the collection of personally identifiable information (PII) from individuals.</P>
        <P>
          <E T="03">Privacy Impact Assessment:</E>No impact(s).</P>
        <P>
          <E T="03">Needs and Uses:</E>On April 6, 2011, in document FCC 11-54, the Commission released a<E T="03">Report and Order,</E>published at 76 FR 24393, May 2, 2011, adopting final rules designed to eliminate the waste, fraud and abuse that has plagued the VRS program and had threatened its ability to continue serving Americans who use it and its long-term viability. The Report and Order contains information collection requirements with respect to the following eight requirements, all of which aims to ensure the sustainability and integrity of the TRS program and the TRS Fund. Though the Report and Order emphasizes VRS, many of the requirements also apply to other or all forms of TRS—which includes the adoption of the interim rule, several new information collection requirements; and all the proposed information collection requirements, except the “Transparency and the Disclosure of Provider Financial and Call Data” requirement, as previously proposed and published at 75 FR 51735, August 23, 2010.</P>
        <P>(a)<E T="03">Provider Certification Under Penalty of Perjury.</E>The Chief Executive Officer (CEO), Chief Financial Officer (CFO), or other senior executive of a TRS provider shall certify, under penalty of perjury, that: (1) Minutes submitted to the Interstate TRS Fund (Fund) administrator for compensation were handled in compliance with section 225 of the Act and the Commission's rules and orders, and are not the result of impermissible financial incentives, or payments or kickbacks, to generate calls, and (2) cost and demand data submitted to the Fund administrator related to the determination of compensation rates or methodologies are true and correct.</P>
        <P>(b)<E T="03">Requiring Providers To Submit Information About New and Existing Call Centers.</E>VRS providers shall submit a written statement to the Commission and the TRS Fund administrator containing the locations of all of their call centers that handle VRS calls, including call centers located outside the United States, twice a year, on April 1st and October 1st. In addition to the street address of each call center, the rules require that these statements contain (1) The number of individual CAs and CA managers employed at each call center; and (2) the name and contact information (phone number and e-mail address) for the managers at each call center. (3) VRS providers shall notify the Commission and the TRS Fund administrator in writing at least 30 days prior to any change to their call centers' locations, including the opening, closing, or relocation of any center.</P>
        <P>(c)<E T="03">Data Filed With the Fund Administrator To Support Payment<PRTPAGE P="45797"/>Claims.</E>VRS providers shall provide the following data associated with each VRS call for which a VRS provider seeks compensation in its filing with the Fund Administrator: (1) The call record ID sequence; (2) CA ID number; (3) session start and end times; (4) conversation start and end times; (5) incoming telephone number and IP address (if call originates with an IP-based device) at the time of call; (6) outbound telephone number and IP address (if call terminates with an IP-based device) at the time of call; (7) total conversation minutes; (8) total session minutes; (9) the call center (by assigned center ID number) that handles the call; and (10) the URL address through which the call was initiated.</P>
        <P>(2) All VRS and IP Relay providers shall submit speed of answer compliance data to the Fund administrator.</P>
        <P>(d)<E T="03">Automated Call Data Collection.</E>TRS providers shall use an automated record keeping system to capture the following data when seeking compensation from the Fund: (1) The call record ID sequence; (2) CA ID number; (3) session start and end times, at a minimum to the nearest second; (4) conversation start and end times, at a minimum to the nearest second; (5) incoming telephone number (if call originates with a telephone) and IP address (if call originates with an IP-based device) at the time of the call; (6) outbound telephone number and IP address (if call terminates to an IP-based device) at the time of call; (7) total conversation minutes; (8) total session minutes; and (9) the call center (by assigned center ID number) that handles the call.</P>
        <P>(e)<E T="03">Record Retention.</E>Internet-based TRS providers shall retain the following data that is used to support payment claims submitted to the Fund administrator for a minimum of five years, in an electronic format: (1) The call record ID sequence; (2) CA ID number; (3) session start and end times; (4) conversation start and end times; (5) incoming telephone number and IP address (if call originates with an IP-based device) at the time of call; (6) outbound telephone number and IP address (if call terminates with an IP-based device) at the time of call; (7) total conversation minutes; (8) total session minutes; and (9) the call center (by assigned center ID number) that handles the call.</P>
        <P>(f)<E T="03">Third-party Agreements.</E>(1) VRS providers shall maintain copies of all third-party contracts or agreements so that copies of these agreements will be available to the Commission and the TRS Fund administrator upon request. Such contracts or agreements shall provide detailed information about the nature of the services to be provided by the subcontractor.</P>
        <P>(2) VRS providers shall describe all agreements in connection with marketing and outreach activities, including those involving sponsorships, financial endorsements, awards, and gifts made by the provider to any individual or entity, in the providers' annual submissions to the TRS Fund administrator.</P>
        <P>(g)<E T="03">Whistleblower Protection.</E>TRS providers shall provide information about these TRS whistleblower protections, including the right to notify the Commission's Office of Inspector General or its Enforcement Bureau, to all employees and contractors, in writing. Providers that already disseminate their internal business policies to their employees in writing (<E T="03">e.g.</E>in employee handbooks, policies and procedures manuals, or bulletin board postings—either online or in hard copy) must also explicitly include these TRS whistleblower protections in those written materials.</P>
        <P>(h)<E T="03">Required Submission for Waiver Request.</E>Potential VRS providers wishing to receive a temporary waiver of the provider's eligibility rules, shall provide, in writing, a description of the specific requirement(s) for which it is seeking a waiver, along with documentation demonstrating the applicant's plan and ability to come into compliance with all of these requirements (other than the certification requirement) within a specified period of time, which shall not exceed three months from the date on which the rules become effective. Evidence of the applicant's plan and ability to come into compliance with the new rules shall include the applicant's detailed plan for modifying its business structure and operations in order to meet the new requirements, along with submission of the following relevant documentation to support the waiver request:</P>
        <P>• A copy of each deed or lease for each call center operated by the applicant;</P>
        <P>• A list of individuals or entities that hold at least a 10 percent ownership share in the applicant's business and a description of the applicant's organizational structure, including the names of its executives, officers, partners, and board of directors;</P>
        <P>• A list of all of the names of applicant's full-time and part-time employees;</P>
        <P>• Proofs of purchase or license agreements for use of all equipment and/or technologies, including hardware and software, used by the applicant for its call center functions, including but not limited to, automatic call distribution (ACD) routing, call setup, mapping, call features, billing for compensation from the TRS fund, and registration;</P>
        <P>• Copies of employment agreements for all of the provider's executives and CAs;</P>
        <P>• A list of all financing arrangements pertaining to the provision of Internet-based relay service, including documentation on loans for equipment, inventory, property, promissory notes, and liens;</P>

        <P>• Copies of all other agreements associated with the provision of Internet-based relay service; and a list of all sponsorship arrangements (<E T="03">e.g.,</E>those providing financial support or in-kind interpreting or personnel service for social activities in exchange for brand marketing), including any associated agreements.</P>
        <SIG>
          <FP>Federal Communications Commission.</FP>
          <NAME>Marlene H. Dortch,</NAME>
          <TITLE>Secretary, Office of the Secretary, Office of Managing Director.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19409 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6712-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">FEDERAL ELECTION COMMISSION</AGENCY>
        <DEPDOC>[Notice 2011-10]</DEPDOC>
        <SUBJECT>Filing Dates for the New York Special Election in the 9th Congressional District</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Federal Election Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of filing dates for special election.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>New York has scheduled a Special General Election on September 13, 2011, to fill the U.S. House seat in the 9th Congressional District vacated by Representative Anthony Weiner.</P>
          <P>Committees required to file reports in connection with the Special General Election on September 13, 2011, shall file a 12-day Pre-General Report, and a 30-day Post-General Report.</P>
        </SUM>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Mr. Kevin R. Salley, Information Division, 999 E Street, N.W., Washington, DC 20463;<E T="03">Telephone:</E>(202) 694-1100; Toll Free (800) 424-9530.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P/>
        <HD SOURCE="HD1">Principal Campaign Committees</HD>

        <P>All principal campaign committees of candidates who participate in the New York Special General Election shall file a 12-day Pre-General Report on September 1, 2011, and a 30-day Post-General Report on October 13, 2011.<PRTPAGE P="45798"/>(See chart below for the closing date for each report).</P>
        <P>Note that these reports are in addition to the campaign committee's year-end filing in January 2012. (See chart below for the closing date for each report).</P>
        <HD SOURCE="HD1">Unauthorized Committees (PACs and Party Committees)</HD>
        <P>Political committees filing on a semi-annual basis in 2011 are subject to special election reporting if they make previously undisclosed contributions or expenditures in connection with the New York Special General Election by the close of books for the applicable report(s). (See chart below for the closing date for each report).</P>
        <P>Committees filing monthly that make contributions or expenditures in connection with the New York Special General Election will continue to file according to the monthly reporting schedule.</P>

        <P>Additional disclosure information in connection with the New York Special Election may be found on the FEC Web site at<E T="03">http://www.fec.gov/info/report_dates_2011.shtml.</E>
        </P>
        <HD SOURCE="HD1">Disclosure of Lobbyist Bundling Activity</HD>
        <P>Campaign committees, party committees and Leadership PACs that are otherwise required to file reports in connection with the special elections must simultaneously file FEC Form 3L if they receive two or more bundled contributions from lobbyists/registrants or lobbyist/registrant PACs that aggregate in excess of $16,200 during the special election reporting periods (see charts below for closing date of each period). 11 CFR 104.22(a)(5)(v).</P>
        <GPOTABLE CDEF="s100,10,xls40,10" COLS="4" OPTS="L2,i1">
          <TTITLE>Calendar of Reporting Dates for New York Special Election—Committees Involved in the Special General (09/13/11) Must File</TTITLE>
          <BOXHD>
            <CHED H="1">Report</CHED>
            <CHED H="1">Close of books<SU>1</SU>
            </CHED>
            <CHED H="1">Reg./cert. &amp; overnight mailing deadline</CHED>
            <CHED H="1">Filing deadline</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Pre-General</ENT>
            <ENT>08/24/11</ENT>
            <ENT>08/29/11</ENT>
            <ENT>09/01/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Post-General</ENT>
            <ENT>10/03/11</ENT>
            <ENT>10/13/11</ENT>
            <ENT>10/13/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">October Quarterly</ENT>
            <ENT/>
            <ENT>WAIVED</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Year-End</ENT>
            <ENT>12/31/11</ENT>
            <ENT>01/31/12</ENT>
            <ENT>01/31/12</ENT>
          </ROW>
          <TNOTE>
            <SU>1</SU>These dates indicate the beginning and the end of the reporting period. A reporting period always begins the day after the closing date of the last report filed. If the committee is new and has not previously filed a report, the first report must cover all activity that occurred before the committee registered as a political committee with the Commission up through the close of books for the first report due.</TNOTE>
        </GPOTABLE>
        <SIG>
          <P>On behalf of the Commission,</P>
          
          <DATED>Dated: July 25, 2011.</DATED>
          <NAME>Cynthia L. Bauerly,</NAME>
          <TITLE>Chair, Federal Election Commission.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19311 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6715-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">FEDERAL ELECTION COMMISSION</AGENCY>
        <SUBJECT>Sunshine Act Notice</SUBJECT>
        <PREAMHD>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Federal Election Commission.</P>
        </PREAMHD>
        <PREAMHD>
          <HD SOURCE="HED">DATE AND TIME:</HD>
          <P>
            <E T="03">Thursday, August 4, 2011 at 10 a.m.</E>
          </P>
        </PREAMHD>
        <PREAMHD>
          <HD SOURCE="HED">PLACE:</HD>
          <P>999 E Street, NW., Washington, DC (Ninth Floor)</P>
        </PREAMHD>
        <PREAMHD>
          <HD SOURCE="HED">STATUS:</HD>
          <P>This meeting will be open to the public.</P>
        </PREAMHD>
        <PREAMHD>
          <HD SOURCE="HED">ITEMS TO BE DISCUSSED:</HD>
          <P/>
          
        </PREAMHD>
        <FP SOURCE="FP-1">Correction and Approval of the Minutes for the Meeting of July 21, 2011</FP>
        <FP SOURCE="FP-1">Draft Advisory Opinion 2011-14: Utah Bankers Association and Utah Bankers Association Action PAC</FP>
        <FP SOURCE="FP-1">Proposed Final Audit Report on John Edwards for President</FP>
        <FP SOURCE="FP-1">Audit Division Recommendation Memorandum on Nader for President 2008 (NFP)</FP>
        <FP SOURCE="FP-1">Management and Administrative Matters</FP>
        
        <P>Individuals who plan to attend and require special assistance, such as sign language interpretation or other reasonable accommodations, should contact Shawn Woodhead Werth, Commission Secretary and Clerk, at (202) 694-1040, at least 72 hours prior to the hearing date.</P>
        <PREAMHD>
          <HD SOURCE="HED">PERSON TO CONTACT FOR INFORMATION:</HD>
          <P>Judith Ingram, Press Officer,<E T="03">Telephone:</E>(202) 694-1220.</P>
        </PREAMHD>
        <SIG>
          <NAME>Shawn Woodhead Werth,</NAME>
          <TITLE>Secretary and Clerk of the Commission.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19547 Filed 7-28-11; 4:15 pm]</FRDOC>
      <BILCOD>BILLING CODE 6715-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">FEDERAL ELECTION COMMISSION</AGENCY>
        <DEPDOC>[Notice 2011-11]</DEPDOC>
        <SUBJECT>Policy Statement Regarding a Program for Requesting Consideration of Legal Questions by the Commission</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Federal Election Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Policy Statement.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Federal Election Commission (“Commission”) is adopting a program providing for a means by which persons and entities may have a legal question considered by the Commission earlier in both the report review process and the audit process.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Effective August 1, 2011.</P>
        </DATES>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Lorenzo Holloway, Assistant General Counsel, or Allison T. Steinle, Attorney, 999 E Street, NW., Washington, DC 20463, (202) 694-1650 or (800) 424-9530.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>The Commission is adopting a program providing for a means by which persons and entities may have a legal question considered by the Commission earlier in both the report review process and the audit process. Specifically, when the Office of Compliance (“OC”) (which includes the Reports Analysis Division and the Audit Division) requests that a person or entity take corrective action during the report review or audit process, if the person or entity disagrees with the request based upon a material dispute on a question of law, the person or entity may seek Commission consideration of the issue pursuant to this procedure.</P>
        <HD SOURCE="HD1">I. Procedures</HD>

        <P>Within 15 business days of a determination by the Reports Analysis Division or Audit Division that a person or entity remains obligated to take corrective action to resolve an issue that has arisen during the report review or audit process, the person or entity may seek Commission consideration if a material dispute on a question of law exists with respect to the recommended<PRTPAGE P="45799"/>corrective action.<SU>1</SU>
          <FTREF/>A “determination” for purposes of triggering the 15 business days is either: (1) notification to the person or entity of legal guidance prepared by the Office of General Counsel (“OGC”) at the request of the Reports Analysis Division recommending the corrective action; or (2) the end of the Committee's Audit Exit Conference response period.</P>
        <FTNT>
          <P>
            <SU>1</SU>Many disputes involving corrective action requests hinge on questions of fact rather than questions of law, and thus are not appropriate for this procedure.</P>
        </FTNT>
        <P>Any request for consideration by a Committee during the report review process or the audit process shall be limited to questions of law on material issues, when: (1) The legal issue is novel, complex, or pertains to an unsettled question of law; (2) there has been intervening legislation, rulemaking, or litigation since the Commission last considered the issue; or (3) the request to take corrective action is contrary to or otherwise inconsistent with prior Commission matters dealing with the same issue. The request must specify the question of law at issue and why it is subject to Commission consideration. It should discuss, when appropriate, prior Commission matters raising the same issue, relevant court decisions, and any other analysis of the issue that may assist the Commission in its decision-making. The Commission will not consider factual disputes under this procedure, and any requests for consideration other than on questions of law on material issues will not be granted.</P>
        <P>All requests, including any extension requests, should be directed to the Commission Secretary, Federal Election Commission, 999 E Street, NW., Washington, DC 20463, and must be received within 15 business days of the determination of corrective action. Upon receipt of a request, the Commission Secretary shall forward a copy of any request to each Commissioner, the General Counsel, and the Staff Director.</P>
        <P>Any request for an extension of time to file will be considered on a case-by-case basis and will only be granted if good cause is shown, and the Commission approves the extension request by four affirmative votes within five business days of receipt of the extension request. Within five business days of notification to the Commissioners of a request for consideration of a legal question, if two or more Commissioners agree that the Commission should consider the request, OGC will prepare a recommendation and, within 15 business days thereafter, circulate the recommendation in accordance with all applicable Commission directives.</P>
        <P>After the recommendation is circulated for a Commission vote, in the event of an objection, the matter shall be automatically placed on the next meeting agenda consistent with the Sunshine Act, 5 U.S.C. 552b(g), and applicable Commission regulations, 11 CFR part 2. However, if within 60 business days of the filing of a request for consideration, the Commission has not resolved the issue or provided guidance on how to proceed with the matter by the affirmative vote of four or more Commissioners, the OC may proceed with the matter. After the 60 business days has elapsed, any requestor will be provided a copy of OGC's recommendation memorandum and an accompanying vote certification, or if no such certification exists, a cover page stating the disposition of the memoranda. Confidential information will be redacted as necessary.</P>
        <P>After the request review process has concluded, or a Final Audit Report has been approved, a copy of the request for consideration, as well as the recommendation memorandum and accompanying vote certification or disposition memorandum, will be placed with the Committee's filings or audit documents on the Commission's website within 30 days. These materials will also be placed a Commission webpage dedicated to legal questions considered by the Commission under this program.</P>
        <P>This procedure is not intended to circumvent or supplant the Advisory Opinion process provided under 2 U.S.C. 437f and 11 CFR part 112. Accordingly, any legal issues that qualify for consideration under the Advisory Opinion process are not appropriate for consideration under this new procedure. Additionally, this policy statement does not supersede the procedures regarding eligibility and entitlement to public funds set forth in Commission Directive 24 and 11 CFR 9005.1, 9033.4, 9033.6 or 9033.10.</P>
        <HD SOURCE="HD1">II. Annual Review</HD>
        <P>No later than July 1 of each year, the OC and OGC shall jointly prepare and distribute to the Commission a written report containing a summary of the requests made under the program over the previous year and a summary of the Commission's consideration of those requests and any action taken thereon. The annual report shall also include the Chief Compliance Officer's and the General Counsel's assessment of whether, and to what extent, the program has promoted efficiency and fairness in both the Commission's report review process and in the audit process, as well as their recommendations, if any, for modifications to the program.</P>
        <P>The Commission may terminate or modify this program through additional policy statements at any time by an affirmative vote of four of its members.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Cynthia L. Bauerly,</NAME>
          <TITLE>Chair, Federal Election Commission.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19312 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6715-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">FEDERAL MINE SAFETY AND HEALTH REVIEW COMMISSION</AGENCY>
        <SUBJECT>Sunshine Act Notice</SUBJECT>
        <DATE>July 25, 2011.</DATE>
        <PREAMHD>
          <HD SOURCE="HED">TIME AND DATE:</HD>
          <P>10 a.m., Thursday, August 4, 2011.</P>
        </PREAMHD>
        <PREAMHD>
          <HD SOURCE="HED">PLACE:</HD>
          <P>The Richard V. Backley Hearing Room, 9th Floor, 601 New Jersey Avenue, NW., Washington, DC.</P>
        </PREAMHD>
        <PREAMHD>
          <HD SOURCE="HED">STATUS:</HD>
          <P>Open.</P>
        </PREAMHD>
        <PREAMHD>
          <HD SOURCE="HED">MATTERS TO BE CONSIDERED:</HD>

          <P>The Commission will hear oral argument in the following matters:<E T="03">Big Ridge, Inc.,</E>Docket Nos. LAKE 2011-116-R, et al., and<E T="03">Peabody Midwest Mining, LLC,</E>Docket Nos. LAKE 2011-118-R,<E T="03">et al.</E>(Issues include whether the Commission should grant an application for temporary relief from orders issued by the Secretary of Labor requiring that mine operators provide certain information and records to the Secretary.)</P>
          <P>Any person attending this oral argument who requires special accessibility features and/or auxiliary aids, such as sign language interpreters, must inform the Commission in advance of those needs. Subject to 29 CFR 2706.150(a)(3) and § 2706.160(d).</P>
        </PREAMHD>
        <PREAMHD>
          <HD SOURCE="HED">CONTACT PERSON FOR MORE INFO:</HD>
          <P>Jean Ellen (202) 434-9950 / (202) 708-9300 for TDD Relay / 1-800-877-8339 for toll free.</P>
        </PREAMHD>
        <SIG>
          <NAME>Emogene Johnson,</NAME>
          <TITLE>Administrative Assistant.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19462 Filed 7-28-11; 11:15 am]</FRDOC>
      <BILCOD>BILLING CODE 6735-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">FEDERAL TRADE COMMISSION</AGENCY>
        <SUBJECT>Agency Information Collection Activities; Submission for OMB Review; Comment Request</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Federal Trade Commission (“Commission” or “FTC”).</P>
        </AGY>
        <ACT>
          <PRTPAGE P="45800"/>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice; and request for public comment.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The FTC intends to conduct a survey of consumers to advance its understanding of the prevalence of consumer fraud and to allow the FTC to better serve people who experience fraud. The survey is a follow-up to two previous surveys—the first was conducted in May and June of 2003 and the second in November and December of 2005. Before gathering this information, the FTC is seeking public comments on its proposed consumer research. The information collection requirements described below are being submitted to the Office of Management and Budget (“OMB”) for review, as required by the Paperwork Reduction Act (“PRA”).</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments must be submitted on or before August 31, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Interested parties may file a comment online or on paper, by following the instructions in the “Request for Comment” part of the<E T="02">SUPPLEMENTARY INFORMATION</E>section below. Write “Consumer Fraud Survey, Project No. P105502” on your comment, and file your comment online at:<E T="03">https://ftcpublic.commentworks.com/ftc/fraudsurvey2,</E>by following the instructions on the web-based form. If you prefer to file your comment on paper, mail or deliver your comment to the following address: Federal Trade Commission, Office of the Secretary, Room H-113 (Annex J), 600 Pennsylvania Avenue, NW., Washington, DC 20580.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Requests for additional information should be addressed to Keith B. Anderson, Economist, Bureau of Economics, Federal Trade Commission, 600 Pennsylvania Avenue NW., Mail Stop NJ-4136, Washington, DC 20580. Telephone: (202) 326-3428.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">1. Background</HD>

        <P>On September 1, 2010, the FTC sought comment on the information collection requirements associated with the proposed Fraud Survey (75 FR 53697). No comments were received. Pursuant to the OMB regulations, 5 CFR part 1320, that implement the PRA, 44 U.S.C. 3501-3521, the Commission is providing this second opportunity for public comment. All comments should be filed as prescribed in the<E T="02">ADDRESSES</E>section above, and must be received on or before August 31, 2011.</P>

        <P>In 2003, OMB approved the FTC's request to conduct a survey on consumer fraud. The FTC completed the consumer research in June 2003 and issued its report, “Consumer Fraud in the United States: An FTC Survey,” in August 2004 (<E T="03">http://www.ftc.gov/reports/consumerfraud/040805confraudrpt.pdf</E>).</P>

        <P>In November 2005, OMB approved the Commission's request to reinstate this clearance. The second survey was conducted in November and December 2005. A report, “Consumer Fraud in the United States: The Second FTC Survey,” detailing the results of that survey, was issued in October 2007 (<E T="03">http://www.ftc.gov/opa/2007/10/fraud.pdf</E>). The 2005 survey asked about consumers' experiences during the previous year with 14 specific and two more general types of fraud. Among frauds covered by the survey were whether the person had purchased a weight-loss product that did not work as promised, whether the person had fallen victim to an advance-fee loan scam, and whether the person had paid someone to remove derogatory information from his or her credit report. According to the survey results, 30.2 million adults in the United States—13.5 percent of all adults in the country—had been a victim during the previous year of one or more of the frauds included in the survey.</P>
        <P>Among the 14 specific frauds included in the survey, the most frequently reported was the purchase of a weight-loss product that the seller represented would allow the user to easily lose a substantial amount of weight or lose the weight without diet or exercise. In fact, consumers who tried the product found that they only lost a little of the weight they had expected to lose or failed to lose any weight at all. This was experienced by 4.8 million adults—2.1 percent of the adult population.</P>
        <HD SOURCE="HD3">2. Description of the Collection of Information and Proposed Use</HD>
        <P>The FTC proposes to conduct a telephone survey of 3,600 randomly-selected consumers nationwide age 18 and over—100 in a pretest and 3,500 in the main survey—in order to gather specific information on the incidence of consumer fraud in the general population. To obtain a more reliable picture of the experience of demographic groups that the earlier surveys found to be at an elevated risk of becoming victims of consumer fraud—including Hispanics, African Americans, and Native Americans—the survey may oversample members of these groups. All information will be collected on a voluntary basis, and information on the identities of individual participants will not be collected. Subject to obtaining OMB clearance, the FTC will work with a consumer research firm to identify consumers and conduct the survey. The results will assist the FTC in determining the incidence of consumer fraud in the general population and whether its type or frequency is changing. This information will inform the FTC about how best to combat consumer fraud.</P>
        <P>The FTC intends to use a sample size similar to that used in the 2005 survey. Many of the questions will be similar to the 2005 survey so that the results from it can be used as a baseline for a time-series analysis.<SU>1</SU>
          <FTREF/>The FTC may choose to conduct another follow-up survey in approximately five years.</P>
        <FTNT>
          <P>
            <SU>1</SU>The survey instrument for the 2005 Consumer Fraud Survey is attached to the 2007 report (referenced above) as Appendix B.</P>
        </FTNT>
        <HD SOURCE="HD3">3. Estimated Hours Burden</HD>
        <P>The FTC will pretest the survey on approximately 100 respondents to ensure that all questions are easily understood. This pretest will take approximately 17 minutes per person<SU>2</SU>
          <FTREF/>and 28 hours as a whole (100 respondents × 17 minutes each). Answering the consumer survey will require approximately 15 minutes per respondent and 875 hours as a whole (3,500 respondents × 15 minutes each). Thus, cumulative total burden hours will approximate 903 hours.</P>
        <FTNT>
          <P>
            <SU>2</SU>Staff originally estimated 15 minutes to complete the pretest, the same time as that needed for the actual survey. The revised estimate takes further into account the presumed added time required to respond to questions unique to the pretest itself.</P>
        </FTNT>
        <HD SOURCE="HD3">4. Estimated Cost Burden</HD>
        <P>The cost per respondent should be negligible. Participation is voluntary and will not require start-up, capital, or labor expenditures by respondents.</P>
        <HD SOURCE="HD3">5. Request for Comment</HD>

        <P>You can file a comment online or on paper. For the Commission to consider your comment, we must receive it on or before August 31, 2011. Write “Consumer Fraud Survey, Project No. P105502” on your comment. Your comment—including your name and your state—will be placed on the public record of this proceeding, including, to the extent practicable, on the public Commission Web site, at<E T="03">http://www.ftc.gov/os/publiccomments.shtm.</E>As a matter of discretion, the Commission tries to remove individuals' home contact information from comments before placing them on the Commission Web site.</P>

        <P>Because your comment will be made public, you are solely responsible for making sure that your comment does<PRTPAGE P="45801"/>not include any sensitive personal information, like anyone's Social Security number, date of birth, driver's license number or other state identification number or foreign country equivalent, passport number, financial account number, or credit or debit card number. You are also solely responsible for making sure that your comment does not include any sensitive health information, like medical records or other individually identifiable health information. In addition, do not include any “[t]rade secret or any commercial or financial information which is obtained from any person and which is privileged or confidential,” as provided in Section 6(f) of the FTC Act, 15 U.S.C. 46(f), and FTC Rule 4.10(a)(2), 16 CFR 4.10(a)(2). In particular, do not include competitively sensitive information such as costs, sales statistics, inventories, formulas, patterns, devices, manufacturing processes, or customer names.</P>
        <P>If you want the Commission to give your comment confidential treatment, you must file it in paper form, with a request for confidential treatment, and you have to follow the procedure explained in FTC Rule 4.9(c), 16 CFR 4.9(c).<SU>3</SU>
          <FTREF/>Your comment will be kept confidential only if the FTC General Counsel, in his or her sole discretion, grants your request in accordance with the law and the public interest.</P>
        <FTNT>
          <P>

            <SU>3</SU>In particular, the written request for confidential treatment that accompanies the comment must include the factual and legal basis for the request, and must identify the specific portions of the comment to be withheld from the public record.<E T="03">See</E>FTC Rule 4.9(c), 16 CFR 4.9(c).</P>
        </FTNT>

        <P>Postal mail addressed to the Commission is subject to delay due to heightened security screening. As a result, we encourage you to submit your comments online. To make sure that the Commission considers your online comment, you must file it at<E T="03">https://ftcpublic.commentworks.com/ftc/fraudsurvey2,</E>by following the instructions on the web-based form. If this Notice appears at<E T="03">http://www.regulations.gov/#!home,</E>you also may file a comment through that Web site.</P>
        <P>If you file your comment on paper, write “Consumer Fraud Survey, Project No. P105502” on your comment and on the envelope, and mail or deliver it to the following address: Federal Trade Commission, Office of the Secretary, Room H-113 (Annex J), 600 Pennsylvania Avenue, NW., Washington, DC 20580. If possible, submit your paper comment to the Commission by courier or overnight service.</P>
        <P>Visit the Commission Web site at<E T="03">http://www.ftc.gov</E>to read this Notice and the news release describing it. The FTC Act and other laws that the Commission administers permit the collection of public comments to consider and use in this proceeding as appropriate. The Commission will consider all timely and responsive public comments that it receives on or before August 31, 2011. You can find more information, including routine uses permitted by the Privacy Act, in the Commission's privacy policy, at<E T="03">http://www.ftc.gov/ftc/privacy.htm.</E>
        </P>
        <P>Comments on the information collection requirements subject to review under the PRA should additionally be submitted to OMB. If sent by U.S. mail, they should be addressed to Office of Information and Regulatory Affairs, Office of Management and Budget, Attention: Desk Officer for the Federal Trade Commission, New Executive Office Building, Docket Library, Room 10102, 725 17th Street, NW., Washington, DC 20503. Comments sent to OMB by U.S. postal mail, however, are subject to delays due to heightened security precautions. Thus, comments instead should be sent by facsimile to (202) 395-5167.</P>
        <SIG>
          <NAME>David C. Shonka,</NAME>
          <TITLE>Acting General Counsel.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19367 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6750-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">FEDERAL TRADE COMMISSION</AGENCY>
        <DEPDOC>[File No. 111 0083]</DEPDOC>
        <SUBJECT>Perrigo Company and Paddock Laboratories, Inc.; Analysis of Agreement Containing Consent Orders To Aid Public Comment</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Federal Trade Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Proposed Consent Agreement.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The consent agreement in this matter settles alleged violations of federal law prohibiting unfair or deceptive acts or practices or unfair methods of competition. The attached Analysis to Aid Public Comment describes both the allegations in the draft complaint and the terms of the consent order—embodied in the consent agreement—that would settle these allegations.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments must be received on or before August 26, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Interested parties may file a comment online or on paper, by following the instructions in the Request for Comment part of the<E T="02">SUPPLEMENTARY INFORMATION</E>section below. Write “Perrigo Paddock, File No. 111 0083” on your comment, and file your comment online at<E T="03">https://ftcpublic.commentworks.com/ftc/perrigopaddockconsent,</E>by following the instructions on the Web-based form. If you prefer to file your comment on paper, mail or deliver your comment to the following address: Federal Trade Commission, Office of the Secretary, Room H-113 (Annex D), 600 Pennsylvania Avenue, NW., Washington, DC 20580.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Christine Palumbo (202-326-3330), FTC, Bureau of Competition, 600 Pennsylvania Avenue, NW., Washington, DC 20580.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>

        <P>Pursuant to section 6(f) of the Federal Trade Commission Act, 38 Stat. 721, 15 U.S.C. 46(f), and § 2.34 the Commission Rules of Practice, 16 CFR 2.34, notice is hereby given that the above-captioned consent agreement containing a consent order to cease and desist, having been filed with and accepted, subject to final approval, by the Commission, has been placed on the public record for a period of thirty (30) days. The following Analysis to Aid Public Comment describes the terms of the consent agreement, and the allegations in the complaint. An electronic copy of the full text of the consent agreement package can be obtained from the FTC Home Page (for July 26, 2011), on the World Wide Web, at<E T="03">http://www.ftc.gov/os/actions.shtm.</E>A paper copy can be obtained from the FTC Public Reference Room, Room 130-H, 600 Pennsylvania Avenue, NW., Washington, DC 20580, either in person or by calling (202) 326-2222.</P>

        <P>You can file a comment online or on paper. For the Commission to consider your comment, we must receive it on or before June 10, 2011. Write “Perrigo Paddock, File No. 111 0083” on your comment. Your comment B including your name and your state B will be placed on the public record of this proceeding, including, to the extent practicable, on the public Commission Web site, at<E T="03">http://www.ftc.gov/os/publiccomments.shtm.</E>As a matter of discretion, the Commission tries to remove individuals' home contact information from comments before placing them on the Commission Web site.</P>

        <P>Because your comment will be made public, you are solely responsible for making sure that your comment does not include any sensitive personal information, like anyone's Social Security number, date of birth, driver's license number or other state<PRTPAGE P="45802"/>identification number or foreign country equivalent, passport number, financial account number, or credit or debit card number. You are also solely responsible for making sure that your comment does not include any sensitive health information, like medical records or other individually identifiable health information. In addition, do not include any “[t]rade secret or any commercial or financial information which is obtained from any person and which is privileged or confidential,” as provided in Section 6(f) of the FTC Act, 15 U.S.C. 46(f), and FTC Rule 4.10(a)(2), 16 CFR 4.10(a)(2). In particular, do not include competitively sensitive information such as costs, sales statistics, inventories, formulas, patterns, devices, manufacturing processes, or customer names.</P>
        <P>If you want the Commission to give your comment confidential treatment, you must file it in paper form, with a request for confidential treatment, and you have to follow the procedure explained in FTC Rule 4.9(c), 16 CFR 4.9(c).<SU>1</SU>
          <FTREF/>Your comment will be kept confidential only if the FTC General Counsel, in his or her sole discretion, grants your request in accordance with the law and the public interest.</P>
        <FTNT>
          <P>
            <SU>1</SU>In particular, the written request for confidential treatment that accompanies the comment must include the factual and legal basis for the request, and must identify the specific portions of the comment to be withheld from the public record. See FTC Rule 4.9(c), 16 CFR 4.9(c).</P>
        </FTNT>

        <P>Postal mail addressed to the Commission is subject to delay due to heightened security screening. As a result, we encourage you to submit your comments online. To make sure that the Commission considers your online comment, you must file it at<E T="03">https://ftcpublic.commentworks.com/ftc/perrigopaddockconsent</E>by following the instructions on the Web-based form. If this Notice appears at<E T="03">http://www.regulations.gov/#!home,</E>you also may file a comment through that Web site.</P>
        <P>If you file your comment on paper, write “Perrigo Paddock, File No. 111 0083” on your comment and on the envelope, and mail or deliver it to the following address: Federal Trade Commission, Office of the Secretary, Room H-113 (Annex D), 600 Pennsylvania Avenue, NW., Washington, DC 20580. If possible, submit your paper comment to the Commission by courier or overnight service.</P>
        <P>Visit the Commission Web site at<E T="03">http://www.ftc.gov</E>to read this Notice and the news release describing it. The FTC Act and other laws that the Commission administers permit the collection of public comments to consider and use in this proceeding as appropriate. The Commission will consider all timely and responsive public comments that it receives on or before August 26, 2011. You can find more information, including routine uses permitted by the Privacy Act, in the Commission's privacy policy, at<E T="03">http://www.ftc.gov/ftc/privacy.htm.</E>
        </P>
        <HD SOURCE="HD1">Analysis of Agreement Containing Consent Order To Aid Public Comment</HD>
        <HD SOURCE="HD2">I. Introduction</HD>
        <P>The Federal Trade Commission (“Commission”) has accepted, subject to final approval, an Agreement Containing Consent Orders (“Consent Agreement”) from Perrigo Company (“Perrigo”) and Paddock Laboratories, Inc. (“Paddock”) that is designed to remedy the anticompetitive effects resulting from Perrigo's acquisition of Paddock. Under the terms of the proposed Consent Agreement, the companies would be required to divest to Watson Pharmaceuticals, Inc. (“Watson”) Paddock's rights and assets necessary to manufacture and market generic: (1) Ammonium lactate external cream 12 percent (“ammonium lactate cream”); (2) ammonium lactate topical lotion 12 percent (“ammonium lactate lotion”); (3) ciclopirox shampoo 1 percent (“ciclopirox shampoo”); and (4) promethazine hydrochloride rectal suppository 12.5 mg and 25 mg (“promethazine suppository”). The proposed Consent Agreement also requires the companies to divest to Watson all of Perrigo's rights and assets necessary to manufacture and market generic clobetasol proprionate spray 0.05 percent (“clobetasol spray”) and diclofenac sodium topical solution 1.5 percent (“diclofenac solution”). Further, the proposed Consent Agreement prohibits the companies from accepting certain payments under a backup supply agreement between Paddock and Abbott Laboratories (“Abbott”) for Androgel, the branded version of testosterone gel 1 percent (“testosterone gel”), and entering into any “pay-for-delay” arrangements with Abbott.</P>
        <P>The proposed Consent Agreement has been placed on the public record for thirty days for receipt of comments by interested persons. Comments received during this period will become part of the public record. After thirty days, the Commission will again review the proposed Consent Agreement and the comments received, and will decide whether it should withdraw from the proposed Consent Agreement, modify it, or make final the Decision and Order (“Order”).</P>
        <P>Pursuant to a Purchase Agreement dated January 20, 2011, Perrigo plans to acquire substantially all of Paddock's assets for $540 million. The Commission's Complaint alleges that the proposed acquisition, if consummated, would violate Section 7 of the Clayton Act, as amended, 15 U.S.C. 18, and Section 5 of the FTC Act, as amended, 15 U.S.C. 45, by substantially lessening competition in the U.S. markets for the manufacture and sale of the following generic pharmaceuticals: (1) Ammonium lactate cream; (2) ammonium lactate lotion; (3) ciclopirox shampoo; (4) promethazine suppository; (5) clobetasol spray; (6) diclofenac solution (collectively, the “Products”); and (7) testosterone gel. The proposed Consent Agreement will remedy the alleged violations in each of these markets.</P>
        <HD SOURCE="HD2">II. The Products and Structure of the Markets</HD>
        <P>The proposed acquisition would reduce the number of generic suppliers in six generic drug markets. The number of generic suppliers has a direct and substantial impact on generic pricing, as each additional generic supplier can have a competitive impact on the market. Because there are multiple generic equivalents for each of the products at issue here and the branded products are substantially more expensive than the generic versions, the branded versions no longer significantly constrain the generics' pricing.</P>
        <P>The proposed acquisition would reduce the number of competitors from three to two in four markets: (1) Ammonium lactate cream; (2) ammonium lactate lotion; (3) ciclopirox shampoo; and (4) promethazine suppository. The structure of each of these markets is as follows:</P>

        <P>• The ammonium lactate cream and lotion products are both prescription moisturizers used to treat dry, scaly skin conditions, and help relieve itching. In 2010, annual sales of ammonium lactate cream were approximately $9.7 million, while sales of the ammonium lactate lotion totaled $19 million. The same firms compete in both markets—Perrigo, Paddock, and Taro Pharmaceutical Industries Ltd. (“Taro”), although Paddock has temporarily withdrawn its products from the U.S. market. Perrigo leads the market for ammonium lactate cream with a 70 percent share in the United States. Paddock has 17 percent of the market and Taro has 12 percent. In the market for ammonium lactate cream, the combined firm would account for 87 percent after the proposed acquisition. Perrigo and Paddock are the leading U.S. suppliers<PRTPAGE P="45803"/>of ammonium lactate lotion, with 43 percent and 50 percent of the market, respectively. Taro has only captured a 5 percent market share to date. Post-acquisition, Perrigo's share would increase to 93 percent of the market.</P>
        <P>• Ciclopirox shampoo is a prescription shampoo used to treat seborrheic dermatitis, an inflammatory condition that causes flaky scales and patches on the scalp. Paddock is the leading supplier in the $14.5 million market for ciclopirox shampoo, with a share of approximately 83 percent. Perrigo, with a share of 16 percent, and E. Fougera &amp; Co., with a 1 percent share, are the only other U.S. suppliers of the product. The proposed acquisition, therefore, would result in a combined market share of 99 percent.</P>
        <P>• Promethazine suppository is indicated for a variety of uses, including to treat allergic reactions, to prevent and control motion sickness, and to relieve nausea and vomiting associated with surgery. Sales of the 12.5 mg and 25 mg strengths were approximately $7.9 million and $36.1 million in 2010, respectively. Perrigo, Paddock, and G&amp;W Laboratories, Inc. (“G&amp;W”) are the only U.S. suppliers of both strengths. For the 12.5 mg strength, Perrigo has 15 percent of the market, Paddock has 19 percent, and G&amp;W has 66 percent. For the 25 mg strength, Perrigo has 15 percent of the market, Paddock has 20 percent, and G&amp;W has 65 percent. A combined Perrigo and Paddock would possess 34 percent of the 12.5 mg market and 35 percent of the 25 mg market.</P>
        <P>Both Perrigo and Paddock also are developing products for two future generic drug markets: (1) Clobetasol spray and (2) diclofenac solution. Clobetasol spray is a topical steroid used to treat moderate to severe psoriasis in adults. Diclofenac solution is a non-steroidal anti-inflammatory drug used to treat osteoarthritis of the knee. Perrigo and Paddock are among a limited number of suppliers that are capable of, and interested in, entering these markets in a timely manner. Accordingly, the proposed acquisition would eliminate important future competition in these markets.</P>
        <P>Finally, the proposed acquisition also could inhibit important future competition in the testosterone gel market. Testosterone gel, marketed by Abbott under the brand name Androgel, is a prescription gel used to treat adult males with a testosterone deficiency. Perrigo is one of a limited number of suppliers capable of entering this future generic market in a timely manner. Pursuant to an agreement between Par Pharmaceutical Companies, Inc. (“Par”), Paddock, and Solvay Pharmaceuticals, the former owner of Androgel, Par agreed to delay introducing a generic version of Androgel in exchange for, among other things, payments under a backup supply agreement. That agreement has since been transferred to Paddock. The proposed acquisition would make Perrigo a party to that agreement, thereby enhancing Abbott's and Perrigo's ability to coordinate to delay the introduction of Perrigo's product.</P>
        <HD SOURCE="HD2">III. Entry</HD>
        <P>Entry into the markets for the manufacture and sale of the products would not be timely, likely, or sufficient in its magnitude, character, and scope to deter or counteract the anticompetitive effects of the acquisition. Entry would not take place in a timely manner because the combination of generic drug development times and U.S. Food and Drug Administration (“FDA”) drug approval requirements take a minimum of two years. Furthermore, entry would not be likely because many of the relevant markets are small, so the limited sales opportunities available to a new entrant would likely be insufficient to warrant the time and investment necessary to enter.</P>
        <HD SOURCE="HD2">IV. Effects of the Acquisition</HD>
        <P>The proposed acquisition would cause significant anticompetitive harm to consumers in the U.S. markets for ammonium lactate cream, ammonium lactate lotion, ciclopirox shampoo, and promethazine suppository. In generic pharmaceutical markets, pricing is heavily influenced by the number of competitors that participate in a given market. The evidence shows that with the entry of each additional competitor, the prices of the generic products at issue have decreased. Customers consistently state that the price of a generic drug decreases with the entry of the second, third, and even fourth competitor. In these markets, the proposed acquisition would eliminate one of only three competitors. The evidence indicates that anticompetitive effects—both unilateral and coordinated—are likely to result from a decrease in the number of independent competitors in these markets, thereby increasing the likelihood that customers will pay higher prices.</P>
        <P>The proposed acquisition also eliminates or delays important future competition between Perrigo and Paddock in the U.S. markets for clobetasol spray and diclofenac solution. Perrigo's and Paddock's independent entry into these markets likely would have resulted in lower prices for customers. The proposed acquisition would deprive customers of the expected price decrease that would occur upon the parties' entry into these markets.</P>
        <P>Similarly, the proposed acquisition increases the likelihood and degree of coordinated interaction between Perrigo and Abbott in the U.S. testosterone gel market. Perrigo would become a party to the Par/Paddock backup supply agreement, thereby enhancing Abbott's and Perrigo's ability to coordinate to delay the introduction of Perrigo's product. Perrigo's independent entry into the market likely would result in lower prices for customers. The proposed acquisition could therefore deprive customers of the expected price decrease that would ensue upon Perrigo's timely entry into the market.</P>
        <HD SOURCE="HD2">V. The Consent Agreement</HD>
        <P>The proposed Consent Agreement effectively remedies the acquisition's anticompetitive effects in the relevant product markets by requiring a divestiture of the Products to a Commission-approved acquirer no later than ten days after the acquisition. The acquirer of the divested assets must receive the prior approval of the Commission. The Commission's goal in evaluating a possible purchaser of divested assets is to maintain the competitive environment that existed prior to the acquisition.</P>
        <P>The Consent Agreement requires that the parties divest rights and assets related to the Products to Watson. Watson is the third largest generic drug manufacturer in the United States, and well-situated to manufacture and market the acquired products. Watson has extensive experience in the development, manufacturing, and distribution of generic pharmaceuticals, as well as experience transferring assets from other pharmaceutical companies. Watson has approximately 325 active products and an active product development pipeline. Moreover, Watson's acquisition of the divested assets does not in itself present competitive concerns because Watson does not compete, nor does it have plans to independently enter, any of the markets affected by the proposed transaction. With its resources, capabilities, strong reputation, and experience manufacturing and marketing generic products, Watson is well-positioned to replicate the competition that would be lost with the acquisition.</P>

        <P>If the Commission ultimately determines that Watson is not an acceptable acquirer of the assets to be divested, or that the manner of the<PRTPAGE P="45804"/>divestitures to Watson is not acceptable, the parties must unwind the sale and divest the Products within six months of the date the Order becomes final to another Commission-approved acquirer. If the parties fail to divest within six months, the Commission may appoint a trustee to divest the Product assets.</P>
        <P>The proposed remedy contains several provisions to ensure that the divestitures are successful. The Order requires Perrigo and Paddock to provide transitional services to enable Watson to obtain all of the necessary approvals from the FDA. These transitional services include technology transfer assistance to manufacture the Products in substantially the same manner and quality employed or achieved by Perrigo and Paddock. In addition, the parties must supply Watson with the Products pursuant to a supply agreement while they transfer the manufacturing technology to a third-party manufacturer of Watson's choice.</P>
        <P>The Consent Agreement also preserves competition in the market for testosterone gel by prohibiting the parties from: (1) receiving any payments that accrue after the initial term of the backup supply agreement aside from those for manufacturing the product; and (2) entering into any anticompetitive pay-for-delay arrangements with Abbott regarding the testosterone gel product.</P>
        <P>The Commission has appointed F. William Rahe of Quantic Regulatory Services, LLC (“Quantic”) as the Interim Monitor to oversee the asset transfer and to ensure Perrigo and Paddock's compliance with the provisions of the proposed Consent Agreement. Mr. Rahe is a senior consultant at Quantic and has several years of experience in the pharmaceutical industry. He is a highly-qualified expert on FDA regulatory matters and currently advises Quantic clients on achieving satisfactory regulatory compliance and interfacing with the FDA. In order to ensure that the Commission remains informed about the status of the proposed divestitures and the transfers of assets, the proposed Consent Agreement requires the parties to file reports with the Commission periodically until the divestitures and transfers are accomplished.</P>
        <P>The purpose of this analysis is to facilitate public comment on the proposed Consent Agreement, and it is not intended to constitute an official interpretation of the proposed Order or to modify its terms in any way.</P>
        <SIG>
          <P>By direction of the Commission.</P>
          <NAME>Richard C. Donohue,</NAME>
          <TITLE>Acting Secretary.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19422 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 6750-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <DEPDOC>[Document Identifier: OS-0990-New; 60-day Notice]</DEPDOC>
        <SUBJECT>Agency Information Collection Request; 60-Day Public Comment Request</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Office of the Secretary, HHS.</P>
        </AGY>
        
        <P>In compliance with the requirement of section 3506(c)(2)(A) of the Paperwork Reduction Act (PRA) of 1995, the Office of the Secretary (OS), Department of Health and Human Services, is publishing the following summary of a proposed information collection request for public comment. Interested persons are invited to send comments regarding this burden estimate or any other aspect of this collection of information, including any of the following subjects: (1) The necessity and utility of the proposed information collection for the proper performance of the agency's functions; (2) the accuracy of the estimated burden; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden.</P>

        <P>To obtain copies of the supporting statement and any related forms for the proposed paperwork collections referenced above, e-mail your request, including your address, phone number, OMB number, and OS document identifier, to<E T="03">Sherette.funncoleman@hhs.gov,</E>or call the Reports Clearance Office on (202) 690-6162. Written comments and recommendations for the proposed information collections must be directed to the OS Paperwork Clearance Officer at the above e-mail address within 60 days.</P>
        <P>
          <E T="03">Proposed Project:</E>Descriptive information of solutions provided to the Federal government in response to Challenge and Competition solicitations posted on<E T="03">Challenge.gov.</E>— OMB No. 0990-New-Immediate Office of the Secretary.</P>
        <P>
          <E T="03">Abstract:</E>This request is to seek generic clearance for the collection of routine information requested of responders to solicitations the Federal government makes during the issuance of challenges and competitions posted on the General Service Administration (GSA)'s<E T="03">Challenge.gov</E>Web site. Since passage of the America COMPETES Act of 2011, challenge competitions are increasingly being used by Federal agencies to solve complex problems and obtain innovative solutions. In this role, the Federal government places a description of a problem and parameters of the solution on the<E T="03">Challenge.gov</E>Web site. The solutions are evaluated by the submitting agency and typically prizes (monetary and non-monetary) are awarded to the winning entries.</P>
        <P>This clearance applies to challenges posted on Challenge.gov which uses a common platform for the solicitation of challenges from the public. Each agency designs the criteria for its solicitations based on the goals of the challenge and the specific needs of the agency. There is no standard submission format for solution providers to follow.</P>
        <P>We anticipate that approximately 100 challenges would be issued each year by HHS, with an average of 15 submissions to each challenge solicitation. It is expected that other federal agencies will issue a similar number of challenges. There is no set schedule for the issuance of challenges; they are developed and issued on an “as needs” basis in response to issues the federal agency wishes to solve. The respondents to the challenges, who are participating voluntarily, are unlikely to reply to more than one or several of the challenges.</P>
        <P>Although in recent memoranda the GSA and Office of Management and Budget (OMB) described circumstances whereby OMB approval of a PRA request is not needed, program officials at HHS have identified several sets of information that will typically need to be requested of solution providers to enable the solutions to be adequately evaluated by the federal agency issuing the challenge. These requests for additional information have been suggested to require a PRA review as they represent structured data requests.</P>
        <P>There are three types of additional data that will be routinely requested by the federal agencies. These include the following:</P>
        
        <EXTRACT>
          <P>
            <E T="03">Title of the submission.</E>Due to the nature of the submission and evaluation processes, it is important that a title be requested and submitted for each submission in order to ensure the solution is correctly identified with its provider.</P>
          <P>
            <E T="03">Identification of data resources.</E>In many cases, the solution to a problem will require the solution provider to use data resources. Often, the nature of the data sets will be derived from Federal data resources, such as data.gov. Evaluations of solutions will often depend on the understanding of the selection of the data resource(s) used in the solution.<PRTPAGE P="45805"/>
          </P>
          <P>
            <E T="03">Description of methodology.</E>For effective judging and evaluation, a description of the development methods for the solution to the challenge will be requested. For instance, a prize may be awarded to the solution of a challenge to develop an algorithm that enables reliable prediction of a certain event. A responder could submit the correct algorithm, but without the methodology, the evaluation process could not be adequately performed.</P>
        </EXTRACT>
        
        <GPOTABLE CDEF="s50,r50,12,12,12,12" COLS="6" OPTS="L2,i1">
          <TTITLE>Estimated Annualized Burden Table</TTITLE>
          <BOXHD>
            <CHED H="1">Forms</CHED>
            <CHED H="1">Type of respondent</CHED>
            <CHED H="1">No. of<LI>respondents</LI>
            </CHED>
            <CHED H="1">No. of responses per respondent</CHED>
            <CHED H="1">Average burden (in hours) per response</CHED>
            <CHED H="1">Total burden hours</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Challenge Template A</ENT>
            <ENT>Individuals or Households</ENT>
            <ENT>500</ENT>
            <ENT>1</ENT>
            <ENT>10/60</ENT>
            <ENT>83.3</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Challenge Template A</ENT>
            <ENT>Organizations</ENT>
            <ENT>500</ENT>
            <ENT>1</ENT>
            <ENT>10/60</ENT>
            <ENT>83.3</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Challenge Template A</ENT>
            <ENT>Businesses</ENT>
            <ENT>500</ENT>
            <ENT>1</ENT>
            <ENT>10/60</ENT>
            <ENT>83.3</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Challenge Template A</ENT>
            <ENT>State, territory, tribal or local governments</ENT>
            <ENT>30</ENT>
            <ENT>1</ENT>
            <ENT>10/60</ENT>
            <ENT>5</ENT>
          </ROW>
          <ROW RUL="n,n,s">
            <ENT I="01">Challenge Template A</ENT>
            <ENT>Federal government</ENT>
            <ENT>30</ENT>
            <ENT>1</ENT>
            <ENT>10/60</ENT>
            <ENT>5</ENT>
          </ROW>
          <ROW>
            <ENT I="03">Total</ENT>
            <ENT/>
            <ENT>1,560</ENT>
            <ENT/>
            <ENT/>
            <ENT>255.9</ENT>
          </ROW>
        </GPOTABLE>
        <SIG>
          <NAME>Mary Forbes,</NAME>
          <TITLE>Paperwork Reduction Act Clearance Officer, Office of the Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19323 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4150-03-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBJECT>Calculation of Annual Federal Medical Assistance Percentages for Indian Tribes for Use in the Title IV-E Foster Care, Adoption Assistance, and Kinship Guardianship Assistance Programs</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Office of the Secretary, DHHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>This notice finalizes the methodology that will be used to calculate reimbursement rates applicable to fiscal years 2010 and beyond for assistance payments under the tribal Foster Care, Adoption Assistance and Guardianship Assistance Programs authorized by title IV-E of the Social Security Act. A Notice with Comment Period on this topic was previously published on October 8, 2010.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>
            <E T="03">Effective Date.</E>The methodology described in this Notice is effective upon publication.</P>
        </DATES>
        <HD SOURCE="HD1">A. Background</HD>
        <P>The Fostering Connections to Success and Increasing Adoptions Act of 2008 (“Fostering Connections Act, ” Pub. L. 110-351), authorizes Indian tribes, tribal organizations and tribal consortia to receive funding directly for Foster Care, Adoption Assistance, and Kinship Guardianship Assistance Programs under title IV-E of the Social Security Act (42 U.S.C. 679c). Such direct funding was authorized to begin in fiscal year (FY) 2010 for Indian tribes, tribal organizations or tribal consortia with approved title IV-E plans, or eligible Indian tribes may submit plans to operate such programs at any time in the future. Indian tribes not operating their own programs may receive title IV-E funds through cooperative agreements or contracts with the States within which they are located. The methodology described in this notice is also applicable in calculating reimbursement rates under such agreements beginning in FY 2010.</P>
        <P>The Federal share of assistance payments for the Title IV-E Foster Care, Adoption Assistance and Kinship Guardianship Assistance Programs is calculated using the Federal Medical Assistance Percentage (FMAP), a match rate calculated annually for each State by the Department of Health and Human Services (HHS) according to a formula specified in statute (section 1905(b) of the Social Security Act, 42 U.S.C. 1396d(b)). The FMAP formula involves comparing the State's average per capita income over a three year period with the average per capita income of the U.S. as a whole for the same three year period, and results in FMAP rates that vary between statutory minimum and maximum levels of 50 and 83 percent. The formula produces higher Federal matching rates for jurisdictions with lower per capita incomes relative to the U.S. as a whole.</P>
        <P>Indian tribes previously have not been authorized to directly administer Federal programs that use FMAPs and therefore tribal FMAPs have not previously been calculated. However, the Fostering Connections Act requires HHS to establish FMAP rates for Indian tribes, tribal organizations, or tribal consortia (Pub. L. 110-351, section 301(d); 42 U.S.C. 679c(d)). The Act further specifies that each Tribe's annual FMAP shall be based on the per capita income of the service population of the Indian tribe, tribal organization, or tribal consortium. However, no tribal FMAP shall be lower than the FMAP of any State in which the Indian tribe, tribal organization, or tribal consortium is located.</P>
        <P>The FMAP rates calculated using the methodology described here will be used for Indian tribes' title IV-E Foster Care, Adoption Assistance, and Kinship Guardianship Assistance programs whether they are administered directly by the Indian tribe or through an agreement or contract with a title IV-E State agency per sections 474(a)(1) and (2) of the Social Security Act, 42 U.S.C. 674(a)(1) and (2). Thus, a State may also claim reimbursement for title IV-E allowable assistance payments made on behalf of tribal children served through agreements or contracts with Indian tribes at the higher of the FMAP rate applicable to the State or the FMAP rate for the involved Indian tribe.</P>
        <HD SOURCE="HD1">B. Outreach Regarding the October 8, 2010, Federal Register Notice and Comments Received</HD>
        <P>On October 8, 2010, HHS published a<E T="04">Federal Register</E>Notice requesting comments on its proposed methodology for calculating FMAP for Indian tribes. A 60-day comment period was provided. HHS mailed copies of the Notice to tribal chairman of all federally recognized Indian tribes and posted the Notice to several electronic listserves operated by the Department's Administration for Children and Families that are most relevant to tribal child welfare programs. Each of the letters and postings provided dates and call-in instructions for four conference calls that were to be held to describe the content of the Notice and answer any questions Tribes may have had about it. These calls were held on November 3, 4, 9 and 10, 2010.</P>

        <P>A single set of written comments was received on the content of the<E T="04">Federal<PRTPAGE P="45806"/>Register</E>Notice and the methodology for calculating tribal FMAP rates. These comments, from the National Indian Child Welfare Association (NICWA), supported several specific aspects of the proposed methodology. These include: (1) The use of the standard FMAP formula to calculate rates for Indian tribes, substituting the Indian tribe's per capita income in place of the State's; (2) the proposal to round each Indian tribe's rate up to the next higher whole number; (3) the extension of temporary FMAP increases as specified in Section 5001 of Public Law 111-5, “the American Recovery and Reinvestment Act of 2009” and Section 201 of Public Law 111-226, the “Education, Jobs and Medicaid Assistance Act” to Indian tribes as they apply to States; and (4) our recommendation to use, as a default, data for the population identified as American Indian or Alaska Native only in the Indian tribe's service area to calculate the FMAP rate, while being open to discussion if the Indian tribe believes another formulation better represents its service population.</P>
        <P>The NICWA comments also expressed guarded support for our proposed methodology for calculating FMAP rates for consortia or tribal organizations serving multiple Indian tribes, noting the methodology “may be appropriate” but noting that individual situations may produce complicating factors of which NICWA is unaware. Neither we nor NICWA has yet identified specific cases in which the proposed methodology is problematic. However, we acknowledge that no methodology is guaranteed to work in all situations and remain willing to work with tribal organizations and consortia to consider alternate methods in cases where the proposed methodology proves inadequate.</P>
        <P>NICWA did express the concern that our proposed data source for FMAP calculations for fiscal year 2012 and beyond involves 5-year per capita income estimates from the American Community Survey (ACS). These data were unavailable before the comment period closed. NICWA, supported by a resolution from the National Congress of American Indians, suggested that we extend the comment period for several months in order to allow a thorough examination of the new data, which was scheduled for release in December, 2010. By the time the NICWA comments were received on the last day of the comment period, it was too late to extend the comment period under the existing Federal Register Notice. We did consider re-opening the comment period and also considered finalizing only rates for 2010 and 2011 while asking anew for comments on the methodology for 2012 and beyond. However, we have decided not to reopen the comment period for two reasons. First, an examination of these new data, published December 14, 2010, reveal few differences between the rates produced using the ACS 5-year estimates and those produced using the 2000 decennial Census data NICWA supported. Second, while NICWA expressed apprehension because the new data was as yet unseen, neither NICWA nor any other organization has identified a viable alternative to these data for routine use. While individual Indian tribes may have alternative data sources, and we have said consistently that we will consider such alternative data as an Indian tribe may choose to submit, the 5-year ACS data is the only data set we have been able to identify that provides consistent information on the per capita incomes of the range of Indian tribes eligible to participate in the title IV-E Foster Care, Adoption Assistance, and Guardianship Assistance Programs. Without a viable alternative to consider, and new evidence that the proposed data source is viable for FY 2012 and beyond, we have decided to finalize the methodology as proposed. A fuller analysis of the 5-year ACS estimates and their implications for tribal FMAP rates appears below. A look-up table for 2012 FMAP rates, equivalent to the table for FYs 2010 and 2011 that appeared in the previous Federal Register Notice, appears at the end of this Notice. We also repeat at the end of this notice the lookup table for the FMAP rates applicable to FYs 2010 and 2011.</P>
        <P>During the conference calls we held with Indian tribes to explain the proposed methodology we did receive questions on the data sources used to calculate the rate, i.e., the 2000 Decennial Census and the ACS, both produced by the U.S. Census Bureau. Specifically, we were asked whether the Census Bureau's definition of income includes tribal payments to members (it does) and whether the data source makes any adjustments to account for the high cost of living in Alaska (it does not). In addition, several callers asked us to provide them with the per capita income data for their Indian tribe, and the associated FMAP rate calculated using the proposed methodology. We provided this information in each case. One caller also asked for clarification regarding which components of the title IV-E Program are matched using the FMAP. We noted that FMAP is used to match assistance payments, which are primarily room and board costs for children in foster care and payments to families under the adoption assistance and kinship guardianship assistance programs. Other costs, particularly administrative and training costs, are matched at other statutorily defined match rates, 50 percent in the case of administrative costs, and 55 to 75 percent in the case of eligible training costs.</P>
        <HD SOURCE="HD1">C. Analysis of American Community Survey 5-Year Estimates for 2005-2009</HD>

        <P>As noted above, the first 5-year ACS estimates were published by the Census Bureau on December 14, 2010. We have conducted an analysis of these data to determine FMAP rates under our proposed methodology for 162 Indian tribes and Alaska native communities that have, to date, either expressed interest in participating in title IV-E programs directly or have agreements or contracts with states under which they operate title IV-E programs. We considered as “interested” those Indian tribes that currently operate title IV-E programs through agreements with States as well as those that either applied for a title IV-E planning grant from the Children's Bureau, or that submitted a letter of intent to the Children's Bureau indicating they are considering the submission of a title IV-E plan. Such letters of intent were solicited by the Children's Bureau in a program instruction in December, 2008 (<E T="03">http://www.acf.hhs.gov/programs/cb/laws_policies/policy/pi/2008/pi0806.htm</E>). Our analysis of ACS 5-year estimates in conjunction with the FMAP calculation methodology has revealed the following:</P>
        <P>• All 11 Indian tribes with current title IV-E planning grants would receive the maximum FMAP under the proposed methodology using the newly released 5-year ACS data, as they did under the 2000 Decennial Census data.</P>
        <P>• Of the 162 Indian tribes and Alaska native communities examined, 5-year ACS data was found to be available covering 151 of these Indian tribes and Alaska native communities. Of the 151, data for those on tribal lands identifying themselves as American Indian or Alaska Native (AI/AN) was available for 143. For the remaining 8 Indian tribes data is available for persons of all races residing in the tribal area, but not for the AI/AN population specifically.</P>

        <P>• The data established that, using AI/AN data when it is available and data for all persons where it is not, a total of 128 of the 151 Indian tribes and Alaska native communities for which ACS data is available would receive the maximum FMAP of 83 percent.<PRTPAGE P="45807"/>
        </P>
        <P>• Twenty-four other Indian tribes that have expressed interest in the title IV-E program were determined to have higher per capita income and as a result the applicable Tribal FMAP would be lower than the maximum rate. These 24 include four tribes that would receive rates of between 80 and 83 percent, 10 that would receive rates between 70 and 79 percent, seven that would receive rates between 60 and 69 percent and two that would receive rates between 50 and 59 percent. In only three cases (two in Oklahoma and one in Michigan) was the calculated FMAP for the Indian tribe lower than that of the State within which the Indian tribe is located. In these three cases, the Indian tribe would receive the State's higher FMAP rate.</P>
        <P>• Per capita income data is not available in the 5-year ACS data for 11 very small Indian tribes that have previously expressed an interest in the title IV-E programs, but which have not yet submitted a title IV-E plan or received a title IV-E plan development grant. Some of these Indian tribes currently receive title IV-E funds under a contract or cooperative agreement with the State(s) within which they are located. As described in section E below, we have modified our proposal to provide a method of calculating FMAP for Indian tribes for which no ACS data is available.</P>
        <P>• FMAP rates calculated using the 5-year ACS data are largely consistent with those calculated using the older 2000 Decennial Census data. Of the 147 Indian tribes for which we examined FMAP rates and for which income estimates are available in both data sets, 121 result in the same FMAP rates using both data sources, while 6 would receive slightly higher rates using the more recent data and 20 would receive slightly lower rates. This fluctuation is to be expected and likely reflects differential economic development since 2000. For instance, the Indian tribe may have opened a casino or other industry since 2000 that has improved its per capita income relative to the nation as a whole. Conversely, the Indian tribe may have been disproportionately affected by the recession if local industry was particularly hard hit relative to other parts of the nation.</P>
        <FP>The 5-year ACS data are the most recent data available for almost all of the Indian tribes that we are aware are considering participating in title IV-E programs and therefore represents the best measure of the current per capita income for each Indian tribe. The consistency with earlier Census data provides further confidence that the ACS data is suitable for the purpose of calculating FMAP rates for Indian tribes.</FP>
        <HD SOURCE="HD1">D. Calculation of FMAP for Indian Tribes for Use Matching Program Claims for Fiscal Years 2010 and 2011</HD>
        <P>In the October 8<E T="04">Federal Register</E>Notice we proposed to adapt the standard FMAP formula used for States by substituting each participating Indian tribe's per capita income for that of the State, that is to use the formula 1-0.45((Indian Tribe's Per Capita Income)<SU>2</SU>/(U.S. Per Capita Income)<SU>2</SU>). We further proposed that minimum and maximum FMAP rates would apply to Indian tribes as they do to States, noting that we had no legal authority to waive these limits. We proposed to use 2000 Decennial Census data to calculate the FMAP rates for FYs 2010 and 2011, noting that it was the only data source we identified that included per capita income data for all the Indian tribes that had expressed interest in participating in the Title IV-E programs. We proposed to use data for those living on tribal lands who identified themselves solely as American Indian or Alaska Native when that data is available, and data for all persons in the tribal area when it is not. Finally, we had proposed that rather than use decimal places, tribal FMAP rates would be rounded up to the next highest whole number (up to a maximum of 83 percent).</P>
        <P>Having received one supportive comment and no negative comments on each of the above components of our proposed methodology and no information about alternative data sources, we are finalizing this proposal with respect to calculating the FMAP rates for FYs 2010 and 2011.</P>
        <P>The calculations using this methodology are to be the default method to be used to calculate FMAP for Indian tribes. However, as spelled out in the statute, if in any case the tribal FMAP rate calculated in this manner is lower than that of any State in which the Indian tribe is located, the Indian tribe would receive the higher State rate instead. In addition, also as directed by statute, HHS will consider using supplemental data identified by an Indian tribe, tribal organization or tribal consortium rather than 2000 Decennial Census data on per capita income if the Indian tribe, tribal organization or tribal consortium can demonstrate that the supplemental data better represents the per capita income of its service population. See section H below for further information on how HHS will evaluate the suitability of supplemental data.</P>
        <HD SOURCE="HD1">E. Calculation of FMAP for Indian Tribes for Use Matching Program Claims for Fiscal Years 2012 and Beyond</HD>
        <P>For fiscal years 2012 and beyond we had proposed to use the same methodology for calculating the FMAP rate for participating Indian tribes, but had proposed to use more recent data on tribal per capita incomes—5-year estimates from the Census Bureau's American Community Survey, the first of which were to be released in December 2010. As was the case with the 2000 Decennial Census data, we had proposed to use data for those on tribal lands identifying themselves only as American Indian or Alaska Native where it is available, and data for all persons on tribal lands where it is not. The 5-year estimates for 2005-2009 were released as scheduled on December 14, 2010. These estimates will be updated annually by the Census Bureau by adding a new year's data and dropping the oldest year. As described above, the new data result in FMAP rates that are substantially similar to those produced by the earlier 2000 Decennial Census data they replace. Decennial census data for 2010 and beyond will not include the per capita income data needed for the FMAP formula.</P>
        <P>We are finalizing this proposal with respect to calculating the FMAP rates for FY 2012 and subsequent FYs. The FY 2012 FMAP rates for Indian tribes will thus be calculated using the ACS 5-year estimates for 2005-2009 published on December 14, 2010. The tribal FMAP rates for each subsequent FY will utilize the most recent update of the ACS 5-year estimates available as of June 30 of the prior FY. As with the calculations for fiscal years 2010 and 2011, no Indian tribe will receive an FMAP rate less than that of any State in which the Indian tribe is located, and any supplemental data provided by the Indian tribe will be considered.</P>

        <P>As noted above, once the first 5-year ACS estimates were published on December 14, 2010, it became clear that for a few small Indian tribes, even 5-year ACS estimates would not be sufficient to produce per capita income estimates for either the AI/AN alone population or for persons of all races living on tribal lands. In these cases, we will use as a third choice the per capita income of all individuals in the State who identify themselves as American Indian/Alaska Native as an estimate of the Indian tribe's per capita income. If the Indian tribe operates in multiple States, we will weigh the per capita income of the AI/AN population in each<PRTPAGE P="45808"/>State by the proportion of the Indian tribe's service population in the State. In establishing FMAP for Indian tribes for which ACS data is unavailable we will take care to consult with the Indian tribe regarding the availability of alternate data.</P>
        <HD SOURCE="HD1">F. Calculation of FMAP for Consortia and Tribal Organizations Serving Multiple Tribes</HD>
        <P>In the October 8, 2010<E T="04">Federal Register</E>Notice we had proposed to calculate FMAP rates for consortia and tribal organizations serving multiple Indian tribes by weighting the per capita income data according to the proportional representation of each Indian tribe's service population relative to the total service population of the organization or consortium. Receiving no comments opposing the proposed methodology and having no alternatives suggested, this now becomes our established method for producing FMAP for organizations and consortia serving multiple Indian tribes. Again, consistent with NICWA's comments, we will consult with organizations and consortia as the issue comes up to ensure this method accurately represents the program's service population.</P>
        <HD SOURCE="HD1">G. Procedures for Producing Annual Updates to Federal Medical Assistance Percentages for Indian Tribes</HD>

        <P>As noted above, we will use as our default source of per capita income data the 5-year estimates the American Community Survey. These data will be updated annually by the Census Bureau on a rolling basis by dropping the earliest of the 5 years and adding the latest. For fiscal year 2012 rates we will use ACS data for 2005-2009. For fiscal year 2013 we will update to using data for 2006-2010, and so forth. The formula for the calculation will remain as described above. In the third quarter of each fiscal year ACF regional office staff will communicate with each Indian tribe, tribal organization, or tribal consortium with an approved title IV-E plan their tribal FMAP rate for the upcoming fiscal year. Those States reporting title IV-E claims for Tribe-State agreement assistance payments will also be informed by the ACF regional office staff of the calculated FMAP rates for Indian tribes located in their State. Because most Indian tribes will be receiving the maximum FMAP rate, the calculation formula provides for rounding up to the next highest full percentage point and per capita incomes do not tend to change rapidly, it is likely that many programs will see little, if any, matching rate shifts from year to year. A link to a table similar to the ones at the end of this notice will be posted annually on ACF's Web site (<E T="03">http://www.acf.hhs.gov</E>) displaying the per capita income thresholds for each FMAP rate for the fiscal year.</P>
        <HD SOURCE="HD1">H. Consideration of Supplemental Data</HD>
        <P>As noted in our previous<E T="04">Federal Register</E>Notice, before finalizing new FMAP rates for a year, HHS will consider any additional relevant data on its per capita income submitted by a Indian tribe, tribal organization or tribal consortium. In the absence of supplemental data, HHS will use the data and procedures described above to calculate the applicable FMAP for the grantee. Additional data submitted by Indian tribes, tribal organizations and tribal consortia will be evaluated by the Division of Mandatory Grants in the Office of Grants Management at ACF. Such data may be submitted to the attention of Joseph Lonergan, Director, Division of Mandatory Grant, ACF Office of Grants Management, at 202-401-6603 (phone); 202-401-5644 (fax); or email:<E T="03">tribalfmap@hhs.gov.</E>Supplemental data may relate to matters such as the per capita income of the Indian tribe, tribal organization or consortium, the numbers and/or geographic locations of its service population, and/or defining the grantee's service population to include individuals other than those who identified themselves solely as American Indian to be considered for the purposes of calculating the applicable per capita income.</P>
        <P>The suitability of supplemental data submissions from Indian Tribes, tribal organizations and tribal consortia will be evaluated based on criteria that include: Whether the Decennial Census or American Community Survey data that would otherwise be used is either missing or has a high margin of error; if the supplemental data reflects the same or similar definitions of income as do the national data, such as what types of income are included and excluded; if the data have been collected and tabulated in a reliable manner; and if the data are current or more recently updated than the data that would otherwise be used and therefore reflect more current economic conditions of the Indian tribe's service population.</P>
        <P>Data to be considered for a given fiscal year's calculation should be submitted no later than 30 days before the beginning of the next fiscal year (September 1) in order to provide sufficient time for the Department to evaluate the suitability of the additional data. The tribal FMAP rate for the next fiscal year calculated from the ACS 5-year data will be in effect beginning on October 1 of that year unless and until a decision is made by the Department to revise it based on the supplemental data previously provided by the Indian tribe, tribal organization, or tribal consortium. Tribal leadership will be consulted prior to a final decision by the Department regarding the suitability of any supplemental data submitted. The Department will also work closely with tribal leaders before establishing a final FMAP for the upcoming fiscal year.</P>
        <HD SOURCE="HD1">I. Application of Temporary Increases to Tribal Federal Medical Assistance Percentages</HD>
        <P>As proposed in our previous<E T="04">Federal Register</E>Notice, to the extent permitted by law we will extend to Tribes any temporary adjustments to FMAP that apply to States. Temporary FMAP rates that applied to states in Fiscal Year 2010 and 2011 (i.e., those authorized by Public Law 111-5 and Public Law 111-226) will apply to Indian tribes. The applicability of any future FMAP adjustments to Indian tribes, tribal organizations, and tribal consortia will depend on the specific statutory language enacting such adjustments.</P>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Laura Radel, Office of the Assistant Secretary for Planning and Evaluation, Room 404-E—Hubert H. Humphrey Building, 200 Independence Avenue, SW., Washington, DC 20201; 202-690-5938;<E T="03">Laura.Radel@hhs.gov.</E>
          </P>
          
          <EXTRACT>
            <FP>(Catalog of Federal Domestic Assistance Program Nos. 93.658: Foster Care Title IV-E; 93.659: Adoption Assistance; 93.090: Guardianship Assistance)</FP>
          </EXTRACT>
          <SIG>
            <DATED>Dated: May 20, 2011.</DATED>
            <NAME>Kathleen Sebelius,</NAME>
            <TITLE>Secretary.</TITLE>
          </SIG>
          <BILCOD>BILLING CODE 4150-05-P</BILCOD>
          <GPH DEEP="520" SPAN="3">
            <PRTPAGE P="45809"/>
            <GID>EN01AU11.034</GID>
          </GPH>
          <GPH DEEP="520" SPAN="3">
            <PRTPAGE P="45810"/>
            <GID>EN01AU11.035</GID>
          </GPH>
        </FURINF>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19358 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4150-05-C</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBJECT>National Committee on Vital and Health Statistics: Meeting</SUBJECT>
        <P>Pursuant to the Federal Advisory Committee Act, the Department of Health and Human Services (HHS) announces the following advisory committee meeting.</P>
        <FP SOURCE="FP-2">Name: National Committee on Vital and Health Statistics (NCVHS), Full Committee Meeting.</FP>
        <FP SOURCE="FP-2">Time and Date: August 26, 2011: 3 p.m.-5 p.m., E.D.T.</FP>
        <FP SOURCE="FP-2">Place: Teleconference. Dial-In Number: 1-877-939-9305, participant code is 4431134.</FP>
        <FP SOURCE="FP-2">Status: Open.</FP>
        <FP SOURCE="FP-2">Purpose: This teleconference is being held to discuss a letter to the HHS Secretary regarding the President's Council of Advisors on Science and Technology (PCAST) Report on Health Information Technology and to approve the final draft.</FP>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Substantive program information as well as summaries of meetings and a roster of committee members may be obtained from Marjorie S. Greenberg, Executive Secretary, NCVHS, National Center for Health Statistics, Centers for Disease Control and Prevention, 3311 Toledo Road, Room 2402, Hyattsville, Maryland 20782, telephone (301) 458-4245. Information also is available on the NCVHS home page of the HHS Web<PRTPAGE P="45811"/>site:<E T="03">http://www.ncvhs.hhs.gov/,</E>where further information including an agenda will be posted when available.</P>
          <P>Should you require reasonable accommodation, please contact the CDC Office of Equal Employment Opportunity on (301) 458-4EEO (4336) as soon as possible.</P>
          <SIG>
            <DATED>Dated: July 25, 2011.</DATED>
            <NAME>James Scanlon,</NAME>
            <TITLE>Deputy Assistant Secretary for Science and Data Policy, Office of the Assistant Secretary for Planning and Evaluation.</TITLE>
          </SIG>
        </FURINF>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19359 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4151-05-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>Food and Drug Administration</SUBAGY>
        <DEPDOC>[Docket No. FDA-2011-N-0548]</DEPDOC>
        <SUBJECT>Animal Drug User Fee Rates and Payment Procedures for Fiscal Year 2012</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Food and Drug Administration, HHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Food and Drug Administration (FDA) is announcing the rates and payment procedures for fiscal year (FY) 2012 animal drug user fees. The Federal Food, Drug, and Cosmetic Act (the FD&amp;C Act), as amended by the Animal Drug User Fee Act of 2003 (ADUFA) and the Animal Drug User Fee Amendments of 2008 (ADUFA II), authorizes FDA to collect user fees for certain animal drug applications and supplements, on certain animal drug products, on certain establishments where such products are made, and on certain sponsors of such animal drug applications and/or investigational animal drug submissions. This notice establishes the fee rates for FY 2012.</P>
        </SUM>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Visit FDA's Web site at<E T="03">http://www.fda.gov/ForIndustry/UserFees/AnimalDrugUserFeeActADUFA/default.htm</E>or contact Lisa Kable, Center for Veterinary Medicine (HFV-10), Food and Drug Administration, 7529 Standish Pl., Rockville, MD 20855, 240-276-9718. For general questions, you may also e-mail the Center for Veterinary Medicine (CVM) at:<E T="03">cvmadufa@fda.hhs.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P/>
        <HD SOURCE="HD1">I. Background</HD>
        <P>Section 740 of the FD&amp;C Act (21 U.S.C. 379j-12) establishes four different kinds of user fees: (1) Fees for certain types of animal drug applications and supplements, (2) annual fees for certain animal drug products, (3) annual fees for certain establishments where such products are made, and (4) annual fees for certain sponsors of animal drug applications and/or investigational animal drug submissions (21 U.S.C. 379j-12(a)). When certain conditions are met, FDA will waive or reduce fees (21 U.S.C. 379j-12(d)).</P>
        <P>For FY 2009 through FY 2013, the FD&amp;C Act establishes aggregate yearly base revenue amounts for each of these fee categories. Base revenue amounts established for years after FY 2009 are subject to adjustment for workload. Fees for applications, establishments, products, and sponsors are to be established each year by FDA so that the revenue for each fee category will approximate the level established in the statute, after the level has been adjusted for workload.</P>
        <P>For FY 2012, the animal drug user fee rates are: $372,100 for an animal drug application; $186,050 for a supplemental animal drug application for which safety or effectiveness data is required and for an animal drug application subject to the criteria set forth in section 512(d)(4) of the FD&amp;C Act (21 U.S.C. 360b(d)(4)); $7,935 for an annual product fee; $93,050 for an annual establishment fee; and $67,200 for an annual sponsor fee. FDA will issue invoices for FY 2012 product, establishment, and sponsor fees by December 31, 2011, and these invoices will be due and payable within 30 days of issuance of the invoice. The application fee rates are effective for applications submitted on or after October 1, 2011, and will remain in effect through September 30, 2012. Applications will not be accepted for review until FDA has received full payment of application fees and any other animal drug user fees owed.</P>
        <HD SOURCE="HD1">II. Revenue Amount for FY 2012</HD>
        <HD SOURCE="HD2">A. Statutory Fee Revenue Amounts</HD>
        <P>ADUFA II (Pub. L. 110-316 signed by the President on August 14, 2008) specifies that the aggregate revenue amount for FY 2012 for each of the four animal drug user fee categories is $5,442,000 before any adjustment for workload is made. (See 21 U.S.C. 379j-12(b)(1) through (b)(4).)</P>
        <HD SOURCE="HD2">B. Inflation Adjustment to Fee Revenue Amount</HD>
        <P>The amounts established in ADUFA II for each year for FY 2009 through FY 2013 include an inflation adjustment; so, no further inflation adjustment is required.</P>
        <HD SOURCE="HD2">C. Workload Adjustment to Inflation Adjusted Fee Revenue Amount</HD>
        <P>For each FY beginning in FY 2010, ADUFA provides that fee revenue amounts shall be further adjusted to reflect changes in review workload (21 U.S.C. 379j-12(c)(1)).</P>
        <P>FDA calculated the average number of each of the five types of applications and submissions specified in the workload adjustment provision (animal drug applications, supplemental animal drug applications for which data with respect to safety or efficacy are required, manufacturing supplemental animal drug applications, investigational animal drug study submissions, and investigational animal drug protocol submissions) received over the 5-year period that ended on September 30, 2002 (the base years), and the average number of each of these types of applications and submissions over the most recent 5-year period that ended on June 30, 2011.</P>

        <P>The results of these calculations are presented in the first two columns of table 1 of this document. Column 3 reflects the percent change in workload over the two 5-year periods. Column 4 shows the weighting factor for each type of application, reflecting how much of the total FDA animal drug review workload was accounted for by each type of application or submission in the table during the most recent 5 years. Column 5 of table 1 of this document is the weighted percent change in each category of workload, and was derived by multiplying the weighting factor in each line in column 4 by the percent change from the base years in column 3. At the bottom right of the table the sum of the values in column 5 is added, reflecting a total change in workload of negative 31 percent for FY 2012. This is the workload adjuster for FY 2012.<PRTPAGE P="45812"/>
        </P>
        <GPOTABLE CDEF="s60,10,10,10,10,10" COLS="6" OPTS="L2,i1">
          <TTITLE>Table 1—Workload Adjuster Calculation</TTITLE>
          <TDESC>[Numbers may not add due to rounding]</TDESC>
          <BOXHD>
            <CHED H="1">Application<LI>type</LI>
            </CHED>
            <CHED H="1">Column 1<LI>5-year avg.</LI>
              <LI>(base years)</LI>
            </CHED>
            <CHED H="1">Column 2<LI>Latest 5-year avg.</LI>
            </CHED>
            <CHED H="1">Column 3<LI>Percent</LI>
              <LI>change</LI>
            </CHED>
            <CHED H="1">Column 4<LI>Weighting</LI>
              <LI>factor</LI>
            </CHED>
            <CHED H="1">Column 5<LI>Weighted</LI>
              <LI>percent change</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">New Animal Drug Applications (NADA's)</ENT>
            <ENT>28.8</ENT>
            <ENT>13.0</ENT>
            <ENT>−55</ENT>
            <ENT>0.0296</ENT>
            <ENT>−2</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Supplemental NADA's with Safety or Efficacy Data</ENT>
            <ENT>23.4</ENT>
            <ENT>11.2</ENT>
            <ENT>−52</ENT>
            <ENT>0.0234</ENT>
            <ENT>−1</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Manufacturing Supplements</ENT>
            <ENT>366.6</ENT>
            <ENT>427.6</ENT>
            <ENT>17</ENT>
            <ENT>0.1385</ENT>
            <ENT>2</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Investigational Study Submissions</ENT>
            <ENT>336.6</ENT>
            <ENT>215.8</ENT>
            <ENT>−36</ENT>
            <ENT>0.6023</ENT>
            <ENT>−22</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Investigational Protocol Submissions</ENT>
            <ENT>292.4</ENT>
            <ENT>173.8</ENT>
            <ENT>−41</ENT>
            <ENT>0.2063</ENT>
            <ENT>−8</ENT>
          </ROW>
          <ROW>
            <ENT I="03">FY 2012 Workload Adjuster</ENT>
            <ENT/>
            <ENT/>
            <ENT/>
            <ENT/>
            <ENT>−31</ENT>
          </ROW>
        </GPOTABLE>
        <P>ADUFA specifies that the workload adjuster may not result in fees that are less than the fee revenue amount in the statute (21 U.S.C. 379j-12(c)(1)(B)). Because applying the FY 2012 workload adjuster would result in fees less than the statutory amount, the workload adjustment will not be applied in FY 2012. As a result, the statutory revenue target amount for each of the four categories of fees remains at $5,442,000 with the new total revenue target for fees in FY 2012 being $21,768,000.</P>
        <HD SOURCE="HD1">III. Adjustment for Excess Collections in Previous Years</HD>
        <P>ADUFA II amended the annual offset provision of ADUFA I to require one offset when FY 2013 fees are set in August of 2012, if aggregate collections from FY 2009 through 2011 plus the amount of fees estimated to be collected for FY 2012 exceed aggregate appropriations over the same period (21 U.S.C. 379j-12(g)(4), as amended by ADUFA II). Therefore FDA is not offsetting for excess collections at this time.</P>
        <HD SOURCE="HD1">IV. Application Fee Calculations for FY 2012</HD>
        <P>The terms “animal drug application” and “supplemental animal drug application” are defined in section 739 of the FD&amp;C Act (21 U.S.C. 379j-11(1) and (2)).</P>
        <HD SOURCE="HD2">A. Application Fee Revenues and Numbers of Fee-Paying Applications</HD>
        <P>The application fee must be paid for any animal drug application or supplemental animal drug application that is subject to fees under ADUFA and that is submitted on or after September 1, 2003. The application fees are to be set so that they will generate $5,442,000 in fee revenue for FY 2012. This is the amount set out in the statute and no adjustments are required for FY 2012. The fee for a supplemental animal drug application for which safety or effectiveness data are required and for an animal drug application subject to criteria set forth in section 512(d)(4) of the FD&amp;C Act is to be set at 50 percent of the animal drug application fee. (See 21 U.S.C. 379j-12(a)(1)(A)(ii), as amended by ADUFA II.)</P>
        <P>To set animal drug application fees and supplemental animal drug application fees to realize $5,442,000, FDA must first make some assumptions about the number of fee-paying applications and supplements the agency will receive in FY 2012.</P>
        <P>The agency knows the number of applications that have been submitted in previous years. That number fluctuates significantly from year to year. In estimating the fee revenue to be generated by animal drug application fees in FY 2012, FDA is assuming that the number of applications that will pay fees in FY 2012 will equal the average number of submissions over the four most recent completed years (FY 2007-FY 2010). This may not fully account for possible year to year fluctuations in numbers of fee-paying applications, but FDA believes that this is a reasonable approach after 8 years of experience with this program.</P>
        <P>Over the 4 most recent completed years, the average number of animal drug applications that would have been subject to the full fee was 8.25. Over this same period, the average number of supplemental applications and applications subject to the criteria set forth in section 512(d)(4) of the FD&amp;C Act that would have been subject to half of the full fee was 12.75.</P>
        <P>Thus, for FY 2012, FDA estimates receipt of 8.25 fee paying original applications and 12.75 fee-paying supplemental animal drug applications and applications subject to the criteria set forth is section 512(d)(4) of the FD&amp;C Act which pay half of the full fee.</P>
        <HD SOURCE="HD2">B. Fee Rates for FY 2012</HD>
        <P>FDA must set the fee rates for FY 2012 so that the estimated 8.25 applications that pay the full fee and the estimated 12.75 supplements and applications subject to the criteria set forth in section 512(d)(4) of the FD&amp;C Act that pay half of the full fee will generate a total of $5,442,000. To generate this amount, the fee for an animal drug application, rounded to the nearest hundred dollars, will have to be $372,100, and the fee for a supplemental animal drug application for which safety or effectiveness data are required and for applications subject to the criteria set forth in section 512(d)(4) of the FD&amp;C Act will have to be $186,050.</P>
        <HD SOURCE="HD1">V. Product Fee Calculations for FY 2012</HD>
        <HD SOURCE="HD2">A. Product Fee Revenues and Numbers of Fee-Paying Products</HD>
        <P>The animal drug product fee (also referred to as the product fee) must be paid annually by the person named as the applicant in a new animal drug application or supplemental new animal drug application for an animal drug product submitted for listing under section 510 of the FD&amp;C Act (21 U.S.C. 360), and who had an animal drug application or supplemental animal drug application pending at FDA after September 1, 2003. (See 21 U.S.C. 379j-12(a)(2).) The term “animal drug product” is defined in 21 U.S.C. 379j-11(3). The product fees are to be set so that they will generate $5,442,000 in fee revenue for FY 2012. This is the amount set out in the statute and no adjustments are required for FY 2012.</P>

        <P>To set animal drug product fees to realize $5,442,000, FDA must make some assumptions about the number of products for which these fees will be paid in FY 2012. FDA developed data on all animal drug products that have been submitted for listing under section 510 of the FD&amp;C Act, and matched this to the list of all persons who had an animal drug application or supplement pending after September 1, 2003. As of July 2011, FDA estimates that there are a total of 762 products submitted for listing by persons who had an animal drug application or supplemental animal drug application pending after September 1, 2003. Based on this, FDA estimates that a total of 762 products will be subject to this fee in FY 2012.<PRTPAGE P="45813"/>
        </P>
        <P>In estimating the fee revenue to be generated by animal drug product fees in FY 2012, FDA is again assuming that 10 percent of the products invoiced, or about 76, will not pay fees in FY 2012 due to fee waivers and reductions. Based on experience with other user fee programs and the first 8 years of ADUFA, FDA believes that this is a reasonable basis for estimating the number of fee-paying products in FY 2012.</P>
        <P>Accordingly, the agency estimates that a total of 686 (762 minus 76) products will be subject to product fees in FY 2012.</P>
        <HD SOURCE="HD2">B. Product Fee Rates for FY 2012</HD>
        <P>FDA must set the fee rates for FY 2012 so that the estimated 686 products that pay fees will generate a total of $5,442,000. To generate this amount will require the fee for an animal drug product, rounded to the nearest 5 dollars, to be $7,935.</P>
        <HD SOURCE="HD1">VI. Establishment Fee Calculations for FY 2012</HD>
        <HD SOURCE="HD2">A. Establishment Fee Revenues and Numbers of Fee-Paying Establishments</HD>
        <P>The animal drug establishment fee (also referred to as the establishment fee) must be paid annually by the person who: (1) Owns or operates, directly or through an affiliate, an animal drug establishment; (2) is named as the applicant in an animal drug application or supplemental animal drug application for an animal drug product submitted for listing under section 510 of the FD&amp;C Act; (3) had an animal drug application or supplemental animal drug application pending at FDA after September 1, 2003; and (4) whose establishment engaged in the manufacture of the animal drug product during the fiscal year. (See 21 U.S.C. 379j-12(a)(3).) An establishment subject to animal drug establishment fees is assessed only one such fee per fiscal year. (See 21 U.S.C. 379j-12(a)(3).) The term “animal drug establishment” is defined in 21 U.S.C. 379j-11(4). The establishment fees are to be set so that they will generate $5,442,000 in fee revenue for FY 2012. This is the amount set out in the statute and no adjustments are required for FY 2012.</P>
        <P>To set animal drug establishment fees to realize $5,442,000, FDA must make some assumptions about the number of establishments for which these fees will be paid in FY 2012. FDA developed data on all animal drug establishments and matched this to the list of all persons who had an animal drug application or supplement pending after September 1, 2003. As of July 2011, FDA estimates that there are a total of 65 establishments owned or operated by persons who had an animal drug application or supplemental animal drug application pending after September 1, 2003. Based on this, FDA believes that 65 establishments will be subject to this fee in FY 2012.</P>
        <P>In estimating the fee revenue to be generated by animal drug establishment fees in FY 2012, FDA is assuming that 10 percent of the establishments invoiced, or 6.5, will not pay fees in FY 2012 due to fee waivers and reductions. Based on experience with the first 8 years of ADUFA, FDA believes that this is a reasonable basis for estimating the number of fee-paying establishments in FY 2012.</P>
        <P>Accordingly, the agency estimates that a total of 58.5 establishments (65 minus 6.5) will be subject to establishment fees in FY 2012.</P>
        <HD SOURCE="HD2">B. Establishment Fee Rates for FY 2012</HD>
        <P>FDA must set the fee rates for FY 2012 so that the estimated 58.5 establishments that pay fees will generate a total of $5,442,000. To generate this amount will require the fee for an animal drug establishment, rounded to the nearest 50 dollars, to be $93,050.</P>
        <HD SOURCE="HD1">VII. Sponsor Fee Calculations for FY 2012</HD>
        <HD SOURCE="HD2">A. Sponsor Fee Revenues and Numbers of Fee-Paying Sponsors</HD>
        <P>The animal drug sponsor fee (also referred to as the sponsor fee) must be paid annually by each person who: (1) Is named as the applicant in an animal drug application, except for an approved application for which all subject products have been removed from listing under section 510 of the FD&amp;C Act or has submitted an investigational animal drug submission that has not been terminated or otherwise rendered inactive; and (2) had an animal drug application, supplemental animal drug application, or investigational animal drug submission pending at FDA after September 1, 2003. (See 21 U.S.C. 379j-11(6) and 379j-12(a)(4).) An animal drug sponsor is subject to only one such fee each fiscal year. (See 21 U.S.C. 379j-12(a)(4).) The sponsor fees are to be set so that they will generate $5,442,000 in fee revenue for FY 2012. This is the amount set out in the statute, and no adjustments are required for FY 2012.</P>
        <P>To set animal drug sponsor fees to realize $5,442,000, FDA must make some assumptions about the number of sponsors who will pay these fees in FY 2012. Based on the number of firms that would have met this definition in each of the past 8 years, FDA estimates that a total of 172 sponsors will meet this definition in FY 2012.</P>
        <P>Careful review indicates that about one third or 33 percent of all of these sponsors will qualify for minor use/minor species waiver or reduction (21 U.S.C. 379j-12(d)(1)(C)). Based on the agency's experience to date with sponsor fees, FDA's current best estimate is that an additional 20 percent will qualify for other waivers or reductions, for a total of 53 percent of the sponsors invoiced, or 91, who will not pay fees in FY 2012 due to fee waivers and reductions. FDA believes that this is a reasonable basis for estimating the number of fee-paying sponsors in FY 2012.</P>
        <P>Accordingly, the agency estimates that a total of 81 sponsors (172 minus 91) will be subject to and pay sponsor fees in FY 2012.</P>
        <HD SOURCE="HD2">B. Sponsor Fee Rates for FY 2012</HD>
        <P>FDA must set the fee rates for FY 2012 so that the estimated 81 sponsors that pay fees will generate a total of $5,442,000. To generate this amount will require the fee for an animal drug sponsor, rounded to the nearest 50 dollars, to be $67,200.</P>
        <HD SOURCE="HD1">VIII. Fee Schedule for FY 2012</HD>
        <P>The fee rates for FY 2012 are summarized in table 2 of this document.</P>
        <GPOTABLE CDEF="s150,12" COLS="2" OPTS="L2,i1">
          <TTITLE>Table 2—FY 2012 Fee Rates</TTITLE>
          <BOXHD>
            <CHED H="1">Animal drug user fee category</CHED>
            <CHED H="1">Fee rate for FY 2012</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Animal Drug Application Fees</ENT>
            <ENT>$372,100</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Animal Drug Application</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Supplemental Animal Drug Application for which Safety or Effectiveness Data are Required or Animal Drug Application Subject to the Criteria Set Forth in Section 512(d)(4) of the FD&amp;C Act</ENT>
            <ENT>186,050</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Animal Drug Product Fee</ENT>
            <ENT>7,935</ENT>
          </ROW>
          <ROW>
            <PRTPAGE P="45814"/>
            <ENT I="01">Animal Drug Establishment Fee<SU>1</SU>
            </ENT>
            <ENT>93,050</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Animal Drug Sponsor Fee<SU>2</SU>
            </ENT>
            <ENT>67,200</ENT>
          </ROW>
          <TNOTE>
            <SU>1</SU>An animal drug establishment is subject to only one such fee each fiscal year.</TNOTE>
          <TNOTE>
            <SU>2</SU>An animal drug sponsor is subject to only one such fee each fiscal year.</TNOTE>
        </GPOTABLE>
        <HD SOURCE="HD1">IX. Procedures for Paying the FY 2012 Fees</HD>
        <HD SOURCE="HD2">A. Application Fees and Payment Instructions</HD>
        <P>The appropriate application fee established in the new fee schedule must be paid for an animal drug application or supplement subject to fees under ADUFA that is submitted after September 30, 2011. Payment must be made in U.S. currency by check, bank draft, or U.S. postal money order payable to the order of the Food and Drug Administration, by wire transfer, or electronically using Pay.gov. (The Pay.gov payment option is available to you after you submit a cover sheet. Click the “Pay Now” button.) On your check, bank draft, or U.S. postal money order, please write your application's unique Payment Identification Number (PIN), beginning with the letters AD, from the upper right-hand corner of your completed Animal Drug User Fee Cover Sheet. Also write the FDA post office box number (P.O. Box 953877) on the enclosed check, bank draft, or money order. Your payment and a copy of the completed Animal Drug User Fee Cover Sheet can be mailed to: Food and Drug Administration, P.O. Box 953877, St. Louis, MO 63195-3877.</P>
        <P>If payment is made by wire transfer, send payment to: U.S. Department of Treasury, TREAS NYC, 33 Liberty St., New York, NY 10045, FDA Deposit Account Number: 75060099, U.S. Department of Treasury routing/transit number: 021030004, SWIFT Number: FRNYUS33. You are responsible for any administrative costs associated with the processing of a wire transfer. Contact your bank or financial institution regarding additional fees.</P>

        <P>If you prefer to send a check by a courier such as Federal Express (FEDEX) or United Parcel Service (UPS), the courier may deliver the check and printed copy of the cover sheet to: U.S. Bank, Attn: Government Lockbox 953877, 1005 Convention Plaza, St. Louis, MO 63101. (<E T="04">Note:</E>This address is for courier delivery only. If you have any questions concerning courier delivery contact the U.S. Bank at 314-418-4821. This telephone number is only for questions about courier delivery.)</P>

        <P>The tax identification number of the Food and Drug Administration is 530196965. (<E T="04">Note:</E>In no case should the payment for the fee be submitted to FDA with the application.)</P>
        <P>It is helpful if the fee arrives at the bank at least a day or two before the application arrives at FDA's CVM. FDA records the official application receipt date as the later of the following: The date the application was received by FDA's CVM, or the date U.S. Bank notifies FDA that your payment in the full amount has been received, or when the U.S. Treasury notifies FDA of receipt of an electronic or wire transfer payment. U.S. Bank and the U.S. Treasury are required to notify FDA within one working day, using the PIN described previously.</P>
        <HD SOURCE="HD2">B. Application Cover Sheet Procedures</HD>

        <P>Step One—Create a user account and password. Log on to the ADUFA Web site at<E T="03">http://www.fda.gov/ForIndustry/UserFees/AnimalDrugUserFeeActADUFA/default.htm</E>and under Tools and Resources click “The Animal Drug User Fee Cover Sheet” and then click “Create ADUFA User Fee Cover Sheet.” For security reasons, each firm submitting an application will be assigned an organization identification number, and each user will also be required to set up a user account and password the first time you use this site. Online instructions will walk you through this process.</P>
        <P>Step Two—Create an Animal Drug User Fee Cover Sheet, transmit it to FDA, and print a copy. After logging into your account with your user name and password, complete the steps required to create an Animal Drug User Fee Cover Sheet. One cover sheet is needed for each animal drug application or supplement. Once you are satisfied that the data on the cover sheet is accurate and you have finalized the cover sheet, you will be able to transmit it electronically to FDA and you will be able to print a copy of your cover sheet showing your unique PIN.</P>
        <P>Step Three—Send the payment for your application as described in section IX.A of this document.</P>
        <P>Step Four—Please submit your application and a copy of the completed Animal Drug User Fee Cover Sheet to the following address: Food and Drug Administration, Center for Veterinary Medicine, Document Control Unit (HFV-199), 7500 Standish Pl., Rockville, MD 20855.</P>
        <HD SOURCE="HD2">C. Product, Establishment, and Sponsor Fees</HD>
        <P>By December 31, 2011, FDA will issue invoices and payment instructions for product, establishment, and sponsor fees for FY 2012 using this Fee Schedule. Payment will be due and payable within 30 days of issuance of the invoice. FDA will issue invoices in November 2012 for any products, establishments, and sponsors subject to fees for FY 2012 that qualify for fees after the December 2011 billing.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Leslie Kux,</NAME>
          <TITLE>Acting Assistant Commissioner for Policy.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19336 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4160-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>Food and Drug Administration</SUBAGY>
        <DEPDOC>[Docket No. FDA-2011-N-0547]</DEPDOC>
        <SUBJECT>Animal Generic Drug User Fee Rates and Payment Procedures for Fiscal Year 2012</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Food and Drug Administration, HHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>The Food and Drug Administration (FDA) is announcing the rates and payment procedures for fiscal year (FY) 2012 generic new animal drug user fees. The Federal Food, Drug, and Cosmetic Act (the FD&amp;C Act), as amended by the Animal Generic Drug User Fee Act of 2008 (AGDUFA), authorizes FDA to collect user fees for certain abbreviated applications for generic new animal drugs, on certain generic new animal drug products, and on certain sponsors of such abbreviated applications for generic new animal drugs and/or investigational<PRTPAGE P="45815"/>submissions for generic new animal drugs. This notice establishes the fee rates for FY 2012.</P>
        </SUM>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Visit FDA's Web site at<E T="03">http://www.fda.gov/ForIndustry/UserFees/AnimalGenericDrugUserFeeActAGDUFA/default.htm</E>or contact Lisa Kable, Center for Veterinary Medicine (HFV-10), Food and Drug Administration, 7529 Standish Pl., Rockville, MD 20855, 240-276-9718. For general questions, you may also email the Center for Veterinary Medicine (CVM) at:<E T="03">cvmagdufa@fda.hhs.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P/>
        <HD SOURCE="HD1">I. Background</HD>
        <P>Section 741 of the FD&amp;C Act (21 U.S.C. 379j-21) establishes three different kinds of user fees: (1) Fees for certain types of abbreviated applications for generic new animal drugs, (2) annual fees for certain generic new animal drug products, and (3) annual fees for certain sponsors of abbreviated applications for generic new animal drugs and/or investigational submissions for generic new animal drugs (21 U.S.C. 379j-21(a)). When certain conditions are met, FDA will waive or reduce fees for generic new animal drugs intended solely to provide for a minor use or minor species indication (21 U.S.C. 379j-21(d)).</P>
        <P>For FY 2009 through FY 2013, the FD&amp;C Act establishes aggregate yearly base revenue amounts for each of these fee categories. Base revenue amounts established for years after FY 2009 may be adjusted for workload. Fees for applications, products, and sponsors are to be established each year by FDA so that the revenue for each fee category will approximate the level established in the statute, after the level has been adjusted for workload.</P>
        <P>For FY 2012, the generic new animal drug user fee rates are: $124,900 for each abbreviated application for a generic new animal drug; $6,200 for each generic new animal drug product; $54,350 for each generic new animal drug sponsor paying 100 percent of the sponsor fee; $40,763 for each generic new animal drug sponsor paying 75 percent of the sponsor fee; and $27,175 for each generic new animal drug sponsor paying 50 percent of the sponsor fee. FDA will issue invoices for FY 2012 product and sponsor fees by December 31, 2011. These fees will be due and payable within 30 days of the issuance of the invoices. The application fee rates are effective for all abbreviated applications for a generic new animal drug submitted on or after October 1, 2011, and will remain in effect through September 30, 2012. Applications will not be accepted for review until FDA has received full payment of related application fees and any other fees owed under the Animal Generic Drug User Fee program.</P>
        <HD SOURCE="HD1">II. Revenue Amount for FY 2012</HD>
        <HD SOURCE="HD2">A. Statutory Fee Revenue Amounts</HD>
        <P>AGDUFA (Title II of Pub. L. 110-316 signed by the President on August 14, 2008) specifies that the aggregate revenue amount for FY 2012 for abbreviated application fees is $1,712,000 and each of the other two generic new animal drug user fee categories, annual product fees and annual sponsor fees, is $1,997,000 each, before any adjustment for workload is made (see 21 U.S.C. 379j-21(b)).</P>
        <HD SOURCE="HD2">B. Inflation Adjustment to Fee Revenue Amount</HD>
        <P>The amounts established in AGDUFA for each year for FY 2009 through FY 2013 include an inflation adjustment; so, no inflation adjustment is required.</P>
        <HD SOURCE="HD2">C. Workload Adjustment to Inflation Adjusted Fee Revenue Amount</HD>
        <P>For each FY beginning after FY 2009, AGDUFA provides that statutory fee revenue amounts shall be further adjusted to reflect changes in review workload (21 U.S.C. 379j-21(c)(1)).</P>
        <P>FDA calculated the average number of each of the four types of applications and submissions specified in the workload adjustment provision (abbreviated applications for generic new animal drugs, manufacturing supplemental abbreviated applications for generic new animal drugs, investigational generic new animal drug study submissions, and investigational generic new animal drug protocol submissions) received over the 5-year period ended on September 30, 2008 (the base years), and the average number of each of these types of applications and submissions over the most recent 5-year period that ended on June 30, 2011.</P>
        <P>The results of these calculations are presented in the first two columns of table 1 of this document. Column 3 reflects the percent change in workload over the two 5-year periods. Column 4 shows the weighting factor for each type of application, reflecting how much of the total FDA generic new animal drug review workload was accounted for by each type of application or submission in the table during the most recent 5 years. Column 5 of table 1 is the weighted percent change in each category of workload and was derived by multiplying the weighting factor in each line in column 4 by the percent change from the base years in column 3. At the bottom right of table 1, the sum of the values in column 5 is calculated, reflecting a total change in workload of negative 25.7 percent for FY 2012. This is the workload adjuster for FY 2012.</P>
        <GPOTABLE CDEF="s60,10,10,10,10,10" COLS="6" OPTS="L2,i1">
          <TTITLE>Table 1—Workload Adjuster Calculation</TTITLE>
          <BOXHD>
            <CHED H="1">Application type</CHED>
            <CHED H="1">Column 1<LI>5-Year</LI>
              <LI>average</LI>
              <LI>(base years)</LI>
            </CHED>
            <CHED H="1">Column 2<LI>Latest</LI>
              <LI>5-year</LI>
              <LI>average</LI>
            </CHED>
            <CHED H="1">Column 3<LI>Percent change</LI>
            </CHED>
            <CHED H="1">Column 4<LI>Weighting factor</LI>
            </CHED>
            <CHED H="1">Column 5<LI>Weighted percent change</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Abbreviated New Animal Drug Applications (ANADAs)</ENT>
            <ENT>44.2</ENT>
            <ENT>25.4</ENT>
            <ENT>−43</ENT>
            <ENT>50%</ENT>
            <ENT>−21.3</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Manufacturing Supplements ANADAs</ENT>
            <ENT>114.6</ENT>
            <ENT>118.4</ENT>
            <ENT>3</ENT>
            <ENT>22%</ENT>
            <ENT>0.7</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Generic Investigational Study Submissions</ENT>
            <ENT>17.4</ENT>
            <ENT>17.0</ENT>
            <ENT>−2</ENT>
            <ENT>10%</ENT>
            <ENT>−0.2</ENT>
          </ROW>
          <ROW RUL="n,s">
            <ENT I="01">Generic Investigational Protocol Submissions</ENT>
            <ENT>21.6</ENT>
            <ENT>15.6</ENT>
            <ENT>−28</ENT>
            <ENT>17%</ENT>
            <ENT>−4.8</ENT>
          </ROW>
          <ROW>
            <ENT I="03">FY 2012 AGDUFA Workload Adjuster</ENT>
            <ENT/>
            <ENT/>
            <ENT/>
            <ENT/>
            <ENT>−25.7</ENT>
          </ROW>
        </GPOTABLE>

        <P>AGDUFA specifies that the workload adjuster may not result in fees for a fiscal year that are less than the statutory revenue amount (21 U.S.C. 379j-21(c)(1)(B)) for that fiscal year. Because applying the workload adjuster for FY 2012 would result in fees less than the statutory amount, the workload adjustment will not be applied in FY 2012. As a result, the statutory revenue amount for each category of fees for FY 2012 ($1,712,000 for application fees and $1,997,000 for both product and sponsor fees) becomes the revenue target for the fees in FY 2012, for a total<PRTPAGE P="45816"/>fee revenue target in FY 2012 of $5,706,000 for fees from all three categories.</P>
        <HD SOURCE="HD1">III. Abbreviated Application Fee Calculations for FY 2012</HD>
        <P>The term “abbreviated application for a generic new animal drug” is defined in 21 U.S.C. 379j-21(k)(1).</P>
        <HD SOURCE="HD2">A. Application Fee Revenues and Numbers of Fee-Paying Applications</HD>
        <P>The application fee must be paid for abbreviated applications for a generic new animal drug that is subject to fees under AGDUFA and that is submitted on or after July 1, 2008. The application fees are to be set so that they will generate $1,712,000 in fee revenue for FY 2012. This is the amount set out in the statute.</P>
        <P>To set fees for abbreviated applications for generic new animal drugs to realize $1,712,000, FDA must first make some assumptions about the number of fee-paying abbreviated applications it will receive during FY 2012.</P>
        <P>The Agency knows the number of applications that have been submitted in previous years. That number fluctuates significantly from year to year. FDA is making estimates and applying different assumptions for two types of submissions: Original submissions of abbreviated applications for generic new animal drugs and “reactivated” submissions of abbreviated applications for generic new animal drugs. Any original submissions of abbreviated applications for generic new animal drugs that were received by FDA before July 1, 2008, were not assessed fees (21 U.S.C. 379j-21(a)(1)(A)). Some of these non-fee-paying submissions were later resubmitted after July 1 because the initial submission was not approved by FDA (i.e., FDA marked the submission as incomplete and requested additional nonadministrative information) or because the original submission was withdrawn by the sponsor. Because these abbreviated applications for generic new animal drugs are resubmitted after July 1, 2008, they are assessed fees. In this notice, FDA refers to these resubmitted applications as “reactivated” applications.</P>
        <P>Regarding original submissions of abbreviated applications for generic new animal drugs, FDA is assuming that the number of applications that will pay fees in FY 2012 will equal 30 percent less than the average number of submissions over the 5 most recent completed years (2006-2010). This 30-percent reduction is made because of the anticipated impact of fees on the number of submissions. The average number of original submissions of abbreviated applications for generic new animal drugs over the 5 most recent completed years is 14.4. Applying a 30-percent reduction to the 14.4 average, the estimate for original submissions of abbreviated applications for generic new animal drugs for FY 2012 is 10.1. (If the number of original submissions of abbreviated applications for generic new animal drugs does not increase over the next year, a higher percent reduction will have to be applied next year when fees are set for FY 2013.)</P>
        <P>Regarding reactivated submissions of abbreviated applications for generic new animal drugs, FDA is applying a 75-percent reduction. This is based on the fact that there were a limited number of original submissions of abbreviated applications for generic new animal drugs received by FDA before July 1, 2008, which were not assessed fees. For these original submissions that were not approved before July 1, 2008, resubmission to FDA would trigger an application fee (21 U.S.C. 379j-21(a)(1)(A)). Once these initial original submissions of abbreviated applications for generic new animal drugs received by FDA before July 1, 2008, have either been withdrawn or resubmitted, “reactivation submissions” will cease completely. This reduction is consistent with estimates made when this user fee program was in the development process. The average number of receipts for reactivated submissions of abbreviated applications for generic new animal drugs is 14.5 per year, which is the average of the 5 most recent completed years. Applying a 75-percent reduction to the 14.5 average, the estimate for reactivated submissions of abbreviated applications for generic new animal drugs for FY 2012 is 3.6. These reductions may not fully account for possible year to year fluctuations in numbers of fee-paying applications, but FDA believes that this is a reasonable approach after years of experience with other user fee programs.</P>
        <P>Based on the previous assumptions, FDA is estimating that it will receive a total of 13.7 fee-paying generic new animal drug applications in FY 2012 (10.1 original applications and 3.6 reactivations).</P>
        <HD SOURCE="HD2">B. Fee Rates for FY 2012</HD>
        <P>FDA must set the fee rates for FY 2012 so that the estimated 13.7 abbreviated applications that pay the fee will generate a total of $1,712,000. To generate this amount, the fee for a generic new animal drug application, rounded to the nearest hundred dollars, will have to be $124,900.</P>
        <HD SOURCE="HD1">IV. Generic New Animal Drug Product Fee Calculations for FY 2012</HD>
        <HD SOURCE="HD2">A. Product Fee Revenues and Numbers of Fee-Paying Products</HD>
        <P>The generic new animal drug product fee (also referred to as the product fee) must be paid annually by the person named as the applicant in an abbreviated new animal drug application or supplemental abbreviated application for generic new animal drugs for an animal drug product submitted for listing under section 510 of the FD&amp;C Act (21 U.S.C. 360), and who had an abbreviated application for a generic new animal drug or supplemental abbreviated application for a generic new animal drug pending at FDA after September 1, 2008 (see 21 U.S.C. 379j-21(a)(2)). The term “generic new animal drug product” means each specific strength or potency of a particular active ingredient or ingredients in final dosage form marketed by a particular manufacturer or distributor, which is uniquely identified by the labeler code and product code portions of the national drug code, and for which an abbreviated application for a generic new animal drug or supplemental abbreviated application for a generic new animal drug has been approved (21 U.S.C. 379j-21(k)(6)). The product fees are to be set so that they will generate $1,997,000 in fee revenue for FY 2012. This is the amount set out in the statute and no further adjustments are required for FY 2012.</P>
        <P>To set generic new animal drug product fees to realize $1,997,000, FDA must make some assumptions about the number of products for which these fees will be paid in FY 2012. FDA gathered data on all generic new animal drug products that have been submitted for listing under section 510 of the FD&amp;C Act and matched this to the list of all persons who FDA estimated would have an abbreviated new animal drug application or supplemental abbreviated application pending after September 1, 2008. FDA estimates a total of 358 products submitted for listing by persons who had an abbreviated application for a generic new animal drug or supplemental abbreviated application for a generic new animal drug pending after September 1, 2008. Based on this, FDA believes that a total of 358 products will be subject to this fee in FY 2012.</P>

        <P>In estimating the fee revenue to be generated by generic new animal drug product fees in FY 2012, FDA is assuming that approximately 10 percent of the products invoiced, or 36, will not pay fees in FY 2012 due to fee waivers<PRTPAGE P="45817"/>and reductions. Based on experience with other user fee programs and the first 3 years of AGDUFA, FDA believes that this is a reasonable basis for estimating the number of fee-paying products in FY 2012.</P>
        <P>Accordingly, the Agency estimates that a total of 322 (358 minus 36) products will be subject to product fees in FY 2012.</P>
        <HD SOURCE="HD2">B. Product Fee Rates for FY 2012</HD>
        <P>FDA must set the fee rates for FY 2012 so that the estimated 322 products that pay fees will generate a total of $1,997,000. To generate this amount will require the fee for a generic new animal drug product, rounded to the nearest 5 dollars, to be $6,200.</P>
        <HD SOURCE="HD1">V. Generic New Animal Drug Sponsor Fee Calculations for FY 2012</HD>
        <HD SOURCE="HD2">A. Sponsor Fee Revenues and Numbers of Fee-Paying Sponsors</HD>
        <P>The generic new animal drug sponsor fee (also referred to as the sponsor fee) must be paid annually by each person who: (1) Is named as the applicant in an abbreviated application for a new generic animal drug, except for an approved application for which all subject products have been removed from listing under section 510 of the FD&amp;C Act, or has submitted an investigational submission for a generic new animal drug that has not been terminated or otherwise rendered inactive; and (2) had an abbreviated application for a generic new animal drug, supplemental abbreviated application for a generic new animal drug, or investigational submission for a generic new animal drug pending at FDA after September 1, 2008 (see 21 U.S.C. 379j-21(k)(7) and 379j-21(a)(3)). A generic new animal drug sponsor is subject to only one such fee each fiscal year (see 21 U.S.C. 379j-21(a)(3)(B)). Applicants with more than 6 approved abbreviated applications will pay 100 percent of the sponsor fee, applicants with 2 to 6 approved abbreviated applications will pay 75 percent of the sponsor fee, and applicants with 1 or fewer approved abbreviated applications will pay 50 percent of the sponsor fee (see 21 U.S.C. 379j-21(a)(3)(B)). The sponsor fees are to be set so that they will generate $1,997,000 in fee revenue for FY 2012. This is the amount set out in the statute and no adjustments are required for FY 2012.</P>
        <P>To set generic new animal drug sponsor fees to realize $1,997,000, FDA must make some assumptions about the number of sponsors who will pay these fees in FY 2012. Based on the number of firms that meet this definition, FDA estimates that in FY 2012, 12 sponsors will pay 100 percent fees, 13 sponsors will pay 75 percent fees, and 38 sponsors will pay 50 percent fees. That totals the equivalent of 40.75 full sponsor fees (12 times 100 percent or 12, plus 13 times 75 percent or 9.75, plus 38 times 50 percent or 19).</P>
        <P>FDA estimates that about 10 percent of all of these sponsors, or 4, may qualify for a minor use/minor species waiver.</P>
        <P>Accordingly, the Agency estimates that the equivalent of 36.75 full sponsor fees (40.75 minus 4) are likely to be paid in FY 2012.</P>
        <HD SOURCE="HD2">B. Sponsor Fee Rates for FY 2012</HD>
        <P>FDA must set the fee rates for FY 2012 so that the estimated equivalent of 36.75 full sponsor fees will generate a total of $1,997,000. To generate this amount will require the 100-percent fee for a generic new animal drug sponsor, rounded to the nearest $50, to be $54,350. Accordingly, the fee for those paying 75 percent of the full sponsor fee will be $40,763, and the fee for those paying 50 percent of the full sponsor fee will be $27,175.</P>
        <HD SOURCE="HD1">VI. Fee Schedule for FY 2012</HD>
        <P>The fee rates for FY 2012 are summarized in table 2 of this document.</P>
        <GPOTABLE CDEF="s100,12" COLS="2" OPTS="L2,i1">
          <TTITLE>Table 2—FY 2012 Fee Rates</TTITLE>
          <BOXHD>
            <CHED H="1">Generic new animal drug user fee category</CHED>
            <CHED H="1">Fee rate for FY 2012</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Abbreviated Application Fee for Generic New Animal Drug Application</ENT>
            <ENT>$124,900</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Generic New Animal Drug Product Fee</ENT>
            <ENT>6,200</ENT>
          </ROW>
          <ROW>
            <ENT I="01">100 Percent Generic New Animal Drug Sponsor Fee<SU>1</SU>
            </ENT>
            <ENT>54,350</ENT>
          </ROW>
          <ROW>
            <ENT I="01">75 Percent Generic New Animal Drug Sponsor Fee<SU>1</SU>
            </ENT>
            <ENT>40,763</ENT>
          </ROW>
          <ROW>
            <ENT I="01">50 Percent Generic New Animal Drug Sponsor Fee<SU>1</SU>
            </ENT>
            <ENT>27,175</ENT>
          </ROW>
          <TNOTE>
            <SU>1</SU>An animal drug sponsor is subject to only one such fee each fiscal year.</TNOTE>
        </GPOTABLE>
        <HD SOURCE="HD1">VII. Procedures for Paying FY 2012 Generic New Animal Drug User Fees</HD>
        <HD SOURCE="HD2">A. Abbreviated Application Fees and Payment Instructions</HD>

        <P>The FY 2012 fee established in the new fee schedule must be paid for an abbreviated new animal drug application subject to fees under AGDUFA that is submitted on or after October 1, 2011. Payment must be made in U.S. currency by check, bank draft, or U.S. postal money order payable to the order of the Food and Drug Administration, by wire transfer, or by automatic clearing house using<E T="03">Pay.gov.</E>(The<E T="03">Pay.gov</E>payment option is available to you after you submit a cover sheet. Click the “Pay Now” button). On your check, bank draft, or U.S. postal money order, please write your application's unique Payment Identification Number (PIN), beginning with the letters “AG”, from the upper right-hand corner of your completed Animal Generic Drug User Fee Cover Sheet. Also write the FDA post office box number (PO Box 953877) on the enclosed check, bank draft, or money order. Your payment and a copy of the completed Animal Generic Drug User Fee Cover Sheet can be mailed to: Food and Drug Administration, P.O. Box 953877, St. Louis, MO 63195-3877.</P>

        <P>If payment is made via wire transfer, send payment to U. S. Department of the Treasury, TREAS NYC, 33 Liberty St., New York, NY 10045,<E T="03">Account Name: Food and Drug Administration, account number:</E>75060099,<E T="03">routing number:</E>021030004,<E T="03">SWIFT number:</E>FRNYUS33. You are responsible for any administrative costs associated with the processing of a wire transfer. Contact your bank or financial institution regarding the amount of the fees that need to be paid in addition to the wire transfer amount.</P>

        <P>If you prefer to send a check by a courier such as Federal Express (FEDEX) or United Parcel Service (UPS), the courier may deliver the check and printed copy of the cover sheet to: U.S. Bank,<E T="03">Attn:</E>Government Lockbox 953877, 1005 Convention Plaza, St. Louis, MO 63101.</P>
        <NOTE>
          <HD SOURCE="HED">(Note:</HD>
          <P>This address is for courier delivery only. If you have any questions concerning courier delivery, contact the U.S. Bank at 314-418-4821. This telephone number is only for questions about courier delivery.)</P>
        </NOTE>
        <P>The tax identification number of the Food and Drug Administration is 530196965.</P>
        <NOTE>
          <HD SOURCE="HED">(Note:</HD>
          <P>In no case should the payment for the fee be submitted to FDA with the application.)</P>
        </NOTE>

        <P>It is helpful if the fee arrives at the bank at least a day or two before the abbreviated application arrives at FDA's Center for Veterinary Medicine. FDA records the official abbreviated application receipt date as the later of the following: The date the application was received by FDA's CVM, or the date U.S. Bank notifies FDA that your payment in the full amount has been received, or when the U.S. Treasury notifies FDA of payment. U.S. Bank and the U.S. Treasury are required to notify FDA within 1 working day, using the PIN described previously.<PRTPAGE P="45818"/>
        </P>
        <HD SOURCE="HD2">B. Application Cover Sheet Procedures</HD>

        <P>Step One—Create a user account and password. Log onto the AGDUFA Web site at<E T="03">http://www.fda.gov/ForIndustry/UserFees/AnimalGenericDrugUserFeeActAGDUFA/ucm137049.htm</E>and scroll down the page until you find the link “Create AGDUFA User Fee Cover Sheet.” Click on that link and follow the directions. For security reasons, each firm submitting an application will be assigned an organization identification number, and each user will also be required to set up a user account and password the first time you use this site. Online instructions will walk you through this process.</P>
        <P>Step Two—Create an Animal Generic Drug User Fee Cover Sheet, transmit it to FDA, and print a copy. After logging into your account with your user name and password, complete the steps required to create an Animal Generic Drug User Fee Cover Sheet. One cover sheet is needed for each abbreviated animal drug application. Once you are satisfied that the data on the cover sheet is accurate and you have finalized the cover sheet, you will be able to transmit it electronically to FDA and you will be able to print a copy of your cover sheet showing your unique PIN.</P>
        <P>Step Three—Send the payment for your application as described in section VII.A of this document.</P>
        <P>Step Four—Please submit your application and a copy of the completed Animal Generic Drug User Fee Cover Sheet to the following address: Food and Drug Administration, Center for Veterinary Medicine, Document Control Unit (HFV-199), 7500 Standish Pl., Rockville, MD 20855.</P>
        <HD SOURCE="HD2">C. Product and Sponsor Fees</HD>
        <P>By December 31, 2011, FDA will issue invoices and payment instructions for product and sponsor fees for FY 2012 using this fee schedule. Fees will be due and payable 30 days after the issuance of the invoices. FDA will issue invoices in November 2012 for any products and sponsors subject to fees for FY 2012 that qualify for fees after the December 2011 billing.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Leslie Kux,</NAME>
          <TITLE>Acting Assistant Commissioner for Policy.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19334 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4160-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>Food and Drug Administration</SUBAGY>
        <DEPDOC>[Docket No. FDA-2011-N-0529]</DEPDOC>
        <SUBJECT>Burden of Food and Drug Administration Food Safety Modernization Act Fee Amounts on Small Business; Request for Comments</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Food and Drug Administration, HHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice; Request for comments and information.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Food and Drug Administration (FDA) is announcing the establishment of a docket to obtain information that will be used to formulate a proposed set of guidelines in consideration of the burden of fee amounts on small business, as set forth in the FDA Food Safety Modernization Act (FSMA). FSMA provides the Agency with authority under the Federal Food, Drug, and Cosmetic Act (the FD&amp;C Act) to assess and collect user fees, including those for costs associated with certain domestic and foreign facility reinspections, failure to comply with a recall order, and importer reinspections. The Agency is seeking public comment on what burdens these fees impose on small business, and whether and how the Agency should alleviate such burdens. In particular, the Agency is seeking public comments on whether a reduction of fees or other consideration for small business is appropriate, and if so, what factors the Agency should consider for each. In addition, the Agency is seeking public comment on how small business should be defined or recognized. FDA is establishing this docket in order to provide an opportunity for interested parties to provide data and share views that will inform future Agency actions with respect to these matters.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Submit either electronic or written comments by October 17, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>Submit electronic comments to<E T="03">http://www.regulations.gov.</E>Submit written comments to the Division of Dockets Management (HFA-305). Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Alexis Nazario-Negron, Office of Financial Management, Food and Drug Administration, 1350 Piccard Dr., rm. 210E,Rockville, MD 20850, 301-796-7223,<E T="03">Alexis.Nazario-Negron@fda.hhs.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P/>
        <HD SOURCE="HD1">I. Background</HD>
        <P>Each year about 48 million people (1 in 6 Americans) are sickened, 128,000 are hospitalized, and 3,000 die from food borne diseases, according to recent data from the Centers for Disease Control and Prevention (Refs. 1 and 2). This is a significant public health burden that is largely preventable.</P>
        <P>FSMA (Pub. L. 111-353), signed into law by President Obama on January 4, 2011, enables FDA to better protect public health by helping to ensure the safety and security of the food supply. It enables FDA to focus more on preventing food safety problems rather than reacting to problems after they occur. The law also provides FDA with new enforcement authorities to help it achieve higher rates of compliance with prevention- and risk-based food safety standards and to better respond to problems when they do occur. The law also gives FDA important new tools to better ensure the safety of imported foods and directs FDA to build an integrated national food safety system in partnership with State and local authorities.</P>
        <P>Among the new authorities Congress provided in FSMA, the Secretary of Health and Human Services (and by delegation, FDA) is to assess and collect fees from industry for FDA's costs associated with certain activities. Section 107(a) of FSMA (which amends the FD&amp;C Act by adding section 743 (21 U.S.C. 379j-31)) mandates that FDA assess and collect fees for costs associated with certain domestic and foreign facility reinspections, failure to comply with a recall order under sections 423 and 412(f) of the FD&amp;C Act (21 U.S.C. 350l and 350a(f)), and certain importer reinspections (section 743(a)(1) of the FD&amp;C Act).<SU>1</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>1</SU>FDA is not soliciting comments, in this<E T="04">Federal Register</E>notice, on the burdens to small businesses that participate in the voluntary qualified importer program (VQIP) under section 743(a)(1)(C) of the FD&amp;C Act. FDA intends to consider such burdens at the time the VQIP is established.</P>
        </FTNT>

        <P>Section 743(b)(2)(A) of the FD&amp;C Act specifies that the Agency must base these fees on an estimation of 100 percent of the costs of the various activities which are described in section 743(a)(1), for the fiscal year. These fees must be published in the<E T="04">Federal Register</E>not later than 60 days before the start of each fiscal year. Elsewhere in this issue of the<E T="04">Federal Register</E>, FDA is publishing notice of these fees.</P>

        <P>Congress directed FDA to publish, within 180 days of enactment of FSMA, a proposed set of guidelines in consideration of the burden of fee<PRTPAGE P="45819"/>amounts on small business (section 743(b)(2)(B)(iii) of the FD&amp;C Act). Such consideration may include reduced fee amounts for small businesses. However, FDA would like to gather additional information before publishing such guidelines. Therefore, the Agency is publishing this notice to request public input to help the Agency understand what factors should be taken into account when drafting the proposed guidelines. The Agency intends to consider the comments received and then publish for comment a proposed set of guidelines on the considerations of the burden of fee amounts on small business.</P>
        <P>Any adjustment to the fee schedule for small business must be done through notice and comment rulemaking (section 743(b)(2)(B)(iii) of the FD&amp;C Act). Thus, the Agency would consider the proposed set of guidelines, and comments on such guidelines, in any future rulemaking should it decide to propose to adjust the fee schedule for small business.</P>
        <HD SOURCE="HD1">II. Request for Comments and Information</HD>
        <P>In order to better inform the Agency, the Agency seeks comment on the following questions, although any additional comments that can inform the guidelines are welcome.</P>
        <HD SOURCE="HD2">A. Is a fee reduction or other consideration for small business appropriate? Please explain</HD>
        <P>Section 743(b)(2)(B)(iii) of the FD&amp;C Act states that the proposed set of guidelines may include consideration of reduced fee amounts for small business, but consideration of reduced fee amounts is not required.</P>
        <P>1. What is the impact, if any, of fee amounts on small business, in general, or to specific types of small businesses, that FDA should consider in the proposed set of guidelines? Please explain.</P>
        <P>2. Should the Agency consider the type of fee collected when considering the burdens to small business? For example, do the types of activities for which a fee is collected for reinspection have a different impact to a small business than those collected based on a failure to comply with a recall order? Please explain.</P>
        <P>3. Assuming there is an impact of fee amounts to small business, or certain types of small businesses, should the Agency consider a reduction in the fees for such small businesses in the proposed set of guidelines? If so, should the Agency consider the reduction in fees to all small businesses, or for only those small businesses that have a demonstrated need for reduced fees? Please explain. If the Agency should not consider a reduction in the fees for small business, why not? Please explain.</P>
        <P>4. Are there ways to alleviate any burden on small business other than a fee reduction? Please explain.</P>
        <HD SOURCE="HD2">B. How should small business be defined or recognized for the purpose of the proposed guidelines?</HD>
        <P>Several provisions in FSMA require FDA to define small and very small business. For example, section 103(a) of FSMA amends the FD&amp;C Act by adding section 418 (21 U.S.C. 350g) regarding “Hazard Analysis and Risk-Based Preventive Controls.” Section 418(n)(1)(B) of the FD&amp;C Act requires FDA to define “small business” and “very small business” for the purpose of the preventive control regulations for facilities. Similarly, FSMA section 105(a) amends the FD&amp;C Act by adding section 419 (21 U.S.C. 350h) regarding standards for produce safety. Section 419(a)(3)(F) of the FD&amp;C Act requires FDA to define “small business” and “very small business” for the purpose of the produce safety regulations.</P>
        <P>In addition, the Agency has issued a number of final rules where the Agency considered business size when considering the regulatory impact of the rule to industry, including the following final rules:</P>
        <P>• “Procedures for the Safe and Sanitary Processing and Importing of Fish and Fishery Products” (60 FR 65096, December 18, 1995) (Docket No. FDA-1993-N-0065 (formerly Docket No. 1993N-0195));</P>
        <P>• “Hazard Analysis and Critical Control Point (HAACP); Procedures for the Safe and Sanitary Processing and Importing of Juice” (66 FR 6138, January 19, 2001) (Docket No. FDA-1997-N-0505 (formerly Docket No. 1997N-0511));</P>
        <P>• “Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements” (72 FR 34752, June 25, 2007) (Docket No. FDA-1996-N-0028 (formerly Docket No. 1996N-0417 or 97N-0417));</P>
        <P>• “Food Labeling, Safe Handling Statements, Labeling of Shell Eggs; Refrigeration of Shell Eggs Held for Retail Distribution” (65 FR 76092, December 5, 2000) (Docket No. FDA-1998-N-0087 (formerly Docket No. 1998N-1230); Docket No. FDA-1996-P-0025 (formerly Docket No. 96P-0418); and Docket No. FDA-1997-P-0017 (formerly Docket No. 1997P-0197));</P>
        <P>• “Prevention of Salmonella Enteritidis in Shell Eggs During Production, Storage, and Transportation” (74 FR 33030, July 9, 2009) (Docket No. FDA-2000-N-0190 (formerly Docket No. 2000N-0504)).</P>
        <P>FDA seeks comment on how a small business should be defined or recognized for purposes of the proposed set of guidelines in consideration of the burden of fee amounts on small business. More specifically, the Agency requests comment on the following questions.</P>
        <P>1. If FDA has defined, by regulation under other FSMA or non-FSMA authorities, an entity as a small or a very small business, should such a definition be considered in the proposed set of guidelines to identify the businesses that may be burdened by the fee amounts under section 743 of the FD&amp;C Act or should the Agency consider a separate definition of small business for purposes of considering the burden of fee amounts? Please explain.</P>
        <P>2. If the Agency relies on an existing regulatory definition of small or very small business that the Agency established under other FSMA or non-FSMA authorities, should any such definition apply in any circumstance where a fee is imposed or only where the fee derives from the rule where such business is defined as a small business? For example, if a facility is reinspected for a violation of the preventive controls regulations, should the Agency consider adjustments to the fee only if the facility meets the definition of small business under the preventive controls regulations, or should the Agency consider such adjustments if the facility meets any definition of small business under any FDA regulation? Please explain.</P>

        <P>3. There may be circumstances where no regulatory definition of small business exists for a given facility. Under these circumstances, what factors or characteristics should FDA use to identify small businesses for which FDA may consider the burden of fee amounts? Please explain. Factors to consider could include, but are not limited to, the segment of the food supply chain to which the entity belongs (<E T="03">e.g.,</E>growers, processors, importers and distributors, retailers,<E T="03">etc.</E>); the sector to which the entity belongs (<E T="03">e.g.,</E>seafood, produce, dairy, eggs, juice, dietary supplements,<E T="03">etc.</E>); the number of employees; the gross revenue, net income, net assets, market liquidity, or other financial measures or ratios; and whether the entity has a subsidiary or is a subsidiary of a parent company.<PRTPAGE P="45820"/>
        </P>
        <HD SOURCE="HD2">C. If FDA considers reduced fee amounts in the proposed set of guidelines, what factors should FDA consider in establishing the amount by which fees could be reduced?</HD>
        <P>1. Should FDA consider the following:</P>
        <P>• A waiver of all of the fees;</P>
        <P>• A percentage reduction of the fees; or</P>
        <P>• A fixed dollar reduction of the fees?</P>
        <P>2. Are there circumstances that justify one approach over another? Please explain.</P>
        <P>3. Are there other approaches that should be considered? Please explain.</P>
        <HD SOURCE="HD1">III. Comments</HD>

        <P>Interested persons may submit to the Division of Dockets Management (see<E T="02">ADDRESSES</E>) either electronic or written comments regarding this document. It is only necessary to send one set of comments. It is no longer necessary to send two copies of mailed comments. Identify comments with the docket number found in brackets in the heading of this document. Received comments may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.</P>
        <HD SOURCE="HD1">IV. References</HD>

        <P>The following references have been placed on display in the Division of Dockets Management (see<E T="02">ADDRESSES</E>) and may be seen by interested persons between 9 a.m. and 4 p.m., Monday through Friday. (FDA has verified the Web site addresses, but FDA is not responsible for any subsequent changes to the Web sites after this document publishes in the<E T="04">Federal Register</E>.)</P>
        

        <FP SOURCE="FP-2">1. Scallan E., R.M. Hoekstra, F.J. Angulo, R.V. Tauxe, M-A. Widdowson, S.L. Roy,<E T="03">et al.,</E>“Foodborne Illness Acquired in the United States—Major Pathogens,”<E T="03">Emerging Infectious Diseases,</E>17(1):7-15, 2011. Available at<E T="03">http://www.cdc.gov/EID/content/17/1/7.htm.</E>
        </FP>

        <FP SOURCE="FP-2">2. Scallan E., P.M. Griffin, F.J. Angulo, R.V. Tauxe, R.M. Hoekstra, “Foodborne Illness Acquired in the United States—Unspecified Agents,”<E T="03">Emerging Infectious Diseases,</E>17(1):16-22, 2011. Available at<E T="03">http://www.cdc.gov/EID/content/17/1/16.htm.</E>
        </FP>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Leslie Kux,</NAME>
          <TITLE>Acting Assistant Commissioner for Policy.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19333 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4160-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>Food and Drug Administration</SUBAGY>
        <DEPDOC>[Docket No. FDA-2011-N-0528]</DEPDOC>
        <SUBJECT>Food Safety Modernization Act Domestic and Foreign Facility Reinspections, Recall, and Importer Reinspection User Fee Rates for Fiscal Year 2012</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Food and Drug Administration, HHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Food and Drug Administration (FDA) is announcing the fiscal year (FY) 2012 fee rates for certain domestic and foreign facility reinspections, failure to comply with a recall order, and importer reinspections that are mandated in the Federal Food, Drug, and Cosmetic Act (the FD&amp;C Act), amended by the FDA Food Safety Modernization Act (FSMA). These fees are effective on October 1, 2011, and will remain in effect through September 30, 2012. Invoices for these fees for FY 2012 will be issued using the fee schedule established in this document. FDA is accepting comments to this document and intends to consider such comments in implementing these user fees in FY 2013.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Submit either electronic or written comments by October 31, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>Submit electronic comments to<E T="03">http://www.regulations.gov.</E>Submit written comments to the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Amy Waltrip, 12420 Parklawn Dr., Rm. 2012, Rockville, MD 20857, 301-796-8811, email:<E T="03">Amy.Waltrip@fda.hhs.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <HD SOURCE="HD1">I. Background</HD>
        <P>FSMA (Pub. L. 111-353), section 743 of the FD&amp;C Act (21 U.S.C. 379j-31), establishes three different kinds of fees. The fees are assessed for the costs of the following activities: (1) Certain domestic and foreign facility reinspections (section 743(a)(1)(A)), (2) failure to comply with a recall order under section 423 or 412(f) of the FD&amp;C Act (section 743(a)(1)(B)), and (3) certain importer reinspections (section 743(a)(1)(D)).</P>
        <P>Fees for each of these activities are to be established to capture 100 percent of the costs of each activity for each year (sections 743(b)(2)(A), (B), and (D) of the FD&amp;C Act), and must be made available solely to pay for the costs of each activity for which the fee was incurred (section 743(b)(3) of the FD&amp;C Act.</P>
        <P>These fees are effective on October 1, 2011, and will remain in effect through September 30, 2012. FDA is accepting comments to this document and intends to consider such comments, as well as experience and additional data gained in implementing these user fees in FY 2012, in implementing these user fees in FY 2013.</P>
        <HD SOURCE="HD1">II. Estimating the Average Cost of a Supported Direct FDA Work Hour for FY 2012</HD>
        <P>FDA is required to estimate 100 percent of its cost for each activity and assess fees for FY 2012. In each year, the costs of salary (or personnel compensation) and benefits for FDA employees account for between 50 and 60 percent of the funds available to, and used by, FDA. Almost all of the remaining funds (or the operating funds) available to FDA are used to support FDA employees for paying rent, travel, utility, information technology, and other operating costs.</P>
        <HD SOURCE="HD2">A. Estimating the Full Cost Per Direct Work Hour in FY 2010</HD>

        <P>In general, the starting point for estimating the full cost per direct work hour is to estimate the cost of a full-time-equivalent (FTE) or paid staff year for the relevant activity. This is most reasonably done by dividing the total funds allocated to the elements of FDA primarily responsible for carrying out the activities for which fees are being collected by the total FTEs allocated to those activities, using information from the most recent FY for which data are available. For the purposes of the FSMA fee provisions, primary responsibility for the activities for which fees will be collected rests with FDA's Office of Regulatory Affairs (ORA), which carries out inspection and other field-based activities on behalf of FDA's product centers, including the Center for Food Safety and Applied Nutrition (CFSAN) and the Center for Veterinary Medicine (CVM), which have FSMA implementation responsibilities. Thus, as the starting point for estimating the full cost per direct work hour, FDA will use the total funds allocated to ORA for CFSAN and CVM related field activities. The most recent FY with available data is FY 2010. In that year, FDA obligated a total of $626,095,116 for the Office of Regulatory Affairs (ORA) in carrying out work related to programs of the CFSAN and CVM, excluding the costs of foreign inspection travel. These are the staff primarily conducting the work related to the reinspection and recall activities<PRTPAGE P="45821"/>for which fees would be charged. The obligated total amount paid for salary, benefits, and operating costs of 2,701 FTEs or paid staff years utilized by ORA in FY 2010, but exclude the cost of foreign inspection travel. Dividing $626,095,116 by 2,701 FTEs, results in an average cost of $231,801 per paid staff year, excluding the costs of foreign inspection travel.</P>
        <P>Not all of the FTEs required to support the activities for which fees will be collected are conducting direct work such as inspecting or reinspecting facilities, examining imports, or monitoring recalls. Data collected over a number of years and used consistently in other FDA user fee programs (e.g., under the Prescription Drug User Fee Act (PDUFA) and the Medical Device User Fee and Modernization Act (MDUFMA)) show that every seven FTEs who perform direct FDA work require three indirect and supporting FTEs. These indirect and supporting FTEs function in budget, facility, human resource, information technology, planning, security, administrative support, legislative liaison, legal counsel, program management, and other essential program areas. On average, two of these indirect and supporting FTEs are located in ORA or the FDA center where the direct work is being conducted, and one of them is located in the Office of the Commissioner. To get the fully supported cost of an FTE, FDA needs to multiply the average cost of an FTE by 1.43, to take into account the indirect and supporting functions. The 1.43 factor is derived by dividing the 10 fully supported FTEs by 7 direct FTEs. In FY 2010, the average cost of an FTE was $231,801. Multiplying this amount by 1.43 results in an average fully supported cost of $331,476 per FTE, excluding the cost of foreign inspection travel.</P>
        <P>To calculate an hourly rate, FDA must divide the average fully supported cost of $331,476 per FTE by the average number of supported direct FDA work hours. See table 1.</P>
        <GPOTABLE CDEF="s50,12" COLS="2" OPTS="L2,p1,8/9,i1">
          <TTITLE>Table 1—Supported Direct FDA Work Hours in a Paid Staff Year</TTITLE>
          <BOXHD>
            <CHED H="1"/>
            <CHED H="1"/>
          </BOXHD>
          <ROW>
            <ENT I="01">Total number of hours in a paid staff year</ENT>
            <ENT>2,080</ENT>
          </ROW>
          <ROW>
            <ENT I="22">Less:</ENT>
          </ROW>
          <ROW>
            <ENT I="02">10 paid holidays</ENT>
            <ENT>80</ENT>
          </ROW>
          <ROW>
            <ENT I="02">20 days of annual leave</ENT>
            <ENT>160</ENT>
          </ROW>
          <ROW>
            <ENT I="02">10 days of sick leave</ENT>
            <ENT>80</ENT>
          </ROW>
          <ROW>
            <ENT I="02">10 days of training</ENT>
            <ENT>80</ENT>
          </ROW>
          <ROW>
            <ENT I="02">2 hours of meetings per week</ENT>
            <ENT>80</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Net Supported Direct FDA Work Hours Available for Assignments</ENT>
            <ENT>1,600</ENT>
          </ROW>
        </GPOTABLE>
        <P>Dividing the average fully supported cost of an FTE in FY 2010 ($331,476) by the total number of supported direct work hours available for assignment (1,600) results in an average fully supported cost of $207 (rounded to the nearest dollar), excluding foreign inspection travel costs, per supported direct work hour in FY 2010—the last FY for which data are available.</P>
        <HD SOURCE="HD2">B. Adjusting FY 2010 Costs for Inflation to Estimate FY 2012 Costs</HD>
        <P>To adjust the hourly rate for FY 2012, FDA must estimate cost of inflation in each year for FY 2011 and FY 2012. FDA uses the method prescribed for estimating inflationary costs under the PDUFA provisions of the FD&amp;C Act (section 736(c)(1) (21 U.S.C. 379h(c)(1))), the only provision the FD&amp;C Act that provides a method for estimating future inflationary costs. The inflationary adjustment specified in these provisions, since FY 2008, is the greater of the following amounts: (1) The total percentage change that occurred in the Consumer Price Index (CPI) (all items; U.S. city average) during the 12-month period ending June 30 preceding the FY for which fees are being set; (2) the total percentage pay change for the previous FY for Federal employees stationed in the Washington, DC metropolitan area; or (3) the average annual change in cost, per FDA FTE, of all personnel compensation and benefits paid per FTE over the previous five of the most recent six FYs. PDUFA IV provides for this adjustment to be cumulative and compounded annually after FY 2008 (see section 736(c)(1)).</P>

        <P>For FY 2012, the first factor is the CPI increase for the 12-month period ending in June 2011. The CPI for June 2011 was 225.722 and the CPI for June 2010 was 217.965. (These CPI figures are available on the Bureau of Labor Statistics Web site at<E T="03">http://data.bls.gov/cgi-bin/surveymost?bls</E>by checking the first box under “Price Indexes” and then clicking “Retrieve Data” at the bottom of the page. FDA has verified the Web site addresses throughout this document, but is not responsible for any subsequent changes to the Web sites after this document publishes in the<E T="04">Federal Register</E>.) The CPI for June 2011 is 3.559 percent higher than the CPI for the previous 12-month period.</P>

        <P>The second factor for the FY 2012 inflationary increase is the increase in pay for the previous FY (FY 2011 in this case) for Federal employees stationed in the Washington, DC metropolitan area. (This figure is published by the Office of Personnel Management, and can be found on the Web site at<E T="03">http://www.opm.gov/oca/11tables/html/dcb.asp</E>above the salary table. For FY 2011, the inflationary increase was 0.00 percent.</P>
        <P>For FY 2012, the third factor is the average change in FDA's cost for compensation and benefits per FTE over the previous five of the most recent six FYs (FY 2006 through FY 2010). The data on total compensation and benefits paid and numbers of FTEs paid, from which the average cost per FTE can be derived, are published in FDA's Justification of Estimates for Appropriations Committees. Table 2 of this document summarizes the actual costs and FTE data for the specified FYs, and provides the percent changes from the previous FYs and the average percent change over the previous five of the most recent six FYs, which is 3.72 percent.</P>
        <GPOTABLE CDEF="s25,13,13,13,13,13,13,10" COLS="8" OPTS="L2,p7,7/8,i1">
          <TTITLE>Table 2—FDA Personnel Compensation and Benefits (PC&amp;B) Each Year and Percent Change</TTITLE>
          <BOXHD>
            <CHED H="1"/>
            <CHED H="1">FY 2005</CHED>
            <CHED H="1">FY 2006</CHED>
            <CHED H="1">FY 2007</CHED>
            <CHED H="1">FY 2008</CHED>
            <CHED H="1">FY 2009</CHED>
            <CHED H="1">FY 2010</CHED>
            <CHED H="1">Average<LI>for latest</LI>
              <LI>5 years</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Total PC&amp;B</ENT>
            <ENT>$1,077,604,000</ENT>
            <ENT>$1,114,704,000</ENT>
            <ENT>$1,144,369,000</ENT>
            <ENT>$1,215,627,000</ENT>
            <ENT>$1,464,445,000</ENT>
            <ENT>$1,634,108,000</ENT>
            <ENT/>
          </ROW>
          <ROW>
            <ENT I="01">Total FTE</ENT>
            <ENT>9,910</ENT>
            <ENT>9,698</ENT>
            <ENT>9,569</ENT>
            <ENT>9,811</ENT>
            <ENT>11,413</ENT>
            <ENT>12,526</ENT>
            <ENT/>
          </ROW>
          <ROW>
            <ENT I="01">PC&amp;B per FTE</ENT>
            <ENT>$108,739</ENT>
            <ENT>$114,942</ENT>
            <ENT>$119,591</ENT>
            <ENT>$123,905</ENT>
            <ENT>$128,314</ENT>
            <ENT>$130,457</ENT>
            <ENT/>
          </ROW>
          <ROW>
            <ENT I="01">% Change from Previous Year</ENT>
            <ENT>5.75%</ENT>
            <ENT>5.70%</ENT>
            <ENT>4.05%</ENT>
            <ENT>3.61%</ENT>
            <ENT>3.56%</ENT>
            <ENT>1.67%</ENT>
            <ENT>3.72%</ENT>
          </ROW>
        </GPOTABLE>

        <P>Taking all three factors into consideration, the inflationary increase for FY 2012 is 3.72 percent. The average percent change over the previous five of the most recent six FYs is 3.72 percent which is greater than the CPI change<PRTPAGE P="45822"/>during the 12-month period ending June 30 preceding the FY for which fees are being set (3.559 percent), and the increase in pay for the previous FY (FY 2011 in this case) for Federal employees stationed in the Washington, DC metropolitan area (0.00 percent). Therefore, the average percent change in PC&amp;B cost per FTE (3.72 percent) becomes the inflation adjustment for the fee revenue for FY 2012.</P>
        <P>The inflationary adjustment for FY 2011 under the same provisions in section 736(c)(1) of the FD&amp;C Act was 4.53 percent—the average percent change over the previous five of the most recent six FYs (FY 2005 through FY 2009). This 4.53 percent is greater than the CPI increase during the 12-month period ending June 30 preceding the FY for which fees were being set on June 30, 2010 (1.053 percent), and the increase in pay for FY 2010 for Federal employees stationed in Washington, DC (2.42 percent).</P>
        <P>Section 736(c)(1) of the FD&amp;C Act requires the inflationary adjustment to be cumulative and compounded. This factor for FY 2012 (3.72 percent) is compounded by adding 1 and then multiplying by 1 plus the inflationary adjustment factor for FY 2011 (4.53 percent), to account for the 2 years of inflationary adjustments since FY 2010. The result of this multiplication (1.0372 times 1.0453) becomes the inflationary adjustment for FY 2012, which is 1.0842, or an increase of 8.42 percent over FY 2010 costs.</P>
        <P>Increasing FY 2010 average fully supported cost per supported direct FDA work hour of $207 (excluding foreign inspection travel costs) by 8.42 percent yields an inflationary adjusted cost of $224 per a supported direct work hour in FY 2012, excluding foreign inspection travel costs. This is the unit cost that FDA will use in billing the reinspection and the recall activities for FY 2012 if no foreign travel is required for the activity.</P>
        <P>In FY 2010, ORA spent a total of $1,010,900 on a total of 91 foreign inspection trips related to FDA's food and veterinary medicine programs, which averaged a total of $11,109 per foreign inspection trip. These trips averaged 3 weeks (or 120 paid hours) per trip. Dividing $11,109 per trip by 120 hours per trip results in a total and an additional cost of $93 per paid hour spent for foreign inspection travel costs in FY 2010. To adjust $93 for inflationary increases in FY 2011 and FY 2012, FDA must multiply it by the same inflation factor mentioned previously in this document (1.0842) which results in an estimated cost of $101 dollars per paid hour in addition to $224 for a total of $335 per paid hour ($224 plus $101) for each direct hour of work requiring foreign inspection travel. These are the rates that FDA will use in charging fees in FY 2012 when foreign travel is required.</P>
        <GPOTABLE CDEF="s100,10" COLS="2" OPTS="L2,i1">
          <TTITLE>Table 3—FSMA Fee Schedule for FY 2012</TTITLE>
          <BOXHD>
            <CHED H="1">Fee category</CHED>
            <CHED H="1">Fee rates for FY 2012</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Hourly rate if no foreign travel is required</ENT>
            <ENT>$224</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Hourly rate if foreign travel is required</ENT>
            <ENT>335</ENT>
          </ROW>
        </GPOTABLE>

        <P>Congress directed FDA to publish, within 180 days of enactment of FSMA, a proposed set of guidelines in consideration of the burden of fee amounts on small business (section 743(b)(2)(B)(iii) of the FD&amp;C Act). Such consideration may include reduced fee amounts for small businesses. FDA believes it is important to gather additional information before publishing such guidelines. Therefore, the Agency is publishing a separate document in this issue of the<E T="04">Federal Register</E>requesting public input to help the Agency understand what factors should be taken into account when drafting the proposed guidelines. The Agency intends to consider the comments received and then publish for comment a proposed set of guidelines on the considerations of the burden of fee amounts on small business. Any adjustment to the fee schedule for small business must be done through notice and comment rulemaking (see section 743(b)(2)(B)(iii)). Thus, there will be no separate small business fees published for FY 2012 (table 3 of this document) and the published fees in this document will apply to all businesses in FY 2012.</P>
        <P>FDA recognizes, however, that for some small businesses the full cost recovery of FDA reinspection or recall oversight could impose severe economic hardship, and there may be unique circumstances in which some relief would be appropriate. Thus, during FY 2012, FDA will consider waiving in limited cases some or all of an invoiced fee based on a severe economic hardship, the nature and extent of the underlying violation, and other relevant factors.</P>
        <HD SOURCE="HD1">III. Fees for Reinspections of Domestic or Foreign Facilities Under Section 743(a)(1)(A)</HD>
        <HD SOURCE="HD2">A. What will cause this fee to be assessed?</HD>
        <P>The fee will be assessed for a reinspection conducted under section 704 of the FD&amp;C Act to determine whether corrective actions have been implemented and are effective and compliance has been achieved to the Secretary of Health and Human Services' (the Secretary) (and, by delegation, FDA's) satisfaction at a facility that manufactures, processes, packs or holds food<SU>1</SU>
          <FTREF/>for consumption necessitated as a result of a previous inspection (also conducted under section 704) of this facility which had a final classification of Official Action Indicated (OAI) conducted by or on behalf of FDA, when FDA determined the non-compliance was materially related to food safety requirements of the FD&amp;C Act. FDA considers such non-compliance to include non-compliance with a statutory or regulatory requirement under section 402 of the FD&amp;C Act (21 U.S.C. 342) and section 403(w) of the FD&amp;C Act (21 U.S.C. 343(w)). However, FDA does not consider non-compliance that is materially related to a food safety requirement to include circumstances where the non-compliance is of a technical nature and not food safety related (e.g., failure to comply with a food standard or incorrect font size on a food label). Determining when non-compliance, other than under section 402 and 403(w) of the FD&amp;C Act, is materially related to food safety may depend on the facts of a particular situation. FDA may consider issuing guidance to provide additional information about the circumstances under which FDA would consider when non-compliance is materially related to a food safety requirement.</P>
        <FTNT>
          <P>
            <SU>1</SU>The term “food” for purposes of this document has the same meaning as such term in section 201(f) of the FD&amp;C Act (21 U.S.C. 321(f)).</P>
        </FTNT>
        <P>Under section 743(a)(1)(A) of the FD&amp;C Act, FDA shall assess and collect fees from “the responsible party for each domestic facility (as defined in section 415(b) (21 U.S.C. 350d)) and the United States agent for each foreign facility subject to a reinspection” to cover reinspection-related costs.</P>
        <P>Section 743(a)(2)(A)(i) of the FD&amp;C Act defines the term “reinspection” with respect to domestic facilities as “1 or more inspections conducted under section 704 subsequent to an inspection conducted under such provision which identified non-compliance materially related to a food safety requirement of th[e] Act, specifically to determine whether compliance has been achieved to the Secretary's satisfaction.”</P>

        <P>The FD&amp;C Act does not contain a definition of “reinspection” specific to foreign facilities. In order to give meaning to the language in section<PRTPAGE P="45823"/>743(a)(1)(A) of the FD&amp;C Act to collect fees from the United States agent of a foreign facility subject to a reinspection, the Agency is using the following definition, of “reinspection,” for purposes of assessing and collecting fees under section 743(a)(1)(A) of the FD&amp;C Act, with respect to a foreign facility: “1 or more inspections conducted by officers or employees duly designated by the Secretary subsequent to such an inspection which identified non-compliance materially related to a food safety requirement of the FD&amp;C Act, specifically to determine whether compliance has been achieved to the Secretary's (and, by delegation, FDA's) satisfaction.”</P>
        <P>This definition allows FDA to fulfill the mandate to assess and collect fees from the United States agent of a foreign facility in the event that an inspection reveals non-compliance materially-related to a food safety requirement causing one or more subsequent inspections to determine whether compliance has been achieved to the Secretary's (and, by delegation, FDA's) satisfaction. By requiring the initial inspection to be conducted by officers or employees duly designated by the Secretary, the definition ensures that a foreign facility would be subject to fees only in the event that FDA, or an entity designated to act on its behalf, has made the requisite identification at an initial inspection of non-compliance materially related to a food-safety requirement of the FD&amp;C Act. The definition of “reinspection-related costs,” as defined in section 743(a)(2)(B) of the FD&amp;C Act, relates to both a domestic facility reinspection and a foreign facility reinspection, as described in section 743(a)1)(A) of the FD&amp;C Act.</P>
        <HD SOURCE="HD2">B. Who will be responsible for paying this fee?</HD>
        <P>The FD&amp;C Act states that this fee is to be paid by the responsible party for each domestic facility (as defined in section 415(b) of the FD&amp;C Act) and by the United States agent for each foreign facility (section 743(a)(1)(A) of the FD&amp;C Act). This is the party to whom FDA will send the invoice for any fees that are assessed under this section.</P>
        <HD SOURCE="HD2">C. How much will this fee be?</HD>
        <P>The fee is based on the number of direct hours spent on such reinspections, including time spent conducting the physical surveillance and/or compliance reinspection at the facility, or whatever components of such an inspection are deemed necessary, making preparations and arrangements for the reinspection, traveling to and from the facility, preparing any reports, analyzing any samples or examining any labels if required, and performing other activities as part of the OAI reinspection until the facility is again determined to be in compliance. The direct hours spent on each such reinspection will be billed at the appropriate hourly rate shown in table 3 of this document.</P>
        <HD SOURCE="HD1">IV. Fees for Non-Compliance With a Recall Order Under Section 743(a)(1)(B)</HD>
        <HD SOURCE="HD2">A. What will cause this fee to be assessed?</HD>
        <P>The fee will be assessed for not complying with a recall order under section 423(d) or 412(f) of the FD&amp;C Act to cover food recall activities associated with such order performed by the Secretary (and by delegation, FDA) (section 743(a)(1)(B) of the FD&amp;C Act). Noncompliance may include the following: (1) Not initiating a recall as ordered by FDA; (2) not conducting the recall in the manner specified by FDA in the recall order; or (3) not providing FDA with requested information regarding the recall, as ordered by FDA.</P>
        <HD SOURCE="HD2">B. Who will be responsible for paying this fee?</HD>
        <P>Section 743(a)(1)(B) of the FD&amp;C Act states that the fee is to be paid by the responsible party for a domestic facility (as defined in section 415(b) of the FD&amp;C Act and an importer who does not comply with a recall order under section 423 or under section 412(f) of the FD&amp;C Act. In other words, the party paying the fee would be the party that received the recall order.</P>
        <HD SOURCE="HD2">C. How much will this fee be?</HD>
        <P>The fee is based on the number of direct hours spent on taking action in response to the firm's failure to comply with a recall order. Types of activities could include conducting recall audit checks, reviewing periodic status reports, analyzing the status reports and the results of the audit checks, conducting inspections, traveling to and from locations, and monitoring product disposition. The direct hours spent on each such recall will be billed at the appropriate hourly rate shown in table 3 of this document.</P>
        <HD SOURCE="HD1">V. Fees for Import Reinspection/Reexamination Under Section 743(a)(1)(D)</HD>
        <HD SOURCE="HD2">A. What will cause this fee to be assessed?</HD>
        <P>Under section 743(a)(2)(A)(ii) of the FD&amp;C Act, for a fee to be assessed, there must be two sets of examinations. First, there must be an examination conducted under section 801 of the FD&amp;C Act (21 U.S.C. 381), which must identify noncompliance materially related to a food safety requirement of the FD&amp;C Act.</P>
        <P>Second, subsequent to the first examination, there must be 1 or more additional examinations conducted under section 801. These additional examinations must be conducted specifically to determine whether compliance has been achieved to the Secretary's (and, by delegation, FDA's) satisfaction. Moreover, per section 743(a)(1)(D) of the FD&amp;C Act, an importer subject to a reinspection will be assessed a fee to cover reinspection-related costs.</P>
        <P>FDA has determined that at least the following four specific situations will cause a fee to be assessed:</P>
        <HD SOURCE="HD3">1. Reconditioning of Imported Food</HD>
        <P>FDA reviews food that is imported or offered for import to determine admissibility into the United States (see, e.g., section 801(a) of the FD&amp;C Act). Food is subject to refusal of admission if, among other reasons, (a) it appears to be adulterated or misbranded, or (b) if it is a dietary supplement subject to section 761 of the FD&amp;C Act (21 U.S.C. 379aa-1), FDA has credible evidence or information indicating that the responsible person has not complied with a requirement of that section or has not allowed access to records described in that section. When FDA initiates a refusal of admission, often referred to as detaining the product, notice is given to the owner or consignee. If the detention is based on one of the reasons just described, the owner or consignee of the food may request permission to recondition the food under section 801(b) of the FD&amp;C Act. When the basis is that the food appears to be adulterated or misbranded, the request can be to bring the food into compliance by relabeling or other action, such as heat treatment, or to render it other than a food, drug, device, or cosmetic. When the basis relates to section 761 (serious adverse event reporting for dietary supplements), the request can be for the responsible person, as defined in section 761, to take action to ensure that the responsible person is in compliance with section 761.</P>

        <P>A request for reconditioning is made after FDA has determined that the food is subject to refusal of admission under section 801(a) of the FD&amp;C Act. For the purpose of section 743 of the FD&amp;C Act, FDA considers its review of information for the purpose of determining whether an article of food is admissible to be “an examination conducted under section 801.” If that review leads FDA to determine that the food is subject to<PRTPAGE P="45824"/>refusal of admission under section 801(a), FDA considers that to mean that its examination “identified noncompliance” for the purpose of section 743. This examination could involve, for example, a laboratory analysis of physical samples of the product or a review of the product's label. It could also involve reviewing other information FDA obtains, such as reviewing sample results from a reliable third party, relevant epidemiological evidence, or the results from an FDA or third party inspection of a facility where the food was processed. A detention without physical examination could also be based on information contained in an import alert.</P>
        <P>When food is on an import alert, it typically means that FDA has concluded there is sufficient evidence or other information to detain without physical examination of future shipments of the imported food (e.g., that future shipments appear to be adulterated or misbranded) and they are subject to refusal unless the owner or consignee shows the product is compliant (e.g., through third-party laboratory analysis). FDA considers situations where FDA's review of information leads it to conclude that food should be placed on an import alert for detention without physical examination to be “an examination conducted under section 801 [that] identified noncompliance” for the purposes of section 743. FDA's Regulatory Procedures Manual (RPM), Chap. 9, discusses the types of reviews FDA conducts, and the types of information it reviews, in determining whether to detain a product or to place a product on an import alert.</P>
        <P>For a fee to be assessed under section 743, FDA's determination that the food is subject to refusal of admission must be on a basis materially related to food safety requirements (see section III.A of this document for a discussion about “materially related to food safety requirements”).</P>
        <P>If FDA authorizes a request for reconditioning, the reconditioning operations are carried out under the supervision of either FDA or U.S. Customs and Border Protection (CBP) (section 801(b) of the FD&amp;C Act; 21 CFR 1.96(a)). FDA considers the review and approval of the request, as well as this supervision to be “1 or more examinations conducted under section 801 * * * specifically to determine whether compliance has been achieved” to FDA's satisfaction.</P>
        <HD SOURCE="HD3">2. Importer Seeking Admission of an Article That Has Been Detained</HD>
        <P>If FDA has determined that an article of food is subject to refusal of admission under section 801(a) of the FD&amp;C Act, FDA gives notice of this to the owner or consignee, who then has an opportunity to introduce evidence regarding the admissibility of the food (section 801(a) of the FD&amp;C Act; 21 CFR 1.94(a)). As discussed previously in this document, where FDA has reviewed information for the purpose of admissibility and determined that the food is subject to refusal of admission under section 801, FDA considers that it has conducted “an examination conducted under section 801 [that] identified noncompliance.” This includes situations where FDA's review determines that food should be placed on an import alert for detention without physical examination.</P>
        <P>If the owner or consignee chooses to submit evidence regarding admissibility, FDA reviews the information to determine whether—despite the appearance that the product is adulterated, misbranded, or otherwise subject to refusal of admission—the food is compliant and admissible into the United States. The evidence the owner or consignee submits varies. Depending on the circumstances, it could include, for example, the results of laboratory analyses of samples conducted on the owner/consignee's behalf to show the product is not contaminated. FDA considers its review of the evidence submitted to be “1 or more examinations conducted under section 801 * * * specifically to determine whether compliance has been achieved” to FDA's satisfaction.</P>
        <P>Not all situations where the owner/consignee provides information or evidence to demonstrate compliance will result in the assessment of a fee. An example is if a food, not subject to an Import Alert, is detained based on an appearance of adulteration or misbranding, but information is presented that demonstrates that the food is not adulterated or misbranded. FDA considers such a situation to be one in which a fee is not assessed.</P>
        <P>A fee may or may not be assessed under certain circumstances related to food that is detained based on an import alert for detention without physical examination covering food from a particular geographic region or country. FDA may place a region or country on an import alert if there appears to be an ongoing problem or condition in that region or country such that it causes the appearance of a violation for future shipments of imported articles originating there. If food from a region or country is subject to an import alert and is subsequently detained based on the overarching import alert, the owner or consignee may seek admission by providing evidence that the problem or conditions regarding the food it is importing have been resolved. Alternatively, the owner or consignee may provide evidence that the problems or conditions that led to the alert, even if widespread in the region or country, did not apply to its food and, thus, it did not need to resolve any compliance-related issues. FDA considers the latter situation to be one in which a fee is not assessed. A fee may be assessed, however, when FDA reviews compliance information specific to the food being imported or specific to a particular processor in determining whether to issue a region- or country-wide import alert. An example is a situation where FDA analyzed samples of food from Processor A and found it to be contaminated, the food is later placed on a region- or country-wide import alert, and the owner or consignee is now importing or offering for import food from Processor A. If the owner or consignee seeks admission of the food by providing third party laboratory analyses to show the food is not contaminated, FDA's review of this information would be “1 or more examinations conducted under section 801 * * * specifically to determine whether compliance has been achieved” to FDA's satisfaction.</P>
        <HD SOURCE="HD3">3. Entity Requesting Removal From an Import Alert for Detention Without Physical Examination</HD>
        <P>Once placed on import alert, food imported from a particular firm, region, or country may remain in this status until FDA has sufficient evidence or other information, such as information that removes the appearance of the violation that led to the initial placement on import alert. Depending on the situation that led to the import alert, FDA's RPM Chapter 9 or the import alert itself may explain the types of information that should be provided.</P>
        <P>As discussed previously in this document, where FDA has reviewed information and determined that food should be placed on an import alert for detention without physical examination, it considers that it has conducted 1 or more examinations conducted under section 801 that identified noncompliance.</P>

        <P>Where an entity requests removal of food from an import alert and provides supporting information, FDA considers its review of this information, along with any other related examination it undertakes in considering the request, to be “1 or more examinations conducted under section 801 * * * specifically to determine whether compliance has been achieved” to FDA's satisfaction.<PRTPAGE P="45825"/>
        </P>
        <P>As discussed in section V.A.2 of this document, some requests for removal from region- or country-wide import alerts will not lead to the assessment of a fee. Fees would only be assessed in situations where, in issuing the alert, FDA reviewed compliance information specific to a particular person or entity sufficiently related to the request for removal. An example of such a situation is where FDA analyzed samples of food from Processor A and found it to be contaminated, the food is then placed on a region- or country-wide import alert, and FDA receives a request to remove food from Processor A from the import alert.</P>
        <HD SOURCE="HD3">4. Destruction of Food That Has Been Refused Admission</HD>
        <P>If a product is refused admission under section 801(a) of the FD&amp;C Act, it must be exported within 90 days of the document of refusal or it is subject to destruction by CBP (section 801(a) of the FD&amp;C Act). In practice, when a product is destroyed, destruction is often conducted by the owner or consignee under the supervision of FDA or CBP. Where FDA conducts a review and/or approves a destruction proposal and such supervision of destruction occurs, FDA considers this to be “1 or more examinations conducted under section 801 * * * specifically to determine whether compliance has been achieved” to FDA's satisfaction.</P>
        <HD SOURCE="HD2">B. Who will be responsible for paying this fee?</HD>
        <P>The importer that is subject to the additional examinations that are described in section V.A of this document is responsible for paying the fee, according to section 743(a)(1)(D) of the FD&amp;C Act.</P>
        <HD SOURCE="HD3">1. Reconditioning of Imported Food</HD>
        <P>For reconditioning, the entity that is responsible for the reconditioning is responsible for paying the fee. The request for reconditioning can only be made by the owner or consignee of the food (21 CFR 1.95). If ownership changes, the new owner will be responsible for the reconditioning if that new owner executes a bond and obtains a new authorization (21 CFR 1.96(d)).</P>
        <HD SOURCE="HD3">2. Importer Seeking Admission of an Article That Has Been Detained</HD>
        <P>The entity that introduces evidence regarding admissibility is responsible for paying this fee. This is the owner or consignee of the food that is being imported or offered for import. (Section 801(a) of the FD&amp;C Act; 21 CFR 1.83(b) and 1.94(a).)</P>
        <HD SOURCE="HD3">3. Entity Requesting Removal From an Import Alert for Detention Without Physical Examination.</HD>
        <P>FDA considers the entity that requests removal of the food from the import alert to be the importer subject to the examination and, thus, responsible for paying this fee.</P>
        <HD SOURCE="HD3">4. Destruction of Food That Has Been Refused Admission</HD>
        <P>FDA considers the entity that destroys the product under FDA or CBP supervision to be the importer subject to the examination and, thus, responsible for paying this fee.</P>
        <HD SOURCE="HD2">C. How much will this fee be?</HD>
        <P>The fee is to cover all expenses incurred in connection with arranging, conducting, and evaluating the results of the one or more additional examinations that are described in section V.A of this document.</P>
        <P>For reconditioning, section 801(c) of the FD&amp;C Act directs the owner or consignee to pay all expenses in connection with the supervision of reconditioning with respect to food and certain other FDA-regulated products. Those parties have been paying these expenses, but FDA did not have authority to retain those fees. FDA considers the enactment of section 743 of the FD&amp;C Act to mean that, for food, FDA is now authorized to assess and retain these fees, but only with respect to the reconditioning of food and only if the other conditions of section 743 are met. If a fee is authorized under section 743 for a particular article of food, FDA considers this to mean it cannot collect a fee related to reconditioning that article under section 801(c).</P>
        <P>For destruction, section 801(c) of the FD&amp;C Act also directs the owner or consignee to pay all expenses in connection with the destruction of food and certain other FDA-regulated products under section 801(a). However, neither FDA nor CBP have had the authority to retain those fees. FDA considers the enactment of section 743 of the FD&amp;C Act to mean that, for food, FDA is now authorized to assess and retain these fees, but only with respect to the destruction of food and only if the other conditions of section 743 are met. If a fee is authorized under section 743 for a particular article of food, FDA considers this to mean it cannot collect a fee related to destruction of that article under section 801(c) of the FD&amp;C Act.</P>
        <P>The direct hours spent on each such import reinspections will be billed at the appropriate hourly rate shown in table 3 of this document.</P>
        <HD SOURCE="HD1">VI. How must the fees be paid?</HD>
        <P>An invoice will be sent to the responsible party for paying the fee after FDA completes the work on which the invoice is based. Payment must be made within 30 days of the invoice date in U.S. currency by check, bank draft, or U.S. postal money order payable to the order of the Food and Drug Administration. Detailed payment information will be included with the invoice when it is issued.</P>
        <HD SOURCE="HD1">VII. What are the consequences of not paying these user fees?</HD>
        <P>Under section 743(e)(2) of the FD&amp;C Act, any fee that is not paid within 30 days after it is due shall be treated as a claim of the United States Government subject to provisions of subchapter II of chapter 37 of title 31, United States Code.</P>
        <HD SOURCE="HD1">VIII. Comments</HD>

        <P>Interested persons may submit to the Division of Dockets Management (see<E T="02">ADDRESSES</E>) either electronic or written comments regarding this document. It is only necessary to send one set of comments. It is no longer necessary to send two copies of mailed comments. Identify comments with the docket number found in brackets in the heading of this document. Received comments may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Leslie Kux,</NAME>
          <TITLE>Acting Assistant Commissioner for Policy.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19331 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4160-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>Food and Drug Administration</SUBAGY>
        <DEPDOC>[Docket No. FDA-2011-N-0556]</DEPDOC>
        <SUBJECT>Center for Devices and Radiological Health 510(k) Clearance Process; Institute of Medicine Report: “Medical Devices and the Public's Health, The FDA 510(k) Clearance Process at 35 Years;” Request for Comments</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Food and Drug Administration, HHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Request for comments.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>The Food and Drug Administration (FDA) is requesting comments on the Institute of Medicine (IOM) report entitled: “Medical Devices and the Public's Health, The FDA 510(k) Clearance Process at 35 Years.” The establishment of this public docket does<PRTPAGE P="45826"/>not signify FDA endorsement or concurrence with any of the conclusions or recommendations contained within the report. FDA may, in the future, take additional measures to solicit public input in the report and specific recommendations contained therein. FDA will not adopt any of the recommendations contained in the report before the close of this comment period.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Submit either electronic or written comments on the report by September 30, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>See the<E T="02">SUPPLEMENTARY INFORMATION</E>section for electronic access to the document. Submit electronic comments on the preliminary report to<E T="03">http://www.regulations.gov.</E>Submit written comments to the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. Identify comments with the docket number found in brackets in the heading of this document.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Philip Desjardins, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, rm. 5452, Silver Spring, MD 20993-0002, 301-796-5678.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P/>
        <HD SOURCE="HD1">I. Background</HD>

        <P>In September 2009, CDRH convened an internal 510(k) Working Group as part of a two-pronged, comprehensive assessment of the 510(k) process. The first prong of this evaluation consisted of an internal evaluation of the 510(k) process, resulting in the publication of the CDRH preliminary internal evaluation entitled: “510(k) Working Group Preliminary Report and Recommendations” (<E T="03">http://www.fda.gov/downloads/AboutFDA/CentersOffices/CDRH/CDRHReports/UCM220784.pdf</E>). This preliminary report was intended to communicate preliminary findings and recommendations regarding the 510(k) program and actions CDRH might take to address identified areas of concern. The report was issued on August 5, 2010 (75 FR 47307). After reviewing public comment, CDRH issued a plan of action for implementation of the previously announced recommendations on January 19, 2011 (<E T="03">http://www.fda.gov/downloads/AboutFDA/CentersOffices/CDRH/CDRHReports/UCM239450.pdf</E>).</P>
        <P>The second prong of the comprehensive assessment of the 510(k) process was an independent study by the IOM. At the request of FDA, IOM has evaluated the 510(k) clearance process and made recommendations aimed at protecting the health of the public and making available a mechanism to achieve timely access of medial devices to the market. On July 29, 2011, IOM released the report “Medical Devices and the Public's Health, The FDA 510(k) Clearance Process at 35 Years.” While FDA has not yet had the opportunity to fully evaluate this report, the agency does recognize the strong public interest in the comprehensive assessment of the 510(k) process and the IOM report. For this reason, FDA is opening a public docket and requesting public comment on the report. The establishment of this public docket does not signify agency endorsement or concurrence with any of the conclusions or recommendations contained within the report. FDA may, in the future, take additional measures to solicit public input in the report and specific recommendations contained therein. FDA will not adopt any of the recommendations contained in the report before the close of this comment period.</P>
        <HD SOURCE="HD1">II. Comments</HD>

        <P>Interested persons may submit to the Division of Dockets Management (see<E T="02">ADDRESSES</E>) either electronic or written comments regarding this document. It is only necessary to send one set of comments. It is no longer necessary to send two copies of mailed comments. Identify comments with the docket number found in brackets in the heading of this document. Received comments may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.</P>
        <HD SOURCE="HD1">III. Electronic Access</HD>

        <P>The IOM report entitled: “Medical Devices and the Public's Health, The FDA 510(k) Clearance Process at 35 Years” can be obtained from the IOM Web site at<E T="03">http://www.iom.edu/Activities/PublicHealth/510KProcess.aspx.</E>
        </P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Nancy K. Stade,</NAME>
          <TITLE>Deputy Director for Policy, Center for Devices and Radiological Health.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19353 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4160-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>Food and Drug Administration</SUBAGY>
        <DEPDOC>[Docket No. FDA-2011-N-0542]</DEPDOC>
        <SUBJECT>Medical Device User Fee Rates for Fiscal Year 2012</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Food and Drug Administration, HHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Food and Drug Administration (FDA) is announcing the fee rates and payment procedures for medical device user fees for fiscal year (FY) 2012. The Federal Food, Drug, and Cosmetic Act (the FD&amp;C Act), as amended by the Medical Device User Fee Amendments of 2007 (title II of the Food and Drug Administration Amendments Act of 2007 (FDAAA)), authorizes FDA to collect user fees for certain medical device submissions, and annual fees for certain periodic reports and for certain establishments subject to registration. The FY 2012 fee rates are provided in this document. These fees apply from October 1, 2011, through September 30, 2012. To avoid delay in the review of your application, you should pay the fee before or at the time you submit your application to FDA. The fee you must pay is the fee that is in effect on the later of the date that your application is received by FDA or the date your fee payment is received. In order to pay a reduced small business fee, you must qualify as a small business before you make your submission to FDA; if you do not qualify as a small business before you make your submission to FDA, you will be required to pay the higher standard fee. This document provides information on how the fees for FY 2012 were determined, the payment procedures you should follow, and how you may qualify for reduced small business fees.</P>
        </SUM>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>
            <E T="03">For information on the Medical Device User Fee and Modernization Act (MDUFMA):</E>visit FDA's Web site,<E T="03">http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Overview/MedicalDeviceUserFeeandModernizationActMDUFMA/default.htm.</E>
          </P>
          <P>
            <E T="03">For questions relating to this notice:</E>Contact David Miller, Office of Financial Management (HFA-100), Food and Drug Administration, 1350 Piccard Dr., Rockville, MD 20850, 301-796-7103.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:<PRTPAGE P="45827"/>
        </HD>
        <HD SOURCE="HD1">I. Background</HD>
        <P>Section 738 of the FD&amp;C Act (21 U.S.C. 379j) establishes fees for certain medical device applications, submissions, supplements, and notices (for simplicity, this document refers to these collectively as “submissions”); for periodic reporting on class III devices; and for the registration of certain establishments. Under statutorily-defined conditions, a qualified applicant may receive a fee waiver or may pay a lower small business fee. (See 21 U.S.C. 379j(d) and (e)).</P>
        <P>Under the FD&amp;C Act, the fee rate for each type of submission is set at a specified percentage of the standard fee for a premarket application (a premarket application is a premarket approval application (PMA), a product development protocol (PDP), or a biologics license application (BLA)). The FD&amp;C Act specifies the standard fee for a premarket application for each year from FY 2008 through FY 2012; however, the standard fee for a premarket application received by FDA during FY 2012, which is set in the statute ($256,384), is adjusted in accordance with the offset provisions of the FD&amp;C Act. Using this adjusted fee rate for FY 2012 as a starting point, this document establishes FY 2012 fee rates for other types of submissions, and for periodic reporting, by applying criteria specified in the FD&amp;C Act.</P>
        <P>The FD&amp;C Act specifies the annual fee for establishment registration for each year from FY 2008 through FY 2012; the registration fee for FY 2012 is $2,364, which is also adjusted in accordance with the offset provisions of the FD&amp;C Act. There is no reduction in the registration fee for small businesses. An establishment must pay the registration fee if it is any of the following types of establishment:</P>
        <P>• Manufacturer—An establishment that makes by any means any article that is a device, including an establishment that sterilizes or otherwise makes such article for or on behalf of a specification developer or any other person.</P>
        <P>• Single-Use Device Reprocessor—An establishment that performs additional processing and manufacturing operations on a single-use device that has previously been used on a patient.</P>
        <P>• Specification Developer—An establishment that develops specifications for a device that is distributed under the establishment's name but which performs no manufacturing, including an establishment that, in addition to developing specifications, also arranges for the manufacturing of devices labeled with another establishment's name by a contract manufacturer.</P>
        <HD SOURCE="HD1">II. Offsetting Fee Amounts for Collections in Excess of Appropriations in FY 2008 through FY 2011</HD>
        <P>Under the offset provision of the FD&amp;C Act (see section 739(h)(4) (21 U.S.C. 379j-11(h)(4))), if the cumulative amount of fees collected during FY 2008 through FY 2010, together with the estimated amount to be collected in FY 2011, exceeds the aggregate amounts specified to be appropriated in these four FYs in section 739(h)(3) of the FD&amp;C Act, the aggregate amount in excess shall be credited to the appropriation account of FDA and subtracted from the amount of fees that would otherwise be collected in FY 2012. Table 1 of this document presents the amount of MDUFMA fees collected during FY 2008 through FY 2010 (actuals), and the amount estimated to be collected in FY 2011, and compares those amounts with the fees specified to be appropriated in these four FYs in section 739(h)(3) of the FD&amp;C Act.</P>
        <GPOTABLE CDEF="s50,12,12,12" COLS="4" OPTS="L2,i1">
          <TTITLE>Table 1—Statement of Fees Appropriated, Fees Collected, and Differences as of September 30, 2010</TTITLE>
          <BOXHD>
            <CHED H="1">Fiscal year</CHED>
            <CHED H="1">Fees appropriated</CHED>
            <CHED H="1">Fees collected</CHED>
            <CHED H="1">Difference</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">2008 Actual</ENT>
            <ENT>$48,431,000</ENT>
            <ENT>$49,314,691</ENT>
            <ENT>$883,691</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2009 Actual</ENT>
            <ENT>52,547,000</ENT>
            <ENT>59,731,482</ENT>
            <ENT>7,184,482</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2010 Actual</ENT>
            <ENT>57,014,000</ENT>
            <ENT>66,949,587</ENT>
            <ENT>9,935,587</ENT>
          </ROW>
          <ROW RUL="n,s">
            <ENT I="01">2011 Estimate</ENT>
            <ENT>61,860,000</ENT>
            <ENT>61,860,000</ENT>
            <ENT>0</ENT>
          </ROW>
          <ROW RUL="s">
            <ENT I="03">Cumulative Total</ENT>
            <ENT/>
            <ENT/>
            <ENT>18,003,760</ENT>
          </ROW>
          <ROW>
            <ENT I="03">Unearned Revenue Included in Above Amount</ENT>
            <ENT/>
            <ENT/>
            <ENT>8,491,930</ENT>
          </ROW>
          <ROW>
            <ENT I="03">Excess Collections Less Unearned Revenue (Offset Amount)</ENT>
            <ENT/>
            <ENT/>
            <ENT>9,511,830</ENT>
          </ROW>
        </GPOTABLE>
        <P>The total amount FDA expects to have collected in excess of appropriations by the end of FY 2011 is $18,003,760. However, of that amount, a total of $8,491,930 represents unearned revenue—primarily fees paid for applications that have not yet been received. The unearned revenue is held in reserve either to refund, if no application is submitted, or to apply toward the future FY when the application is received. The net of these two figures, $9,511,830, is the amount that FDA has received in excess of appropriations that is available for obligation, and the amount by which fee revenue will be offset in FY 2012.</P>
        <P>For FY 2012, the statute authorizes $67,118,000 in user fees (see section 738(h)(3)(E)). In order to determine the revised collection amount, we deduct the net excess collection amount of $9,511,830 from $67,118,000, and the revised revenue target for FY 2012 becomes $57,606,170. Stated as a percent, this is 85.8281 percent of the original revenue target for FY 2012. Accordingly, if we multiply this percentage by the revenue amounts for the two fees set in statute, $256,384 for a Premarket Application fee and $2,364 for an Establishment Registration Fee (see 21 U.S.C. 379j(b)), the reduced fees for FY 2012 are $220,050 for a premarket application fee and $2,029 for the annual establishment registration fee.</P>
        <P>It is important to note that the appropriation for FY 2012 still must be $67,118,000 as specified in the statute, so that the $9,511,830 in user fees collected in prior years is appropriated and available for obligation.</P>
        <HD SOURCE="HD1">III. Fees for FY 2012</HD>
        <P>Under the FD&amp;C Act, all submission fees and the periodic reporting fee are set as a percent of the standard (full) fee for a premarket application (see 21 U.S.C. 379j(a)(2)(A)), and the offset fee for the standard premarket application, including a BLA, a premarket report, and an efficacy supplement, for FY 2012. As calculated previously, the FY 2012 premarket application fee is $220,050. This is referred to as the “base fee.” The fees set by reference to the base fee are as follows:</P>

        <P>• For a panel-track supplement, 75 percent of the base fee;<PRTPAGE P="45828"/>
        </P>
        <P>• For a 180-day supplement, 15 percent of the base fee;</P>
        <P>• For a real-time supplement, 7 percent of the base fee;</P>
        <P>• For a 30-day notice, 1.6 percent of the base fee;</P>
        <P>• For a 510(k) premarket notification, 1.84 percent of the base fee;</P>
        <P>• For a 513(g) (21 U.S.C. 360(c)(g)) request for classification information, 1.35 percent of the base fee; and</P>
        <P>• For an annual fee for periodic reporting concerning a class III device, 3.5 percent of the base fee.</P>
        <P>For all submissions other than a 510(k) premarket notification, a 30-day notice, and a 513(g) request for classification information, the small business fee is 25 percent of the standard (full) fee. (See 21 U.S.C. 379j(d)(2)(C).) For a 510(k) premarket notification submission, a 30-day notice, and a 513(g) request for classification information, the small business fee is 50 percent of the standard (full) fee. (See 21 U.S.C. 379j(d)(2)(C) and 379j(e)(2)(C).)</P>
        <P>The annual fee for establishment registration, after reduction as calculated in the previous section, is $2,029 in FY 2012. There is no small business rate for the annual establishment registration fee; all establishments pay the same fee. The statute authorizes increases in the annual establishment fee for FY 2011 and subsequent years if the estimated number of establishments submitting fees for FY 2009 is fewer than 12,250. (See 21 U.S.C. 379j(c)(2)(A).) The number of establishments submitting fees in FY 2009 was in excess of 12,250, so no establishment fee increase is warranted under this provision of the statute.</P>
        <P>Table 2 of this document sets out the FY 2012 rates for all medical device fees.</P>
        <GPOTABLE CDEF="s100,r50,12,12" COLS="4" OPTS="L2,i1">
          <TTITLE>Table 2—Medical Device Fees for FY 2012</TTITLE>
          <BOXHD>
            <CHED H="1">Application fee type</CHED>
            <CHED H="1">Standard Fee, as a Percent of the standard fee for a premarket<LI>application</LI>
            </CHED>
            <CHED H="1">FY 2012 standard fee</CHED>
            <CHED H="1">FY 2012 small business fee</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Premarket application (a PMA submitted under section 515(c)(1) of the FD&amp;C Act (21 U.S.C. 360e(c)(1)), a PDP submitted under section 515(f) of the FD&amp;C Act, or a BLA submitted under section 351 of the Public Health Service (PHS) Act (42 U.S.C. 262))</ENT>
            <ENT>Set in statute at $256,382, but offset by multiplying by 85.8281 percent</ENT>
            <ENT>$220,050</ENT>
            <ENT>$55,013</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Premarket report (submitted under section 515(c)(2) of the FD&amp;C Act)</ENT>
            <ENT>100%</ENT>
            <ENT>220,050</ENT>
            <ENT>55,013</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Efficacy supplement (to an approved BLA under section 351 of the PHS Act)</ENT>
            <ENT>100%</ENT>
            <ENT>220,050</ENT>
            <ENT>55,013</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Panel-track supplement</ENT>
            <ENT>75%</ENT>
            <ENT>165,038</ENT>
            <ENT>41,259</ENT>
          </ROW>
          <ROW>
            <ENT I="01">180-day supplement</ENT>
            <ENT>15%</ENT>
            <ENT>33,008</ENT>
            <ENT>8,252</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Real-time supplement</ENT>
            <ENT>7%</ENT>
            <ENT>15,404</ENT>
            <ENT>3,851</ENT>
          </ROW>
          <ROW>
            <ENT I="01">510(k) premarket notification submission</ENT>
            <ENT>1.84%</ENT>
            <ENT>4,049</ENT>
            <ENT>2,024</ENT>
          </ROW>
          <ROW>
            <ENT I="01">30-day notice</ENT>
            <ENT>1.6%</ENT>
            <ENT>3,521</ENT>
            <ENT>1,760</ENT>
          </ROW>
          <ROW RUL="s">
            <ENT I="01">513(g) (21 U.S.C. 360c(g)) request for classification information</ENT>
            <ENT>1.35%</ENT>
            <ENT>2,971</ENT>
            <ENT>1,485</ENT>
          </ROW>
          <ROW EXPSTB="03" RUL="s">
            <ENT I="21">Annual Fee Type</ENT>
          </ROW>
          <ROW EXPSTB="00">
            <ENT I="01">Annual fee for periodic reporting on a class III device</ENT>
            <ENT>3.5%</ENT>
            <ENT>7,702</ENT>
            <ENT>1,925</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Annual establishment registration fee (to be paid by each establishment that is a manufacturer, a single-use device reprocessor, or a specification developer, as defined by 21 U.S.C. 379i(13))</ENT>
            <ENT>Set in statute at $2,364, but offset by multiplying by 85.8281 percent</ENT>
            <ENT>2,029</ENT>
            <ENT>2,029</ENT>
          </ROW>
        </GPOTABLE>
        <HD SOURCE="HD1">IV. How to Qualify as a Small Business for Purposes of Medical Device Fees</HD>
        <P>If your business has gross receipts or sales of no more than $100 million for the most recent tax year, you may qualify for reduced small business fees. If your business has gross sales or receipts of no more than $30 million, you may also qualify for a waiver of the fee for your first premarket application (PMA, PDP, or BLA) or premarket report. You must include the gross receipts or sales of all of your affiliates along with your own gross receipts or sales when determining whether you meet the $100 million or $30 million threshold. In order to pay the small business fee rate for a submission, or to receive a waiver of the fee for your first premarket application or premarket report, you should submit the materials showing you qualify as a small business 60 days before you send your submission to FDA. If you make a submission before FDA finds that you qualify as a small business, you must pay the standard fee for that submission.</P>
        <P>If your business qualified as a small business for FY 2011, your status as a small business will expire at the close of business on September 30, 2011. You must re-qualify for FY 2012 in order to pay small business fees during FY 2012.</P>
        <P>If you are a domestic (U.S.) business, and wish to qualify as a small business for FY 2012, you must submit the following to FDA:</P>

        <P>1. A completed FY 2012 MDUFMA Small Business Qualification Certification (Form FDA 3602). This form is provided in FDA's guidance document, “FY 2012 Medical Device User Fee Small Business Qualification and Certification,” available on FDA's Web site at<E T="03">http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Overview/MedicalDeviceUserFeeandModernizationActMDUFMA/default.htm.</E>This form is not available separate from the guidance document.</P>
        <P>2. A certified copy of your Federal (U.S.) Income Tax Return for the most recent tax year. The most recent tax year will be 2011, except:</P>
        <P>• If you submit your FY 2012 MDUFMA Small Business Qualification before April 15, 2012, and you have not yet filed your return for 2011, you may use tax year 2010.</P>
        <P>• If you submit your FY 2012 MDUFMA Small Business Qualification on or after April 15, 2012, and have not yet filed your 2011 return because you obtained an extension, you may submit your most-recent return filed prior to the extension.</P>
        <P>3. For each of your affiliates, either:</P>
        <P>• If the affiliate is a domestic (U.S.) business, a certified copy of the affiliate's Federal (U.S.) income tax return for the most recent tax year, or</P>

        <P>• If the affiliate is a foreign business and cannot submit a Federal (U.S.) Income Tax Return, a National Taxing Authority Certification completed by, and bearing the official seal of, the<PRTPAGE P="45829"/>National Taxing Authority of the country in which the firm is headquartered. The National Taxing Authority is the foreign equivalent of the U.S. Internal Revenue Service. This certification must show the amount of gross receipts or sales for the most recent tax year, in both U.S. dollars and the local currency of the country, the exchange rate used in converting the local currency to U.S. dollars, and the dates of the gross receipts or sales collected. The applicant should also submit a statement signed by the head of the applicant's firm or by its chief financial officer that the applicant has submitted certifications for all of its affiliates, identifying the name of each affiliate, or that the applicant has no affiliates.</P>
        <P>If you are a foreign business, and wish to qualify as a small business for FY 2012, you must submit the following:</P>

        <P>1. A completed FY 2012 MDUFMA Foreign Small Business Qualification Certification (Form FDA 3602A). This form is provided in FDA's guidance document, “FY 2012 Medical Device User Fee Small Business Qualification and Certification,” available on FDA's Web site at<E T="03">http://www.fda.gov/cdrh/mdufma.</E>This form is not available separate from the guidance document.</P>
        <P>2. A National Taxing Authority Certification, completed by, and bearing the official seal of, the National Taxing Authority of the country in which the firm is headquartered. This Certification must show the amount of gross receipts or sales for the most recent tax year, in both U.S. dollars and the local currency of the country, the exchange rate used in converting the local currency to U.S. dollars, and the dates of the gross receipts or sales collected.</P>
        <P>3. For each of your affiliates, either:</P>
        <P>• If the affiliate is a domestic (U.S.) business, a certified copy of the affiliate's Federal (U.S.) Income Tax Return for the most recent tax year (2010 or later), or</P>
        <P>• If the affiliate is a foreign business and cannot submit a Federal (U.S.) Income Tax Return, a National Taxing Authority Certification completed by, and bearing the official seal of, the National Taxing Authority of the country in which the firm is headquartered. The National Taxing Authority is the foreign equivalent of the U.S. Internal Revenue Service. This certification must show the amount of gross receipts or sales for the most recent tax year, in both U.S. dollars and the local currency of the country, the exchange rate used in converting the local currency to U.S. dollars, and the dates for the gross receipts or sales collected. The applicant should also submit a statement signed by the head of the applicant's firm or by its chief financial officer that the applicant has submitted certifications for all of its affiliates, identifying the name of each affiliate, or that the applicant has no affiliates.</P>
        <HD SOURCE="HD1">V. Procedures for Paying Application Fees</HD>
        <P>If your application or submission is subject to a fee and your payment is received by FDA from October 1, 2011, through September 30, 2012, you must pay the fee in effect for FY 2012. The later of the date that the application is received in the reviewing center's document room or the date that the check is received by U.S. Bank determines whether the fee rates for FY 2011 or FY 2012 apply. FDA must receive the correct fee at the time that an application is submitted, or the application will not be accepted for filing or review.</P>

        <P>FDA requests that you follow the steps in the paragraphs that follow when submitting a medical device application subject to a fee to ensure that FDA links the fee with the correct application. (<E T="04">Note:</E>In no case should the check for the fee be submitted to FDA with the application.)</P>
        <HD SOURCE="HD2">A. Step One—Secure a Payment Identification Number (PIN) and Medical Device User Fee Cover Sheet From FDA Before Submitting Either the Application or the Payment. Both the FY 2011 and FY 2012 Fee Rates Will Be Available on the User Fee Web Site Beginning on the Date of Publication of This Document, and Only the FY 2012 Rates Will Appear After September 30, 2011)</HD>
        <P>Log on to the MDUFMA Web site at:<E T="03">http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Overview/MedicalDeviceUserFeeandModernizationActMDUFMA/default.htm</E>and under the MDUFMA Forms heading, click on the link “Create a User Fee Cover Sheet.” Complete the Medical Device User Fee cover sheet. Be sure you choose the correct application submission date range (two choices will be offered until October 1, 2011. One choice is for applications that will be received on or before September 30, 2011, which are subject to FY 2011 fee rates. A second choice is for applications that will be received on or after October 1, 2011, which are subject to FY 2012 fee rates.) After completing data entry, print a copy of the Medical Device User Fee cover sheet and note the unique PIN located in the upper right-hand corner of the printed cover sheet.</P>
        <HD SOURCE="HD2">B. Step Two—Electronically Transmit a Copy of the Printed Cover Sheet With the PIN to FDA's Office of Financial Management</HD>
        <P>Once you are satisfied that the data on the cover sheet is accurate, electronically transmit that data to FDA according to instructions on the screen. Because electronic transmission is possible, applicants are required to set up a user account and use passwords to assure data security in the creation and electronic submission of cover sheets.</P>
        <HD SOURCE="HD2">C. Step Three—Submit Payment for the Completed Medical Device User Fee Cover Sheet as Described in This Section, Depending on the Method You Will Use to Make Payment</HD>
        <P>1. If paying with a paper check:</P>
        <P>• All paper checks must be in U.S. currency from a U.S. bank and made payable to the Food and Drug Administration. (FDA's tax identification number is 53-0196965, should your accounting department need this information.)</P>
        <P>• Please write your application's unique PIN, from the upper right-hand corner of your completed Medical Device User Fee cover sheet, on your check.</P>
        <P>• Mail the paper check and a copy of the completed cover sheet to: Food and Drug Administration, P.O. Box 956733, St. Louis, MO, 63195-6733. (Please note that this address is for payments of application and annual report fees only and is not to be used for payment of annual establishment registration fees.)</P>

        <P>If you prefer to send a check by a courier (such as Federal Express (FEDEX), DHL, United Parcel Service (UPS), etc.), the courier may deliver the check to: U.S. Bank, Attn: Government Lockbox 956733, 1005 Convention Plaza, St. Louis, MO 63101. (<E T="04">Note:</E>This address is for courier delivery only. Contact the U.S. Bank at 314-418-4821 if you have any questions concerning courier delivery.)</P>
        <P>FDA records the official application receipt date as the later of the following: (1) The date the application was received by FDA or (2) the date U.S. Bank receives the payment. It is helpful if the fee arrives at the bank at least 1 day before the application arrives at FDA. U.S. Bank is required to notify FDA within 1 working day, using the PIN described previously in this document.</P>
        <P>2. If paying with a credit card or electronic check (Automated Clearing House (ACH)):</P>

        <P>FDA has partnered with the U.S. Department of the Treasury to utilize Pay.gov, a Web based payment system,<PRTPAGE P="45830"/>for online electronic payment. You may make a payment via electronic check or credit card after submitting your coversheet. To pay online, select the “Pay Now” button. Credit card transactions for cover sheets are limited to $5,000.</P>
        <P>3. If paying with a wire transfer:</P>
        <P>• Please include your application's unique PIN, from the upper right-hand corner of your completed Medical Device User Fee cover sheet, in your wire transfer. Without the PIN, your payment may not be applied to your cover sheet and review of your application will be delayed.</P>
        <P>• The originating financial institution may charge a wire transfer fee between $15 and $35. Please ask your financial institution about the fee and include it with your payment to ensure that your cover sheet is fully paid.</P>
        <P>Use the following account information when sending a wire transfer: New York Federal Reserve Bank, U.S. Department of Treasury, TREAS NYC, 33 Liberty St, New York, NY 10045, Acct. No. 75060099, Routing No. 021030004, SWIFT: FRNYUS33, Beneficiary: FDA, 1350 Piccard Dr., Rockville, MD 20850.</P>
        <HD SOURCE="HD2">D. Step Four—Submit Your Application to FDA With a Copy of the Completed Medical Device User Fee Cover Sheet</HD>
        <P>Please submit your application and a copy of the completed Medical Device User Fee cover sheet to one of the following addresses:</P>
        <P>1. Medical device applications should be submitted to: Food and Drug Administration, Center for Devices and Radiological Health, Document Mail Center— WO66, rm. 0609, 10903 New Hampshire Ave., Silver Spring, MD 20993-0002.</P>
        <P>2. Biologic applications should be sent to: Food and Drug Administration, Center for Biologics Evaluation and Research, Document Control Center (HFM-99), suite 200N, 1401 Rockville Pike, Rockville, MD 20852-1448.</P>
        <HD SOURCE="HD1">VI. Procedures for Paying the Annual Fee for Periodic Reporting</HD>
        <P>As of FY 2011, you are no longer able to create a cover sheet and obtain a PIN to pay the MDUFMA Annual Fee for Periodic Reporting. Instead, you will be invoiced at the end of the quarter in which your PMA Periodic Report is due. Invoices will be sent based on the details included on your PMA file; you are responsible to ensure your billing information are kept up-to-date (you can update your contact for the PMA by submitting an amendment).</P>
        <P>1. If paying with a paper check:</P>
        <P>• All paper checks must be in U.S. currency from a U.S. bank and made payable to the Food and Drug Administration. (FDA's tax identification number is 53-0196965, should your accounting department need this information.)</P>
        <P>• Please write your invoice number.</P>
        <P>• Mail the paper check and a copy of invoice to: Food and Drug Administration, P.O. Box 956733, St. Louis, MO, 63195-6733. (Please note that this address is for payments of application and annual report fees only and is not to be used for payment of annual establishment registration fees.)</P>

        <P>If you prefer to send a check by a courier (such as Federal Express (FEDEX), DHL, United Parcel Service (UPS), etc.), the courier may deliver the check to: U.S. Bank, Attn: Government Lockbox 956733, 1005 Convention Plaza, St. Louis, MO 63101. (<E T="04">Note:</E>This address is for courier delivery only. Contact the U.S. Bank at 314-418-4821 if you have any questions concerning courier delivery.)</P>
        <P>2. If paying with a wire transfer:</P>
        <P>• Please include your invoice number in your wire transfer. Without the invoice number, your payment may not be applied and you may be referred to collections.</P>
        <P>• The originating financial institution may charge a wire transfer fee between $15 and $35. Please ask your financial institution about the fee and include it with your payment to ensure that your invoice is fully paid.</P>
        <P>Use the following account information when sending a wire transfer: New York Federal Reserve Bank, U.S. Department of Treasury, TREAS NYC, 33 Liberty St., New York, NY 10045, Acct. No. 75060099, Routing No. 021030004, SWIFT: FRNYUS33, Beneficiary: FDA, 1350 Piccard Dr., Rockville, MD 20850.</P>
        <HD SOURCE="HD1">VII. Procedures for Paying Annual Establishment Fees</HD>

        <P>In order to pay the annual establishment fee, firms must access the Device Facility User Fee (DFUF) Web site at<E T="03">https://userfees.fda.gov/OA_HTML/furls.jsp.</E>(FDA has verified the Web site address, but FDA is not responsible for any subsequent changes to the Web site after this document publishes in the<E T="04">Federal Register</E>). The Web site includes a short interactive questionnaire to help you ascertain whether an annual registration payment is required for your type of facility. If you are required to pay an annual establishment registration fee, you must pay for each establishment prior to registration. You will create a DFUF order and you will be issued a PIN once you place your order. After payment has been processed, you will be issued a payment confirmation number (PCN). You will not be able to register your establishment if you do not have a PIN and a PCN. An establishment required to pay an annual establishment registration fee is not legally registered in FY 2012 until it has completed the steps in the paragraphs that follow to register and pay any applicable fee. (See 21 U.S.C. 379j(f)(2).)</P>
        <P>Companies that do not manufacture any product other than a licensed biologic are required to register in the Blood Establishment Registration (BER) system. FDA's Center for Biologics Evaluation and Research (CBER) will send establishment registration fee invoices annually to these companies.</P>
        <HD SOURCE="HD2">A. Step One—Submit a Device Facility User Fee (DFUF) Order With a PIN From FDA Before Registering or Submitting Payment</HD>
        <P>To submit a DFUF order, you must create or have previously created a user account and password through the User Fee Web site listed previously in this section. After creating a user name and password, log into the Establishment Registration User Fee 2012 store. Complete the DFUF order by entering the number of establishments you are registering that require payment. Once you are satisfied that the data on the order is accurate, electronically transmit that data to FDA according to instructions on the screen. Print a copy of the final DFUF order and note the unique PIN located in the upper right-hand corner of the printed order.</P>
        <HD SOURCE="HD2">B. Step Two—Pay For Your Device Facility User Fee Order</HD>
        <P>Unless paying by credit card, all payments must be in U. S. currency and drawn on a U.S. bank.</P>
        <P>1. If paying with a credit card or electronic check (ACH):</P>
        <P>The DFUF order will include payment information, including details on how you can pay online using a credit card or electronic checks. Follow the instructions provided to make an electronic payment.</P>
        <P>2. If paying with a paper check:</P>

        <P>If you prefer not to pay online, you may pay by a check, in U.S. dollars and drawn on a U.S. bank, mailed to: U.S. Bank, Attn: Government Lockbox 979108, St. Louis, MO 63197-9000. (<E T="04">Note:</E>This address is different from the address for payments of application and annual report fees and is to be used only for payment of annual establishment registration fees.)</P>

        <P>If a check is sent by a courier that requests a street address, the courier can<PRTPAGE P="45831"/>deliver the check to: U.S. Bank, Attn: Government Lockbox 979108, 1005 Convention Plaza, St. Louis, MO 63101. (<E T="04">Note:</E>This U.S. Bank address is for courier delivery only; do not send mail to this address.)</P>
        <P>Please make sure that both of the following are written on your check: (1) The FDA lockbox number (Lockbox 979108) and (2) the PIN that is printed on your order. A copy of your printed order should also be mailed along with your check. FDA's tax identification number is 53-0196965.</P>
        <P>3. If paying with a wire transfer:</P>
        <P>Wire transfers may also be used to pay annual establishment fees. To send a wire transfer, please read and comply with the following information:</P>
        <P>• Include your order's unique PIN, from the upper right-hand corner of your completed Medical Device User Fee order, in your wire transfer. Without the PIN your payment may not be applied to your facility and your registration will be delayed.</P>
        <P>• The originating financial institution usually charges a wire transfer fee between $15 and $35. Please ask your financial institution about the fee and include it with your payment to ensure that your order is fully paid. Use the following account information when sending a wire transfer: New York Federal Reserve Bank, U.S. Dept of Treasury, TREAS NYC, 33 Liberty St., New York, NY 10045, Acct. No. 75060099, Routing No. 021030004, SWIFT: FRNYUS33, Beneficiary: FDA, 5600 Fishers Lane, Rockville, MD 20857.</P>
        <HD SOURCE="HD2">C. Step Three—Complete the Information Online To Update Your Establishment's Annual Registration for FY 2012, or to Register a New Establishment for FY 2012</HD>
        <P>Go to CDRH's Web site at<E T="03">http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/HowtoMarketYourDevice/RegistrationandListing/default.htm</E>and click the “Access Electronic Registration” link on the left of the page. This opens up a new page with important information about the FDA Unified Registration and Listing System (FURLS). After reading this information, click on the link (Access Electronic Registration) at the bottom of the page. This link takes you to an FDA Industry Systems page with tutorials that demonstrate how to create a new FURLS user account if your establishment did not create an account in FY 2010 or FY 2011. Biologics manufacturers should register in the BER system at<E T="03">http://www.fda.gov/BiologicsBloodVaccines/GuidanceComplianceRegulatoryInformation/EstablishmentRegistration/BloodEstablishmentRegistration/default.htm.</E>
        </P>

        <P>Enter your existing account ID and password to log into FURLS. From the FURLS/FDA Industry Systems menu, click on the Device Registration and Listing Module (DRLM) of FURLS button. New establishments will need to register and existing establishments will update their annual registration using selections on the DRLM menu. Once you choose to register or update your annual registration, the system will prompt you through the entry of information about your establishment and your devices. If you have any problems with this process, e-mail:<E T="03">reglist@cdrh.fda.gov</E>or call 301-796-7400 for assistance. (<E T="04">Note:</E>this e-mail address and this telephone number are for assistance with establishment registration only, and not for any other aspects of medical device user fees.) Problems with BER should be directed to<E T="03">bloodregis@fda.hhs.gov</E>or call 301-827-3546.</P>
        <HD SOURCE="HD2">D. Step Four—Enter Your DFUF Order PIN and PCN</HD>
        <P>After completing your annual or initial registration and device listing, you will be prompted to enter your DFUF order PIN and PCN, when applicable. This process does not apply to licensed biologic devices. CBER will send invoices for payment of the establishment registration fee to companies who only manufacture licensed biologics devices. Fees are only required for those establishments defined in section I of this document.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Leslie Kux,</NAME>
          <TITLE>Acting Assistant Commissioner for Policy.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19335 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4160-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>Food and Drug Administration</SUBAGY>
        <DEPDOC>[Docket No. FDA-2011-N-0559]</DEPDOC>
        <SUBJECT>Prescription Drug User Fee Rates for Fiscal Year 2012</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Food and Drug Administration, HHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Food and Drug Administration (FDA) is announcing the rates for prescription drug user fees for fiscal year (FY) 2012. The Federal Food, Drug, and Cosmetic Act (the FD&amp;C Act), as amended by the Prescription Drug User Fee Amendments of 2007 (Title 1 of the Food and Drug Administration Amendments Act of 2007 (FDAAA)) (PDUFA IV), authorizes FDA to collect user fees for certain applications for approval of drug and biological products, on establishments where the products are made, and on such products. Base revenue amounts to be generated from PDUFA fees were established by PDUFA IV, with provisions for certain adjustments. Fee revenue amounts for applications, establishments, and products are to be established each year by FDA so that one-third of the PDUFA fee revenues FDA collects each year will be generated from each of these categories. This document establishes fee rates for FY 2012 for application fees for an application requiring clinical data ($1,841,500), for an application not requiring clinical data or a supplement requiring clinical data ($920,750), for establishment fees ($520,100), and for product fees ($98,970). These fees are effective on October 1, 2011, and will remain in effect through September 30, 2012. For applications and supplements that are submitted on or after October 1, 2011, the new fee schedule must be used. Invoices for establishment and product fees for FY 2012 will be issued in August 2011, using the new fee schedule.</P>
        </SUM>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>David Miller, Office of Financial Management (HFA-100),  Food and Drug Administration,  1350 Picard Dr., PI50, Rm. 210J,  Rockville, MD 20850,  301-796-7103.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P/>
        <HD SOURCE="HD1">I. Background</HD>
        <P>Sections 735 and 736 of the FD&amp;C Act (21 U.S.C. 379g and 379h, respectively), establish three different kinds of user fees. Fees are assessed on the following: (1) Certain types of applications and supplements for approval of drug and biological products, (2) certain establishments where such products are made, and (3) certain products (section 736(a) of the FD&amp;C Act). When certain conditions are met, FDA may waive or reduce fees (section 736(d) of the FD&amp;C Act).</P>

        <P>For FY 2008 through FY 2012, the base revenue amounts for the total revenues from all PDUFA fees are established by PDUFA IV. The base revenue amount for FY 2008 is to be adjusted for workload, and that adjusted amount becomes the base amount for the remaining 4 FYs. That adjusted base revenue amount is increased for drug safety enhancements by $10,000,000 in each of the subsequent 4 FYs, and the increased total is further adjusted each year for inflation and workload. Fees for<PRTPAGE P="45832"/>applications, establishments, and products are to be established each year by FDA so that revenues from each category will provide one-third of the total revenue to be collected each year.</P>

        <P>This document uses the fee base revenue amount for FY 2008 published in the<E T="04">Federal Register</E>of October 12, 2007 (72 FR 58103) (the October 2007 notice); adjusts it for the FY 2009, FY 2010, FY 2011, and FY 2012 drug safety increases (see section 736(b)(4) of the FD&amp;C Act), for inflation, and for workload, for excess collections through FY 2011, and for a final year adjustment; and then establishes the application, establishment, and product fees for FY 2012. These fees are effective on October 1, 2011, and will remain in effect through September 30, 2012.</P>
        <HD SOURCE="HD1">II. Fee Revenue Amount for FY 2012</HD>
        <P>The total fee revenue amount for FY 2012 is $702,172,000, based on the fee revenue amount specified in the statute, including additional fee funding for drug safety and adjustments for inflation, changes in workload, offset for excess collections and the final year adjustment. The statutory amount and a one-time base adjustment are described in sections II.A and II.B of this document. The adjustment for inflation is described in section II.C of this document, and the adjustment for changes in workload in section II.D of this document. The adjustment for estimated excess collections through FY 2012 is described in section III of this document, and the final year adjustment is described in section IV of this document.</P>
        <HD SOURCE="HD2">A. FY 2012 Statutory Fee Revenue Amounts Before Adjustments</HD>
        <P>PDUFA IV specifies that the fee revenue amount before adjustments for FY 2012 for all fees is $457,783,000 ($392,783,000 specified in section 736(b)(1) of the FD&amp;C Act plus an additional $65,000,000 for drug safety in FY 2012 specified in section 736(b)(4)).</P>
        <HD SOURCE="HD2">B. Base Adjustment to Statutory Fee Revenue Amount</HD>
        <P>The statute also specifies that $354,893,000 of the base amount is to be further adjusted for workload increases through FY 2007 (see section 736(b)(1)(B) of the FD&amp;C Act). The workload adjustment on this amount is to be made in accordance with the workload adjustment provisions that were in effect for FY 2007, except that the adjustment for investigational new drug (IND) workload is based on the number of INDs with a submission in the previous 12 months rather than on the number of new commercial INDs submitted in the same 12-month period. This adjustment was explained in detail in the October 2007 notice. Increasing the statutorily specified amount of $354,893,000 by the specified workload adjuster (11.73 percent) results in an increase of $41,629,000, rounded to the nearest thousand. Adding this amount to the $457,783,000 statutorily specified amount from section II.A of this document, results in a total adjusted PDUFA IV base revenue amount of $499,412,000, before further adjustment for inflation and changes in workload after FY 2007.</P>
        <HD SOURCE="HD2">C. Inflation Adjustment to FY 2012 Fee Revenue Amount</HD>
        <P>PDUFA IV provides that fee revenue amounts for each FY after FY 2008 shall be adjusted for inflation. The adjustment must reflect the greater of the following amounts: (1) The total percentage change that occurred in the Consumer Price Index (CPI) (all items; U.S. city average) during the 12-month period ending June 30 preceding the FY for which fees are being set; (2) the total percentage pay change for the previous FY for Federal employees stationed in the Washington, DC metropolitan area; or (3) the average annual change in cost, per FDA full time equivalent (FTE), of all personnel compensation and benefits paid for the first 5 of the previous 6 FYs. PDUFA IV provides for this annual adjustment to be cumulative and compounded annually after FY 2008 (see section 736(c)(1) of the FD&amp;C Act).</P>

        <P>The first factor is the CPI increase for the 12-month period ending in June 2011. The CPI for June 2011 was 225.722 and the CPI for June 2010 was 217.965. (These CPI figures are available on the Bureau of Labor Statistics (BLS) Web site at<E T="03">http://data.bls.gov/cgi-bin/surveymost?bls</E>by checking the first box under “Price Indexes” and then clicking “Retrieve Data” at the bottom of the page. FDA has verified the Web site address, but FDA is not responsible for any subsequent changes to the Web site after this document publishes in the<E T="04">Federal Register.</E>) The CPI for June 2011 is 3.559 percent higher than the CPI for the previous 12-month period.</P>

        <P>The second factor is the increase in pay for the previous FY (FY 2011 in this case) for Federal employees stationed in the Washington, DC metropolitan area. This figure is published by the Office of Personnel Management (OPM), and found on their Web site at<E T="03">http://www.opm.gov/oca/11tables/html/dcb.asp</E>above the salary table. (FDA has verified the Web site address, but FDA is not responsible for any subsequent changes to the Web site after this document publishes in the<E T="04">Federal Register.</E>) For FY 2011 it was 0.00 percent.</P>
        <P>The third factor is the average change in FDA cost for compensation and benefits per FTE over the previous 5 of the most recent 6 FYs (FY 2006 through FY 2010). The data on total compensation paid and numbers of FTE paid, from which the average cost per FTE can be derived, are published in FDA's Justification of Estimates for Appropriations Committees. Table 1 of this document summarizes that actual cost and FTE use data for the specified FYs, and provides the percent change from the previous FY and the average percent change over the most 5 recent FYs, which is 3.72 percent.</P>
        <GPOTABLE CDEF="s60,14,14,14,14,14,14" COLS="7" OPTS="L2,i1">
          <TTITLE>Table 1—FDA Personnel Compensation and Benefits (PC&amp;B) Each Year and Percent Change</TTITLE>
          <BOXHD>
            <CHED H="1"/>
            <CHED H="1">FY2006</CHED>
            <CHED H="1">FY2007</CHED>
            <CHED H="1">FY2008</CHED>
            <CHED H="1">FY2009</CHED>
            <CHED H="1">FY2010</CHED>
            <CHED H="1">Annual average increase for<LI>latest 5 years</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Total PC&amp;B</ENT>
            <ENT>$1,114,704,000</ENT>
            <ENT>$1,144,369,000</ENT>
            <ENT>$1,215,627,000</ENT>
            <ENT>$1,464,445,000</ENT>
            <ENT>$1,634,108,000</ENT>
            <ENT/>
          </ROW>
          <ROW>
            <ENT I="01">Total FTE</ENT>
            <ENT>9,698</ENT>
            <ENT>9,569</ENT>
            <ENT>9,811</ENT>
            <ENT>11,413</ENT>
            <ENT>12,256</ENT>
            <ENT/>
          </ROW>
          <ROW>
            <ENT I="01">PC&amp;B per FTE</ENT>
            <ENT>$114,942</ENT>
            <ENT>$119,591</ENT>
            <ENT>$123,905</ENT>
            <ENT>$128,314</ENT>
            <ENT>$130,457</ENT>
            <ENT/>
          </ROW>
          <ROW>
            <ENT I="01">Percent Change from Previous Year</ENT>
            <ENT>5.70</ENT>
            <ENT>4.05</ENT>
            <ENT>3.61</ENT>
            <ENT>3.56</ENT>
            <ENT>1.67</ENT>
            <ENT>3.72</ENT>
          </ROW>
        </GPOTABLE>

        <P>The inflation increase for FY 2012 is 3.72 percent. This is the greater of the CPI change during the 12-month period ending June 30 preceding the FY for which fees are being set (3.559 percent), the increase in pay for the previous FY (FY 2011 in this case) for Federal employees stationed in the Washington, DC metropolitan area (0.00 percent), and<PRTPAGE P="45833"/>the average annual change in cost, per FDA FTE, of all personnel compensation and benefits paid for the first 5 of the previous 6 FYs (3.72 percent). Because the average change in pay per FTE (3.72 percent) is the highest of the three factors, it becomes the inflation adjustment for total fee revenue for FY 2012.</P>
        <P>The inflation adjustment for FY 2009 was 5.64 percent. This is the greater of the CPI increase during the 12-month period ending June 30 preceding the FY for which fees were being set (June 30, 2008, which was 5.05 percent), the increase in pay for FY 2008 for Federal employees stationed in Washington, DC (4.49 percent), or the average annual change in cost, per FDA FTE, of all personnel compensation and benefits paid for the first 5 of the previous 6 FYs (5.64 percent).</P>
        <P>The inflation adjustment for FY 2010 was 5.54 percent. This is the greater of the CPI increase during the 12-month period ending June 30 preceding the FY for which fees were being set (June 30, 2009) (negative 1.43 percent), the increase in pay for FY 2009 for Federal employees stationed in Washington, DC (4.78 percent), or the average annual change in cost, per FDA FTE, of all personnel compensation and benefits paid for the first 5 of the previous 6 FYs (5.54 percent).</P>
        <P>The inflation adjustment for FY 2011 was 4.53 percent. This is the greater of the CPI increase during the 12-month period ending June 30 preceding the FY for which fees were being set (June 30, 2010) (1.053 percent), the increase in pay for FY 2010 for Federal employees stationed in Washington, DC (2.42 percent), or the average annual change in cost, per FDA FTE, of all personnel compensation and benefits paid for the first 5 of the previous 6 FYs (4.53 percent).</P>
        <P>PDUFA IV provides for this inflation adjustment to be cumulative and compounded annually after FY 2008 (see section 736(c)(1) of the FD&amp;C Act). This factor for FY 2012 (3.72 percent) is compounded by adding one to it and then multiplying it by one plus the inflation adjustment factor for FY 2011 (4.53 percent) and by one plus the inflation adjustment factor for FY 2010 (5.54 percent) and by one plus the inflation adjustment factor for FY 2009 (5.64 percent). The result of this multiplication of the inflation factors for the 4 years since FY 2008 (1.0372 times 1.0453 times 1.0554 times 1.0564 percent) becomes the inflation adjustment for FY 2012. This inflation adjustment for FY 2012 is 20.88 percent.</P>
        <P>Increasing the FY 2012 fee revenue base of $499,412,000, by 20.88 percent yields an inflation-adjusted fee revenue amount for FY 2012 of $603,689,000, rounded to the nearest thousand dollars, before the application of the FY 2012 workload adjustment.</P>
        <HD SOURCE="HD2">D. Workload Adjustment to the FY 2012 Inflation Adjusted Fee Revenue Amount</HD>

        <P>PDUFA IV does not allow FDA to adjust the total revenue amount for workload beginning in FY 2010, unless an independent accounting firm study is complete (see section 736(c)(2)(C) of the FD&amp;C Act). That study, conducted by Deloitte Touche, LLP, was completed on March 31, 2009, and is available online at<E T="03">http://www.fda.gov/ForIndustry/UserFees/PrescriptionDrugUserFee/ucm164339.htm.</E>The study found that the adjustment methodology used by FDA reasonably captures changes in workload for reviewing human drug applications under PDUFA IV. Accordingly, FDA continues to use the workload adjustment methodology prescribed in PDUFA IV.</P>
        <P>For each fiscal year beginning in FY 2009, PDUFA IV provides that fee revenue amounts, after they have been adjusted for inflation, shall be further adjusted to reflect changes in workload for the process for the review of human drug applications (see section 736(c)(2) of the FD&amp;C Act). PDUFA IV continues the Prescription Drug User Fee Amendments of 2002 (PDUFA III) workload adjustment with modifications, and provides for a new additional adjustment for changes in review activity.</P>
        <P>FDA calculated the average number of each of the four types of applications specified in the workload adjustment provision: (1) Human drug applications, (2) active commercial INDs (applications that have at least one submission during the previous 12 months), (3) efficacy supplements, and (4) manufacturing supplements received over the 5-year period that ended on June 30, 2007 (base years), and the average number of each of these types of applications over the most recent 5-year period that ended June 30, 2011.</P>
        <P>The calculations are summarized in table 2 of this document. The 5-year averages for each application category are provided in Column 1 (“5-Year Average Base Years 2002-2007”) and Column 2a (“5-Year Average 2007-2011”).</P>
        <P>PDUFA IV specifies that FDA make additional adjustments for changes in review activities to human drug applications and active commercial INDs. These adjustments, specified under PDUFA IV, are summarized in columns 2b and 2c in table 2 of this document. The number in the new drug applications/biologics license applications (NDAs/BLAs) line of column 2b of table 2 of this document is the percent by which the average workload for meetings, annual reports, and labeling supplements for NDAs and BLAs has changed from the 5-year period 2002 through 2007, to the 5-year period 2007 through 2011. Likewise, the number in the “Active commercial INDs” line of column 2b of table 2 of this document is the percent by which the workload for meetings and special protocol assessments for active commercial INDs has changed from the 5-year period 2002 through 2007, to the 5-year period 2007 through 2011. There is no entry in the last two lines of column 2b because the adjustment for changes in review workload does not apply to the workload for efficacy supplements and manufacturing supplements.</P>

        <P>Column 3 of table 2 of this document reflects the percent change in workload from column 1 to column 2c. Column 4 of table 2 of this document shows the weighting factor for each type of application, estimating how much of the total FDA drug review workload was accounted for by each type of application in the table during the most recent 5 years. Column 5 of table 2 of this document is the weighted percent change in each category of workload. This was derived by multiplying the weighting factor in each line in column 4 by the percent change from the base years in column 3. At the bottom right of table 2 of this document is the sum of the values in column 5 that are added, reflecting an increase in workload of 8.12 percent for FY 2012 when compared to the base years.<PRTPAGE P="45834"/>
        </P>
        <GPOTABLE CDEF="s60,9.2,9.1,10,9.1,10,10,10" COLS="8" OPTS="L2,i1">
          <TTITLE>Table 2—Workload Adjuster Calculation for FY 2012</TTITLE>
          <BOXHD>
            <CHED H="1">Application type</CHED>
            <CHED H="1">Column 1<LI>5-year</LI>
              <LI>average base years</LI>
              <LI>2002-2007</LI>
            </CHED>
            <CHED H="1">Column 2a<LI>5-year</LI>
              <LI>average</LI>
              <LI>2007-2011</LI>
            </CHED>
            <CHED H="1">Column 2b<LI>Adjustment for changes in review activity</LI>
            </CHED>
            <CHED H="1">Column 2c<LI>(Column 2a increased by column 2b)</LI>
            </CHED>
            <CHED H="1">Column 3<LI>Percent change</LI>
              <LI>(column 1 to column 2c)</LI>
            </CHED>
            <CHED H="1">Column 4<LI>Weighting factor</LI>
            </CHED>
            <CHED H="1">Column 5<LI>Weighted percent change</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">NDAs/BLAs</ENT>
            <ENT>123.8</ENT>
            <ENT>130.8</ENT>
            <ENT>−0.01%</ENT>
            <ENT>130.8</ENT>
            <ENT>5.6%</ENT>
            <ENT>35.3%</ENT>
            <ENT>1.99%</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Active commercial INDs</ENT>
            <ENT>5,528.2</ENT>
            <ENT>6520.6</ENT>
            <ENT>−2.41</ENT>
            <ENT>6363.2</ENT>
            <ENT>15.1</ENT>
            <ENT>42.4</ENT>
            <ENT>6.40</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Efficacy supplements</ENT>
            <ENT>163.4</ENT>
            <ENT>157.4</ENT>
            <ENT>NA</ENT>
            <ENT>157.4</ENT>
            <ENT>−3.7</ENT>
            <ENT>9.9</ENT>
            <ENT>−0.36</ENT>
          </ROW>
          <ROW RUL="n,s">
            <ENT I="01">Manufacturing supplements</ENT>
            <ENT>2589.2</ENT>
            <ENT>2606.8</ENT>
            <ENT>NA</ENT>
            <ENT>2606.8</ENT>
            <ENT>0.7</ENT>
            <ENT>12.4</ENT>
            <ENT>0.08</ENT>
          </ROW>
          <ROW>
            <ENT I="03">FY 2012 Workload Adjuster</ENT>
            <ENT/>
            <ENT/>
            <ENT/>
            <ENT/>
            <ENT/>
            <ENT/>
            <ENT>8.12</ENT>
          </ROW>
        </GPOTABLE>
        <P>The FY 2012 workload adjuster reflected in the calculations in table 3 of this document is 8.12 percent. Therefore the inflation-adjusted revenue amount of $603,689,000 from section II.C of this document will be increased by the FY 2012 workload adjuster of 8.12 percent, resulting in a total adjusted revenue amount in FY 2012 of $652,709,000, rounded to the nearest thousand dollars.</P>
        <HD SOURCE="HD2">E. Rent and Rent-Related Adjustment to the FY 2011 Adjusted Fee Revenue Amount</HD>
        <P>PDUFA specifies that for FY 2010 and each subsequent FY, the revenue amount will be decreased if the actual cost paid for rent and rent-related expenses for preceding FYs are less than estimates made for such FYs in FY 2006 (see section 736(c)(3) of the FD&amp;C Act). Table 3 of this document shows the estimates of rent and rent-related costs for FY 2008 through FY 2010 made in 2006 and the actual costs for these 3 FYs, the only FYs for which complete data are available at this time.</P>
        <GPOTABLE CDEF="s25,11,11,11,12,11,11,11,12" COLS="9" OPTS="L2,p7,7/8,i1">
          <TTITLE>Table 3—Comparison of Actual and Estimated Rent and Rent-Related Expenses for the Center for Drug Evaluation and Research (CDER) and the Center for Biologics Evaluation and Research (CBER)</TTITLE>
          <BOXHD>
            <CHED H="1"/>
            <CHED H="1">Estimates made in 2006</CHED>
            <CHED H="2">FY 2008</CHED>
            <CHED H="2">FY 2009</CHED>
            <CHED H="2">FY 2010</CHED>
            <CHED H="2">Total</CHED>
            <CHED H="1">Actual amounts paid</CHED>
            <CHED H="2">FY 2008</CHED>
            <CHED H="2">FY 2009</CHED>
            <CHED H="2">FY 2010</CHED>
            <CHED H="2">Total</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">CDER</ENT>
            <ENT>$46,732,000</ENT>
            <ENT>$40,415,000</ENT>
            <ENT>$41,589,000</ENT>
            <ENT>$128,736,000</ENT>
            <ENT>$51,619,000</ENT>
            <ENT>$64,687,250</ENT>
            <ENT>$58,049,000</ENT>
            <ENT>$174,355,250</ENT>
          </ROW>
          <ROW RUL="n,s">
            <ENT I="01">CBER</ENT>
            <ENT>22,295,000</ENT>
            <ENT>23,067,000</ENT>
            <ENT>25,652,000</ENT>
            <ENT>71,014,000</ENT>
            <ENT>26,715,000</ENT>
            <ENT>26,966,750</ENT>
            <ENT>27,815,000</ENT>
            <ENT>81,496,750</ENT>
          </ROW>
          <ROW>
            <ENT I="03">Total</ENT>
            <ENT>69,027,000</ENT>
            <ENT>63,482,000</ENT>
            <ENT>67,241,000</ENT>
            <ENT>199,750,000</ENT>
            <ENT>78,334,000</ENT>
            <ENT>91,654,000</ENT>
            <ENT>85,864,000</ENT>
            <ENT>255,852,000</ENT>
          </ROW>
        </GPOTABLE>
        <P>Because FY 2008 through FY 2010 costs for rent and rent-related items in total ($255,852,000) exceeded the estimates of these costs made in FY 2006 ($199,750,000), no decrease in the FY 2012 estimated PDUFA revenues is required under this provision of PDUFA.</P>
        <HD SOURCE="HD1">III. Offset for Excess Collections Through FY 2011</HD>
        <P>Under the provisions of PDUFA III, which applies to user fees collected for FY 2002 through FY 2007, if the amount of fees collected for a FY exceeds the amount of fees specified in appropriation acts for that FY, the excess amount shall be credited to FDA's appropriation account and shall be subtracted from the amount of fees that would otherwise be authorized to be collected in a subsequent FY (See 21 U.S.C. 379h(g)(4) as amended by PDUFA III). In setting PDUFA fees for FY 2007 in August of 2006, some offsets were made under these provisions, but some offsets still need to be made based on final collection data for that period. Table 4 shows the amount of fees specified in FDA's annual appropriation for each year from FY 2003 through FY 2007; the amounts FDA has collected for each year; the amount of offset previously taken; and the cumulative difference. FDA will take this difference as an offset against FY 2012 fee collections.</P>
        <GPOTABLE CDEF="s50,12,12,12,12" COLS="5" OPTS="L2,i1">
          <TTITLE>Table 4—Offsets Remaining To Be Taken for PDUFA III, FY 2003-2007</TTITLE>
          <BOXHD>
            <CHED H="1">Fiscal year</CHED>
            <CHED H="1">Fees<LI>appropriated</LI>
            </CHED>
            <CHED H="1">Fees collected</CHED>
            <CHED H="1">Excess collections offset under section 736(g)(4) of the FD&amp;C Act when 2007 fees were set</CHED>
            <CHED H="1">Remaining<LI>excess</LI>
              <LI>collections</LI>
              <LI>to be offset</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">2003</ENT>
            <ENT>$222,900,000</ENT>
            <ENT>$218,302,684</ENT>
            <ENT/>
            <ENT/>
          </ROW>
          <ROW>
            <ENT I="01">2004</ENT>
            <ENT>249,825,000</ENT>
            <ENT>258,333,700</ENT>
            <ENT>$7,230,906</ENT>
            <ENT>$1,277,794</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2005</ENT>
            <ENT>284,394,000</ENT>
            <ENT>287,178,231</ENT>
            <ENT/>
            <ENT>2,784,231</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2006</ENT>
            <ENT>305,332,000</ENT>
            <ENT>313,514,278</ENT>
            <ENT/>
            <ENT>8,209,278</ENT>
          </ROW>
          <ROW RUL="n,s">
            <ENT I="01">2007</ENT>
            <ENT>352,200,000</ENT>
            <ENT>370,934,966</ENT>
            <ENT/>
            <ENT>18,734,966</ENT>
          </ROW>
          <ROW>
            <ENT I="03">Cumulative difference to be offset against FY 2012 collections</ENT>
            <ENT/>
            <ENT/>
            <ENT/>
            <ENT>30,974,959</ENT>
          </ROW>
        </GPOTABLE>
        <PRTPAGE P="45835"/>
        <P>In addition, under the provisions of PDUFA, as amended by PDUFA IV, if the sum of the cumulative amount of the fees collected for FY 2008 through 2010, and the amount of fees estimated to be collected under this section III of the document for FY 2011, exceeds the cumulative amount appropriated for fees for FYs 2008 through 2011, the excess will be credited to FDA's appropriation account and subtracted from the amount of fees that FDA would otherwise be authorized to collect for FY 2012 under the FD&amp;C Act (21 U.S.C. 379h(g)(4) as amended by PDUFA IV).</P>

        <P>Table 5 of this document shows the amounts specified in appropriation acts for each year from FY 2008 through FY 2011, and the amounts FDA has collected for FYs 2008, 2009, and 2010 as of March 31, 2011, and the amount that FDA estimated it would collect in FY 2011 when it published the notice of FY 2011 fees in the<E T="04">Federal Register</E>on August 4, 2010 (75 FR 46956). In FY 2011, application fee revenues to date are less than anticipated when fees were set in August 2010. The bottom line of table 5 of this document shows the estimated cumulative difference between fee amounts specified in appropriation acts for FY 2008 through FY 2011 and PDUFA fee amounts collected.</P>
        <GPOTABLE CDEF="s50,12,12,12" COLS="4" OPTS="L2,i1">
          <TTITLE>Table 5—Offsets To Be Taken for the PDUFA IV Period, FY 2008-2011 for FY 2008-2010, Fees Collected Through 3/31/2011; for FY 2011, Estimate as of 3/31/2011</TTITLE>
          <BOXHD>
            <CHED H="1">Fiscal year</CHED>
            <CHED H="1">Fees appropriated</CHED>
            <CHED H="1">Fees collected</CHED>
            <CHED H="1">Difference</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">2008</ENT>
            <ENT>$459,412,000</ENT>
            <ENT>$479,582,086</ENT>
            <ENT>$20,170,086</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2009</ENT>
            <ENT>510,665,000</ENT>
            <ENT>521,496,042</ENT>
            <ENT>10,831,042</ENT>
          </ROW>
          <ROW>
            <ENT I="01">2010</ENT>
            <ENT>578,162,000</ENT>
            <ENT>567,877,548</ENT>
            <ENT>(10,284,452)</ENT>
          </ROW>
          <ROW RUL="n,s">
            <ENT I="01">2011 estimate</ENT>
            <ENT>667,057,000</ENT>
            <ENT>619,070,000</ENT>
            <ENT>(47,987,000)</ENT>
          </ROW>
          <ROW>
            <ENT I="03">Cumulative difference</ENT>
            <ENT/>
            <ENT/>
            <ENT>(27,270,324)</ENT>
          </ROW>
        </GPOTABLE>
        <P>The cumulative fees collected for FYs 2008 through 2011 are estimated to be more than $27 million less than the cumulative fee amounts specified in appropriation acts during this same period. Under section 736(g)(4) of the FD&amp;C Act, an offset is only made if the cumulative fees collected exceed cumulative fee appropriations for this period. Accordingly, there will be no offset of fees attributable to the PDUFA IV period of FYs 2008 through 2012. The only offset will be for the $30,974,959 for the PDUFA III period. Reducing the inflation and workload adjusted estimate of total revenue of $652,709,000 by the PDUFA III offset of $30,975,000 (rounded to the nearest thousand dollars) results in a revenue estimate of $621,734,000, before the final year adjustment.</P>
        <HD SOURCE="HD1">IV. Final Year Adjustment</HD>
        <P>Under the provisions of PDUFA, as amended, the Secretary of Health and Human Services may, in addition to the inflation and workload adjustments, further increase the fees and fee revenues if such an adjustment is necessary to provide for not more than 3 months of operating reserves of carryover user fees for the process for the review of human drug applications for the first 3 months of FY 2013. The rationale for the amount of this increase shall be contained in the annual notice establishing fee revenues and fees for FY 2012 (see 21 U.S.C. 379h(c)(4)).</P>
        <GPOTABLE CDEF="s100,12" COLS="2" OPTS="L2,p1,8/9,i1">
          <TTITLE>Table 6—Estimated Carryover Balance at the End of FY 2012, After Deduction of Estimated FY 2011-2012 Operating Costs</TTITLE>
          <BOXHD>
            <CHED H="1"/>
            <CHED H="1"/>
          </BOXHD>
          <ROW>
            <ENT I="01">Total carryover balance end of FY 2010</ENT>
            <ENT>$150,611,598</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Used for offset in 2012</ENT>
            <ENT>30,975,000</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Used for additional 53 FTE (FDAAA drug safety), FY 2011-2012</ENT>
            <ENT>29,771,000</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Reserve for refunds</ENT>
            <ENT>2,500,000</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Used for CBER move to White Oak</ENT>
            <ENT>37,896,000</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Used to cover 2011 estimated revenue shortfalls</ENT>
            <ENT>8,382,000</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Used to cover 2012 estimated revenue shortfalls</ENT>
            <ENT>8,694,000</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Estimated 2012 end of FY carryover balance</ENT>
            <ENT>32,393,598</ENT>
          </ROW>
        </GPOTABLE>
        <P>As of September 30, 2010, FDA had cash carryover balances of $150,611,598. However, of this amount, a total of $30,975,000 will be used to cover the cost of the reduction in fee revenue that will result from the offset in fees for excess collections during PDUFA III. A total of $29,771,000 will be used in FY 2011 and FY 2012 to cover the cost of additional FTEs allocated in FY 2009 to address increased PDUFA workload associated with new drug safety provisions under FDAAA. A total of $2,500,000 is not available to FDA to obligate because it represents the minimum amount FDA will need to keep in reserve for refunds that will need to be made. A total of $37,896,000 is expected to be used for the CBER move to the White Oak campus in FY 2012-2014. Based on FDA's experience in FY 2010 when about 17 fewer paid full application fees were received by FDA than expected, causing a revenue shortfall, FDA is assuming that about 5.5 fewer full applications will be received in both FY 2011 and FY 2012, resulting in shortfalls of over $8,382,000 and $8,694,000 each year, respectively, that will have to be covered from the carryover balances. Thus the amount of carry-over balance FDA expects to be available for obligation at the end of FY 2012 is $32,393,598, as shown in the last line of table 6 of this document.</P>
        <GPOTABLE CDEF="s100,12" COLS="2" OPTS="L2,p1,8/9,i1">
          <TTITLE>Table 7—Estimated Fee Revenue Needed To Sustain FY 2012 Operations for the First 3 Months of FY 2013</TTITLE>
          <BOXHD>
            <CHED H="1"/>
            <CHED H="1"/>
          </BOXHD>
          <ROW>
            <ENT I="01">Estimated total spending from fees in FY 2012</ENT>
            <ENT>$652,709,000</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Estimated FY 2013 inflation costs at 3.72%</ENT>
            <ENT>24,280,775</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Estimated FY 2013 funds to sustain FY 2012 operations</ENT>
            <ENT>676,989,755</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Estimated fees needed for 3 months in FY 2013</ENT>
            <ENT>169,247,444</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Estimated end-of-FY 2012 carryover balance</ENT>
            <ENT>32,393,598</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Additional revenue needed for 3 months in FY 2013</ENT>
            <ENT>136,854,000</ENT>
          </ROW>
        </GPOTABLE>

        <P>In FY 2012, FDA expects to spend a total of $652,709,000, as noted at the end of section III of this document. To sustain current operations in FY 2012, with an anticipated inflation rate of 3.72 percent, FDA expects to obligate a total of $676,989,775 in FY 2013—or a total of about $169,247,444 during the first 3 months of FY 2013. The available<PRTPAGE P="45836"/>carryover balance at the beginning of FY 2013 is estimated at $32,393,598. Thus FDA would need an additional $136,854,000 ($169,247,444 minus $32,393,598, rounded to the nearest thousand dollars) as the final year adjustment to assure sufficient operating reserves for the first 3 months of FY 2013.</P>
        <P>FDA recognizes that adding $136,854,000 to the fee revenue costs in FY 2012 poses a substantial burden on the regulated industry at a time when it is undergoing significant financial strain. In light of this, and in light of the fact that the legislative language authorizing the final year adjustment allows FDA discretion in whether to make this adjustment for a full 3 months of operating reserves or for a shorter period, FDA has decided to balance its own risks with the amount of burden the final year adjustment will place on the industry. In making this decision, FDA has decided to assume more risk, making the final year adjustment to allow for only 2 months of operating reserves instead of for 3 months of operating reserves. Accordingly FDA will make the final year adjustment for a lesser amount, as derived in table 8 of this document.</P>
        <GPOTABLE CDEF="s100,15" COLS="2" OPTS="L2,p1,8/9">
          <TTITLE>Table 8—Estimated Fee Revenue Needed To Sustain FY 2012 Operations for the First 2 Months of FY 2013</TTITLE>
          <BOXHD>
            <CHED H="1"/>
            <CHED H="1"/>
          </BOXHD>
          <ROW>
            <ENT I="01">Estimated total spending from fees in FY 2012</ENT>
            <ENT>$652,709,000</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Estimated FY 2013 inflation costs at 3.72%</ENT>
            <ENT>24,280,775</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Estimated 2013 funds to sustain 2012 operations</ENT>
            <ENT>676,989,775</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Estimated fees needed for 2 months in FY 2013</ENT>
            <ENT>112,831,629</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Estimated 2012 end of FY carryover balance</ENT>
            <ENT>32,393,598</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Additional revenue needed for 2 months in 2013</ENT>
            <ENT>80,438,031</ENT>
          </ROW>
        </GPOTABLE>
        <P>Rounding this amount to the nearest thousand dollars results in a final year adjustment of $80,438,000. Adding this amount to the total of $621,743,000, the total after the offset adjustment at the end of section III of this document, results in a total revenue target of $702,172,000, rounded to the nearest thousand dollars, for FY 2012.</P>
        <P>PDUFA specifies that one-third of the total fee revenue is to be derived from application fees, one-third from establishment fees, and one-third from product fees (see section 736(b)(2) of the FD&amp;C Act). Accordingly, one-third of the total revenue amount (rounded to the nearest thousand dollars), or a total of $234,057,000 is the total amount of fee revenue that will be derived from each of these fee categories: Application Fees, Establishment Fees, and Product Fees.</P>

        <P>While the fee revenue amount anticipated in FY 2012 is $702,172,000, as the previous paragraph shows, FDA assumes that the fee appropriation for FY 2012 will be 5 percent higher, or $737,281,000, rounded to the nearest thousand dollars. The PDUFA IV 5-Year Financial Plan, (which can be found at<E T="03">http://www.fda.gov/ForIndustry/UserFees/PrescriptionDrugUserFee/ucm153456.htm</E>) states in Assumption 14 (Fee Revenue and Annual Appropriation Amount) that the PDUFA workload adjuster is a lagging adjustment dampened by averages over five years, and will not help FDA keep up with workload if there are sudden increases in the number of applications to be reviewed in the current fiscal year. Appropriated amounts for PDUFA fee revenue each year are estimated at 5 percent higher than estimated fee revenues for each year, to provide FDA with the ability to cope with surges in application review workload should that occur. If FDA collects less than the fee estimate at the beginning of the year and less than the fee appropriation, then collections rather than appropriations set the upper limit on how much FDA may actually keep and spend. If, however, FDA collects more than fee estimates at the beginning of the year, due to a workload surge, a slightly higher fee appropriation will permit FDA to keep and spend the higher collections in order to respond to a real surge in review workload that caused the increased collections—an unexpected increase in the number of applications that FDA must review in accordance with PDUFA goals. For this reason, in most FY since 1993, actual appropriations have slightly exceeded PDUFA fee revenue estimates made each year.</P>
        <HD SOURCE="HD1">V. Application Fee Calculations</HD>
        <HD SOURCE="HD2">A. Application Fee Revenues and Application Fees</HD>
        <P>Application fees will be set to generate one-third of the total fee revenue amount, or $234,057,000, in FY 2012, as calculated previously in this document.</P>
        <HD SOURCE="HD2">B. Estimate of the Number of Fee-Paying Applications and the Establishment of Application Fees</HD>
        <P>For FY 2008 through FY 2012, FDA will estimate the total number of fee-paying full application equivalents (FAEs) it expects to receive the next FY by averaging the number of fee-paying FAEs received in the 5 most recent fiscal years. Using a rolling average of the 5 most recent fiscal years is the same method that has been applied for the last 8 years.</P>
        <P>In estimating the number of fee-paying FAEs that FDA will receive in FY 2012, the 5-year rolling average for the most recent 5 years will be based on actual counts of fee-paying FAEs received for FY 2007 through FY 2011. For FY 2011, FDA is estimating the number of fee-paying FAEs for the full year based on the actual count for the first 9 months and estimating the number for the final 3 months, as we have done for the past 8 years.</P>

        <P>Table 9 of this document shows, in column 1, the total number of each type of FAE received in the first 9 months of FY 2011, whether fees were paid or not. Column 2 shows the number of FAEs for which fees were waived or exempted during this period, and column 3 shows the number of fee-paying FAEs received through June 30, 2011. Column 4 estimates the 12-month total fee-paying FAEs for FY 2011 based on the applications received through June 30, 2011. All of the counts are in FAEs. A full application requiring clinical data counts as one FAE. An application not requiring clinical data counts as one-half an FAE, as does a supplement requiring clinical data. An application that is withdrawn, or refused for filing, counts as one-fourth of an FAE if the applicant initially paid a full application fee, or one-eighth of an FAE if the applicant initially paid one-half of the full application fee amount.<PRTPAGE P="45837"/>
        </P>
        <GPOTABLE CDEF="s60,6.3,7.2,6.3,7.2" COLS="5" OPTS="L2,i1">
          <TTITLE>Table 9—FY 2011 Full Application Equivalents Received Through June 30, 2011, and Projected Through September 30, 2011</TTITLE>
          <BOXHD>
            <CHED H="1"/>
            <CHED H="1">Column 1<LI>Total</LI>
              <LI>received through</LI>
              <LI>6/30/2011</LI>
            </CHED>
            <CHED H="1">Column 2<LI>Fees exempted or waived through</LI>
              <LI>6/30/2011</LI>
            </CHED>
            <CHED H="1">Column 3<LI>Total fee paying through</LI>
              <LI>6/30/2011</LI>
            </CHED>
            <CHED H="1">Column 4<LI>12-Month fee paying projection</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Applications requiring clinical data</ENT>
            <ENT>55</ENT>
            <ENT>18</ENT>
            <ENT>37</ENT>
            <ENT>49.33</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Applications not requiring clinical data</ENT>
            <ENT>9.5</ENT>
            <ENT>5.5</ENT>
            <ENT>4</ENT>
            <ENT>5.33</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Supplements requiring clinical data</ENT>
            <ENT>44.5</ENT>
            <ENT>9</ENT>
            <ENT>35.5</ENT>
            <ENT>47.88</ENT>
          </ROW>
          <ROW RUL="n,s">
            <ENT I="01">Withdrawn or refused to file</ENT>
            <ENT>1.625</ENT>
            <ENT>1.25</ENT>
            <ENT>.375</ENT>
            <ENT>.5</ENT>
          </ROW>
          <ROW>
            <ENT I="03">Total</ENT>
            <ENT>110.625</ENT>
            <ENT>33.75</ENT>
            <ENT>76.875</ENT>
            <ENT>102.5</ENT>
          </ROW>
        </GPOTABLE>
        <P>In the first 9 months of FY 2011, FDA received 110.625 FAEs, of which 76.875 were fee-paying. Based on data from the last 10 FYs, on average, 25 percent of the applications submitted each year come in the final 3 months. Dividing 76.875 by 3 and multiplying by 4 extrapolates the amount to the full 12 months of the FY and projects the number of fee-paying FAEs in FY 2011 at 102.5.</P>
        <P>As table 10 of this document shows, the average number of fee-paying FAEs received annually in the most recent 5-year period, and including our estimate for FY 2011, is 127.1 FAEs. FDA will set fees for FY 2011 based on this estimate as the number of full application equivalents that will pay fees.</P>
        <GPOTABLE CDEF="s50,10C,10C,10C,10C,10C,10C" COLS="7" OPTS="L2,i1">
          <TTITLE>Table 10—Fee-Paying FAE 5-Year Average</TTITLE>
          <BOXHD>
            <CHED H="1">Fiscal year</CHED>
            <CHED H="1">2007</CHED>
            <CHED H="1">2008</CHED>
            <CHED H="1">2009</CHED>
            <CHED H="1">2010</CHED>
            <CHED H="1">2011<LI>estimate</LI>
            </CHED>
            <CHED H="1">5-Year<LI>average</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Fee-Paying FAEs</ENT>
            <ENT>134.4</ENT>
            <ENT>140.0</ENT>
            <ENT>140.3</ENT>
            <ENT>118.4</ENT>
            <ENT>102.5</ENT>
            <ENT>127.1</ENT>
          </ROW>
        </GPOTABLE>
        <P>The FY 2012 application fee is estimated by dividing the average number of full applications that paid fees over the latest 5 years, 127.1, into the fee revenue amount to be derived from application fees in FY 2012, $234,057,000. The result, rounded to the nearest $100, is a fee of $1,841,500 per full application requiring clinical data, and $920,750 per application not requiring clinical data or per supplement requiring clinical data.</P>
        <HD SOURCE="HD1">VI. Fee Calculations for Establishment and Product Fees</HD>
        <HD SOURCE="HD2">A. Establishment Fees</HD>
        <P>At the beginning of FY 2011, the establishment fee was based on an estimate that 415 establishments would be subject to, and would pay, fees. By the end of FY 2011, FDA estimates that 475 establishments will have been billed for establishment fees, before all decisions on requests for waivers or reductions are made. FDA estimates that a total of 10 establishment fee waivers or reductions will be made for FY 2011. In addition, FDA estimates that another 15 full establishment fees will be exempted this year based on the orphan drug exemption in FDAAA (see section 736(k) of the FD&amp;C Act). Subtracting 25 establishments (10 waivers, plus the estimated 15 establishments under the orphan exemption) from 450 leaves a net of 415 fee-paying establishments. FDA will use 450 for its FY 2012 estimate of establishments paying fees, after taking waivers and reductions into account. The fee per establishment is determined by dividing the adjusted total fee revenue to be derived from establishments ($234,057,000) by the estimated 450 establishments, for an establishment fee rate for FY 2012 of $520,100 (rounded to the nearest $100).</P>
        <HD SOURCE="HD2">B. Product Fees</HD>
        <P>At the beginning of FY 2011, the product fee was based on an estimate that 2,385 products would be subject to and would pay product fees. By the end of FY 2011, FDA estimates that 2,450 products will have been billed for product fees, before all decisions on requests for waivers, reductions, or exemptions are made. FDA assumes that there will be 55 waivers and reductions granted. In addition, FDA estimates that another 30 product fees will be exempted this year based on the orphan drug exemption in FDAAA (see section 736(k) of the FD&amp;C Act). FDA estimates that 2,365 products will qualify for product fees in FY 2011, after allowing for waivers and reductions, including the orphan drug products eligible under the FDAAA exemption, and will use this number for its FY 2012 estimate. The FY 2012 product fee rate is determined by dividing the adjusted total fee revenue to be derived from product fees ($234,057,000) by the estimated 2,365 products for a FY 2012 product fee of $98,970 (rounded to the nearest $10).</P>
        <HD SOURCE="HD1">VII. Fee Schedule for FY 2012</HD>
        <P>The fee rates for FY 2012 are set out in table 11 of this document.</P>
        <GPOTABLE CDEF="s100,12" COLS="2" OPTS="L2,i1">
          <TTITLE>Table 11—Fee Schedule for FY 2012</TTITLE>
          <BOXHD>
            <CHED H="1">Fee category</CHED>
            <CHED H="1">Fee rates for FY 2012</CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Applications</ENT>
            <ENT/>
          </ROW>
          <ROW>
            <ENT I="03">Requiring clinical data</ENT>
            <ENT>$1,841,500</ENT>
          </ROW>
          <ROW>
            <ENT I="03">Not requiring clinical data</ENT>
            <ENT>920,750</ENT>
          </ROW>
          <ROW>
            <ENT I="03">Supplements requiring clinical data</ENT>
            <ENT>920,750</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Establishments</ENT>
            <ENT>520,100</ENT>
          </ROW>
          <ROW>
            <ENT I="01">Products</ENT>
            <ENT>98,970</ENT>
          </ROW>
        </GPOTABLE>
        <HD SOURCE="HD1">IX. Fee Payment Options and Procedures</HD>
        <HD SOURCE="HD2">A. Application Fees</HD>

        <P>The appropriate application fee established in the new fee schedule must be paid for any application or supplement subject to fees under PDUFA that is received after September 30, 2011. Payment must be made in U.S. currency by check, bank draft, or U.S. postal money order payable to the order of the Food and Drug Administration. Please include the user fee<PRTPAGE P="45838"/>identification (ID) number on your check, bank draft, or postal money order. Your payment can be mailed to: Food and Drug Administration, P.O. Box 979107, St. Louis, MO 63197-9000.</P>

        <P>If checks are to be sent by a courier that requests a street address, the courier can deliver the checks to: U.S. Bank, Attention: Government Lockbox 979107, 1005 Convention Plaza, St. Louis, MO 63101. (<E T="04">Note:</E>This U.S. Bank address is for courier delivery only.)</P>
        <P>Please make sure that the FDA post office box number (P.O. Box 979107) is written on the check, bank draft, or postal money order.</P>
        <P>Wire transfer payment may also be used. Please reference your unique user fee ID number when completing your transfer. The originating financial institution may charge a wire transfer fee between $15.00 and $35.00. Please ask your financial institution about the fee and include it with your payment to ensure that your fee is fully paid. The account information is as follows: New York Federal Reserve Bank, U.S. Dept of Treasury, TREAS NYC, 33 Liberty St., New York, NY 10045, Acct. No.: 75060099, Routing No.: 021030004, SWIFT: FRNYUS33, Beneficiary: FDA, 1350 Piccard Dr., Rockville, MD, 20850.</P>
        <P>Application fees can also be paid online with an electronic check (ACH). FDA has partnered with the U.S. Department of the Treasury to utilize Pay.gov, a Web-based payment application, for online electronic payment. The Pay.gov feature is available on the FDA Web site after the user fee ID number is generated.</P>
        <P>The tax identification number of the Food and Drug Administration is 53-0196965.</P>
        <HD SOURCE="HD2">B. Establishment and Product Fees</HD>
        <P>FDA will issue invoices for establishment and product fees for FY 2012 under the new fee schedule in August 2011. Payment will be due on October 1, 2011. FDA will issue invoices in November 2012 for any products and establishments subject to fees for FY 2012 that qualify for fee assessments after the August 2011 billing.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Leslie Kux,</NAME>
          <TITLE>Acting Assistant Commissioner for Policy.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19332 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4160-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>National Institutes of Health</SUBAGY>
        <SUBJECT>Government-Owned Inventions; Availability for Licensing</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>National Institutes of Health, Public Health Service, HHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The inventions listed below are owned by an agency of the U.S. Government and are available for licensing in the U.S. in accordance with 35 U.S.C. 207 to achieve expeditious commercialization of results of federally-funded research and development. Foreign patent applications are filed on selected inventions to extend market coverage for companies and may also be available for licensing.</P>
        </SUM>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>Licensing information and copies of the U.S. patent applications listed below may be obtained by writing to the indicated licensing contact at the Office of Technology Transfer, National Institutes of Health, 6011 Executive Boulevard, Suite 325, Rockville, Maryland 20852-3804; telephone: 301-496-7057; fax: 301-402-0220. A signed Confidential Disclosure Agreement will be required to receive copies of the patent applications.</P>
        </ADD>
        <HD SOURCE="HD1">Combination Cancer Therapy Using an IL13-Targeted Toxin and a Vaccine</HD>
        <P>
          <E T="03">Description of Technology:</E>Typical cancer treatments such as chemotherapy, radiation therapy and surgical resection are non-specific processes that kill healthy cells as well as diseased cells, ultimately resulting in discomfort and undesirable side-effects for patients. In an effort to reduce the burden on cancer patients, a tremendous effort has been placed on developing ways to increase the specificity of cancer treatments. One way to increase specificity is to identify proteins which are present on the surface of cancer cells but absent on normal healthy cells, and use that protein as a target for delivering a therapeutic agent. Because the therapeutic agent only reaches the diseased cell, patients are less likely to experience non-specific side-effects, reducing their pain burden during treatment.</P>

        <P>IL13-receptor-alpha-2 (IL13-Rα2) is a cell surface protein that is selectively expressed on certain diseased cells, including cancer cells. IL13-Rα2 binds to the cytokine IL13, suggesting that a therapeutic agent fused to IL13 can target and kill only those cancer cells which express IL13-Rα2. Our inventors previously constructed fusion proteins comprising (1) IL13 and (2) an active fragment of the bacterial toxin<E T="03">Pseudomonas</E>exotoxin A (PE). These IL13-PE fusion proteins demonstrated the ability to selectively kill cancer cells that overexpressed IL13-Rα2, as well as other types of diseased cells (asthma, pulmonary fibrosis) which overexpressed IL13-Rα2. This suggested that IL13-PE fusion proteins were excellent candidates for new therapeutic agents.</P>
        <P>The inventors recently sought methods to increase the effectiveness of these IL13-PE fusion proteins in the treatment of disease. This technology is directed to a combination therapy comprising (a) a DNA vaccine against IL13-Rα2 and (b) an IL13-PE fusion protein. By combining these therapeutic approaches it is possible to kill certain cell types that express IL13-Rα2 at high levels (such as cancer cells), making this combinatorial approach an attractive potential therapeutic.</P>
        <P>
          <E T="03">Applications:</E>
        </P>
        <P>• Treatment of diseases associated with the increased expression of IL13-Rα2</P>
        <P>• Relevant diseases include pulmonary fibrosis, asthma and cancers such as pancreatic cancer, glioblastoma multiforme and other head and neck cancers</P>
        <P>
          <E T="03">Advantages:</E>
        </P>
        <P>• The DNA vaccine only affects cells where IL13-Rα2 expression is increased, limiting their effects to diseased cells</P>
        <P>• IL13-PE fusion proteins also only kill cells that overexpress IL13-Rα2, allowing specific targeting of treatment</P>
        <P>• Targeted treatment decreases non-specific killing of healthy, essential cells, resulting in fewer side-effects and healthier patients</P>
        <P>
          <E T="03">Development Status:</E>Preclinical stage of development.</P>
        <P>
          <E T="03">Inventors:</E>Puri<E T="03">et al.</E>(FDA).</P>
        <P>
          <E T="03">Patent Status:</E>US provisional application 61/451,331 (HHS reference E-104-2011/0-US-01).</P>
        <P>
          <E T="03">For more information, see:</E>
        </P>
        <P>• US Patents 5,614,191, 5,919,456 and 6,518,061 (HHS technology reference E-266-1994/0)</P>
        <P>• US Patent Publication US 20040136959 A1 (HHS technology reference E-032-2000/0)</P>
        <P>• US Patent 7,541,040 (HHS technology reference E-296-2001/0)</P>
        <P>
          <E T="03">Licensing Status:</E>Available for licensing.</P>
        <P>
          <E T="03">Licensing Contact:</E>David A. Lambertson, PhD; 301-435-4632;<E T="03">lambertsond@mail.nih.gov.</E>
          <PRTPAGE P="45839"/>
        </P>
        <HD SOURCE="HD1">Combination Cancer Therapy Using an IL13-Targeted Toxin and an HDAC Inhibitor</HD>
        <P>
          <E T="03">Description of Technology:</E>Typical cancer treatments such as chemotherapy, radiation therapy and surgical resection are non-specific processes that kill healthy cells as well as diseased cells, ultimately resulting in discomfort and undesirable side-effects for patients. In an effort to reduce the burden on cancer patients, a tremendous effort has been placed on developing ways to increase the specificity of cancer treatments. One way to increase specificity is to identify proteins which are present on the surface of cancer cells but absent on normal healthy cells, and use that protein as a target for delivering a therapeutic agent. Because the therapeutic agent only reaches the diseased cell, patients are less likely to experience non-specific side-effects, reducing their pain burden during treatment.</P>

        <P>IL13-receptor-alpha-2 (IL13-Rα2) is a cell surface protein that is selectively expressed on certain diseased cells, including cancer cells. IL13-Rα2 binds to the cytokine IL13, suggesting that a therapeutic agent fused to IL13 can target and kill only those cancer cells which express IL13-Rα2. Our inventors previously constructed fusion proteins comprising (1) IL13 and (2) an active fragment of the bacterial toxin<E T="03">Pseudomonas</E>exotoxin A (PE). These IL13-PE fusion proteins demonstrated the ability to selectively kill cancer cells that overexpressed IL13-Rα2, as well as other types of diseased cells (asthma, pulmonary fibrosis) which overexpressed IL13-Rα2. This suggested that IL13-PE fusion proteins were excellent candidates for new therapeutic agents.</P>
        <P>In an effort to increase the effectiveness of these IL13-PE fusion proteins, the inventors sought ways to increase the expression of IL13-Rα2 on cancer cells, thereby increasing the rate at which the therapeutic agent could kill the diseased cell. Histone deacetylase (HDAC) inhibitors have been employed as anti-cancer agents for several years, and a number of HDAC inhibitors are currently in clinical trials. Although the exact mechanism by which HDAC inhibitors function is unclear, it is believed that the ability of these molecules to increase the expression of anti-cancer genes is behind their therapeutic effect.</P>
        <P>This invention concerns a means of improving specific cancer therapy through the combination of (a) IL13-PE fusion proteins and (b) HDAC inhibitors. The inventors surprisingly found that the expression of IL13-Rα2 increased in several types of pancreatic cancer cells in response to HDAC inhibitors, whereas normal, healthy cells did not experience such an increase in IL13-Rα2 expression. The use of IL13-PE fusion proteins in combination with HDAC inhibitors improved specific killing of pancreatic cancer cells relative to the use of IL13-PE fusion proteins in the absence of the HDAC inhibitors. This suggested that the use of IL13-PE fusion proteins along with HDAC inhibitors was a strong candidate combinatorial therapeutic for the treatment of various cancers (e.g., pancreatic, glioblastoma multiforme) and other diseases characterized by overexpression of IL13-Rα2 (e.g., asthma, pulmonary fibrosis).</P>
        <P>
          <E T="03">Applications:</E>
        </P>
        <P>• Treatment of diseases associated with the increased expression of IL13-Rα2</P>
        <P>• Relevant diseases include pulmonary fibrosis, asthma and cancers such as pancreatic cancer, glioblastoma multiforme and other head and neck cancers</P>
        <P>
          <E T="03">Advantages:</E>
        </P>
        <P>• HDAC inhibitors only increased IL13-Rα2 expression in diseased cells, leaving normal healthy cells unaltered</P>
        <P>• IL13-PE fusion proteins only kill cells that overexpress IL13-Rα2, allowing specific targeting of treatment</P>
        <P>• Targeted treatment decreases non-specific killing of healthy, essential cells, resulting in fewer side-effects and healthier patients</P>
        <P>
          <E T="03">Development Status:</E>Preclinical stage of development</P>
        <P>
          <E T="03">Inventors:</E>Puri<E T="03">et al.</E>(FDA)</P>
        <P>
          <E T="03">Patent Status:</E>US provisional application 61/494,779 (HHS reference E-107-2011/0-US-01)</P>
        <P>
          <E T="03">For more information, see:</E>
        </P>
        <P>• US Patents 5,614,191, 5,919,456 and 6,518,061 (HHS technology reference E-266-1994/0)</P>
        <P>• US Patent Publication US 20040136959 A1 (HHS technology reference E-032-2000/0)</P>
        <P>• US Patent 7,541,040 (HHS technology reference E-296-2001/0)</P>
        <P>
          <E T="03">Licensing Status:</E>Available for licensing</P>
        <P>
          <E T="03">Licensing Contact:</E>David A. Lambertson, PhD; 301-435-4632;<E T="03">lambertsond@mail.nih.gov</E>
        </P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Richard U. Rodriguez,</NAME>
          <TITLE>Director, Division of Technology Development and Transfer, Office of Technology Transfer, National Institutes of Health.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19378 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4140-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>National Institutes of Health</SUBAGY>
        <SUBJECT>Government-Owned Inventions; Availability for Licensing</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>National Institutes of Health, Public Health Service, HHS.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The inventions listed below are owned by an agency of the U.S. Government and are available for licensing in the U.S. in accordance with 35 U.S.C. 207 to achieve expeditious commercialization of results of federally-funded research and development. Foreign patent applications are filed on selected inventions to extend market coverage for companies and may also be available for licensing.</P>
        </SUM>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Licensing information and copies of the U.S. patent applications listed below may be obtained by writing to the indicated licensing contact at the Office of Technology Transfer, National Institutes of Health, 6011 Executive Boulevard, Suite 325, Rockville, Maryland 20852-3804;<E T="03">telephone:</E>301-496-7057;<E T="03">fax:</E>301-402-0220. A signed Confidential Disclosure Agreement will be required to receive copies of the patent applications.</P>
        </ADD>
        <HD SOURCE="HD1">Methods and Software for the Quantitative Assessment of Vasculature in Allantois and Retina Explants</HD>
        <P>
          <E T="03">Description of Technology:</E>The invention relates to methods and software that can facilitate and improve quantification, accuracy and standardization in the assessment of vasculature in angiogenesis assays such as in the allantois explants and the retina explants assays. The software of this invention can aid in the analysis of images resulting from these assays and thus enhance the accuracy and effectiveness of research in the area of angiogenesis. This in turn will lead to enhanced progress in the development of medical methods and drugs to treat diseases related to angiogenesis such as cancer, macular degeneration, and some pregnancy disorders.</P>
        <P>
          <E T="03">Applications:</E>The software can be integrated with a variety of imaging systems used in conjunction with angiogenesis assays to enhance the assessment and the quality of research in the area of angiogenesis.</P>
        <P>
          <E T="03">Advantages:</E>
        </P>

        <P>• The method and software of the invention will make analysis of angiogenesis assays more accurate, better standardized, and less<PRTPAGE P="45840"/>cumbersome than existing analysis systems.</P>
        <P>• This method and software will eliminate the user-dependent bias which is characteristic of existing methods.</P>
        <P>• This method and software will generally improve the quality of analysis of angiogenesis assays.</P>
        <P>• The software is suitable for integration in a variety of existing imaging systems and software as well as readily usable as an independent complementary technology in the research and biomedical fields.</P>
        <P>
          <E T="03">Development Status:</E>The software is fully developed.</P>
        <P>
          <E T="03">Inventor:</E>Enrique Zudaire (NCI).</P>
        <P>Relevant Publications:</P>
        <P>1. Pitulescu ME, Schmidt I, Benedito R, Adams RH. Inducible gene targeting in the neonatal vasculature and analysis of retinal angiogenesis in mice. Nat Protoc. 2010 Sep;5(9):1518-1534. [PMID: 20725067].</P>
        <P>2. Gambardella L,<E T="03">et al.</E>PI3K signaling through the dual GTPase-activating protein ARAP3 is essential for developmental angiogenesis. Sci Signal 2010 Oct 26;3(145):ra76. [PMID: 20978237].</P>
        <P>3. Zudaire E, Gambardella L, Kurcz C, Vermeren S. A computational tool for quantitative analysis of vascular networks. PLoS One (Submitted).</P>
        <P>
          <E T="03">Patent Status:</E>HHS Reference No. E-176-2011/0—Software/Research Tool. Patent protection is not being pursued for this technology.</P>
        <P>
          <E T="03">Licensing Status:</E>The software is available for licensing.</P>
        <P>Licensing Contacts:</P>
        <P>• Uri Reichman, Ph.D., MBA; 301-435-4616;<E T="03">UR7a@nih.gov.</E>
        </P>
        <P>• Michael Shmilovich,<E T="03">Esq.;</E>301-435-5019;<E T="03">shmilovm@mail.nih.gov</E>.</P>
        <HD SOURCE="HD1">Pyruvate as a Transient Hypoxia Inducer for Anti-cancer Therapies</HD>
        <P>
          <E T="03">Description of Technology:</E>Human solid tumors, such as breast cancer, lung cancer, ovarian cancer, pancreatic cancer and prostate cancer, etc. frequently have substantial volumes with low oxygen concentration, i.e. hypoxic. These hypoxic tumors show resistance to radiation and chemotherapies. To overcome such resistance, novel classes of agents have been designed and developed that are specifically active or activated under hypoxic conditions, in hypoxic tumors. The instant invention describes a novel idea to improve anti-cancer effect of hypoxia-sensitive therapeutics by using a rapidly oxidized reducing agent such as pyruvate or succinate. In the instant invention, the NIH investigators found that pyruvate, an endogenous substrate for energy production by mitochondria, induced severe hypoxia in tumors within 30 minutes of intravenous injection, and the tumor oxygen level reversibly returned to basal level within a few hours. Since pyruvate seems to induce only transient hypoxia, and its safety profiles are known, it may have significant advantages over other hypoxia inducers reported to date for improving the efficacy of hypoxia-sensitive anti-cancer therapies.</P>
        <P>Applications:</P>
        <P>• Provide a novel way to target various cancers, especially solid tumors for treatment;</P>
        <P>• Improve the efficacy of using hypoxic toxins for cancer treatment;</P>
        <P>•<E T="03">In vivo</E>screening of oxygen-status dependent drugs.</P>
        <P>
          <E T="03">Market:</E>Cancer is the second leading cause of death in the U.S. The National Cancer Institute estimates the overall annual costs for cancer in the U.S. at $107 billion; $37 billion for direct medical costs, $11 billion for morbidity costs (cost of lost productivity), and $59 billion for mortality costs. There is an ongoing need for innovative approaches to anticancer therapy.</P>
        <P>
          <E T="03">Development Status:</E>Pre-clinical stage of development.</P>
        <P>
          <E T="03">Inventors:</E>Drs. Shingo Matsumoto (NCI), James B. Mitchell (NCI), and Robert J. Gillies (H. Lee Moffitt Cancer Center and Research Institute)<E T="03">et al.</E>
        </P>
        <P>
          <E T="03">Publication:</E>Poster presentation in the International Society for Magnetic Resonance in Medicine (ISMRM) meeting in May 2011. Manuscript is<E T="03">in press.</E>
        </P>
        <P>
          <E T="03">Patent Status:</E>U.S. Provisional Application No. 61/478,465 filed April 22, 2011 (HHS Reference No. E-144-2011/0-US-01).</P>
        <P>
          <E T="03">Licensing Status:</E>Available for licensing.</P>
        <P>
          <E T="03">Licensing Contact:</E>Betty B. Tong, PhD; 301-594-6565;<E T="03">tongb@mail.nih.gov</E>.</P>
        <HD SOURCE="HD1">Multivalent Vaccines for Rabies Virus and Filoviruses</HD>
        <P>
          <E T="03">Description of Technology:</E>No vaccine candidates against Ebola virus (EBOV) or Marburg virus (MARV) are nearing licensure and the need to develop a safe and efficacious vaccine against filoviruses continues. Whereas several preclinical vaccine candidates against EBOV or MARV exist, their further development is a major challenge based on safety concerns, pre-existing vector immunity, and issues such as manufacturing, dosage, and marketability. The inventors have developed a new platform based on live or chemically inactivated (killed) rabies virus (RABV) virions containing EBOV glycoprotein (GP) in their envelope. In preclinical trials, immunization with such recombinant RABV virions provided excellent protection in mice against lethal challenge with the mouse adapted EBOV and RABV. More specifically, the inventors have developed a trivalent filovirus vaccine based on killed rabies virus virions for use in humans to confer protection from all medically relevant filoviruses and RABV. Two additional vectors containing EBOV Sudan GP or MARV GP are planned to be constructed in addition to the previously developed EBOV Zaire GP containing vaccine. The efficiency of these vaccines against challenge with EBOV, MARV and RABV will be studied in multiple preclinical studies. Live attenuated vaccines are being developed for use in at risk nonhuman primate populations in Africa and inactivated vaccines are being developed for use in humans.</P>
        <P>
          <E T="03">Potential Commercial Applications:</E>
        </P>
        <P>• Biodefense vaccine.</P>
        <P>• Developing country vaccine.</P>
        <P>• Multivalent prophylactic Ebola/Marburg/rabies vaccine.</P>
        <P>
          <E T="03">Competitive Advantages:</E>
        </P>
        <P>• Vaccines are replication deficient and/or inactivated.</P>
        <P>• Protection against rabies and Ebola.</P>
        <P>• Reliable and cost-effective manufacture.</P>
        <P>• No preexisting immunity to vectors.</P>
        <P>• No potential vaccine reactogenicity.</P>
        <P>
          <E T="03">Development Stage:</E>
        </P>
        <P>• Pre-clinical.</P>
        <P>•<E T="03">In vitro</E>data available.</P>
        <P>•<E T="03">In vivo</E>data available (animal).</P>
        <P>
          <E T="03">Inventors:</E>Joseph Blaney, Jason Paragas, Peter Jahrling, Reed Johnson (NIAID).</P>
        <P>
          <E T="03">Intellectual Property:</E>HHS Reference No. E-032-2011/0 — U.S. Patent Application No. 61/439,046 filed 03 Feb 2011.</P>
        <P>
          <E T="03">Licensing Contact:</E>Peter A. Soukas, J.D.; 301-435-4646;<E T="03">soukasp@mail.nih.gov.</E>
        </P>
        <HD SOURCE="HD1">Layered Electrophoretic Transfer for Analysis of Low or Medium Abundant Proteins in Tissue Samples</HD>
        <P>
          <E T="03">Description of Technology:</E>The subject invention is a method to selectively process the protein content from a two dimensional sample, such as a tissue section, for more detailed analysis. It is particularly useful for analysis of a subset of proteins from a complex protein mixture. The method employs a layer of polyacrylamide gels and an electric field. Proteins from the sample are transferred and sieved through a stack of polyacrylamide gels of varying concentrations. Thus, it is possible to analyze specific subsets of<PRTPAGE P="45841"/>proteins in the different gel layers and maintain the two dimensional location of the proteins within the original sample. One of the advantages of this technology is that it allows for isolation and subsequent analysis of low abundant or medium abundant proteins by a number of different methodologies such as imaging mass spectrometry.</P>
        <P>
          <E T="03">Applications:</E>
        </P>
        <P>• Protein Analysis of Tissue Samples.</P>
        <P>• Histology and Pathology.</P>
        <P>
          <E T="03">Advantages:</E>
        </P>
        <P>• Isolation of low or moderately-abundant proteins in tissue sections.</P>
        <P>• Method maintains 2-dimensional location of proteins in tissue samples.</P>
        <P>
          <E T="03">Development Status: In vitro</E>data can be provided upon request.</P>
        <P>
          <E T="03">Market:</E>
        </P>
        <P>• Diagnostic.</P>
        <P>• Pathology.</P>
        <P>• Basic Research.</P>
        <P>
          <E T="03">Inventors:</E>Michael Emmert-Buck, Liang Zhu, and Michael Tangrea (NCI).</P>
        <P>
          <E T="03">Publication:</E>Zhu L, Tangrea MA, Mukherjee S, Emmert-Buck MR. Layered electrophoretic transfer—A method for pre-analytic processing of histological sections. Proteomics. 2011 Mar;11(5):883-889. [PMID: 21280224].</P>
        <P>
          <E T="03">Patent Status:</E>U.S. Provisional Application No. 61/420,258 filed December 6, 2010 (HHS Reference No. E-020-2011/0-US-01).</P>
        <P>
          <E T="03">Licensing Status:</E>Available for licensing.</P>
        <P>
          <E T="03">Licensing Contact:</E>Kevin W. Chang, PhD; 301-435-5018;<E T="03">changke@mail.nih.gov.</E>
        </P>
        <P>
          <E T="03">Collaborative Research Opportunity:</E>The Center for Cancer Research, Laboratory of Pathology, Pathogenetics Unit, is seeking statements of capability or interest from parties interested in collaborative research to further develop, evaluate, or commercialize layered electrophoretic transfer (LET). Please contact John Hewes, PhD at 301-435-3121 or hewesj<E T="03">@mail.nih.gov</E>for more information.</P>
        <HD SOURCE="HD1">Pertussis Vaccine</HD>
        <P>
          <E T="03">Description of Technology:</E>Despite mass vaccination, reported pertussis cases have increased in the United States and other parts of the world, probably because of increased awareness, improved diagnostic means, and waning vaccine-induced immunity among adolescents and adults. Licensed vaccines do not kill the organism directly; the addition of a component inducing bactericidal antibodies would improve vaccine efficacy. This application claims<E T="03">Bordetella pertussis</E>and<E T="03">Bordetella bronchiseptica</E>LPS-derived core oligosaccharide (OS) protein conjugates.<E T="03">B. pertussis</E>and<E T="03">B. bronchiseptica</E>core OS were bound to aminooxylated BSA via their terminal Kdo residues. The two conjugates induced similar anti-<E T="03">B. pertussis</E>LPS IgG levels in mice. Conjugate-induced antisera were bactericidal against<E T="03">B. pertussis.</E>
        </P>
        <P>
          <E T="03">Potential Commercial Applications:</E>
        </P>
        <P>• Pertussis prophylactic conjugate vaccine.</P>
        <P>• Use of vaccine to generate neutralizing antibodies.</P>
        <P>
          <E T="03">Competitive Advantages:</E>Conjugates are easy to prepare and standardize; added to a recombinant pertussis toxoid, they may induce antibacterial and antitoxin immunity.</P>
        <P>
          <E T="03">Development Stage:</E>
        </P>
        <P>• Pre-clinical.</P>
        <P>•<E T="03">In vitro</E>data available.</P>
        <P>•<E T="03">In vivo</E>data available (animal).</P>
        <P>
          <E T="03">Inventors:</E>Joanna Kubler-Kielb (NICHD), Rachel Schneerson (NICHD), John B. Robbins (NICHD), Ariel Ginzberg (NICHD), Teresa Lagergard (NICHD),<E T="03">et al.</E>
        </P>
        <P>
          <E T="03">Publication:</E>Kubler-Kielb J, Vinogradov E, Lagergård T, Ginzberg A, King JD, Preston A, Maskell DJ, Pozsgay V, Keith JM, Robbins JB, Schneerson R. Oligosaccharide conjugates of Bordetella pertussis and bronchiseptica induce bactericidal antibodies, an addition to pertussis vaccine. Proc Natl Acad Sci U S A. 2011 Mar 8;108(10):4087-4092. [PMID: 21367691].</P>
        <P>
          <E T="03">Intellectual Property:</E>HHS Reference No. E-006-2011/0—U.S. Application No. 61/438,190 filed 31 Jan 2011.</P>
        <P>
          <E T="03">Related Technology:</E>HHS Reference No. E-183-2005/0 —U.S. Application No. 12/309,428 filed 16 Jan 2009.</P>
        <P>
          <E T="03">Licensing Contact:</E>Peter A. Soukas, J.D.; 301-435-4646;<E T="03">soukasp@mail.nih.gov.</E>
        </P>
        <P>
          <E T="03">Collaborative Research Opportunity:</E>The NICHD is seeking statements of capability or interest from parties interested in collaborative research to further develop, evaluate, or commercialize vaccines against pertussis. For collaboration opportunities, please contact Joseph Conrad, III, PhD at<E T="03">jmconrad@mail.nih.gov.</E>
        </P>
        <HD SOURCE="HD1">Novel Methods for the Reversible Incorporation of Functional Groups Into RNA and DNA: Synthesis and Uses for 2′-O-aminooxymethyl Nucleoside Derivatives</HD>
        <P>
          <E T="03">Description of Technology:</E>The delivery of DNA/RNA therapeutic drugs is still a major hurdle for the clinical application of DNA/RNA-based drugs. Also, developments in silencing the expression of specific genes, through RNA interference pathways, have led to an increased demand for synthetic RNA sequences and have created a pressing need for rapid and efficient methods for RNA synthesis. Recently, FDA scientists have developed a novel phosphoramidite, 2′-O-aminooxymethyl ribonucleoside (2′-O-protected compounds). The 2′-O-aminooxymethyl ribonucleoside can be modified with any type of functional group using an oximation reaction as long as the functional group contains an aldehyde, ketone, or acetal group. Modification of the 2′-O-aminooxymethyl with an aldehyde results in a conjugated 2′-phosphoramidite that could be readily converted back to the native ribonucleoside and its corresponding by-product. On the other hand, the oximation of 2′-O-aminooxymethy with a ketone results in an irreversible conjugated form of the phosphoramidite.</P>
        <P>The 2′-O-protected compounds of the present technology have several advantages, for example, the 2′-O-protected compound is stable during the various reaction steps involved in oligonucleotide synthesis; and the protecting group can be easily removed after the synthesis of the oligonucleotide, for example, by reaction with tetrabutylammonium fluoride; and the O-protected groups do not generate DNA/RNA alkylating side products, which have been reported during removal of 2′-O-(2-cyanoethyl)oxymethyl or 2′-O-[2-(4-tolylsulfonyl)ethoxymethyl groups under similar conditions.</P>
        <P>
          <E T="03">Applications:</E>
        </P>
        <P>• Incorporation of a potentially large array of functional groups into RNA and DNA oligonucleotides for diagnostic and/or therapeutic applications.</P>
        <P>• Conjugation of a variety of sugars or complex carbohydrates to DNA/RNA therapeutic oligonucleotides.</P>
        <P>• Attachment of cell membrane-penetrating peptides to therapeutic DNA/RNA oligonucleotides.</P>
        <P>
          <E T="03">Inventors:</E>Serge L. Beaucage and Jacek Cieslak (FDA).</P>
        <P>
          <E T="03">Patent Status:</E>U.S. Provisional Application No. 61/471,451 filed 04 April 2011 (HHS Reference No. E-262-2010/0-US-01).</P>
        <P>
          <E T="03">Licensing Status:</E>Available for licensing.</P>
        <P>
          <E T="03">Licensing Contact:</E>Suryanarayana Vepa, PhD, J.D.; 301-435-5020;<E T="03">vepas@mail.nih.gov.</E>
        </P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Richard U. Rodriguez,</NAME>
          <TITLE>Director, Division of Technology Development and Transfer, Office of Technology Transfer, National Institutes of Health.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19377 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4140-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <PRTPAGE P="45842"/>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>National Institutes of Health</SUBAGY>
        <SUBJECT>Center for Scientific Review Notice of Closed Meetings</SUBJECT>
        <P>Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of the following meetings.</P>
        <P>The meetings will be closed to the public in accordance with the  provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5  U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy.</P>
        
        <EXTRACT>
          <P>
            <E T="03">Name of Committee:</E>Center for Scientific Review Special Emphasis Panel, Member Conflict: Topics in Microbial Pathogenesis and Immunity.</P>
          <P>
            <E T="03">Date:</E>August 18-19, 2011.</P>
          <P>
            <E T="03">Time:</E>8:30 a.m. to 5 p.m.</P>
          <P>
            <E T="03">Agenda:</E>To review and evaluate grant applications.</P>
          <P>
            <E T="03">Place:</E>National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892, (Virtual Meeting).</P>
          <P>
            <E T="03">Contact Person:</E>Kenneth Izumi, PhD, Scientific Review Officer, IDM IRG, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 3204, MSC 7808, Bethesda, MD 20892, 301-496-6980,<E T="03">izumikm@csr.nih.gov.</E>
          </P>
          
          <P>
            <E T="03">Name of Committee:</E>Center for Scientific Review Special Emphasis Panel, Member Conflict: Health and Behavior.</P>
          <P>
            <E T="03">Date:</E>August 22, 2011.</P>
          <P>
            <E T="03">Time:</E>12 to 1:30 p.m.</P>
          <P>
            <E T="03">Agenda:</E>To review and evaluate grant applications.</P>
          <P>
            <E T="03">Place:</E>National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892, (Telephone Conference Call).</P>
          <P>
            <E T="03">Contact Person:</E>Martha M. Faraday, PhD, Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 3110,  MSC 7808, Bethesda, MD 20892, 301-435-3575,<E T="03">faradaym@csr.nih.gov.</E>
          </P>
          
          <P>
            <E T="03">Name of Committee:</E>Center for Scientific Review Special Emphasis Panel, Member Conflict: Oral Microbiology, Biofilm and  Periodontology.</P>
          <P>
            <E T="03">Date:</E>August 24, 2011.</P>
          <P>
            <E T="03">Time:</E>2 to 4 p.m.</P>
          <P>
            <E T="03">Agenda:</E>To review and evaluate grant applications.</P>
          <P>
            <E T="03">Place:</E>National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892, (Telephone Conference Call).</P>
          <P>
            <E T="03">Contact Person:</E>Baljit S Moonga, PhD, Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 4214, MSC 7806, Bethesda, MD 20892, 301-435-1777,<E T="03">moongabs@mail.nih.gov.</E>
          </P>
          
          <P>
            <E T="03">Name of Committee:</E>Center for Scientific Review Special Emphasis Panel, Member Conflict: Vascular Hematology.</P>
          <P>
            <E T="03">Date:</E>August 25, 2011.</P>
          <P>
            <E T="03">Time:</E>1 to 2:30 p.m.</P>
          <P>
            <E T="03">Agenda:</E>To review and evaluate grant applications.</P>
          <P>
            <E T="03">Place:</E>National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892, (Telephone Conference Call).</P>
          <P>
            <E T="03">Contact Person:</E>Anshumali Chaudhari, PhD, Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 4124, MSC 7802, Bethesda, MD 20892, (301) 435-1210,<E T="03">chaudhaa@csr.nih.gov.</E>
          </P>
          
          <FP>(Catalogue of Federal Domestic Assistance Program Nos. 93.306, Comparative Medicine; 93.333, Clinical Research, 93.306, 93.333, 93.337, 93.393-93.396, 93.837-93.844, 93.846-93.878, 93.892, 93.893, National Institutes of Health, HHS)</FP>
        </EXTRACT>
        <SIG>
          <DATED>Dated: July 22, 2011.</DATED>
          <NAME>Anna P. Snouffer,</NAME>
          <TITLE>Deputy Director, Office of Federal Advisory Committee Policy.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19375 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4140-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>National Institutes of Health</SUBAGY>
        <SUBJECT>National Library of Medicine Notice of Meetings</SUBJECT>
        <P>Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended(5 U.S.C. App), notice is hereby given of meetings of the Board of Regents of theNational Library of Medicine.</P>
        <P>The meeting will be open to the public as indicated below, with attendance limited to space available. Individuals who plan to attend and need special assistance, such as sign language interpretation or other reasonable accommodations, should notify the Contact Person listed below in advance of the meeting.</P>
        <P>The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable materials, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy.</P>
        
        <EXTRACT>
          <P>
            <E T="03">Name of Committee:</E>Board of Regents of the National Library of Medicine EP Subcommittee.</P>
          <P>
            <E T="03">Date:</E>October 3, 2011.</P>
          <P>
            <E T="03">Closed:</E>4 p.m. to 5:30 p.m.</P>
          <P>
            <E T="03">Agenda:</E>Grant Applications.</P>
          <P>
            <E T="03">Place:</E>National Library of Medicine, Building 38, 2nd Floor, Conference Room B, 8600 Rockville Pike, Bethesda, MD 20892.</P>
          <P>
            <E T="03">Contact Person:</E>Donald A.B. Lindberg, MD, Director, National Library of Medicine, 8600 Rockville Pike, Bethesda, MD 20892, 301-496-6221,<E T="03">lindberg@mail.nih.gov.</E>
          </P>
          
          <P>
            <E T="03">Name of Committee:</E>Board of Regents of the National Library of Medicine; Subcommittee on Outreach and Public Information.</P>
          <P>
            <E T="03">Date:</E>October 4, 2011.</P>
          <P>
            <E T="03">Open:</E>7:30 a.m. to 8:45 a.m.</P>
          <P>
            <E T="03">Agenda:</E>Outreach Activities.</P>
          <P>
            <E T="03">Place:</E>National Library of Medicine, Building 38, 2nd Floor, Conference Room B, 8600 Rockville Pike, Bethesda, MD 20892.</P>
          <P>
            <E T="03">Contact Person:</E>Donald A.B. Lindberg, MD, Director, National Library of Medicine, 8600 Rockville Pike, Bethesda, MD 20892, 301-496-6221,<E T="03">lindberg@mail.nih.gov.</E>
          </P>
          
          <P>
            <E T="03">Name of Committee:</E>Board of Regents of the National Library of Medicine.</P>
          <P>
            <E T="03">Date:</E>October 4-5, 2011.</P>
          <P>
            <E T="03">Open:</E>October 4, 2011, 9 a.m. to 4:30 p.m.</P>
          <P>
            <E T="03">Agenda:</E>Program Discussion.</P>
          <P>
            <E T="03">Place:</E>National Library of Medicine, Building 38, 2nd Floor, Board Room, 8600 Rockville Pike, Bethesda, MD 20892.</P>
          <P>
            <E T="03">Closed:</E>October 4, 2011, 4:30 p.m. to 5 p.m.</P>
          <P>
            <E T="03">Agenda:</E>To review and evaluate grant applications.</P>
          <P>
            <E T="03">Place:</E>National Library of Medicine, Building 38, 2nd Floor, Board Room, 8600 Rockville Pike, Bethesda, MD 20892.</P>
          <P>
            <E T="03">Open:</E>October 5, 2011, 9 a.m. to 12 p.m.</P>
          <P>
            <E T="03">Agenda:</E>Program Discussion.</P>
          <P>
            <E T="03">Place:</E>National Library of Medicine, Building 38, 2nd Floor, Board Room, 8600 Rockville Pike, Bethesda, MD 20892.</P>
          <P>
            <E T="03">Contact Person:</E>Donald A.B. Lindberg, MD, Director, National Library of Medicine, 8600 Rockville Pike, Bethesda, MD 20892, 301-496-6221,<E T="03">lindberg@mail.nih.gov.</E>
          </P>
          
          <P>Any interested person may file written comments with the committee by forwarding the statement to the Contact Person listed on this notice. The statement should include the name, address, telephone number and when applicable, the business or professional affiliation of the interested person.</P>
          <P>In the interest of security, NIH has instituted stringent procedures for entrance onto the NIH campus. All visitor vehicles, including taxicabs, hotel, and airport shuttles will be inspected before being allowed on campus. Visitors will be asked to show one form of identification (for example, a government-issued photo ID, driver's license, or passport) and to state the purpose of their visit.</P>

          <P>Information is also available on the Institute's/Center's home page:<E T="03">http://www.nlm.nih.gov/od/bor/bor.html,</E>where an agenda and any additional information for the meeting will be posted when available.</P>
          
          <FP>(Catalogue of Federal Domestic Assistance Program No. 93.879, Medical Library Assistance, National Institutes of Health, HHS).</FP>
        </EXTRACT>
        <SIG>
          <PRTPAGE P="45843"/>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Anna P. Snouffer,</NAME>
          <TITLE>Deputy Director, Office of Federal Advisory Committee Policy.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19374 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4140-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>National Institutes of Health</SUBAGY>
        <SUBJECT>National Heart, Lung, and Blood Institute Notice of Closed Meeting</SUBJECT>
        <P>Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of a meeting of the National Heart, Lung, and Blood Advisory Council.</P>
        <P>The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy.</P>
        
        <EXTRACT>
          <P>
            <E T="03">Name of Committee:</E>National Heart, Lung, and Blood Advisory Council.</P>
          <P>
            <E T="03">Date:</E>September 9, 2011.</P>
          <P>
            <E T="03">Time:</E>1 p.m. to 3 p.m.</P>
          <P>
            <E T="03">Agenda:</E>To review and evaluate grant applications.</P>
          <P>
            <E T="03">Place:</E>National Institutes of Health, Building 31, 31 Center Drive, C-Wing, Room 10, Bethesda, MD 20892 (Telephone Conference Call).</P>
          <P>
            <E T="03">Contact Person:</E>Stephen C. Mockrin, PhD, Director, Division of Extramural Research Activities, National Heart, Lung, and Blood Institute, National Institutes of Health, 6701 Rockledge Drive, Room 7100, Bethesda, MD 20892, (301) 435-0260,<E T="03">mockrins@nhlbi.nih.gov.</E>
          </P>

          <P>Information is also available on the Institute's/Center's home page:<E T="03">http://www.nhlbi.nih.gov/meetings/index.htm,</E>where an agenda and any additional information for the meeting will be posted when available.</P>
          
          <FP>(Catalogue of Federal Domestic Assistance Program Nos. 93.233, National Center for Sleep Disorders Research; 93.837, Heart and Vascular Diseases Research; 93.838, Lung Diseases Research; 93.839, Blood Diseases and Resources Research, National Institutes of Health, HHS)</FP>
        </EXTRACT>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Jennifer S. Spaeth,</NAME>
          <TITLE>Director, Office of Federal Advisory Committee Policy.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19373 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4140-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HEALTH AND HUMAN SERVICES</AGENCY>
        <SUBAGY>National Institutes of Health</SUBAGY>
        <SUBJECT>Center for Scientific Review Notice of Closed Meeting</SUBJECT>
        <P>Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of the following meeting.</P>
        <P>The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy.</P>
        
        <EXTRACT>
          <P>
            <E T="03">Name of Committee:</E>Center for Scientific Review Special Emphasis Panel; Member Conflict: NeuroAIDS and HIVAN Applications.</P>
          <P>
            <E T="03">Date:</E>August 9, 2011.</P>
          <P>
            <E T="03">Time:</E>2 p.m. to 5 p.m.</P>
          <P>
            <E T="03">Agenda:</E>To review and evaluate grant applications.</P>
          <P>
            <E T="03">Place:</E>National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892 (Telephone Conference Call).</P>
          <P>
            <E T="03">Contact Person:</E>Mary Clare Walker, PhD, Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 5208, MSC 7852, Bethesda, MD 20892, (301) 435-1165,<E T="03">walkermc@csr.nih.gov.</E>
          </P>
          
          <P>This notice is being published less than 15 days prior to the meeting due to the timing limitations imposed by the review and funding cycle.</P>
          
          <FP>(Catalogue of Federal Domestic Assistance Program Nos. 93.306, Comparative Medicine; 93.333, Clinical Research; 93.306, 93.333, 93.337, 93.393-93.396, 93.837-93.844, 93.846-93.878, 93.892, 93.893, National Institutes of Health, HHS)</FP>
        </EXTRACT>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Jennifer S. Spaeth,</NAME>
          <TITLE>Director, Office of Federal Advisory Committee Policy.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19369 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4140-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF HOMELAND SECURITY</AGENCY>
        <SUBAGY>U.S. Citizenship and Immigration Services</SUBAGY>
        <DEPDOC>[OMB Control No. 1615-0092]</DEPDOC>
        <SUBJECT>Agency Information Collection Activities: E-Verify Program</SUBJECT>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>60-Day Notice: Correction.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>In accordance with the Paperwork Reduction Act of 1995 (PRA), on July 13, 2011, USCIS published a 60-day notice, “Memorandum of Understanding to Participate in the Basic Pilot Employment Eligibility Program; Verify Employment Eligibility Status” in the<E T="04">Federal Register</E>at 76 FR 41279. USCIS is correcting two errors in this notice. First, the title incorrectly read “Memorandum of Understanding to Participate in the Basic Pilot Employment Eligibility Program; Verify Employment Eligibility Status”. Instead it should read “E-Verify Program.” Second, comments are not requested on the E-Verify Memorandum of Understanding as previously published. Instead, comments are requested on the burden for enrolling in E-Verify (and modifying an ID/IQ contract if applicable), inputting information directly from Form I-9, Employment Eligibility Verification into the E-Verify web interface, and performing initial and secondary queries (for example: referring and resolving tentative nonconfirmations.).</P>

          <P>Written comments and/or suggestions regarding the item(s) contained in this notice, especially regarding the estimated public burden and associated response time, should be directed to the Department of Homeland Security (DHS), USCIS, Chief, Regulatory Products Division, Office of the Executive Secretariat, 20 Massachusetts Avenue, NW., Washington, DC 20529-2020. Comments may also be submitted to DHS via facsimile to 202-272-0997 or via e-mail at<E T="03">USCISFRComment@dhs.gov.</E>When submitting comments by e-mail please make sure to add OMB Control Number 1615-0092 in the subject box.</P>
          <P>The public comment period is unchanged and ends September 12, 2011, as cited in the previously published 60-day notice at 76 FR 41279 on July 13, 2011.</P>
        </SUM>
        <NOTE>
          <HD SOURCE="HED">Note:</HD>

          <P>The address listed in this notice should be used only to submit comments concerning this information collection. Please do not submit requests for individual case status inquiries to this address. If you are seeking information about the status of<PRTPAGE P="45844"/>your individual case, please check “My Case Status” online at<E T="03">https://egov.uscis.gov/cris/Dashboard.do,</E>or call the USCIS National Customer Service Center at 1-800-375-5283 (TTY 1-800-767-1833).</P>
        </NOTE>
        <P>Written comments and suggestions from the public and affected agencies should address one or more of the following four points:</P>
        <P>(1) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility;</P>
        <P>(2) Evaluate the accuracy of the agency's estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used;</P>
        <P>(3) Enhance the quality, utility, and clarity of the information to be collected; and</P>
        <P>(4) Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses.</P>
        <HD SOURCE="HD1">Overview of This Information Collection</HD>
        <P>1.<E T="03">Type of Information Collection:</E>Revision of a currently approved information collection.</P>
        <P>2.<E T="03">Title of the Form/Collection:</E>E-Verify Program.</P>
        <P>3.<E T="03">Agency form number, if any, and the applicable component of the Department of Homeland Security sponsoring the collection:</E>No Agency Form Number; File OMB-18. U.S. Citizenship and Immigration Services.</P>
        <P>4.<E T="03">Affected public who will be asked or required to respond, as well as a brief abstract: Primary:</E>Business or other for profit. E-Verify allows employers to electronically verify the employment eligibility status of newly hired employees.</P>
        <P>5.<E T="03">An estimate of the total number of respondents and the amount of time estimated for an average respondent to respond:</E>125,015 completing the E-Verify web interface at 17 responses at .86 hours (52 minutes) per response; 521,134 employers registering to participate in the program at 2.26 hours (2 hours and 15 minutes) per response; 3,333 requiring ID/IQ modification at 2 hours per response; 4,094,955 initial queries at .12 hours (7 minutes) per response; 195,329 secondary queries at 1.94 hours (1 hour 56 minutes) per response.</P>
        <P>6.<E T="03">An estimate of the total public burden (in hours) associated with the collection:</E>3,882,482 annual burden hours.</P>

        <P>If you need a copy of the supporting statement, please visit the Web site at:<E T="03">http://www.regulations.gov/.</E>
        </P>
        <P>We may also be contacted at: USCIS, Regulatory Products Division, Office of the Executive Secretariat, 20 Massachusetts Avenue, NW., Washington, DC 20529-2020, Telephone number 202-272-8377.</P>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>Sunday Aigbe,</NAME>
          <TITLE>Chief, Regulatory Products Division, Office of the Executive Secretariat, U.S. Citizenship and Immigration Services, Department of Homeland Security.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19423 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 9111-97-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HOMELAND SECURITY</AGENCY>
        <SUBAGY>U.S. Citizenship and Immigration Services</SUBAGY>
        <SUBJECT>Agency Information Collection Activities: Form N-426, Extension of a Currently Approved Information Collection; Comment Request</SUBJECT>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>30-Day Notice of Information Collection Under Review: Form N-426, Request for Certification of Military or Naval Service.</P>
        </ACT>

        <P>The Department of Homeland Security, U.S. Citizenship and Immigration Services (USCIS) will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and clearance in accordance with the Paperwork Reduction Act of 1995. The information collection was previously published in the<E T="04">Federal Register</E>on May 10, 2011, at 76 FR 27078, allowing for a 60-day public comment period. USCIS did not receive any comments.</P>
        <P>The purpose of this notice is to allow an additional 30 days for public comments. Comments are encouraged and will be accepted until August 31, 2011. This process is conducted in accordance with 5 CFR 1320.10.</P>

        <P>Written comments and/or suggestions regarding the item(s) contained in this notice, especially regarding the estimated public burden and associated response time, should be directed to the Department of Homeland Security (DHS), and to the Office of Information and Regulatory Affairs, Office of Management and Budget (OMB), USCIS Desk Officer. Comments may be submitted to: USCIS, Chief, Regulatory Products Division, 20 Massachusetts Avenue, NW., Washington, DC 20529. Comments may also be submitted to DHS via facsimile to 202-272-8352 or via e-mail at<E T="03">uscisfrcomment@dhs.gov</E>, and to the OMB USCIS Desk Officer via facsimile at 202-395-5806 or via e-mail at<E T="03">oira_submission@omb.eop.gov.</E>
        </P>
        <P>When submitting comments by e-mail, please make sure to add OMB Control No. 1615-0053 in the subject box. Written comments and suggestions from the public and affected agencies should address one or more of the following four points:</P>
        <P>(1) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility;</P>
        <P>(2) Evaluate the accuracy of the agency's estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used;</P>
        <P>(3) Enhance the quality, utility, and clarity of the information to be collected; and</P>
        <P>(4) Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses.</P>
        <P>
          <E T="03">Overview of this information collection:</E>
        </P>
        <P>(1)<E T="03">Type of Information Collection:</E>Extension of a currently approved information collection.</P>
        <P>(2)<E T="03">Title of the Form/Collection:</E>Request for Certification of Military or Naval Service.</P>
        <P>(3)<E T="03">Agency form number, if any, and the applicable component of the Department of Homeland Security sponsoring the collection:</E>Form N-426. U.S. Citizenship and Immigration Services.</P>
        <P>(4)<E T="03">Affected public who will be asked or required to respond, as well as a brief abstract:</E>
        </P>
        <P>
          <E T="03">Primary:</E>Individuals or Households. This form will be used by USCIS to request a verification of the military or naval service claim by an applicant filing for naturalization on the basis of honorable service in the U.S. armed forces.</P>
        <P>(5)<E T="03">An estimate of the total number of respondents and the amount of time estimated for an average respondent to respond:</E>45,000 responses at 20 minutes (.333) per response.<PRTPAGE P="45845"/>
        </P>
        <P>(6)<E T="03">An estimate of the total public burden (in hours) associated with the collection:</E>14,985 annual burden hours.</P>

        <P>If you have additional comments, suggestions, or need a copy of the proposed information collection instrument with instructions, or additional information, please visit:<E T="03">http://www.regulations.gov/search/index.jsp.</E>
        </P>
        <P>If additional information is required contact: USCIS, Regulatory Products Division, 20 Massachusetts Avenue, NW., Washington, DC 20529-2020, telephone (202) 272-8377.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Sunday Aigbe,</NAME>
          <TITLE>Chief, Regulatory Products Division, Office of the Executive Secretariat, U.S. Citizenship and Immigration Services, Department of Homeland Security.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19316 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 9111-97-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HOMELAND SECURITY</AGENCY>
        <SUBAGY>U.S. Citizenship and Immigration Services</SUBAGY>
        <SUBJECT>Agency Information Collection Activities: Form I-777, Extension of a Currently Approved Information Collection; Comment Request</SUBJECT>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>30-Day Notice of Information Collection Under Review: Form I-777, Application for Replacement of Northern Mariana Card.</P>
        </ACT>

        <P>The Department of Homeland Security, U.S. Citizenship and Immigration Services (USCIS) will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and clearance in accordance with the Paperwork Reduction Act of 1995. The information collection was previously published in the<E T="04">Federal Register</E>on May 19, 2011, at 76 FR 28800, allowing for a 60-day public comment period. USCIS received one comment for this information collection.</P>
        <P>The purpose of this notice is to allow an additional 30 days for public comments. Comments are encouraged and will be accepted until August 31, 2011. This process is conducted in accordance with 5 CFR 1320.10.</P>

        <P>Written comments and/or suggestions regarding the item(s) contained in this notice, especially regarding the estimated public burden and associated response time, should be directed to the Department of Homeland Security (DHS), and to the Office of Information and Regulatory Affairs, Office of Management and Budget (OMB), USCIS Desk Officer. Comments may be submitted to: USCIS, Chief, Regulatory Products Division, 20 Massachusetts Avenue, NW., Washington, DC 20529-2020. Comments may also be submitted to DHS via facsimile to 202-272-0997 or via e-mail at<E T="03">uscisfrcomment@dhs.gov,</E>and to the OMB USCIS Desk Officer via facsimile at 202-395-5806 or via e-mail at<E T="03">oira_submission@omb.eop.gov.</E>
        </P>
        <P>When submitting comments by e-mail please make sure to add OMB Control Number 1615-0042 in the subject box. Written comments and suggestions from the public and affected agencies should address one or more of the following four points:</P>
        <P>(1) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility;</P>
        <P>(2) Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used;</P>
        <P>(3) Enhance the quality, utility, and clarity of the information to be collected; and</P>
        <P>(4) Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses.</P>
        <P>
          <E T="03">Overview of this information collection:</E>
        </P>
        <P>(1)<E T="03">Type of Information Collection:</E>Extension of a currently approved information collection.</P>
        <P>(2)<E T="03">Title of the Form/Collection:</E>Application for Replacement of Northern Mariana Card.</P>
        <P>(3)<E T="03">Agency form number, if any, and the applicable component of the Department of Homeland Security sponsoring the collection:</E>Form I-777; U.S. Citizenship and Immigration Services.</P>
        <P>(4)<E T="03">Affected public who will be asked or required to respond, as well as a brief abstract: Primary: Individuals or Households.</E>Form I-777 is used by applicants applying for a Northern Marina identification card if they received United States citizenship pursuant to Public law 94-241 (covenant to establish a Commonwealth of the Northern Mariana Islands).</P>
        <P>(5)<E T="03">An estimate of the total number of respondents and the amount of time estimated for an average respondent to respond:</E>100 responses at .50 hours (30 minutes) per response.</P>
        <P>(6)<E T="03">An estimate of the total public burden (in hours) associated with the collection:</E>50 annual burden hours.</P>

        <P>If you need a copy of the information collection instrument, please visit the Web site at:<E T="03">http://www.regulations.gov.</E>
        </P>
        <P>We may also be contacted at: USCIS, Regulatory Products Division, 20 Massachusetts Avenue, NW., Washington, DC 20529-2020; Telephone 202-272-8377.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Sunday Aigbe,</NAME>
          <TITLE>Chief, Regulatory Products Division, Office of the Executive Secretariat, U.S. Citizenship and Immigration Services, Department of Homeland Security.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19317 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 9111-97-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF HOMELAND SECURITY</AGENCY>
        <SUBAGY>U.S. Customs and Border Protection</SUBAGY>
        <SUBJECT>Notice of Issuance of Final Determination Concerning a Certain Patient Transport Chair</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>U.S. Customs and Border Protection, Department of Homeland Security.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of final determination.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>This document provides notice that U.S. Customs and Border Protection (“CBP”) has issued a final determination concerning the country of origin of a certain patient transport chair. Based upon the facts presented, CBP has concluded in the final determination that the U.S. is the country of origin of the patient transport chair for purposes of U.S. government procurement.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATE:</HD>
          <P>The final determination was issued on July 26, 2011. A copy of the final determination is attached. Any party-at-interest, as defined in 19 CFR 177.22(d), may seek judicial review of this final determination on or before August 31, 2011.</P>
        </DATES>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Elif Eroglu, Valuation and Special Programs Branch: (202) 325-0277.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>

        <P>Notice is hereby given that on July 26, 2011, pursuant to subpart B of part 177, Customs Regulations (19 CFR part 177, subpart B), CBP issued a final determination concerning the country of origin of the BREEZ patient transport chair which may be offered to the U.S. Government under an undesignated government procurement contract. This final determination, Headquarters<PRTPAGE P="45846"/>Ruling Letter (“HQ”) H156919, was issued at the request of Electro Kinetic Technologies under procedures set forth at 19 CFR part 177, subpart B, which implements Title III of the Trade Agreements Act of 1979, as amended (19 U.S.C. 2511-18). In the final determination, CBP has concluded that, based upon the facts presented, the assembly of the BREEZ patient transport chair in the U.S., from parts made in China, Canada, France, and the U.S., constitutes a substantial transformation, such that the U.S. is the country of origin of the finished article for purposes of U.S. government procurement.</P>

        <P>Section 177.29, Customs Regulations (19 CFR 177.29), provides that notice of final determinations shall be published in the<E T="04">Federal Register</E>within 60 days of the date the final determination is issued. Section 177.30, CBP Regulations (19 CFR 177.30), provides that any party-at-interest, as defined in 19 CFR 177.22(d), may seek judicial review of a final determination within 30 days of publication of such determination in the<E T="04">Federal Register</E>.</P>
        <SIG>
          <DATED>Dated: July 26, 2011.</DATED>
          <NAME>Sandra L. Bell,</NAME>
          <TITLE>Executive Director,  Regulations and Rulings,  Office of International Trade.</TITLE>
        </SIG>
        <HD SOURCE="HD1">Attachment</HD>
        <FP SOURCE="FP-2">HQ H156919</FP>
        <FP SOURCE="FP-2">July 26, 2011</FP>
        <FP SOURCE="FP-2">OT:RR:CTF:VS H156919 EE</FP>
        <FP SOURCE="FP-2">CATEGORY: Marking</FP>
        <FP SOURCE="FP-2">Robert Gardenier</FP>
        <FP SOURCE="FP-2">M.E. Dey &amp; Co., Inc.</FP>
        <FP SOURCE="FP-2">700 W Virginia Street Suite 300</FP>
        <FP SOURCE="FP-2">Milwaukee, WI 53204</FP>
        <FP SOURCE="FP-2">RE: U.S. Government Procurement; Title III, Trade Agreements Act of 1979 (19 U.S.C. § 2511); Subpart B, Part 177, CBP Regulations; Patient Transport Chair</FP>
        <FP SOURCE="FP-2">Dear Mr. Gardenier:</FP>

        <P>This is in response to your correspondence of March 14, 2011, telephone conference on June 10, 2011, and additional information you submitted on July 21, 2011, requesting a final determination on behalf of Electro Kinetic Technologies (“Electro Kinetic”), pursuant to subpart B of part 177, U.S. Customs and Border Protection (“CBP”) Regulations (19 C.F.R. § 177.21<E T="03">et seq</E>.). Under the pertinent regulations, which implement Title III of the Trade Agreements Act of 1979, as amended (19 U.S.C. § 2511<E T="03">et seq</E>.), CBP issues country of origin advisory rulings and final determinations as to whether an article is or would be a product of a designated country or instrumentality for the purpose of granting waivers of certain “Buy American” restrictions in U.S. law or practice for products offered for sale to the U.S. Government.</P>
        <P>This final determination concerns the country of origin of the BREEZ patient transport chair. We note that Electro Kinetic is a party-at-interest within the meaning of 19 C.F.R. § 177.22(d)(1) and is entitled to request this final determination.</P>
        
        <FP SOURCE="FP-2">FACTS:</FP>
        <P>Electro Kinetic, headquartered in Germantown, Wisconsin, designs and manufactures ergonomically focused products used to transport people and materials within the retail, healthcare, and material handling industries. The merchandise at issue is the Electro Kinetic BREEZ patient transport chair engineered and assembled in the U.S. from U.S. and foreign components.</P>
        <P>The BREEZ transport chair is intended to transport patients or mobility impaired individuals. With the drive system integrated into the wheelchair, the patient transport chair can be maneuvered through tight or crowded hallways, elevators and rooms, transporting patients up to 750 lbs.</P>
        <P>The patient transport chair is produced in the U.S. from approximately 481 components. All of the components are of U.S., Chinese, Canadian, or French origin. The majority of the components are assembled in the U.S. into 26 subassemblies which are ultimately assembled with the remaining components into the final product.</P>
        <P>You submitted the costed bill of materials for the patient transport chair. The significant materials which comprise the patient transport chair include: wheels, casters, arm weldments, anti-tip weldments, swivel locks, 17 cable assemblies, a transaxle subassembly (which includes a Chinese-origin transaxle), a circuit breaker, a guard plate, a static strap subassembly, a Chinese-origin frame base weldment, a garment rod, a control box subassembly (which includes a French-origin handle circuit board, a control box, a key switch subassembly, and a forward/reverse switch subassembly), an s-drive subassembly, tire assemblies (which include wheel rims and foam filled tires), a charger subassembly (which includes a Canadian-origin charger), a control box plate, a high back flip seat, and batteries. It takes approximately six and a half hours to produce the finished patient transport chair.</P>
        <P>You state that the production of the BREEZ patient transport chair in the U.S. begins with the production of 17 cable subassemblies which include: positive and negative battery cable subassemblies, a handle cable subassembly, an emergency stop switch subassembly, a horn potentiometer subassembly, a speed potentiometer subassembly, a brake cable subassembly, a black horn cable subassembly, a controller cable subassembly, a brown horn cable subassembly, a charger cable subassembly, a motor cable subassembly, and a battery jumper subassembly.</P>
        <P>Next, the s-drive, which is part of s-drive subassembly, is programmed for acceleration, deceleration, and speed profiles. The transaxle subassembly, static strap subassembly, control box subassembly, keyswitch subassembly, forward/reverse switch subassembly, s-drive subassembly, tire assemblies, and charger assembly are produced. The wheels are added to the transaxle subassembly and assembled onto the frame. The control box subassembly, circuit breaker, charger assembly, horn and battery subassemblies are then installed onto the frame.</P>
        <P>In the final assembly stage, the rear casters, front anti-tip casters, seat, seat belt, headrest, arm rests, foot rests and the IV pole are installed.</P>
        <P>You provided a copy of the product brochure for the BREEZ patient transport chair.</P>
        
        <FP>ISSUE:</FP>
        <P>What is the country of origin of the BREEZ patient transport chair for the purpose of U.S. government procurement?</P>
        
        <FP>LAW AND ANALYSIS:</FP>
        <P>Pursuant to subpart B of part 177, 19 C.F.R. § 177.21 et seq., which implements Title III of the Trade Agreements Act of 1979, as amended (19 U.S.C. § 2511 et seq.), CBP issues country of origin advisory rulings and final determinations as to whether an article is or would be a product of a designated country or instrumentality for the purposes of granting waivers of certain “Buy American” restrictions in U.S. law or practice for products offered for sale to the U.S. Government.</P>
        <P>Under the rule of origin set forth under 19 U.S.C. § 2518(4)(B):</P>

        <P>An article is a product of a country or instrumentality only if (i) it is wholly the growth, product, or manufacture of that country or instrumentality, or (ii) in the case of an article which consists in whole or in part of materials from another country or instrumentality, it has been substantially transformed into a new and different article of commerce with a name, character, or use distinct from that of the article or articles from which it was so transformed.<PRTPAGE P="45847"/>
        </P>
        <P>See also, 19 C.F.R. § 177.22(a).</P>
        <P>In rendering advisory rulings and final determinations for purposes of U.S. government procurement, CBP applies the provisions of subpart B of part 177 consistent with the Federal Acquisition Regulations. See 19 C.F.R. § 177.21. In this regard, CBP recognizes that the Federal Acquisition Regulations restrict the U.S. Government's purchase of products to U.S.-made or designated country end products for acquisitions subject to the TAA. See 48 C.F.R. § 25.403(c)(1). The Federal Acquisition Regulations define “U.S.-made end product” as:</P>
        <P>* * *an article that is mined, produced, or manufactured in the United States or that is substantially transformed in the United States into a new and different article of commerce with a name, character, or use distinct from that of the article or articles from which it was transformed.</P>
        <P>48 C.F.R. § 25.003.</P>
        <P>In order to determine whether a substantial transformation occurs when components of various origins are assembled into completed products, CBP considers the totality of the circumstances and makes such determinations on a case-by-case basis. The country of origin of the item's components, extent of the processing that occurs within a country, and whether such processing renders a product with a new name, character, and use are primary considerations in such cases. Additionally, factors such as the resources expended on product design and development, extent and nature of post-assembly inspection and testing procedures, and the degree of skill required during the actual manufacturing process may be relevant when determining whether a substantial transformation has occurred. No one factor is determinative.</P>
        <P>In Headquarters Ruling Letter (“HQ”) H095239, dated June 2, 2010, CBP held that certain upright and recumbent exercise bikes, assembled in the U.S., were products of the U.S. for purposes of U.S. government procurement. The exercise bikes were assembled from a range of U.S. and foreign components and subassemblies. With the exception of the standard console assembly, all of the subassemblies, which were ultimately assembled to produce the final product, were produced in the U.S. In finding that the imported components were substantially transformed in the U.S., CBP stated that the assembly process that occurred in the U.S. was complex and meaningful, required the assembly of a large number of components, and rendered the final article with a new name, character, and use.</P>
        <P>As in HQ H095239, the BREEZ patient transport chair comprises the assembly of a large number of components, namely, 481 components. The majority of the components are assembled in the U.S. into 26 subassemblies which are then assembled with the remaining components into the finished patient transport chair. It takes approximately six and a half hours to produce the finished patient transport chair. We find that under the described assembly process, the foreign components lose their individual identities and become an integral part of the article, the patient transport chair, possessing a new name, character and use. The assembly process that occurs in the U.S. is complex and meaningful, involving the assembly of components into subassemblies which are then made into the final product. Therefore, based upon the information before us, we find that the imported components that are used to manufacture the patient transport chair are substantially transformed as a result of the assembly operations performed in the U.S. and that the country of origin of the patient transport chair for government procurement purposes is the U.S.</P>
        
        <FP>HOLDING:</FP>
        <P>The imported components that are used to manufacture the BREEZ patient transport chair are substantially transformed as a result of the assembly operations performed in the U.S. Therefore, we find that the country of origin of the BREEZ patient transport chair for government procurement purposes is the U.S.</P>
        <P>Notice of this final determination will be given in the Federal Register, as required by 19 C.F.R. § 177.29. Any party-at-interest other than the party which requested this final determination may request, pursuant to 19 C.F.R. § 177.31, that CBP reexamine the matter anew and issue a new final determination. Pursuant to 19 C.F.R. § 177.30, any party-at-interest may, within 30 days after publication of the Federal Register notice referenced above, seek judicial review of this final determination before the Court of International Trade.</P>
        <P>Sincerely,</P>
        <P>Sandra L. Bell, Executive Director, Regulations and Rulings, Office of International Trade</P>
        
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19400 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF THE INTERIOR</AGENCY>
        <SUBAGY>Office of the Secretary</SUBAGY>
        <SUBJECT>Vendor Outreach Workshop for Small Businesses in New Mexico of the United States</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Office of the Secretary, Interior.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Office of Small and Disadvantaged Business Utilization of the Department of the Interior and the Department of Agriculture are hosting a Vendor Outreach Workshop for small businesses in the State of New Mexico of the United States that are interested in doing business with each agency. This outreach workshop will review market contracting opportunities for the attendees. Business owners will be able to share their individual perspectives with Contracting Officers, Program Managers and Small Business Specialists from the Department.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>The workshop will be held on September 15, 2011, from 8:30 a.m. to 4 p.m.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>The workshop will be held at the Albuquerque Convention Center, 401 Second Street, Albuquerque, New Mexico 87102. Register online at:<E T="03">http://www.doi.gov/osdbu.</E>
          </P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Mark Oliver, Director, Office of Small and Disadvantaged Business Utilization, 1951 Constitution Ave., NW., MS-320 SIB, Washington, DC 20240, telephone 1-877-375-9927 (Toll-Free).</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>In accordance with the Small Business Act, as amended by Public Law 95-507, the Department has the responsibility to promote the use of small and small disadvantaged business for its acquisition of goods and services. The Department is proud of its accomplishments in meeting its business goals for small, small disadvantaged, 8(a), woman-owned, HUBZone, and service-disabled veteran-owned businesses. In Fiscal Year 2010, the Department awarded 50 percent of its $2.6 billion in contracts to small businesses.</P>

        <P>This fiscal year, the Office of Small and Disadvantaged Business Utilization are reaching out to our internal stakeholders and the Department's small business community by conducting several vendor outreach workshops. The Department's presenters will focus on contracting and subcontracting opportunities and how small businesses can better market services and products. Over 3,000 small businesses have been targeted for this event. If you are a small business interested in working with the<PRTPAGE P="45848"/>Department, we urge you to register online at:<E T="03">http://www.doi.gov/osdbu</E>and attend the workshop.</P>

        <P>These outreach events are a new and exciting opportunity for the Department's bureaus and offices to improve their support for small business. Additional scheduled events are posted on the Office of Small and Disadvantaged Business Utilization Web site at<E T="03">http://www.doi.gov/osdbu.</E>
        </P>
        <SIG>
          <NAME>Mark Oliver,</NAME>
          <TITLE>Director, Office of Small and Disadvantaged Business Utilization.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19360 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4210-RK-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF THE INTERIOR</AGENCY>
        <SUBAGY>Bureau of Land Management</SUBAGY>
        <DEPDOC>[LLOR-936000-L14300000-ET0000; HAG-11-0220; OROR-66533]</DEPDOC>
        <SUBJECT>Notice of Application for Withdrawal and Public Meeting; Oregon</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Bureau of Land Management, Interior.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The United States Forest Service (USFS) has filed an application with the Bureau of Land Management (BLM) requesting the Secretary of the Interior to withdraw approximately 5,610 acres of National Forest System lands, for a period of 5 years in aid of legislation to protect certain lands along the Chetco Wild and Scenic River. This notice temporarily segregates the lands for up to 2 years from location and entry under the United States mining laws, and from operation of the mineral and geothermal leasing laws, while the withdrawal application is being processed. This notice also gives an opportunity to comment on the application and announces the date, time, and location of a public meeting.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments must be received by October 31, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>Comments should be sent to the Oregon/Washington State Director, BLM, P.O. Box 2965, Portland, Oregon 97208-2965, or 333 SW. 1st Avenue, Portland, Oregon 97204.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Charles R. Roy, BLM Oregon/Washington State Office, 503-808-6189, or William C. Drummond, USFS Pacific Northwest Region, 503-808-2420. Persons who use a telecommunications device for the deaf (TDD) may call the Federal Information Relay Service (FIRS) at 1-800-877-8339 to contact the above individual during normal business hours. The FIRS is available 24 hours a day, 7 days a week, to leave a message or question with the above individual. You will receive a reply during normal business hours.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>The USFS has filed an application requesting that the Secretary of the Interior withdraw, for a 5-year period, the following described National Forest System lands from location and entry under the United States mining laws (30 U.S.C. ch. 2), and operation of the mineral and geothermal leasing laws, subject to valid existing rights.</P>
        <P>The application applies only to the Federal lands within the following described lands. The intent of this description is to follow the outer boundary of the Chetco Wild and Scenic River corridor, downstream of the western boundary of the Kalmiopsis Wilderness, as said corridor is described in the official boundary package certified by the USFS, Regional Forester, Region 6, on December 18, 1998, and available for public review at 333 SW. 1st Avenue, Portland, Oregon 97204. The wild and scenic corridor contains approximately 5,610 acres in Curry County and lies within the following sections:</P>
        <EXTRACT>
          <HD SOURCE="HD1">Willamette Meridian</HD>
          <FP SOURCE="FP-2">T. 38 S., R. 11 W.,</FP>
          <FP SOURCE="FP1-2">secs. 5 to 7, inclusive, and sec. 18.</FP>
          <FP SOURCE="FP-2">T. 38 S., R. 12 W.,</FP>
          <FP SOURCE="FP1-2">secs. 9 to 16, inclusive, sec. 21, secs. 27 to 29, inclusive, secs. 32 and 33.</FP>
          <FP SOURCE="FP-2">T. 39 S., R. 12 W.,</FP>
          <FP SOURCE="FP1-2">secs. 4, 5, 8, 9, 16, 17, 20, 29, 30, and 31.</FP>
        </EXTRACT>
        
        <P>The purpose of the withdrawal is to temporarily segregate the lands in aid of legislation.</P>
        <P>No suitable alternative sites were considered, as the pending legislation is to protect the lands specified in this notice. The use of a right-of-way, interagency agreement, or cooperative agreement would not provide adequate protection. The USFS would not need to acquire water rights to fulfill the purpose of the requested withdrawal.</P>
        <P>Temporary land uses may be permitted during this segregative period, including licenses, permits, rights-of-way, and disposal of vegetative resources; however, the lands will be segregated from appropriation under the mining law.</P>
        <P>Records related to the application may be examined by contacting Charles R. Roy at the above address or phone number.</P>
        <P>On or before October 31, 2011, all persons who wish to submit comments, suggestions, or objections in connection with the application may present their views in writing to the BLM State Director at the address indicated above.</P>
        <P>Comments, including names and street addresses of respondents, will be available for public review at the address indicated above during regular business hours. Before including your address, phone number, e-mail address, or other personal identifying information in your comment, be advised that your entire comment—including your personal identifying information—may be made publicly available at any time. While you can ask us in your comment to withhold from public review your personal identifying information, we cannot guarantee that we will be able to do so.</P>
        <P>Notice is hereby given that a public meeting in connection with the application for withdrawal will be held on September 15, 2011 from 5 p.m. to 7 p.m. at the USFS, Gold Beach District Office located at 539 SW. Chetco Avenue, Brookings, Oregon. Interested parties may make oral statements at the meeting and/or may file written statements with the BLM. All statements received will be considered before any recommendation concerning the withdrawal is submitted to the Assistant Secretary—Land and Minerals Management for final action.</P>
        <P>The application will be processed in accordance with the regulations set forth in 43 CFR part 2300.</P>
        <AUTH>
          <HD SOURCE="HED">Authority:</HD>
          <P>43 CFR 2310.3-1.</P>
        </AUTH>
        <SIG>
          <NAME>Fred O'Ferrall,</NAME>
          <TITLE>Chief, Branch of Land, Mineral, and Energy Resources.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19302 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 3410-11-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF THE INTERIOR</AGENCY>
        <SUBAGY>National Park Service</SUBAGY>
        <SUBJECT>Draft Environmental Impact Statement on a Denali Park Road Vehicle Management Plan for Denali National Park and Preserve</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>National Park Service, Interior.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice of availability of the Draft Environmental Impact Statement on a Denali Park Road Vehicle Management Plan for Denali National Park and Preserve.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>The National Park Service announces the availability of a Draft Environmental Impact Statement (DEIS) on a Denali Park Road Vehicle Management Plan for Denali National Park and Preserve. The document describes and analyzes the environmental impacts of a no action alternative and two action alternatives for management of vehicle use on the Denali Park Road. This notice<PRTPAGE P="45849"/>announces the public comment period, the locations of public meetings, and solicits comments on the DEIS.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Comments on the DEIS must be received no later than September 30, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>Written comments on the DEIS should be submitted to Miriam Valentine, Park Planner, Denali National Park and Preserve, P.O. Box 588, Talkeetna, AK 99676.</P>

          <P>Submit comments electronically through the NPS Planning, Environment and Public Comment system (PEPC) at<E T="03">http://parkplanning.nps.gov.</E>The DEIS may be viewed and retrieved at this Web site as well. Hard copies of the DEIS are available by request from the aforementioned address. See Supplementary Information for the locations of public meetings.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Miriam Valentine, Park Planner, Denali National Park and Preserve,<E T="03">miriam_valentine@nps.gov,</E>Telephone: 907-733-9102.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>The purpose of the DEIS is to analyze the effects of the alternatives for managing vehicle use along the Park Road in Denali National Park. Since the mid-1920s, visitors have been able to travel the approximately 90-mile Park Road on buses operated by the park concessioner. Starting in 1972, when private vehicle traffic was restricted beyond mile 15 of the road, visitors have used the mandatory visitor transportation system. The present approach for managing vehicles on the Park Road is based on the park's 1986 general management plan, which established a seasonal limit of 10,512 vehicles beyond mile 15 between approximately Memorial Day and a week after Labor Day. As tourism in Alaska has increased, so have demands for visits along the Park Road. This plan evaluates how to manage vehicle use, while continuing to provide high quality visitor experience, opportunities to view wildlife in natural habitats and to access the park's wilderness. The Denali Park Road Vehicle Management Plan is intended to guide park managers over the next 20 years with management of vehicles on the Park Road. The DEIS considers a reasonable range of alternatives based on management objectives, park resources and values, and public input.</P>
        <P>
          <E T="03">Alternative A:</E>(No Action): This alternative would continue current management of vehicle use on the Park Road. In addition to a seasonal limit of 10,512 vehicles past mile 15, there would continue to be specific seasonal and daily limits to tour buses, shuttle buses, inholder traffic, professional photographer vehicles, NPS administrative vehicles and other categories of vehicles.</P>
        <P>
          <E T="03">Alternative B:</E>This alternative would use an adaptive management framework for vehicle use based on indicators and standards for visitor experiences and resource protection. While adhering to these standards, management would maximize seating on all transit and tour vehicles to offer the largest number of visitors the opportunity to travel the Park Road. This adaptive management framework would include options for reducing or scheduling non-bus traffic to allow for additional visitor use.</P>
        <P>
          <E T="03">Alternative C:</E>This alternative would use an adaptive management framework for vehicle use based on indicators and standards for visitor experiences and resource protection. While adhering to these standards, management would promote a wide variety of visitor opportunities that would include brief experiences in the park's entrance area, short visits along segments of the Park Road, special interest tours, and multiday experiences in the park's backcountry. This adaptive management framework would include options for reducing or scheduling non-bus traffic to allow for additional visitor use.</P>
        <P>At this time, the NPS does not have a preferred alternative, and public comment is sought to inform selection of a preferred alternative in the final EIS.</P>
        <P>Public meetings are scheduled in Alaska at the following locations: Anchorage, Fairbanks, and Denali National Park. The specific dates and times of the public meetings will be announced in local media.</P>
        <P>If you include your address, phone number, e-mail address, or other personal identifying information in your comment, you should be aware that your entire comment—including your personal identifying information—may be made publicly available at any time. While you can ask us in your comment to withhold your personal identifying information from public review, we cannot guarantee that we will be able to do so.</P>
        <SIG>
          <DATED>Dated: May 6, 2011.</DATED>
          <NAME>Sue E. Masica,</NAME>
          <TITLE>Regional Director, Alaska.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19310 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4310-PF-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF THE INTERIOR</AGENCY>
        <SUBAGY>Office of Surface Mining Reclamation and Enforcement</SUBAGY>
        <SUBJECT>Notice of Proposed Information Collection</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Office of Surface Mining Reclamation and Enforcement, Interior.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice and request for comments.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>In compliance with the Paperwork Reduction Act of 1995, the Office of Surface Mining Reclamation and Enforcement (OSM) is announcing its intention to renew the approval for the collection of information under 30 CFR part 842 which allows the collection and processing of citizen complaints and requests for inspection. The collection described below has been forwarded to the Office of Management and Budget (OMB) for review and approval. The information collection request describes the nature of the information collection and the expected burden and cost.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>OMB has up to 60 days to approve or disapprove the information collection but may respond after 30 days. Therefore, public comments should be submitted to OMB by August 31, 2011, in order to be assured of consideration.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Submit comments to the Office of Information and Regulatory Affairs, Office of Management and Budget, Attention: Department of Interior Desk Officer, by telefax at (202) 395-5806 or via e-mail to<E T="03">OIRA_Docket@omb.eop.gov.</E>Also, please send a copy of your comments to John Trelease, Office of Surface Mining Reclamation and Enforcement, 1951 Constitution Ave., NW., Room 202—SIB, Washington, DC 20240, or electronically to<E T="03">jtrelease@osmre.gov.</E>Please refer to OMB Control Number 1029-0118 in your correspondence.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>To receive a copy of the information collection request contact John Trelease at (202) 208-2783, or electronically at<E T="03">jtrelease@osmre.gov.</E>You may also review this collection by going to<E T="03">http://www.reginfo.gov</E>(Information Collection Review, Currently Under Review, Agency is Department of the Interior, DOI-OSMRE).</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>

        <P>OMB regulations at 5 CFR part 1320, which implement provisions of the Paperwork Reduction Act of 1995 (Pub. L. 104-13), require that interested members of the public and affected agencies have an opportunity to comment on information<PRTPAGE P="45850"/>collection and recordkeeping activities [see 5 CFR 1320.8(d)]. OSM has submitted a request to OMB to approve the collection of information in 30 CFR part 842—Federal inspections and monitoring. OSM is requesting a 3-year term of approval for this information collection activity.</P>

        <P>An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. The OMB control number for this collection of information, 1029-0118, has been placed on the electronic citizen complaint form that may be found on OSM's home page at<E T="03">http://vvww.osmre.gov/citizen.htm.</E>
        </P>
        <P>As required under 5 CFR 1320.8(d), a<E T="04">Federal Register</E>notice soliciting comments on this collection of information was published on May 11, 2011 (76 FR 27346). No comments were received. This notice provides the public with an additional 30 days in which to comment on the following information collection activity:</P>
        <P>
          <E T="03">Title:</E>30 CFR 842—Federal inspections and monitoring.</P>
        <P>
          <E T="03">OMB Control Number:</E>1029-0118.</P>
        <P>
          <E T="03">Summary:</E>For purposes of information collection, this part establishes the procedures for any person to notify the Office of Surface Mining in writing of any violation that may exist at a surface coal mining operation. The information will be used to investigate potential violations of the Act or applicable State regulations.</P>
        <P>
          <E T="03">Bureau Form Number:</E>None.</P>
        <P>
          <E T="03">Frequency of Collection:</E>Once.</P>
        <P>
          <E T="03">Description of Respondents:</E>Citizens.</P>
        <P>
          <E T="03">Total Annual Responses:</E>50.</P>
        <P>
          <E T="03">Total Annual Burden Hours:</E>184 hours.</P>
        <P>
          <E T="03">Total Annual Non-Wage Cost:</E>$0.</P>

        <P>Send comments on the need for the collection of information for the performance of the functions of the agency; the accuracy of the agency's burden estimates; ways to enhance the quality, utility and clarity of the information collection; and ways to minimize the information collection burden on respondents, such as use of automated means of collection of the information, to the addresses listed under<E T="02">ADDRESSES</E>. Please refer to the appropriate OMB control number 1029-0118 in your correspondence.</P>
        <P>Before including your address, phone number, email address, or other personal identifying information in your comment, you should be aware that your entire comment, including your personal identifying information, may be made publicly available at any time. While you can ask us in your comment to withhold your personal identifying information from public review, we cannot guarantee that we will be able to do so.</P>
        <SIG>
          <DATED>Dated: July 22, 2011.</DATED>
          <NAME>Stephen M. Sheffield,</NAME>
          <TITLE>Acting Chief, Division of Regulatory Support.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19295 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4310-05-M</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">INTERNATIONAL TRADE COMMISSION</AGENCY>
        <SUBJECT>Notice of Receipt of Complaint; Solicitation of Comments Relating to the Public Interest</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>U.S. International Trade Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>Notice is hereby given that the U.S. International Trade Commission has received a complaint entitled<E T="03">In Re Certain Products Containing Interactive Program Guide and Parental Controls Technology,</E>DN 2836; the Commission is soliciting comments on any public interest issues raised by the complaint.</P>
        </SUM>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>James R. Holbein, Secretary to the Commission, U.S. International Trade Commission, 500 E Street, SW., Washington, DC 20436, telephone (202) 205-2000. The public version of the complaint can be accessed on the Commission's electronic docket (EDIS) at<E T="03">http://edis.usitc.gov,</E>and will be available for inspection during official business hours (8:45 a.m. to 5:15 p.m.) in the Office of the Secretary, U.S. International Trade Commission, 500 E Street, SW., Washington, DC 20436, telephone (202) 205-2000.</P>

          <P>General information concerning the Commission may also be obtained by accessing its Internet server (<E T="03">http://www.usitc.gov</E>). The public record for this investigation may be viewed on the Commission's electronic docket (EDIS) at<E T="03">http://edis.usitc.gov.</E>Hearing-impaired persons are advised that information on this matter can be obtained by contacting the Commission's TDD terminal on (202) 205-1810.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>The Commission has received a complaint filed on behalf of Rovi Corporation, Rovi Guides, Inc., United Video Properties, Inc., and Gemstar Development Corporation on July 26, 2011. The complaint alleges violations of section 337 of the Tariff Act of 1930 (19 U.S.C. 1337) in the importation into the United States, the sale for importation, and the sale within the United States after importation of certain products containing interactive program guide and parental controls technology. The complaint names as respondents Sharp Corporation of Japan; Sharp Electronics Corporation of NJ; and Sharp Electronics Manufacturing Company of America, Inc. of NJ.</P>
        <P>The complainant, proposed respondents, other interested parties, and members of the public are invited to file comments, not to exceed five pages in length, on any public interest issues raised by the complaint. Comments should address whether issuance of an exclusion order and/or a cease and desist order in this investigation would negatively affect the public health and welfare in the United States, competitive conditions in the United States economy, the production of like or directly competitive articles in the United States, or United States consumers.</P>
        <P>In particular, the Commission is interested in comments that:</P>
        <P>(i) Explain how the articles potentially subject to the orders are used in the United States;</P>
        <P>(ii) Identify any public health, safety, or welfare concerns in the United States relating to the potential orders;</P>
        <P>(iii) Indicate the extent to which like or directly competitive articles are produced in the United States or are otherwise available in the United States, with respect to the articles potentially subject to the orders; and</P>
        <P>(iv) Indicate whether Complainant, Complainant's licensees, and/or third party suppliers have the capacity to replace the volume of articles potentially subject to an exclusion order and a cease and desist order within a commercially reasonable time.</P>

        <P>Written submissions must be filed no later than by close of business, five business days after the date of publication of this notice in the<E T="04">Federal Register</E>. There will be further opportunities for comment on the public interest after the issuance of any final initial determination in this investigation.</P>

        <P>Persons filing written submissions must file the original document and 12 true copies thereof on or before the deadlines stated above with the Office of the Secretary. Submissions should refer to the docket number (“Docket No. 2836”) in a prominent place on the cover page and/or the first page. The Commission's rules authorize filing submissions with the Secretary by facsimile or electronic means only to the extent permitted by section 201.8 of the rules (see Handbook for Electronic Filing Procedures,<E T="03">http://www.usitc.gov/<PRTPAGE P="45851"/>secretary/fed_reg_notices/rules/documents/handbook_on_electronic_filing.pdf</E>). Persons with questions regarding electronic filing should contact the Secretary (202-205-2000).</P>

        <P>Any person desiring to submit a document to the Commission in confidence must request confidential treatment. All such requests should be directed to the Secretary to the Commission and must include a full statement of the reasons why the Commission should grant such treatment.<E T="03">See</E>19 CFR 201.6. Documents for which confidential treatment by the Commission is properly sought will be treated accordingly. All nonconfidential written submissions will be available for public inspection at the Office of the Secretary.</P>
        <P>This action is taken under the authority of section 337 of the Tariff Act of 1930, as amended (19 U.S.C. 1337), and of sections 201.10 and 210.50(a)(4) of the Commission's Rules of Practice and Procedure (19 CFR 201.10, 210.50(a)(4)).</P>
        <SIG>
          <P>By order of the Commission.</P>
          
          <DATED>Issued: July 26, 2011.</DATED>
          <NAME>James R. Holbein,</NAME>
          <TITLE>Secretary to the Commission.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19355 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 7020-02-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">INTERNATIONAL TRADE COMMISSION</AGENCY>
        <DEPDOC>[Investigation Nos. 701-TA-442-443 and 731-TA-1095-1097 (Review)]</DEPDOC>
        <SUBJECT>Certain Lined Paper School Supplies From China, India, and Indonesia—Institution of Five-Year Reviews Concerning the Countervailing Duty Orders on Certain Lined Paper School Supplies From India and Indonesia and the Antidumping Duty Orders on Certain Lined Paper School Supplies From China, India, and Indonesia</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>United States International Trade Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Commission hereby gives notice that it has instituted reviews pursuant to section 751(c) of the Tariff Act of 1930 (19 U.S.C. 1675(c)) (the Act) to determine whether revocation of the countervailing duty orders on certain lined paper school supplies from India and Indonesia and the antidumping duty orders on certain lined paper school supplies from China, India, and Indonesia would be likely to lead to continuation or recurrence of material injury. Pursuant to section 751(c)(2) of the Act, interested parties are requested to respond to this notice by submitting the information specified below to the Commission;<SU>1</SU>
            <FTREF/>to be assured of consideration, the deadline for responses is August 31, 2011. Comments on the adequacy of responses may be filed with the Commission by October 14, 2011. For further information concerning the conduct of these reviews and rules of general application, consult the Commission's Rules of Practice and Procedure, part 201, subparts A through E (19 CFR part 201), and part 207, subparts A, D, E, and F (19 CFR part 207), as most recently amended at 74 FR 2847 (January 16, 2009).</P>
          <FTNT>
            <P>
              <SU>1</SU>No response to this request for information is required if a currently valid Office of Management and Budget (OMB) number is not displayed; the OMB number is 3117-0016/USITC No. 11-5-254, expiration date June 30, 2014. Public reporting burden for the request is estimated to average 15 hours per response. Please send comments regarding the accuracy of this burden estimate to the Office of Investigations, U.S. International Trade Commission, 500 E Street, SW., Washington, DC 20436.</P>
          </FTNT>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATED:</HD>
          <P>
            <E T="03">Effective Date:</E>August 1, 2011.</P>
        </DATES>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Mary Messer (202-205-3193), Office of Investigations, U.S. International Trade Commission, 500 E Street, SW., Washington, DC 20436. Hearing-impaired persons can obtain information on this matter by contacting the Commission's TDD terminal on 202-205-1810. Persons with mobility impairments who will need special assistance in gaining access to the Commission should contact the Office of the Secretary at 202-205-2000. General information concerning the Commission may also be obtained by accessing its Internet server (<E T="03">http://www.usitc.gov</E>). The public record for these reviews may be viewed on the Commission's electronic docket (EDIS) at<E T="03">http://edis.usitc.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>
          <E T="03">Background.</E>—On September 28, 2006, the Department of Commerce (“Commerce”) issued countervailing duty orders on certain lined paper school supplies from India and Indonesia and antidumping duty orders on certain lined paper school supplies from China, India, and Indonesia (71 FR 56949). On April 14, 2011, Commerce amended in part the antidumping duty order on subject imports from India (76 FR 20954). The Commission is conducting reviews to determine whether revocation of the orders would be likely to lead to continuation or recurrence of material injury to the domestic industry within a reasonably foreseeable time. It will assess the adequacy of interested party responses to this notice of institution to determine whether to conduct full or expedited reviews. The Commission's determinations in any expedited reviews will be based on the facts available, which may include information provided in response to this notice.</P>
        <P>
          <E T="03">Definitions.</E>—The following definitions apply to these reviews:</P>
        <P>(1)<E T="03">Subject Merchandise</E>is the class or kind of merchandise that is within the scope of the five-year reviews, as defined by the Department of Commerce.</P>
        <P>(2) The<E T="03">Subject Countries</E>in these reviews are China, India, and Indonesia.</P>
        <P>(3) The<E T="03">Domestic Like Product</E>is the domestically produced product or products which are like, or in the absence of like, most similar in characteristics and uses with, the<E T="03">Subject Merchandise.</E>In its original determinations, the Commission found one<E T="03">Domestic Like Product</E>consisting of all lined paper products, regardless of dimension.</P>
        <P>(4) The<E T="03">Domestic Industry</E>is the U.S. producers as a whole of the<E T="03">Domestic Like Product,</E>or those producers whose collective output of the<E T="03">Domestic Like Product</E>constitutes a major proportion of the total domestic production of the product. In its original determinations, the Commission found one<E T="03">Domestic Industry</E>consisting of all domestic producers of lined paper products. The Commission also found during the original investigations that circumstances were appropriate to exclude two domestic producers, American Scholar and CPP, from the domestic industry under the related parties provision.</P>
        <P>(5) The<E T="03">Order Date</E>is the date that the antidumping and countervailing duty orders under review became effective. In these reviews, the<E T="03">Order Date</E>is September 28, 2006.</P>
        <P>(6) An<E T="03">Importer</E>is any person or firm engaged, either directly or through a parent company or subsidiary, in importing the<E T="03">Subject Merchandise</E>into the United States from a foreign manufacturer or through its selling agent.</P>
        <P>
          <E T="03">Participation in the reviews and public service list.</E>—Persons, including industrial users of the<E T="03">Subject Merchandise</E>and, if the merchandise is sold at the retail level, representative consumer organizations, wishing to participate in the reviews as parties must file an entry of appearance with the Secretary to the Commission, as provided in section 201.11(b)(4) of the Commission's rules, no later than 21 days after publication of this notice in<PRTPAGE P="45852"/>the<E T="04">Federal Register.</E>The Secretary will maintain a public service list containing the names and addresses of all persons, or their representatives, who are parties to the reviews.</P>
        <P>Former Commission employees who are seeking to appear in Commission five-year reviews are advised that they may appear in a review even if they participated personally and substantially in the corresponding underlying original investigation. The Commission's designated agency ethics official has advised that a five-year review is not considered the ``same particular matter'' as the corresponding underlying original investigation for purposes of 18 U.S.C. 207, the post employment statute for Federal employees, and Commission rule 201.15(b) (19 CFR 201.15(b)), 73 FR 24609 (May 5, 2008). This advice was developed in consultation with the Office of Government Ethics. Consequently, former employees are not required to seek Commission approval to appear in a review under Commission rule 19 CFR 201.15, even if the corresponding underlying original investigation was pending when they were Commission employees. For further ethics advice on this matter, contact Carol McCue Verratti, Deputy Agency Ethics Official, at 202-205-3088.</P>
        <P>
          <E T="03">Limited disclosure of business proprietary information (BPI) under an administrative protective order (APO) and APO service list.</E>—Pursuant to section 207.7(a) of the Commission's rules, the Secretary will make BPI submitted in these reviews available to authorized applicants under the APO issued in the reviews, provided that the application is made no later than 21 days after publication of this notice in the<E T="04">Federal Register</E>. Authorized applicants must represent interested parties, as defined in 19 U.S.C. 1677(9), who are parties to the reviews. A separate service list will be maintained by the Secretary for those parties authorized to receive BPI under the APO.</P>
        <P>
          <E T="03">Certification.</E>—Pursuant to section 207.3 of the Commission's rules, any person submitting information to the Commission in connection with these reviews must certify that the information is accurate and complete to the best of the submitter's knowledge. In making the certification, the submitter will be deemed to consent, unless otherwise specified, for the Commission, its employees, and contract personnel to use the information provided in any other reviews or investigations of the same or comparable products which the Commission conducts under Title VII of the Act, or in internal audits and investigations relating to the programs and operations of the Commission pursuant to 5 U.S.C. Appendix 3.</P>
        <P>
          <E T="03">Written submissions.</E>—Pursuant to section 207.61 of the Commission's rules, each interested party response to this notice must provide the information specified below. The deadline for filing such responses is August 31, 2011. Pursuant to section 207.62(b) of the Commission's rules, eligible parties (as specified in Commission rule 207.62(b)(1)) may also file comments concerning the adequacy of responses to the notice of institution and whether the Commission should conduct expedited or full reviews. The deadline for filing such comments is October 14, 2011. All written submissions must conform with the provisions of sections 201.8 and 207.3 of the Commission's rules and any submissions that contain BPI must also conform with the requirements of sections 201.6 and 207.7 of the Commission's rules. The Commission's rules do not authorize filing of submissions with the Secretary by facsimile or electronic means, except to the extent permitted by section 201.8 of the Commission's rules, as amended, 67 FR 68036 (November 8, 2002). Also, in accordance with sections 201.16(c) and 207.3 of the Commission's rules, each document filed by a party to the reviews must be served on all other parties to the reviews (as identified by either the public or APO service list as appropriate), and a certificate of service must accompany the document (if you are not a party to the reviews you do not need to serve your response).</P>
        <P>
          <E T="03">Inability to provide requested information.</E>—Pursuant to section 207.61(c) of the Commission's rules, any interested party that cannot furnish the information requested by this notice in the requested form and manner shall notify the Commission at the earliest possible time, provide a full explanation of why it cannot provide the requested information, and indicate alternative forms in which it can provide equivalent information. If an interested party does not provide this notification (or the Commission finds the explanation provided in the notification inadequate) and fails to provide a complete response to this notice, the Commission may take an adverse inference against the party pursuant to section 776(b) of the Act in making its determinations in the reviews.</P>
        <P>
          <E T="03">INFORMATION TO BE PROVIDED IN RESPONSE TO THIS NOTICE OF INSTITUTION:</E>If you are a domestic producer, union/worker group, or trade/business association; import/export<E T="03">Subject Merchandise</E>from more than one<E T="03">Subject Country;</E>or produce<E T="03">Subject Merchandise</E>in more than one<E T="03">Subject Country,</E>you may file a single response. If you do so, please ensure that your response to each question includes the information requested for each pertinent<E T="03">Subject Country.</E>As used below, the term ``firm'' includes any related firms.</P>
        <P>(1) The name and address of your firm or entity (including World Wide Web address) and name, telephone number, fax number, and E-mail address of the certifying official.</P>

        <P>(2) A statement indicating whether your firm/entity is a U.S. producer of the<E T="03">Domestic Like Product,</E>a U.S. union or worker group, a U.S. importer of the<E T="03">Subject Merchandise,</E>a foreign producer or exporter of the<E T="03">Subject Merchandise,</E>a U.S. or foreign trade or business association, or another interested party (including an explanation). If you are a union/worker group or trade/business association, identify the firms in which your workers are employed or which are members of your association.</P>
        <P>(3) A statement indicating whether your firm/entity is willing to participate in these reviews by providing information requested by the Commission.</P>

        <P>(4) A statement of the likely effects of the revocation of the antidumping and countervailing duty orders on the<E T="03">Domestic Industry</E>in general and/or your firm/entity specifically. In your response, please discuss the various factors specified in section 752(a) of the Act (19 U.S.C. § 1675a(a)) including the likely volume of subject imports, likely price effects of subject imports, and likely impact of imports of<E T="03">Subject Merchandise</E>on the<E T="03">Domestic Industry.</E>
        </P>

        <P>(5) A list of all known and currently operating U.S. producers of the<E T="03">Domestic Like Product.</E>Identify any known related parties and the nature of the relationship as defined in section 771(4)(B) of the Act (19 U.S.C. 1677(4)(B)).</P>

        <P>(6) A list of all known and currently operating U.S. importers of the<E T="03">Subject Merchandise</E>and producers of the<E T="03">Subject Merchandise</E>in each<E T="03">Subject Country</E>that currently export or have exported<E T="03">Subject Merchandise</E>to the United States or other countries since the<E T="03">Order Date.</E>
        </P>

        <P>(7) A list of 3-5 leading purchasers in the U.S. market for the<E T="03">Domestic Like Product</E>and the<E T="03">Subject Merchandise</E>(including street address, World Wide Web address, and the name, telephone number, fax number, and E-mail address of a responsible official at each firm).</P>

        <P>(8) A list of known sources of information on national or regional prices for the<E T="03">Domestic Like Product</E>or<PRTPAGE P="45853"/>the<E T="03">Subject Merchandise</E>in the U.S. or other markets.</P>
        <P>(9) If you are a U.S. producer of the<E T="03">Domestic Like Product,</E>provide the following information on your firm's operations on that product during calendar year 2010, except as noted (report quantity data in pieces and value data in U.S. dollars, f.o.b. plant). If you are a union/worker group or trade/business association, provide the information, on an aggregate basis, for the firms in which your workers are employed/which are members of your association.</P>

        <P>(a) Production (quantity) and, if known, an estimate of the percentage of total U.S. production of the<E T="03">Domestic Like Product</E>accounted for by your firm's(s') production;</P>
        <P>(b) Capacity (quantity) of your firm to produce the<E T="03">Domestic Like Product</E>(i.e., the level of production that your establishment(s) could reasonably have expected to attain during the year, assuming normal operating conditions (using equipment and machinery in place and ready to operate), normal operating levels (hours per week/weeks per year), time for downtime, maintenance, repair, and cleanup, and a typical or representative product mix);</P>

        <P>(c) the quantity and value of U.S. commercial shipments of the<E T="03">Domestic Like Product</E>produced in your U.S. plant(s);</P>

        <P>(d) the quantity and value of U.S. internal consumption/company transfers of the<E T="03">Domestic Like Product</E>produced in your U.S. plant(s); and</P>

        <P>(e) the value of (i) net sales, (ii) cost of goods sold (COGS), (iii) gross profit, (iv) selling, general and administrative (SG&amp;A) expenses, and (v) operating income of the<E T="03">Domestic Like Product</E>produced in your U.S. plant(s) (include both U.S. and export commercial sales, internal consumption, and company transfers) for your most recently completed fiscal year (identify the date on which your fiscal year ends).</P>

        <P>(10) If you are a U.S. importer or a trade/business association of U.S. importers of the<E T="03">Subject Merchandise</E>from the<E T="03">Subject Country(ies),</E>provide the following information on your firm's(s') operations on that product during calendar year 2010 (report quantity data in pieces and value data in U.S. dollars). If you are a trade/business association, provide the information, on an aggregate basis, for the firms which are members of your association.</P>

        <P>(a) The quantity and value (landed, duty-paid but not including antidumping or countervailing duties) of U.S. imports and, if known, an estimate of the percentage of total U.S. imports of<E T="03">Subject Merchandise</E>from each<E T="03">Subject Country</E>accounted for by your firm's(s') imports;</P>

        <P>(b) the quantity and value (f.o.b. U.S. port, including antidumping and/or countervailing duties) of U.S. commercial shipments of<E T="03">Subject Merchandise</E>imported from each<E T="03">Subject Country;</E>and</P>

        <P>(c) the quantity and value (f.o.b. U.S. port, including antidumping and/or countervailing duties) of U.S. internal consumption/company transfers of<E T="03">Subject Merchandise</E>imported from each<E T="03">Subject Country.</E>
        </P>

        <P>(11) If you are a producer, an exporter, or a trade/business association of producers or exporters of the<E T="03">Subject Merchandise</E>in the<E T="03">Subject Country(ies),</E>provide the following information on your firm's(s') operations on that product during calendar year 2010 (report quantity data in pieces and value data in U.S. dollars, landed and duty-paid at the U.S. port but not including antidumping or countervailing duties). If you are a trade/business association, provide the information, on an aggregate basis, for the firms which are members of your association.</P>

        <P>(a) Production (quantity) and, if known, an estimate of the percentage of total production of<E T="03">Subject Merchandise</E>in each<E T="03">Subject Country</E>accounted for by your firm's(s') production;</P>
        <P>(b) Capacity (quantity) of your firm to produce the<E T="03">Subject Merchandise</E>in each<E T="03">Subject Country</E>(i.e., the level of production that your establishment(s) could reasonably have expected to attain during the year, assuming normal operating conditions (using equipment and machinery in place and ready to operate), normal operating levels (hours per week/weeks per year), time for downtime, maintenance, repair, and cleanup, and a typical or representative product mix); and</P>

        <P>(c) the quantity and value of your firm's(s') exports to the United States of<E T="03">Subject Merchandise</E>and, if known, an estimate of the percentage of total exports to the United States of<E T="03">Subject Merchandise</E>from each<E T="03">Subject Country</E>accounted for by your firm's(s') exports.</P>

        <P>(12) Identify significant changes, if any, in the supply and demand conditions or business cycle for the<E T="03">Domestic Like Product</E>that have occurred in the United States or in the market for the<E T="03">Subject Merchandise</E>in the<E T="03">Subject Country(ies)</E>since the<E T="03">Order Date,</E>and significant changes, if any, that are likely to occur within a reasonably foreseeable time. Supply conditions to consider include technology; production methods; development efforts; ability to increase production (including the shift of production facilities used for other products and the use, cost, or availability of major inputs into production); and factors related to the ability to shift supply among different national markets (including barriers to importation in foreign markets or changes in market demand abroad). Demand conditions to consider include end uses and applications; the existence and availability of substitute products; and the level of competition among the<E T="03">Domestic Like Product</E>produced in the United States,<E T="03">Subject Merchandise</E>produced in the<E T="03">Subject Country(ies),</E>and such merchandise from other countries.</P>

        <P>(13) (OPTIONAL) A statement of whether you agree with the above definitions of the<E T="03">Domestic Like Product</E>and<E T="03">Domestic Industry;</E>if you disagree with either or both of these definitions, please explain why and provide alternative definitions.</P>
        <AUTH>
          <HD SOURCE="HED">Authority:</HD>
          <P>This review is being conducted under authority of title VII of the Tariff Act of 1930; this notice is published pursuant to section 207.61 of the Commission's rules.</P>
        </AUTH>
        <SIG>
          <P>By order of the Commission.</P>
          <DATED>Issued: July 26, 2011.</DATED>
          <NAME>James R. Holbein,</NAME>
          <TITLE>Secretary to the Commission.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19314 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 7020-02-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">INTERNATIONAL TRADE COMMISSION</AGENCY>
        <DEPDOC>[Investigation Nos. 731-TA-344 and 391A-393A (Third Review)]</DEPDOC>
        <SUBJECT>Certain Bearings From China, France, Germany, and Italy; Institution of Five-Year Reviews Concerning the Antidumping Duty Orders on Certain Bearings From China, France, Germany, and Italy</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>United States International Trade Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>The Commission hereby gives notice that it has instituted reviews pursuant to section 751(c) of the Tariff Act of 1930 (19 U.S.C. 1675(c)) (the Act) to determine whether revocation of the antidumping duty orders on certain bearings from China, France, Germany, and Italy would be likely to lead to continuation or recurrence of material injury. Pursuant to section 751(c)(2) of the Act, interested parties are requested to respond to this notice by submitting the information specified below to the<PRTPAGE P="45854"/>Commission;<SU>1</SU>
            <FTREF/>to be assured of consideration, the deadline for responses is August 31, 2011. Comments on the adequacy of responses may be filed with the Commission by October 14, 2011. For further information concerning the conduct of these reviews and rules of general application, consult the Commission's Rules of Practice and Procedure, part 201, subparts A through E (19 CFR part 201), and part 207, subparts A, D, E, and F (19 CFR part 207), as most recently amended at 74 FR 2847 (January 16, 2009).</P>
          <FTNT>
            <P>
              <SU>1</SU>No response to this request for information is required if a currently valid Office of Management and Budget (OMB) number is not displayed; the OMB number is 3117-0016/USITC No. 11-5-253, expiration date June 30, 2014. Public reporting burden for the request is estimated to average 15 hours per response. Please send comments regarding the accuracy of this burden estimate to the Office of Investigations, U.S. International Trade Commission, 500 E Street, SW., Washington, DC 20436.</P>
          </FTNT>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>
            <E T="03">Effective Date:</E>August 1, 2011.</P>
        </DATES>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Mary Messer (202-205-3193), Office of Investigations, U.S. International Trade Commission, 500 E Street SW., Washington, DC 20436. Hearing-impaired persons can obtain information on this matter by contacting the Commission's TDD terminal on 202-205-1810. Persons with mobility impairments who will need special assistance in gaining access to the Commission should contact the Office of the Secretary at 202-205-2000. General information concerning the Commission may also be obtained by accessing its internet server (<E T="03">http://www.usitc.gov</E>). The public record for these reviews may be viewed on the Commission's electronic docket (EDIS) at<E T="03">http://edis.usitc.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>
          <E T="03">Background.</E>On June 15, 1987, the Department of Commerce (“Commerce”) issued an antidumping duty order on imports of tapered roller bearings from China (52 FR 22667). On May 15, 1989, Commerce issued antidumping duty orders on imports of ball bearings from France, Germany, and Italy (54 FR 20900, 20902, and 20903). Following first and second five-year reviews by Commerce and the Commission, effective July 11, 2000 and September 15, 2006, respectively, Commerce issued continuations of the antidumping duty orders on imports of certain bearings from China, France, Germany, and Italy (65 FR 42665 and 71 FR 54469). The Commission is now conducting third reviews to determine whether revocation of the orders would be likely to lead to continuation or recurrence of material injury to the domestic industry within a reasonably foreseeable time. It will assess the adequacy of interested party responses to this notice of institution to determine whether to conduct full or expedited reviews. The Commission's determinations in any expedited reviews will be based on the facts available, which may include information provided in response to this notice.</P>
        <P>
          <E T="03">Definitions.</E>The following definitions apply to these reviews:</P>
        <P>(1)<E T="03">Subject Merchandise</E>is the class or kind of merchandise that is within the scope of the five-year reviews, as defined by the Department of Commerce.</P>
        <P>(2) The<E T="03">Subject Countries</E>in these reviews are China, France, Germany, and Italy.</P>
        <P>(3) The<E T="03">Domestic Like Product</E>is the domestically produced product or products which are like, or in the absence of like, most similar in characteristics and uses with, the<E T="03">Subject Merchandise.</E>In its original determination concerning tapered roller bearings from China (Investigation No. 731-TA-344), the Commission found one<E T="03">Domestic Like Product:</E>tapered roller bearings and parts thereof—finished or unfinished; flange, take-up cartridge, and hanger units incorporating tapered roller bearings, and tapered roller housings (except pillow blocks) incorporating tapered rollers, with or without spindles, and whether or not for automotive use. In its original determinations concerning ball bearings from France, Germany, and Italy (Investigation Nos. 731-TA-391A-393A), the Commission found ball bearings to be a single<E T="03">Domestic Like Product.</E>One Commissioner defined the<E T="03">Domestic Like Product</E>differently in the original ball bearings final determinations. In its full first and second five-year review determinations concerning the existing orders on certain bearings, the Commission defined ball bearings and tapered roller bearings as separate<E T="03">Domestic Like Products,</E>coextensive with Commerce's scope definitions for each type of bearing. For purposes of this notice, you should report information separately on each of the following two<E T="03">Domestic Like Products:</E>(1) ball bearings and (2) tapered roller bearings.</P>
        <P>(4) The<E T="03">Domestic Industry</E>is the U.S. producers as a whole of the<E T="03">Domestic Like Product,</E>or those producers whose collective output of the<E T="03">Domestic Like Product</E>constitutes a major proportion of the total domestic production of the product. In its original determination concerning tapered roller bearings from China (Inv. No. 731-TA-344), the Commission found one<E T="03">Domestic Industry</E>devoted to the production of the<E T="03">Domestic Like Product,</E>as defined above. In its original determinations concerning ball bearings from France, Germany, and Italy (Investigation Nos. 731-TA-391A-393A), the Commission found one<E T="03">Domestic Industry</E>devoted to the production of ball bearings. One Commissioner defined the<E T="03">Domestic Industry</E>differently in the original ball bearings final determinations. In its full first and second five-year review determinations concerning the existing orders on tapered roller bearings and ball bearings, the Commission found two separate<E T="03">Domestic Industries,</E>each devoted to the production of one of the two<E T="03">Domestic Like Products,</E>as defined above. For purposes of this notice, you should report information on two<E T="03">Domestic Industries,</E>each devoted to the production of one of the following two<E T="03">Domestic Like Products:</E>(1) Ball bearings and (2) tapered roller bearings.</P>
        <P>(5) An<E T="03">Importer</E>is any person or firm engaged, either directly or through a parent company or subsidiary, in importing the<E T="03">Subject Merchandise</E>into the United States from a foreign manufacturer or through its selling agent.</P>
        <P>
          <E T="03">Participation in the reviews and public service list.</E>—Persons, including industrial users of the<E T="03">Subject Merchandise</E>and, if the merchandise is sold at the retail level, representative consumer organizations, wishing to participate in the reviews as parties must file an entry of appearance with the Secretary to the Commission, as provided in section 201.11(b)(4) of the Commission's rules, no later than 21 days after publication of this notice in the<E T="04">Federal Register</E>. The Secretary will maintain a public service list containing the names and addresses of all persons, or their representatives, who are parties to the reviews.</P>

        <P>Former Commission employees who are seeking to appear in Commission five-year reviews are advised that they may appear in a review even if they participated personally and substantially in the corresponding underlying original investigation. The Commission's designated agency ethics official has advised that a five-year review is not considered the “same particular matter” as the corresponding underlying original investigation for purposes of 18 U.S.C. 207, the post employment statute for Federal employees, and Commission rule 201.15(b)(19 CFR 201.15(b)), 73 FR 24609 (May 5, 2008). This advice was developed in consultation with the Office of Government Ethics. Consequently, former employees are not<PRTPAGE P="45855"/>required to seek Commission approval to appear in a review under Commission rule 19 CFR 201.15, even if the corresponding underlying original investigation was pending when they were Commission employees. For further ethics advice on this matter, contact Carol McCue Verratti, Deputy Agency Ethics Official, at 202-205-3088.</P>
        <P>
          <E T="03">Limited disclosure of business proprietary information (BPI) under an administrative protective order (APO) and APO service list.</E>Pursuant to section 207.7(a) of the Commission's rules, the Secretary will make BPI submitted in these reviews available to authorized applicants under the APO issued in the reviews, provided that the application is made no later than 21 days after publication of this notice in the<E T="04">Federal Register</E>. Authorized applicants must represent interested parties, as defined in 19 U.S.C. 1677(9), who are parties to the reviews. A separate service list will be maintained by the Secretary for those parties authorized to receive BPI under the APO.</P>
        <P>
          <E T="03">Certification.</E>Pursuant to section 207.3 of the Commission's rules, any person submitting information to the Commission in connection with these reviews must certify that the information is accurate and complete to the best of the submitter's knowledge. In making the certification, the submitter will be deemed to consent, unless otherwise specified, for the Commission, its employees, and contract personnel to use the information provided in any other reviews or investigations of the same or comparable products which the Commission conducts under Title VII of the Act, or in internal audits and investigations relating to the programs and operations of the Commission pursuant to 5 U.S.C. Appendix 3.</P>
        <P>
          <E T="03">Written submissions.</E>Pursuant to section 207.61 of the Commission's rules, each interested party response to this notice must provide the information specified below. The deadline for filing such responses is August 31, 2011. Pursuant to section 207.62(b) of the Commission's rules, eligible parties (as specified in Commission rule 207.62(b)(1)) may also file comments concerning the adequacy of responses to the notice of institution and whether the Commission should conduct expedited or full reviews. The deadline for filing such comments is October 25, 2011. All written submissions must conform with the provisions of sections 201.8 and 207.3 of the Commission's rules and any submissions that contain BPI must also conform with the requirements of sections 201.6 and 207.7 of the Commission's rules. The Commission's rules do not authorize filing of submissions with the Secretary by facsimile or electronic means, except to the extent permitted by section 201.8 of the Commission's rules, as amended, 67 FR 68036 (November 8, 2002). Also, in accordance with sections 201.16(c) and 207.3 of the Commission's rules, each document filed by a party to the reviews must be served on all other parties to the reviews (as identified by either the public or APO service list as appropriate), and a certificate of service must accompany the document (if you are not a party to the reviews you do not need to serve your response).</P>
        <P>
          <E T="03">Inability to provide requested information.</E>Pursuant to section 207.61(c) of the Commission's rules, any interested party that cannot furnish the information requested by this notice in the requested form and manner shall notify the Commission at the earliest possible time, provide a full explanation of why it cannot provide the requested information, and indicate alternative forms in which it can provide equivalent information. If an interested party does not provide this notification (or the Commission finds the explanation provided in the notification inadequate) and fails to provide a complete response to this notice, the Commission may take an adverse inference against the party pursuant to section 776(b) of the Act in making its determinations in the reviews.</P>
        <P>
          <E T="03">Information To Be Provided in Response to this Notice of Institution:</E>Please provide the requested information separately for each<E T="03">Domestic Like Product,</E>as defined by the Commission in its determinations, and for each of the products identified by Commerce as<E T="03">Subject Merchandise.</E>If you are a domestic producer, union/worker group, or trade/business association; import/export<E T="03">Subject Merchandise</E>from more than one<E T="03">Subject Country;</E>or produce<E T="03">Subject Merchandise</E>in more than one<E T="03">Subject Country,</E>you may file a single response. If you do so, please ensure that your response to each question includes the information requested for each pertinent<E T="03">Subject Country.</E>As used below, the term “firm” includes any related firms.</P>
        <P>(1) The name and address of your firm or entity (including World Wide Web address) and name, telephone number, fax number, and E-mail address of the certifying official.</P>

        <P>(2) A statement indicating whether your firm/entity is a U.S. producer of a<E T="03">Domestic Like Product,</E>a U.S. union or worker group, a U.S. importer of the<E T="03">Subject Merchandise,</E>a foreign producer or exporter of the<E T="03">Subject Merchandise,</E>a U.S. or foreign trade or business association, or another interested party (including an explanation). If you are a union/worker group or trade/business association, identify the firms in which your workers are employed or which are members of your association.</P>
        <P>(3) A statement indicating whether your firm/entity is willing to participate in these reviews by providing information requested by the Commission.</P>

        <P>(4) A statement of the likely effects of the revocation of the antidumping duty orders on the<E T="03">Domestic Industries</E>in general and/or your firm/entity specifically. In your response, please discuss the various factors specified in section 752(a) of the Act (19 U.S.C. 1675a(a)) including the likely volume of subject imports, likely price effects of subject imports, and likely impact of imports of<E T="03">Subject Merchandise</E>on the<E T="03">Domestic Industries.</E>
        </P>

        <P>(5) A list of all known and currently operating U.S. producers of each<E T="03">Domestic Like Product.</E>Identify any known related parties and the nature of the relationship as defined in section 771(4)(B) of the Act (19 U.S.C. 1677(4)(B)).</P>

        <P>(6) A list of all known and currently operating U.S. importers of the<E T="03">Subject Merchandise</E>and producers of the<E T="03">Subject Merchandise</E>in each<E T="03">Subject Country</E>that currently export or have exported<E T="03">Subject Merchandise</E>to the United States or other countries after 2005.</P>

        <P>(7) A list of 3-5 leading purchasers in the U.S. market for each<E T="03">Domestic Like Product</E>and the<E T="03">Subject Merchandise</E>(including street address, World Wide Web address, and the name, telephone number, fax number, and E-mail address of a responsible official at each firm).</P>

        <P>(8) A list of known sources of information on national or regional prices for each<E T="03">Domestic Like Product</E>or the<E T="03">Subject Merchandise</E>in the U.S. or other markets.</P>
        <P>(9) If you are a U.S. producer of a<E T="03">Domestic Like Product,</E>provide the following information on your firm's operations on that product during calendar year 2010, except as noted (report quantity data in units and value data in U.S. dollars, f.o.b. plant). If you are a union/worker group or trade/business association, provide the information, on an aggregate basis, for the firms in which your workers are employed/which are members of your association.</P>

        <P>(a) Production (quantity) and, if known, an estimate of the percentage of total U.S. production of each<E T="03">Domestic<PRTPAGE P="45856"/>Like Product</E>accounted for by your firm's(s') production;</P>
        <P>(b) Capacity (quantity) of your firm to produce each<E T="03">Domestic Like Product</E>(i.e., the level of production that your establishment(s) could reasonably have expected to attain during the year, assuming normal operating conditions (using equipment and machinery in place and ready to operate), normal operating levels (hours per week/weeks per year), time for downtime, maintenance, repair, and cleanup, and a typical or representative product mix);</P>

        <P>(c) the quantity and value of U.S. commercial shipments of each<E T="03">Domestic Like Product</E>produced in your U.S. plant(s);</P>

        <P>(d) the quantity and value of U.S. internal consumption/company transfers of each<E T="03">Domestic Like Product</E>produced in your U.S. plant(s); and</P>

        <P>(e) the value of (i) net sales, (ii) cost of goods sold (COGS), (iii) gross profit, (iv) selling, general and administrative (SG&amp;A) expenses, and (v) operating income of each<E T="03">Domestic Like Product</E>produced in your U.S. plant(s) (include both U.S. and export commercial sales, internal consumption, and company transfers) for your most recently completed fiscal year (identify the date on which your fiscal year ends).</P>

        <P>(10) If you are a U.S. importer or a trade/business association of U.S. importers of the<E T="03">Subject Merchandise</E>from the<E T="03">Subject Country(ies),</E>provide the following information on your firm's(s') operations on that product during calendar year 2010 (report quantity data in units and value data in U.S. dollars). If you are a trade/business association, provide the information, on an aggregate basis, for the firms which are members of your association.</P>

        <P>(a) The quantity and value (landed, duty-paid but not including antidumping duties) of U.S. imports and, if known, an estimate of the percentage of total U.S. imports of<E T="03">Subject Merchandise</E>from each<E T="03">Subject Country</E>accounted for by your firm's(s') imports;</P>

        <P>(b) the quantity and value (f.o.b. U.S. port, including antidumping duties) of U.S. commercial shipments of<E T="03">Subject Merchandise</E>imported from each<E T="03">Subject Country;</E>and</P>

        <P>(c) the quantity and value (f.o.b. U.S. port, including antidumping duties) of U.S. internal consumption/company transfers of<E T="03">Subject Merchandise</E>imported from each<E T="03">Subject Country.</E>
        </P>

        <P>(11) If you are a producer, an exporter, or a trade/business association of producers or exporters of the<E T="03">Subject Merchandise</E>in the<E T="03">Subject Country(ies),</E>provide the following information on your firm's(s') operations on that product during calendar year 2010 (report quantity data in units and value data in U.S. dollars, landed and duty-paid at the U.S. port but not including antidumping duties). If you are a trade/business association, provide the information, on an aggregate basis, for the firms which are members of your association.</P>

        <P>(a) Production (quantity) and, if known, an estimate of the percentage of total production of<E T="03">Subject Merchandise</E>in each<E T="03">Subject Country</E>accounted for by your firm's(s') production;</P>
        <P>(b) Capacity (quantity) of your firm to produce the<E T="03">Subject Merchandise</E>in each<E T="03">Subject Country</E>(i.e., the level of production that your establishment(s) could reasonably have expected to attain during the year, assuming normal operating conditions (using equipment and machinery in place and ready to operate), normal operating levels (hours per week/weeks per year), time for downtime, maintenance, repair, and cleanup, and a typical or representative product mix); and</P>

        <P>(c) the quantity and value of your firm's(s') exports to the United States of<E T="03">Subject Merchandise</E>and, if known, an estimate of the percentage of total exports to the United States of<E T="03">Subject Merchandise</E>from each<E T="03">Subject Country</E>accounted for by your firm's(s') exports.</P>

        <P>(12) Identify significant changes, if any, in the supply and demand conditions or business cycle for the<E T="03">Domestic Like Products</E>that have occurred in the United States or in the market for the<E T="03">Subject Merchandise</E>in the<E T="03">Subject Countries</E>after 2005, and significant changes, if any, that are likely to occur within a reasonably foreseeable time. Supply conditions to consider include technology; production methods; development efforts; ability to increase production (including the shift of production facilities used for other products and the use, cost, or availability of major inputs into production); and factors related to the ability to shift supply among different national markets (including barriers to importation in foreign markets or changes in market demand abroad). Demand conditions to consider include end uses and applications; the existence and availability of substitute products; and the level of competition among the<E T="03">Domestic Like Products</E>produced in the United States,<E T="03">Subject Merchandise</E>produced in the<E T="03">Subject Countries,</E>and such merchandise from other countries.</P>

        <P>(13) (OPTIONAL) A statement of whether you agree with the above definitions of the<E T="03">Domestic Like Products and</E>
          <E T="03">Domestic Industries;</E>if you disagree with either or both of these definitions, please explain why and provide alternative definitions.</P>
        <AUTH>
          <HD SOURCE="HED">Authority:</HD>
          <P>These reviews are being conducted under authority of title VII of the Tariff Act of 1930; this notice is published pursuant to section 207.61 of the Commission's rules.</P>
        </AUTH>
        <SIG>
          <DATED>Issued: July 26, 2011.</DATED>
          
          <P>By order of the Commission.</P>
          <NAME>James R. Holbein,</NAME>
          <TITLE>Secretary to the Commission.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19318 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 7020-02-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">INTERNATIONAL TRADE COMMISSION</AGENCY>
        <DEPDOC>[Investigation Nos. 731-TA-671-673 (Third Review)]</DEPDOC>
        <SUBJECT>Silicomanganese From Brazil, China, and Ukraine Institution of a Five-Year Review Concerning the Antidumping Duty Orders on Silicomanganese From Brazil, China, and Ukraine</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>United States International Trade Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Commission hereby gives notice that it has instituted reviews pursuant to section 751(c) of the Tariff Act of 1930 (19 U.S.C. 1675(c)) (the Act) to determine whether revocation of the antidumping duty orders on silicomanganese from Brazil, China, and Ukraine would be likely to lead to continuation or recurrence of material injury. Pursuant to section 751(c)(2) of the Act, interested parties are requested to respond to this notice by submitting the information specified below to the Commission;<SU>1</SU>
            <FTREF/>to be assured of consideration, the deadline for responses is August 31, 2011. Comments on the adequacy of responses may be filed with the Commission by October 14, 2011. For further information concerning the conduct of these reviews and rules of general application, consult the Commission's Rules of Practice and Procedure, part 201, subparts A through E (19 CFR part 201), and part 207, subparts A, D, E, and F (19 CFR part 207), as most recently amended at 74 FR 2847 (January 16, 2009).</P>
          <FTNT>
            <P>
              <SU>1</SU>No response to this request for information is required if a currently valid Office of Management and Budget (OMB) number is not displayed; the OMB number is 3117-0016/USITC No. 11-5-255, expiration date June 30, 2011. Public reporting burden for the request is estimated to average 15 hours per response. Please send comments regarding the accuracy of this burden estimate to the Office of Investigations, U.S. International Trade Commission, 500 E Street, SW., Washington, DC 20436.</P>
          </FTNT>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>
            <E T="03">Effective Date:</E>August 1, 2011.</P>
        </DATES>
        <FURINF>
          <PRTPAGE P="45857"/>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Mary Messer (202-205-3193), Office of Investigations, U.S. International Trade Commission, 500 E Street, SW., Washington, DC 20436. Hearing-impaired persons can obtain information on this matter by contacting the Commission's TDD terminal on 202-205-1810. Persons with mobility impairments who will need special assistance in gaining access to the Commission should contact the Office of the Secretary at 202-205-2000. General information concerning the Commission may also be obtained by accessing its internet server (<E T="03">http://www.usitc.gov</E>). The public record for these reviews may be viewed on the Commission's electronic docket (EDIS) at<E T="03">http://edis.usitc.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P SOURCE="NPAR">
          <E T="03">Background.</E>—On October 31, 1994, the Department of Commerce (“Commerce”) suspended an antidumping duty investigation on imports of silicomanganese from Ukraine (59 FR 60951, November 29, 1994). On December 22, 1994, Commerce issued antidumping duty orders on imports of silicomanganese from Brazil and China (59 FR 66003). Following first five-year reviews by Commerce and the Commission, effective February 16, 2001, Commerce issued a continuation of the antidumping duty orders on imports of silicomanganese from Brazil and China and the suspended investigation on imports of silicomanganese from Ukraine (66 FR 10669). On July 19, 2001, the Government of Ukraine requested termination of the suspension agreement on silicomanganese from Ukraine and, effective September 17, 2001, Commerce issued an antidumping duty order (66 FR 43838, August 21, 2001). Following second five-year reviews by Commerce and the Commission, effective September 14, 2006, Commerce issued a continuation of the antidumping duty orders on imports of silicomanganese from Brazil, China, and Ukraine (71 FR 54272). The Commission is now conducting third reviews to determine whether revocation of the orders would be likely to lead to continuation or recurrence of material injury to the domestic industry within a reasonably foreseeable time. It will assess the adequacy of interested party responses to this notice of institution to determine whether to conduct full or expedited reviews. The Commission's determinations in any expedited reviews will be based on the facts available, which may include information provided in response to this notice.</P>
        <P>
          <E T="03">Definitions.</E>—The following definitions apply to these reviews:</P>
        <P>(1)<E T="03">Subject Merchandise</E>is the class or kind of merchandise that is within the scope of the five-year reviews, as defined by the Department of Commerce.</P>
        <P>(2) The<E T="03">Subject Countries</E>in these reviews are Brazil, China, and Ukraine.</P>
        <P>(3) The<E T="03">Domestic Like Product</E>is the domestically produced product or products which are like, or in the absence of like, most similar in characteristics and uses with, the<E T="03">Subject Merchandise.</E>In its original determinations, its full first five-year review determinations, and its expedited second five-year review determinations, the Commission defined the<E T="03">Domestic Like Product</E>as all silicomanganese, coextensive with Commerce's scope.</P>
        <P>(4) The<E T="03">Domestic Industry</E>is the U.S. producers as a whole of the<E T="03">Domestic Like Product,</E>or those producers whose collective output of the<E T="03">Domestic Like Product</E>constitutes a major proportion of the total domestic production of the product. In its original determinations, its full first five-year review determinations, and its expedited second five-year review determinations, the Commission defined the<E T="03">Domestic Industry</E>as all domestic producers of silicomanganese.</P>
        <P>(5) An<E T="03">Importer</E>is any person or firm engaged, either directly or through a parent company or subsidiary, in importing the<E T="03">Subject Merchandise</E>into the United States from a foreign manufacturer or through its selling agent.</P>
        <P>
          <E T="03">Participation in the reviews and public service list.</E>—Persons, including industrial users of the<E T="03">Subject Merchandise</E>and, if the merchandise is sold at the retail level, representative consumer organizations, wishing to participate in the reviews as parties must file an entry of appearance with the Secretary to the Commission, as provided in section 201.11(b)(4) of the Commission's rules, no later than 21 days after publication of this notice in the<E T="04">Federal Register.</E>The Secretary will maintain a public service list containing the names and addresses of all persons, or their representatives, who are parties to the reviews.</P>
        <P>Former Commission employees who are seeking to appear in Commission five-year reviews are advised that they may appear in a review even if they participated personally and substantially in the corresponding underlying original investigation. The Commission's designated agency ethics official has advised that a five-year review is not considered the “same particular matter” as the corresponding underlying original investigation for purposes of 18 U.S.C. 207, the post employment statute for Federal employees, and Commission rule 201.15(b) (19 CFR 201.15(b)), 73 FR 24609 (May 5, 2008). This advice was developed in consultation with the Office of Government Ethics. Consequently, former employees are not required to seek Commission approval to appear in a review under Commission rule 19 CFR § 201.15, even if the corresponding underlying original investigation was pending when they were Commission employees. For further ethics advice on this matter, contact Carol McCue Verratti, Deputy Agency Ethics Official, at 202-205-3088.</P>
        <P>
          <E T="03">Limited disclosure of business proprietary information (BPI) under an administrative protective order (APO) and APO service list.</E>—Pursuant to section 207.7(a) of the Commission's rules, the Secretary will make BPI submitted in these reviews available to authorized applicants under the APO issued in the reviews, provided that the application is made no later than 21 days after publication of this notice in the<E T="04">Federal Register</E>. Authorized applicants must represent interested parties, as defined in 19 U.S.C. 1677(9), who are parties to the reviews. A separate service list will be maintained by the Secretary for those parties authorized to receive BPI under the APO.</P>
        <P>
          <E T="03">Certification.</E>—Pursuant to section 207.3 of the Commission's rules, any person submitting information to the Commission in connection with these reviews must certify that the information is accurate and complete to the best of the submitter's knowledge. In making the certification, the submitter will be deemed to consent, unless otherwise specified, for the Commission, its employees, and contract personnel to use the information provided in any other reviews or investigations of the same or comparable products which the Commission conducts under Title VII of the Act, or in internal audits and investigations relating to the programs and operations of the Commission pursuant to 5 U.S.C. Appendix 3.</P>
        <P>
          <E T="03">Written submissions.</E>—Pursuant to section 207.61 of the Commission's rules, each interested party response to this notice must provide the information specified below. The deadline for filing such responses is August 31, 2011. Pursuant to section 207.62(b) of the Commission's rules, eligible parties (as specified in Commission rule 207.62(b)(1)) may also file comments<PRTPAGE P="45858"/>concerning the adequacy of responses to the notice of institution and whether the Commission should conduct expedited or full reviews. The deadline for filing such comments is October 14, 2011. All written submissions must conform with the provisions of sections 201.8 and 207.3 of the Commission's rules and any submissions that contain BPI must also conform with the requirements of sections 201.6 and 207.7 of the Commission's rules. The Commission's rules do not authorize filing of submissions with the Secretary by facsimile or electronic means, except to the extent permitted by section 201.8 of the Commission's rules, as amended, 67 FR 68036 (November 8, 2002). Also, in accordance with sections 201.16(c) and 207.3 of the Commission's rules, each document filed by a party to the reviews must be served on all other parties to the reviews (as identified by either the public or APO service list as appropriate), and a certificate of service must accompany the document (if you are not a party to the reviews you do not need to serve your response).</P>
        <P>
          <E T="03">Inability to provide requested information.</E>—Pursuant to section 207.61(c) of the Commission's rules, any interested party that cannot furnish the information requested by this notice in the requested form and manner shall notify the Commission at the earliest possible time, provide a full explanation of why it cannot provide the requested information, and indicate alternative forms in which it can provide equivalent information. If an interested party does not provide this notification (or the Commission finds the explanation provided in the notification inadequate) and fails to provide a complete response to this notice, the Commission may take an adverse inference against the party pursuant to section 776(b) of the Act in making its determinations in the reviews.</P>
        <P>
          <E T="03">INFORMATION TO BE PROVIDED IN RESPONSE TO THIS NOTICE OF INSTITUTION:</E>If you are a domestic producer, union/worker group, or trade/business association; import/export<E T="03">Subject Merchandise</E>from more than one<E T="03">Subject Country;</E>or produce<E T="03">Subject Merchandise</E>in more than one<E T="03">Subject Country,</E>you may file a single response. If you do so, please ensure that your response to each question includes the information requested for each pertinent<E T="03">Subject Country.</E>As used below, the term “firm” includes any related firms.</P>
        <P>(1) The name and address of your firm or entity (including World Wide Web address) and name, telephone number, fax number, and E-mail address of the certifying official.</P>

        <P>(2) A statement indicating whether your firm/entity is a U.S. producer of the<E T="03">Domestic Like Product,</E>a U.S. union or worker group, a U.S. importer of the<E T="03">Subject Merchandise,</E>a foreign producer or exporter of the<E T="03">Subject Merchandise,</E>a U.S. or foreign trade or business association, or another interested party (including an explanation). If you are a union/worker group or trade/business association, identify the firms in which your workers are employed or which are members of your association.</P>
        <P>(3) A statement indicating whether your firm/entity is willing to participate in these reviews by providing information requested by the Commission.</P>

        <P>(4) A statement of the likely effects of the revocation of the antidumping duty orders on the Domestic Industry in general and/or your firm/entity specifically. In your response, please discuss the various factors specified in section 752(a) of the Act (19 U.S.C. 1675a(a)) including the likely volume of subject imports, likely price effects of subject imports, and likely impact of imports of<E T="03">Subject Merchandise</E>on the<E T="03">Domestic Industry.</E>
        </P>

        <P>(5) A list of all known and currently operating U.S. producers of the<E T="03">Domestic Like Product.</E>Identify any known related parties and the nature of the relationship as defined in section 771(4)(B) of the Act (19 U.S.C. 1677(4)(B)).</P>

        <P>(6) A list of all known and currently operating U.S. importers of the<E T="03">Subject Merchandise</E>and producers of the<E T="03">Subject Merchandise</E>in each<E T="03">Subject Country</E>that currently export or have exported<E T="03">Subject Merchandise</E>to the United States or other countries after 2005.</P>

        <P>(7) A list of 3-5 leading purchasers in the U.S. market for the<E T="03">Domestic Like Product</E>and the<E T="03">Subject Merchandise</E>(including street address, World Wide Web address, and the name, telephone number, fax number, and E-mail address of a responsible official at each firm).</P>

        <P>(8) A list of known sources of information on national or regional prices for the<E T="03">Domestic Like Product</E>or the<E T="03">Subject Merchandise</E>in the U.S. or other markets.</P>
        <P>(9) If you are a U.S. producer of the<E T="03">Domestic Like Product,</E>provide the following information on your firm's operations on that product during calendar year 2010, except as noted (report quantity data in short tons and value data in U.S. dollars, f.o.b. plant). If you are a union/worker group or trade/business association, provide the information, on an aggregate basis, for the firms in which your workers are employed/which are members of your association.</P>

        <P>(a) Production (quantity) and, if known, an estimate of the percentage of total U.S. production of the<E T="03">Domestic Like Product</E>accounted for by your firm's(s') production;</P>
        <P>(b) Capacity (quantity) of your firm to produce the<E T="03">Domestic Like Product</E>(i.e., the level of production that your establishment(s) could reasonably have expected to attain during the year, assuming normal operating conditions (using equipment and machinery in place and ready to operate), normal operating levels (hours per week/weeks per year), time for downtime, maintenance, repair, and cleanup, and a typical or representative product mix);</P>

        <P>(c) the quantity and value of U.S. commercial shipments of the<E T="03">Domestic Like Product</E>produced in your U.S. plant(s);</P>

        <P>(d) the quantity and value of U.S. internal consumption/company transfers of the<E T="03">Domestic Like Product</E>produced in your U.S. plant(s); and</P>

        <P>(e) the value of (i) net sales, (ii) cost of goods sold (COGS), (iii) gross profit, (iv) selling, general and administrative (SG&amp;A) expenses, and (v) operating income of the<E T="03">Domestic Like Product</E>produced in your U.S. plant(s) (include both U.S. and export commercial sales, internal consumption, and company transfers) for your most recently completed fiscal year (identify the date on which your fiscal year ends).</P>

        <P>(10) If you are a U.S. importer or a trade/business association of U.S. importers of the<E T="03">Subject Merchandise</E>from the<E T="03">Subject Country(ies),</E>provide the following information on your firm's(s') operations on that product during calendar year 2010 (report quantity data in short tons and value data in U.S. dollars). If you are a trade/business association, provide the information, on an aggregate basis, for the firms which are members of your association.</P>

        <P>(a) The quantity and value (landed, duty-paid but not including antidumping duties) of U.S. imports and, if known, an estimate of the percentage of total U.S. imports of<E T="03">Subject Merchandise</E>from each<E T="03">Subject Country</E>accounted for by your firm's(s') imports;</P>

        <P>(b) the quantity and value (f.o.b. U.S. port, including antidumping duties) of U.S. commercial shipments of<E T="03">Subject Merchandise</E>imported from each<E T="03">Subject Country;</E>and</P>

        <P>(c) the quantity and value (f.o.b. U.S. port, including antidumping duties) of U.S. internal consumption/company transfers of<E T="03">Subject Merchandise</E>imported from each<E T="03">Subject Country.</E>
          <PRTPAGE P="45859"/>
        </P>

        <P>(11) If you are a producer, an exporter, or a trade/business association of producers or exporters of the<E T="03">Subject Merchandise</E>in the<E T="03">Subject Country(ies),</E>provide the following information on your firm's(s') operations on that product during calendar year 2010 (report quantity data in short tons and value data in U.S. dollars, landed and duty-paid at the U.S. port but not including antidumping duties). If you are a trade/business association, provide the information, on an aggregate basis, for the firms which are members of your association.</P>

        <P>(a) Production (quantity) and, if known, an estimate of the percentage of total production of<E T="03">Subject Merchandise</E>in each<E T="03">Subject Country</E>accounted for by your firm's(s') production;</P>
        <P>(b) Capacity (quantity) of your firm to produce the<E T="03">Subject Merchandise</E>in each<E T="03">Subject Country</E>(i.e., the level of production that your establishment(s) could reasonably have expected to attain during the year, assuming normal operating conditions (using equipment and machinery in place and ready to operate), normal operating levels (hours per week/weeks per year), time for downtime, maintenance, repair, and cleanup, and a typical or representative product mix); and</P>

        <P>(c) the quantity and value of your firm's(s') exports to the United States of<E T="03">Subject Merchandise</E>and, if known, an estimate of the percentage of total exports to the United States of<E T="03">Subject Merchandise</E>from each<E T="03">Subject Country</E>accounted for by your firm's(s') exports.</P>

        <P>(12) Identify significant changes, if any, in the supply and demand conditions or business cycle for the<E T="03">Domestic Like Product</E>that have occurred in the United States or in the market for the<E T="03">Subject Merchandise</E>in the<E T="03">Subject Country(ies)</E>after 2005, and significant changes, if any, that are likely to occur within a reasonably foreseeable time. Supply conditions to consider include technology; production methods; development efforts; ability to increase production (including the shift of production facilities used for other products and the use, cost, or availability of major inputs into production); and factors related to the ability to shift supply among different national markets (including barriers to importation in foreign markets or changes in market demand abroad). Demand conditions to consider include end uses and applications; the existence and availability of substitute products; and the level of competition among the<E T="03">Domestic Like Product</E>produced in the United States,<E T="03">Subject Merchandise</E>produced in the<E T="03">Subject Country(ies),</E>and such merchandise from other countries.</P>

        <P>(13) (OPTIONAL) A statement of whether you agree with the above definitions of the<E T="03">Domestic Like Product</E>and<E T="03">Domestic Industry;</E>if you disagree with either or both of these definitions, please explain why and provide alternative definitions.</P>
        <AUTH>
          <HD SOURCE="HED">Authority:</HD>
          <P>These reviews are being conducted under authority of title VII of the Tariff Act of 1930; this notice is published pursuant to section 207.61 of the Commission's rules.</P>
        </AUTH>
        <SIG>
          <P>By order of the Commission.</P>
          
          <DATED>Issued: July 26, 2011.</DATED>
          <NAME>James R. Holbein,</NAME>
          <TITLE>Secretary to the Commission.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19315 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 7020-02-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">INTERNATIONAL TRADE COMMISSION</AGENCY>
        <DEPDOC>[Inv. No. 337-TA-795]</DEPDOC>
        <SUBJECT>In the Matter of Certain Video Analytics Software, Systems, Components Thereof, and Products Containing Same; Notice of Institution of Investigation; Institution of Investigation Pursuant to 19 U.S.C. 1337</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>U.S. International Trade Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>Notice is hereby given that a complaint was filed with the U.S. International Trade Commission on June 29, 2011, under section 337 of the Tariff Act of 1930, as amended, 19 U.S.C. 1337, on behalf of ObjectVideo, Inc. of Reston, Virginia. The complaint alleges violations of section 337 based upon the importation into the United States, the sale for importation, and the sale within the United States after importation of certain video analytics software, systems, components thereof, and products containing same by reason of infringement of certain claims of U.S. Patent No 6,696,945 (“the '945 patent”); U.S. Patent No. 6,970,083 (“the '083 patent”); U.S. Patent No. 7,613,324 (“the '324 patent”); U.S. Patent No. 7,424,175 (“the '175 patent”); U.S. Patent No. 7,868,912 (“the '912 patent”); and U.S. Patent No. 7,932,923 (“the '923 patent”). The complaint further alleges that an industry in the United States exists as required by subsection (a)(2) of section 337.</P>
          <P>The complainant requests that the Commission institute an investigation and, after the investigation, issue an exclusion order and cease and desist orders.</P>
        </SUM>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>The complaint, except for any confidential information contained therein, is available for inspection during official business hours (8:45 a.m. to 5:15 p.m.) in the Office of the Secretary, U.S. International Trade Commission, 500 E Street, SW., Room 112, Washington, DC 20436, telephone (202) 205-2000. Hearing impaired individuals are advised that information on this matter can be obtained by contacting the Commission's TDD terminal on (202) 205-1810. Persons with mobility impairments who will need special assistance in gaining access to the Commission should contact the Office of the Secretary at (202) 205-2000. General information concerning the Commission may also be obtained by accessing its internet server at<E T="03">http://www.usitc.gov.</E>The public record for this investigation may be viewed on the Commission's electronic docket (EDIS) at<E T="03">http://edis.usitc.gov.</E>
          </P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>The Office of Unfair Import Investigations, U.S. International Trade Commission, telephone (202) 205-2560.</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>The authority for institution of this investigation is contained in section 337 of the Tariff Act of 1930, as amended, and in section 210.10 of the Commission's Rules of Practice and Procedure, 19 CFR 210.10 (2011).</P>
            <P>
              <E T="03">Scope of Investigation:</E>Having considered the complaint, the U.S. International Trade Commission, on July 26, 2011,<E T="03">ordered that</E>—</P>
            <P>(1) Pursuant to subsection (b) of section 337 of the Tariff Act of 1930, as amended, an investigation be instituted to determine whether there is a violation of subsection (a)(1)(B) of section 337 in the importation into the United States, the sale for importation, or the sale within the United States after importation of certain video analytics software, systems, components thereof, and products containing same that infringe one or more of claims 1-8, 11-14, 17, and 24-37 of the '945 patent; claims 1-28 of the '083 patent; claims 1-3, 6, and 7 of the '324; claims 2 and 3 of the '175 patent; claims 1-3 and 6-22 of the '912 patent; and claims 1-7, 9-13, and 15-28 of the '923 patent, and whether an industry in the United States exists as required by subsection (a)(2) of section 337;</P>
            <P>(2) For the purpose of the investigation so instituted, the following are hereby named as parties upon which this notice of investigation shall be served:</P>
            <P>(a) The complainant is: ObjectVideo, Inc., 11600 Sunrise Valley Drive, Suite 290, Reston, VA 20191.</P>

            <P>(b) The respondents are the following entities alleged to be in violation of<PRTPAGE P="45860"/>section 337, and are the parties upon which the complaint is to be served:</P>
          </AUTH>
          
          <FP SOURCE="FP-2">Robert Bosch GmbH, Postfach 106050, D-70049 Stuttgart, Germany.</FP>
          <FP SOURCE="FP-2">Bosch Security Systems, Inc., 130 Perinton Parkway, Fairpoint, NY 14450-9107.</FP>
          <FP SOURCE="FP-2">Samsung Techwin Co., Ltd., 657-9, Yeoksam-Dong, Kangnam-gu, Seoul 135-080, Korea.</FP>
          <FP SOURCE="FP-2">Samsung Opto-Electronics America, Inc. (d/b/a Samsung Techwin America, Inc.), 100 Challenger Road, Suite 700, Ridgefield Park, NJ 07660.</FP>
          <FP SOURCE="FP-2">Sony Corporation, 1-7-1 Konan, Minato-ku, Tokyo 108-0075, Japan.</FP>
          <FP SOURCE="FP-2">Sony Electronics, Inc., 16530 Via Esprillo, San Diego, CA 92127.</FP>
          <P>(c) The Office of Unfair Import Investigations, U.S. International Trade Commission, 500 E Street, SW., Suite 401, Washington, DC 20436; and</P>
          <P>(3) For the investigation so instituted, the Chief Administrative Law Judge, U.S. International Trade Commission, shall designate the presiding Administrative Law Judge.</P>
          <P>Responses to the complaint and the notice of investigation must be submitted by the named respondents in accordance with section 210.13 of the Commission's Rules of Practice and Procedure, 19 CFR 210.13. Pursuant to 19 CFR 201.16(d)-(e) and 210.13(a), such responses will be considered by the Commission if received not later than 20 days after the date of service by the Commission of the complaint and the notice of investigation. Extensions of time for submitting responses to the complaint and the notice of investigation will not be granted unless good cause therefor is shown.</P>
          <P>Failure of a respondent to file a timely response to each allegation in the complaint and in this notice may be deemed to constitute a waiver of the right to appear and contest the allegations of the complaint and this notice, and to authorize the administrative law judge and the Commission, without further notice to the respondent, to find the facts to be as alleged in the complaint and this notice and to enter an initial determination and a final determination containing such findings, and may result in the issuance of an exclusion order or a cease and desist order or both directed against the respondent.</P>
          <SIG>
            <P>By order of the Commission.</P>
            
            <DATED>Issued: July 27, 2011.</DATED>
            <NAME>James R. Holbein,</NAME>
            <TITLE>Secretary to the Commission.</TITLE>
          </SIG>
        </FURINF>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19357 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 7020-02-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">INTERNATIONAL TRADE COMMISSION</AGENCY>
        <DEPDOC>[Inv. No. 337-TA-794]</DEPDOC>
        <SUBJECT>In the Matter of Certain Electronic Devices, Including Wireless Communication Devices, Portable Music and Data Processing Devices, and Tablet Computers; Notice of Institution of Investigation; Institution of Investigation Pursuant to 19 U.S.C. 1337</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>U.S. International Trade Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>Notice is hereby given that a complaint was filed with the U.S. International Trade Commission on June 28, 2011, under section 337 of the Tariff Act of 1930, as amended, 19 U.S.C. 1337, on behalf of Samsung Electronics Co., Ltd. of Korea and Samsung Telecommunications America, LLC of Richardson, Texas. Supplements were filed on July 7 and July 15, 2011. The complaint alleges violations of section 337 based upon the importation into the United States, the sale for importation, and the sale within the United States after importation of certain electronic devices, including wireless communication devices, portable music and data processing devices, and tablet computers by reason of infringement of certain claims of U.S. Patent No. 7,706,348 (“the `348 patent”); U.S. Patent No. 7,486,644 (“the `644 patent”); U.S. Patent No. 6,771,980 (“the `980 patent”); U.S. Patent No. 6,879,843 (“the `843 patent”); and U.S. Patent No. 7,450,114 (“the `114 patent”). The complaint further alleges that an industry in the United States exists or is in the process of being established as required by subsection (a)(2) of section 337.</P>
          <P>The complainants request that the Commission institute an investigation and, after the investigation, issue an exclusion order and a cease and desist order.</P>
        </SUM>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>The complaint and supplements, except for any confidential information contained therein, are available for inspection during official business hours (8:45 a.m. to 5:15 p.m.) in the Office of the Secretary, U.S. International Trade Commission, 500 E Street, SW., Room 112, Washington, DC 20436, telephone (202) 205-2000. Hearing impaired individuals are advised that information on this matter can be obtained by contacting the Commission's TDD terminal on (202) 205-1810. Persons with mobility impairments who will need special assistance in gaining access to the Commission should contact the Office of the Secretary at (202) 205-2000. General information concerning the Commission may also be obtained by accessing its internet server at<E T="03">http://www.usitc.gov.</E>The public record for this investigation may be viewed on the Commission's electronic docket (EDIS) at<E T="03">http://edis.usitc.gov.</E>
          </P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>The Office of Unfair Import Investigations, U.S. International Trade Commission, telephone (202) 205-2560.</P>
          <AUTH>
            <HD SOURCE="HED">Authority:</HD>
            <P>The authority for institution of this investigation is contained in section 337 of the Tariff Act of 1930, as amended, and in section 210.10 of the Commission's Rules of Practice and Procedure, 19 CFR 210.10 (2011).</P>
          </AUTH>
          
          <P>
            <E T="03">Scope of Investigation:</E>Having considered the complaint, the U.S. International Trade Commission, on July 26, 2011,<E T="03">ordered that</E>—</P>
          <P>(1) Pursuant to subsection (b) of section 337 of the Tariff Act of 1930, as amended, an investigation be instituted to determine whether there is a violation of subsection (a)(1)(B) of section 337 in the importation into the United States, the sale for importation, or the sale within the United States after importation of certain electronic devices, including wireless communication devices, portable music and data processing devices, and tablet computers that infringe one or more of claims 75-78 and 82-84 of the `348 patent; claims 9-16 of the `644 patent; claims 5-7 and 9-13 of the `980 patent; claims 1-11 of the `843 patent; and claims 1-5 of the `114 patent, and whether an industry in the United States exists as required by subsection (a)(2) of section 337;</P>
          <P>(2) For the purpose of the investigation so instituted, the following are hereby named as parties upon which this notice of investigation shall be served:</P>
          <P>(a) The complainants are:</P>
          
          <FP SOURCE="FP-2">Samsung Electronics Co., Ltd., 416 Maetan-3dong, Yeongtong-gu, Suwon-City, Gyeonggi-do, Korea 443-742;</FP>
          <FP SOURCE="FP-2">Samsung Telecommunications America, LLC, 1301 East Lookout Drive, Richardson, TX 75082.</FP>
          <P>(b) The respondent is the following entity alleged to be in violation of section 337, and is the party upon which the complaint is to be served: Apple Inc., 1 Infinite Loop, Cupertino, CA 95014.</P>

          <P>(c) The Office of Unfair Import Investigations, U.S. International Trade Commission, 500 E Street, SW., Suite 401, Washington, DC 20436; and<PRTPAGE P="45861"/>
          </P>
          <P>(3) For the investigation so instituted the Chief Administrative Law Judge, U.S. International Trade Commission, shall designate the presiding Administrative Law Judge.</P>
          <P>Responses to the complaint and the notice of investigation must be submitted by the named respondent in accordance with section 210.13 of the Commission's Rules of Practice and Procedure, 19 CFR 210.13. Pursuant to 19 CFR 201.16(d)-(e) and 210.13(a), such responses will be considered by the Commission if received not later than 20 days after the date of service by the Commission of the complaint and the notice of investigation. Extensions of time for submitting responses to the complaint and the notice of investigation will not be granted unless good cause therefor is shown.</P>
          <P>Failure of the respondent to file a timely response to each allegation in the complaint and in this notice may be deemed to constitute a waiver of the right to appear and contest the allegations of the complaint and this notice, and to authorize the administrative law judge and the Commission, without further notice to the respondent, to find the facts to be as alleged in the complaint and this notice and to enter an initial determination and a final determination containing such findings, and may result in the issuance of an exclusion order or a cease and desist order or both directed against the respondent.</P>
          <SIG>
            <P>By order of the Commission.</P>
            
            <DATED>Issued: July 27, 2011.</DATED>
            <NAME>James R. Holbein,</NAME>
            <TITLE>Secretary to the Commission.</TITLE>
          </SIG>
        </FURINF>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19356 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 7020-02-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF JUSTICE</AGENCY>
        <DEPDOC>[OMB Number 1122-New]</DEPDOC>
        <SUBJECT>Agency Information Collection Activities: New Collection; Semi-Annual Progress Report for Grantees from the Children and Youth Exposed to Violence Program</SUBJECT>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>30-Day Notice of Information Collection Under Review.</P>
        </ACT>

        <P>The Department of Justice, Office on Violence Against Women (OVW) will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The proposed information collection is published to obtain comments from the public and affected agencies. This proposed information collection was previously published in the<E T="04">Federal Register</E>Volume 76, Number 101, page 30389, on May 25, 2011, allowing for a 60-day comment period.</P>
        <P>The purpose of this notice is to allow for an additional 30 days for public comment until August 31, 2011. This process is conducted in accordance with 5 CFR 1320.10.</P>

        <P>Written comments concerning this information collection should be sent to the Office of Information and Regulatory Affairs, Office of Management and Budget,<E T="03">Attn:</E>DOJ Desk Officer. The best way to ensure your comments are received is to e-mail them to<E T="03">oira_submission@omb.eop.gov</E>or fax them to 202-395-7285. All comments should reference the 8 digit OMB number for the collection or the title of the collection. If you have questions concerning the collection, please call Cathy Poston at 202-514-5430 or the DOJ Desk Officer at 202-395-3176.</P>
        <P>Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address one or more of the following four points:</P>
        <P>(1) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility;</P>
        <P>(2) Evaluate the accuracy of the agency's estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used;</P>
        <P>(3) Enhance the quality, utility, and clarity of the information to be collected; and</P>

        <P>(4) Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology,<E T="03">e.g.,</E>permitting electronic submission of responses.</P>
        <HD SOURCE="HD1">Overview of This Information Collection</HD>
        <P>(1)<E T="03">Type of Information Collection:</E>New collection.</P>
        <P>(2)<E T="03">Title of the Form/Collection:</E>Semi-Annual Progress Report for Grantees from the Children and Youth Exposed to Violence Program.</P>
        <P>(3)<E T="03">Agency form number, if any, and the applicable component of the Department of Justice sponsoring the collection:</E>Form Number: 1122-XXXX. U.S. Department of Justice, Office on Violence Against Women.</P>

        <P>(4) Affected public who will be asked or required to respond, as well as a brief abstract: The affected public includes the approximately 25 grantees of the Children and Youth Exposed to Violence Program, created by the<E T="03">Violence Against Women Act of 2005</E>(VAWA 2005), creates a unique opportunity for communities to increase the resources, services, and advocacy available to children, youth and their nonabusing parent or caretaker, when a child has been exposed to incidences of sexual assault, domestic violence, dating violence, or stalking.</P>
        <P>(5) An estimate of the total number of respondents and the amount of time estimated for an average respondent to respond/reply: It is estimated that it will take the approximately 25 respondents (grantees from the Children and Youth Exposed to Violence Program) approximately one hour to complete a semi-annual progress report. The semi-annual progress report is divided into sections that pertain to the different types of activities in which grantees may engage. A Children and Youth Exposed to Violence Program grantee will only be required to complete the sections of the form that pertain to its own specific activities.</P>
        <P>(6) An estimate of the total public burden (in hours) associated with the collection: The total annual hour burden to complete the data collection forms is 50 hours, that is 25 grantees completing a form twice a year with an estimated completion time for the form being one hour.</P>
        <P>If additional information is required contact: Jerri Murray, Department Clearance Officer, United States Department of Justice, Justice Management Division, Policy and Planning Staff, Two Constitution Square, 145 N Street, NE., Room 2E-508, Washington, DC 20530.</P>
        <SIG>
          <NAME>Jerri Murray,</NAME>
          <TITLE>Department Clearance Officer, United States Department of Justice.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19345 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4410-FX-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF JUSTICE</AGENCY>
        <DEPDOC>[OMB Number 1103-NEW]</DEPDOC>
        <SUBJECT>Agency Information Collection Activities: Proposed Collection; Comments Requested; Generic Information Collection Review of Customer Outreach and Information</SUBJECT>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>30-Day Notice of Information Collection Under Review.</P>
        </ACT>
        <PRTPAGE P="45862"/>

        <P>The Department of Justice (DOJ) Office of Community Oriented Policing Services (COPS) will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The proposed information collection is published to obtain comments from the public and affected agencies. This information collection was previously published in the<E T="04">Federal Register</E>Volume 76, Number 101, on May 25, 2011, allowing for a 60-day comment period.</P>
        <P>The purpose of this notice is to allow for 30 days for public comment until August 31, 2011. This process is conducted in accordance with 5 CFR 1320.10.</P>

        <P>Written comments concerning this information collection should be sent to the Office of  Information and Regulatory Affairs, Office of Management and Budget, Attn: DOJ Desk Officer. The best way to ensure your comments are received is to e-mail them to<E T="03">oira_submission@omb.eop.gov</E>or fax them to 202-395-7285. All comments should reference the 8 digit OMB number for the collection or the title of the collection. If you have questions concerning the collection, please call Ashley Hoornstra at (202) 616-1314 or the DOJ Desk Officer at 202-395-3176.</P>
        <P>If you have comments especially on the estimated public burden or associated response time, suggestions, or need a copy of the proposed information collection instrument with instructions or additional information, please contact Ashley Hoornstra, Department of Justice Office of Community Oriented Policing Services, 145 N Street, NE., Washington, DC 20530.</P>
        <P>Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address one or more of the following four points:</P>
        
        <FP SOURCE="FP-1">—Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility;</FP>
        <FP SOURCE="FP-1">—Evaluate the accuracy of the agency's estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used;</FP>
        <FP SOURCE="FP-1">—Enhance the quality, utility, and clarity of the information to be collected; and</FP>

        <FP SOURCE="FP-1">—Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology,<E T="03">e.g.,</E>permitting electronic submission of responses.</FP>
        <HD SOURCE="HD1">Overview of This Information Collection</HD>
        <P>(1)<E T="03">Type of Information Collection:</E>Proposed collection; comments requested.</P>
        <P>(2)<E T="03">Title of the Form/Collection:</E>Generic Information Collection Review of Customer Outreach and Information.</P>
        <P>(3)<E T="03">Agency form number, if any, and the applicable component of the Department sponsoring the collection:</E>None. U.S. Department of Justice Office of Community Oriented Policing Services.</P>
        <P>(4)<E T="03">Affected public who will be asked or required to respond, as well as a brief abstract:</E>Primary: Law enforcement and public safety agencies, institutions of higher learning and non-profit organizations.</P>
        <P>(5)<E T="03">An estimate of the total number of respondents and the amount of time estimated for an average respondent to respond/reply:</E>It is estimated that approximately 2000 respondents will participate in the survey annually in an average of 28 minutes.</P>
        <P>(6)<E T="03">An estimate of the total public burden (in hours) associated with the collection:</E>933 total burden hours.</P>
        <P>If additional information is required contact: Jerri Murray, Department Clearance Officer, United States Department of Justice, Justice Management Division, Policy and Planning Staff, Two Constitution Square, 145 N Street, NE., Room 2E-508, Washington, DC 20530.</P>
        <SIG>
          <NAME>Jerri Murray,</NAME>
          <TITLE>Department Clearance Officer, PRA,  U.S. Department of Justice.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19371 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4410-AT-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF JUSTICE</AGENCY>
        <DEPDOC>[OMB Number 1122—New]</DEPDOC>
        <SUBJECT>Agency Information Collection Activities: New Collection; Semi-Annual Progress Report for Grantees From the Services, Training, Education and Policies To Reduce Domestic Violence, Dating Violence, Sexual Assault and Stalking in Secondary Schools Grant Program</SUBJECT>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>30-Day Notice of Information Collection Under Review.</P>
        </ACT>

        <P>The Department of Justice, Office on Violence Against Women (OVW) will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The proposed information collection is published to obtain comments from the public and affected agencies. This proposed information collection was previously published in the<E T="04">Federal Register</E>Volume 76, Number 101, page 30388-30389, on May 25, 2011, allowing for a 60-day comment period.</P>
        <P>The purpose of this notice is to allow for an additional 30 days for public comment until August 31, 2011. This process is conducted in accordance with 5 CFR 1320.10.</P>

        <P>Written comments concerning this information collection should be sent to the Office of Information and Regulatory Affairs, Office of Management and Budget,<E T="03">Attn:</E>DOJ Desk Officer. The best way to ensure your comments are received is to e-mail them to<E T="03">oira_submission@omb.eop.gov</E>or fax them to 202-395-7285. All comments should reference the 8 digit OMB number for the collection or the title of the collection. If you have questions concerning the collection, please call Cathy Poston at 202-514-5430 or the DOJ Desk Officer at  202-395-3176.</P>
        <P>Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address one or more of the following four points:</P>
        <P>(1) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility;</P>
        <P>(2) Evaluate the accuracy of the agency's estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used;</P>
        <P>(3) Enhance the quality, utility, and clarity of the information to be collected; and</P>

        <P>(4) Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology,<E T="03">e.g.,</E>permitting electronic submission of responses.</P>
        <HD SOURCE="HD1">Overview of This Information Collection</HD>
        <P>(1)<E T="03">Type of Information Collection:</E>New collection.<PRTPAGE P="45863"/>
        </P>
        <P>(2)<E T="03">Title of the Form/Collection:</E>Semi-Annual Progress Report for Grantees from the Services, Training, Education and Policies to Reduce Domestic Violence, Dating Violence, Sexual Assault and Stalking in Secondary Schools Grant Program (STEP).</P>
        <P>(3)<E T="03">Agency form number, if any, and the applicable component of the Department of Justice sponsoring the collection:</E>Form Number: 1122-XXXX. U.S. Department of Justice, Office on Violence Against Women.</P>

        <P>(4) Affected public who will be asked or required to respond, as well as a brief abstract: The affected public includes the approximately 10 grantees of the STEP Program. The STEP Program, created by the<E T="03">Violence Against Women Act of 2005</E>(VAWA 2005), will support middle and high schools to develop and implement effective training, services, prevention strategies, policies, and coordinated community responses for student victims of domestic violence, dating violence, sexual assault, or stalking.</P>
        <P>(5) An estimate of the total number of respondents and the amount of time estimated for an average respondent to respond/reply: It is estimated that it will take the approximately 10 respondents (grantees from the STEP Program) approximately one hour to complete a semi-annual progress report. The semi-annual progress report is divided into sections that pertain to the different types of activities in which grantees may engage. A STEP Program grantee will only be required to complete the sections of the form that pertain to its own specific activities.</P>
        <P>(6) An estimate of the total public burden (in hours) associated with the collection: The total annual hour burden to complete the data collection forms is 20 hours, that is 10 grantees completing a form twice a year with an estimated completion time for the form being one hour.</P>
        <P>If additional information is required contact: Jerri Murray, Department Clearance Officer, United States Department of Justice, Justice Management Division, Policy and Planning Staff, Two Constitution Square, 145 N Street, NE., Room 2E-508, Washington, DC 20530.</P>
        <SIG>
          <NAME>Jerri Murray,</NAME>
          <TITLE>Department Clearance Officer, PRA, United States Department of Justice.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19346 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4410-FX-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF JUSTICE</AGENCY>
        <SUBAGY>Bureau of Alcohol, Tobacco, Firearms and Explosives</SUBAGY>
        <DEPDOC>[OMB Number 1140-0020]</DEPDOC>
        <SUBJECT>Agency Information Collection Activities; Proposed Collection; Comments Requested: Firearms Transaction Record, Part 1, Over-the-Counter; Extension Without Change of a Currently Approved Information Collection</SUBJECT>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>30-Day Notice and requests for comments.</P>
        </ACT>

        <P>The Department of Justice (DOJ), Bureau of Alcohol, Tobacco, Firearms and Explosives (ATF) will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The proposed information collection is published to obtain comments from the public and affected agencies. This proposed information collection was previously published in the<E T="04">Federal Register</E>Volume 76, Number 99, page 29791-29792, on May 23, 2011, allowing for a 60 day comment period.</P>
        <P>The purpose of this notice is to allow for an additional 30 days for public comment until August 31, 2011. This process is conducted in accordance with 5 CFR 1320.10.</P>

        <P>Written comments concerning this information collection should be sent to the Office of Information and Regulatory Affairs, Office of Management and Budget, Attn: DOJ Desk Officer. The best way to ensure your comments are received is to email them to<E T="03">oria_submission@omb.eop.gov</E>or fax them to 202-395-7285. All comments should reference the 8 digit OMB number for the collection or the title of the collection. If you have questions concerning the collection, please call Barbara A. Terrell, at 202-648-7122 or the DOJ Desk Officer at 202-395-3176.</P>
        <P>Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address one or more of the following four points:</P>
        
        <FP SOURCE="FP-1">—Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility;</FP>
        <FP SOURCE="FP-1">—Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used;</FP>
        <FP SOURCE="FP-1">—Enhance the quality, utility, and clarity of the information to be collected; and</FP>
        <FP SOURCE="FP-1">—Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses.</FP>
        <HD SOURCE="HD1">Summary of Collection</HD>
        <P>(1)<E T="03">Type of Information Collection:</E>Extension without change of a currently approved collection.</P>
        <P>(2)<E T="03">Title of the Form/Collection:</E>Firearms Transaction Record, Part 1, Over-the-Counter.</P>
        <P>(3)<E T="03">Agency form number, if any, and the applicable component of the Department of Justice sponsoring the collection:</E>Form Number: ATF F 4473 (5300.9) Part 1, Bureau of Alcohol, Tobacco, Firearms and Explosives.</P>
        <P>(4)<E T="03">Affected public who will be asked or required to respond, as well as a brief abstract:</E>Primary: Individuals or households. Other: Business or other for-profit.</P>
        <HD SOURCE="HD1">Need for Collection</HD>
        <P>The form is used to determine the eligibility (under the Gun Control Act) of a person to receive a firearm from a Federal firearm licensee and to establish the identity of the buyer. It is also used in law enforcement investigations/inspections to trace firearms.</P>
        <P>(5)<E T="03">An estimate of the total number of respondents and the amount of time estimated for an average respondent to respond:</E>ATF estimates that 112,073 respondents will respond to the collection and that the total amount of time to read the instructions and complete the form on average is 25 minutes.</P>
        <P>(6)<E T="03">An estimate of the total burden (in hours) associated with the collection:</E>ATF estimates 56,037 annual total burden hours associated with this collection.</P>

        <P>If additional information is required contact: Jerri Murray at<E T="03">http://www.DOJ.PRA@usdoj.gov</E>, Department Clearance Officer, Policy and Planning Staff, Justice Management Division, Department of Justice, Two Constitution Square, 145 N Street, NE., Room 2E-508, Washington, DC 20530.</P>
        <SIG>
          <NAME>Jerri Murray,</NAME>
          <TITLE>Department Clearance Officer, PRA,  United States Department of Justice.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19370 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4410-FY-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <PRTPAGE P="45864"/>
        <AGENCY TYPE="S">DEPARTMENT OF JUSTICE</AGENCY>
        <SUBAGY>Drug Enforcement Administration</SUBAGY>
        <SUBJECT>Shannon L. Gallentine, D.P.M.; Denial of Application</SUBJECT>
        <P>On June 25, 2010, the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, issued an Order to Show Cause to Shannon Gallentine, D.P.M. (Respondent), of Maypearl, Texas. The Show Cause Order proposed the denial of Respondent's pending application for a DEA Certificate of Registration as a practitioner, on the grounds that he had materially falsified his application and that his “registration would be inconsistent with the public interest.” Show Cause Order at 1 (citing 21 U.S.C. 824(a)(1) &amp; 823 (f)).</P>

        <P>With respect to the material falsification ground, the Show Cause Order alleged that on October 1, 2007, Respondent had surrendered his DEA registration. Show Cause Order at 1. The Order further alleged that on July 16, 2009, Respondent had applied for a new DEA registration, but had failed to disclose that he had surrendered his prior registration.<E T="03">Id.</E>The Order thus alleged that Respondent had materially falsified his application by failing to disclose the surrender and that this was ground to deny his application.<E T="03">Id.</E>(citing 21 U.S.C. 824(a)(1)).</P>

        <P>As for the public interest ground, the Show Cause Order alleged that between various dates beginning in May 2004 through September 2007, Respondent prescribed controlled substances to six patients (M.P., H.G., D.C., P.P., K.B., N.B.), “without a legitimate medical purpose and/or outside the course of professional practice.”<E T="03">Id.</E>at 1-2. The Order further alleged that on October 1, 2007, a federal search warrant was executed at Respondent's registered location and that “no records were found to adequately support the prescribing of control substances to” these patients.<E T="03">Id.</E>at 2.</P>
        <P>As evidenced by the signed return receipt card, on July 2, 2010, the Show Cause Order, which also notified Respondent of his right to request a hearing or to submit a written statement in lieu of a hearing, the procedures for doing either, and the consequences for failing to do either, was served on him. GX 4. Respondent did not, however, file his request for a hearing<SU>1</SU>
          <FTREF/>with the Office of Administrative Law Judges until August 5, 2010, which was three days<SU>2</SU>
          <FTREF/>after it was due.<E T="03">See</E>GX 5, at 1; 21 CFR 1301.43(a);<E T="03">id.</E>1316.45.</P>
        <FTNT>
          <P>
            <SU>1</SU>Respondent's request was dated August 2, 2010.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>2</SU>The thirty-day period for filing a request for a hearing ended on August 1, 2010. However, because that day fell on a Sunday, Respondent's request was not due until August 2, 2010, when the Office of Administrative Law Judges was open for business.</P>
        </FTNT>

        <P>On August 12, 2010, the ALJ issued an order, a copy of which was not included in the record submitted to this Office. However, based on a subsequent order of the ALJ, it appears that the Government had previously filed a motion to terminate, and that in the initial order, the ALJ had provided Respondent with until August 23rd to file a response to the Government's motion.<E T="03">See</E>GX 7, at 1 (Order Adjusting Deadlines for the Filing of Prehearing Statements).</P>

        <P>On August 16, 2010, the Government moved to deny Respondent's request for a hearing on the ground that it was untimely. GX 6. Therein, the Government argued that the ALJ does not have jurisdiction to grant a hearing when a hearing request is not timely filed, and that in any event, Respondent had not established “good cause” for his untimely filing.<E T="03">Id.</E>at 2.</P>
        <P>On August 18, 2010, the ALJ issued a new order extending the deadlines for each party to file its prehearing statement. GX 7, at 1 (Order Adjusting Deadlines for the Filing of Prehearing Statements).</P>

        <P>On August 23, 2010, Respondent filed a “Motion To Establish Proceedings.” GX 8, at 2. Therein, Respondent stated that he did not receive the Government's Motion to Terminate. Respondent further stated that he had received the Order to Show Cause on July 2, 2010, and asserted that he had “provided a timely request for hearing, dated August 2, 2010.”<E T="03">Id.</E>Respondent further argued that because he did not receive the Government's Motion to Terminate, he “was not given [an] opportunity to respond to” the Motion.<E T="03">Id.</E>
        </P>

        <P>On August 24, 2010, the ALJ issued an Amended Order Granting the Government's Motion to Terminate Proceedings.<E T="03">See</E>GX 10, at 1 (Order Granting Respondent's Request To Stay Termination Of Proceedings And Consenting To Allowance Of Interlocutory Appeal). However, two days later, Respondent filed a Request To Stay Termination Of Proceedings.<E T="03">Id.</E>Therein, Respondent stated that he was “currently in bankruptcy proceedings” and was “unable to afford legal counsel.” GX 9, at 1 (Request To Stay Termination Of Proceedings). Respondent further argued that because he is not an attorney, he “understood the due date of the request for hearing as needing to be dated within 30 days” and “pray[ed that] the court not terminate the proceedings.”<E T="03">Id.</E>
        </P>

        <P>On August 30, 2010, the ALJ granted Respondent's request. Noting that his ruling terminating the proceeding constituted a departure from a prior Agency decision, the ALJ authorized Respondent to file an interlocutory appeal of his Amended Termination Order. GX 10, at 1-2 (Order Granting Respondent's Request To State Termination Of Proceedings And Consenting To Allowance Of Interlocutory Appeal) (citing<E T="03">Garth A.A. Clark, M.D.,</E>63 FR 54733 (1998)). The ALJ further ordered that Respondent file his interlocutory appeal with my Office no later than September 20, 2010; the ALJ also ordered that Respondent serve a copy of his filing on him and Government counsel.<E T="03">Id.</E>at 2 &amp; n.2.</P>

        <P>Respondent did not, however, file an interlocutory appeal. Instead, on September 20, 2010, Respondent filed a Request for Extension of Time to File an Interlocutory Appeal [and] Request for Appointment of Legal Counsel Due to Financial Hardship. GX 12. Therein, Respondent noted that because he is not an attorney, he “does not know how to file an interlocutory appeal,” and sought the appointment of counsel “because of the financial inability” to retain counsel.<E T="03">Id.</E>Respondent also sought “an extension of time after appointment of legal counsel in which to file an interlocutory appeal.”<E T="03">Id.</E>
        </P>

        <P>Thereafter, the ALJ denied Respondent's motion for appointed counsel, noting that he lacked authority to do so. GX 11, at 1-2 (Order Denying Respondent's Request for An Extension Of Time To File An Interlocutory Appeal And His Motion For Appointment Of Legal Counsel). The ALJ also denied Respondent's request for an extension, noting that the sole basis for it was to obtain appointed counsel.<E T="03">Id.</E>The ALJ further held that because Respondent had failed to file an interlocutory appeal, the stay of the Amended Termination Order “ha[d] expired by its own terms” and the Order had “become[] immediately effective.”<E T="03">Id.</E>at 2.</P>

        <P>The Government then filed a Request for Final Agency Action with my Office and submitted various documents as evidence in support of its request. Having considered the record, I conclude that Respondent did not submit a timely request for a hearing as required by 21 CFR 1301.43(a), and that he has not established good cause for his failure to do so.<E T="03">Id.</E>1301.43(d). I therefore find that Respondent has waived his right to a hearing.<E T="03">Id.</E>
          <PRTPAGE P="45865"/>
        </P>
        <P>As to the merits, I find that Respondent materially falsified his application for registration; I also find that Respondent's registration “would be inconsistent with the public interest” because he issued numerous prescriptions for controlled substances which lacked a legitimate medical purpose and thus violated 21 CFR 1306.04(a). 21 U.S.C. 823(f). Accordingly, Respondent's application will be denied. I make the following findings of fact.</P>
        <HD SOURCE="HD1">Findings</HD>
        <P>Respondent is a podiatrist licensed by the Texas State Board of Podiatric Medical Examiners (TSBPME). Respondent previously held DEA Certificate of Registration BG6902919, which authorized him to dispense controlled substances in schedules II through V, as a practitioner, at the registered location of 2700 Pleasant Run Road, Suite 360, Lancaster, Texas.</P>
        <P>According to the Affidavit of a DEA Diversion Investigator (DI), on November 6, 2006, DEA received information from the TSBPME which prompted it to investigate Respondent's prescribing practices. During the course of the investigation, Respondent was found to have authorized numerous prescriptions to six patients for narcotics such as codeine with acetaminophen (apap) and hydrocodone/apap, both of which are schedule III controlled substances. 21 CFR 1308.13(e)(1). More specifically, the Investigators obtained records from various pharmacies and found that Respondent had prescribed to: (1) M.P., a total of 4,230 dosage units [hereinafter, d.u.] of codeine/apap from January 3, 2005 through September 14, 2007; (2) H.G., a total of 3,180 d.u. of codeine #4/apap from May 29, 2004 through November 27, 2006; (3) D.C., a total of 2,260 d.u. of hydrocodone/apap from April 4, 2005 through September 18, 2007; (4) P.P., a total of 3,330 d.u. of hydrocodone/apap from January 24, 2005 through January 9, 2007; (5) K.B., a total of 1,500 d.u. of hydrocodone/apap from February 21, 2005 through December 4, 2006; (6) N.B., a total of 1,515 d.u. of hydrocodone/apap from October 4, 2004 through May 3, 2006. GXs 13-18.</P>
        <P>On October 1, 2007, federal and state Investigators executed a search warrant at Respondent's registered location of 2700 Pleasant Run Road, Suite 360, Lancaster, Texas. During the course of the search, Respondent stated that no other person had access to his prescription pad and that he personally signed all of his prescriptions. Respondent also stated that he only prescribed hydrocodone to patients who had a traumatic injury.</P>
        <P>Moreover, of the six patients identified above, Respondent did not have medical records for H.G., M.P., K.B., and N.B. While Respondent had records for D.C. and P.P., the records for D.C. consisted largely of billing records which listed various conditions and their reimbursement codes, as well as progress notes which were blank except for such information as the date, D.C.'s name, his date of birth, and age. P.P.'s record also consisted largely of billing records and progress notes. Moreover, only one of the progress notes (dated February 19, 2007) documented that P.P. had a medical condition and had pain.<SU>3</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>3</SU>The records for D.C. and P.P. also contained medication flow sheets listing each patient's prescriptions and refills, some prescriptions, as well as various refill authorization forms sent to Respondent by the patient's pharmacy. For both D.C. and P.P., there were no such records prior to 2007.</P>
        </FTNT>

        <P>Upon reviewing Respondent's records during the search, DEA Investigators asked Respondent if he would voluntarily surrender his DEA registration. Respondent agreed to do so and executed a form DEA-104, Voluntary Surrender of Controlled Substances Privileges. GX 2, at 5. Therein, Respondent acknowledged that he was voluntarily surrendering his Certificate of Registration, “[i]n view of [his] alleged failure to comply with the Federal requirements pertaining to controlled substances.”<E T="03">Id.</E>According to an Agency Investigator, “Respondent was fully aware that the surrender of [his registration] was based upon alleged violations of the Controlled Substances Act.” Declaration of DI, at 4.</P>
        <P>On July 14, 2009, Respondent applied for a new DEA registration. On the application form, Respondent was required to answer four questions. The second of these questions asked: “Has the applicant ever surrendered (for cause) or had a federal controlled substance registration revoked, suspended, restricted or denied, or is any such action pending?” Respondent entered “N” for no.</P>
        <HD SOURCE="HD1">Discussion</HD>
        <P>Section 303(f) of the Controlled Substances Act provides that an application for a practitioner's registration may be denied upon a determination “that the issuance of such registration would be inconsistent with the public interest.” 21 U.S.C. 823(f). In making the public interest determination, the CSA requires the consideration of the following factors:</P>
        
        <EXTRACT>
          <P>(1) The recommendation of the appropriate State licensing board or professional disciplinary authority.</P>
          <P>(2) The applicant's experience in dispensing * * * controlled substances.</P>
          <P>(3) The applicant's conviction record under Federal or State laws relating to the manufacture, distribution, or dispensing of controlled substances.</P>
          <P>(4) Compliance with applicable State, Federal, or local laws relating to controlled substances.</P>
          <P>(5) Such other conduct which may threaten the public health and safety.</P>
        </EXTRACT>
        
        <FP>
          <E T="03">Id.</E>
        </FP>
        
        <P>“These factors are * * * considered in the disjunctive.”<E T="03">Robert A. Leslie, M.D.,</E>68 FR 15227, 15230 (2003). I “may rely on any one or a combination of factors, and may give each factor the weight [I] deem[] appropriate in determining whether * * * an application for registration [should be] denied.”<E T="03">Id.</E>Moreover, case law establishes that I am “not required to make findings as to all of the factors.”<E T="03">Hoxie</E>v.<E T="03">DEA,</E>419 F.3d 477, 482 (6th Cir. 2005);<E T="03">see also Morall</E>v.<E T="03">DEA,</E>412 F.3d 165, 173-74 (2005).</P>

        <P>Furthermore, under Section 304(a)(1), a registration may be revoked or suspended “upon a finding that the registrant * * * has materially falsified any application filed pursuant to or required by this subchapter.” 21 U.S.C. 824(a)(1). Under agency precedent, the various grounds for revocation or suspension of an existing registration that Congress enumerated in section 304(a), 21 U.S.C. 824(a), are also properly considered in deciding whether to grant or deny an application under section 303.<E T="03">See Anthony D. Funches,</E>64 FR 14267, 14268 (1999);<E T="03">Alan R. Schankman,</E>63 FR 45260 (1998);<E T="03">Kuen H. Chen,</E>58 FR 65401, 65402 (1993).</P>

        <P>Thus, the allegation that Respondent materially falsified his application is properly considered in this proceeding.<E T="03">See Samuel S. Jackson,</E>72 FR 23848, 23852 (2007). Just as materially falsifying an application provides a basis for revoking an existing registration without proof of any other misconduct,<E T="03">see</E>21 U.S.C. 824(a)(1), it also provides an independent and adequate ground for denying an application.<E T="03">Cf. Bobby Watts, M.D.,</E>58 FR 46995 (1993).</P>
        <HD SOURCE="HD2">The Material Falsification Allegation</HD>

        <P>As found above, on October 1, 2007, Respondent voluntarily surrendered his registration upon being questioned by Investigators, who were executing a search warrant, regarding whether he had adequate documentation to support the controlled substance prescriptions he issued to six patients. However, on<PRTPAGE P="45866"/>his July 14, 2009 application for a new DEA registration, in answering the application's question which asked whether he had previously surrendered for cause his DEA registration, Respondent answered “no.”</P>

        <P>Respondent's answer was a material falsification of his application. As the Supreme Court has explained, “[t]he most common formulation” of the concept of materiality “is that a concealment or misrepresentation is material if it `has a natural tendency to influence, or was capable of influencing, the decision of' the decisionmaking body to which it was addressed.”<E T="03">Kungys</E>v.<E T="03">United States,</E>485 U.S. 759, 770 (1988) (quoting<E T="03">Weinstock</E>v.<E T="03">United States,</E>231 F.2d 699, 701 (D.C. Cir. 1956)) (other citation omitted);<E T="03">see also United States</E>v.<E T="03">Wells,</E>519 U.S. 482, 489 (1997) (quoting<E T="03">Kungys,</E>485 U.S. at 770). The evidence must be “clear, unequivocal, and convincing.”<E T="03">Kungys,</E>485 U.S. at 772. However, “the ultimate finding of materiality turns on an interpretation of substantive law.”<E T="03">Id.</E>at 772 (int. quotations and other citation omitted).</P>

        <P>DEA has previously held that “[t]he provision of truthful information on applications is absolutely essential to effectuating [the] statutory purpose” of determining whether the granting of an application is consistent with the public interest.<E T="03">See Peter H. Ahles,</E>71 FR 50097, 50098 (2006). More specifically, the public interest inquiry under section 303(f) requires,<E T="03">inter alia,</E>that the Agency examine “[t]he applicant's experience in dispensing * * * controlled substances,” his “[c]ompliance with applicable State, Federal, or local laws relating to controlled substances,” and whether he has committed other “conduct which may threaten public health and safety.” 21 U.S.C. 823(f). Because Respondent's voluntary surrender was for cause and arose out of an investigation into whether he had violated the Controlled Substance Act by issuing prescriptions outside of the usual course of professional practice and which lacked a legitimate medical purpose, 21 CFR 1306.04(a), his failure to disclose the surrender was capable of influencing the Agency's evaluation of his experience in dispensing controlled substances, his compliance with Federal and State laws relating to controlled substances, and whether he had engaged in other conduct which may threaten public health and safety.</P>

        <P>That the Agency did not rely on Respondent's false statement and grant his application does not make the statement immaterial. As the First Circuit has noted with respect to the material falsification requirement under 18 U.S.C. 1001, “[i]t makes no difference that a specific falsification did not exert influence so long as it had the capacity to do so.”<E T="03">United States</E>v.<E T="03">Alemany Rivera,</E>781 F.2d 229, 234 (1st Cir. 1985).<E T="03">See also United States</E>v.<E T="03">Norris,</E>749 F.2d 1116, 1121 (4th Cir. 1984) (“There is no requirement that the false statement influence or effect the decisionmaking process of a department of the United States Government.”).</P>
        <P>I further conclude that Respondent's false statement cannot be attributed to a good faith misunderstanding as to whether he had surrendered his registration for cause (as he maintained in his letter requesting a hearing). On the date he completed the application, less than two years had passed since the search warrant was executed and Respondent surrendered his registration. Given the circumstances of the surrender, during which he was confronted with questions by the Investigators about his prescribing practices and lack of documentation to justify his prescriptions, Respondent cannot claim that he did not surrender his registration for cause. Moreover, on the voluntary surrender form, Respondent acknowledged that he was doing so “[i]n view of [his] alleged failure to comply with the Federal requirements pertaining to controlled substances.” Accordingly, I conclude that Respondent knew that he had surrendered his registration for cause and that he knowingly materially falsified his July 14, 2009 application for a new Certificate of Registration. This conclusion provides reason alone to deny his application.</P>
        <HD SOURCE="HD2">The Public Interest Grounds</HD>
        <P>Having considered all of the public interest factors, I conclude that the evidence with respect to Respondent's experience in dispensing controlled substances (factor two), his compliance with laws related to controlled substances (factor four), and whether he has committed other conduct which may threaten public health and safety (factor five) establishes that Respondent's registration “would be inconsistent with the public interest.”<SU>4</SU>
          <FTREF/>21 U.S.C. 823(f). This conclusion provides an additional ground for denying Respondent's application.</P>
        <FTNT>
          <P>

            <SU>4</SU>I acknowledge that the investigative record contains no evidence that Respondent's state podiatrist's license or state controlled substances registration (factor one) have been suspended or revoked. However, DEA has long held that while possessing state authority is a necessary condition for obtaining and maintaining a DEA registration, the possession of state authority is not dispositive of the public interest.<E T="03">See Mortimer B. Levin, D.O.,</E>55 FR 8209, 8210 (1990). DEA has also held that the absence of a criminal conviction of a Federal or State offense related to the manufacture, distribution, or dispensing of a controlled substance (factor three) is not dispositive.<E T="03">See Edmund Chein, M.D.,</E>72 FR 6580, 6593 n.22 (2007).</P>
        </FTNT>

        <P>Under a longstanding DEA regulation, a prescription for a controlled substance is not “effective” unless it is “issued for a legitimate medical purpose by an individual practitioner acting in the usual course of his professional practice.” 21 CFR 1306.04(a). This regulation further provides that “an order purporting to be a prescription issued not in the usual course of professional treatment * * * is not a prescription within the meaning and intent of [21 U.S.C. 829] and * * * the person issuing it, shall be subject to the penalties provided for violations of the provisions of law related to controlled substances.”<E T="03">Id. See also</E>21 U.S.C. 802(10) (defining the term “dispense” as meaning “to deliver a controlled substance to an ultimate user by, or pursuant to<E T="03">the lawful order of, a practitioner,</E>including the prescribing and administering of a controlled substance”) (emphasis added).</P>

        <P>As the Supreme Court has explained, “the prescription requirement * * * ensures patients use controlled substances under the supervision of a doctor so as to prevent addiction and recreational abuse. As a corollary, [it] also bars doctors from peddling to patients who crave the drugs for those prohibited uses.”<E T="03">Gonzales</E>v.<E T="03">Oregon,</E>546 U.S. 243, 274 (2006) (citing<E T="03">United States</E>v.<E T="03">Moore,</E>423 U.S. 122, 135, 143 (1975)). Under the CSA, it is fundamental that a practitioner must establish and maintain a bonafide doctor-patient relationship in order to act “in the usual course of * * * professional practice” and to issue a prescription for a “legitimate medical purpose.”<E T="03">Laurence T. McKinney,</E>73 FR 43260, 43265 n.22 (2008);<E T="03">see also Moore,</E>423 U.S. at 142-43 (noting that evidence established that physician “exceeded the bounds of `professional practice,' ” when “he gave inadequate physical examinations or none at all,” “ignored the results of the tests he did make,” and “took no precautions against * * * misuse and diversion”). The CSA, however, generally looks to state law to determine whether a doctor and patient have established a bonafide doctor-patient relationship.<E T="03">See Kamir Garces-Mejias,</E>72 FR 54931, 54935 (2007);<E T="03">United Prescription Services, Inc.,</E>72 FR 50397, 50407-08 (2007).</P>

        <P>Under the rules of the Texas State Board of Podiatric Medical Examiners, “[a]ll podiatric physicians shall make, maintain, and keep accurate records of<PRTPAGE P="45867"/>the diagnosis made and the treatment performed for and upon each of his or her patients for reference and for protection of the patient for at least five years following the completion of treatment.” Tex. Admin Code tit. 22, § 375.21(a). When, however, Investigators executed the search warrant at Respondent's registered location, Respondent did not have any medical records for M.P., H.G., K.B., and N.B., even though he had prescribed large quantities of codeine/apap to M.P. (4,230 d.u.) and H.G. (3,180 d.u.) and large quantities of hydrocodone/apap to K.B. (1,500 d.u.) and N.B. (1,515 d.u.). Moreover, Respondent had prescribed to these persons for between a year and a half (in N.B.'s case) and two and a half years (in M.P.'s case). Based on Respondent's failure to maintain any medical records, let alone document a diagnosis to support his prescribing of controlled substances to M.P., H.G., K.B., and N.B., I conclude that Respondent acted outside of the usual course of professional practice and lacked a legitimate medical purpose when he prescribed controlled substances to these patients and thus violated the CSA. 21 U.S.C. 841(a)(1); 21 CFR 1306.04(a). I also conclude that Respondent violated the Texas Board's regulation requiring that he “make, maintain, and keep accurate records of the diagnosis made and the treatment performed for” each of these patients. Tex. Admin Code tit. 22, § 375.21(a).</P>
        <P>As for D.C., while the Investigators found a medical record, the progress notes did not document a diagnosis and contained no information other than D.C.'s name, date of birth, his age, and the date of the visit. Notwithstanding his failure to document a diagnosis, Respondent issued D.C. prescriptions for 2,260 d.u. of hydrocodone/apap over a nearly two and one half year period. Here again, I conclude that Respondent acted outside of the usual course of professional practice and lacked a legitimate medical purpose in prescribing hydrocodone/apap to D.C. and violated the CSA in doing so. 21 U.S.C. 841(a)(1); 21 CFR 1306.04(a). Here too, Respondent also violated the Texas Board's rule.</P>
        <P>While P.P.'s medical record contained a progress note documenting a diagnosis, this note was dated February 19, 2007. However, Respondent had prescribed hydrocodone/apap to her since February 2005, and had authorized the dispensing of more than 3,300 dosage units to her before he even documented a diagnosis. Here again, I conclude that these prescriptions were issued outside of the usual course of professional practice and lacked a legitimate medical purpose and thus violated the CSA. 21 U.S.C. 841(a)(1); 21 CFR 1306.04(a). And here too, Respondent violated the Board's rule by failing to document a diagnosis between February 2005 and February 2007.</P>
        <P>I therefore conclude that Respondent's experience in dispensing controlled substances (factor two), his failure to comply with the CSA's prescription requirement, 21 CFR 1306.04(a) (factor four) and his failure to comply with the Texas Board's rule (factor five<SU>5</SU>
          <FTREF/>), establish that Respondent's registration “would be inconsistent with the public interest.” 21 U.S.C. 823(f). This conclusion provides an additional and independent ground for denying Respondent's application. Accordingly, Respondent's application for a new DEA Certificate of Registration will be denied.</P>
        <FTNT>
          <P>

            <SU>5</SU>As the Texas rule states, “All podiatric physicians shall make, maintain, and keep accurate records of the diagnosis made and the treatment performed for and upon each of his or her patients for reference and<E T="03">for protection of the patient</E>for at least five years following the completion of treatment.” Tex. Admin Code tit. 22, § 375.21(a). DEA has also held that a practitioner's failure to maintain medical records required by state law constitutes such other conduct which may threaten public health and safety.<E T="03">See Robert L. Dougherty,</E>60 FR 55047, 55050-51 (1995).</P>

          <P>The Government also asserts that Respondent materially falsified his application for a state controlled substances registration because he failed to disclose the surrender of his DEA registration. Req. for Final Agency Action, at 14. This allegation was not, however, made in the Order to Show Cause, and the ALJ's various orders make clear that the Government did not file a Pre-Hearing Statement, in which it might have provided the requisite notice.<E T="03">See CBS Wholesale Distributors,</E>74 FR 36746, 36749-50 (2009);<E T="03">see also</E>5 U.S.C. § 554(b) (“Persons entitled to notice of an agency hearing shall be timely informed of * * * the matters of fact and law asserted.”). I therefore do not consider it.</P>
        </FTNT>
        <HD SOURCE="HD1">Order</HD>
        <P>Pursuant to the authority vested in me by 21 U.S.C. 823(f), as well as 28 CFR 0.100(b), I order that the application of Shannon L. Gallentine, D.P.M., for a DEA Certificate of Registration as a practitioner, be, and it hereby is, denied. This Order is effective immediately.</P>
        <SIG>
          <DATED>Dated: July 22, 2011.</DATED>
          <NAME>Michele M. Leonhart,</NAME>
          <TITLE>Administrator.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19381 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4410-09-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF JUSTICE</AGENCY>
        <SUBAGY>Drug Enforcement Administration</SUBAGY>
        <DEPDOC>[Docket No. 10-39]</DEPDOC>
        <SUBJECT>Michael S. Moore, M.D.; Suspension of Registration</SUBJECT>
        <P>On October 4, 2010, Administrative Law Judge John H. Mulrooney, II, issued the attached recommended decision. Neither party filed exceptions to the decision.</P>
        <P>Having reviewed the record in its entirety, I have decided to adopt the ALJ's rulings, findings of fact, and conclusions of law except for his conclusion regarding the applicability of factor five.<SU>1</SU>
          <FTREF/>
          <E T="03">See</E>ALJ Dec. at 21-22.<SU>2</SU>
          <FTREF/>For the reasons explained below, I adopt in part and reject in part the ALJ's recommended order that I suspend Respondent's registration for a period of six months and impose various conditions on his registration. Instead, I conclude that Respondent's registration should be suspended for a period of one year and impose two of the four conditions recommended by the ALJ.</P>
        <FTNT>
          <P>

            <SU>1</SU>In light of the conduct proved on the record, a finding under factor five is not necessary to conclude that Respondent has committed acts which render his registration inconsistent with the public interest.<E T="03">See Hoxie</E>v.<E T="03">DEA,</E>419 F.3d 477, 482 (6th Cir. 2005) (The Agency is “not required to make findings as to all of the factors[.]”).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>2</SU>All citations to the ALJ's Recommended Decision are to the slip opinion as issued on October 4, 2010.</P>
        </FTNT>
        <P>The record in this case establishes that Respondent was convicted of a felony offense under Wisconsin law “relating to any substance defined in [the Controlled Substances Act] as a controlled substance.”<SU>3</SU>

          <FTREF/>21 U.S.C. 824(a)(2). More specifically, Respondent has been convicted of the felony offense of unlawful manufacture, distribution or delivery of “[t]wo hundred grams or less, or 4 or fewer plants containing tetrahydrocannabinols,” in violation of Wis. Stat. § 961.41(1)(h)(1). ALJ Dec. at 4. Moreover, while Respondent was allowed to plead no contest to this charge, the evidence showed that Respondent had in his possession at least 1725 grams of marijuana, plus marijuana seeds, four marijuana plants, and the equipment needed to grow<PRTPAGE P="45868"/>marijuana hydroponically.<E T="03">Id.</E>at 8-9. The evidence also showed that Respondent had in his possession multiple marijuana pipes and pipe cleaners.<SU>4</SU>
          <FTREF/>GX 7, at 30.</P>
        <FTNT>
          <P>

            <SU>3</SU>On July 14, 2011, Respondent's counsel notified this Office that he had completed his probation and that his conviction has been reduced to a misdemeanor. Be that as it may, under the public interest inquiry, DEA is also required to consider Respondent's compliance with applicable Federal and State laws related to controlled substances.<E T="03">See</E>21 U.S.C. 823(f)(4). As explained above, notwithstanding Respondent's completion of his probation and the reduction of his conviction to a misdemeanor, his conduct still constitutes a felony offense under Federal law.<E T="03">See</E>21 U.S.C. 841(a) &amp; (b)(1)(D).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>4</SU>Respondent was also convicted of possession of drug paraphernalia, a misdemeanor offense under Wisconsin law. ALJ Dec. at 4 (citing Wis. Stat. § 961.573(1)).</P>
        </FTNT>

        <P>The evidence further showed that on numerous occasions, Respondent's niece (who was the legal ward of his wife) smoked marijuana with two boyfriends at Respondent's house and that on some occasions she provided the marijuana. GX 7, at 1, 7-8. Moreover, one of the boyfriends reported to the police that on two occasions, he observed marijuana leafs drying in the bedroom closet of Respondent's niece.<E T="03">Id.</E>at 7.</P>
        <P>As the ALJ recognized, the Government established a<E T="03">prima facie</E>case for revocation on two separate grounds: (1) his felony conviction for manufacturing marijuana, and (2) his having committed acts which render his registration inconsistent with the public interest. ALJ at 22 (citing 21 U.S.C. 824(a)(2) &amp; (4)). The ALJ correctly recognized that the burden then shifted to Respondent to demonstrate why revocation of his registration would be inappropriate and that he was “required not only to accept responsibility for [his] misconduct, but also to demonstrate what corrective measures [he has] undertaken to prevent the reoccurrence of similar acts.”<E T="03">Id.</E>(quoting<E T="03">Jeri Hassman, M.D.,</E>75 FR 8194, 8236 (2010)).</P>

        <P>DEA has also repeatedly held that a registrant's candor during both an investigation and the hearing itself is an important factor to be considered in determining both whether he has accepted responsibility as well as the appropriate sanction.<E T="03">Robert F. Hunt, D.O.,</E>75 FR 49995, 50004 (2010);<E T="03">see also Hassman,</E>75 FR at 8236 (quoting<E T="03">Hoxie</E>v.<E T="03">DEA,</E>419 F.3d 477, 483 (6th Cir. 2005) (“Candor during DEA investigations, regardless of the severity of the violations alleged, is considered by the DEA to be an important factor when assessing whether a physician's registration is consistent with the public interest[.]”) Moreover, in assessing an appropriate sanction, DEA also properly considers the need to deter others from engaging in similar acts and the egregiousness of the misconduct.<E T="03">See Joseph Gaudio,</E>74 FR 10083, 10094 (2009);<E T="03">Southwood Pharmaceuticals, Inc.,</E>72 FR 36487, 36504 (2007) (citing<E T="03">Butz</E>v.<E T="03">Glover Livestock Commission Co., Inc.,</E>411 U.S. 182, 187-88 (1973)).</P>

        <P>Here, the ALJ found that Respondent credibly testified that he was in compliance with the terms of his probation, as well as the terms of the Order of the Wisconsin Medical Board, which include that he undergo treatment and be subject to random drug testing. ALJ at 22. While the ALJ found that Respondent “demonstrate[d] an acknowledgement that his actions were illegal,” he further observed that “Respondent's testimony at the hearing did not reflect a high level of contrition,” and that “true remorse, to the extent Respondent may possess it, was not patently evident from his presentation at the hearing.”<E T="03">Id.</E>at 23. As the ALJ further explained, “[d]uring his testimony, the Respondent gave the distinct impression that he was not so much sorry about his transgression as he was sorry that he got caught and was laboring under the criminal and administrative consequences of that reality.”<E T="03">Id.</E>
        </P>
        <P>In addition, I note that in his testimony, Respondent maintained that he “never” provided marijuana to his niece, that she had obtained it behind his back, and that he had no knowledge that she was using marijuana and doing so with others prior to when the police searched his house. Tr. 47-48. However, the ALJ found this testimony “implausibl[e],” ALJ at 11, as do I.<SU>5</SU>
          <FTREF/>Based on the ALJ's finding, I further find that Respondent's testimony was not entirely candid. Thus, even giving weight to the ALJ's findings regarding Respondent's rehabilitation and his acceptance of responsibility, Respondent's lack of candor supports a substantial period of suspension.</P>
        <FTNT>
          <P>
            <SU>5</SU>Having observed Respondent testify, the ALJ"s finding is entitled to substantial deference. Beyond this, the finding is consistent with other evidence of record including the statement of one of the informants that whenever the subject of the marijuana plants would come up, Respondent's niece “would say that she couldn't talk about it”; that on at least two occasions, he observed marijuana leaves drying in her closet; and that on another occasion, when he and the niece needed marijuana, she left the bedroom and returned with a large bud which “was packed down dried.” GX 7, at 13. Thus, it is clear that his niece had ready access to Respondent's marijuana; moreover, Respondent offered no explanation as to why he allowed his niece to have access to it. In any event, Respondent's testimony that he was unaware that she was using marijuana begs credulity.</P>
        </FTNT>

        <P>In seeking the revocation of Respondent's registration, the Government cited three cases, each of which the ALJ distinguished on the grounds that the various practitioners had engaged in far more egregious misconduct either because they also “had significant * * * prescribing anomalies,” or because they were found to have grown far larger amounts of marijuana than Respondent. ALJ at 23-24. However, possession of a four pound stash of a schedule I controlled substance is nothing to sneeze at, and indeed, under Federal law, it is a felony offense punishable by up to five years imprisonment and a $250,000 fine.<E T="03">See</E>21 U.S.C. 841(a) &amp; (b)(1)(D). Moreover, as explained above, this is not simply a case of self-abuse. Rather, the evidence is clear that Respondent distributed the marijuana to his wife,<SU>6</SU>
          <FTREF/>and whether he actually physically delivered the drug to his niece, it is clear that she had ready access to it and also distributed it to at least one of her boyfriends.</P>
        <FTNT>
          <P>
            <SU>6</SU>Respondent likewise maintained that his wife used marijuana because she thought it eased a medical condition, but then acknowledged that “[s]he would have smoked it anyway.” Tr. 61. Moreover, Wisconsin does not permit the so-called “medical” use of marijuana.</P>
        </FTNT>
        <P>In short, while many cases brought under sections 303 and 304 of the Controlled Substances Act,<SU>7</SU>
          <FTREF/>involve registrants who have engaged in substantial unlawful distributions to others, Respondent's felonious conduct is nonetheless sufficiently egregious to warrant the revocation of his registration.<SU>8</SU>
          <FTREF/>
          <E T="03">See</E>21 U.S.C. 824(a)(2) (authorizing Agency to suspend or revoke a registration based on conviction for felony related to controlled substance). Moreover, even though Respondent now appears to acknowledge most of his illegal behavior and has been in compliance with the State Board's Order, I agree with the ALJ that the Agency's interest in deterring similar misconduct on the part of others warrants a substantial period of outright suspension. However, because I disagree with the ALJ's recommendation that a six-month suspension sufficiently protects the Agency's interest in deterring misconduct on the part of others and also note Respondent's less than candid testimony regarding his niece's access and use of marijuana, I will order that Respondent's registration be suspended for a period of one year.<SU>9</SU>

          <FTREF/>Further, while Respondent's renewal application will be granted (subject to the suspension of<PRTPAGE P="45869"/>his registration as set forth above), I further adopt the following conditions as recommended by the ALJ:</P>
        <FTNT>
          <P>
            <SU>7</SU>21 U.S.A. 823 and 824.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>8</SU>Indeed, in<E T="03">Alan H. Olefsky,</E>57 FR 928 (1992), DEA revoked a practitioner's registration based on his have in presented (in a single act) two fraudulent prescriptions to a pharmacist for filling. Respondent's conduct is at least as egregious as, if not considerably more so than, the conduct which warranted revocation in<E T="03">Olefsky.</E>
          </P>
        </FTNT>
        <FTNT>
          <P>
            <SU>9</SU>In determining the appropriate sanction, I have also considered the June 14, 2011 letter written by the Langlade County District Attorney on Respondent's behalf which was submitted to this Office on July 14, 2011. However, other than the information that Respondent has completed his probation and the terms of his sentence, the remainder of the letter does not constitute newly discovered evidence and I give it no weight.</P>
        </FTNT>
        <P>(1) The Respondent will comply with the terms and conditions of his criminal sentence and the Order of the Wisconsin Medical Board that are currently in effect, as well as any conditions which may be imposed in the future by either the state court or the Wisconsin Medical Board; Respondent shall provide a copy of all reports which he is required to submit to the Wisconsin Medical Board or the Department Monitor to the local DEA office within five business days of the submission.</P>
        <P>(2) Respondent shall agree and ensure that copies of all drug screening test results are submitted to the local DEA office, whether those tests are ordered by the state court, the Wisconsin Medical Board, or the approved drug and alcohol monitoring program in which he has enrolled pursuant to the Final Order of the Wisconsin Board.<SU>10</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>10</SU>Because the Wisconsin Board imposed extensive drug testing on Respondent in its final order, and Respondent has passed each of these tests, I conclude that it is unnecessary to subject Respondent to additional drug testing. For this reason, as well as that there is no evidence that Respondent has diverted controlled substances in his professional capacity, I conclude that is unnecessary to require as a condition of his registration, that he agree to warrantless searches of his residence and principal place of business.</P>
        </FTNT>
        <HD SOURCE="HD1">Order</HD>
        <P>Pursuant to the authority vested in me by 21 U.S.C. 823(f) and 824(a), as well as 28 CFR 0.100(b) and 0.104, I hereby order that the application of Michael S. Moore, M.D., to renew his DEA Certificate of Registration be, and it hereby is, granted subject to the conditions set forth above. I further order that the registration of Michael S. Moore, M.D., be, and it hereby is, suspended for a period of one year. This Order is effective August 31, 2011.</P>
        <SIG>
          <DATED>Dated: July 21, 2011.</DATED>
          <NAME>Michele M. Leonhart,</NAME>
          <TITLE>Administrator.</TITLE>
        </SIG>
        <EXTRACT>
          <FP>
            <E T="03">James Hambuechen, Esq.,</E>for the Government;</FP>
          
          <FP>
            <E T="03">David Madison, Esq.,</E>for the Respondent.</FP>
        </EXTRACT>
        <HD SOURCE="HD1">Recommended Rulings, Findings of Fact, Conclusions of Law, and Decision of the Administrative Law Judge</HD>
        <P>John J. Mulrooney, II, Administrative Law Judge. On February 26, 2010, the Drug Enforcement Administration (DEA) Deputy Assistant Administrator issued an Order to Show Cause (OSC) seeking revocation of the Respondent's Certificate of Registration (COR), Number BM6464147, as a practitioner, pursuant to 21 U.S.C. 824(a)(2) and (a)(4), and denial of any pending applications for renewal or modification of such registration, pursuant to 21 U.S.C. 823(f), alleging that the Respondent has been convicted of a felony and misdemeanor involving controlled substances, and that his continued registration is otherwise inconsistent with the public interest, as that term is used in 21 U.S.C. § 823(f). On March 23, 2010, the Respondent timely requested a hearing, which was conducted in Arlington, Virginia, on August 31, 2010.<SU>11</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>11</SU>Following the unexpected and unfortunate passing of the Gene Linehan, Esq., who had represented the Respondent at and prior to the hearing in this matter, representation was undertaken by current counsel, David Madison, Esq., an attorney who was associated with Mr. Linehan's law firm.</P>
        </FTNT>
        <P>The issue ultimately to be adjudicated by the Deputy Administrator, with the assistance of this recommended decision, is whether the record as a whole establishes by substantial evidence that Respondent's registration with the DEA should be revoked as inconsistent with the public interest as that term is used in 21 U.S.C. 823(f) and 824(a)(4). The Respondent's DEA COR is set to expire by its terms on January 31, 2011.</P>
        <P>After carefully considering the testimony elicited at the hearing, the admitted exhibits, the arguments of counsel, and the record as a whole, I have set forth my recommended findings of fact and conclusions below.</P>
        <HD SOURCE="HD1">The Evidence</HD>
        <P>The OSC issued by the Government alleges that revocation of the Respondent's COR is appropriate because of the Respondent's April 9, 2009 no contest plea to a felony charge of manufacturing and delivering tetrahydrocannabinols (THC),<SU>12</SU>
          <FTREF/>and a misdemeanor charge of possession of drug paraphernalia, both of which, according to the Government's allegations, constitute criminal convictions that “arose from [the Respondent] growing large amounts of marijuana at [Respondent's] home, which was discovered upon the execution of a search warrant on August 3, 2007.”<SU>13</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>12</SU>A Schedule I controlled substance. 21 U.S.C. 812; 21 CFR 1308.11.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>13</SU>Initially, the OSC also alleged that a positive urinalysis result rendered the Respondent in violation of the terms of an October 17, 2007 Final Decision and Order of the State of Wisconsin Medical Examining Board (Wisconsin Medical Board), requiring him to abstain from the personal use of controlled substances without a legitimate prescription. At the outset of the hearing, however, the Government withdrew that allegation. ALJ Ex. 11; Tr. at 12-14, 82.</P>
        </FTNT>

        <P>At the hearing, the Government presented the testimony of DEA Diversion Investigator (DI) Thomas B. Hill, in support of its case for revocation. Through DI Hill's testimony, the Government introduced the Final Decision and Order relative to the Respondent which was issued by the Wisconsin Medical Examining Board (Wisconsin Medical Board) on October 17, 2007. Gov't Ex. 3; Resp't Ex. 7; Tr. at 20. That document contains the Respondent's stipulation to the Wisconsin Medical Board's factual finding that, on August 3, 2007, he “possess[ed] tetrahydrocannabinol, a Schedule I controlled substance, not in the course of professional practice, and without any other authorization to do so,” and that said conduct “violated Wis. Stat. § 961.41(3g) [possession of controlled substance], Wis. Adm. Code § Med 10.02(2)(p) [obtaining controlled substance outside legitimate practice], and (z) [violation of related law or rule],” and that “[s]uch conduct constitutes unprofessional conduct within the meaning of the Code and statutes.” Gov't Ex. 3 at 1-2; Resp't Ex. 7 at 1-2. As a result of these factual findings and conclusions of law, the Respondent's state medical license was indefinitely suspended for a period of at least five years, subject to a stay of that suspension, which was conditioned upon the Respondent remaining in compliance with certain conditions and limitations contained in the Order. The conditions of the stay include rehabilitation, drug monitoring, and treatment regimens, all of which are directed to be conducted at his expense. The regimens set forth in the Wisconsin Medical Board's Order require the Respondent to,<E T="03">inter alia,</E>attend individual and/or group therapy sessions, attend weekly Narcotics and/or Alcoholic Anonymous meetings, abstain from all personal use of alcohol, abstain from controlled substances “except when prescribed, dispensed or administered by a practitioner for a legitimate medical condition,” notify his designated treating physician and the Department Monitor within twenty-four hours of ingestion or administration of any and all medications and drugs, provide those officials with any associated prescription, and submit to drug and alcohol urinalysis screens at a frequency of not less than ninety-six times per year for the first year of the program. Gov't Ex. 3 at 3-4; Resp't Ex. 7 at 3-4. With respect to practice limitations, the Wisconsin Medical Board's Order limits the Respondent's practice of medicine to serving as an emergency physician in a Board-approved setting, and prohibits him from prescribing or ordering<PRTPAGE P="45870"/>controlled substances outside of that setting. Furthermore, the Order forbids the Respondent from the administering or dispensing of all controlled substances, and provides that all controlled substance orders issued by Respondent through his practice as an emergency physician “shall be reviewed by another physician within twenty-four hours of issuance, in a manner which documents the review.” Gov't Ex. 3 at 4; Resp't Ex. 7 at 4.</P>
        <P>Through the testimony of DI Hill, the Government also introduced various documents obtained from the Wisconsin Court system relative to the Respondent's state criminal case, which arose out of the same conduct at issue in the state medical board proceedings. Gov't Ex. 6. Those documents reflect that on April 9, 2009, the Respondent entered a no contest plea<SU>14</SU>
          <FTREF/>to Wisc. Stat. § 961.41(1)(h)(1), Manufacturing or Delivering<SU>15</SU>

          <FTREF/>less than or equal to 200 grams of THC (a felony), and Wisc. Stat. § 961.573(1), Possession of Drug Paraphernalia (a misdemeanor), and, pursuant to that plea, was found guilty of both charges.<E T="03">Id.</E>The documents reflect that the Respondent was sentenced to probation (sentence withheld two years), conditioned upon serving thirty days at Langlade County Jail with work-release privileges, 160 hours of community service, a monetary fine, a six month suspension of his driver's license, and several other terms.<E T="03">Id.</E>at 3-4.</P>
        <FTNT>
          <P>
            <SU>14</SU>A plea of no contest or<E T="03">nolo contendere</E>that results in a judgment of conviction constitutes a conviction for purposes of the Controlled Substances Act (CSA).<E T="03">Pearce</E>v.<E T="03">DEA,</E>867 F.2d 253, 255 (6th Cir. 1988);<E T="03">Noell</E>v.<E T="03">Bensinger,</E>586 F.2d 554, 556-57 (5th Cir. 1978);<E T="03">Sokoloff</E>v.<E T="03">Saxbe,</E>501 F.2d 571, 575 (2d Cir. 1974).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>15</SU>A Plea Questionnaire/Waiver of Rights form subsequently entered into the record through Respondent's testimony reflects that the Respondent only pleaded guilty to the manufacturing of THC, rather than the statutory elements relating to delivery/distribution. Resp't Ex. 3 at 3; see also Tr. at 21-22, 67-70. Accordingly, the disposition of this charge is referenced hereinafter as a felony conviction for controlled substance manufacturing.</P>
        </FTNT>
        <P>The transcript of the state court guilty plea was offered by the Respondent and received into evidence.<SU>16</SU>
          <FTREF/>Tr. at 67; Resp't Ex. 1. Although at his sentencing hearing, the Respondent provided an unsworn statement assuring the criminal trial judge that he “never sold [marijuana and] never shared it,”<SU>17</SU>
          <FTREF/>the record contains the following comments from the trial judge on the subject:</P>
        <FTNT>
          <P>
            <SU>16</SU>The Respondent initially marked individual pages of the state court sentencing transcript as separate proposed exhibits, but the entire transcript was relatively brief and was received into evidence as a single exhibit.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>17</SU>Resp't Ex. 1 at 23.</P>
        </FTNT>
        
        <EXTRACT>
          <P>I don't totally accept that [the Respondent] was growing simply for his own use. I think it was for probably, in all likelihood, him and his guests of like mind, his wife, but I do agree I am looking at this, and I see to a large extent these are plants, seeds, stems. Looks to me that there's probably some processed here. Looks to be down to the buds that are in the plastic bags, and probably more than you would normally find.</P>
        </EXTRACT>
        
        <FP>Resp't Ex. 1 at 26.</FP>
        <P>The criminal sentencing transcript also reflects an acknowledgement by the trial court that, under Wisconsin law, the Respondent, upon successful completion of his probation, may apply to have the felony conviction reduced to a misdemeanor. Resp't Ex. 1 at 3. Although there is no indication in the record that such an application has been granted, is pending, or has even been submitted to competent state officials for action,<SU>18</SU>

          <FTREF/>it is worthy of note that Agency precedent has long held that even a subsequent dismissal would not undermine the validity of a criminal conviction for purposes of the CSA.<E T="03">Edson W. Redard, M.D.,</E>65 FR 30616, 30618 (2000);<E T="03">Stanley Alan Azen, M.D.,</E>61 FR 57893, 57895 (1996). Thus, following his plea to felony manufacturing of tetrahydrocannabinol (THC), Respondent remains a convicted felon, “convicted of a felony under [the law of Wisconsin] relating to * * * a controlled substance. * * *”<SU>19</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>18</SU>Tr. at 90.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>19</SU>21 U.S.C. 824(a)(2).</P>
        </FTNT>
        <P>The Government, through the testimony of DI Hill, also introduced a packet containing information related to the state criminal case that culminated in the convictions that form the basis of the Wisconsin Board Order. Gov't Ex. 7. Specifically, the Government provided the search and arrests warrants associated with the August 3, 2007 arrest that resulted in the Respondent's conviction of felony manufacturing of THC and misdemeanor possession of drug paraphernalia, as well as the associated affidavits prepared by the executing state law enforcement officers.<SU>20</SU>

          <FTREF/>Gov't Ex. 7 at 1-5. The Government also supplied numerous investigation reports, inventories and allied documents prepared by members of two local county law enforcement entities, and sworn, hand-written statements from current and former boyfriends of the Respondent's niece.<E T="03">Id.</E>at 6-31, 42-46. Also included in the packet were numerous documents that the Government alleged were seized at the Respondent's residence in connection with the search warrant execution, and which, according to the Government, demonstrated the Respondent's participation in a significant marijuana growing operation.<E T="03">Id.</E>at 32-41.</P>
        <FTNT>
          <P>
            <SU>20</SU>The Government did not produce live testimonyfrom any of the state law enforcement officers.</P>
        </FTNT>

        <P>It is well-settled that hearsay may be correctly considered at an administrative hearing and may even support a finding of substantial evidence.<E T="03">Richardson</E>v.<E T="03">Perales,</E>402 U.S. 389, 402 (1971) (signed reports prepared by licensed physicians correctly admitted at Social Security disability hearing);<E T="03">Keller</E>v.<E T="03">Sullivan,</E>928 F.2d 227, 230 (7th Cir. 1991) (insurance company investigative reports correctly admitted in Social Security disability hearing where sufficient indicia of reliability established);<E T="03">Calhoun</E>v.<E T="03">Bailar,</E>626 F.2d 145, 149 (9th Cir. 1980) (hearsay affidavits correctly admitted where indicia of reliability established). However, there are limits that circumscribe the admission and utility of hearsay evidence before an administrative tribunal. The touchstone is that before it may be used to support of finding of substantial evidence, the offered hearsay evidence must have sufficient reliability and credibility. Divining the correct use of hearsay evidence requires a balancing of four factors: (1) Whether the out-of-court declarant was not biased and had no interest in the outcome of the case; (2) whether the opposing party could have obtained the information contained in the hearsay before the hearing and could have subpoenaed the declarant; (3) whether the information was inconsistent on its face; and (4) whether the information has been recognized by the courts as inherently reliable.<E T="03">J.A.M. Builders</E>v.<E T="03">Herman,</E>233 F.3d 1350, 1354 (11th Cir. 2000).</P>
        <P>Government Exhibit 7 divides analytically into five general categories of evidence: (1) A signed search and arrest warrant with its underlying supporting affidavit (executed by a local law enforcement officer) and some blank affiliated paperwork;<SU>21</SU>
          <FTREF/>(2) two sworn statements apparently procured by local law enforcement personnel, signed by two individuals whom claim, respectively, to be the current and former boyfriend of the Respondent's niece (the boyfriends);<SU>22</SU>

          <FTREF/>(3) unsigned typewritten police reports prepared by named local law enforcement personnel with apparent personal knowledge of the events contained therein, along with an apparently affiliated narcotics field<PRTPAGE P="45871"/>test report<SU>23</SU>
          <FTREF/>and documents that appear to reflect an inventory of items seized from the Respondent's residence on the night the search warrant was executed;<SU>24</SU>
          <FTREF/>(4) documents purportedly seized from the Respondent's residence;<SU>25</SU>
          <FTREF/>and (5) unsigned, handwritten notes that may have been prepared by law enforcement personnel on the scene of the search warrant executed at the Respondent's home.<SU>26</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>21</SU>Gov't Ex. 7 at 1-5.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>22</SU>
            <E T="03">Id.</E>at 13-14.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>23</SU>
          </P>Although at least part of the Respondent'sobjection to the field test portion of the exhibit was founded in counsel's assertion that the type of field test employed was not adequately identified, Tr. at 30, the police paperwork indicates that a Nark II test 05 was utilized. Gov't Ex. 7 at 15.</FTNT>
        <FTNT>
          <P>
            <SU>24</SU>
            <E T="03">Id.</E>at 6-12, 15-31.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>25</SU>
            <E T="03">Id.</E>at 32-41.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>26</SU>
            <E T="03">Id.</E>at 44-46.</P>
        </FTNT>
        <P>Regarding the fifth category (handwritten police notes), the documents are intermittently legible, insufficiently explained by any witness with personal knowledge, were excluded from consideration at the hearing,<SU>27</SU>
          <FTREF/>and will play no role in the disposition of this case.</P>
        <FTNT>
          <P>
            <SU>27</SU>Tr. at 38-39.</P>
        </FTNT>

        <P>The documents offered by the Government in the fourth category (seized from the Respondent's residence) were authenticated by the Respondent, himself, who testified that he prepared the handwritten notes in the packet related to preparing for and monitoring the progress of his marijuana grow. Tr. at 50. Some of the seized notes related to information the Respondent accumulated to help him select the most effective lighting to maximize his marijuana yield.<E T="03">Id.</E>at 49-50; Gov't Ex. 7 at 32. There are other notes that the Respondent indicated were taken from a book he read regarding marijuana grow methods,<SU>28</SU>
          <FTREF/>and still more notes reflected his careful monitoring of the growth progress of his marijuana plants. Tr. at 49-51; Gov't Ex. 7 at 35-36. The Respondent identified a portion of the documents as an Internet recipe for preparing “hash,” an enterprise that he apparently attempted in vain. Tr. at 52; Gov't Ex. 7 at 37-41. The Respondent's marijuana research notes and materials were sufficiently authenticated and relevant to merit admission and consideration in these proceedings and clearly demonstrate a high level of planning in his efforts to circumvent the CSA.</P>
        <FTNT>
          <P>
            <SU>28</SU>Gov't Ex. 7 at 33-34.</P>
        </FTNT>

        <P>Regarding the other documents in Government Exhibit 7, the first three<E T="03">J.A.M. Builders</E>factors militate in favor of admission. There is no indication of bias on the part of the local law enforcement officers who swore out the warrant affidavits, prepared the investigative reports, and took the sworn statements from the two boyfriends. Likewise, no bias is readily apparent regarding the statements from the boyfriends.<SU>29</SU>
          <FTREF/>The Respondent clearly had the opportunity to subpoena<SU>30</SU>
          <FTREF/>any of the authors of any of the documents but elected (presumably for tactical reasons) not to do so. The documents are internally consistent and essentially consistent with one another.</P>
        <FTNT>
          <P>
            <SU>29</SU>
          </P>To the extent that bias borne of jealousy or unrequited affection may have existed, it was not developed, elicited, or argued by any party to this litigation. To assign bias on the current record would be to engage in unwarranted and unfair speculation.</FTNT>
        <FTNT>
          <P>
            <SU>30</SU>
          </P>In fact, the Prehearing Ruling, which was issued after service of the Government's Prehearing statement outlining its evidence, set a date by which subpoena requests were due. ALJ Ex. 7 at 4. No subpoena requests from the Respondent were filed.</FTNT>
        <P>Consideration of the fourth factor, that is, whether the information has been recognized by the courts as inherently reliable, is something of a mixed bag regarding Government Exhibit 7. In this administrative setting, the inventory log is reliable to the same extent generally accorded to records prepared in the regular course of business,<SU>31</SU>
          <FTREF/>and courts routinely rely on sworn affidavits to support searches, seizures, and other intrusions,<SU>32</SU>

          <FTREF/>but there is no precedential basis to accord any special weight to police reports. In<E T="03">Richardson,</E>
          <SU>33</SU>

          <FTREF/>the Supreme Court squarely based its holding on the narrow fact that the party opposing admission never used the available procedural devices to seek the personal appearances of the declarants, but the<E T="03">Richardson</E>court took pains to point out that the case dealt with the admission of medical reports, each of which was “prepared by a practicing physician who had examined [the opponent of admission and where each of whom had] set[] forth his medical findings in his area of competence. * * *” 402 U.S. 389, 402 (1971). As the post-<E T="03">Richardson</E>cases have evolved, the emphasis has increasingly focused on whether the opponent could have subpoenaed the declarant but declined to do so, and whether the hearsay is reliable and trustworthy. In<E T="03">U.S. Pipe &amp; Foundry Co.</E>v.<E T="03">Webb,</E>595 F.2d 264, 270 (5th Cir. 1979), the court re-emphasized that medical reports are inherently reliable and trustworthy. In<E T="03">Klinestiver</E>v.<E T="03">DEA,</E>606 F.2d 1128, 1130 (D.C. Cir. 1979), the court held that hearsay at a DEA administrative hearing may constitute substantial evidence where the opponent of the evidence could have subpoenaed the declarant but declined to do so, and that the controlling guidance regarding admission is found in the DEA regulations. The current DEA regulations provide for the admission of evidence that is “competent, relevant, material, and not unduly repetitious.” 21 CFR 1316.59(a).</P>
        <FTNT>
          <P>
            <SU>31</SU>This heightened level of reliability is based on the likelihood that inventory logs reflecting seized property have been accurately kept, given that such logs are judicially-mandated pursuant to Fed. R. Crim. P. 41(f)(1)(b) (or, as is relevant to this case, the equivalent Wisconsin state criminal procedural rule, i.e. Wisc. Stat. § 968.17) and routinely relied on for a property itemization and accounting purpose by the courts, law enforcement, and the person whose property was seized.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>32</SU>
            <E T="03">See</E>Fed. R. Crim. P. 41(d).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>33</SU>402 U.S. 389 (1971).</P>
        </FTNT>
        <P>Balancing the<E T="03">J.A.M. Builders</E>factors, the sworn statements, police reports, and allied paperwork (excluding the withdrawn, illegible handwritten notes) were admitted and considered, albeit with the heightened scrutiny correctly attached to evidence that has not been exposed to the rigors of cross-examination.<E T="03">Cf.</E>21 CFR 1301.43(c) (DEA regulations provide for the consideration of waiver-related statements to be “considered in light of the lack of opportunity for cross-examination in determining the weight to be attached to matters of fact asserted therein.”). Government Exhibit 7, as admitted, establishes that the search warrant and ultimate arrest was the result of an investigation initiated based on information gleaned from a former boyfriend of the Respondent's niece. The niece was living in the Respondent's home and apparently smoking and sharing marijuana with guests, including (by their own accounts and at different times) the two boyfriends. When officers executed the state-authorized<SU>34</SU>
          <FTREF/>search warrant, they uncovered a hidden, locked room with elaborate equipment utilized for the growing of marijuana, as well as multiple bags and other containers that held marijuana plant parts and seeds. According to the paperwork, 4.76 pounds<SU>35</SU>
          <FTREF/>of marijuana were identified, tested,<SU>36</SU>

          <FTREF/>and seized from the Respondent's residence. Gov't Ex. 7 at 17-18. Additionally, the executing officers seized some paperwork they believed to be related to the growing of marijuana, and through a previous, separate authorization, learned that the Respondent's power bill, at least in the opinion of the state investigators, was<PRTPAGE P="45872"/>unusually large.<SU>37</SU>
          <FTREF/>
          <E T="03">Id.</E>at 1. The officers observed and seized what they characterized as “four large stalks [of marijuana] in the hydroponic growing stages.”<SU>38</SU>
          <FTREF/>
          <E T="03">Id.</E>at 9.</P>
        <FTNT>
          <P>
            <SU>34</SU>The search warrant was authorized by a Langlade County Court Commissioner. Gov't Ex. 7 at 2-3.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>35</SU>DI Hill testified that 1,725 grams were seized, Tr. at 16, which would be a little less than four pounds.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>36</SU>Gov't Ex. 7 at 15.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>37</SU>Presumably this information was included on the affidavit in support of the search warrant under the theory that it was consistent with the power required to run electrical equipment associated with a marijuana grow operation.</P>
        </FTNT>
        <FTNT>
          <P>

            <SU>38</SU>Although the police paperwork indicates that both still and video photographs of the hidden room, marijuana, and paraphernalia were generated at the scene contemporaneous with the search warrant execution, the Government, inexplicably, did not offer any of this evidence at the hearing. During his testimony, DI Hill initially testified that three (3) marijuana plants were seized from the Respondent's residence. Tr. at 39-40. This is curious in light of the fact that he readily maintained that all his knowledge about the case was obtained through the paperwork he provided,<E T="03">Id.</E>at 19, 41, and the paperwork indicates that four (4) plants were seized. Gov't Ex. 7 at 9. In his testimony, the Respondent confirmed that four (4) plants were seized. Tr. at 46.</P>
        </FTNT>
        <P>Inasmuch as DI Hill gleaned all the information he had about the case from documents that he obtained from local law enforcement officers and a court database check, the factual aspects of the case depend less on the credibility of his testimony than the truth of the facts established by the Government's exhibits introduced through Hill's testimonial foundations. Furthermore, even considering that the acknowledgement of virtually all the factual matters asserted in the paperwork by the Respondent in his testimony further diminishes the significance of Hill's testimony, it is worth noting that DI Hill provided testimony that was sufficiently detailed, plausible, and internally consistent to be deemed credible.</P>
        <P>The Respondent testified at the hearing.<SU>39</SU>
          <FTREF/>By his own account, the Respondent, who lives with his wife, two small children,<SU>40</SU>

          <FTREF/>and his niece, has quite a history with marijuana. He recalled smoking marijuana most days he attended college, most non-working days after college, and several times a week through his medical residency program. Tr. at 44-45. After presumably purchasing marijuana on a regular basis for most of his adult life, the Respondent testified that he began growing his own marijuana during the 2004-2005 time frame.<E T="03">Id.</E>at 46. At the time his house was searched, his current marijuana crop (grow) had four (4) plants, the yield of which, at least according to his testimony, was reserved for use by himself and his wife.<E T="03">Id.</E>at 47. The Respondent acknowledged that he and his wife share their family home with their two children, ages nine and eleven, as well as a niece, and that his in-laws were the only people outside his home who knew about his foray into the world of marijuana production.<E T="03">Id.</E>at 47. While the Respondent did not dispute the accounts in the police paperwork that ascribe significant marijuana consumption to his niece, he testified that this information came as a surprise to him.<E T="03">Id.</E>at 47-48.</P>
        <FTNT>
          <P>
            <SU>39</SU>Although the Respondent noticed himself as a witness, he testified as a witness called by the Government.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>40</SU>Tr. at 56.</P>
        </FTNT>

        <P>Regarding his conviction, the Respondent freely acknowledged all the attendant facts raised in the court records and the police paperwork, as well as the illegality of his conduct and the propriety of the conviction.<E T="03">Id.</E>at 55, 77, 79. The Respondent represented that he intended to avoid violating controlled substance laws in the future.<E T="03">Id.</E>at 76. In response to questioning by the Government, the Respondent agreed that marijuana is an illegal substance and concurred that his conviction was not unfair.<E T="03">Id.</E>at 55. When asked why he elected to grow marijuana (after an adult lifetime of presumably acquiring the substance by other means), the Respondent related that he lived in a small community and would likely be easily identified as a physician during any exploit to purchase marijuana from those “on the street” in his local area willing to sell it.<SU>41</SU>
          <FTREF/>
          <E T="03">Id.</E>at 78.</P>
        <FTNT>
          <P>
            <SU>41</SU>During his criminal sentencing hearing, theRespondent's counsel argued that he chose to grow marijuana to help his wife with a digestive disorder and as a way to withhold support from Mexican drug cartels. Resp't Ex. 1 at 19. The Respondent's response at his DEA administrative hearing appears to be a more candid and plausible handling of the issue.</P>
        </FTNT>

        <P>The Respondent credibly testified that he has complied with the conditions fixed by the Wisconsin Medical Board during the first three years of the five-year duration of its Order.<E T="03">Id.</E>at 58-59. In particular, the Respondent testified that he has complied with the Order's mandate of random urinalysis, including one directive to provide a random sample which serendipitously arose while he was traveling to the hearing of this case.<E T="03">Id.</E>at 59.</P>

        <P>The Respondent also elaborated on the community service that he provided at the direction of the Wisconsin Medical Board. Although he performed work at a hospice as directed by the criminal court, the Respondent also indicated that he continues to contribute his time to the nun-operated hospice, even after the community service time in his sentence has been completed.<E T="03">Id.</E>at 64-65. The Respondent also testified that he had performed volunteer work at the hospice before his conviction.<E T="03">Id.</E>
        </P>

        <P>The Respondent characterized his community as “sparsely populated,” discussed his perception that physician recruitment was problematic in the area, and indicated that he would be unable to provide his emergency room services if rendered unauthorized to handle controlled substances.<E T="03">Id.</E>at 65-66.</P>
        <P>While the Respondent implausibly testified that the marijuana he produced was only consumed by himself and his wife, and that he was surprised to learn that his niece (who was also the legal ward of his wife) was also smoking his pot by herself and with company, the bulk of his other testimony, though admittedly self-serving, was sufficiently plausible, detailed, and internally consistent to be deemed generally credible for purposes of this recommended decision.</P>

        <P>The Respondent offered letters of support from various medical practitioners in his community. Resp't Exs. 8-11. A carefully-worded letter authored by Noel N. Deep, M.D., F.A.C.P., the Chief of Staff at the Langlade Hospital, relates that the Respondent has “scored high on patient satisfaction surveys, that his “professionalism and clinical skills” have won praise from members of the hospital staff, that he has volunteered to serve in numerous capacities in the hospital, and that Dr. Deep has “never been aware of any adverse clinical outcomes or patient care concerns” related to the Respondent's work. Resp't Ex. 8. The principal thrust of Dr. Deep's letter is to essentially highlight the potential impact that would be felt by Langlade Hospital and the rural community surrounding it should one of its four emergency room physicians be deprived access to controlled substance handling authority by DEA.<E T="03">Id.</E>In particular, the letter indicates that an adverse DEA decision in this regard “would burden the other three physicians who currently share the Emergency Room call rotation with [the Respondent].”<E T="03">Id.</E>
        </P>

        <P>Another Langlade Hospital administrator, David Schneider, the executive director, also provided a letter of support. Resp't Ex. 10. Like the wording in Dr. Deep's letter, this hospital official references the Respondent's patient satisfaction survey scores, and indicates that there have been “[n]o clinical adverse issues” associated with the Respondent's practice at the hospital, which (like the survey results) Mr. Schneider characterizes as “at the upper end of quality scales.”<E T="03">Id.</E>Mr. Schneider, like Dr. Deep, spends a significant portion of his letter seeking leniency for the Respondent, based upon community<PRTPAGE P="45873"/>impact, stating that “Langlade Hospital serves a medically underserved area [where] it has been and is increasingly difficult to obtain and maintain skilled practitioners in full-time [emergency room] service.”<E T="03">Id.</E>
        </P>
        <P>A third letter admitted into evidence is co-signed by the three emergency medicine physicians who, according to the Respondent,<SU>42</SU>
          <FTREF/>are his partners at Northwoods Emergency Physicians, LLP (the Northwoods Group), a medical entity that provides emergency room physicians to Langlade Hospital. Resp't Ex. 9; Tr. at 63. The letter from the Respondent's associates details the conditions fixed by the Wisconsin Medical Board in its Order, and (somewhat self-servingly) concludes that “[t]hese are adequate measures to assure patient safety.” Resp't Ex. 9. Like the other letters, there is a reference to the doctors' perception that the area surrounding Langlade Hospital is “underserved” and currently benefits by the Respondent's presence there, and presumably also his access to controlled substances.</P>
        <FTNT>
          <P>
            <SU>42</SU>Tr. at 73.</P>
        </FTNT>

        <P>The Respondent also provided a letter from Sister Dolores Demulling, R.N., M.S., the Administrator at the LeRoyer Hospice affiliated with the hospital where the Respondent serves in the emergency room. Resp. Ex. 11. Sr. Demulling confirmed the Respondent's representations that he has volunteered his time doing hospice work and provides her estimation that the Respondent's “medical care in the emergency room has always been very satisfactory.”<E T="03">Id.</E>
        </P>
        <P>In evaluating the weight to be attached to the representations in the letters provided by the Respondent's hospital administrators and peers, it can hardly escape notice that, in addition to the fact that the authors were not subjected to the rigors of cross examination, each source has a significant influencing consideration that bears caution. The emergency room doctors are the Respondent's partners. As partner-members to a group which is contracted to cover Langlade Hospital, it is not improbable that the doctors would likely be understandably reluctant to question the abilities of one of their own. Criticism of a member's ability to safely continue to serve the hospital would perforce call into question the Northwoods Group's ability to continue to staff the emergency room. Similarly, the hospital administrators who have elected to allow the Northwoods Group to continue to utilize the Respondent's services for patient care would be virtually unable to provide an unflattering assessment of any concerns they possess without exposing the institution to significant potential past and future tort and/or regulatory liability. However, even bearing these concerns in mind, the letters can, should, and will nevertheless provide evidence that other medical professionals and administrators feel sufficiently confident in the Respondent and his level of professional commitment that they believe his continued authorization to handle controlled substances will not pose an unacceptable risk to the patients served by Langlade Hospital.</P>
        <P>Other evidence required for a disposition of this issue is set forth in the analysis portion of this decision.</P>
        <HD SOURCE="HD1">The Analysis</HD>
        <P>The Deputy Administrator<SU>43</SU>

          <FTREF/>may revoke a registrant's DEA Certification upon a finding that the registrant has been convicted of a felony relating to a CSA-designated controlled substance. 21 U.S.C. § 824(a)(2). As discussed<E T="03">supra,</E>a conviction resulting from a<E T="03">nolo contendere,</E>or “no contest” plea, is a conviction providing a sufficient basis for the revocation of a DEA COR under section 824(a)(2).<E T="03">Pearce</E>v.<E T="03">DEA,</E>867 F.2d 253, 255 (6th Cir. 1988);<E T="03">Noell</E>v.<E T="03">Bensinger,</E>586 F.2d 554, 556-57 (5th Cir. 1978);<E T="03">Sokoloff</E>v.<E T="03">Saxbe,</E>501 F.2d 571, 574-75 (2d Cir. 1974);<E T="03">Edson W. Redard, M.D.,</E>65 FR 30616, 30618 (2000). Furthermore, inasmuch as the Agency has consistently held that a deferred adjudication of guilt following a guilty plea, even where the proceedings are later dismissed, still constitutes a conviction within the statutory meaning of the CSA,<SU>44</SU>

          <FTREF/>the potential for some future reduction of the Respondent's conviction before the Wisconsin state courts bears little on any issue relevant to a disposition of this administrative case. Hence, inasmuch as the uncontroverted evidence of record conclusively establishes that the Respondent has been convicted of a state felony relating to controlled substances,<E T="03">to wit,</E>the manufacture of a Schedule I controlled substance (marijuana), the Government has established a basis under which the revocation relief it seeks may be evaluated to determine whether it constitutes a provident exercise of discretion.<E T="03">Pearce,</E>867 F.2d at 256.</P>
        <FTNT>
          <P>
            <SU>43</SU>This authority has been delegated pursuant to 28 CFR 0.100(b) and 0.104.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>44</SU>
            <E T="03">Vincent J. Scolaro, D.O.,</E>67 FR 42060, 42065 (2002) (citing<E T="03">Yu-To Hsu, M.D.,</E>62 FR 12840 (1997));<E T="03">Redard</E>, 65 FR at 30618;<E T="03">Stanley Alan Azen, M.D.</E>, 61 FR 57893, 57895 (1996). Agency precedent has previously validated the position that to hold otherwise would mean “the conviction could only be considered between its date and the date of subsequent dismissal * * * [which would be] inconsistent with holdings in other show cause cases that the passage of time since misconduct affects only the weight to be given the evidence.”<E T="03">Edson W. Redard, M.D.</E>, 65 FR 30616, 30618 (2000) (citing<E T="03">Mark Binette, M.D.</E>, 64 FR 42977, 42980 (1999));<E T="03">Thomas H. McCarthy, D.O.</E>, 54 FR 20938 (1989),<E T="03">aff'd</E>No. 89-3496 (6th Cir. Apr. 5, 1990).</P>
        </FTNT>
        <P>In addition to the controlled-substance-related felony conviction basis that the Government established in support of the revocation it seeks, under 21 U.S.C. 824(a)(4), the Deputy Administrator may also revoke a registrant's DEA COR if persuaded that the registrant “has committed such acts that would render * * * registration under section 823 * * * inconsistent with the public interest * * *” The following factors have been provided by Congress in determining “the public interest:”</P>
        
        <EXTRACT>
          <P>(1) The recommendation of the appropriate State licensing board or professional disciplinary authority.</P>
          <P>(2) The applicant's experience in dispensing, or conducting research with respect to controlled substances.</P>
          <P>(3) The applicant's conviction record under Federal or State laws relating to the manufacture, distribution, or dispensing of controlled substances.</P>
          <P>(4) Compliance with applicable State, Federal or local laws relating to controlled substances.</P>
          <P>(5) Such other conduct which may threaten the public health and safety.</P>
        </EXTRACT>
        
        <FP>21 U.S.C. 823(f).</FP>
        <P>“[T]hese factors are considered in the disjunctive.”<E T="03">Robert A. Leslie, M.D.,</E>68 FR 15227, 15230 (2003). Any one or a combination of factors may be relied upon, and when exercising authority as an impartial adjudicator, the Deputy Administrator may properly give each factor whatever weight she deems appropriate in determining whether an application for a registration should be denied.<E T="03">Id.; David H. Gillis, M.D.,</E>58 FR 37507, 37508 (1993);<E T="03">see also Joy's Ideas,</E>70 FR 33195, 33197 (2005);<E T="03">Henry J. Schwarz, Jr., M.D.,</E>54 FR 16422 (1989). Moreover, the Deputy Administrator is “not required to make findings as to all of the factors * * * .”<E T="03">Hoxie</E>v.<E T="03">DEA,</E>419 F.3d 477, 482 (6th Cir. 2005);<E T="03">see also Morall</E>v.<E T="03">DEA,</E>412 F.3d 165, 173-74 (D.C. Cir. 2005). The Deputy Administrator is not required to discuss consideration of each factor in equal detail, or even every factor in any given level of detail.<E T="03">Trawick</E>v.<E T="03">DEA,</E>861 F.2d 72, 76 (4th Cir. 1988) (Administrator's obligation to explain the decision rationale may be satisfied even if only minimal consideration is given to the relevant factors and remand is required only when it is unclear whether the relevant factors were<PRTPAGE P="45874"/>considered at all). The balancing of the public interest factors “is not a contest in which score is kept; the Agency is not required to mechanically count up the factors and determine how many favor the Government and how many favor the registrant. Rather, it is an inquiry which focuses on protecting the public interest * * * .”<E T="03">Jayam Krishna-Iyer, M.D.,</E>74 FR 459, 462 (2009).</P>

        <P>In an action to revoke a registrant's DEA Certificate of Registration, the DEA has the burden of proving that the requirements for revocation are satisfied. 21 CFR 1301.44(e). Once DEA has made its prima facie case for revocation of the registrant's DEA COR, the burden of production then shifts to the Respondent to show that, given the totality of the facts and circumstances in the record, revoking the registrant's registration would not be appropriate.<E T="03">Morall,</E>412 F.3d at 174;<E T="03">Humphreys</E>v.<E T="03">DEA,</E>96 F.3d 658, 661 (3d Cir. 1996);<E T="03">Shatz</E>v.<E T="03">U.S. Dept. of Justice,</E>873 F.2d 1089, 1091 (8th Cir. 1989);<E T="03">Thomas E. Johnston,</E>45 FR 72311, 72311 (1980). Further, “to rebut the Government's<E T="03">prima facie</E>case, [the Respondent] is required not only to accept responsibility for [the established] misconduct, but also to demonstrate what corrective measures [have been] undertaken to prevent the reoccurrence of similar acts.”<E T="03">Jeri Hassman, M.D.,</E>75 FR 8194, 8236 (2010).</P>

        <P>Where the Government has sustained its burden and established that a registrant has committed acts inconsistent with the public interest, that registrant must present sufficient mitigating evidence to assure the Deputy Administrator that he or she can be entrusted with the responsibility commensurate with such a registration.<E T="03">Steven M. Abbadessa, D.O.,</E>74 FR 10077 (2009);<E T="03">Medicine Shoppe-Jonesborough,</E>73 FR 364, 387 (2008);<E T="03">Samuel S. Jackson, D.D.S.,</E>72 FR 23848, 23853 (2007). Normal hardships to the practitioner, and even the surrounding community, that are attendant upon the lack of registration are not a relevant consideration.<E T="03">Abbadessa,</E>74 FR at 10078;<E T="03">see also Gregory D. Owens, D.D.S.,</E>74 FR 36751, 36757 (2009).</P>

        <P>The Agency's conclusion that past performance is the best predictor of future performance has been sustained on review in the courts,<E T="03">Alra Labs.</E>v.<E T="03">DEA,</E>54 F.3d 450, 452 (7th Cir. 1995), as has the Agency's consistent policy of strongly weighing whether a registrant who has committed acts inconsistent with the public interest has accepted responsibility and demonstrated that he or she will not engage in future misconduct.<E T="03">Hoxie,</E>419 F.3d at 483;<E T="03">George C. Aycock, M.D.,</E>74 FR 17529, 17543 (2009);<E T="03">Abbadessa,</E>74 FR at 10078;<E T="03">Krishna-Iyer,</E>74 FR at 463;<E T="03">Medicine Shoppe,</E>73 FR at 387.</P>

        <P>While the burden of proof at this administrative hearing is a preponderance-of-the-evidence standard,<E T="03">see Steadman</E>v.<E T="03">SEC,</E>450 U.S. 91, 100-01 (1981), the Deputy Administrator's factual findings will be sustained on review to the extent they are supported by “substantial evidence.”<E T="03">Hoxie,</E>419 F.3d at 481. While “the possibility of drawing two inconsistent conclusions from the evidence” does not limit the Deputy Administrator's ability to find facts on either side of the contested issues in the case,<E T="03">Shatz,</E>873 F.2d<E T="03"/>at 1092;<E T="03">Trawick,</E>861 F.2d at 77, all “important aspect[s] of the problem,” such as a respondent's defense or explanation that runs counter to the Government's evidence, must be considered.<E T="03">Wedgewood Village Pharm.</E>v.<E T="03">DEA,</E>509 F.3d 541, 549 (D.C. Cir. 2007);<E T="03">Humphreys,</E>96 F.3d at 663. The ultimate disposition of the case must be in accordance with the weight of the evidence, not simply supported by enough evidence to justify, if the trial were to a jury, a refusal to direct a verdict when the conclusion sought to be drawn from it is one of fact for the jury.<E T="03">Steadman,</E>450 U.S. at 99 (internal quotation marks omitted).</P>

        <P>Regarding the exercise of discretionary authority, the courts have recognized that gross deviations from past agency precedent must be adequately supported,<E T="03">Morall,</E>412 F.3d at 183, but mere unevenness in application does not, standing alone, render a particular discretionary action unwarranted.<E T="03">Chein</E>v.<E T="03">DEA,</E>533 F.3d 828, 835 (D.C. Cir. 2008) (citing<E T="03">Butz</E>v.<E T="03">Glover Livestock Comm. Co., Inc.,</E>411 U.S. 182, 188 (1973)),<E T="03">cert. denied,</E>__ U.S. __, 129 S. Ct. 1033 (2009). It is well-settled that since the Administrative Law Judge has had the opportunity to observe the demeanor and conduct of hearing witnesses, the factual findings set forth in this recommended decision are entitled to significant deference,<E T="03">Universal Camera Corp.</E>v.<E T="03">NLRB,</E>340 U.S. 474, 496 (1951), and that this recommended decision constitutes an important part of the record that must be considered in the Deputy Administrator's decision,<E T="03">Morall,</E>412 F.3d at 179. However, any recommendations set forth herein regarding the exercise of discretion are by no means binding on the Deputy Administrator and do not limit the exercise of that discretion. 5 U.S.C. § 557(b);<E T="03">River Forest Pharm., Inc.</E>v.<E T="03">DEA,</E>501 F.2d 1202, 1206 (7th Cir. 1974);<E T="03">Attorney General's Manual on the Administrative Procedure Act</E>8 (1947).</P>
        <HD SOURCE="HD1">Factor 1: The Recommendation of the Appropriate State Licensing Board or Professional Disciplinary Authority</HD>
        <P>The present record reflects that the Wisconsin Medical Board, by issuing a suspension that was stayed with conditions, implicitly determined that with the imposition of a number of arguably arduous monitoring and supervision conditions the Respondent could continue to practice medicine and handle controlled substances. Gov't Ex. 3; Resp't Ex. 7.</P>

        <P>Action taken by a state medical board is an important, though not dispositive, factor in determining whether the continuation of a DEA COR is consistent with the public interest.<E T="03">Patrick W. Stodola, M.D.,</E>74 FR 20727, 20730 (2009);<E T="03">Jayam Krishna-Iyer,</E>74 FR at 461. The considerations employed by, and the public responsibilities of, a state medical board in determining whether a practitioner may continue to practice within its borders are not coextensive with those attendant upon the determination that must be made by the DEA relative to continuing a registrant's authority to handle controlled substances. It is well-established Agency precedent that a “state license is a necessary, but not a sufficient condition for registration.”<E T="03">Leslie,</E>68 FR at 15230;<E T="03">John H. Kennedy, M.D.,</E>71 FR 35705, 35708 (2006). Even the reinstatement of a state medical license does not affect the DEA's independent responsibility to determine whether a registration is in the public interest.<E T="03">Mortimer B. Levin, D.O.,</E>55 FR 9209, 8210 (1990). The ultimate responsibility to determine whether a registration is consistent with the public interest has been delegated exclusively to the DEA, not to entities within state government.<E T="03">Edmund Chein, M.D.,</E>72 FR 6580, 6590 (2007),<E T="03">aff'd, Chein</E>v.<E T="03">DEA,</E>533 F.3d 828 (D.C. Cir. 2008),<E T="03">cert. denied,</E>__ U.S. __, 129 S. Ct. 1033 (2009). Congress vested authority to enforce the CSA in the Attorney General and not state officials.<E T="03">Stodola,</E>74 FR at 20375. On the issue of revocation, consideration of this first factor presents something of a mixed bag. By its own terms, the Order suspends the Respondent's medical license indefinitely, but stays that action, contingent on the satisfaction of numerous conditions. Gov't Ex. 3 at 3; Resp't Ex. 7 at 2. In exercising its public safety responsibilities and medical oversight authority relative to the Respondent, the Order of the Wisconsin Medical Board reflected the judgment of that body that the Respondent's transgressions, while sufficiently grave to warrant a complete preclusion of all medical privileges, were not of a nature<PRTPAGE P="45875"/>that precluded the safe treatment of patients and handling of controlled substances, so long as significant monitoring and oversight were mandated. This factor weighs in favor of a significant sanction, but also lends some possible support to the consideration of a less stringent alternative to the complete COR revocation sought by the Government.</P>
        <HD SOURCE="HD1">Factor 3: The Applicant's Conviction Record Under Federal or State Laws Relating to the Manufacture, Distribution, or Dispensing of Controlled Substances</HD>
        <P>The record reflects the Respondent was convicted of felony manufacture of marijuana, as referenced under the 21 U.S.C. 824(a)(2) analysis. Consistent with his plea, the Respondent was also convicted of a state misdemeanor offense related to the possession of drug paraphernalia.</P>
        <P>By its own terms, as expressed in the record of conviction, the Respondent's marijuana manufacture felony conviction is clearly related to the manufacture of controlled substances. That the Respondent was convicted of illegally manufacturing a Schedule I controlled substance in a clandestine partition within the bedroom closet of his residence while he was operating under a DEA COR is, without a doubt, logically repugnant to the notion that he should ever again be entrusted with the responsibilities of a DEA registrant, and therefore militates strongly in favor of the revocation sought by the Government.</P>

        <P>As clear as the pendulum under Factor 3 swings regarding the Respondent's manufacturing conviction, the picture is somewhat murkier regarding his misdemeanor conviction for drug paraphernalia. While the paraphernalia conviction undoubtedly relates to controlled substances, Agency precedent is less clear on whether such a conviction relates to the manufacture, distribution, or dispensing of controlled substances under the third public interest factor. For example, with respect to convictions involving possession of actual narcotics, in<E T="03">Stanley Alan Azen, M.D.,</E>61 FR 57893, 57895 (1996),<E T="03">aff'd, Azen</E>v.<E T="03">DEA,</E>76 F.3d 384 (9th Cir. 1996), a state felony conviction for possession of cocaine was held to be relevant to Factor 3. Likewise, in<E T="03">Jeffrey Martin Ford, D.D.S.,</E>68 FR 10750, 10753 (2003), a cocaine possession felony conviction was held to implicate this factor. On the contrary, in<E T="03">Super-Rite Drugs,</E>56 FR 46014 (1991), the Agency determined that a cocaine possession conviction did not implicate Factor 3 based on the reasoning that “[a]lthough [the respondent] entered a guilty plea to a drug-related felony,<E T="03">his actions did not relate to the manufacture, distribution, or dispensing</E>of controlled substances.”<E T="03">Id.</E>(emphasis supplied). Ironically, although<E T="03">Super-Rite Drugs</E>is the more dated precedent, it is the most persuasive and should be followed. The analysis in<E T="03">Azen</E>centered on the subsequent state court reversal of the conviction, and in<E T="03">Ford,</E>the decision actually omitted the phrase “relating to the manufacture, distribution, or dispensing” when addressing the issue. A contrary interpretation would eviscerate the difference between public interest Factors 3 and 5 and ignore the specific language inserted by Congress. Guidance can be found in the accepted maxims of statutory interpretation that “a statute of specific intention takes precedence over one of general intention,”<E T="03">United States</E>v.<E T="03">Dozier,</E>555 F.3d 1136, 1140 n.7 (10th Cir. 2009) (citing<E T="03">NISH</E>v.<E T="03">Rumsfeld,</E>348 F.3d 1263, 1272 (10th Cir. 2003)), that “words should ordinarily be given their ordinary meaning,”<E T="03">Moskal</E>v.<E T="03">United States,</E>498 U.S. 103, 108 (1990), and that “where language is clear and unambiguous, it must be followed, except in the most extraordinary situation where the language leads to an absurd result contrary to clear legislative intent.”<E T="03">United States</E>v.<E T="03">Plots,</E>347 F.3d 873, 876 (10th Cir. 2003) (citing<E T="03">United States.</E>v.<E T="03">Tagore,</E>158 F.3d 1124, 1128 (10th Cir. 1998)); s<E T="03">ee Griffin</E>v.<E T="03">Oceanic Contractors,</E>458 U.S. 564, 572 (1982);<E T="03">Comm'r</E>v.<E T="03">Brown,</E>380 U.S. 563, 571 (1965). The ordinary meaning of the clear, unambiguous, specifically limiting words “relating to the manufacture, distribution, or dispensing of controlled substances” set forth in 21 U.S.C. 823(f) compels the result that a conviction that is related to illegal drugs generally, but not to manufacturing, distributing, or dispensing specifically, is not relevant to public interest Factor 3.</P>

        <P>In evaluating the Respondent's paraphernalia conviction within this analytical framework, even assuming,<E T="03">arguendo,</E>that a possession of drug paraphernalia conviction stemming from items<E T="03">used</E>to manufacture a controlled substance could conceivably fall within a broad reading of the conduct contemplated under Factor 3, the record in the instant case, as it stands, does not provide a sufficient basis to make such a finding. The lack of factual development and associated evidence presented at the hearing concerning details regarding the specific items of alleged drug paraphernalia upon which the conviction was premised (and the purpose for which said items were utilized, i.e. for personal use, manufacture, distribution, etc.) simply does not provide a means to determine whether the conviction relates to the manufacture, distribution, or dispensing of controlled substances as contemplated under the statutory language employed under Factor 3 and as interpreted by Agency precedent.</P>
        <P>Accordingly, although an analysis of the Respondent's two convictions present some mixed considerations regarding Factor 3, the gravity and circumstances of the manufacturing felony conviction so profoundly tip the scales against the Respondent's continued registration that consideration of this factor weighs strongly in favor of revocation.</P>
        <HD SOURCE="HD1">Factors 2 and 4: The Respondent's Experience in Dispensing Controlled Substances and Compliance With Applicable State, Federal or Local Laws Relating to Controlled Substances</HD>
        <P>The evidence of record in this case raises issues regarding both Factor 2 (experience dispensing<SU>45</SU>
          <FTREF/>controlled substances) and Factor 4 (compliance with federal and state law relating to controlled substances). Regarding Factor 2, neither party to the litigation introduced any evidence relevant to the quality of the controlled substance dispensing that the Respondent has engaged in relative to his medical practice.<SU>46</SU>

          <FTREF/>Ordinarily, the qualitative manner and the quantitative volume in which a registrant has engaged in the dispensing of controlled substances, and how long he has been in the business of doing so are factors to be evaluated in reaching a determination as to whether he should be entrusted with a DEA certificate. In some cases, viewing a registrant's actions against a backdrop of how he has performed activity within the scope of the certificate can provide a contextual lens to assist in a fair adjudication of whether continued registration is in the public interest. However, the Agency has taken the reasonable position that although evidence that a practitioner may have conducted a significant level of sustained activity within the scope of the registration for a sustained period is a relevant and correct consideration, this factor can be outweighed by acts<PRTPAGE P="45876"/>held to be inconsistent with the public interest.<E T="03">Jayam Krishna-Iyer,</E>74 FR at 463.</P>
        <FTNT>
          <P>
            <SU>45</SU>The statutory definition of the term “dispense” includes the prescribing and administering of controlled substances. 21 U.S.C. 802(10).</P>
        </FTNT>
        <FTNT>
          <P>

            <SU>46</SU>The record does reflect that the controlled substance prescription monitoring condition imposed on the Respondent by the Wisconsin Medical Board has yielded no negative feedback as of April 9, 2010.<E T="03">See</E>Resp't Ex. 9.</P>
        </FTNT>
        <P>While true that the record is devoid of evidence related to the Respondent's prescribing practices at work, at home he was producing a significant amount of marijuana, a Schedule I controlled substance, and distributing it (at a minimum) to himself and his wife. Tr. at 47; Resp't Ex. 1 at 26. The record also contains significant evidence that, even if the Respondent's dubious testimony that he was surprised that his niece was using marijuana is credited, it is clear that any safeguards deployed to ensure against that eventuality were sadly lacking. Virtually the only evidence of any dispensing of controlled substance on the part of the Respondent is that he dispensed marijuana to himself and his wife, and in the process lacked the ability and/or inclination to keep the drug from his niece and her friends. Thus, consideration of the Respondent's dispensing history, at least as it relates to his marijuana harvest, militates in favor of revocation.<SU>47</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>47</SU>Although the record contains evidence that a .38 caliber handgun was located near the entrance to the secret room that contained the Respondent's marijuana grow and associated equipment, and that marijuana was found in many small paper and plastic bags and other containers with other bags readily accessible, the evidence was not developed sufficiently to allow any relevant inference (such as an escalated likelihood that these types of items are often linked with distribution activity) from those factors. Gov't Ex. 7 at 9, 17, 19, 23-31. Accordingly, no such inference can fairly be drawn on this record.</P>
        </FTNT>

        <P>Regarding Factor 4, to effectuate the dual goals of conquering drug abuse and controlling both legitimate and illegitimate traffic in controlled substances, “Congress devised a closed regulatory system making it unlawful to manufacture, distribute, dispense, or possess any controlled substance except in a manner authorized by the CSA.”<E T="03">Gonzales</E>v.<E T="03">Raich,</E>545 U.S. 1, 13 (2005). Every DEA registrant serves as a guardian of the closed regulatory system, with specific obligations aimed at protecting against improper diversion. It would be difficult to imagine a more deliberate, flagrant disregard to the Respondent's obligations as a registrant than his decision to convert a portion of his residence into a marijuana factory for himself and his family. While there is no doubt that there was room for some elaboration of the evidence on the part of the Government, the record clearly demonstrates that this was not a single marijuana plant growing in a tiny pot on the Respondent's bedroom window. The Respondent pled guilty to a felony-level conviction for the manufacture of a Schedule I controlled substance, which was conducted in a specially-constructed secret room, with sophisticated equipment, detailed instructions, and documented monitoring. Gov't Ex. 7. Consideration of the Respondent's compliance with state and federal laws related to controlled substances (Factor 4) militates strongly in favor of revocation.</P>
        <HD SOURCE="HD1">Factor 5: Such Other Conduct Which May Threaten the Public Health and Safety</HD>

        <P>Under Factor 5, the Deputy Administrator is authorized to consider “other conduct which may threaten the public health and safety.” 21 U.S.C. 823(f)(5). It is settled Agency precedent that, “offenses or wrongful acts committed by a registrant outside of his professional practice, but which relate to controlled substances may constitute sufficient grounds for the revocation of a registrant's DEA Certificate of Registration.”<E T="03">David E. Trawick, D.D.S.,</E>53 FR 5326 (1988);<E T="03">Jose Antonio Pla-Cisneros, M.D.,</E>52 FR 42154 (1987);<E T="03">Walker L. Whaley, M.D.,</E>51 FR 15556 (1986). As discussed above, the Respondent produced a significant yield of a Schedule I controlled substance and distributed it to himself and (at least) his wife. While any action that undermines the closed regulatory system by the intentional and secretive production of a controlled substance arguably has the potential to adversely impact public safety in a broad sense, the issue under Factor 5 is not merely whether the public safety was adversely impacted to any extent, but rather, whether consideration of any threat to public safety militates in favor of revocation. In other words, consideration of evidence under Factor 5 is less of a litmus test for conceivable public impact than it is a question of degree. The credible, unrefuted evidence of record establishes that the fruits of the Respondent's marijuana grow were being abused by not only himself and his wife, but also by his niece and at least two of her suitors. Gov't Ex. 7 at 13-14. Admittedly, no admissible evidence established the age of the Respondent's niece,<SU>48</SU>
          <FTREF/>and no evidence indicated that the Respondent's minor children were exposed to the illegal fruits of his grow, but it is beyond dispute that the marijuana he was growing was being regularly and continuously abused by persons other than the Respondent. The Respondent grew marijuana plants, abused marijuana himself, and shared it with his wife and niece. His niece shared it with others. However, although the public safety was arguably affected, the issue here is not so narrow. Even acknowledging the reality that any leak in the closed system of controlled substances cannot occur without some diminishment of the public safety in general, a consideration of this Factor (public health and safety threat), under these circumstances, does not support the revocation sought by the Government.</P>
        <FTNT>
          <P>
            <SU>48</SU>According to the police reports, the Respondent's spouse indicated that she is the legal guardian of the Respondent's niece. Gov't Ex. 7 at 20.</P>
        </FTNT>
        <HD SOURCE="HD1">Recommendation</HD>

        <P>A balancing of the public interest factors militates sufficiently in favor of revocation to compel the conclusion that the Government has borne its burden to establish a<E T="03">prima facie</E>case for revocation under 21 U.S.C. 824(a)(4) as well as (a)(2). Inasmuch as the Government has made out a<E T="03">prima facie</E>case for revocation, to avoid this sanction, the burden shifts to the Respondent to demonstrate that COR revocation is inappropriate.<E T="03">Morall,</E>412 F.3d at 174;<E T="03">Humphreys</E>v.<E T="03">DEA,</E>96 F.3d 658, 661 (3d Cir. 1996);<E T="03">Shatz</E>v.<E T="03">U.S. Dept. of Justice,</E>873 F.2d 1089, 1091 (8th Cir. 1989);<E T="03">Thomas E. Johnston,</E>45 FR 72311 (1980). Further, to meet this burden “to rebut the Government's<E T="03">prima facie</E>case, [the Respondent] is required not only to accept responsibility for [the established] misconduct, but also to demonstrate what corrective measures [have been] undertaken to prevent the reoccurrence of similar acts.”<E T="03">Jeri Hassman, M.D.,</E>75 FR 8194, 8236 (2010).</P>
        <P>The Respondent credibly testified that he is complying with the conditions of his criminal sentence, including the terms of his probation, and that he is complying with the monitoring terms fixed by the Order of the Wisconsin Medical Board, including mandated substance abuse treatment<SU>49</SU>

          <FTREF/>and a regimen of random drug tests that have thus far yielded no adverse results. Tr. at 58-59. The Respondent testified that he accepts the wrongfulness of his conduct and that he has resolved not to violate drug laws in the future.<E T="03">Id.</E>at 77-79.</P>
        <FTNT>
          <P>
            <SU>49</SU>However, the Respondent introduced no input from anyone connected with any drug rehabilitation program in which he has participated.</P>
        </FTNT>

        <P>While the Respondent, with the words of acceptance he carefully employed in his testimony, has satisfied the Agency-created condition precedent to seek amelioration of the sanction of revocation, his words of acceptance are at least somewhat fortified by his<PRTPAGE P="45877"/>apparent level of uneventful compliance with a significant level of restrictions and monitoring. Still, his actions regarding his in-home marijuana factory, at least as they are depicted in the record evidence, are remarkable in the extent to which they reflect a high level of planning and deliberation to thwart the CSA. This was not an accidental occurrence or a brief dalliance, but an elaborate, secretive, deliberate, liberally-financed plan to undermine the CSA—the Act that authorizes the COR that was issued to the Respondent as a registrant. This is the same COR upon which, according to his testimony, he bases his livelihood as a physician. Tr. at 65. Under the circumstances presented here, the Agency has an interest in both assuring that the Respondent can be entrusted with the responsibilities attendant upon a COR registrant and (notwithstanding the non-punitive nature of these proceedings) the Agency's legitimate interest in deterring others from similar acts.<E T="03">Hassman,</E>75 FR at 10094;<E T="03">Joseph Gaudio, M.D.,</E>74 FR 10083, 10095 (2009);<E T="03">Southwood Pharms., Inc.,</E>72 F.R at 36504 (citing<E T="03">Butz</E>v.<E T="03">Glover Livestock Commission Co., Inc.,</E>411 U.S. 182, 187-88 (1973)). Therefore, the appropriate sanction must factor in the Respondent's acknowledgement of wrongdoing and efforts at demonstrating sufficient contrition and rehabilitation efforts, while also incorporating the Agency's interests in the integrity of the closed system and deterrence of like conduct.</P>

        <P>The Government, in its Proposed Findings of Fact and Conclusions of Law (Government Closing Brief), maintains that the nature of the marijuana activity as well as what it perceives as a lack of remorse, supports revocation. Gov't Closing. Br. at 4. As discussed,<E T="03">supra,</E>the Respondent expressed an acknowledgement of wrongdoing at the hearing. Tr. at 77-79. Thus, the Government's argument in this regard is essentially that the Respondent has not said sufficiently that he regrets his actions, i.e., he is not sorry<E T="03">enough.</E>While, admittedly, the tenor of the Respondent's testimony at the hearing did not reflect a high level of contrition, he did demonstrate an acknowledgement that his actions were illegal and that the punishments meted out by the criminal justice system were not unfair. Similarly, his thus-far unblemished compliance with conditions imposed by the Wisconsin Medical Board and the criminal court sentence demonstrates at least some level of commitment to rehabilitation. Even so, true remorse, to the extent that Respondent may possess it, was not patently evident from his presentation at the hearing. During his testimony, the Respondent gave the distinct impression that he was not so much sorry about his transgressions as he was sorry that he got caught and was laboring under the criminal and administrative consequences of that reality.</P>

        <P>In support of its argument that Agency precedent calls for revocation, in its Closing Brief, the Government cites three cases, all of which are distinguishable from the present case. In<E T="03">Arthur C. Rosenblatt, M.D.,</E>55 FR 25901 (1990) and<E T="03">Robert G. Crummie, M.D.</E>, 55 FR 5303 (1990), the Agency determined that the respondents not only grew marijuana, but also had significant controlled substance prescribing anomalies. The revocation issued in<E T="03">Alan L. Ager, D.P.M.,</E>63 FR 54732 (1998) was the result of sustained allegations that the respondent, less than a year and a half after being convicted of growing 1,719 marijuana plants, was caught (and ultimately convicted) of growing 135 more marijuana plants.<E T="03">Id.</E>Not only was the respondent in<E T="03">Ager</E>a recidivist who obviously learned nothing from his first conviction, but he produced marijuana in quantities far in excess of the established levels in this case.<SU>50</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>

            <SU>50</SU>This was also true in regarding the respondent in the<E T="03">Crummie</E>case, who was caught growing fifty marijuana plants. 55 FR at 5304.</P>
        </FTNT>

        <P>The cases cited in the Government's Closing Brief are distinguishable on other grounds as well, apart from the disparities in marijuana production scale and illegal prescribing practices. The respondent in<E T="03">Crummie</E>untruthfully testified that he never used, possessed, or manufactured marijuana, and he never accepted responsibility or remorse for his misconduct. 55 FR at 5304. Relatedly, the respondent in<E T="03">Ager</E>failed to offer an explanation for his misconduct, to accept responsibility or remorse, or to provide assurances he would no longer illegally manufacture marijuana in the future. 63 FR 54733. Unlike the cited cases, the Respondent in the instant case, despite his lukewarm remorse, explained the reasons for his illegal misconduct and at least articulated his assurance that he would never manufacture marijuana again.</P>
        <P>The Government also cites in its closing brief<E T="03">Gordon M. Acker, D.M.D.,</E>52 FR 9962 (1987) for the proposition that DEA possesses the authority to revoke a registration for a registrant's felony conviction involving controlled substances, even if the respondent did not use his registration in the commission of his felonious actions. While the Government is certainly correct to the extent a felony conviction related to controlled substances is a factor to be considered in deciding whether revocation is appropriate, the facts of each matter are the operative elements which militate in favor of, or against, revocation. In<E T="03">Acker,</E>the respondent participated during his dental school years in the largest cocaine organization ever prosecuted in Philadelphia.<E T="03">Acker,</E>FR at 9963. The organization profited by millions of dollars per month, and the respondent acted as a redistributor, carrier, and money launderer for the enterprise.<E T="03">Id.</E>Here, the Respondent's criminal behavior, while significant, pales in comparison to that of<E T="03">Acker.</E>There is no evidence that the Respondent ever sold the marijuana he produced, nor is there evidence that the Respondent was part of a large scale, interstate criminal operation. Accordingly, because the facts of<E T="03">Acker</E>and the present case as distinguishable,<E T="03">Acker</E>does not compel the same result in this case.</P>

        <P>That the cases cited by the Government do not compel the revocation it seeks is not to say that such an outcome would be undeserved or unauthorized. The evidence in this case supports a finding that the Government has established that the Respondent has been convicted of a felony under Wisconsin state law related to a Schedule I controlled substance and that he has also committed acts that are inconsistent with the public interest. Although the nature of the Respondent's controlled substance-related felony conviction and a careful balancing of the statutory public interest factors support the revocation of the Respondent's COR, the determination rendered by the Wisconsin State Medical Board that fastidious monitoring can sufficiently protect its interests in public safety, coupled with the Respondent's satisfactory compliance with the restrictions placed on him by the state criminal courts and the Wisconsin State Medical Board, add sufficient indicia of reliability to his professed acceptance of responsibility to support consideration of a sanction less than outright revocation. Accordingly, although the Government's petition for revocation is not wholly unreasonable under the circumstances, the legitimate interests of the Agency can be attained with the imposition of COR restrictions coupled with a period of suspension for a period no less than six (6) months from the<PRTPAGE P="45878"/>date that the Agency issues a final order in this matter.<SU>51</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>51</SU>The Respondent's current COR expires by its own terms on January 31, 2011. In the event that a timely COR renewal application is filed pending final Agency action in this matter in accordance with 21 CFR 1301.36(i) and that application is granted in the final Agency decision, the period of suspension and restricted conditions set forth in this recommended decision may and should be applied to the COR as renewed.</P>
        </FTNT>
        <P>The Respondent's COR shall be restricted and conditioned in the following manner:</P>
        <P>(1) The Respondent will comply with the terms of his criminal sentence and the conditions that are currently in effect, or are subsequently imposed by the criminal sentencing court and/or the Wisconsin Medical Board,<SU>52</SU>
          <FTREF/>and render monthly reports demonstrating such compliance to an official designated by the DEA (designated DEA official) in a manner and format directed by DEA;</P>
        <FTNT>
          <P>
            <SU>52</SU>Thus, the conditions fixed by the Order of the Wisconsin Medical Board and the terms of the Respondent's criminal probation are adopted and incorporated herein as conditions of the restricted COR.</P>
        </FTNT>
        <P>(2) The Respondent will provide the DEA designated official with the results of any and all urinalysis and/or toxicology reports related to drug screening tests administered during the period of the suspension and the restricted COR, irrespective of whether such tests have been or are directed by the criminal sentencing court, the Wisconsin Medical Board, and/or any other source, including (but not limited to) tests mandated by liability carriers and/or other regulatory bodies;</P>
        <P>(3) The Respondent, at his own expense, will participate in such drug screening tests as may be, from time to time, required by the designated DEA official;</P>
        <P>(4) Within a reasonable period, not to exceed thirty (30) days after the issuance of a final Agency decision in this case, the Respondent will execute a document consenting to any and all inspections of the Respondent's home and/or principal place of business conducted by DEA during the period of suspension; and,</P>
        <P>(5) Any other reasonable conditions consistent with this decision that may be imposed by the Deputy Administrator in the final Agency decision issued in this case.</P>
        <P>Failure to comply with any of the conditions specified above shall be grounds for the further suspension or revocation of the Respondent's registration.</P>

        <P>Accordingly, the Respondent's Certificate of Registration should be<E T="03">suspended</E>and<E T="03">restricted</E>as set forth in this recommended decision.</P>
        
        <SIG>
          <DATED>Dated: October 4, 2010</DATED>
          <NAME>John J. Mulrooney, II</NAME>
          <TITLE>U.S. Administrative Law Judge</TITLE>
        </SIG>
        
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19376 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4410-09-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF LABOR</AGENCY>
        <SUBAGY>Employment and Training Administration</SUBAGY>
        <DEPDOC>[TA-W-73,420; TA-W-73,420A; TA-W-73,420B]</DEPDOC>
        <SUBJECT>Alticor, Inc., Including Access Business Group International LLC and Amway Corporation, Buena Park, CA; Alticor, Inc., Including Access Business Group International LLC and Amway Corporation, Including On-Site Leased Workers From Otterbase, Manpower, KForce and Robert Half, Ada, MI; Alticor, Inc., Including Access Business Group International LLC and Amway Corporation, Including On-Site Leased Workers From Helpmates, Lakeview, CA; Amended Certification Regarding Eligibility To Apply for Worker Adjustment Assistance</SUBJECT>

        <P>In accordance with section 223 of the Trade Act of 1974, as amended (“Act”), 19 U.S.C. 2273, the Department of Labor issued a Certification of Eligibility to Apply for Worker Adjustment Assistance on April 12, 2010, applicable to workers of Alticor, Inc., including Access Business Group International LLC and Amway Corporation, Buena Park, California. The workers are engaged in activities related to financial and procurement services. The Department's Notice of determination was published in the<E T="04">Federal Register</E>on May 20, 2010 (75 FR 28300).</P>

        <P>The Notice was amended on April 28, 2010 to include the Ada, Michigan location of the subject firm and on May 24, 2010 to include leased workers on-site at the Ada, Michigan location. The amended Notices were published in the<E T="04">Federal Register</E>on May 12, 2010 (75 FR 26794-26795) and June 7, 2010 (75 FR 32221), respectively.</P>
        <P>At the request of a State agency, the Department reviewed the certification for workers of the subject firm.</P>
        <P>New findings show that the intent of the petitioner was to cover the Buena Park, California, Ada, Michigan, and Lakeview, California locations of the subject firm. The relevant data supplied by the subject firm to the Department during the initial investigation combined the aforementioned locations. Information reveals that workers leased from Helpmates were employed on-site at the Lakeview, California location of the subject firm. The Department has determined that on-site workers from Helpmates were sufficiently under the control of the subject firm to be covered by this certification.</P>
        <P>Accordingly, the Department is amending the certification to include workers of the Lakeview, California location of Alticor, Inc., including Access Business Group International LLC and Amway Corporation and including on-site leased workers from Helpmates.</P>
        <P>The intent of the Department's certification is to include all workers of the subject firm who were adversely affected by a shift in financial and procurement services to Costa Rica.</P>
        <P>The amended notice applicable to TA-W-73,420, TA-W-73,420A and TA-W-73,420B are hereby issued as follows:</P>
        
        <EXTRACT>
          <P>All workers of Alticor, Inc., including Access Business Group International LLC and Amway Corporation, Buena Park, California (TA-W-73,420) and Alticor, Inc., including Access Business Group International LLC and Amway Corporation, including on-site leased workers from Otterbase, Manpower, Kforce and Robert Half, Ada, Michigan, (TA-W-73,420A), and Alticor, Inc., including Access Business Group International LLC and Amway Corporation, including on-site leased workers from Helpmates, Lakeview, California (TA-W-73,420B), who became totally or partially separated from employment on or after February 1, 2009, through April 12, 2012, and all workers in the group threatened with total or partial separation from employment on date of certification through two years from the date of certification, are eligible to apply for adjustment assistance under Chapter 2 of Title II of the Trade Act of 1974, as amended.</P>
        </EXTRACT>
        <SIG>
          <DATED>Signed in Washington, DC, this 18th day of July 2010.</DATED>
          <NAME>Del Min Amy Chen,</NAME>
          <TITLE>Certifying Officer, Office of Trade Adjustment Assistance.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19343 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4510-FN-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <PRTPAGE P="45879"/>
        <AGENCY TYPE="S">DEPARTMENT OF LABOR</AGENCY>
        <SUBAGY>Employment and Training Administration</SUBAGY>
        <DEPDOC>[TA-W-73,644]</DEPDOC>
        <SUBJECT>Cinram Manufacturing, LLC, a Subsidiary of Cinram International, Including On-Site Leased Workers From OneSource Staffing Solutions, Canteen, Division of Compass Group and IKON Office Solutions, a Ricoh Company, Olyphant, PA; Amended Certification Regarding Eligibility To Apply for Worker Adjustment Assistance</SUBJECT>

        <P>In accordance with section 223 of the Trade Act of 1974, as amended (“Act”), 19 U.S.C. 2273, the Department of Labor (Department) issued a Certification of Eligibility to Apply for Worker Adjustment Assistance on July 16, 2010, applicable to workers of Cinram Manufacturing, LLC, a subsidiary of Cinram International, including on-site leased workers from OneSource Staffing Solutions, Olyphant, Pennsylvania. The workers are engaged in employment related to the production of optical media devices. The Department's Notice was published in the<E T="04">Federal Register</E>on August 2, 2010 (75 FR 45162). On February 24, 2011, the Notice was amended to include on-site leased workers from Canteen, a division of Compass Group. The Department's amended Notice was published in the<E T="04">Federal Register</E>on March 14, 2011 (76 FR 13668).</P>
        <P>At the request of the State of Pennsylvania Department of Labor and Industry, the Department reviewed the certification for workers of the subject firm.</P>
        <P>The company reports that workers leased from IKON Office Solutions, a Ricoh Company, were employed on-site at the Olyphant, Pennsylvania location of Cinram Manufacturing, LLC, a subsidiary of Cinram International. The Department has determined that these workers were sufficiently under the control of the subject firm to be considered leased workers.</P>
        <P>Based on these findings, the Department is amending this certification to include workers leased from IKON Office Solutions, a Ricoh Company, working on-site at the Olyphant, Pennsylvania location of Cinram Manufacturing, LLC, a subsidiary of Cinram International.</P>
        <P>The amended notice applicable to TA-W-73,644 is hereby issued as follows:</P>
        
        <EXTRACT>
          <P>All workers of Cinram Manufacturing, LLC, a subsidiary of Cinram International, including on-site leased workers from OneSource Staffing Solutions, Canteen, a division of Compass Group, and IKON Office Solutions, A Ricoh Company, Olyphant, Pennsylvania, who became totally or partially separated from employment on or after March 4, 2009, through July 16, 2012, and all workers in the group threatened with total or partial separation from employment on the date of certification through two years from the date of certification, are eligible to apply for adjustment assistance under Chapter 2 of Title II of the Trade Act of 1974, as amended.</P>
        </EXTRACT>
        <SIG>
          <DATED>Signed at Washington, DC, this 20th day of July, 2011.</DATED>
          <NAME>Del Min Amy Chen,</NAME>
          <TITLE>Certifying Officer, Office of Trade Adjustment Assistance.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19339 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4510-FN-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF LABOR</AGENCY>
        <SUBAGY>Employment and Training Administration</SUBAGY>
        <DEPDOC>[TA-W-73,198]</DEPDOC>
        <SUBJECT>West, a Thomson Reuters Business, Thomson Reuters Legal, Including On-Site Leased Workers From Adecco, Including a Teleworker Located in Albuquerque, NM Reporting to Eagan, MN; Amended Certification Regarding Eligibility To Apply for Worker Adjustment Assistance</SUBJECT>

        <P>In accordance with section 223 of the Trade Act of 1974, as amended (“Act”), 19 U.S.C. 2273, the Department of Labor (Department) issued a Certification of Eligibility to Apply for Worker Adjustment Assistance on June 21, 2010, applicable to workers of West, A Thomson Reuters Legal, including on-site leased workers from Adecco, Eagan, Minnesota. The workers are engaged in activities related to legal, business and regulatory print and electronic information published services. The Department's Notice was published in the<E T="04">Federal Register</E>on July 7, 2010 (75 FR 39048).</P>
        <P>At the request of the petitioner, the Department reviewed the certification for workers of the subject firm.</P>
        <P>New information shows that a worker separation occurred involving a teleworker (Robert Louie) located in Albuquerque, New Mexico who reported to Eagan, Minnesota. Mr. Louie provided various activities related to legal, business and regulatory print and electronic information publishing services.</P>
        <P>Based on these findings, the Department is amending this certification to include an employee of the subject firm who teleworked and reported to the Eagan, Minnesota facility.</P>
        <P>The intent of the Department's certification is to include all workers of the subject firm who were adversely affected by a shift in legal, business and regulatory information publishing services to India and the Philippines.</P>
        <P>The amended notice applicable to TA-W-73,198 is hereby issued as follows:</P>
        
        <EXTRACT>
          <P>All workers of West, A Thomson Reuters Business, Thomson Reuter Legal, including on-site leased workers from Adecco, including a teleworker located in Albuquerque, New Mexico reporting to Eagan, Minnesota, who became totally or partially separated from employment on or after December 30, 2008 through June 21, 2012, and all workers in the group threatened with total or partial separation from employment on date of certification through two years from the date of certification, are eligible to apply for adjustment assistance under Chapter 2 of Title II of the Trade Act of 1974, as amended.</P>
        </EXTRACT>
        <SIG>
          <DATED>Signed in Washington, DC, this 20th day of July, 2011.</DATED>
          <NAME>Del Min Amy Chen,</NAME>
          <TITLE>Certifying Officer, Office of Trade Adjustment Assistance.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19342 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4510-FN-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF LABOR</AGENCY>
        <SUBAGY>Employment and Training Administration</SUBAGY>
        <SUBJECT>Notice of Determinations Regarding Eligibility To Apply for Worker Adjustment Assistance and Alternative Trade Adjustment Assistance</SUBJECT>
        <P>In accordance with section 223 of the Trade Act of 1974, as amended (19 U.S.C. 2273) the Department of Labor herein presents summaries of determinations regarding eligibility to apply for trade adjustment assistance for workers (TA-W) number and alternative trade adjustment assistance (ATAA) by (TA-W) number issued during the period of July 11, 2011 through July 15, 2011.</P>
        <P>In order for an affirmative determination to be made for workers of a primary firm and a certification issued regarding eligibility to apply for worker adjustment assistance, each of the group eligibility requirements of Section 222(a) of the Act must be met.</P>
        <P>I. Section (a)(2)(A) all of the following must be satisfied:</P>

        <P>A. a significant number or proportion of the workers in such workers' firm, or an appropriate subdivision of the firm, have become totally or partially separated, or are threatened to become totally or partially separated;<PRTPAGE P="45880"/>
        </P>
        <P>B. the sales or production, or both, of such firm or subdivision have decreased absolutely; and</P>
        <P>C. increased imports of articles like or directly competitive with articles produced by such firm or subdivision have contributed importantly to such workers' separation or threat of separation and to the decline in sales or production of such firm or subdivision; or</P>
        <P>II. Section (a)(2)(B) both of the following must be satisfied:</P>
        <P>A. a significant number or proportion of the workers in such workers' firm, or an appropriate subdivision of the firm, have become totally or partially separated, or are threatened to become totally or partially separated;</P>
        <P>B. there has been a shift in production by such workers' firm or subdivision to a foreign country of articles like or directly competitive with articles which are produced by such firm or subdivision; and</P>
        <P>C. One of the following must be satisfied:</P>
        <P>1. the country to which the workers' firm has shifted production of the articles is a party to a free trade agreement with the United States;</P>
        <P>2. the country to which the workers' firm has shifted production of the articles to a beneficiary country under the Andean Trade Preference Act, African Growth and Opportunity Act, or the Caribbean Basin Economic Recovery Act; or</P>
        <P>3. there has been or is likely to be an increase in imports of articles that are like or directly competitive with articles which are or were produced by such firm or subdivision.</P>
        <P>Also, in order for an affirmative determination to be made for secondarily affected workers of a firm and a certification issued regarding eligibility to apply for worker adjustment assistance, each of the group eligibility requirements of Section 222(b) of the Act must be met.</P>
        <P>(1) significant number or proportion of the workers in the workers' firm or an appropriate subdivision of the firm have become totally or partially separated, or are threatened to become totally or partially separated;</P>
        <P>(2) the workers' firm (or subdivision) is a supplier or downstream producer to a firm (or subdivision) that employed a group of workers who received a certification of eligibility to apply for trade adjustment assistance benefits and such supply or production is related to the article that was the basis for such certification; and</P>
        <P>(3) either—</P>
        <P>(A) the workers' firm is a supplier and the component parts it supplied for the firm (or subdivision) described in paragraph (2) accounted for at least 20 percent of the production or sales of the workers' firm; or</P>
        <P>(B) a loss of business by the workers' firm with the firm (or subdivision) described in paragraph (2) contributed importantly to the workers' separation or threat of separation.</P>
        <P>In order for the Division of Trade Adjustment Assistance to issue a certification of eligibility to apply for Alternative Trade Adjustment Assistance (ATAA) for older workers, the group eligibility requirements of Section 246(a)(3)(A)(ii) of the Trade Act must be met.</P>
        <P>1. Whether a significant number of workers in the workers' firm are 50 years of age or older.</P>
        <P>2. Whether the workers in the workers' firm possess skills that are not easily transferable.</P>
        <P>3. The competitive conditions within the workers' industry (i.e., conditions within the industry are adverse).</P>
        <HD SOURCE="HD1">Affirmative Determinations for Worker Adjustment Assistance</HD>
        <P>The following certifications have been issued. The date following the company name and location of each determination references the impact date for all workers of such determination.</P>
        <P>
          <E T="03">None</E>.</P>
        <HD SOURCE="HD1">Affirmative Determinations for Worker Adjustment Assistance and Alternative Trade Adjustment Assistance</HD>
        <P>The following certifications have been issued. The date following the company name and location of each determination references the impact date for all workers of such determination.</P>
        <P>The following certifications have been issued. The requirements of Section 222(a)(2)(A) (increased imports) and Section 246(a)(3)(A)(ii) of the Trade Act have been met.</P>
        
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,128; Wheeler Logging, White Swan, WA: April 21, 2010</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,201; Bradington-Young LLC, Hickory, NC: February 19, 2011</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,201A; Bradington-Young LLC, Cherryville, NC: February 19, 2011</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,201B; Bradington-Young LLC, Hickory, NC: May 25, 2010</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,201C; Bradington-Young LLC, Hickory, NC: February 19, 2011</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,212; Unlimited Services, Inc., Oconto, WI: June 1, 2010</E>
        </FP>
        
        <P>The following certifications have been issued. The requirements of Section 222(a)(2)(B) (shift in production) and Section 246(a)(3)(A)(ii) of the Trade Act have been met.</P>
        
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,096; Metal Textiles Corporation, Edison, NJ: April 8, 2010</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,113; Diversey, Inc., Sturtevant, WI: April 15, 2010 TA-W-80,123; Harman, Washington, MO: April 18, 2010</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,182; Palmer Johnson Yacht's LLC, Sturgeon Bay, WI: May 4, 2010</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,193; Vicount Industries, Inc., Farmington Hills, MI: May 23, 2010</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,196; T-Shirt International, Inc., Franklin, WI: May 23, 2010</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,196A; T-Shirt International, Inc., Oak Creek, WI: May 23, 2010</E>
        </FP>
        <HD SOURCE="HD1">Negative Determinations for Worker Adjustment Assistance and Alternative Trade Adjustment Assistance</HD>
        <P>In the following cases, the investigation revealed that the eligibility criteria for worker adjustment assistance have not been met for the reasons specified.</P>
        <P>Because the workers of the firm are not eligible to apply for TAA, the workers cannot be certified eligible for ATAA.</P>
        <P>The investigation revealed that criteria (a)(2)(A)(I.A.) and (a)(2)(B)(II.A.) (employment decline) have not been met.</P>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,091; G &amp; G Garments, New York, NY</E>
        </FP>
        
        <P>The investigation revealed that criteria (a)(2)(A)(I.C.) (increased imports) and (a)(2)(B)(II.B.) (shift in production to a foreign country) have not been met.</P>
        
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,204; Starks Manufacturing LLC, Paris, AR</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,204A; Starks Manufacturing LLC, Russellville, AR</E>
        </FP>
        
        <P>The workers' firm does not produce an article as required for certification under Section 222 of the Trade Act of 1974.</P>
        
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,036; Jabil Circuit of Texas, McAllen, TX</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,141; Bank of America, Fort Wayne, IN</E>
        </FP>
        <FP SOURCE="FP-2">
          <E T="03">TA-W-80,144; Paramount Home Furnishings, Inc., Greensboro, NC</E>
        </FP>
        
        <HD SOURCE="HD1">Determinations Terminating Investigations of Petitions for Worker Adjustment Assistance</HD>
        <P>After notice of the petitions was published in the<E T="04">Federal Register</E>and on the Department's Web site, as required by Section 221 of the Act (19 U.S.C. 2271), the Department initiated investigations of these petitions.</P>
        <P>
          <E T="03">None</E>.</P>

        <P>I hereby certify that the aforementioned determinations were issued during the period of July 11, 2011 through July 15, 2011. Copies of<PRTPAGE P="45881"/>these determinations may be requested under The Freedom of Information Act. Requests may be submitted by fax, courier services, or mail to FOIA Disclosure Officer, Office of Trade Adjustment Assistance (ETA), U.S. Department of Labor, 200 Constitution Avenue, NW., Washington, DC 20210 or<E T="03">tofoiarequest@dol.gov.</E>These determinations also are available on the Department's Web site at<E T="03">http://www.doleta.gov/tradeact</E>under the searchable listing of determinations.</P>
        <SIG>
          <DATED>Dated: July 22, 2011.</DATED>
          <NAME>Michael W. Jaffe,</NAME>
          <TITLE>Certifying Officer, Office, Trade Adjustment Assistance.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19341 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4510-FN-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF LABOR</AGENCY>
        <SUBAGY>Employment and Training Administration</SUBAGY>
        <SUBJECT>Investigations Regarding Certifications of Eligibility To Apply for Worker Adjustment Assistance and Alternative Trade Adjustment Assistance</SUBJECT>
        <P>Petitions have been filed with the Secretary of Labor under section 221(a) of the Trade Act of 1974 (“the Act”) and are identified in the Appendix to this notice. Upon receipt of these petitions, the Director of the Division of Trade Adjustment Assistance, Employment and Training Administration, has instituted investigations pursuant to Section 221(a) of the Act.</P>
        <P>The purpose of each of the investigations is to determine whether the workers are eligible to apply for adjustment assistance under Title II, Chapter 2, of the Act. The investigations will further relate, as appropriate, to the determination of the date on which total or partial separations began or threatened to begin and the subdivision of the firm involved.</P>
        <P>The petitioners or any other persons showing a substantial interest in the subject matter of the investigations may request a public hearing, provided such request is filed in writing with the Director, Office of Trade Adjustment Assistance.</P>
        <P>Interested persons are invited to submit written comments regarding the subject matter of the investigations to the Director, Office of Trade Adjustment Assistance, at the address shown below, not later than August 11, 2011.</P>
        <P>The petitions filed in this case are available for inspection at the Office of the Director, Office of Trade Adjustment Assistance, Employment and Training Administration, U.S. Department of Labor, Room N-5428, 200 Constitution Avenue, NW., Washington, DC 20210.</P>
        <SIG>
          <DATED>Signed at Washington, DC, this 21st day of July 2011.</DATED>
          <NAME>Michael W. Jaffe,</NAME>
          <TITLE>Certifying Officer, Office of Trade Adjustment Assistance.</TITLE>
        </SIG>
        <GPOTABLE CDEF="xs54,r100,r50,12,12" COLS="5" OPTS="L2,i1">
          <TTITLE>Appendix</TTITLE>
          <TDESC>[18 TAA petitions instituted between 7/11/11 and 7/15/11]</TDESC>
          <BOXHD>
            <CHED H="1">TA-W</CHED>
            <CHED H="1">Subject firm (petitioners)</CHED>
            <CHED H="1">Location</CHED>
            <CHED H="1">Date of<LI>institution</LI>
            </CHED>
            <CHED H="1">Date of<LI>petition</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">80274</ENT>
            <ENT>OmniVision Technologies Inc. (State/One-Stop)</ENT>
            <ENT>Boulder, CO</ENT>
            <ENT>07/11/11</ENT>
            <ENT>07/08/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80275</ENT>
            <ENT>Pfizer, Inc. (State/One-Stop)</ENT>
            <ENT>Groton, CT</ENT>
            <ENT>07/11/11</ENT>
            <ENT>07/08/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80276</ENT>
            <ENT>Foster Needle Company Inc. (Company)</ENT>
            <ENT>Manitowoc, WI</ENT>
            <ENT>07/11/11</ENT>
            <ENT>06/30/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80277</ENT>
            <ENT>Vermont Transformer (Workers)</ENT>
            <ENT>Saint Albans, VT</ENT>
            <ENT>07/11/11</ENT>
            <ENT>07/07/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80278</ENT>
            <ENT>Wells Fargo Home Mortgage (State/One-Stop)</ENT>
            <ENT>Costa Mesa, CA</ENT>
            <ENT>07/11/11</ENT>
            <ENT>07/06/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80279</ENT>
            <ENT>Paris Accessories, Inc. (State/One-Stop)</ENT>
            <ENT>Yellville, AR</ENT>
            <ENT>07/12/11</ENT>
            <ENT>07/11/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80280</ENT>
            <ENT>Client Services, Inc. (Workers)</ENT>
            <ENT>Denison, TX</ENT>
            <ENT>07/12/11</ENT>
            <ENT>07/11/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80281</ENT>
            <ENT>Priceline.com (State/One-Stop)</ENT>
            <ENT>Grand Rapids, MI</ENT>
            <ENT>07/12/11</ENT>
            <ENT>06/21/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80282</ENT>
            <ENT>GH Metals Solutions (State/One-Stop)</ENT>
            <ENT>Fort Payne, AL</ENT>
            <ENT>07/12/11</ENT>
            <ENT>06/16/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80283</ENT>
            <ENT>Craftwood, Inc. (Company)</ENT>
            <ENT>High Point, NC</ENT>
            <ENT>07/13/11</ENT>
            <ENT>07/13/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80284</ENT>
            <ENT>Duro Bag Manufacturing Company (Company)</ENT>
            <ENT>Richmond, VA</ENT>
            <ENT>07/13/11</ENT>
            <ENT>07/12/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80285</ENT>
            <ENT>ETS Tan (Company)</ENT>
            <ENT>Indianapolis, IN</ENT>
            <ENT>07/13/11</ENT>
            <ENT>07/13/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80286</ENT>
            <ENT>The Columbus Dispatch (Workers)</ENT>
            <ENT>Columbus, OH</ENT>
            <ENT>07/13/11</ENT>
            <ENT>07/12/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80287</ENT>
            <ENT>Anthony Temperment (Workers)</ENT>
            <ENT>Alsip, IL</ENT>
            <ENT>07/14/11</ENT>
            <ENT>07/13/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80288</ENT>
            <ENT>Croscill Acquisition, LLC (Company)</ENT>
            <ENT>Oxford, NC</ENT>
            <ENT>07/14/11</ENT>
            <ENT>06/14/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80289</ENT>
            <ENT>SAFC Biosciences Inc. (Company)</ENT>
            <ENT>Denver, PA</ENT>
            <ENT>07/14/11</ENT>
            <ENT>07/13/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80290</ENT>
            <ENT>MGM Resorts International Operations, Inc. (Workers)</ENT>
            <ENT>Las Vegas, NV</ENT>
            <ENT>07/15/11</ENT>
            <ENT>07/14/11</ENT>
          </ROW>
          <ROW>
            <ENT I="01">80291</ENT>
            <ENT>Iridio Color Services (State/One-Stop)</ENT>
            <ENT>Seattle, WA</ENT>
            <ENT>07/15/11</ENT>
            <ENT>07/14/11</ENT>
          </ROW>
        </GPOTABLE>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19340 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4510-FN-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">NATIONAL FOUNDATION ON THE ARTS AND THE HUMANITIES</AGENCY>
        <SUBJECT>National Endowment for the Arts;  Proposed Collection; Comment Request</SUBJECT>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The National Endowment for the Arts (NEA), as part of its continuing effort to reduce paperwork and respondent burden, conducts a preclearance consultation program to provide the general public and federal agencies with an opportunity to comment on proposed and/or continuing collections of information in accordance with the Paperwork Reduction Act of 1995 (PRA95) [44 U.S.C. 3506(c)(A)]. This program helps to ensure that requested data can be provided in the desired format, reporting burden (time and financial resources) is minimized, collection instruments are clearly understood, and the impact of collection requirements on respondents can be properly assessed. Currently, the NEA is soliciting comments concerning the proposed information collection on grant applicant satisfaction with application guidance and materials provided on the NEA website and by NEA staff. A copy of the current information collection request can be obtained by contacting the office listed below in the address section of this notice.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>

          <P>Written comments must be submitted to the office listed in the address section below on or before September 1, 2011. The NEA is<PRTPAGE P="45882"/>particularly interested in comments which:</P>
          <P>• Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility;</P>
          <P>• Evaluate the accuracy of the agency's estimate of the burden of the proposed collection of information including the validity of the methodology and assumptions used;</P>
          <P>• Enhance the quality, utility, and clarity of the information to be collected; and</P>

          <P>• Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology,<E T="03">e.g.,</E>permitting electronic submissions of responses.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>Sunil Iyengar, National Endowment for the Arts, 1100 Pennsylvania Avenue, NW., Room 616, Washington, DC 20506-0001, telephone (202) 682-5424 (this is not a toll-free number), fax (202) 682-5677.</P>
        </ADD>
        <SIG>
          <NAME>Kathleen Edwards,</NAME>
          <TITLE>Director, Administrative Services,  National Endowment for the Arts.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19298 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 7537-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">NATIONAL LABOR RELATIONS BOARD</AGENCY>
        <SUBJECT>Sunshine Act Meetings: August 2011</SUBJECT>
        <PREAMHD>
          <HD SOURCE="HED">TIME AND DATES:</HD>
          <P>All meetings are held at 2:30 p.m.Wednesday, August 3;Wednesday, August 10;Wednesday, August 17;Wednesday, August 24;Wednesday, August 31.</P>
        </PREAMHD>
        <PREAMHD>
          <HD SOURCE="HED">PLACE:</HD>
          <P>Board Agenda Room, No. 11820,1099 14th St., NW.,Washington DC 20570.</P>
        </PREAMHD>
        <PREAMHD>
          <HD SOURCE="HED">STATUS:</HD>
          <P>Closed.</P>
        </PREAMHD>
        <PREAMHD>
          <HD SOURCE="HED">MATTERS TO BE CONSIDERED:</HD>
          <P>Pursuant to § 102.139(a) of the Board's Rules and Regulations, the Board or a panel thereof will consider “the issuance of a subpoena, the Board's participation in a civil action or proceeding or an arbitration, or the initiation, conduct, or disposition  * * *  of particular representation or unfair labor practice proceedings under section 8, 9, or 10 of the [National Labor Relations] Act, or any court proceedings collateral or ancillary thereto.” See also 5 U.S.C. 552b(c)(10).</P>
        </PREAMHD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>
            <E T="03">Henry S. Breiteneicher,</E>(202) 273-2917.</P>
          <SIG>
            <DATED>Dated: July 28, 2011.</DATED>
            <NAME>Henry S. Breiteneicher,</NAME>
            <TITLE>Associate Executive Secretary.</TITLE>
          </SIG>
        </FURINF>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19486 Filed 7-28-11; 4:15 pm]</FRDOC>
      <BILCOD>BILLING CODE 7545-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">POSTAL REGULATORY COMMISSION</AGENCY>
        <DEPDOC>[Docket No. A2011-28; Order No. 771]</DEPDOC>
        <SUBJECT>Post Office Closing</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Postal Regulatory Commission.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>This document informs the public that an appeal of the closing of the Goodwin, Arkansas post office has been filed. It identifies preliminary steps and provides a procedural schedule. Publication of this document will allow the Postal Service, petitioners, and others to take appropriate action.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>
            <E T="03">Administrative record due (from Postal Service</E>): August 8, 2011;<E T="03">deadline for notices to intervene:</E>August 22, 2011.<E T="03">See</E>the Procedural Schedule in the<E T="02">SUPPLEMENTARY INFORMATION</E>section for other dates of interest.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>

          <P>Submit comments electronically by accessing the “Filing Online” link in the banner at the top of the Commission's Web site (<E T="03">http://www.prc.gov</E>) or by directly accessing the Commission's Filing Online system at<E T="03">https://www.prc.gov/prc-pages/filing-online/login.aspx.</E>Commenters who cannot submit their views electronically should contact the person identified in the<E T="02">FOR FURTHER INFORMATION CONTACT</E>section as the source for case-related information for advice on alternatives to electronic filing.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Stephen L. Sharfman, General Counsel, at 202-789-6820 (case-related information) or<E T="03">DocketAdmins@prc.gov</E>(electronic filing assistance).</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P>Notice is hereby given that, pursuant to 39 U.S.C. 404(d), on July 22, 2011, the Commission received a petition for review of the Postal Service's determination to close the post office in Goodwin, Arkansas. The petition was filed by Randy Jones (Petitioner). The Commission hereby institutes a proceeding under 39 U.S.C. 404(d)(5) and establishes Docket No. A2011-28 to consider Petitioner's appeal. If Petitioner would like to further explain his position with supplemental information or facts, Petitioner may either file a Participant Statement on PRC Form 61 or file a brief with the Commission no later than August 26, 2011.</P>
        <P>
          <E T="03">Categories of issues apparently raised.</E>Petitioner contends that: (1) The Postal Service failed to adequately consider the economic savings resulting from the closure (<E T="03">see</E>39 U.S.C. 404(d)(2)(A)(iv)); and (2) that the Postal Service failed to consider whether or not it will continue to provide a maximum degree of effective and regular postal services to the community (<E T="03">see</E>39 U.S.C. 404(d)(2)(A)(iii)).</P>

        <P>After the Postal Service files the administrative record and the Commission reviews it, the Commission may find that there are more legal issues than those set forth above, or that the Postal Service's determination disposes of one or more of those issues. The deadline for the Postal Service to file the applicable administrative record with the Commission is August 8, 2011.<E T="03">See</E>39 CFR 3001.113. In addition, the due date for any responsive pleading by the Postal Service to this Notice is August 8, 2011.</P>
        <P>
          <E T="03">Availability; Web site posting.</E>The Commission has posted the appeal and supporting material on its Web site at<E T="03">http://www.prc.gov.</E>Additional filings in this case and participants' submissions also will be posted on the Commission's Web site, if provided in electronic format or amenable to conversion, and not subject to a valid protective order. Information on how to use the Commission's Web site is available online or by contacting the Commission's webmaster via telephone at 202-789-6873 or via electronic mail at<E T="03">prc-webmaster@prc.gov.</E>
        </P>

        <P>The appeal and all related documents are also available for public inspection in the Commission's docket section. Docket section hours are 8 a.m. to 4:30 p.m., Monday through Friday, except on Federal government holidays. Docket section personnel may be contacted via electronic mail at<E T="03">prc-dockets@prc.gov</E>or via telephone at 202-789-6846.</P>
        <P>
          <E T="03">Filing of documents.</E>All filings of documents in this case shall be made using the Internet (Filing Online) pursuant to Commission rules 9(a) and 10(a) at the Commission's Web site,<E T="03">http://www.prc.gov,</E>unless a waiver is obtained.<E T="03">See</E>39 CFR 3001.9(a) and 3001.10(a). Instructions for obtaining an account to file documents online may be found on the Commission's Web site or by contacting the Commission's docket section at<E T="03">prc-dockets@prc.gov</E>or via telephone at 202-789-6846.</P>

        <P>The Commission reserves the right to redact personal information which may infringe on an individual's privacy<PRTPAGE P="45883"/>rights from documents filed in this proceeding.</P>
        <P>
          <E T="03">Intervention.</E>Persons, other than the Petitioner and respondent, wishing to be heard in this matter are directed to file a notice of intervention.<E T="03">See</E>39 CFR 3001.111(b). Notices of intervention in this case are to be filed on or before August 22, 2011. A notice of intervention shall be filed using the Internet (Filing Online) at the Commission's Web site unless a waiver is obtained for hardcopy filing.<E T="03">See</E>39 CFR 3001.9(a) and 3001.10(a).</P>
        <P>
          <E T="03">Further procedures.</E>By statute, the Commission is required to issue its decision within 120 days from the date it receives the appeal.<E T="03">See</E>39 U.S.C. 404(d)(5). A procedural schedule has been developed to accommodate this statutory deadline. In the interest of expedition, in light of the 120-day decision schedule, the Commission may request the Postal Service or other participants to submit information or memoranda of law on any appropriate issue. As required by the Commission rules, if any motions are filed, responses are due 7 days after any such motion is filed.<E T="03">See</E>39 CFR 3001.21.</P>
        <P>
          <E T="03">It is ordered:</E>
        </P>
        <P>1. The Postal Service shall file the applicable administrative record regarding this appeal no later than August 8, 2011.</P>
        <P>2. Any responsive pleading by the Postal Service to this Notice is due no later than August 8, 2011.</P>
        <P>3. The procedural schedule listed below is hereby adopted.</P>
        <P>4. Pursuant to 39 U.S.C. 505, Cassandra L. Hicks is designated officer of the Commission (Public Representative) to represent the interests of the general public.</P>

        <P>5. The Secretary shall arrange for publication of this Notice and Order in the<E T="04">Federal Register</E>.</P>
        <GPOTABLE CDEF="xs100,r100" COLS="2" OPTS="L2,p1,8/9,i1">
          <TTITLE>Procedural Schedule</TTITLE>
          <BOXHD>
            <CHED H="1"/>
            <CHED H="1"/>
          </BOXHD>
          <ROW>
            <ENT I="01">July 22, 2011</ENT>
            <ENT>Filing of Appeal.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">August 8, 2011</ENT>
            <ENT>Deadline for the Postal Service to file the applicable administrative record in this appeal.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">August 8, 2011</ENT>
            <ENT>Deadline for the Postal Service to file any responsive pleading.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">August 22, 2011</ENT>
            <ENT>Deadline for notices to intervene (<E T="03">see</E>39 CFR 3001.111(b)).</ENT>
          </ROW>
          <ROW>
            <ENT I="01">August 26, 2011</ENT>

            <ENT>Deadline for Petitioners' Form 61 or initial brief in support of petition (<E T="03">see</E>39 CFR 3001.115(a) and (b)).</ENT>
          </ROW>
          <ROW>
            <ENT I="01">September 15, 2011</ENT>

            <ENT>Deadline for answering brief in support of the Postal Service (<E T="03">see</E>39 CFR 3001.115(c)).</ENT>
          </ROW>
          <ROW>
            <ENT I="01">September 30, 2011</ENT>

            <ENT>Deadline for reply briefs in response to answering briefs (<E T="03">see</E>39 CFR 3001.115(d)).</ENT>
          </ROW>
          <ROW>
            <ENT I="01">October 7, 2011</ENT>

            <ENT>Deadline for motions by any party requesting oral argument; the Commission will schedule oral argument only when it is a necessary addition to the written filings (<E T="03">see</E>39 CFR 3001.116).</ENT>
          </ROW>
          <ROW>
            <ENT I="01">November 21, 2011</ENT>

            <ENT>Expiration of the Commission's 120-day decisional schedule (<E T="03">see</E>39 U.S.C. 404(d)(5)).</ENT>
          </ROW>
        </GPOTABLE>
        <SIG>
          <P>By the Commission.</P>
          <NAME>Shoshana M. Grove,</NAME>
          <TITLE>Secretary.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19380 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 7710-FW-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">SECURITIES AND EXCHANGE COMMISSION</AGENCY>
        <DEPDOC>[Release No. 34-64961; File No. SR-FINRA-2011-026]</DEPDOC>
        <SUBJECT>Self-Regulatory Organizations; Financial Industry Regulatory Authority, Inc.; Notice of Filing and Immediate Effectiveness of Proposed Rule Change Regarding Cancellation or Rescheduling Fees for Qualification Examinations and Continuing Education Sessions</SUBJECT>
        <DATE>July 26, 2011.</DATE>
        <P>Pursuant to Section 19(b)(1) of the Securities Exchange Act of 1934 (“Act”)<SU>1</SU>
          <FTREF/>and Rule 19b-4 thereunder,<SU>2</SU>
          <FTREF/>notice is hereby given that on July 15, 2011, Financial Industry Regulatory Authority, Inc. (“FINRA”) filed with the Securities and Exchange Commission (“SEC” or “Commission”) the proposed rule change as described in Items I, II, and III below, which Items have been prepared by FINRA. The Commission is publishing this notice to solicit comments on the proposed rule change from interested persons.</P>
        <FTNT>
          <P>
            <SU>1</SU>15 U.S.C. 78s(b)(1).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>2</SU>17 CFR 240.19b-4.</P>
        </FTNT>
        <HD SOURCE="HD1">I. Self-Regulatory Organization's Statement of the Terms of Substance of the Proposed Rule Change</HD>
        <P>FINRA is proposing to amend Section 4(c) of Schedule A to the FINRA By-Laws to address cancellation/rescheduling fees for qualification examinations and continuing education sessions. Specifically, the proposed rule change would (1) Establish a fee for individuals who cancel or reschedule a qualification examination or Regulatory Element Continuing Education (“Regulatory Element”) session three to ten business days prior to the appointment date, and (2) add a reference to the fee for individuals who fail to timely appear for a scheduled Regulatory Element session or who cancel or reschedule such a session within two business days prior to the appointment date.</P>

        <P>The text of the proposed rule change is available on FINRA's Web site at<E T="03">http://www.finra.org,</E>at the principal office of FINRA, and at the Commission's Public Reference Room.</P>
        <HD SOURCE="HD1">II. Self-Regulatory Organization's Statement of the Purpose of, and Statutory Basis for, the Proposed Rule Change</HD>
        <P>In its filing with the Commission, FINRA included statements concerning the purpose of and basis for the proposed rule change and discussed any comments it received on the proposed rule change. The text of these statements may be examined at the places specified in Item IV below. FINRA has prepared summaries, set forth in sections A, B, and C below, of the most significant aspects of such statements.</P>
        <HD SOURCE="HD2">A. Self-Regulatory Organization's Statement of the Purpose of, and Statutory Basis for, the Proposed Rule Change</HD>
        <HD SOURCE="HD3">1. Purpose</HD>
        <P>As discussed in further detail below, the proposed rule change amends Section 4(c) of Schedule A to the FINRA By-Laws to (1) Establish a fee for individuals who cancel or reschedule a qualification examination or Regulatory Element session three to ten business days prior to the appointment date, and (2) add a reference to the fee for individuals who fail to timely appear for a scheduled Regulatory Element session or who cancel or reschedule such a session within two business days prior to the appointment date.</P>
        <HD SOURCE="HD3">Three- to Ten-Day Cancellation/Rescheduling Fee</HD>

        <P>Pursuant to NASD Rules 1021 and 1031, any person engaged in the investment banking or securities business of a FINRA member must register with FINRA in the category of registration appropriate to the function<PRTPAGE P="45884"/>the individual will be performing. As part of the registration process, securities professionals must pass a qualification examination to demonstrate competence in the areas in which they will work. In addition, such individuals must complete the appropriate Regulatory Element program subsequent to their initial qualification and registration with FINRA, as set forth in NASD Rule 1120.<SU>3</SU>
          <FTREF/>The qualification examinations and Regulatory Element programs cover a broad range of subjects regarding financial markets and products, individual responsibilities, securities industry rules, and regulatory structure. FINRA develops, maintains, and delivers all qualification examinations and Regulatory Element programs for individuals who are registered or seeking registration with FINRA. FINRA also delivers examinations sponsored by the North American Securities Administrators Association, the National Futures Association, the Federal Deposit Insurance Corporation, and others. FINRA currently administers examinations and Regulatory Element programs via computer at testing centers operated by vendors under contract with FINRA.</P>
        <FTNT>
          <P>

            <SU>3</SU>The SEC has approved the adoption of NASD Rule 1120 (Continuing Education Requirements) as FINRA Rule 1250 (Continuing Education Requirements) in the consolidated FINRA rulebook with certain changes.<E T="03">See</E>Securities Exchange Act Release No. 64687 (June 16, 2011), 76 FR 36586 (June 22, 2011) (Order Approving SR-FINRA-2011-013). FINRA will issue a<E T="03">Regulatory Notice</E>announcing the effective date of FINRA Rule 1250 in the near future.</P>
        </FTNT>
        <P>To request and schedule an appointment for a qualification examination, a FINRA member must file a Form U4 (Uniform Application for Securities Industry Registration or Transfer) through the Central Registration Depository (“Web CRD®”).<SU>4</SU>
          <FTREF/>After the request is processed, a scheduling window will be posted on Web CRD. For Regulatory Element programs, registered persons in covered registration categories will automatically become enrolled for the requisite program on the second anniversary of their initial securities registration and every three years thereafter. Once an individual or an individual's firm receives the enrollment notification for an examination or Regulatory Element session, the individual may then contact a FINRA authorized testing center to schedule an appointment.</P>
        <FTNT>
          <P>
            <SU>4</SU>Individuals who are not employed or associated with a FINRA member must file a Form U10 (Uniform Examination Request for Non-FINRA candidates) with FINRA to schedule an examination.</P>
        </FTNT>
        <P>After an examination or Regulatory Element session has been scheduled, an individual may cancel or reschedule the appointment by contacting the testing center. Currently, FINRA does not impose a fee for cancelling or rescheduling an appointment if it is done by noon two business days before the scheduled appointment. FINRA charges a cancellation fee equal to the examination or Regulatory Element session fee if this deadline is not met, if an individual does not appear for an appointment, or if an individual arrives so late for an appointment that the examination or Regulatory Element session cannot begin without disrupting the testing center's schedule.<SU>5</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>

            <SU>5</SU>Further information about the cancellation policy can be found on FINRA's Web site at<E T="03">http://www.finra.org/Industry/Compliance/Registration/QualificationsExams/RegisteredReps/Qualifications/P120071.</E>
          </P>
        </FTNT>
        <P>FINRA has determined that individuals who cancel or reschedule an appointment more than two business days before the scheduled appointment date also place an administrative burden on test-delivery vendors and degrade the efficiency of test center resource utilization. To discourage such behavior, FINRA is proposing to implement a fee for individuals who cancel or reschedule a qualification examination or Regulatory Element session within three to ten business days of a scheduled appointment date.<SU>6</SU>
          <FTREF/>The amount of the proposed fee would be one-half of the fee of the examination or Regulatory Element session being cancelled or rescheduled.<SU>7</SU>
          <FTREF/>FINRA believes that this fee will help to control the overall costs associated with the delivery of examinations and Regulatory Element programs and the resultant examination and Regulatory Element session fees charged to individuals for examinations and Regulatory Element programs.</P>
        <FTNT>
          <P>
            <SU>6</SU>The cancellation/rescheduling fee will be assessed for the qualification examinations set forth in Section 4(c) of Schedule A to the FINRA By-Laws and all Regulatory Element programs. In addition, depending on the terms of agreement, the fee also may apply for those qualification examinations that FINRA delivers for other entities.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>7</SU>The fee must be paid at the time of cancellation or rescheduling. In those circumstances where the fee is not paid in a timely manner, FINRA, instead, will assess a fee equal to the examination or Regulatory Element session fee if the individual does not appear for the scheduled appointment.</P>
        </FTNT>
        <HD SOURCE="HD3">Continuing Education Failure To Timely Appear/Late Cancellation or Rescheduling Fee</HD>
        <P>As previously mentioned, FINRA assesses a fee equal to the examination or Regulatory Element session fee to individuals who fail to timely appear for an appointment or who cancel or reschedule an examination or Regulatory Element session within two business days of the scheduled appointment date.<SU>8</SU>

          <FTREF/>Although Section 4(c) of Schedule A to the FINRA By-Laws currently sets forth this fee for qualification examinations, it does not set forth the fee with respect to the Regulatory Element program. Consequently, FINRA is proposing to amend Section 4(c) of Schedule A to the FINRA By-Laws to add a reference to this Regulatory Element program fee. The proposed rule change would also specifically reference the time period for which this fee applies (<E T="03">i.e.,</E>within two business days prior to the appointment date).</P>
        <FTNT>
          <P>

            <SU>8</SU>FINRA considers an individual who fails to cancel or reschedule an examination or Regulatory Element session by noon two business days before the scheduled appointment to have failed timely to cancel or reschedule the appointment under Section 4(c)(2) of Schedule A to the FINRA By-Laws.<E T="03">See supra</E>note 7.</P>
        </FTNT>
        <P>FINRA has filed the proposed rule change for immediate effectiveness. FINRA is proposing that the implementation date of the proposed rule change will be September 1, 2011.</P>
        <HD SOURCE="HD3">2. Statutory Basis</HD>
        <P>FINRA believes that the proposed rule change is consistent with the provisions of Section 15A of the Act,<SU>9</SU>
          <FTREF/>in general, and with Section 15A(b)(5) of the Act,<SU>10</SU>

          <FTREF/>in particular, in that it provides for the equitable allocation of reasonable dues, fees and other charges among members and issuers and other persons using any facility or system which FINRA operates or controls. FINRA believes that it is an equitable allocation to assess a fee on those individuals who cancel a qualification examination or Regulatory Element session within three to ten business days of a scheduled appointment date, because such behavior places an administrative burden on test-delivery vendors and degrades the efficiency of test center resource utilization. FINRA further believes that the amount of the fee, which is one-half of the current fee for individuals who fail to appear for a scheduled appointment or who cancel/reschedule an appointment within two business days of a scheduled appointment date, is reasonable because it will help to control the overall costs associated with the delivery of examinations and Regulatory Element programs while also recognizing the lesser burden that results from those individuals who provide additional notice by cancelling/rescheduling an appointment three to ten business days<PRTPAGE P="45885"/>before the scheduled appointment date. FINRA further believes that the amount of the fee is reasonable because it will dissuade individuals from cancelling or rescheduling an appointment three to ten business days before the scheduled appointment date.</P>
        <FTNT>
          <P>
            <SU>9</SU>15 U.S.C. 78<E T="03">o</E>-3(b)(5).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>10</SU>
            <E T="03">Id.</E>
          </P>
        </FTNT>
        <HD SOURCE="HD2">B. Self-Regulatory Organization's Statement on Burden on Competition</HD>
        <P>FINRA does not believe that the proposed rule change will result in any burden on competition that is not necessary or appropriate in furtherance of the purposes of the Act.</P>
        <HD SOURCE="HD2">C. Self-Regulatory Organization's Statement on Comments on the Proposed Rule Change Received From Members, Participants, or Others</HD>
        <P>Written comments were neither solicited nor received.</P>
        <HD SOURCE="HD1">III. Date of Effectiveness of the Proposed Rule Change and Timing for Commission Action</HD>
        <P>The foregoing rule change has become effective pursuant to Section 19(b)(3)(A) of the Act<SU>11</SU>
          <FTREF/>and paragraph (f)(2) of Rule 19b-4 thereunder.<SU>12</SU>
          <FTREF/>At any time within 60 days of the filing of the proposed rule change, the Commission summarily may temporarily suspend such rule change if it appears to the Commission that such action is necessary or appropriate in the public interest, for the protection of investors, or otherwise in furtherance of the purposes of the Act. If the Commission takes such action, the Commission shall institute proceedings to determine whether the proposed rule should be approved or disapproved.</P>
        <FTNT>
          <P>
            <SU>11</SU>15 U.S.C. 78s(b)(3)(A).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>12</SU>17 CFR 240.19b-4(f)(2).</P>
        </FTNT>
        <HD SOURCE="HD1">IV. Solicitation of Comments</HD>
        <P>Interested persons are invited to submit written data, views, and arguments concerning the foregoing, including whether the proposed rule change is consistent with the Act. Comments may be submitted by any of the following methods:</P>
        <HD SOURCE="HD2">Electronic Comments</HD>
        <P>• Use the Commission's Internet comment form (<E T="03">http://www.sec.gov/rules/sro.shtml</E>); or</P>
        <P>• Send an e-mail to<E T="03">rule-comments@sec.gov.</E>Please include File Number SR-FINRA-2011-026 on the subject line.</P>
        <HD SOURCE="HD2">Paper Comments</HD>
        <P>• Send paper comments in triplicate to Elizabeth M. Murphy, Secretary, Securities and Exchange Commission, 100 F Street, NE., Washington, DC 20549-1090.</P>
        

        <P>All submissions should refer to File Number SR-FINRA-2011-026. This file number should be included on the subject line if e-mail is used. To help the Commission process and review your comments more efficiently, please use only one method. The Commission will post all comments on the Commission's Internet Web site (<E T="03">http://www.sec.gov/rules/sro.shtml</E>). Copies of the submission, all subsequent amendments, all written statements with respect to the proposed rule change that are filed with the Commission, and all written communications relating to the proposed rule change between the Commission and any person, other than those that may be withheld from the public in accordance with the provisions of 5 U.S.C. 552, will be available for Web site viewing and printing in the Commission's Public Reference Room, 100 F Street, NE., Washington, DC 20549, on official business days between the hours of 10 a.m. and 3 p.m. Copies of such filing also will be available for inspection and copying at the principal office of FINRA. All comments received will be posted without change; the Commission does not edit personal identifying information from submissions. You should submit only information that you wish to make publicly available. All submissions should refer to File Number SR-FINRA-2011-026 and should be submitted on or before August 22, 2011.</P>
        <SIG>
          <P>For the Commission, by the Division of Trading and Markets, pursuant to delegated authority.<SU>13</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>13</SU>17 CFR 200.30-3(a)(12).</P>
          </FTNT>
          <NAME>Elizabeth M. Murphy,</NAME>
          <TITLE>Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19324 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 8011-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">SECURITIES AND EXCHANGE COMMISSION</AGENCY>
        <DEPDOC>[Release No. 34-64967; File No. SR-NYSEArca-2011-48]</DEPDOC>
        <SUBJECT>Self-Regulatory Organizations; NYSE Arca, Inc.; Notice of Filing of Proposed Rule Change To List and Trade Shares of the Teucrium Wheat Fund, the Teucrium Soybean Fund and the Teucrium Sugar Fund Under NYSE Arca Equities Rule 8.200, Commentary .02</SUBJECT>
        <DATE>July 26, 2011.</DATE>
        <P>Pursuant to Section 19(b)(1) of the Securities Exchange Act of 1934 (the “Act”)<SU>1</SU>
          <FTREF/>and Rule 19b-4 thereunder,<SU>2</SU>
          <FTREF/>notice is hereby given that, on July 11, 2011, NYSE Arca, Inc. (“NYSE Arca” or the “Exchange”) filed with the Securities and Exchange Commission (the “Commission”) the proposed rule change as described in Items I and II below, which Items have been prepared by the Exchange. The Commission is publishing this notice to solicit comments on the proposed rule change from interested persons.</P>
        <FTNT>
          <P>
            <SU>1</SU>15 U.S.C. 78s(b)(1).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>2</SU>17 CFR 240.19b-4.</P>
        </FTNT>
        <HD SOURCE="HD1">I. Self-Regulatory Organization's Statement of the Terms of Substance of the Proposed Rule Change</HD>

        <P>The Exchange proposes to list and trade shares of the Teucrium Wheat Fund, the Teucrium Soybean Fund and the Teucrium Sugar Fund under NYSE Arca Equities Rule 8.200. The text of the proposed rule change is available on the Exchange's Web site at<E T="03">http://www.nyse.com,</E>at the Exchange's principal office and at the Commission's Public Reference Room.</P>
        <HD SOURCE="HD1">II. Self-Regulatory Organization's Statement of the Purpose of, and Statutory Basis for, the Proposed Rule Change</HD>
        <P>In its filing with the Commission, the self-regulatory organization included statements concerning the purpose of, and basis for, the proposed rule change and discussed any comments it received on the proposed rule change. The text of those statements may be examined at the places specified in Item IV below. The Exchange has prepared summaries, set forth in sections A, B, and C below, of the most significant parts of such statements.</P>
        <HD SOURCE="HD2">A. Self-Regulatory Organization's Statement of the Purpose of, and the Statutory Basis for, the Proposed Rule Change</HD>
        <HD SOURCE="HD3">1. Purpose</HD>
        <P>NYSE Arca Equities Rule 8.200, Commentary .02 permits the trading of Trust Issued Receipts (“TIRs”) either by listing or pursuant to unlisted trading privileges (“UTP”).<SU>3</SU>

          <FTREF/>The Exchange proposes to list and trade shares (“Shares”) of the Teucrium Wheat Fund, the Teucrium Soybean Fund and the Teucrium Sugar Fund (each a<PRTPAGE P="45886"/>“Fund” and, collectively, the “Funds”) pursuant to NYSE Arca Equities Rule 8.200.</P>
        <FTNT>
          <P>
            <SU>3</SU>Commentary .02 to NYSE Arca Equities Rule 8.200 applies to TIRs that invest in “Financial Instruments.” The term “Financial Instruments,” as defined in Commentary .02(b)(4) to NYSE Arca Equities Rule 8.200, means any combination of investments, including cash; securities; options on securities and indices; futures contracts; options on futures contracts; forward contracts; equity caps, collars and floors; and swap agreements.</P>
        </FTNT>
        <P>The Exchange notes that the Commission has previously approved the listing and trading of other issues of TIRs on the American Stock Exchange LLC,<SU>4</SU>
          <FTREF/>trading on NYSE Arca pursuant to UTP,<SU>5</SU>
          <FTREF/>and listing on NYSE Arca.<SU>6</SU>
          <FTREF/>Among these is the Teucrium Corn Fund, a series of the Teucrium Commodity Trust (“Trust”).<SU>7</SU>
          <FTREF/>In addition, the Commission has approved the listing and trading of other exchange-traded fund-like products linked to the performance of underlying commodities.<SU>8</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>4</SU>
            <E T="03">See, e.g.,</E>Securities Exchange Act Release No. 58161 (July 15, 2008), 73 FR 42380 (July 21, 2008) (SR-Amex-2008-39).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>5</SU>
            <E T="03">See, e.g.,</E>Securities Exchange Act Release No. 58163 (July 15, 2008), 73 FR 42391 (July 21, 2008) (SR-NYSEArca-2008-73).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>6</SU>
            <E T="03">See, e.g.,</E>Securities Exchange Act Release No. 58457 (September 3, 2008), 73 FR 52711 (September 10, 2008) (SR-NYSEArca-2008-91).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>7</SU>
            <E T="03">See</E>Securities Exchange Act Release No. 62213 (June 3, 2010), 75 FR 32828 (June 9, 2010) (SR-NYSEArca-2010-22) (order approving listing on the Exchange of Teucrium Corn Fund).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>8</SU>
            <E T="03">See, e.g.,</E>Securities Exchange Act Release Nos. 57456 (March 7, 2008), 73 FR 13599 (March 13, 2008) (SR-NYSEArca-2007-91) (order granting accelerated approval for NYSE Arca listing the iShares GS Commodity Trusts); 59781 (April 17, 2009), 74 FR 18771 (April 24, 2009) (SR-NYSEArca-2009-28) (order granting accelerated approval for NYSE Arca listing the ETFS Silver Trust); 59895 (May 8, 2009), 74 FR 22993 (May 15, 2009) (SR-NYSEArca-2009-40) (order granting accelerated approval for NYSE Arca listing the ETFS Gold Trust); 61219 (December 22, 2009), 74 FR 68886 (December 29, 2009) (SR-NYSEArca-2009-95) (order approving listing on NYSE Arca of the ETFS Platinum Trust).</P>
        </FTNT>
        <P>The Shares represent beneficial ownership interests in the Funds, as described in the Registration Statements for the Funds.<SU>9</SU>
          <FTREF/>The Funds are commodity pools that are series of the Trust, a Delaware statutory trust. The Funds are managed and controlled by Teucrium Trading, LLC (“Sponsor”). The Sponsor is a Delaware limited liability company that is registered as a commodity pool operator (“CPO”) with the Commodity Futures Trading Commission (“CFTC”) and is a member of the National Futures Association.</P>
        <FTNT>
          <P>
            <SU>9</SU>
            <E T="03">See</E>Amendment No. 3 to Form S-1 for Teucrium Commodity Trust, dated June 3, 2011 (File No. 333-167591) relating to the Teucrium Wheat Fund; Amendment No. 3 to Form S-1 for Teucrium Commodity Trust, dated June 3, 2011 (File No. 333-167590) relating to the Teucrium Soybean Fund; and Amendment No. 3 to Form S-1 for Teucrium Commodity Trust, dated June 3, 2011 (File No. 333-167585) relating to the Teucrium Sugar Fund (each, a “Registration Statement,” and, collectively, the “Registration Statements”). The discussion herein relating to the Trust and the Shares is based, in part, on the Registration Statements.</P>
        </FTNT>
        <HD SOURCE="HD3">Teucrium Wheat Fund</HD>
        <P>According to the Registration Statement, the investment objective of the Fund is to have the daily changes in percentage terms of the Shares' net asset value (“NAV”) reflect the daily changes in percentage terms of a weighted average of the closing settlement prices for three futures contracts for wheat (wheat futures contracts generally referred to herein as “Wheat Futures Contracts”) that are traded on the Chicago Board of Trade (“CBOT”), specifically: (1) The second-to-expire CBOT Wheat Futures Contract, weighted 35%, (2) the third-to-expire CBOT Wheat Futures Contract, weighted 30%, and (3) the CBOT Wheat Futures Contract expiring in the December following the expiration month of the third-to-expire contract, weighted 35%. (This weighted average of the three referenced Wheat Futures Contracts is referred to herein as the “Wheat Benchmark,” and the three Wheat Futures Contracts that at any given time make up the Wheat Benchmark are referred to herein as the “Wheat Benchmark Component Futures Contracts”).<SU>10</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>10</SU>Wheat futures volume on CBOT for 2010 and 2011 (through April 29, 2011) was 23,058,783 contracts and 8,860,135 contracts, respectively. As of April 29, 2011, open interest for wheat futures was 456,851 contracts. The contract price was $40,062.50 (801.25 cents per bushel and 5,000 bushels per contract). The approximate value of all outstanding contracts was $18.3 billion. The position limits for all months is 6,500 contracts and the total value of contracts if position limits were reached would be approximately $260.4 million (based on the $40,062.50 contract price).</P>
        </FTNT>
        <P>The Fund seeks to achieve its investment objective by investing under normal market conditions<SU>11</SU>
          <FTREF/>in Wheat Benchmark Component Futures Contracts or, in certain circumstances, in other Wheat Futures Contracts traded on the CBOT, the Kansas City Board of Trade (“KCBT”), or the Minneapolis Grain Exchange (“MGEX”), or Wheat Futures Contracts traded on foreign exchanges. In addition, and to a limited extent, the Fund also may invest in exchange-traded options on Wheat Futures Contracts, and in wheat-based swap agreements that are cleared through the CBOT or its affiliated provider of clearing services (“Cleared Wheat Swaps”) in furtherance of the Fund's investment objective.<SU>12</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>11</SU>The term “under normal market conditions” includes, but is not limited to, the absence of extreme volatility or trading halts in the fixed income markets or the financial markets generally; operational issues causing dissemination of inaccurate market information; or force majeure type events such as systems failure, natural or man-made disaster, act of God, armed conflict, act of terrorism, riot or labor disruption or any similar intervening circumstance.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>12</SU>According to the Registration Statement, a swap agreement is a bilateral contract to exchange a periodic stream of payments determined by reference to a notional amount, with payment typically made between the parties on a net basis. For example, in the case of a wheat swap, the Fund may be obligated to pay a fixed price per bushel of wheat and be entitled to receive an amount per bushel equal to the current value of an index of wheat prices, the price of a specified Wheat Futures Contract, or the average price of a group of Wheat Futures Contracts such as the Wheat Benchmark.</P>
        </FTNT>

        <P>Specifically, once position limits in CBOT Wheat Futures Contracts are reached, the Fund's intention is to invest first in Cleared Wheat Swaps to the extent permitted under the position limits applicable to Cleared Wheat Swaps and appropriate in light of the liquidity in the Cleared Wheat Swaps market, and then, using its commercially reasonable judgment, in other Wheat Futures Contracts (<E T="03">i.e.,</E>Wheat Futures Contracts traded on KCBT, MGEX or traded on foreign exchanges) or instruments such as cash-settled options on Wheat Futures Contracts and forward contracts, swaps other than Cleared Wheat Swaps, and other over-the-counter transactions that are based on the price of wheat and Wheat Futures Contracts (collectively, “Other Wheat Interests,” and together with Wheat Futures Contracts and Cleared Wheat Swaps, “Wheat Interests”). By utilizing certain or all of these investments, the Sponsor will endeavor to cause the Fund's performance to closely track that of the Wheat Benchmark. The circumstances under which such investments in Other Wheat Interests may be utilized (<E T="03">e.g.,</E>imposition of position limits) are discussed below.</P>
        <P>Wheat Futures Contracts traded on the CBOT expire on a specified day in five different months: March, May, July, September and December. For example, in terms of the Wheat Benchmark, in June of a given year the next-to-expire or “spot month” Wheat Futures Contract will expire in July of that year, and the Wheat Benchmark Component Futures Contracts will be the contracts expiring in September of that year (the second-to-expire contract), December of that year (the third-to-expire contract), and December of the following year. As another example, in November of a given year, the Wheat Benchmark Component Futures Contracts will be the contracts expiring in March, May and December of the following year.</P>

        <P>According to the Registration Statement, the Fund seeks to achieve its investment objective primarily by investing in Wheat Interests such that daily changes in the Fund's NAV will be<PRTPAGE P="45887"/>expected to closely track the changes in the Wheat Benchmark. The Fund's positions in Wheat Interests will be changed or “rolled” on a regular basis in order to track the changing nature of the Wheat Benchmark. For example, five times a year (on the date on which a Wheat Futures Contract expires), the second-to-expire Wheat Futures Contract will become the next-to-expire Wheat Futures Contract and will no longer be a Wheat Benchmark Component Futures Contract, and the Fund's investments will have to be changed accordingly.<SU>13</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>13</SU>For each of the Funds, in order that the Fund's trading does not cause unwanted market movements and to make it more difficult for third parties to profit by trading based on such expected market movements, the Fund's investments typically will not be rolled entirely on that day, but rather will typically be rolled over a period of several days.</P>
        </FTNT>
        <P>Consistent with achieving the Fund's investment objective of closely tracking the Wheat Benchmark, the Sponsor may for certain reasons cause the Fund to enter into or hold Cleared Wheat Swaps and/or Other Wheat Interests. For example, certain Cleared Wheat Swaps have standardized terms similar to, and are priced by reference to, a corresponding Wheat Benchmark Component Futures Contract. Additionally, Other Wheat Interests that do not have standardized terms and are not exchange-traded (“over-the-counter” Wheat Interests), can generally be structured as the parties desire. Therefore, the Fund might enter into multiple Cleared Wheat Swaps and/or over-the-counter Wheat Interests intended to exactly replicate the performance of each of the three Wheat Benchmark Component Futures Contracts, or a single over-the-counter Wheat Interest designed to replicate the performance of the Wheat Benchmark as a whole. According to the Registration Statement, assuming that there is no default by a counterparty to an over-the-counter Wheat Interest, the performance of the over-the-counter Wheat Interest will necessarily correlate exactly with the performance of the Wheat Benchmark or the applicable Wheat Benchmark Component Futures Contract.<SU>14</SU>
          <FTREF/>The Fund might also enter into or hold over-the-counter Wheat Interests to facilitate effective trading, consistent with the discussion of the Fund's “roll” strategy in the preceding paragraph. In addition, the Fund might enter into or hold over-the-counter Wheat Interests that would be expected to alleviate overall deviation between the Fund's performance and that of the Wheat Benchmark that may result from certain market and trading inefficiencies or other reasons.</P>
        <FTNT>
          <P>
            <SU>14</SU>According to the Registration Statements, the Funds face the risk of non-performance by the counterparties to over-the-counter contracts. Unlike in futures contracts, the counterparty to these contracts is generally a single bank or other financial institution, rather than a clearing organization backed by a group of financial institutions. As a result, there will be greater counterparty credit risk in these transactions. The creditworthiness of each potential counterparty will be assessed by the Sponsor. The Sponsor will assess or review, as appropriate, the creditworthiness of each potential or existing counterparty to an over-the-counter contract pursuant to guidelines approved by the Sponsor. The creditworthiness of existing counterparties will be reviewed periodically by the Sponsor.</P>
        </FTNT>
        <P>The Fund will invest in Wheat Interests to the fullest extent possible without being leveraged or unable to satisfy its expected current or potential margin or collateral obligations with respect to its investments in Wheat Interests.<SU>15</SU>
          <FTREF/>After fulfilling such margin and collateral requirements, the Fund will invest the remainder of its proceeds from the sale of baskets in obligations of the United States government (“Treasury Securities”) or cash equivalents, and/or hold such assets in cash (generally in interest-bearing accounts). Therefore, the focus of the Sponsor in managing the Fund is investing in Wheat Interests and in Treasury Securities, cash and/or cash equivalents. Each of the Funds will earn interest income from the Treasury Securities and/or cash equivalents that it purchases and on the cash it holds through each Fund's custodian, the Bank of New York Mellon (the “Custodian” and the “Administrator”).</P>
        <FTNT>
          <P>
            <SU>15</SU>The Sponsor represents that the Fund will invest in Wheat Interests in a manner consistent with the Fund's investment objective and not to achieve additional leverage.</P>
        </FTNT>

        <P>The Sponsor endeavors to place the Fund's trades in Wheat Interests and otherwise manage the Fund's investments so that the Fund's average daily tracking error against the Wheat Benchmark will be less than 10 percent over any period of 30 trading days. More specifically, the Sponsor will endeavor to manage the Fund so that A will be within plus/minus 10 percent of B, where A is the average daily change in the Fund's NAV for any period of 30 successive valuation days,<E T="03">i.e.,</E>any trading day as of which the Fund calculates its NAV, and B is the average daily change in the Wheat Benchmark over the same period.<SU>16</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>16</SU>For each of the Funds, the Sponsor believes that market arbitrage opportunities will cause each Fund's respective Share price on the NYSE Arca to closely track the Fund's NAV per Share. The Sponsor believes that the net effect of this expected relationship and the expected relationship described above between the Fund's respective NAV and the respective benchmark will be that the changes in the price of the Fund's Shares on the NYSE Arca will closely track, in percentage terms, changes in such benchmark, less expenses.</P>
        </FTNT>
        <P>According to the Registration Statement, the Sponsor employs a “neutral” investment strategy intended to track the changes in the Wheat Benchmark regardless of whether the Wheat Benchmark goes up or goes down. The Fund's “neutral” investment strategy is designed to permit investors generally to purchase and sell the Fund's Shares for the purpose of investing indirectly in the wheat market in a cost-effective manner. Such investors may include participants in the wheat industry and other industries seeking to hedge the risk of losses in their wheat-related transactions, as well as investors seeking exposure to the wheat market. The Sponsor does not intend to operate the Fund in a fashion such that its per Share NAV will equal, in dollar terms, the spot price of a bushel or other unit of wheat or the price of any particular Wheat Futures Contract.</P>
        <P>According to the Registration Statement, the CFTC and U.S. designated contract markets such as the CBOT may establish position limits on the maximum net long or net short futures contracts in commodity interests that any person or group of persons under common trading control (other than as a hedge) may hold, own or control.<SU>17</SU>
          <FTREF/>For example, the current position limit for investments at any one time in CBOT Wheat Futures Contracts are 600 spot month contracts, 5,000 contracts expiring in any other single month, and 6,500 contracts total for all months. Cleared Wheat Swaps are subject to position limits that are substantially identical to, but measured separately from, the limits on Wheat Futures Contracts. Position limits are fixed ceilings that the Fund would not be able to exceed without specific exchange authorization. Under current law, all Wheat Futures Contracts traded on a particular exchange that are held under the control of the Sponsor, including those held by any future series of the Trust, are aggregated in determining the application of applicable position limits.</P>
        <FTNT>
          <P>
            <SU>17</SU>According to the Registration Statement, position limits generally impose a fixed ceiling on aggregate holdings in futures contracts relating to a particular commodity, and may also impose separate ceilings on contracts expiring in any one month, contracts expiring in the spot month, and/or contracts in certain specified final days of trading.</P>
        </FTNT>

        <P>In addition to position limits, the exchanges may establish daily price fluctuation limits on futures contracts. The daily price fluctuation limit establishes the maximum amount that<PRTPAGE P="45888"/>the price of futures contracts may vary either up or down from the previous day's settlement price. Once the daily price fluctuation limit has been reached in a particular futures contract, no trades may be made at a price beyond that limit.<SU>18</SU>
          <FTREF/>Position limits, accountability levels, and daily price fluctuation limits set by the exchanges have the potential to cause tracking error, which could cause the price of Shares to substantially vary from the Wheat Benchmark and prevent an investor from being able to effectively use the Fund as a way to hedge against wheat-related losses or as a way to indirectly invest in wheat.</P>
        <FTNT>
          <P>
            <SU>18</SU>For example, the CBOT imposes a $3,000 per contract price fluctuation limit for Wheat Futures Contracts. This limit is initially based off of the previous trading day's settlement price. If two or more Wheat Futures Contract months within the first five listed non-spot contracts close at the limit, the daily price limit increases to $4,500 per contract for the next business day and to $6,750 for the next business day.</P>
        </FTNT>
        <P>The Fund does not intend to limit the size of the offering and will attempt to expose substantially all of its proceeds to the wheat market utilizing Wheat Interests. If the Fund encounters position limits, accountability levels, or price fluctuation limits for Wheat Futures Contracts and/or Cleared Wheat Swaps on the CBOT, it may then, if permitted under applicable regulatory requirements, purchase Other Wheat Interests and/or Wheat Futures Contracts listed on other domestic or foreign exchanges. However, the Wheat Futures Contracts available on such foreign exchanges may have different underlying sizes, deliveries, and prices. In addition, the Wheat Futures Contracts available on these exchanges may be subject to their own position limits and accountability levels. In any case, notwithstanding the potential availability of these instruments in certain circumstances, position limits could force the Fund to limit the number of Creation Baskets (as defined below) that it sells.<SU>19</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>19</SU>With respect to each of the Funds, there will be no specified limit on the maximum amount of Creation Baskets that can be sold. At some point, however, applicable position limits may practically limit the number of Creation Baskets that will be sold if the Sponsor determines that the other investment alternatives available to a Fund at that time will not enable it to meet its stated investment objective.</P>
        </FTNT>
        <HD SOURCE="HD3">Teucrium Soybean Fund</HD>

        <P>According to the Registration Statement, the investment objective of the Fund is to have the daily changes in percentage terms of the Shares' NAV reflect the daily changes in percentage terms of a weighted average of the closing settlement prices for three futures contracts for soybeans (soybean futures contracts generally referred to herein as “Soybean Futures Contracts”) that are traded on the CBOT. Except as described in the following paragraph, the three Soybean Futures Contracts will be: (1) Second-to-expire CBOT Soybean Futures Contract, weighted 35%, (2) the third-to-expire CBOT Soybean Futures Contract, weighted 30%, and (3) the CBOT Soybean Futures Contract expiring in the November following the expiration month of the third-to-expire contract, weighted 35%. The weighted average of the three Soybean Futures Contracts is referred to herein as the “Soybean Benchmark,” and the three Soybean Futures Contracts that at any given time make up the Soybean Benchmark are referred to herein as the “Soybean Benchmark Component Futures Contracts.” The circumstances under which such investments in Other Soybean Interests may be utilized (<E T="03">e.g.,</E>imposition of position limits) are discussed below.<SU>20</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>20</SU>Soybean futures volume on CBOT for 2010 and 2011 (through April 29, 2011) was 36,962,868 contracts and 16,197,385 contracts, respectively. As of April 29, 2011, open interest for soybean futures was 572,959 contracts. The contract price was $69,700.00 (1394 cents per bushel and 5,000 bushels per contract). The approximate value of all outstanding contracts was $39.9 billion. The position limits for all months is 6,500 contracts and the total value of contracts if position limits were reached would be approximately $453 million (based on the $69,700.00 contract price).</P>
        </FTNT>
        <P>Soybean Futures Contracts traded on the CBOT expire on a specified day in seven different months: January, March, May, July, August, September and November. However, there is generally a less liquid market for the Soybean Futures Contracts expiring in August (the “August Contract”) and September (the “September Contract” and, together with the August Contract, the “Excluded Contracts”), and the Sponsor has determined not to incorporate the Excluded Contracts into the Soybean Benchmark calculation. Accordingly, during the period when the Excluded Contracts are the second-to-expire and third-to-expire Soybean Futures Contract, the fourth-to-expire and fifth-to-expire Soybean Futures Contracts will take the place of the second-to-expire and third-to-expire Soybean Futures Contracts, respectively, as Soybean Benchmark Component Futures Contracts. Similarly, when the August Contract is the third-to-expire Soybean Futures Contract, the fifth-to-expire Soybean Futures Contract will take the place of the August Contract as a Soybean Benchmark Component Futures Contract, and when the September Contract is the second-to-expire Soybean Futures Contract, the third-to-expire and fourth-to-expire Soybean Futures Contracts will be Soybean Benchmark Component Futures Contracts.<SU>21</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>21</SU>
            <E T="03">See</E>the Registration Statement for additional information regarding specific Soybean Futures Contracts that will be used in the calculation of the Soybean Benchmark at any point in a given year, based on the same 35%/30%/35% weighting methodology described above.</P>
        </FTNT>
        <P>According to the Registration Statement, the Fund seeks to achieve its investment objective by investing under normal market conditions in Soybean Benchmark Component Futures Contracts or, in certain circumstances, in other Soybean Futures Contracts traded on CBOT or Soybean Futures Contracts traded on foreign exchanges. In addition, and to a limited extent, the Fund also may invest in exchange-traded options on Soybean Futures Contracts and in soybean-based swap agreements that are cleared through the CBOT or its affiliated provider of clearing services (“Cleared Soybean Swaps”) in furtherance of the Fund's investment objective.</P>

        <P>Specifically, once CBOT position limits in Soybean Futures Contracts are reached, the Fund's intention is to invest first in Cleared Soybean Swaps to the extent permitted under the CBOT position limits applicable to Cleared Soybean Swaps and appropriate in light of the liquidity in the Cleared Soybean Swaps market, and then, using its commercially reasonable judgment, in other Soybean Futures Contracts (<E T="03">i.e.,</E>Soybean Futures Contracts traded on foreign exchanges) and instruments such as cash-settled options on Soybean Futures Contracts and forward contracts, swaps other than Cleared Soybean Swaps, and other over-the-counter transactions that are based on the price of soybeans and Soybean Futures Contracts (collectively, “Other Soybean Interests,” and together with Soybean Futures Contracts and Cleared Soybean Swaps, “Soybean Interests”).</P>

        <P>The Fund seeks to achieve its investment objective primarily by investing in Soybean Interests such that daily changes in the Fund's NAV will be expected to closely track the changes in the Soybean Benchmark. The Fund's positions in Soybean Interests will be changed or “rolled” on a regular basis in order to track the changing nature of the Soybean Benchmark. For example, five times a year (on the date on which certain Soybean Futures Contracts expire), a particular Soybean Futures Contract will no longer be a Soybean Benchmark Component Futures Contract, and the Fund's investments will have to be changed accordingly.<PRTPAGE P="45889"/>
        </P>
        <P>According to the Registration Statement, consistent with achieving the Fund's investment objective of closely tracking the Soybean Benchmark, the Sponsor may for certain reasons cause the Fund to enter into or hold Cleared Soybean Swaps and/or Other Soybean Interests. For example, certain Cleared Soybean Swaps have standardized terms similar to, and are priced by reference to, a corresponding Soybean Benchmark Component Futures Contract. Additionally, Other Soybean Interests that do not have standardized terms and are not exchange-traded (“over-the-counter” Soybean Interests) can generally be structured as the parties desire. Therefore, the Fund might enter into multiple Cleared Soybean Swaps and/or over-the-counter Soybean Interests intended to exactly replicate the performance of each of the three Soybean Benchmark Component Futures Contracts, or a single over-the-counter Soybean Interest designed to replicate the performance of the Soybean Benchmark as a whole. According to the Registration Statement, assuming that there is no default by a counterparty to an over-the-counter Soybean Interest, the performance of the over-the-counter Soybean Interest will necessarily correlate exactly with the performance of the Soybean Benchmark or the applicable Soybean Benchmark Component Futures Contract. The Fund might also enter into or hold over-the-counter Soybean Interests to facilitate effective trading, consistent with the discussion of the Fund's “roll” strategy in the preceding paragraph. In addition, the Fund might enter into or hold over-the-counter Soybean Interests that would be expected to alleviate overall deviation between the Fund's performance and that of the Soybean Benchmark that may result from certain market and trading inefficiencies or other reasons.</P>
        <P>The Fund will invest in Soybean Interests to the fullest extent possible without being leveraged or unable to satisfy its expected current or potential margin or collateral obligations with respect to its investments in Soybean Interests.<SU>22</SU>
          <FTREF/>After fulfilling such margin and collateral requirements, the Fund will invest the remainder of its proceeds from the sale of baskets in Treasury Securities or cash equivalents, and/or hold such assets in cash (generally in interest-bearing accounts). Therefore, the focus of the Sponsor in managing the Fund is investing in Soybean Interests and in Treasury Securities, cash and/or cash equivalents.</P>
        <FTNT>
          <P>
            <SU>22</SU>The Sponsor represents that the Fund will invest in Soybean Interests in a manner consistent with the Fund's investment objective and not to achieve additional leverage.</P>
        </FTNT>

        <P>The Sponsor endeavors to place the Fund's trades in Soybean Interests and otherwise manage the Fund's investments so that the Fund's average daily tracking error against the Soybean Benchmark will be less than 10 percent over any period of 30 trading days. More specifically, the Sponsor will endeavor to manage the Fund so that A will be within plus/minus 10 percent of B, where A is the average daily change in the Fund's NAV for any period of 30 successive valuation days,<E T="03">i.e.,</E>any trading day as of which the Fund calculates its NAV, and B is the average daily change in the Soybean Benchmark over the same period.</P>
        <P>The Sponsor employs a “neutral” investment strategy intended to track the changes in the Soybean Benchmark regardless of whether the Soybean Benchmark goes up or goes down. The Fund's “neutral” investment strategy is designed to permit investors generally to purchase and sell the Fund's Shares for the purpose of investing indirectly in the soybean market in a cost-effective manner. Such investors may include participants in the soybean industry and other industries seeking to hedge the risk of losses in their soybean-related transactions, as well as investors seeking exposure to the soybean market. The Sponsor does not intend to operate the Fund in a fashion such that its per Share NAV will equal, in dollar terms, the spot price of a bushel or other unit of soybean or the price of any particular Soybean Futures Contract.</P>
        <P>The CFTC's position limits for Soybean Futures Contracts (including related options) are 600 spot month contracts, 6,500 contracts expiring in any other single month, and 10,000 contracts for all months. Position limits could in certain circumstances effectively limit the number of Creation Baskets that the Fund can sell but, because the Fund is new, it is not expected to reach asset levels that would cause these position limits to be implicated in the near future. Cleared Soybean Swaps are subject to position limits that are substantially identical to, but measured separately from, the positions limits applicable to Soybean Futures Contracts. Under current law, all Soybean Futures Contracts that are held under the control of the Sponsor, including those held by any future series of the Trust, are aggregated in determining the application of applicable position limits.</P>
        <P>According to the Registration Statement, in contrast to position limits, accountability levels are not fixed ceilings, but rather thresholds above which an exchange may exercise greater scrutiny and control over an investor, including by imposing position limits on the investor. In light of the position limits discussed above, the CBOT has not set any accountability levels for Soybean Futures Contracts.</P>
        <P>According to the Registration Statement, the CBOT imposes a $0.70 per bushel ($3,500 per contract) daily price fluctuation limit for Soybean Futures Contracts. Once the daily price fluctuation limit has been reached in a particular Soybean Futures Contract, no trades may be made at a price beyond that limit. If two or more Soybean Futures Contract months within the first seven listed non-spot contracts close at the limit, the daily price limit increases to $1.05 per bushel ($5,250 per contract) the next business day and to $1.60 per bushel ($8,000 per contract) the next business day. These limits are based off the previous trading day's settlement price. Position limits and daily price fluctuation limits set by the CFTC and the exchanges have the potential to cause tracking error, which could cause the price of Shares to substantially vary from the Soybean Benchmark and prevent an investor from being able to effectively use the Fund as a way to hedge against soybean-related losses or as a way to indirectly invest in soybeans.</P>
        <P>The Fund does not intend to limit the size of the offering and will attempt to expose substantially all of its proceeds to the soybean market utilizing Soybean Interests. If the Fund encounters position limits or price fluctuation limits for Soybean Futures Contracts and/or Cleared Soybean Swaps on the CBOT, it may then, if permitted under applicable regulatory requirements, purchase Other Soybean Interests and/or Soybean Futures Contracts listed on foreign exchanges. However, the Soybean Futures Contracts available on such foreign exchanges may have different underlying sizes, deliveries, and prices. In addition, the Soybean Futures Contracts available on these exchanges may be subject to their own position limits or similar restrictions. In any case, notwithstanding the potential availability of these instruments in certain circumstances, position limits could force the Fund to limit the number of Creation Baskets (as defined below) that it sells.<SU>23</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>23</SU>
            <E T="03">See</E>note 19,<E T="03">supra.</E>
          </P>
        </FTNT>
        <HD SOURCE="HD3">Teucrium Sugar Fund</HD>

        <P>According to the Registration Statement, the investment objective of the Fund is to have the daily changes in percentage terms of the Shares' NAV<PRTPAGE P="45890"/>reflect the daily changes in percentage terms of a weighted average of the closing settlement prices for three futures contracts for sugar (sugar futures contracts generally referred to herein as “Sugar Futures Contracts”) that are traded on ICE Futures US (“ICE Futures”), specifically: (1) The second-to-expire Sugar No. 11 Futures Contract (a “Sugar No. 11 Futures Contract”), weighted 35%, (2) the third-to-expire Sugar No. 11 Futures Contract, weighted 30%, and (3) the Sugar No. 11 Futures Contract expiring in the March following the expiration month of the third-to-expire contract, weighted 35%. The weighted average of the three Sugar No. 11 Futures Contracts is referred to herein as the “Sugar Benchmark,” and the three Sugar No. 11 Futures Contracts that at any given time make up the Sugar Benchmark are referred to herein as the “Sugar Benchmark Component Futures Contracts.”<SU>24</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>24</SU>Sugar futures volume on ICE Futures for 2010 and 2011 (through April 29, 2011) was 27,848,391 contracts and 9,045,069 contracts, respectively. As of April 29, 2011, open interest for sugar futures was 570,948 contracts. The contract price was $24,920.00 (22.25 cents per pound and 112,000 pounds per contract). The approximate value of all outstanding contracts was $14.2 billion. The position limits for all months is 15,000 contracts and the total value of contracts if position limits were reached would be approximately $373.8 million (based on the $24,920.00 contract price).</P>
        </FTNT>
        <P>The Fund seeks to achieve its investment objective by investing under normal market conditions in Sugar Benchmark Component Futures Contracts or, in certain circumstances, in other Sugar Futures Contracts traded on ICE Futures or the New York Mercantile Exchange (“NYMEX”), or Sugar Futures Contracts traded on foreign exchanges. In addition, and to a limited extent, the Fund also may invest in exchange-traded options on Sugar Futures Contracts and in sugar-based swap agreements that are cleared through ICE Futures or its affiliated provider of clearing services (“Cleared Sugar Swaps”) in furtherance of the Fund's investment objective.</P>

        <P>Specifically, once accountability levels in Sugar No. 11 Futures Contracts traded on ICE Futures are reached, the Fund's intention is to invest first in Cleared Sugar Swaps to the extent permitted under the accountability levels applicable to Cleared Sugar Swaps and appropriate in light of the liquidity in the Cleared Sugar Swaps market, and then, using its commercially reasonable judgment, in other Sugar Futures Contracts (<E T="03">i.e.,</E>Sugar Futures Contracts traded on the NYMEX or foreign exchanges) and instruments such as cash-settled options on Sugar Futures Contracts and forward contracts, swaps other than Cleared Sugar Swaps, and other over-the-counter transactions that are based on the price of sugar and Sugar Futures Contracts (collectively, “Other Sugar Interests,” and together with Sugar Futures Contracts and Cleared Sugar Swaps, “Sugar Interests”).</P>
        <P>Sugar No. 11 Futures Contracts traded on the ICE Futures expire on a specified day in four different months: March, May, July, and October. For example, in terms of the Sugar Benchmark, in June of a given year (“year 1”) the next-to-expire or “spot month” Sugar No. 11 Futures Contract will expire in July of year 1, and the Sugar Benchmark Component Futures Contracts will be the contracts expiring in October of year 1 (the second-to-expire contract), March of year 2 (the third-to-expire contract), and March of year 3. As another example, in November of year 1 the Sugar Benchmark Component Futures Contracts will be the contracts expiring in May of year 2, July of year 2, and March of year 3.</P>
        <P>The Fund seeks to achieve its investment objective primarily by investing in Sugar Interests such that daily changes in the Fund's NAV will be expected to closely track the changes in the Sugar Benchmark. The Fund's positions in Sugar Interests will be changed or “rolled” on a regular basis in order to track the changing nature of the Sugar Benchmark. For example, four times a year (on the date on which a Sugar No. 11 Futures Contract expires), a particular Sugar No. 11 Futures Contract will no longer be a Sugar Benchmark Component Futures Contract, and the Fund's investments will have to be changed accordingly.</P>
        <P>Consistent with achieving the Fund's investment objective of closely tracking the Sugar Benchmark, the Sponsor may for certain reasons cause the Fund to enter into or hold Cleared Sugar Swaps and/or Other Sugar Interests. For example, certain Cleared Sugar Swaps have standardized terms similar to, and are priced by reference to, a corresponding Sugar Benchmark Component Futures Contract. Additionally, Other Sugar Interests that do not have standardized terms and are not exchange-traded, referred to as “over-the-counter” Sugar Interests, can generally be structured as the parties desire. Therefore, the Fund might enter into multiple Cleared Sugar Swaps and/or over-the-counter Sugar Interests intended to exactly replicate the performance of each of the three Sugar Benchmark Component Futures Contracts, or a single over-the-counter Sugar Interest designed to replicate the performance of the Sugar Benchmark as a whole. According to the Registration Statement, assuming that there is no default by a counterparty to an over-the-counter Sugar Interest, the performance of the over-the-counter Sugar Interest will necessarily correlate exactly with the performance of the Sugar Benchmark or the applicable Sugar Benchmark Component Futures Contract. The Fund might also enter into or hold over-the-counter Sugar Interests other than Sugar Benchmark Component Futures Contracts to facilitate effective trading, consistent with the discussion of the Fund's “roll” strategy in the preceding paragraph. In addition, the Fund might enter into or hold over-the-counter Sugar Interests that would be expected to alleviate overall deviation between the Fund's performance and that of the Sugar Benchmark that may result from certain market and trading inefficiencies or other reasons.</P>
        <P>The Fund will invest in Sugar Interests to the fullest extent possible without being leveraged or unable to satisfy its expected current or potential margin or collateral obligations with respect to its investments in Sugar Interests.<SU>25</SU>
          <FTREF/>After fulfilling such margin and collateral requirements, the Fund will invest the remainder of its proceeds from the sale of baskets in Treasury Securities or cash equivalents, and/or hold such assets in cash (generally in interest-bearing accounts). Therefore, the focus of the Sponsor in managing the Fund is investing in Sugar Interests and in Treasury Securities, cash and/or cash equivalents.</P>
        <FTNT>
          <P>
            <SU>25</SU>The Sponsor represents that the Fund will invest in Sugar Interests in a manner consistent with the Fund's investment objective and not to achieve additional leverage.</P>
        </FTNT>

        <P>The Sponsor endeavors to place the Fund's trades in Sugar Interests and otherwise manage the Fund's investments so that the Fund's average daily tracking error against the Sugar Benchmark will be less than 10 percent over any period of 30 trading days. More specifically, the Sponsor will endeavor to manage the Fund so that A will be within plus/minus 10 percent of B, where A is the average daily change in the Fund's NAV for any period of 30 successive valuation days,<E T="03">i.e.,</E>any trading day as of which the Fund calculates its NAV, and B is the average daily change in the Sugar Benchmark over the same period.</P>

        <P>The Sponsor employs a “neutral” investment strategy intended to track the changes in the Sugar Benchmark regardless of whether the Sugar Benchmark goes up or goes down. The Fund's “neutral” investment strategy is<PRTPAGE P="45891"/>designed to permit investors generally to purchase and sell the Fund's Shares for the purpose of investing indirectly in the sugar market in a cost-effective manner. Such investors may include participants in the sugar industry and other industries seeking to hedge the risk of losses in their sugar-related transactions, as well as investors seeking exposure to the sugar market. The Sponsor does not intend to operate the Fund in a fashion such that its per Share NAV will equal, in dollar terms, the spot price of a pound or other unit of sugar or the price of any particular Sugar Futures Contract.</P>
        <P>U.S. designated contract markets such as the ICE Futures and the NYMEX have established accountability levels on the maximum net long or net short Sugar Futures Contracts that any person or group of persons under common trading control may hold, own or control. For example, the current ICE Futures-established accountability level for investments in Sugar No. 11 Futures Contracts for any one month is 10,000, and the accountability level for all combined months is 15,000. While accountability levels are not fixed ceilings, they are thresholds above which the exchange may exercise greater scrutiny and control over an investor, including limiting an investor to holding no more Sugar No. 11 Futures Contracts than the amount established by the accountability level. Cleared Sugar Swaps are subject to an ICE Futures accountability level of 10,000 swap positions for all months combined. This limit is measured separately from the accountability levels on Sugar No. 11 Futures Contracts. Under current law, all Sugar Futures Contracts traded on a particular exchange that are held under the control of the Sponsor, including those held by any future series of the Trust, are aggregated in determining the application of applicable accountability levels. The Fund does not intend to invest in Sugar Futures Contracts or Cleared Sugar Swaps in excess of any applicable accountability levels.</P>
        <P>According to the Registration Statement, the CFTC has not currently set position limits for Sugar Futures Contracts, and ICE Futures and NYMEX have established such position limits only on spot month Sugar No. 11 Futures Contracts. Cleared Sugar Swaps are subject to ICE Futures position limits that are substantially identical to, but measured separately from, the limits on Sugar No. 11 Futures Contracts. However, because the Fund does not expect to hold spot month contracts at any time when these position limits would be applicable, it is unlikely that these limits will come into play. Currently, the ICE Futures and the NYMEX have not imposed maximum daily price fluctuation limits on Sugar Futures Contracts. Accountability levels, position limits and daily price fluctuation limits set by the CFTC and the exchanges have the potential to cause tracking error, which could cause the price of Shares to substantially vary from the Sugar Benchmark and prevent an investor from being able to effectively use the Fund as a way to hedge against sugar-related losses or as a way to indirectly invest in sugar.</P>
        <P>The Fund does not intend to limit the size of the offering and will attempt to expose substantially all of its proceeds to the sugar market utilizing Sugar Interests. If the Fund encounters accountability levels, position limits, or price fluctuation limits for Sugar Futures Contracts and/or Cleared Sugar Swaps on ICE Futures, it may then, if permitted under applicable regulatory requirements, purchase Other Sugar Interests and/or Sugar Futures Contracts listed on the NYMEX or foreign exchanges. However, the Sugar Futures Contracts available on such foreign exchanges may have different underlying sizes, deliveries, and prices. In addition, the Sugar Futures Contracts available on these exchanges may be subject to their own position limits and accountability levels. In any case, notwithstanding the potential availability of these instruments in certain circumstances, position limits could force the Fund to limit the number of Creation Baskets that it sells.<SU>26</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>26</SU>
            <E T="03">See</E>note 19,<E T="03">supra.</E>
          </P>
        </FTNT>
        <HD SOURCE="HD3">Creation and Redemption of Shares</HD>
        <P>The Funds create and redeem Shares only in blocks called “Creation Baskets” and “Redemption Baskets,” respectively, each consisting of 50,000 Shares. Only Authorized Purchasers may purchase or redeem Creation Baskets or Redemption Baskets. An Authorized Purchaser is under no obligation to create or redeem baskets, and an Authorized Purchaser is under no obligation to offer to the public Shares of any baskets it does create. Baskets are generally created when there is a demand for Shares, including, but not limited to, when the market price per Share is at (or perceived to be at) a premium to the NAV per Share. Similarly, baskets are generally redeemed when the market price per Share is at (or perceived to be at) a discount to the NAV per Share. Retail investors seeking to purchase or sell Shares on any day are expected to effect such transactions in the secondary market, on the NYSE Arca, at the market price per Share, rather than in connection with the creation or redemption of baskets.</P>
        <P>The total deposit required to create each basket (“Creation Basket Deposit”) is the amount of Treasury Securities and/or cash that is in the same proportion to the total assets of each Fund (net of estimated accrued but unpaid fees, expenses and other liabilities) on the purchase order date as the number of Shares to be created under the purchase order is in proportion to the total number of Shares outstanding on the purchase order date. The redemption distribution from each Fund will consist of a transfer to the redeeming Authorized Purchaser of an amount of Treasury Securities and/or cash that is in the same proportion to the total assets of such Fund (net of estimated accrued but unpaid fees, expenses and other liabilities) on the date the order to redeem is properly received as the number of Shares to be redeemed under the redemption order is in proportion to the total number of Shares outstanding on the date the order is received.</P>
        <P>The Funds will meet the initial and continued listing requirements applicable to TIRs in NYSE Arca Equities Rule 8.200 and Commentary .02 thereto. With respect to application of Rule 10A-3<SU>27</SU>
          <FTREF/>under the Act, the Trust relies on the exception contained in Rule 10A-3(c)(7).<SU>28</SU>
          <FTREF/>A minimum of 100,000 Shares for each Fund will be outstanding as of the start of trading on the Exchange.</P>
        <FTNT>
          <P>
            <SU>27</SU>17 CFR 240.10A-3.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>28</SU>17 CFR 240.10A-3(c)(7).</P>
        </FTNT>
        <P>A more detailed description of Wheat Interests, Soybean Interests and Sugar Interests and other aspects of the applicable commodities markets, as well as investment risks, are set forth in the Registration Statements. All terms relating to the Funds that are referred to, but not defined in, this proposed rule change are defined in the Registration Statements.</P>
        <HD SOURCE="HD3">Availability of Information Regarding the Shares</HD>
        <P>The Web site for the Funds (<E T="03">http://www.teucriumwheatfund.com, http://www.teucriumsoybeanfund.com</E>and<E T="03">http://www.teucriumsugarfund.com,</E>respectively) and/or the Exchange, which are publicly accessible at no charge, will contain the following information: (a) The current NAV per Share daily and the prior business day's NAV and the reported closing price; (b) the midpoint of the bid-ask price in<PRTPAGE P="45892"/>relation to the NAV as of the time the NAV is calculated (the “Bid-Ask Price”); (c) calculation of the premium or discount of such price against such NAV; (d) the bid-ask price of Shares determined using the highest bid and lowest offer as of the time of calculation of the NAV; (e) data in chart form displaying the frequency distribution of discounts and premiums of the Bid-Ask Price against the NAV, within appropriate ranges for each of the four (4) previous calendar quarters; (f) the prospectus; and (g) other applicable quantitative information. The Funds will also disseminate the Funds' holdings on a daily basis on the Funds' respective Web sites.</P>
        <P>The NAV for the Funds will be calculated by the Administrator once a day and will be disseminated daily to all market participants at the same time.<SU>29</SU>

          <FTREF/>The Exchange also will disseminate on a daily basis via the Consolidated Tape Association (“CTA”) information with respect to recent NAV, and Shares outstanding. The Exchange will also make available on its Web site daily trading volume of each of the Shares, closing prices of such Shares, and the corresponding NAV. The closing price and settlement prices of the Wheat Futures Contracts and Soybean Futures Contracts are also readily available from the CBOT, and of the Sugar No. 11 Futures Contracts from ICE Futures. In addition, such prices are available from automated quotation systems, published or other public sources, or on-line information services such as Bloomberg or Reuters. Each benchmark will be disseminated by one or more major market data vendors every 15 seconds during the NYSE Arca Core Trading Session of 9:30 a.m. to 4:00 p.m. E.T. Quotation and last-sale information regarding the Shares will be disseminated through the facilities of the CTA. In addition, the Exchange will provide a hyperlink on its Web site at<E T="03">http://www.nyx.com</E>to the Funds' Web sites, which will display all intraday and closing benchmark levels, the intraday Indicative Trust Value (see below), and NAV.</P>
        <FTNT>
          <P>
            <SU>29</SU>For each Fund, the NAV will be calculated by taking the current market value of the Fund's total assets and subtracting any liabilities. Under the Funds' current operational procedures, the Administrator will generally calculate the NAV of the Funds' Shares as of 4:00 p.m. Eastern Time (“E.T.”). The NAV for a particular trading day will be released after 4:15 p.m. E.T.</P>
        </FTNT>

        <P>The daily settlement prices for the Wheat Futures Contracts and Soybeans Futures Contracts are publicly available on the Web site of the CBOT (<E T="03">http://www.cmegroup.com</E>) and, for the Sugar No. 11 Futures Contracts, on the Web site of ICE Futures (<E T="03">http://www.theice.com</E>). In addition, various data vendors and news publications publish futures prices and data. The Exchange represents that quotation and last sale information for the Wheat Futures Contracts, Soybean Futures Contracts and Sugar No. 11 Futures Contracts are widely disseminated through a variety of major market data vendors worldwide, including Bloomberg and Reuters. In addition, the Exchange further represents that complete real-time data for such contracts is available by subscription from Reuters and Bloomberg. The CBOT and ICE Futures also provide delayed futures information on current and past trading sessions and market news free of charge on their Web sites. The specific contract specifications for such contracts are also available at the CBOT and ICE Futures Web sites, as well as other financial informational sources. The spot price of wheat, soybeans and sugar also is available on a 24-hour basis from major market data vendors.</P>
        <P>Each Fund will provide Web site disclosure of portfolio holdings daily and will include, as applicable, the names, quantity, price and market value of Wheat, Soybean and Sugar Benchmark Component Futures Contracts, as applicable, and other financial instruments, if any, and the characteristics of such instruments and cash equivalents, and amount of cash held in the portfolios of the Funds. This Web site disclosure of the portfolio composition of the Funds will occur at the same time as the disclosure by the Sponsor of the portfolio composition to Authorized Purchasers so that all market participants are provided portfolio composition information at the same time. Therefore, the same portfolio information will be provided on the public Web sites as well as in electronic files provided to Authorized Purchasers. Accordingly, each investor will have access to the current portfolio composition of the Funds through the Funds' Web sites.</P>
        <HD SOURCE="HD3">Dissemination of Indicative Trust Value</HD>
        <P>In addition, in order to provide updated information relating to the Funds for use by investors and market professionals, an updated Indicative Trust Value (“ITV”) will be calculated. The ITV is calculated by using the prior day's closing NAV per Share of each Fund as a base and updating that value throughout the trading day to reflect changes in the value of the Wheat, Soybean and Sugar Benchmark Component Futures Contracts, as applicable, and other financial instruments, if any. As stated in the Registration Statements, changes in the value of Treasury Securities and cash equivalents will not be included in the calculation of the ITV. The ITV disseminated during NYSE Arca trading hours should not be viewed as an actual real time update of the NAV, which is calculated only once a day.</P>
        <P>The ITV will be disseminated on a per Share basis by one or more major market data vendors every 15 seconds during the NYSE Arca Core Trading Session. The normal trading hours for Wheat Futures Contracts on the CBOT are 10:30 a.m. E.T. to 2:15 p.m. E.T. The normal trading hours for Soybean Futures Contracts on the CBOT are 10:30 a.m. E.T. to 2:15 p.m. E.T. Thus, there is a gap in time at the end of each day during which the Funds' Shares are traded on the NYSE Arca, but real-time CBOT trading prices for Wheat Futures Contracts and Soybean Futures Contracts traded on CBOT are not available. As a result, during those gaps there will be no update to the ITV. Therefore, a static ITV will be disseminated, between the close of trading on CBOT of Wheat Futures Contracts and Soybean Futures Contracts and the close of the NYSE Arca Core Trading Session.</P>
        <P>The normal trading hours for Sugar No. 11 Futures Contracts on ICE Futures are 3:30 a.m. E.T. to 2:00 p.m. E.T. Thus, there is a gap in time at the end of each day during which the Teucrium Sugar Fund's Shares are traded on NYSE Arca, but real-time ICE Futures trading prices for Sugar Futures Contracts traded on ICE Futures are not available. As a result, during those gaps there will be no update to the ITV. Therefore, a static ITV will be disseminated, between the close of trading on ICE Futures of Sugar No. 11 Futures Contracts and the close of the NYSE Arca Core Trading Session. The value of Shares of each Fund may be influenced by non-concurrent trading hours between NYSE Arca and the CBOT and ICE Futures, as applicable, when such Shares are traded on NYSE Arca after normal trading hours of the applicable futures contracts on CBOT or ICE Futures.</P>
        <P>The Exchange believes that dissemination of the ITV provides additional information regarding each Fund that is not otherwise available to the public and is useful to professionals and investors in connection with the related Shares trading on the Exchange or the creation or redemption of such Shares.</P>
        <HD SOURCE="HD3">Trading Rules</HD>

        <P>The Exchange deems the Shares to be equity securities, thus rendering trading in the Shares subject to the Exchange's<PRTPAGE P="45893"/>existing rules governing the trading of equity securities. Shares will trade on the NYSE Arca Marketplace from 4:00 a.m. to 8:00 p.m. E.T. The Exchange has appropriate rules to facilitate transactions in the Shares during all trading sessions. As provided in NYSE Arca Equities Rule 7.6, Commentary .03, the minimum price variation (“MPV”) for quoting and entry of orders in equity securities traded on the NYSE Arca Marketplace is $0.01, with the exception of securities that are priced less than $1.00 for which the MPV for order entry is $0.0001.</P>
        <P>The trading of the Shares will be subject to NYSE Arca Equities Rule 8.200, Commentary .02(e), which sets forth certain restrictions on ETP Holders acting as registered Market Makers in TIRs to facilitate surveillance. See “Surveillance” below for more information.</P>
        <P>With respect to trading halts, the Exchange may consider all relevant factors in exercising its discretion to halt or suspend trading in the Shares. Trading may be halted because of market conditions or for reasons that, in the view of the Exchange, make trading in the Shares inadvisable. These may include: (1) The extent to which trading is not occurring in the underlying futures contracts, or (2) whether other unusual conditions or circumstances detrimental to the maintenance of a fair and orderly market are present. In addition, trading in Shares will be subject to trading halts caused by extraordinary market volatility pursuant to the Exchange's “circuit breaker” rule<SU>30</SU>
          <FTREF/>or by the halt or suspension of trading of the underlying futures contracts.</P>
        <FTNT>
          <P>
            <SU>30</SU>
            <E T="03">See</E>NYSE Arca Equities Rule 7.12.</P>
        </FTNT>
        <P>The Exchange represents that the Exchange may halt trading during the day in which an interruption to the dissemination of the ITV or the value of the underlying futures contracts or the applicable benchmark occurs. If the interruption to the dissemination of the ITV, the value of the underlying futures contracts or the applicable benchmark persists past the trading day in which it occurred, the Exchange will halt trading no later than the beginning of the trading day following the interruption. In addition, if the Exchange becomes aware that the NAV with respect to the Shares is not disseminated to all market participants at the same time, it will halt trading in the Shares until such time as the NAV is available to all market participants.</P>
        <HD SOURCE="HD3">Surveillance</HD>
        <P>The Exchange intends to utilize its existing surveillance procedures applicable to derivative products, including TIRs, to monitor trading in the Shares. The Exchange represents that these procedures are adequate to properly monitor Exchange trading of the Shares in all trading sessions and to deter and detect violations of Exchange rules and applicable federal securities laws.</P>

        <P>The Exchange's current trading surveillances focus on detecting securities trading outside their normal patterns. When such situations are detected, surveillance analysis follows and investigations are opened, where appropriate, to review the behavior of all relevant parties for all relevant trading violations. The Exchange is able to obtain information regarding trading in the Shares, the physical commodities included in, or options, futures or options on futures on, Shares through ETP Holders, in connection with such ETP Holders' proprietary or customer trades through ETP Holders which they effect on any relevant market. The Exchange can obtain market surveillance information, including customer identity information, with respect to transactions occurring on exchanges that are members of the Intermarket Surveillance Group (“ISG”) or with which the Exchange has in place a comprehensive surveillance sharing agreement. With respect to the Teucrium Wheat Fund, the Exchange can obtain market surveillance information from CBOT, KCBT and MGEX in that CBOT is a member of ISG and the Exchange has in place a comprehensive surveillance sharing agreement with KCBT and MGEX. Likewise, with respect to the Teucrium Soybean Fund, the Exchange can obtain market surveillance information from CBOT as a member of ISG. With respect to the Teucrium Sugar Fund, the Exchange can obtain market surveillance information from NYMEX and ICE Futures in that both such exchanges are ISG members. A list of ISG members is available at<E T="03">http://www.isgportal.org.</E>
          <SU>31</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>31</SU>The Exchange notes that not all Wheat Interests, Soybean Interests and Sugar Interests may trade on markets that are members of ISG or with which the Exchange has in place a comprehensive surveillance sharing agreement.</P>
        </FTNT>
        <P>In addition, with respect to the Funds' futures contracts traded on exchanges, not more than 10% of the weight of such futures contracts in the aggregate shall consist of components whose principal trading market is not a member of ISG or is a market with which the Exchange does not have a comprehensive surveillance sharing agreement.</P>
        <P>The Exchange also has a general policy prohibiting the distribution of material, non-public information by its employees.</P>
        <HD SOURCE="HD3">Information Bulletin</HD>
        <P>Prior to the commencement of trading, the Exchange will inform its ETP Holders in an Information Bulletin of the special characteristics and risks associated with trading the Shares. Specifically, the Information Bulletin will discuss the following: (1) The risks involved in trading the Shares during the Opening and Late Trading Sessions when an updated ITV will not be calculated or publicly disseminated; (2) the procedures for purchases and redemptions of Shares in Creation Baskets and Redemption Baskets (and that Shares are not individually redeemable); (3) NYSE Arca Equities Rule 9.2(a), which imposes a duty of due diligence on its ETP Holders to learn the essential facts relating to every customer prior to trading the Shares; (4) how information regarding the ITV is disseminated; (5) that a static ITV will be disseminated, between the close of trading on the applicable futures exchange and the close of the NYSE Arca Core Trading Session; (6) the requirement that ETP Holders deliver a prospectus to investors purchasing newly issued Shares prior to or concurrently with the confirmation of a transaction; and (7) trading information.</P>
        <P>In addition, the Information Bulletin will advise ETP Holders, prior to the commencement of trading, of the prospectus delivery requirements applicable to the Funds. The Exchange notes that investors purchasing Shares directly from each Fund will receive a prospectus. ETP Holders purchasing Shares from each Fund for resale to investors will deliver a prospectus to such investors. The Information Bulletin will also discuss any exemptive, no-action and interpretive relief granted by the Commission from any rules under the Act.</P>
        <P>In addition, the Information Bulletin will reference that the Funds are subject to various fees and expenses described in the Registration Statements. The Information Bulletin will also reference that the CFTC has regulatory jurisdiction over the trading of wheat, soybean and sugar futures contracts traded on U.S. markets.</P>

        <P>The Information Bulletin will also disclose the trading hours of the Shares of each Fund and that the NAV for the Shares is calculated after 4:00 p.m. E.T. each trading day. The Bulletin will<PRTPAGE P="45894"/>disclose that information about the Shares of each Fund is publicly available on the Funds' Web sites.</P>
        <HD SOURCE="HD3">2. Statutory Basis</HD>
        <P>The basis under the Act for this proposed rule change is the requirement under Section 6(b)(5)<SU>32</SU>
          <FTREF/>that an exchange have rules that are designed to prevent fraudulent and manipulative acts and practices, to promote just and equitable principles of trade, to remove impediments to, and perfect the mechanism of a free and open market and, in general, to protect investors and the public interest.</P>
        <FTNT>
          <P>
            <SU>32</SU>15 U.S.C. 78f(b)(5).</P>
        </FTNT>
        <P>The Exchange believes that the proposed rule change is designed to prevent fraudulent and manipulative acts and practices in that the Shares will be listed and traded on the Exchange pursuant to the initial and continued listing criteria in NYSE Arca Equities Rule 8.200 and Commentary .02 thereto. The Exchange has in place surveillance procedures that are adequate to properly monitor trading in the Shares in all trading sessions and to deter and detect violations of Exchange rules and applicable federal securities laws. The Wheat, Soybean and Sugar Benchmark Component Futures Contracts are traded on futures exchanges that are members of ISG or with which the Exchange has in place a comprehensive surveillance sharing agreement. With respect to the Funds' futures contracts traded on exchanges, not more than 10% of the weight of such futures contracts in the aggregate shall consist of components whose principal trading market is not a member of ISG or is a market with which the Exchange does not have a comprehensive surveillance sharing agreement. The closing price and settlement prices of the Wheat Futures Contracts and Soybean Futures Contracts are readily available from the CBOT, and of the Sugar No. 11 Futures Contracts from ICE Futures. In addition, such prices are available from automated quotation systems, published or other public sources, or on-line information services. Each benchmark will be disseminated by one or more major market data vendors every 15 seconds during the NYSE Arca Core Trading Session of 9:30 a.m. to 4:00 p.m. E.T. Quotation and last-sale information regarding the Shares will be disseminated through the facilities of the CTA. The ITV will be disseminated on a per Share basis by one or more major market data vendors every 15 seconds during the NYSE Arca Core Trading Session. The Exchange may halt trading during the day in which the interruption to the dissemination of the ITV or the value of the underlying futures contracts or applicable benchmark occurs. If the interruption to the dissemination of the ITV, the value of the underlying futures contracts or the applicable benchmark persists past the trading day in which it occurred, the Exchange will halt trading no later than the beginning of the trading day following the interruption. In addition, if the Exchange becomes aware that the NAV with respect to the Shares is not disseminated to all market participants at the same time, it will halt trading in the Shares until such time as the NAV is available to all market participants.</P>
        <P>The proposed rule change is designed to promote just and equitable principles of trade and to protect investors and the public interest in that a large amount of information is publicly available regarding the Funds and the Shares, thereby promoting market transparency. Quotation and last sale information for the Wheat Futures Contracts, Soybean Futures Contracts and Sugar No. 11 Futures Contracts are widely disseminated through a variety of major market data vendors worldwide. Complete real-time data for such contracts is available by subscription from Reuters and Bloomberg. The CBOT and ICE Futures also provide delayed futures information on current and past trading sessions and market news free of charge on their Web sites. Each benchmark will be disseminated by one or more major market data vendors every 15 seconds during the NYSE Arca Core Trading Session of 9:30 a.m. to 4:00 p.m. E.T. The spot price of wheat, soybeans and sugar also is available on a 24-hour basis from major market data vendors. Each Fund will provide Web site disclosure of portfolio holdings daily and will include, as applicable, the names, quantity, price and market value of Wheat, Soybean and Sugar Benchmark Component Futures Contracts, as applicable, and other financial instruments, if any, and the characteristics of such instruments and cash equivalents, and amount of cash held in the portfolios of the Funds. The NAV per Share will be calculated daily and made available to all market participants at the same time. One or more major market data vendors will disseminate for the Funds on a daily basis information with respect to the recent NAV per Share and Shares outstanding. NYSE Arca will calculate and disseminate every 15 seconds throughout the NYSE Arca Core Trading Session an updated ITV.</P>
        <P>The proposed rule change is designed to perfect the mechanism of a free and open market and, in general, to protect investors and the public interest in that it will facilitate the listing and trading of additional types of exchange-traded products that will enhance competition among market participants, to the benefit of investors and the marketplace. As noted above, the Exchange has in place surveillance procedures relating to trading in the Shares and may obtain information via ISG from other exchanges that are members of ISG or with which the Exchange has entered into a comprehensive surveillance sharing agreement. In addition, as noted above, investors will have ready access to information regarding the Funds' holdings, ITV, and quotation and last sale information for the Shares.</P>
        <HD SOURCE="HD2">B. Self-Regulatory Organization's Statement on Burden on Competition</HD>
        <P>The Exchange does not believe that the proposed rule change will impose any burden on competition that is not necessary or appropriate in furtherance of the purposes of the Act.</P>
        <HD SOURCE="HD2">C. Self-Regulatory Organization's Statement on Comments on the Proposed Rule Change Received From Members, Participants, or Others</HD>
        <P>No written comments were solicited or received with respect to the proposed rule change.</P>
        <HD SOURCE="HD1">III. Date of Effectiveness of the Proposed Rule Change and Timing for Commission Action</HD>

        <P>Within 45 days of the date of publication of this notice in the<E T="04">Federal Register</E>or within such longer period (i) As the Commission may designate up to 90 days of such date if it finds such longer period to be appropriate and publishes its reasons for so finding or (ii) as to which the self-regulatory organization consents, the Commission will:</P>
        <P>(A) By order approve or disapprove the proposed rule change, or</P>
        <P>(B) Institute proceedings to determine whether the proposed rule change should be disapproved.</P>
        <HD SOURCE="HD1">IV. Solicitation of Comments</HD>
        <P>Interested persons are invited to submit written data, views, and arguments concerning the foregoing, including whether the proposed rule change is consistent with the Act. Comments may be submitted by any of the following methods:</P>
        <HD SOURCE="HD2">Electronic Comments</HD>
        <P>• Use the Commission's Internet comment form (<E T="03">http://www.sec.gov/rules/sro.shtml</E>); or</P>
        <P>• Send an e-mail to<E T="03">rule-comments@sec.gov.</E>Please include File<PRTPAGE P="45895"/>Number SR-NYSEArca-2011-48 on the subject line.</P>
        <HD SOURCE="HD2">Paper Comments</HD>
        <P>• Send paper comments in triplicate to Elizabeth M. Murphy, Secretary, Securities and Exchange Commission, 100 F Street, NE., Washington, DC 20549-1090.</P>
        

        <FP>All submissions should refer to File Number SR-NYSEArca-2011-48. This file number should be included on the subject line if e-mail is used. To help the Commission process and review your comments more efficiently, please use only one method. The Commission will post all comments on the Commission's Internet Web site (<E T="03">http://www.sec.gov/rules/sro.shtml</E>). Copies of the submission, all subsequent amendments, all written statements with respect to the proposed rule change that are filed with the Commission, and all written communications relating to the proposed rule change between the Commission and any person, other than those that may be withheld from the public in accordance with the provisions of 5 U.S.C. 552, will be available for Web site viewing and printing in the Commission's Public Reference Room, 100 F Street, NE., Washington, DC 20549, on official business days between the hours of 10 a.m. and 3 p.m. Copies of such filing also will be available for inspection and copying at the principal office of the Exchange. All comments received will be posted without change; the Commission does not edit personal identifying information from submissions. You should submit only information that you wish to make available publicly. All submissions should refer to File Number SR-NYSEArca-2011-48 and should be submitted on or August 22, 2011.</FP>
        <SIG>
          <P>For the Commission, by the Division of Trading and Markets, pursuant to delegated authority.<SU>33</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>33</SU>17 CFR 200.30-3(a)(12).</P>
          </FTNT>
          <NAME>Elizabeth M. Murphy,</NAME>
          <TITLE>Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19329 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 8011-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">SECURITIES AND EXCHANGE COMMISSION</AGENCY>
        <DEPDOC>[Release No. 34-64963; File No. SR-EDGX-2011-21]</DEPDOC>
        <SUBJECT>Self-Regulatory Organizations; EDGX Exchange, Inc.; Notice of Filing and Immediate Effectiveness of Proposed Rule Change Relating to Amendments to the EDGX Exchange, Inc. Fee Schedule</SUBJECT>
        <DATE>July 26, 2011.</DATE>
        <P>Pursuant to Section 19(b)(1) of the Securities Exchange Act of 1934 (the “Act”),<SU>1</SU>
          <FTREF/>and Rule 19b-4 thereunder,<SU>2</SU>
          <FTREF/>notice is hereby given that on July 21, 2011, the EDGX Exchange, Inc. (the “Exchange” or the “EDGX”) filed with the Securities and Exchange Commission (“Commission”) the proposed rule change as described in Items I, II, and III below, which items have been prepared by the self-regulatory organization. The Commission is publishing this notice to solicit comments on the proposed rule change from interested persons.</P>
        <FTNT>
          <P>
            <SU>1</SU>15 U.S.C. 78s(b)(1).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>2</SU>17 CFR 240.19b-4.</P>
        </FTNT>
        <HD SOURCE="HD1">I. Self-Regulatory Organization's Statement of the Terms of Substance of the Proposed Rule Change</HD>
        <P>The Exchange proposes to amend its fee schedule applicable to Members<SU>3</SU>

          <FTREF/>and non-members of the Exchange pursuant to EDGX Rule 15.1(a) and (c). Pursuant to the proposed rule change, the Exchange will commence charging fees for Members and non-members for certain logical ports used to receive market data. The Exchange intends to implement this rule proposal effective August 1, 2011. The text of the proposed rule change is available on the Exchange's Internet website at<E T="03">http://www.directedge.com.</E>
        </P>
        <FTNT>
          <P>
            <SU>3</SU>A Member is any registered broker or dealer, or any person associated with a registered broker or dealer, that has been admitted to membership in the Exchange.</P>
        </FTNT>
        <HD SOURCE="HD1">II. Self-Regulatory Organization's Statement of the Purpose of, and Statutory Basis for, the Proposed Rule Change</HD>
        <P>In its filing with the Commission, the self-regulatory organization included statements concerning the purpose of, and basis for, the proposed rule change and discussed any comments it received on the proposed rule change. The text of these statements may be examined at the places specified in Item IV below. The self-regulatory organization has prepared summaries, set forth in sections A, B and C below, of the most significant aspects of such statements.</P>
        <HD SOURCE="HD2">A. Self-Regulatory Organization's Statement of the Purpose of, and Statutory Basis for, the Proposed Rule Change</HD>
        <HD SOURCE="HD3">1. Purpose</HD>
        <P>The Exchange is proposing to charge a monthly fee for logical ports used to receive market data. Currently, ports used to receive or re-transmit market data are provided free of charge. The Exchange currently charges for logical ports (also commonly referred to as TCP/IP ports) established by the Exchange within the Exchange's system that grant Members or non-members the ability to operate a specific application, such as FIX or High Performance API for order entry. The current monthly fee for these logical ports is $500 per month, where members and non-members receive the first ten (10) sessions free of charge for direct (“Direct”) Sessions only. The Exchange is proposing to include logical ports used to receive market data among those logical ports currently charged at $500 per month.<SU>4</SU>
          <FTREF/>Under the proposed change, the quantity of logical ports used to receive market data will be included among those ports used for order entry (FIX, HP-API) or for drop copies (DROP). Exchange customers will continue to receive the first ten (10) sessions free of charge, regardless of the type of logical port used for Direct Sessions (FIX, HP-API, DROP, or data), and thereafter be charged a $500 fee per month per logical port. The charge will apply to Members and non-members. The Exchange notes that the proposed port fees are consistent with similar logical port fees charged by other exchanges.<SU>5</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>4</SU>The Exchange notes that ports used to request a re-transmission of market data from the Exchange will continue to be provided free of charge.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>5</SU>
            <E T="03">See, e.g.,</E>Rule 7015(g) of The NASDAQ Stock Market LLC (“NASDAQ”) (setting forth, among other fees for access services, port fees charged to members and non-members used for market data delivery over the internet); Securities Exchange Act Release No. 63197 (October 27, 2010), 75 FR 67791 (November 3, 2010) (SR-NASDAQ-2010-136) (adopting Access Services fees, including fees for ports used to receive market data) 72 FR 13328 (March 21, 2007) (SR-NASDAQ-2006-064) (increasing Internet port fee from $200 to $600 per Internet port that is used to deliver market data); Securities Exchange Act Release No. 60586 (August 28, 2009), 74 FR 46256 (September 8, 2009) (SR-BATS-2009-026) (establishing fees for ports used by members and non-members to enter orders and receive market data).</P>
        </FTNT>

        <P>The Exchange believes that the imposition of port fees for logical ports used to receive market data will promote efficient use of the ports by market participants, helping the Exchange to continue to maintain and improve its infrastructure, while also encouraging Exchange customers to request and enable only the ports that<PRTPAGE P="45896"/>are necessary for their operations related to the Exchange.</P>
        <P>The Exchange will implement the proposed rule change on August 1, 2011.</P>
        <HD SOURCE="HD3">2. Statutory Basis</HD>
        <P>The Exchange believes that the proposed rule change is consistent with the objectives of Section 6 of the Act,<SU>6</SU>
          <FTREF/>in general, and furthers the objectives of Section 6(b)(4),<SU>7</SU>
          <FTREF/>in particular, as it is designed to provide for the equitable allocation of reasonable dues, fees and other charges among its Members and other persons using its facilities. The Exchange believes that its proposed logical data port fees are reasonable in light of the benefits to members of market data access. In addition, the Exchange believes that its fees are equitably allocated among its constituents based upon the number of access ports that they require to receive data from the Exchange. Furthermore, the fees associated with logical data ports will be equitably allocated to all constituents as the fees will be uniform in application to all Members and non-members. Finally, the Exchange believes that the fees obtained will enable it to cover its infrastructure costs associated with allowing Members and non-members to establish logical ports to connect to the Exchange's systems and continue to maintain and improve its infrastructure, market technology, and services.</P>
        <FTNT>
          <P>
            <SU>6</SU>15 U.S.C. 78f.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>7</SU>15 U.S.C. 78f(b)(4).</P>
        </FTNT>
        <HD SOURCE="HD2">B. Self-Regulatory Organization's Statement on Burden on Competition</HD>
        <P>The proposed rule change does not impose any burden on competition that is not necessary or appropriate in furtherance of the purposes of the Act.</P>
        <HD SOURCE="HD2">C. Self-Regulatory Organization's Statement on Comments on the Proposed Rule Change Received From Members, Participants or Others</HD>
        <P>The Exchange has not solicited, and does not intend to solicit, comments on this proposed rule change. The Exchange has not received any unsolicited written comments from members or other interested parties.</P>
        <HD SOURCE="HD1">III. Date of Effectiveness of the Proposed Rule Change and Timing for Commission Action</HD>
        <P>The foregoing rule change has become effective pursuant to Section 19(b)(3) of the Act<SU>8</SU>
          <FTREF/>and Rule 19b-4(f)(2)<SU>9</SU>
          <FTREF/>thereunder. At any time within 60 days of the filing of such proposed rule change, the Commission summarily may temporarily suspend such rule change if it appears to the Commission that such action is necessary or appropriate in the public interest, for the protection of investors, or otherwise in furtherance of the purposes of the Act.</P>
        <FTNT>
          <P>
            <SU>8</SU>15 U.S.C. 78s(b)(3)(A).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>9</SU>17 CFR 19b-4(f)(2).</P>
        </FTNT>
        <HD SOURCE="HD1">IV. Solicitation of Comments</HD>
        <P>Interested persons are invited to submit written data, views, and arguments concerning the foregoing, including whether the proposed rule change is consistent with the Act. Comments may be submitted by any of the following methods:</P>
        <HD SOURCE="HD2">Electronic Comments</HD>
        <P>• Use the Commission's Internet comment form (<E T="03">http://www.sec.gov/rules/sro.shtml</E>); or</P>
        <P>• Send an e-mail to<E T="03">rule-comments@sec.gov.</E>Please include File Number SR-EDGX-2011-21 on the subject line.</P>
        <HD SOURCE="HD2">Paper Comments</HD>
        <P>• Send paper comments in triplicate to Elizabeth M. Murphy, Secretary, Securities and Exchange Commission, 100 F Street, NE., Washington, DC 20549-1090.</P>
        

        <FP>All submissions should refer to File Number SR-EDGX-2011-21. This file number should be included on the subject line if e-mail is used. To help the Commission process and review your comments more efficiently, please use only one method. The Commission will post all comments on the Commission's Internet website (<E T="03">http://www.sec.gov/rules/sro.shtml</E>). Copies of the submission, all subsequent amendments, all written statements with respect to the proposed rule change that are filed with the Commission, and all written communications relating to the proposed rule change between the Commission and any person, other than those that may be withheld from the public in accordance with the provisions of 5 U.S.C. 552, will be available for website viewing and printing in the Commission's Public Reference Room, 100 F Street, NE., Washington, DC 20549, on official business days between the hours of 10 a.m. and 3 p.m. Copies of the filing also will be available for inspection and copying at the principal office of the Exchange. All comments received will be posted without change; the Commission does not edit personal identifying information from submissions. You should submit only information that you wish to make available publicly. All submissions should refer to File Number SR-EDGX-2011-21 and should be submitted on or before August 22, 2011.</FP>
        <SIG>
          <P>For the Commission, by the Division of Trading and Markets, pursuant to delegated authority.<SU>10</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>10</SU>17 CFR 200.30-3(a)(12).</P>
          </FTNT>
          <NAME>Elizabeth M. Murphy,</NAME>
          <TITLE>Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19325 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 8011-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">SECURITIES AND EXCHANGE COMMISSION</AGENCY>
        <DEPDOC>[Release No. 34-64962; File No. SR-EDGA-2011-21]</DEPDOC>
        <SUBJECT>Self-Regulatory Organizations; EDGA Exchange, Inc.; Notice of Filing And Immediate Effectiveness of Proposed Rule Change To Amend EDGA Rule 11.5(c)(8) Regarding the Description of the Non-Displayed Order Type</SUBJECT>
        <DATE>July 26, 2011.</DATE>
        <P>Pursuant to Section 19(b)(1) of the Securities Exchange Act of 1934 (“Act”)<SU>1</SU>
          <FTREF/>and Rule 19b-4 thereunder,<SU>2</SU>
          <FTREF/>notice is hereby given that on July 15, 2011, EDGA Exchange, Inc. (“EDGA” or the “Exchange”) filed with the Securities and Exchange Commission (“SEC” or “Commission”) the proposed rule change as described in Items I and II below, which Items have been prepared by EDGA. The Commission is publishing this notice to solicit comments on the proposed rule change, from interested persons.</P>
        <FTNT>
          <P>
            <SU>1</SU>15 U.S.C. 78s(b)(1).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>2</SU>17 CFR 240.19b-4.</P>
        </FTNT>
        <HD SOURCE="HD1">I. Self-Regulatory Organization's Statement of the Terms of Substance of the Proposed Rule Change</HD>

        <P>The Exchange proposes to amend EDGA Rule 11.5(c)(8) regarding the description of the Non-Displayed order type. The text of the proposed rule change is available on the Exchange's Web site at<E T="03">http://www.directedge.com,</E>at the Exchange's principal office, at the Public Reference Room of the Commission, and at the Commission's Web site at<E T="03">http://www.sec.gov.</E>
        </P>
        <HD SOURCE="HD1">II. Self-Regulatory Organization's Statement of the Purpose of, and Statutory Basis for, the Proposed Rule Change</HD>

        <P>In its filing with the Commission, the Exchange included statements concerning the purpose of, and basis for, the proposed rule change and discussed any comments it received on the proposed rule change. The text of these statements may be examined at the<PRTPAGE P="45897"/>places specified in Item IV below. The self-regulatory organization has prepared summaries, set forth in Sections A, B and C below, of the most significant aspects of such statements.</P>
        <HD SOURCE="HD2">A. Self-Regulatory Organization's Statement of the Purpose of, and Statutory Basis for, the Proposed Rule Change</HD>
        <HD SOURCE="HD3">1. Purpose</HD>
        <P>The Exchange proposes to amend Rule 11.5(c)(8) to correct an inadvertent error in the definition of “Non-Displayed Orders.”</P>
        <P>Exchange Rule 11.5(c)(8) states, in part, that for a Non-Displayed order, “the System<SU>3</SU>
          <FTREF/>shall not accept a Non-Displayed Order that is priced better than the midpoint of the NBBO.”</P>
        <FTNT>
          <P>
            <SU>3</SU>As defined in Rule 1.5(aa).</P>
        </FTNT>
        <P>However, currently, on EDGA, Non-Displayed orders are accepted and posted on the EDGA Book (“Book” or “EDGA Book”)<SU>4</SU>
          <FTREF/>at their specified limit price for limit orders or executed immediately for market orders. This occurs regardless of whether the Non-Displayed Orders are priced better than the midpoint of the NBBO.</P>
        <FTNT>
          <P>
            <SU>4</SU>As defined in Rule 1.5(d).</P>
        </FTNT>
        <P>The following examples illustrate the operation of Non-Displayed Orders:</P>
        <P>Assume the NBBO is 1.00 x 1.10, and a Non-Displayed Order is entered to sell 100 shares at $1.03. Such Non-Displayed Order will be posted to the EDGA Book at $1.03 or executed if there is contra-side trading interest at $1.03 or higher.<SU>5</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>5</SU>This could include a Non-Displayed buy order or displayed buy order.</P>
        </FTNT>
        <P>Assume the NBBO changes and is now 1.04 x 1.10 and a Non-Displayed Order is entered to sell 100 shares at $1.07. Such Non-Displayed Order will be posted to the EDGA Book at $1.07 or executed if there is contra-side trading interest at $1.07 or higher.</P>
        <P>Assume the NBBO remains at 1.04 x 1.10 and a Non-Displayed Order is entered to sell 100 shares at $1.04. Such Non-Displayed Order will be posted to the EDGA Book at $1.04, executed if there is contra-side trading interest at $1.04 or higher, or routed to an away market if the order is marked eligible for routing.</P>
        <P>The Exchange believes that this proposed amendment provides more transparency regarding the System's processing of this order type by correcting an inadvertent error in the rule text of Non-Displayed Orders.</P>
        <HD SOURCE="HD3">2. Statutory Basis</HD>
        <P>The statutory basis for the proposed rule change is Section 6(b)(5) of the Act,<SU>6</SU>
          <FTREF/>which requires the rules of an exchange to promote just and equitable principles of trade, to remove impediments to and perfect the mechanism of a free and open market and a national market system and, in general, to protect investors and the public interest. The Exchange believes that providing that Non-Displayed orders may be accepted and posted on the Book regardless of whether they are priced better than the midpoint encourages liquidity and potential price improvement for transactions without arbitrarily restricting liquidity from being executed at the Exchange. The Exchange also believes that by correcting an inadvertent error in the definition of “Non-Displayed Orders” in EDGA Rule 11.5(c)(8), the proposed rule promotes the efficient execution of investor transactions, and thus investor confidence, over the long term.</P>
        <FTNT>
          <P>
            <SU>6</SU>15 U.S.C. 78f(b)(5).</P>
        </FTNT>
        <HD SOURCE="HD2">B. Self-Regulatory Organization's Statement on Burden on Competition</HD>
        <P>The Exchange does not believe that the proposed rule change will impose any burden on competition that is not necessary or appropriate in furtherance of the purposes of the Act.</P>
        <HD SOURCE="HD2">C. Self-Regulatory Organization's Statement on Comments on the Proposed Rule Change Received From Members, Participants, or Others</HD>
        <P>The Exchange has neither solicited nor received written comments on the proposed rule change.</P>
        <HD SOURCE="HD1">III. Date of Effectiveness of the Proposed Rule Change and Timing for Commission Action</HD>
        <P>Because the proposed rule change: (i) Does not significantly affect the protection of investors or the public interest; (ii) does not impose any significant burden on competition; and (iii) does not become operative for 30 days after the date of the filing, or such shorter time as the Commission may designate if consistent with the protection of investors and the public interest, the proposed rule change has become effective pursuant to Section 19(b)(3)(A) of the Act<SU>7</SU>
          <FTREF/>and Rule 19b-4(f)(6) thereunder.<SU>8</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>7</SU>15 U.S.C. 78s(b)(3)(A).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>8</SU>17 CFR 240.19b-4(f)(6). In addition, Rule 19b-4(f)(6)(iii) requires that a self-regulatory organization submit to the Commission written notice of its intent to file the proposed rule change, along with a brief description and text of the proposed rule change, at least five business days prior to the date of filing of the proposed rule change, or such shorter time as designated by the Commission. The Exchange has satisfied this requirement.</P>
        </FTNT>
        <P>The Exchange has requested that the Commission waive the 30-day operative delay. The Commission believes that waiving the 30-day operative delay is consistent with the protection of investors and the public interest because other national securities exchanges have adopted similar Non-displayed order types,<SU>9</SU>
          <FTREF/>and this proposal does not raise any novel issues. Therefore, the Commission designates the proposed rule change to be operative upon filing with the Commission.<SU>10</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>9</SU>
            <E T="03">See, e.g.,</E>BATS Rule 11.9(c)(11) and Nasdaq Rule 4751(e)(3).</P>
        </FTNT>
        <FTNT>
          <P>

            <SU>10</SU>For purposes only of waiving the 30-day operative delay, the Commission has considered the proposed rule's impact on efficiency, competition, and capital formation.<E T="03">See</E>15 U.S.C. 78c(f).</P>
        </FTNT>
        <P>At any time within 60 days of the filing of the proposed rule change, the Commission summarily may temporarily suspend such rule change if it appears to the Commission that such action is necessary or appropriate in the public interest, for the protection of investors, or otherwise in furtherance of the purposes of the Act.</P>
        <HD SOURCE="HD1">IV. Solicitation of Comments</HD>
        <P>Interested persons are invited to submit written data, views, and arguments concerning the foregoing, including whether the proposed rule change is consistent with the Act. Comments may be submitted by any of the following methods:</P>
        <HD SOURCE="HD2">Electronic Comments</HD>
        <P>• Use the Commission's Internet comment form (<E T="03">http://www.sec.gov/rules/sro.shtml</E>); or</P>
        <P>• Send an e-mail to<E T="03">rule-comments@sec.gov.</E>Please include File Number SR-EDGA-2011-21 on the subject line.</P>
        <HD SOURCE="HD2">Paper Comments</HD>
        <P>• Send paper comments in triplicate to Elizabeth M. Murphy, Secretary, Securities and Exchange Commission, 100 F Street, NE., Washington, DC 20549-1090.</P>
        

        <FP>All submissions should refer to File Number SR-EDGA-2011-21. This file number should be included on the subject line if e-mail is used. To help the Commission process and review your comments more efficiently, please use only one method. The Commission will post all comments on the Commission's Internet Web site (<E T="03">http://www.sec.gov/rules/sro.shtml</E>). Copies of the submission, all subsequent amendments, all written statements with respect to the proposed rule change that are filed with the Commission, and all written<PRTPAGE P="45898"/>communications relating to the proposed rule change between the Commission and any person, other than those that may be withheld from the public in accordance with the provisions of 5 U.S.C. 552, will be available for Web site viewing and printing in the Commission's Public Reference Room, 100 F Street, NE., Washington, DC 20549, on official business days between the hours of 10:00 a.m. and 3:00 p.m. Copies of such filing also will be available for inspection and copying at the principal office of EDGA. All comments received will be posted without change; the Commission does not edit personal identifying information from submissions. You should submit only information that you wish to make publicly available. All submissions should refer to File Number SR-EDGA-2011-21 and should be submitted on or before August 22, 2011.</FP>
        <SIG>
          <P>For the Commission, by the Division of Trading and Markets, pursuant to delegated authority.<SU>11</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>11</SU>17 CFR 200.30-3(a)(12).</P>
          </FTNT>
          <NAME>Elizabeth M. Murphy,</NAME>
          <TITLE>Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19326 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 8011-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">SECURITIES AND EXCHANGE COMMISSION</AGENCY>
        <DEPDOC>[Release No. 34-64964; File No. SR-EDGA-2011-22]</DEPDOC>
        <SUBJECT>Self-Regulatory Organizations; EDGA Exchange, Inc.; Notice of Filing and Immediate Effectiveness of Proposed Rule Change Relating to Amendments to the EDGA Exchange, Inc. Fee Schedule</SUBJECT>
        <DATE>July 26, 2011.</DATE>
        <P>Pursuant to Section 19(b)(1) of the Securities Exchange Act of 1934 (the “Act”),<SU>1</SU>
          <FTREF/>and Rule 19b-4 thereunder,<SU>2</SU>
          <FTREF/>notice is hereby given that on July 21, 2011, the EDGA Exchange, Inc. (the “Exchange” or the “EDGA”) filed with the Securities and Exchange Commission (“Commission”) the proposed rule change as described in Items I, II, and III below, which items have been prepared by the self-regulatory organization. The Commission is publishing this notice to solicit comments on the proposed rule change from interested persons.</P>
        <FTNT>
          <P>
            <SU>1</SU>15 U.S.C. 78s(b)(1).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>2</SU>17 CFR 240.19b-4.</P>
        </FTNT>
        <HD SOURCE="HD1">I.  Self-Regulatory Organization's Statement of the Terms of Substance of the Proposed Rule Change</HD>
        <P>The Exchange proposes to amend its fee schedule applicable to Members<SU>3</SU>

          <FTREF/>and non-members of the Exchange pursuant to EDGA Rule 15.1(a) and (c). Pursuant to the proposed rule change, the Exchange will commence charging fees for Members and non-members for certain logical ports used to receive market data. The Exchange intends to implement this rule proposal effective August 1, 2011. The text of the proposed rule change is available on the Exchange's Internet Web site at<E T="03">http://www.directedge.com.</E>
        </P>
        <FTNT>
          <P>
            <SU>3</SU>A Member is any registered broker or dealer, or any person associated with a registered broker or dealer, that has been admitted to membership in the Exchange.</P>
        </FTNT>
        <HD SOURCE="HD1">II. Self-Regulatory Organization's Statement of the Purpose of, and Statutory Basis for, the Proposed Rule Change</HD>
        <P>In its filing with the Commission, the self-regulatory organization included statements concerning the purpose of, and basis for, the proposed rule change and discussed any comments it received on the proposed rule change. The text of these statements may be examined at the places specified in Item IV below. The self-regulatory organization has prepared summaries, set forth in sections A, B and C below, of the most significant aspects of such statements.</P>
        <HD SOURCE="HD2">A. Self-Regulatory Organization's Statement of the Purpose of, and Statutory Basis for, the Proposed Rule Change</HD>
        <HD SOURCE="HD3">1. Purpose</HD>
        <P>The Exchange is proposing to charge a monthly fee for logical ports used to receive market data. Currently, ports used to receive or re-transmit market data are provided free of charge. The Exchange currently charges for logical ports (also commonly referred to as TCP/IP ports) established by the Exchange within the Exchange's system that grant Members or non-members the ability to operate a specific application, such as FIX or High Performance API for order entry. The current monthly fee for these logical ports is $500 per month, where members and non-members receive the first ten (10) sessions free of charge for direct (“Direct”) Sessions only. The Exchange is proposing to include logical ports used to receive market data among those logical ports currently charged at $500 per month.<SU>4</SU>
          <FTREF/>Under the proposed change, the quantity of logical ports used to receive market data will be included among those ports used for order entry (FIX, HP-API) or for drop copies (DROP). Exchange customers will continue to receive the first ten (10) sessions free of charge, regardless of the type of logical port used for Direct Sessions (FIX, HP-API, DROP, or data), and thereafter be charged a $500 fee per month per logical port. The charge will apply to Members and non-members. The Exchange notes that the proposed port fees are consistent with similar logical port fees charged by other exchanges.<SU>5</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>4</SU>The Exchange notes that ports used to request a re-transmission of market data from the Exchange will continue to be provided free of charge.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>5</SU>
            <E T="03">See, e.g.,</E>Rule 7015(g) of The NASDAQ Stock Market LLC (“NASDAQ”) (setting forth, among other fees for access services, port fees charged to members and non-members used for market data delivery over the Internet); Securities Exchange Act Release No. 63197 (October 27, 2010), 75 FR 67791 (November 3, 2010) (SR-NASDAQ-2010-136)(adopting Access Services fees, including fees for ports used to receive market data) 72 FR 13328 (March 21, 2007) (SR-NASDAQ-2006-064) (increasing Internet port fee from $200 to $600 per Internet port that is used to deliver market data); Securities Exchange Act Release No. 60586 (August 28, 2009), 74 FR 46256 (September 8, 2009) (SR-BATS-2009-026) (establishing fees for ports used by members and non-members to enter orders and receive market data).</P>
        </FTNT>
        <P>The Exchange believes that the imposition of port fees for logical ports used to receive market data will promote efficient use of the ports by market participants, helping the Exchange to continue to maintain and improve its infrastructure, while also encouraging Exchange customers to request and enable only the ports that are necessary for their operations related to the Exchange.</P>
        <P>The Exchange will implement the proposed rule change on August 1, 2011.</P>
        <HD SOURCE="HD3">2. Statutory Basis</HD>
        <P>The Exchange believes that the proposed rule change is consistent with the objectives of Section 6 of the Act,<SU>6</SU>
          <FTREF/>in general, and furthers the objectives of Section 6(b)(4),<SU>7</SU>

          <FTREF/>in particular, as it is designed to provide for the equitable allocation of reasonable dues, fees and other charges among its Members and other persons using its facilities. The Exchange believes that its proposed logical data port fees are reasonable in light of the benefits to members of market data access. In addition, the Exchange believes that its fees are equitably allocated among its constituents based upon the number of access ports that they require to receive data from the Exchange. Furthermore, the fees associated with logical data ports will be equitably allocated to all<PRTPAGE P="45899"/>constituents as the fees will be uniform in application to all Members and non-members. Finally, the Exchange believes that the fees obtained will enable it to cover its infrastructure costs associated with allowing Members and non-members to establish logical ports to connect to the Exchange's systems and continue to maintain and improve its infrastructure, market technology, and services.</P>
        <FTNT>
          <P>
            <SU>6</SU>15 U.S.C. 78f.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>7</SU>15 U.S.C. 78f(b)(4).</P>
        </FTNT>
        <HD SOURCE="HD2">B. Self-Regulatory Organization's Statement on Burden on Competition</HD>
        <P>The proposed rule change does not impose any burden on competition that is not necessary or appropriate in furtherance of the purposes of the Act.</P>
        <HD SOURCE="HD2">C. Self-Regulatory Organization's Statement on Comments on the Proposed Rule Change Received From Members, Participants or Others</HD>
        <P>The Exchange has not solicited, and does not intend to solicit, comments on this proposed rule change. The Exchange has not received any unsolicited written comments from members or other interested parties.</P>
        <HD SOURCE="HD1">III. Date of Effectiveness of the Proposed Rule Change and Timing for Commission Action</HD>
        <P>The foregoing rule change has become effective pursuant to Section 19(b)(3) of the Act<SU>8</SU>
          <FTREF/>and Rule 19b-4(f)(2)<SU>9</SU>
          <FTREF/>thereunder. At any time within 60 days of the filing of such proposed rule change, the Commission summarily may temporarily suspend such rule change if it appears to the Commission that such action is necessary or appropriate in the public interest, for the protection of investors, or otherwise in furtherance of the purposes of the Act.</P>
        <FTNT>
          <P>
            <SU>8</SU>15 U.S.C. 78s(b)(3)(A).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>9</SU>17 CFR 19b-4(f)(2).</P>
        </FTNT>
        <HD SOURCE="HD1">IV. Solicitation of Comments</HD>
        <P>Interested persons are invited to submit written data, views, and arguments concerning the foregoing, including whether the proposed rule change is consistent with the Act. Comments may be submitted by any of the following methods:</P>
        <HD SOURCE="HD2">Electronic Comments</HD>
        <P>• Use the Commission's Internet comment form (<E T="03">http://www.sec.gov/rules/sro.shtml</E>); or</P>
        <P>• Send an e-mail to<E T="03">rule-comments@sec.gov.</E>Please include File Number SR-EDGA-2011-22 on the subject line.</P>
        <HD SOURCE="HD2">Paper comments</HD>
        <P>• Send paper comments in triplicate to Elizabeth M. Murphy, Secretary, Securities and Exchange Commission, 100 F Street, NE., Washington, DC 20549-1090.</P>
        

        <FP>All submissions should refer to File Number SR-EDGA-2011-22. This file number should be included on the subject line if e-mail is used. To help the Commission process and review your comments more efficiently, please use only one method. The Commission will post all comments on the Commission's Internet Web site (<E T="03">http://www.sec.gov/rules/sro.shtml</E>). Copies of the submission, all subsequent amendments, all written statements with respect to the proposed rule change that are filed with the Commission, and all written communications relating to the proposed rule change between the Commission and any person, other than those that may be withheld from the public in accordance with the provisions of 5 U.S.C. 552, will be available for Web site viewing and printing in the Commission's Public Reference Room, 100 F Street, NE., Washington, DC 20549, on official business days between the hours of 10 a.m. and 3 p.m. Copies of the filing also will be available for inspection and copying at the principal office of the Exchange. All comments received will be posted without change; the Commission does not edit personal identifying information from submissions. You should submit only information that you wish to make available publicly. All submissions should refer to File Number SR-EDGA-2011-22 and should be submitted on or before August 22, 2011.</FP>
        <SIG>
          <P>For the Commission, by the Division of Trading and Markets, pursuant to delegated authority.<SU>10</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>10</SU>17 CFR 200.30-3(a)(12).</P>
          </FTNT>
          <NAME>Elizabeth M. Murphy,</NAME>
          <TITLE>Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19327 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 8011-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">SECURITIES AND EXCHANGE COMMISSION</AGENCY>
        <DEPDOC>[Release No. 34-64966; File No. SR-NYSEAmex-2011-50]</DEPDOC>
        <SUBJECT>Self-Regulatory Organizations; NYSE Amex LLC; Notice of Filing and Immediate Effectiveness of Proposed Rule Change Amending Commentary .07 to NYSE Amex Rule 904 To Increase Position Limits for Options on the SPDR® S&amp;P 500® Exchange-Traded Fund, Which List and Trade Under the Option Symbol SPY, and To Update the Names and One Trading Symbol for the Options Reflected Therein, Including SPY</SUBJECT>
        <DATE>July 26, 2011.</DATE>
        <P>Pursuant to Section 19(b)(1)<SU>1</SU>
          <FTREF/>of the Securities Exchange Act of 1934 (the “Act”)<SU>2</SU>
          <FTREF/>and Rule 19b-4 thereunder,<SU>3</SU>
          <FTREF/>notice is hereby given that, on July 11, 2011, NYSE Amex LLC (the “Exchange” or “NYSE Amex”) filed with the Securities and Exchange Commission (the “Commission”) the proposed rule change as described in Items I and II below, which Items have been prepared by the Exchange. The Commission is publishing this notice to solicit comments on the proposed rule change from interested persons.</P>
        <FTNT>
          <P>
            <SU>1</SU>15 U.S.C.78s(b)(1).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>2</SU>15 U.S.C. 78a.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>3</SU>17 CFR 240.19b-4.</P>
        </FTNT>
        <HD SOURCE="HD1">I. Self-Regulatory Organization's Statement of the Terms of the Substance of the Proposed Rule Change</HD>
        <P>The Exchange proposes to amend Commentary .07 to NYSE Amex Rule 904 to increase position limits for options on the SPDR® S&amp;P 500® exchange-traded fund (“SPY ETF”),<SU>4</SU>

          <FTREF/>which list and trade under the option symbol SPY, and to update the names and one trading symbol for the options reflected therein, including SPY. The text of the proposed rule change is available at the Exchange's Web site at<E T="03">http://www.nyse.com,</E>on the Commission's Web site at<E T="03">http://www.sec.gov</E>, at the Exchange's principal office, and at the Commission's Public Reference Room.</P>
        <FTNT>
          <P>
            <SU>4</SU>“SPDR®,” “Standard &amp; Poor's®,” “S&amp;P®,” “S&amp;P 500®,” and “Standard &amp; Poor's 500” are registered trademarks of Standard &amp; Poor's Financial Services LLC. The SPDR S&amp;P 500 ETF represents ownership in the SPDR S&amp;P 500 Trust, a unit investment trust that generally corresponds to the price and yield performance of the SPDR S&amp;P 500 Index.</P>
        </FTNT>
        <HD SOURCE="HD1">II. Self-Regulatory Organization's Statement of the Purpose of, and Statutory Basis for, the Proposed Rule Change</HD>

        <P>In its filing with the Commission, the self-regulatory organization included<PRTPAGE P="45900"/>statements concerning the purpose of, and basis for, the proposed rule change and discussed any comments it received on the proposed rule change. The text of those statements may be examined at the places specified in Item IV below. The Exchange has prepared summaries, set forth in sections A, B, and C below, of the most significant parts of such statements.</P>
        <HD SOURCE="HD2">A. Self-Regulatory Organization's Statement of the Purpose of, and Statutory Basis for, the Proposed Rule Change</HD>
        <HD SOURCE="HD3">1. Purpose</HD>
        <P>The purpose of the proposal is to amend Commentary .07 to NYSE Amex Rule 904 to increase position limits for SPY options from 300,000 to 900,000 contracts on the same side of the market and to update the names, and one trading symbol, for the options reflected therein, including SPY.<SU>5</SU>
          <FTREF/>The Exchange is basing this proposal on a recently approved rule change by NASDAQ OMX PHLX (“PHLX”).<SU>6</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>5</SU>By virtue of NYSE Amex Rule 905, which is not amended by this filing, exercise limits on SPY options would be the same as position limits for SPY options established in Commentary .07 to NYSE Amex Rule 904.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>6</SU>
            <E T="03">See</E>Securities Exchange Act Release No. 64695 (June 17, 2011), 76 FR 36942 (June 23, 2011) (SR-Phlx-2011-58). The Exchange commented favorably on that PHLX proposal, noting that “the continued disparate treatment of SPY options, which have a position limit and are traded on multiple exchanges, versus SPX options, which have no position limit and are traded exclusively on CBOE [the Chicago Board Options Exchange], only serves to thwart competition and harm the marketplace,” and that the “PHLX's Proposal to increase the position limits for SPY options is a step in the right direction.”<E T="03">See</E>(<E T="03">http://www.sec.gov/comments/sr-phlx-2011-58/phlx201158-1.pdf</E>).</P>
        </FTNT>
        <HD SOURCE="HD3">Background</HD>
        <P>Institutional and retail traders have greatly increased their demand for SPY options for hedging and trading purposes, such that these options have experienced an explosive gain in popularity and have been the most actively traded options in the U.S. in terms of volume for the last two years. For example, SPY options traded a total of 33,341,698 contracts across all exchanges from March 1, 2011 through March 16, 2011. In contrast, over the same time period options on the PowerShares QQQ Trust<SU>SM</SU>, Series 1 (“QQQ”<SU>SM</SU>),<SU>7</SU>
          <FTREF/>the third [sic] most actively traded option, traded a total of 8,730,718 contracts (less than 26.2% of the volume of SPY options).</P>
        <FTNT>
          <P>
            <SU>7</SU>QQQ options were formerly known as options on the Nasdaq-100 Tracking Stock<SU>SM</SU>(former option symbol QQQQ<SU>SM</SU>). NASDAQ, Nasdaq-100 Index, Nasdaq-100 Index Tracking Stock and QQQ are trade/service marks of The Nasdaq Stock Market, Inc. and have been licensed for use by Invesco PowerShares Capital Management LLC.</P>
        </FTNT>
        <P>Currently, SPY options have a position limit of only 300,000 contracts on the same side of the market while QQQ options, which are comparable to SPY options but exhibit significantly lower volume, have a position limit of 900,000 contracts on the same side of the market. The Exchange believes that SPY options should, like options on QQQ, have a position limit of 900,000 contracts. Given the increase in volume and continuous unprecedented demand for trading SPY options, the Exchange believes that the current position limit of 300,000 contracts is entirely too low and is a deterrent to the optimal use of the product for hedging and trading purposes. There are multiple reasons to increase the position limit for SPY options.</P>
        <P>First, traders have informed the Exchange that the current SPY option position limit of 300,000 contracts, which has remained flat for more than five years despite the tremendous trading volume increase, is no longer sufficient for optimal trading and hedging purposes. SPY options are, as noted, used by large institutions and traders as a means to invest in or hedge the overall direction of the market. Second, SPY options are one-tenth the size of options on the S&amp;P 500 Index, traded under the symbol SPX.<SU>8</SU>
          <FTREF/>Thus, a position limit of 300,000 contracts in SPY options is equivalent to a 30,000 contract position limit in options on SPX. Traders who trade SPY options to hedge positions in SPX options (and the SPY ETF) have indicated on several occasions that the current position limit for SPY options is simply too restrictive, which may adversely affect their (and the Exchange's) ability to provide liquidity in this product. Finally, the products that are perhaps most comparable to SPY options, namely options on QQQ, are subject to a 900,000 contract position limit on the same side of the market.<SU>9</SU>
          <FTREF/>This has, in light of the huge run-up in SPY option trading making them the number one nationally-ranked option in terms of volume, resulted in a skewed and unacceptable SPY option position limit. Specifically, the position limit for SPY options at 300,000 contracts is but 33% of the position limit for the less active options on QQQ at 900,000 contracts.<SU>10</SU>
          <FTREF/>The Exchange proposes that SPY options similarly be subject to a position limit of 900,000 contracts.</P>
        <FTNT>
          <P>

            <SU>8</SU>CBOE, which exclusively lists and trades SPX options, has established that there are no position limits on SPX options.<E T="03">See</E>CBOE Rule 24.4 and Securities Exchange Act Release No. 44994 (October 26, 2001), 66 FR 55722 (November 2, 2001) (SR-CBOE-2001-22).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>9</SU>
            <E T="03">See</E>Commentary .07 to Rule 904 and Securities Exchange Act Release No. 57415 (March 3, 2008), 73 FR 12479 (March 7, 2008) (SR-Amex-2008-16).<E T="03">See also</E>Securities Exchange Act Release No. 51316 (March 3, 2005), 70 FR 12251 (March 11, 2005) (SR-Amex-2005-029).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>10</SU>Similarly to SPY options being one-tenth the size of options on SPX, QQQ options are also one-tenth the size of options on the related index NASDAQ-100 Index (option symbol NDX). The position limit for QQQ options and its related index NDX have a comparable relationship to that of SPY options and SPX. That is, the position limit for options on QQQ is 900,000 contracts and there is no position limit for NDX options.</P>
        </FTNT>
        <P>The volume and notional value of SPY options and QQQ options as well as the volume and market capitalizations of their underlying ETFs, are set forth below:</P>
        <GPOTABLE CDEF="xs80,xs80,r25,r35,r55,r35" COLS="6" OPTS="L2,tp0,i1">
          <TTITLE/>
          <BOXHD>
            <CHED H="1">Option national rank 2010</CHED>
            <CHED H="1">Option symbol</CHED>
            <CHED H="1">Name of underlying ETF</CHED>
            <CHED H="1">Option ADV 2010</CHED>
            <CHED H="1">Option notional value* as of<LI>December 31, 2010</LI>
            </CHED>
            <CHED H="1">Current options<LI>position limit</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">1</ENT>
            <ENT>SPY</ENT>
            <ENT>SPDR S&amp;P 500</ENT>
            <ENT>3,625,904 contracts</ENT>
            <ENT>$177,823,76 million</ENT>
            <ENT>300,000 contracts.</ENT>
          </ROW>
          <ROW>
            <ENT I="01">4</ENT>
            <ENT>QQQ</ENT>
            <ENT>Powershares QQQ Trust</ENT>
            <ENT>963,502 contracts</ENT>
            <ENT>$27,141,91 million</ENT>
            <ENT>900,000 contracts.</ENT>
          </ROW>
        </GPOTABLE>
        <GPOTABLE CDEF="xs80,r35,r25,r25,r35" COLS="5" OPTS="L2,tp0,i1">
          <TTITLE/>
          <BOXHD>
            <CHED H="1">ETF Nat'l rank 2010</CHED>
            <CHED H="1">Name of ETF</CHED>
            <CHED H="1">ETF ADV 2010</CHED>
            <CHED H="1">ETF market<LI>capitalization</LI>
              <LI>December 31, 2010</LI>
            </CHED>
            <CHED H="1">ETF average<LI>dollar volume</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">1</ENT>
            <ENT>SPDR S&amp;P 500</ENT>
            <ENT>210,232,241 shares</ENT>
            <ENT>$90,280.71 million</ENT>
            <ENT>$20,794 million</ENT>
          </ROW>
          <ROW>
            <ENT I="01">3</ENT>
            <ENT>Powershares QQQ Trust</ENT>
            <ENT>85,602,200 shares</ENT>
            <ENT>$23,564.8 million</ENT>
            <ENT>$3,593 million</ENT>
          </ROW>
          <TNOTE>* Notional value is calculated as follows: OI × Close × 100; where OI = underlying security's open interest (in contracts), Close = closing price of underlying security on 12/31/2010.</TNOTE>
        </GPOTABLE>
        <PRTPAGE P="45901"/>

        <P>The Exchange notes that the Large Option Position Reporting requirement in NYSE Amex Rule 906 would continue to apply. Rule 906 requires ATP Holders to file a report with the Exchange with respect to each account in which the ATP Holder has an interest; each account of a partner, officer, director, trustee or employee of such ATP Holder; and each customer account that has established an aggregate position (whether long or short) that meets certain determined thresholds (<E T="03">e.g.,</E>200 or more option contracts if the underlying security is a stock or Exchange-Traded Fund Share). Rule 906 also permits the Exchange to impose a higher margin requirement upon the account of an ATP Holder when it determines that the account maintains an under-hedged position. Furthermore, large stock holdings must be disclosed to the Commission by way of Schedules 13D or 13G.<SU>11</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>11</SU>17 CFR 240.13d-1</P>
        </FTNT>
        <P>Monitoring accounts maintaining large positions provides the Exchange with the information necessary to determine whether to impose additional margin and/or whether to assess capital charges upon an ATP Holder carrying the account. In addition, the Commission's net capital rule, Rule 15c3-1 under the Securities Exchange Act of 1934 (“Act”),<SU>12</SU>
          <FTREF/>imposes a capital charge on ATP Holders to the extent of any margin deficiency resulting from the higher margin requirement, which should serve as an additional form of protection.</P>
        <FTNT>
          <P>
            <SU>12</SU>17 CFR 240.15c3-1.</P>
        </FTNT>
        <P>The Exchange believes that position and exercise limits, at their current levels, no longer serve their stated purpose. There has been a steadfast and significant increase over the last decade in the overall volume of exchange-traded options; position limits, however, have not kept up with the volume. Part of this volume is attributable to a corresponding increase in the number of overall market participants, which has, in turn, brought about additional depth and increased liquidity in exchange-traded options.<SU>13</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>

            <SU>13</SU>The Commission has previously observed that: “Since the inception of standardized options trading, the options exchanges have had rules imposing limits on the aggregate number of options contracts that a member or customer could hold or exercise. These rules are intended to prevent the establishment of options positions that can be used or might create incentives to manipulate or disrupt the underlying market so as to benefit the options position. In particular, position and exercise limits are designed to minimize the potential for mini-manipulations and for corners or squeezes of the underlying market. In addition such limits serve to reduce the possibility for disruption of the options market itself, especially in illiquid options classes.”<E T="03">See</E>Securities Exchange Act Release No. 39489 (December 24, 1997), 63 FR 276, 278 (January 5, 1998) (SR-CBOE-97-11) (footnote omitted).</P>
        </FTNT>
        <P>As the anniversary of listed options trading approaches its fortieth year, the Exchange believes that the existing surveillance procedures and reporting requirements at the Exchange, other options exchanges, and at the several clearing firms are capable of properly identifying unusual and/or illegal trading activity. In addition, routine oversight inspections of the Exchange's regulatory programs by the Commission have not uncovered any material inconsistencies or shortcomings in the manner in which the Exchange's market surveillance is conducted. These procedures utilize daily monitoring of market movements via automated surveillance techniques to identify unusual activity in both options and underlying stocks.<SU>14</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>14</SU>These procedures have been effective for the surveillance of SPY options trading and will continue to be employed.</P>
        </FTNT>
        <P>Finally, the Exchange believes that while position limits on options on QQQ, which as noted are similar to SPY options, has been gradually expanded from 75,000 contracts to the current level of 900,000 contracts since 2005, there have been no adverse effects on the market as a result of this position limit increase.<SU>15</SU>
          <FTREF/>Likewise, there have been no adverse effects on the market from expanding the position limit for SPY options from 75,000 contracts to the current level of 300,000 contracts in 2005.<SU>16</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>15</SU>
            <E T="03">See supra</E>note 9.<E T="03">See</E>e-mail from Joseph Corcoran, Chief Counsel, NYSE to Arisa Tinaves, Special Counsel, Division of Trading and Markets, dated July 19, 2011.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>16</SU>
            <E T="03">See</E>Securities Exchange Act Release No. 51043 (January 14, 2005), 70 FR 3402 (January 24, 2005) (SR-Amex-2005-06).</P>
        </FTNT>
        <P>The Exchange believes that restrictive option position limits prevent large customers, such as mutual funds and pension funds, from using options to gain meaningful exposure to and hedging protection through the use of SPY options. This can result in lost liquidity in both the options market and the equity market. The proposed position limit increase would remedy this situation to the benefit of large as well as retail traders, investors, and public customers. The Exchange believes that increasing position and exercise limits for SPY options would lead to a more liquid and competitive market environment for SPY options that would benefit customers interested in this product.</P>
        <HD SOURCE="HD3">Update to Names</HD>
        <P>The Exchange proposes non-substantive technical changes to update the names and one trading symbol for the option products specifically identified within Commentary .07 to NYSE Amex Rule 904. This change would result in Commentary .07 reflecting the current names and symbols by which these products trade in the marketplace as follows: Nasdaq-100 Tracking Stock (QQQQ) changes to PowerShares QQQ Trust<SU>SM</SU>, Series 1 (QQQ); Standard &amp; Poor's Depositary Receipts Trust (SPDR) changes to SPDR® S&amp;P 500® ETF (SPY); and DIAMONDS Trust changes to SPDR® Dow Jones Industrial Average<SU>SM</SU>ETF Trust (DIA).</P>
        <HD SOURCE="HD3">2. Statutory Basis</HD>
        <P>The proposed rule change is consistent with Section 6(b)<SU>17</SU>
          <FTREF/>of the Act, in general, and furthers the objectives of Section 6(b)(5),<SU>18</SU>
          <FTREF/>in particular, in that it is designed to prevent fraudulent and manipulative acts and practices, to promote just and equitable principles of trade, to foster cooperation and coordination with persons engaged in facilitating transactions in securities, to remove impediments to and perfect the mechanism of a free and open market and a national market system and, in general, to protect investors and the public interest. The Exchange is proposing to expand the position limits on SPY options. The Exchange believes that this proposal would be beneficial to large market makers (which generally have the greatest potential and actual ability to provide liquidity and depth in the product), as well as retail traders, investors, and public customers.</P>
        <FTNT>
          <P>
            <SU>17</SU>15 U.S.C. 78f(b).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>18</SU>15 U.S.C. 78f(b)(5).</P>
        </FTNT>
        <HD SOURCE="HD2">B. Self-Regulatory Organization's Statement on Burden on Competition</HD>
        <P>The Exchange does not believe that the proposed rule change will impose any burden on competition that is not necessary or appropriate in furtherance of the purposes of the Act.</P>
        <HD SOURCE="HD2">C. Self-Regulatory Organization's Statement on Comments on the Proposed Rule Change Received From Members, Participants, or Others</HD>
        <P>The Exchange has neither solicited nor received written comments on the proposed rule change.</P>
        <HD SOURCE="HD1">III. Date of Effectiveness of the Proposed Rule Change and Timing for Commission Action</HD>

        <P>Because the proposed rule change does not (i) Significantly affect the protection of investors or the public interest; (ii) impose any significant burden on competition; and (iii) become<PRTPAGE P="45902"/>operative prior to 30 days from the date on which it was filed, or such shorter time as the Commission may designate, if consistent with the protection of investors and the public interest, provided that the self-regulatory organization has given the Commission written notice of its intent to file the proposed rule change at least five business days prior to the date of filing of the proposed rule change or such shorter time as designated by the Commission, the proposed rule change has become effective pursuant to Section 19(b)(3)(A) of the Act<SU>19</SU>
          <FTREF/>and Rule 19b-4(f)(6)(iii) thereunder.<SU>20</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>19</SU>15 U.S.C. 78s(b)(3)(A).</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>20</SU>17 CFR 240.19b-4(f)(6).</P>
        </FTNT>
        <P>A proposed rule change filed under Rule 19b-4(f)(6)<SU>21</SU>
          <FTREF/>normally does not become operative prior to 30 days after the date of the filing. However, pursuant to Rule 19b-4(f)(6)(iii),<SU>22</SU>
          <FTREF/>the Commission may designate a shorter time if such action is consistent with the protection of investors and the public interest. The Exchange has requested that the Commission waive the 30-day operative delay so that the proposal may become operative immediately upon filing. The Commission believes that waiving the 30-day operative delay is consistent with the protection of investors and the public interest, because increasing position and exercise limits for SPY options would lead to a more liquid and competitive market environment that would benefit customers interested in this product. Additionally, it will enable the Exchange's position and exercise limits for SPY options to be consistent with those of other exchanges that have already adopted the higher position and exercise limits. Therefore, the Commission designates the proposal operative upon filing.<SU>23</SU>
          <FTREF/>
        </P>
        <FTNT>
          <P>
            <SU>21</SU>17 CFR 240.19b-4(f)(6). In addition, Rule 19b-4(f)(6)(iii) requires that a self-regulatory organization submit to the Commission written notice of its intent to file the proposed rule change, along with a brief description and text of the proposed rule change, at least five business days prior to the filing of the proposed rule change, or such shorter time as designated by the Commission. The Commission notes that the Exchange has satisfied this requirement.</P>
        </FTNT>
        <FTNT>
          <P>
            <SU>22</SU>17 CFR 240.19b-4(f)(6)(iii).</P>
        </FTNT>
        <FTNT>
          <P>

            <SU>23</SU>For purposes only of waiving the 30-day operative delay, the Commission has considered the proposed rule's impact on efficiency, competition, and capital formation.<E T="03">See</E>15 U.S.C. 78c(f).</P>
        </FTNT>
        <P>At any time within 60 days of the filing of such proposed rule change, the Commission summarily may temporarily suspend such rule change if it appears to the Commission that such action is necessary or appropriate in the public interest, for the protection of investors, or otherwise in furtherance of the purposes of the Act.</P>
        <HD SOURCE="HD1">IV. Solicitation of Comments</HD>
        <P>Interested persons are invited to submit written data, views, and arguments concerning the foregoing, including whether the proposed rule change is consistent with the Act. Comments may be submitted by any of the following methods:</P>
        <HD SOURCE="HD2">Electronic Comments</HD>
        <P>• Use the Commission's Internet comment form (<E T="03">http://www.sec.gov/rules/sro.shtml</E>); or</P>
        <P>• Send an e-mail to<E T="03">rule-comments@sec.gov.</E>Please include File Number SR-NYSEAmex-2011-50 on the subject line.</P>
        <HD SOURCE="HD2">Paper Comments</HD>
        <P>• Send paper comments in triplicate to Elizabeth M. Murphy, Secretary, Securities and Exchange Commission, 100 F Street, NE., Washington DC 20549-1090.</P>
        

        <FP>All submissions should refer to File Number SR-NYSEAmex-2011-50. This file number should be included on the subject line if e-mail is used. To help the Commission process and review your comments more efficiently, please use only one method. The Commission will post all comments on the Commission's Internet Web site (<E T="03">http://www.sec.gov/rules/sro.shtml</E>). Copies of the submission, all subsequent amendments, all written statements with respect to the proposed rule change that are filed with the Commission, and all written communications relating to the proposed rule change between the Commission and any person, other than those that may be withheld from the public in accordance with the provisions of 5 U.S.C. 552, will be available for Web site viewing and printing in the Commission's Public Reference Room, 100 F Street, NE., Washington, DC 20549, on official business days between the hours of 10 a.m. and 3 p.m. Copies of such filing also will be available for inspection and copying at the principal office of the Exchange. All comments received will be posted without change; the Commission does not edit personal identifying information from submissions. You should submit only information that you wish to make available publicly. All submissions should refer to File No. SR-NYSEAmex-2011-50 and should be submitted on or before August 22, 2011.</FP>
        <SIG>
          <P>For the Commission, by the Division of Trading and Markets, pursuant to delegated authority.<SU>24</SU>
            <FTREF/>
          </P>
          <FTNT>
            <P>
              <SU>24</SU>17 CFR 200.30-3(a)(12).</P>
          </FTNT>
          <NAME>Elizabeth M. Murphy,</NAME>
          <TITLE>Secretary.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19328 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 8011-01-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">SOCIAL SECURITY ADMINISTRATION</AGENCY>
        <SUBJECT>Agency Information Collection Activities: Proposed Request and Comment Request</SUBJECT>
        <P>The Social Security Administration (SSA) publishes a list of information collection packages requiring clearance by the Office of Management and Budget (OMB) in compliance with Public Law 104-13, the Paperwork Reduction Act of 1995, effective October 1, 1995. This notice includes revisions and an extension of OMB-approved information collections, and one request for a new information collection.</P>
        <P>SSA is soliciting comments on the accuracy of the agency's burden estimate; the need for the information; its practical utility; ways to enhance its quality, utility, and clarity; and ways to minimize burden on respondents, including the use of automated collection techniques or other forms of information technology. Mail, email, or fax your comments and recommendations on the information collection(s) to the OMB Desk Officer and SSA Reports Clearance Officer at the following addresses or fax numbers.</P>
        

        <FP SOURCE="FP-1">(OMB),  Office of Management and Budget,  Attn: Desk Officer for SSA,  Fax: 202-395-6974, E-mail address:<E T="03">OIRA_Submission@omb.eop.gov.</E>
        </FP>

        <FP SOURCE="FP-1">(SSA) Social Security Administration, DCBFM, Attn: Reports Clearance Officer, 1333 Annex Building, 6401 Security Blvd., Baltimore, MD 21235,  Fax: 410-965-6400,E-mail address:<E T="03">OPLM.RCO@ssa.gov.</E>
        </FP>
        
        <P>I. The information collection below is pending at SSA. SSA will submit it to OMB within 60 days from the date of this notice. To be sure we consider your comments, we must receive them no later than September 30, 2011. Individuals can obtain copies of the collection instrument by calling the SSA Reports Clearance Officer at 410-965-8783 or by writing to the above email address.</P>
        <P>
          <E T="03">Report on Individual with Mental Impairment—20 CFR 404.1513 &amp; 416.913—0960-0058.</E>SSA uses Form SSA-824 to obtain medical evidence from medical sources who have treated a Social Security disability claimant for<PRTPAGE P="45903"/>a mental impairment. SSA uses the information from this form to establish whether a claimant filing for disability benefits has a mental impairment that meets the statutory definition of disability in accordance with the Social Security Act. The respondents are mental impairment treatment providers.</P>
        <P>
          <E T="03">Type of Request:</E>Extension of an OMB-approved information collection.</P>
        <GPOTABLE CDEF="s50,12,12,12,12" COLS="5" OPTS="L2,tp0,i1">
          <TTITLE/>
          <BOXHD>
            <CHED H="1">Type of respondents</CHED>
            <CHED H="1">Number of<LI>respondents</LI>
            </CHED>
            <CHED H="1">Frequency of response</CHED>
            <CHED H="1">Average<LI>burden per</LI>
              <LI>response</LI>
              <LI>(minutes)</LI>
            </CHED>
            <CHED H="1">Total annual burden<LI>(hours)</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Private Sector</ENT>
            <ENT>25,000</ENT>
            <ENT>1</ENT>
            <ENT>36</ENT>
            <ENT>15,000</ENT>
          </ROW>
          <ROW RUL="n,s">
            <ENT I="01">State Disability Determination Services (State/Local Government)</ENT>
            <ENT>25,000</ENT>
            <ENT>1</ENT>
            <ENT>36</ENT>
            <ENT>15,000</ENT>
          </ROW>
          <ROW>
            <ENT I="03">Totals</ENT>
            <ENT>50,000</ENT>
            <ENT/>
            <ENT/>
            <ENT>30,000</ENT>
          </ROW>
        </GPOTABLE>
        <P>II. SSA submitted the information collections below to OMB for clearance. Your comments regarding the information collections would be most useful if OMB and SSA receive them within 30 days from the date of this publication. To be sure we consider your comments, we must receive them no later than August 31, 2011. Individuals can obtain copies of the OMB clearance packages by calling the SSA Reports Clearance Officer at 410-965-8783 or by writing to the above email address.</P>
        <P>1.<E T="03">Social Security's Public Credentialing and Authentication Process—20 CFR 401.45—0960-NEW.</E>Social Security is introducing a stronger citizen authentication process that will enable a new user to experience and access more electronic services.</P>
        <HD SOURCE="HD1">Background</HD>
        <P>Authentication is the foundation for secure, online transactions. Identity authentication is the process of determining with confidence that people are who they claim to be during a remote, automated session. It comprises three distinct factors: something you know, something you have, and something you are. Single-factor authentication uses one of these factors, and multi-factor authentication uses two or more of these factors.</P>
        <HD SOURCE="HD1">SSA's New Authentication Process</HD>
        <P>Social Security's new process features credential issuance, account management, and single- and multi-factor authentication. With this process, we are working toward offering consistent authentication across Social Security's secured online services, and eventually to Social Security's automated telephone services. We will allow our users to maintain one User ID, consisting of a self-selected Username and Password, to access multiple Social Security electronic services. This new process: (1) Enables the authentication of users of Social Security's sensitive electronic services; and (2) streamlines access to those services.</P>
        <P>Social Security is developing a new authentication strategy that will:</P>
        <P>• Issue a single User Identification (ID) for personal, business, and governmental transactions;</P>
        <P>• Offer a variety of authentication options to meet the changing needs of the public;</P>
        <P>• Partner with an external data provider to help us verify the identity of our online customers;</P>
        <P>• Comply with relevant standards;</P>
        <P>• Offer access to some of Social Security's more sensitive workloads online, while providing a high level of confidence in the identity of the person requesting access to these services;</P>
        <P>• Offer an in-person process for those who are uncomfortable with or unable to use the Internet registration process; and</P>
        <P>• Balance security with ease of use.</P>
        <HD SOURCE="HD1">New Authentication Process Features</HD>
        <P>SSA's new process will include the following key components: (1) Registration and identity verification; (2) enhancement of the User ID; and (3) authentication. The registration process is a one-time activity for the respondents. The respondent provides some personal information, and we use this to verify respondent identity. Respondents then select their User ID (Username &amp; Password). Respondents will log in with this User ID each time they access SSA's online services. SSA will also allow respondents to increase the security of their credential by adding a second authentication factor.</P>
        <HD SOURCE="HD1">Information SSA Will Request As Part of the Process</HD>
        <P>SSA will ask for respondents' personal information, which may include:</P>
        
        <FP SOURCE="FP-1">• Name</FP>
        <FP SOURCE="FP-1">• Social Security number (SSN)</FP>
        <FP SOURCE="FP-1">• Date of Birth</FP>
        <FP SOURCE="FP-1">• Address—mailing and residential</FP>
        <FP SOURCE="FP-1">• Telephone number</FP>
        <FP SOURCE="FP-1">• Email address</FP>
        <FP SOURCE="FP-1">• Financial information</FP>
        <FP SOURCE="FP-1">• Cell phone number</FP>
        <FP SOURCE="FP-1">• Responses to an identity quiz (multiple choice format questions keyed to specific data identity thieves will not be able to answer)</FP>
        <FP SOURCE="FP-1">• Password reset questions</FP>
        
        <P>This collection of information, or a subset of it, is required for respondents who want to conduct business with Social Security via the Internet or our automated 800 number. We will collect this information via the Internet on SSA's public-facing website. We also offer an in-person identification verification process for individuals who cannot or are not willing to register online. We do not ask for financial information with the in-person process. In addition, if individuals opt for the enhanced or upgraded account, they will also receive a text message on their cell phones (this serves as the second factor for authentication) each time they log into SSA's online services.</P>
        <HD SOURCE="HD1">Advantages of the New Authentication Strategy</HD>
        <P>This new authentication strategy will provide a user-friendly way for the public to conduct extended business with Social Security online instead of visiting the local servicing office or requesting information over the phone. Individuals will have real-time access to their sensitive Social Security information in a safe and secured web environment.</P>
        <HD SOURCE="HD1">Burden Information</HD>
        <P>The respondents for this information collection request are individuals who choose to use the Internet or Automated Telephone Response System to conduct business with SSA.</P>
        <P>
          <E T="03">Type of Request:</E>Request for a new information collection.<PRTPAGE P="45904"/>
        </P>
        <GPOTABLE CDEF="s50,12,12,12,12" COLS="5" OPTS="L2,tp0,i1">
          <TTITLE/>
          <BOXHD>
            <CHED H="1">Modality of completion</CHED>
            <CHED H="1">Number of<LI>respondents</LI>
            </CHED>
            <CHED H="1">Frequency of response</CHED>
            <CHED H="1">Average<LI>burden per response</LI>
              <LI>(minutes)</LI>
            </CHED>
            <CHED H="1">Total annual burden hours<LI>(hours)</LI>
            </CHED>
          </BOXHD>
          <ROW>
            <ENT I="01">Internet Requestors</ENT>
            <ENT>17,900,000</ENT>
            <ENT>1</ENT>
            <ENT>8</ENT>
            <ENT>2,386,667</ENT>
          </ROW>
          <ROW RUL="n,s">
            <ENT I="01">In-Person (Intranet) Requestors</ENT>
            <ENT>5,800,000</ENT>
            <ENT>1</ENT>
            <ENT>8</ENT>
            <ENT>773,333</ENT>
          </ROW>
          <ROW>
            <ENT I="03">Totals</ENT>
            <ENT>23,700,000</ENT>
            <ENT/>
            <ENT/>
            <ENT>3,160,000</ENT>
          </ROW>
        </GPOTABLE>
        <P>2.<E T="03">Marriage Certification—20 CFR 404.725—0960-0009.</E>SSA uses Form SSA-3 to determine if a spouse claimant has the necessary relationship to the SSN holder (i.e., the worker) to qualify for the worker's Title II benefits. The respondents are applicants for spouse's benefits.  This is a correction notice. SSA published this information collection as an extension on May 26, 2011 at 76 FR 30749. Since we are revising the Privacy Act Statement, this is now a revision of an OMB-approved information collection.</P>
        <P>
          <E T="03">Type of Request:</E>Revision of an OMB-approved information collection.</P>
        <P>
          <E T="03">Number of Respondents:</E>180,000.</P>
        <P>
          <E T="03">Frequency of Response:</E>1.</P>
        <P>
          <E T="03">Average Burden Per Response:</E>5 minutes.</P>
        <P>
          <E T="03">Estimated Annual Burden:</E>15,000 hours.</P>
        <P>3.<E T="03">Statement Regarding Date of Birth and Citizenship—20CFR 404.716—0960-0016.</E>When individuals apply for Social Security benefits and cannot provide preferred methods of proving age or citizenship, SSA uses Form SSA-702 to establish these facts. Specifically, SSA uses the SSA-702 to establish age as a factor of entitlement to Social Security benefits, or U.S. citizenship as a payment factor. Respondents are individuals with knowledge about the date of birth or citizenship of applicants filing for one or more Social Security benefits who need to establish age or citizenship.</P>
        <P>
          <E T="03">Type of Request:</E>Revision of an OMB-approved information collection.</P>
        <P>
          <E T="03">Number of Respondents:</E>1,200.</P>
        <P>
          <E T="03">Frequency of Response:</E>1.</P>
        <P>
          <E T="03">Average Burden per Response:</E>10 minutes.</P>
        <P>
          <E T="03">Estimated Annual Burden:</E>200.</P>
        <SIG>
          <DATED>Dated: July 27, 2011<E T="03">.</E>
          </DATED>
          <NAME>Faye Lipsky,</NAME>
          <TITLE>Reports Clearance Officer,  Center for Reports Clearance,  Social Security Administration.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19406 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4191-02-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF TRANSPORTATION</AGENCY>
        <SUBAGY>Pipeline and Hazardous Materials Safety Administration</SUBAGY>
        <DEPDOC>[Docket No. PHMSA-2011-0178]</DEPDOC>
        <SUBJECT>Pipeline Safety: Information Collection Activities</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Pipeline and Hazardous Materials Safety Administration (PHMSA), DOT.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice and request for comments.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>In accordance with the Paperwork Reduction Act of 1995, PHMSA invites comments on certain information collections pertaining to pipeline safety for which PHMSA intends to request renewal from the Office of Management and Budget (OMB).</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Interested persons are invited to submit comments on or before September 30, 2011.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>Comments may be submitted in the following ways:</P>
          <P>
            <E T="03">E-Gov Web Site: http://www.regulations.gov.</E>This site allows the public to enter comments on any<E T="04">Federal Register</E>notice issued by any agency.</P>
          <P>
            <E T="03">Fax:</E>1-202-493-2251.</P>
          <P>
            <E T="03">Mail:</E>Docket Management Facility; U.S. Department of Transportation, 1200 New Jersey Avenue, SE., West Building, Room W12-140, Washington, DC 20590-0001.</P>
          <P>
            <E T="03">Hand Delivery:</E>Room W12-140 on the ground level of the West Building, 1200 New Jersey Avenue, SE., Washington, DC, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays.</P>
          <P>
            <E T="03">Instructions:</E>Identify the docket number, PHMSA-2011-0178, at the beginning of your comments. Note that all comments received will be posted without change to<E T="03">http://www.regulations.gov,</E>including any personal information provided. You should know that anyone is able to search the electronic form of all comments received into any of our dockets by the name of the individual submitting the comment (or signing the comment, if submitted on behalf of an association, business, labor union, etc.). Therefore, you may want to review DOT's complete Privacy Act Statement in the<E T="04">Federal Register</E>published on April 11, 2000 (65 FR 19477) or visit<E T="03">http://www.regulations.gov</E>before submitting any such comments.</P>
          <P>
            <E T="03">Docket:</E>For access to the docket or to read background documents or comments, go to<E T="03">http://www.regulations.gov</E>at any time or to Room W12-140 on the ground level of the West Building, 1200 New Jersey Avenue, SE., Washington, DC, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays. If you wish to receive confirmation of receipt of your written comments, please include a self-addressed, stamped postcard with the following statement: “Comments on PHMSA-2011-0178.” The Docket Clerk will date stamp the postcard prior to returning it to you via the U.S. mail. Please note that due to delays in the delivery of U.S. mail to Federal offices in Washington, DC, we recommend that persons consider an alternative method (Internet, fax, or professional delivery service) of submitting comments to the docket and ensuring their timely receipt at DOT.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
          <P>Angela Dow by telephone at 202-366-1246, by fax at 202-366-4566, or by mail at U.S. Department of Transportation, Pipeline and Hazardous Materials Safety Administration, 1200 New Jersey Avenue, SE., PHP-30, Washington, DC 20590-0001.</P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>

        <P>Section 1320.8(d), Title 5, Code of Federal Regulations, requires PHMSA to provide interested members of the public and affected agencies an opportunity to comment on information collection and recordkeeping requests. This notice identifies several information collection requests that PHMSA will be submitting to OMB for renewal. The following information is provided for each information collection: (1) Title of the information collection; (2) OMB control number; (3) Current expiration date; (4) Type of request; (5) Abstract of the information collection activity; (6) Description of affected public; (7) Estimate of total annual reporting and recordkeeping burden; and (8) Frequency of collection. PHMSA will<PRTPAGE P="45905"/>request a three-year term of approval for each information collection activity. PHMSA requests comments on the following information collections:</P>
        <P>
          <E T="03">Title:</E>Requirements for Liquefied Natural Gas (LNG) Facilities.</P>
        <P>
          <E T="03">OMB Control Number:</E>2137-0048.</P>
        <P>
          <E T="03">Current Expiration Date:</E>1/31/2012.</P>
        <P>
          <E T="03">Abstract:</E>Operators of liquefied natural gas facilities are required under 49 CFR part 193 to maintain records, make reports, and provide information to PHMSA and State pipeline safety agencies concerning the operations of their facilities. The information aids Federal and state pipeline safety inspectors in conducting compliance inspections and investigating incidents.</P>
        <P>
          <E T="03">Affected Public:</E>Operators of Liquefied Natural Gas Facilities.</P>
        <P>
          <E T="03">Annual Reporting and Recordkeeping Burden:</E>
        </P>
        
        <FP SOURCE="FP-1">
          <E T="03">Total Annual Responses:</E>101.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Total Annual Burden Hours:</E>12,120.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Frequency of Collection:</E>On Occasion.</FP>
        
        <P>
          <E T="03">Title:</E>Record Keeping for Natural Gas Pipeline Operators.</P>
        <P>
          <E T="03">OMB Control Number:</E>2137-0049.</P>
        <P>
          <E T="03">Current Expiration Date:</E>1/31/2012.</P>
        <P>
          <E T="03">Abstract:</E>Operators of gas pipelines are required under 49 CFR part 192 to maintain records, make reports, and provide information to PHMSA and State pipeline safety agencies concerning the operations of their pipelines. The information aids Federal and state pipeline safety inspectors in conducting compliance inspections and investigating incidents.</P>
        <P>
          <E T="03">Affected Public:</E>Operators of Natural Gas Pipeline Systems.</P>
        <P>
          <E T="03">Annual Reporting and Recordkeeping Burden:</E>
        </P>
        
        <FP SOURCE="FP-1">
          <E T="03">Total Annual Responses:</E>2,300.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Total Annual Burden Hours:</E>940,454.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Frequency of collection:</E>On occasion.</FP>
        
        <P>
          <E T="03">Title:</E>Pipeline Safety: Excess Flow Valves—Customer Notification.</P>
        <P>
          <E T="03">OMB Control Number:</E>2137-0593.</P>
        <P>
          <E T="03">Current Expiration Date:</E>1/31/2012.</P>
        <P>
          <E T="03">Abstract:</E>Pipeline operators are required to provide notifications about excess flow valves to service line customers as described in § 192.383. Upon request, an operator must make documentation of compliance available to PHMSA or the appropriate state regulatory agency.</P>
        <P>
          <E T="03">Affected Public:</E>Pipeline Operators.</P>
        <P>
          <E T="03">Annual Reporting and Recordkeeping Burden:</E>
        </P>
        
        <FP SOURCE="FP-1">
          <E T="03">Total Annual Responses:</E>900,000.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Total Annual Burden Hours:</E>18,000.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Frequency of collection:</E>On Occasion.</FP>
        
        <P>
          <E T="03">Title:</E>Customer Owned Service Lines.</P>
        <P>
          <E T="03">OMB Control Number:</E>2137-0594.</P>
        <P>
          <E T="03">Current Expiration Date:</E>1/31/2012.</P>
        <P>
          <E T="03">Abstract:</E>Operators of gas service lines who do not maintain certain buried piping on behalf of their customers must provide notification about maintenance to those customers (§ 192.16). Upon request, an operator must make documentation of compliance available to PHMSA or the appropriate state regulatory agency.</P>
        <P>
          <E T="03">Affected Public:</E>Natural Gas Pipeline Operators.</P>
        <P>
          <E T="03">Annual Reporting and Recordkeeping Burden:</E>
        </P>
        
        <FP SOURCE="FP-1">
          <E T="03">Total Annual Responses:</E>550, 000.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Total Annual Burden Hours:</E>9,167.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Frequency of collection:</E>On Occasion.</FP>
        
        <P>
          <E T="03">Title:</E>Pipeline Safety: Qualification of Pipeline Safety, Training.</P>
        <P>
          <E T="03">OMB Control Number:</E>2137-0600.</P>
        <P>
          <E T="03">Current Expiration Date:</E>2/29/2012.</P>
        <P>
          <E T="03">Abstract:</E>Pipeline operators are required to have continuing programs for qualifying and training personnel performing safety-sensitive functions on pipelines. (49 CFR part 192, Subpart N and 49 CFR part 195, Subpart G). Operators must maintain records, make reports, and provide information to PHMSA and state pipeline safety agencies concerning these programs. The information aids Federal and state pipeline safety inspectors in conducting compliance inspections and investigating incidents.</P>
        <P>
          <E T="03">Affected Public:</E>Pipeline Operators.</P>
        <P>
          <E T="03">Annual Reporting and Recordkeeping Burden:</E>
        </P>
        
        <FP SOURCE="FP-1">
          <E T="03">Total Annual Responses:</E>22,300.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Total Annual Burden Hours:</E>466,667.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Frequency of collection:</E>On Occasion.</FP>
        
        <P>
          <E T="03">Title:</E>Pipeline Safety: Report of Abandoned Underwater Pipelines.</P>
        <P>
          <E T="03">OMB Control Number:</E>2137-0601.</P>
        <P>
          <E T="03">Current Expiration Date:</E>2/29/2012.</P>
        <P>
          <E T="03">Abstract:</E>Pipeline operators are required to report certain information about abandoned underwater pipelines to PHMSA (§ 195.59 and § 192.727). The information aids Federal and state pipeline safety inspectors in conducting compliance inspections and investigating incidents.</P>
        <P>
          <E T="03">Affected Public:</E>Operators of Underwater Pipelines.</P>
        <P>
          <E T="03">Annual Reporting and Recordkeeping Burden:</E>
        </P>
        
        <FP SOURCE="FP-1">
          <E T="03">Annual Responses:</E>10.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Annual Burden Hours:</E>60.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Frequency of collection:</E>On Occasion.</FP>
        
        <P>
          <E T="03">Title:</E>Pipeline Safety: Integrity Management in High Consequence Areas for Operators with more than 500 Miles of Hazardous Liquid Pipelines.</P>
        <P>
          <E T="03">OMB Control Number:</E>2137-0604.</P>
        <P>
          <E T="03">Current Expiration Date:</E>1/31/2012</P>
        <P>
          <E T="03">Abstract:</E>Hazardous liquid operators with pipelines in high consequence areas (<E T="03">i.e.,</E>commercially navigable waterways, high population areas, other populated areas, and unusually sensitive areas as defined in § 195.450) are subject to certain information collection requirements relative to the Integrity Management Program provisions of § 195.452.</P>
        <P>
          <E T="03">Affected Public:</E>Pipeline operators with more than 500 miles of hazardous liquid pipeline located in high consequence areas.</P>
        <P>
          <E T="03">Annual Reporting and Recordkeeping Burden:</E>
        </P>
        
        <FP SOURCE="FP-1">
          <E T="03">Annual Responses:</E>71.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Annual Burden Hours:</E>57,510.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Frequency of collection:</E>On Occasion.</FP>
        
        <P>
          <E T="03">Title:</E>Pipeline Safety: Integrity Management in High Consequence Areas for Operators with Less than 500 Miles of Hazardous Liquid Pipeline.</P>
        <P>
          <E T="03">OMB Control Number:</E>2137-0605.</P>
        <P>
          <E T="03">Current Expiration Date:</E>1/31/2012.</P>
        <P>
          <E T="03">Abstract:</E>Hazardous liquid operators with pipelines in high consequence areas (<E T="03">i.e.,</E>commercially navigable waterways, high population areas, other populated areas, and unusually sensitive areas as defined in § 195.450) are subject to certain information collection requirements relative to the Integrity Management Program provisions of § 195.452.</P>
        <P>
          <E T="03">Affected Public:</E>Pipeline operators with less than 500 miles of hazardous liquid pipeline located in high consequence areas.</P>
        <P>
          <E T="03">Annual Reporting and Recordkeeping Burden:</E>
        </P>
        
        <FP SOURCE="FP-1">
          <E T="03">Annual Responses:</E>132.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Annual Burden Hours:</E>267,960.</FP>
        <FP SOURCE="FP-1">
          <E T="03">Frequency of collection:</E>On Occasion.</FP>
        
        <P>Comments are invited on:</P>
        <P>(a) The need for the proposed collection of information for the proper performance of the functions of the agency, including whether the information will have practical utility;</P>
        <P>(b) The accuracy of the agency's estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used;</P>
        <P>(c) Ways to enhance the quality, utility, and clarity of the information to be collected; and</P>
        <P>(d) Ways to minimize the burden of the collection of information on those who are to respond, including the use of appropriate automated, electronic, mechanical, or other technological collection techniques.</P>
        <SIG>
          <PRTPAGE P="45906"/>
          <DATED>Issued in Washington, DC, on July 27, 2011.</DATED>
          <NAME>Alan K. Mayberry,</NAME>
          <TITLE>Deputy Associate Administrator for Field Operations.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19383 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4910-60-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="N">DEPARTMENT OF THE TREASURY</AGENCY>
        <SUBJECT>Submission for OMB Review; Comment Request</SUBJECT>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice; Correction.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>

          <P>The Department of the Treasury published a document in the<E T="04">Federal Register</E>on July 22, 2011, inviting comments on collections of information submitted to the Office of Management and Budget (OMB) for review. This document contained an incorrect reference.</P>
          <HD SOURCE="HD2">Correction</HD>
          <P>In the<E T="04">Federal Register</E>of July 22, 2011, in FR Doc. 2011-18536, make the following correction:</P>
          <P>• page 44084, in the third column, under<E T="03">OMB Number:</E>1510-0014: replace “1510-0014” with “1510-0004”.</P>
        </SUM>
        <SIG>
          <DATED>Dated: July 27, 2011.</DATED>
          <NAME>Dawn D. Wolfgang,</NAME>
          <TITLE>Treasury PRA Clearance Officer.</TITLE>
        </SIG>
      </PREAMB>
      <FRDOC>[FR Doc. 2011-19344 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4810-35-P</BILCOD>
    </NOTICE>
    <NOTICE>
      <PREAMB>
        <AGENCY TYPE="S">DEPARTMENT OF THE TREASURY</AGENCY>
        <SUBAGY>Internal Revenue Service</SUBAGY>
        <SUBJECT>Proposed Collection; Comment Request for Form W-10</SUBJECT>
        <AGY>
          <HD SOURCE="HED">AGENCY:</HD>
          <P>Internal Revenue Service (IRS), Treasury.</P>
        </AGY>
        <ACT>
          <HD SOURCE="HED">ACTION:</HD>
          <P>Notice and request for comments.</P>
        </ACT>
        <SUM>
          <HD SOURCE="HED">SUMMARY:</HD>
          <P>The Department of the Treasury, as part of its continuing effort to reduce paperwork and respondent burden, invites the general public and other Federal agencies to take this opportunity to comment on proposed and/or continuing information collections, as required by the Paperwork Reduction Act of 1995, Public Law 104-13 (44 U.S.C. 3506(c)(2)(A)). Currently, the IRS is soliciting comments concerning Form W-10, Dependent Care Provider's Identification and Certification.</P>
        </SUM>
        <DATES>
          <HD SOURCE="HED">DATES:</HD>
          <P>Written comments should be received on or before September 30, 2011 to be assured of consideration.</P>
        </DATES>
        <ADD>
          <HD SOURCE="HED">ADDRESSES:</HD>
          <P>Direct all written comments to Yvette B. Lawrence, Internal Revenue Service, room 6129, 1111 Constitution Avenue, NW., Washington, DC 20224.</P>
        </ADD>
        <FURINF>
          <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>

          <P>Requests for additional information or copies of the form and instructions should be directed to Evelyn J. Mack, (202) 622-7381, at Internal Revenue Service, room 6231, 1111 Constitution Avenue, NW., Washington, DC 20224, or through the Internet at<E T="03">Evelyn.J.Mack@irs.gov.</E>
          </P>
        </FURINF>
      </PREAMB>
      <SUPLINF>
        <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
        <P/>
        <P SOURCE="NPAR">
          <E T="03">Title:</E>Dependent Care Provider's Identification and Certification.</P>
        <P>
          <E T="03">OMB Number:</E>1545-XXXX.</P>
        <P>
          <E T="03">Form Number:</E>Form W-10.</P>
        <P>
          <E T="03">Abstract:</E>The proposed collection of information is necessary for the taxpayer to file information about the caretaker of a child or other dependent when a tax credit on a return is claimed or when benefits from a dependent care assistance program is received. Taxpayers are required to obtain the name and address of the dependent care provider, the provider's taxpayer identification number, and a certification from the dependent care provider that the name, address and taxpayer identification number on the form are correct.</P>
        <P>
          <E T="03">Current Actions:</E>This form is being submitted for OMB approval.</P>
        <P>
          <E T="03">Type of Review:</E>Approval of a currently used collection.</P>
        <P>
          <E T="03">Affected Public:</E>Individuals or households, business or other for-profit organizations, and not-for-profit institutions.</P>
        <P>
          <E T="03">Estimated Number of Respondents:</E>39,354.</P>
        <P>
          <E T="03">Estimated Time Per Respondent:</E>1 hour 53 minutes.</P>
        <P>
          <E T="03">Estimated Total Annual Burden Hours:</E>74,773.</P>
        <P>The following paragraph applies to all of the collections of information covered by this notice:</P>
        <P>An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless the collection of information displays a valid OMB control number. Books or records relating to a collection of information must be retained as long as their contents may become material in the administration of any internal revenue law. Generally, tax returns and tax return information are confidential, as required by 26 U.S.C. 6103.</P>
        <P>
          <E T="03">Request For Comments:</E>Comments submitted in response to this notice will be summarized and/or included in the request for OMB approval. All comments will become a matter of public record. Comments are invited on: (a) Whether the collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency's estimate of the burden of the collection of information; (c) ways to enhance the quality, utility, and clarity of the information to be collected; (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology; and (e) estimates of capital or start-up costs and costs of operation, maintenance, and purchase of services to provide information.</P>
        <SIG>
          <DATED>Approved: July 21, 2011.</DATED>
          <NAME>Yvette Lawrence,</NAME>
          <TITLE>IRS Reports Clearance Officer.</TITLE>
        </SIG>
      </SUPLINF>
      <FRDOC>[FR Doc. 2011-19398 Filed 7-29-11; 8:45 am]</FRDOC>
      <BILCOD>BILLING CODE 4830-01-P</BILCOD>
    </NOTICE>
  </NOTICES>
  <VOL>76</VOL>
  <NO>147</NO>
  <DATE>Monday, August 1, 2011</DATE>
  <UNITNAME>Presidential Documents</UNITNAME>
  <PRESDOCS>
    <PRESDOCU>
      <PRNOTICE>
        <TITLE3>Title 3—</TITLE3>
        <PRES>The President<PRTPAGE P="45653"/>
        </PRES>
        <PNOTICE>Notice of July 28, 2011</PNOTICE>
        <HD SOURCE="HED">Continuation of the National Emergency With Respect to Actions of Certain Persons to Undermine the Sovereignty of Lebanon or Its Democratic Processes and Institutions</HD>
        <FP>On August 1, 2007, by Executive Order 13441, the President declared a national emergency and ordered related measures blocking the property of certain persons undermining the sovereignty of Lebanon or its democratic processes or institutions and certain other persons, pursuant to the International Emergency Economic Powers Act (50 U.S.C. 1701-1706).  The President determined that the actions of certain persons to undermine Lebanon's legitimate and democratically elected government or democratic institutions; to contribute to the deliberate breakdown in the rule of law in Lebanon, including through politically motivated violence and intimidation; to reassert Syrian control or contribute to Syrian interference in Lebanon; or to infringe upon or undermine Lebanese sovereignty and contribute to political and economic instability in that country and the region and constitute an unusual and extraordinary threat to the national security and foreign policy of the United States.</FP>
        <FP>Certain ongoing activities, such as continuing arms transfers to Hizballah that include increasingly sophisticated weapons systems, serve to undermine Lebanese sovereignty, contribute to political and economic instability in Lebanon, and continue to pose an unusual and extraordinary threat to the national security and foreign policy of the United States.  Therefore, the national emergency declared on August 1, 2007, and the measures adopted on that date to deal with that emergency, must continue in effect beyond August 1, 2011.  In accordance with section 202(d) of the National Emergencies Act (50 U.S.C. 1622(d)), I am continuing for 1 year the national emergency declared in Executive Order 13441.</FP>
        <FP>This notice shall be published in the<E T="03">Federal Register</E>and transmitted to the Congress.</FP>
        <GPH DEEP="50" HTYPE="RIGHT" SPAN="1">
          <GID>OB#1.EPS</GID>
        </GPH>
        <PSIG/>
        <PLACE>THE WHITE HOUSE,</PLACE>
        <DATE>July 28, 2011.</DATE>
        <FRDOC>[FR Doc. 2011-19490</FRDOC>
        <FILED>Filed 7-29-11; 8:45 am]</FILED>
        <BILCOD>Billing code 3195-W1-P</BILCOD>
      </PRNOTICE>
    </PRESDOCU>
  </PRESDOCS>
  <VOL>76</VOL>
  <NO>147</NO>
  <DATE>Monday, August 1, 2011</DATE>
  <UNITNAME>Proposed Rules</UNITNAME>
  <NEWPART>
    <PTITLE>
      <PRTPAGE P="45907"/>
      <PARTNO>Part II</PARTNO>
      <AGENCY TYPE="P">Department of Homeland Security</AGENCY>
      <SUBAGY>Coast Guard</SUBAGY>
      <CFR>46 CFR Parts 1, 10, 11 et al.</CFR>
      <TITLE>Implementation of the Amendments to the International Convention on Standards of Training, Certification and Watchkeeping for Seafarers, 1978, and Changes to Domestic Endorsements; Proposed Rule</TITLE>
    </PTITLE>
    <PRORULES>
      <PRORULE>
        <PREAMB>
          <PRTPAGE P="45908"/>
          <AGENCY TYPE="S">DEPARTMENT OF HOMELAND SECURITY</AGENCY>
          <SUBAGY>Coast Guard</SUBAGY>
          <CFR>46 CFR Parts 1, 10, 11, 12, 13, 14, and 15</CFR>
          <DEPDOC>[Docket No. USCG-2004-17914]</DEPDOC>
          <RIN>RIN 1625-AA16</RIN>
          <SUBJECT>Implementation of the Amendments to the International Convention on Standards of Training, Certification and Watchkeeping for Seafarers, 1978, and Changes to Domestic Endorsements.</SUBJECT>
          <AGY>
            <HD SOURCE="HED">AGENCY:</HD>
            <P>Coast Guard, DHS.</P>
          </AGY>
          <ACT>
            <HD SOURCE="HED">ACTION:</HD>
            <P>Supplemental notice of proposed rulemaking; notice of public meetings.</P>
          </ACT>
          <SUM>
            <HD SOURCE="HED">SUMMARY:</HD>
            <P>The Coast Guard proposes to amend the existing regulations that implement the International Convention on Standards of Training, Certification and Watchkeeping for Seafarers, 1978, as amended (STCW Convention), as well as the Seafarer's Training, Certification and Watchkeeping Code (STCW Code). The changes proposed in this Supplemental Notice of Proposed Rulemaking (SNPRM) address the comments received from the public response to the Notice of Proposed Rulemaking (NPRM), in most cases through revisions based on those comments, and propose to incorporate the 2010 amendments to the STCW Convention that will come into force on January 1, 2012. In addition, this SNPRM proposes to make other non-STCW changes necessary to reorganize, clarify, and update these regulations.</P>
          </SUM>
          <EFFDATE>
            <HD SOURCE="HED">DATES:</HD>

            <P>Comments and related material must either be submitted to our online docket via<E T="03">http://www.regulations.gov</E>on or before September 30, 2011 or reach the Docket Management Facility by that date. Comments sent to the Office of Management and Budget (OMB) on collection of information must reach OMB on or before September 30, 2011.</P>
          </EFFDATE>
          <ADD>
            <HD SOURCE="HED">ADDRESSES:</HD>
            <P>You may submit comments identified by docket number USCG-2004-17914 using any one of the following methods:</P>
            <P>(1)<E T="03">Federal eRulemaking Portal: http://www.regulations.gov.</E>
            </P>
            <P>(2)<E T="03">Fax:</E>202-493-2251.</P>
            <P>(3)<E T="03">Mail:</E>Docket Management Facility (M-30), U.S. Department of Transportation, West Building Ground Floor, Room W12-140, 1200 New Jersey Avenue SE., Washington, DC 20590-0001.</P>
            <P>(4)<E T="03">Hand delivery:</E>Same as mail address above, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays. The telephone number is 202-366-9329.</P>

            <P>To avoid duplication, please use only one of these four methods. See the “Public Participation and Request for Comments” portion of the<E T="02">SUPPLEMENTARY INFORMATION</E>section below for instructions on submitting comments.</P>
            <P>
              <E T="03">Collection of Information Comments:</E>If you have comments on the collection of information discussed in section VIII.D of this NPRM, you must also send comments to the Office of Information and Regulatory Affairs (OIRA), Office of Management and Budget. To ensure that your comments to OIRA are received on time, the preferred methods are by e-mail to<E T="03">oira_submission@omb.eop.gov</E>(include the docket number and “Attention: Desk Officer for Coast Guard, DHS” in the subject line of the e-mail) or fax at 202-395-6566. An alternate, though slower, method is by U.S. mail to the Office of Information and Regulatory Affairs, Office of Management and Budget, 725 17th Street NW., Washington, DC 20503, ATTN: Desk Officer, U.S. Coast Guard.</P>
            <P>
              <E T="03">Viewing incorporation by reference material:</E>You may inspect the material proposed for incorporation by reference at room 1210, U.S. Coast Guard Headquarters, 2100 Second Street SW., Washington, DC 20593-0001 between 8 a.m. and 4 p.m., Monday through Friday, except Federal holidays. The telephone number is 202-372-1401. Copies of the material are available as indicated in the “Incorporation by Reference” section of this preamble.</P>
          </ADD>
          <FURINF>
            <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD>
            <P>If you have questions on this proposed rule, call or e-mail Ms. Zoe Goss, Maritime Personnel Qualifications Division, Coast Guard; telephone 202-372-1425, e-mail Zoe.A.Goss@uscg.mil. If you have questions on viewing or submitting material to the docket, call Renee V. Wright, Program Manager, Docket Operations, telephone 202-366-9826.</P>
          </FURINF>
        </PREAMB>
        <SUPLINF>
          <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD>
          <HD SOURCE="HD1">Table of Contents for Preamble</HD>
          <EXTRACT>
            <FP SOURCE="FP-2">I. Public Participation and Request for Comments</FP>
            <FP SOURCE="FP1-2">A. Submitting Comments</FP>
            <FP SOURCE="FP1-2">B. Viewing Comments and Documents</FP>
            <FP SOURCE="FP1-2">C. Privacy Act</FP>
            <FP SOURCE="FP1-2">D. Public Meeting</FP>
            <FP SOURCE="FP-2">II. Abbreviations</FP>
            <FP SOURCE="FP-2">III. Regulatory History</FP>
            <FP SOURCE="FP-2">IV. Basis and Purpose</FP>
            <FP SOURCE="FP-2">V. Background</FP>
            <FP SOURCE="FP-2">VI. Discussion of Proposed Rule</FP>
            <FP SOURCE="FP1-2">A. Overview</FP>
            <FP SOURCE="FP1-2">B. Differences Between This SNPRM and the Coast Guard's Current Regulations</FP>
            <FP SOURCE="FP1-2">C. Table of Proposed Changes</FP>
            <FP SOURCE="FP1-2">D. Part 12 Re-Numbering</FP>
            <FP SOURCE="FP-2">VII. Discussion of Comments on the NPRM</FP>
            <FP SOURCE="FP-2">VIII. Incorporation by Reference</FP>
            <FP SOURCE="FP-2">IX. Regulatory Analyses</FP>
            <FP SOURCE="FP1-2">A. Regulatory Planning and Review</FP>
            <FP SOURCE="FP1-2">B. Small Entities</FP>
            <FP SOURCE="FP1-2">C. Assistance for Small Entities</FP>
            <FP SOURCE="FP1-2">D. Collection of Information</FP>
            <FP SOURCE="FP1-2">E. Federalism</FP>
            <FP SOURCE="FP1-2">F. Unfunded Mandates Reform Act</FP>
            <FP SOURCE="FP1-2">G. Taking of Private Property</FP>
            <FP SOURCE="FP1-2">H. Civil Justice Reform</FP>
            <FP SOURCE="FP1-2">I. Protection of Children</FP>
            <FP SOURCE="FP1-2">J. Indian Tribal Governments</FP>
            <FP SOURCE="FP1-2">K. Energy Effects</FP>
            <FP SOURCE="FP1-2">L. Technical Standards</FP>
            <FP SOURCE="FP1-2">M. Environment</FP>
          </EXTRACT>
          <HD SOURCE="HD1">I. Public Participation and Request for Comments</HD>

          <P>We encourage you to participate in this rulemaking by submitting comments and related materials. All comments received will be posted without change to<E T="03">http://www.regulations.gov</E>and will include any personal information you have provided.</P>
          <HD SOURCE="HD2">A. Submitting Comments</HD>
          <P>If you submit a comment, please include the docket number for this rulemaking (USCG-2004-17914), indicate the specific section of this document to which each comment applies, and provide a reason for each suggestion or recommendation. You may submit your comments and material online or by fax, mail, or hand delivery, but please use only one of these means. We recommend that you include your name and a mailing address, an e-mail address, or a phone number in the body of your document so that we can contact you if we have questions regarding your submission.</P>
          <P>To submit your comment online, go to<E T="03">http://www.regulations.gov,</E>click on the “submit a comment” box, which will then become highlighted in blue. In the “Document Type” drop down menu select “Proposed Rule” and insert “USCG-2004-17914” in the “Keyword” box. Click “Search” then click on the balloon shape in the “Actions” column. If you submit your comments by mail or hand delivery, submit them in an unbound format, no larger than 8<FR>1/2</FR>; by 11 inches, suitable for copying and electronic filing. If you submit comments by mail and would like to know that they reached the Facility, please enclose a stamped, self-addressed postcard or envelope.</P>

          <P>We will consider all comments and material received during the comment<PRTPAGE P="45909"/>period and may change this proposed rule based on your comments.</P>
          <HD SOURCE="HD2">B. Additional Request for Comments</HD>
          <P>In addition to encouraging your comments on all of the proposals within this rulemaking, the Coast Guard seeks specific comment on the issues outlined below:</P>
          <P>1. The value of tonnage and route restrictions for engineer endorsements. Current regulations restrict Designated Duty Engineers (DDEs) with 1,000 horsepower (HP) and 4,000 HP limits to inland and near-coastal waters, and all DDEs to 500 gross register tons (GRT) vessels. Also, the limited series of engineer credentials authorize service on vessels less than 1,600 GRT/3,000 gross tonnage (GT), with two classes of chief engineer, one of which authorizes sailing only on near-coastal waters. The Coast Guard seeks comment from the public regarding the possible elimination or retention of these tonnage and route restrictions.</P>
          <P>2. Alternative or additional requirements for limiting engineer authority, such as maintaining current horsepower limits, adding equipment restrictions, or any other alternative requirements.</P>
          <P>3. Potential changes to the qualification requirements for a Designated Examiner (DE) for Towing Officer's Assessment Record (TOARs) to allow mariners to serve as DEs by virtue of their endorsement without any further approval process.</P>
          <P>4. Who, within the mariner population, will take advantage of the alternatives provided to meet the standards of competence, besides formal training, for an STCW endorsement.</P>
          <P>5. The extent to which changes to sea service requirements, particularly in § 10.232, will increase the availability of mariners for service on ocean-going ships.</P>
          <P>6. Possible changes to fee payment options, as proposed in § 10.219, which would eliminate the ability to pay by cash or check.</P>
          <HD SOURCE="HD2">C. Viewing Comments and Documents</HD>

          <P>To view comments, as well as documents mentioned in this preamble as being available in the docket, go to<E T="03">http://www.regulations.gov,</E>click on the “read comments” box, which will then become highlighted in blue. In the “Keyword” box insert “USCG-2004-17914” and click “Search.” Click the “Open Docket Folder” in the “Actions” column. If you do not have access to the internet, you may view the docket online by visiting the Docket Management Facility in Room W12-140 on the ground floor of the Department of Transportation West Building, 1200 New Jersey Avenue SE., Washington, DC 20590, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays. We have an agreement with the Department of Transportation to use the Docket Management Facility.</P>
          <HD SOURCE="HD2">D. Privacy Act</HD>

          <P>Anyone can search the electronic form of comments received into any of our dockets by the name of the individual submitting the comment (or signing the comment, if submitted on behalf of an association, business, labor union, etc.). You may review a Privacy Act notice regarding our public dockets in the January 17, 2008, issue of the<E T="04">Federal Register</E>(73 FR 3316).</P>
          <HD SOURCE="HD2">E. Public Meeting</HD>
          <P>We plan to hold public meetings in Miami, New Orleans, Seattle, and Washington, DC.</P>

          <P>We will be providing the dates, times, and exact locations of those meetings by later<E T="04">Federal Register</E>notice.</P>
          <HD SOURCE="HD1">II. Abbreviations</HD>
          <EXTRACT>
            <FP SOURCE="FP-1">A/BAble Seaman</FP>
            <FP SOURCE="FP-1">ARPAAutomatic Radar Plotting Aid</FP>
            <FP SOURCE="FP-1">ATBArticulated Tug Barge</FP>
            <FP SOURCE="FP-1">BCOBallast Control Operator</FP>
            <FP SOURCE="FP-1">BRMBridge Resource Management</FP>
            <FP SOURCE="FP-1">BSBarge Supervisor</FP>
            <FP SOURCE="FP-1">BSTBasic Safety Training</FP>
            <FP SOURCE="FP-1">CFRCode of Federal Regulations</FP>
            <FP SOURCE="FP-1">COICertificate of Inspection</FP>
            <FP SOURCE="FP-1">COLREGSInternational Regulations for Preventing Collisions at Sea</FP>
            <FP SOURCE="FP-1">CPRCardio-Pulmonary Resuscitation</FP>
            <FP SOURCE="FP-1">DCDamage Control</FP>
            <FP SOURCE="FP-1">DDEDesignated Duty Engineer</FP>
            <FP SOURCE="FP-1">DEDesignated Examiner</FP>
            <FP SOURCE="FP-1">DLDangerous Liquid</FP>
            <FP SOURCE="FP-1">DOTDepartment of Transportation</FP>
            <FP SOURCE="FP-1">ECDISElectronic Chart Display Information System</FP>
            <FP SOURCE="FP-1">EEZExclusive Economic Zone</FP>
            <FP SOURCE="FP-1">ERMEngine Room Resource Management</FP>
            <FP SOURCE="FP-1">FCCFederal Communications Commission</FP>
            <FP SOURCE="FP-1">F.H.Food Handler</FP>
            <FP SOURCE="FP-1">FR<E T="04">Federal Register</E>
            </FP>
            <FP SOURCE="FP-1">GMDSSGlobal Maritime Distress and Safety System</FP>
            <FP SOURCE="FP-1">GRTGross Register Tons</FP>
            <FP SOURCE="FP-1">GTGross Tonnage</FP>
            <FP SOURCE="FP-1">HPHorsepower</FP>
            <FP SOURCE="FP-1">IMDGThe International Maritime Dangerous Goods Code</FP>
            <FP SOURCE="FP-1">IMOInternational Maritime Organization</FP>
            <FP SOURCE="FP-1">IRInterim Rule</FP>
            <FP SOURCE="FP-1">IRFAInitial Regulatory Flexibility Act</FP>
            <FP SOURCE="FP-1">ISMInternational Safety Management Code</FP>
            <FP SOURCE="FP-1">ISOInternational Organization for Standardization</FP>
            <FP SOURCE="FP-1">ISPSInternational Ship and Port Facility Security</FP>
            <FP SOURCE="FP-1">ITBIntegrated Tug Barge</FP>
            <FP SOURCE="FP-1">ITCInternational Tonnage Convention on Tonnage Measurement of Ships, 1969</FP>
            <FP SOURCE="FP-1">KUPKnowledge, Understanding, and Proficiency</FP>
            <FP SOURCE="FP-1">kWKilowatts</FP>
            <FP SOURCE="FP-1">LGLiquefied Gas</FP>
            <FP SOURCE="FP-1">MARADMaritime Administration</FP>
            <FP SOURCE="FP-1">MARPOL 73/78International Convention for the Prevention of Pollution From Ships, 1973 as modified by the Protocol of 1978</FP>
            <FP SOURCE="FP-1">MERPACMerchant Marine Personnel Advisory Committee</FP>
            <FP SOURCE="FP-1">MMCMerchant Mariner Credential</FP>
            <FP SOURCE="FP-1">MMDMerchant Mariner Document</FP>
            <FP SOURCE="FP-1">MODUMobile Offshore Drilling Unit</FP>
            <FP SOURCE="FP-1">NAVSACNavigation Safety Advisory Committee</FP>
            <FP SOURCE="FP-1">NDRNational Driver Register</FP>
            <FP SOURCE="FP-1">NMCU.S. Coast Guard National Maritime Center</FP>
            <FP SOURCE="FP-1">NEPANational Environment Policy Act of 1969</FP>
            <FP SOURCE="FP-1">NPRMNotice of Proposed Rulemaking</FP>
            <FP SOURCE="FP-1">NVICNavigation and Vessel Inspection Circular</FP>
            <FP SOURCE="FP-1">OCMIOfficer in Charge, Marine Inspection</FP>
            <FP SOURCE="FP-1">OICEWOfficer in Charge of an Engineering Watch</FP>
            <FP SOURCE="FP-1">OICNWOfficer in Charge of a Navigational Watch</FP>
            <FP SOURCE="FP-1">OIMOffshore Installation Manager</FP>
            <FP SOURCE="FP-1">OIRAOffice of Information and Regulatory Affairs</FP>
            <FP SOURCE="FP-1">OJTOn-the-job training</FP>
            <FP SOURCE="FP-1">OMBOffice of Management and Budget</FP>
            <FP SOURCE="FP-1">OSVOffshore Supply Vessel</FP>
            <FP SOURCE="FP-1">OUPVOperator of an Uninspected Passenger Vessel</FP>
            <FP SOURCE="FP-1">PICPerson in Charge</FP>
            <FP SOURCE="FP-1">PMSPreventive Maintenance System</FP>
            <FP SOURCE="FP-1">PSCProficiency in Survival Craft</FP>
            <FP SOURCE="FP-1">QAQualified Assessor</FP>
            <FP SOURCE="FP-1">QMEDQualified Member of the Engineering Department</FP>
            <FP SOURCE="FP-1">QSSQuality Standard Systems</FP>
            <FP SOURCE="FP-1">RECRegional Examination Center</FP>
            <FP SOURCE="FP-1">RFARegulatory Flexibility Act</FP>
            <FP SOURCE="FP-1">RFPEWRatings Forming Part of an Engineering Watch</FP>
            <FP SOURCE="FP-1">RFPNWRatings Forming Part of a Navigational Watch</FP>
            <FP SOURCE="FP-1">SHIPSeafarers' Health Improvement Program</FP>
            <FP SOURCE="FP-1">SOLASThe International Convention for the Safety of Life at Sea (1974)</FP>
            <FP SOURCE="FP-1">STCW CodeSeafarer's Training, Certification and Watchkeeping Code</FP>
            <FP SOURCE="FP-1">STCW ConventionInternational Convention on Standards of Training, Certification, and Watchkeeping for Seafarers, 1978, as amended</FP>
            <FP SOURCE="FP-1">STCW-FInternational Convention on Standards of Training, Certification, and Watchkeeping for Fishing Vessel Personnel</FP>
            <FP SOURCE="FP-1">TOARTowing Officer's Assessment Record</FP>
            <FP SOURCE="FP-1">TRBTraining Record Book</FP>
            <FP SOURCE="FP-1">TSATransportation Security Administration</FP>
            <FP SOURCE="FP-1">TSACTowing Safety Advisory Committee</FP>
            <FP SOURCE="FP-1">UPVUninspected Passenger Vessel</FP>
            <FP SOURCE="FP-1">UTVUninspected Towing Vessel</FP>
            <FP SOURCE="FP-1">VSOVessel Security Officer</FP>
          </EXTRACT>
          <HD SOURCE="HD1">III. Regulatory History</HD>

          <P>The Coast Guard first published changes to the regulations governing the credentialing of merchant mariners serving on U.S. flag vessels with an Interim Rule (IR) on June 26, 1997 (62 FR 34505). The 1997 IR ensured that<PRTPAGE P="45910"/>U.S. merchant mariner credentials would meet IMO standards, thereby reducing the possibility of U.S. ships being detained in a foreign port for non-compliance.</P>
          <P>In 2009, The Coast Guard proposed to update the changes made by the 1997 IR through experience gained during the implementation of that rule. To that end, the Coast Guard published a Notice of Proposed Rulemaking (NPRM) on November 17, 2009 (74 FR 59354). The proposed rule sought to incorporate all effective amendments as of that publication date to the STCW Convention and Code. The Coast Guard determined, as a result of comments from the public and federal advisory committees (specifically the Merchant Marine Personnel Advisory Committee (MERPAC)), that more information, including more detailed regulatory text, was required for the affected public, and incorporated those comments as proposals within the NPRM.</P>

          <P>Five public meetings were held to receive comments on the NPRM. These meetings were announced in the<E T="04">Federal Register</E>on November 18, 2009 (74 FR 59502). The comments received during these five meetings are discussed in the “Discussion of Comments on the NPRM” section of this preamble.</P>
          <HD SOURCE="HD1">IV. Basis and Purpose</HD>
          <P>The Coast Guard has identified two basic concerns with the existing mariner credentialing regulations that it intends to remedy with this supplemental proposal. First, the existing regulations, which combine domestic and international requirements, are confusing to mariners and others in the maritime industry. Second, in June 2010 the International Maritime Organization (IMO) amended the International Convention on Standards of Training, Certification and Watchkeeping for Seafarers (STCW), 1978. This proposal intends to clarify the Coast Guard's domestic and international mariner license endorsement regulations, and implement provisions related to the amended STCW Convention.</P>
          <P>The International Convention on Standards of Training, Certification and Watchkeeping for Seafarers, 1978 as amended, sets forth minimum training and demonstrations of proficiency requirements for merchant mariners. The IMO adopted amendments to the STCW in 1995. Those amendments entered into force on February 1, 1997. In 2007, the IMO embarked on a comprehensive review of the entire STCW Convention and STCW Code, which sets forth provisions for implementing provisions from the STCW Convention. Five meetings were held at IMO headquarters in London on the comprehensive review, and the Parties developed draft 2010 amendments to the Convention. The Parties adopted these amendments on June 25, 2010, at the STCW Diplomatic Conference in Manila, Philippines. They will enter into force for all ratifying countries on January 1, 2012. Because these amendments were not adopted until after the previous NPRM was published, they were not included in the NPRM's proposals.</P>
          <P>The Coast Guard is publishing this Supplemental Notice of Proposed Rulemaking (SNPRM) to implement amendments to the STCW, including the 2010 amendments, and ensure that the U.S. is meeting its obligations under the Convention. The Coast Guard considered issuing a Final Rule implementing the 1995 amendments before issuing these proposals but determined it would be less confusing to the mariner to combine into one rule the lessons learned from the implementation of the 1995 amendments and the 2010 amendments.</P>
          <P>In addition, the Coast Guard is issuing the SNPRM to respond to the comments, feedback, and concerns received from the public as a result of the NPRM. In order to address those comments and concerns, the SNPRM will: simplify domestic licensing requirements and separate them from STCW requirements; provide alternative means for demonstrating competence; clarify oversight requirements for approved courses; amend lifeboatmen requirements; allow for acceptance of sea service on vessels serving the Great Lakes and inland waters to meet STCW requirements; and permit acceptance of maritime academies' documentation in compliance with national accreditation bodies to meet STCW requirements. The SNPRM will also give the public an opportunity to comment on these changes.</P>
          <HD SOURCE="HD1">V. Background</HD>
          <P>In 2007, the IMO embarked on a comprehensive review of the entire STCW Convention and STCW Code. The Coast Guard held public meetings prior to each one of the IMO meetings in London for the review to determine what positions U.S. delegations should advocate and to exchange views about amendments to STCW that were under discussion. In addition, the Coast Guard also took advantage of advisory committee meetings, specifically MERPAC, to discuss developments and implementation of the requirements relating to the 2010 amendments. The 2010 amendments resulting from that review were adopted on June 25, 2010.</P>
          <P>The Convention is not self-implementing; therefore, the United States, as a signatory to the STCW Convention, must initiate regulatory changes to ensure full implementation of all amendments to the STCW Convention and STCW Code. The United States implements these provisions under the Convention and under the authority of United States domestic laws at United States Code titles 5, 14, 33 and 46, as cited with the proposed rule text under “Authorities.”</P>
          <P>Parties to the STCW Convention have port state control authority to detain vessels that do not appear to be in compliance with the Convention. If U.S. regulations are non-compliant with the STCW Convention and STCW Code, there is a risk that U.S. ships will be detained in foreign ports by member nations and that U.S. mariners would not be able to seek employment on foreign flag vessels.</P>
          <HD SOURCE="HD1">VI. Discussion of Proposed Rule</HD>
          <HD SOURCE="HD2">A. Overview</HD>
          <P>This proposed rule is a result of ongoing work to ensure that U.S. mariners comply with the standards set forth in the STCW Convention and Code and to clarify and update the regulations of 46 CFR Subchapter B. In responding to the comments, feedback, and concerns received from the public as a result of the 2009 NPRM, and due to the adoption of the 2010 amendments to the STCW Convention and STCW Code, the Coast Guard recognized a need to make substantial changes to the merchant mariner licensing and documentation credentialing program. Because of these substantial changes, we recognize the necessity of developing a more comprehensive rule, and of providing additional opportunity—through this SNPRM—for the public to comment on these changes.</P>

          <P>Most seagoing merchant mariners must comply with the requirements of the STCW Convention and STCW Code. The Coast Guard recognizes that the CFR regulations implementing the STCW Convention and STCW Code requirements have been the subject of different interpretations and that the requirements reflected in the CFR are not currently organized in a manner that is easy to read and understand. This SNPRM seeks to implement all of the provisions in the STCW Convention by taking full advantage of the flexibilities incorporated in the STCW Convention and of the robustness of an existing domestic licensing scheme, without compromising the safety, security and protection of mariners or the marine environment.<PRTPAGE P="45911"/>
          </P>
          <P>This SNPRM also seeks to revise other sections of 46 CFR Subchapter B in order to clarify, address omissions in, and update these regulations.</P>
          <HD SOURCE="HD2">B. Differences Between This SNPRM and the Coast Guard's Current Regulations</HD>
          <P>This list provides a brief summary of the significant changes proposed in this SNPRM. The “Table of Proposed Changes” in part C of this section provides more detailed information and explanation of the key changes in the summarized listing below.</P>
          <HD SOURCE="HD3">1. Separation of STCW and Domestic Endorsements</HD>
          <P>The Coast Guard proposes to clearly separate the two licensing schemes for STCW and domestic endorsements. For STCW endorsements, this proposed rule incorporates the sea service, assessment and training requirements directly from the STCW Convention and STCW Code to ensure consistency and clarity. In addition, the Coast Guard has provided entry paths from domestic endorsements to the equivalent STCW endorsement. These proposed changes would make it easier for mariners to read and understand the requirements for each Merchant Mariner Credential (MMC) STCW endorsement.</P>
          <HD SOURCE="HD3">2. Methods for Demonstrating Competence</HD>
          <P>The Coast Guard proposes to accept various methods for assessment of competence as provided in the Tables of Competence in the STCW Code. This would allow the preservation of the “hawsepipe” program, which permits the use of on-the-job training (OJT) or practical experience, to obtain endorsements, and would foster career paths that were not previously available.</P>
          <P>Implementation of an assessment-based process would provide acceptance of the various methods for demonstrating competence, including, but not limited to: (1) On-the-job training and/or in-service experience; (2) formal training (classroom or distance-learning), including laboratory assessment; and (3) simulator training. The complete list of acceptable methods of demonstrating competence can be found in proposed §§ 11.301, 12.601, and 13.601 accordingly.</P>
          <HD SOURCE="HD3">3. Sea Service Credit for Great Lakes and Inland Mariners</HD>
          <P>The Coast Guard proposes to add provisions to grant sea service credit towards STCW and domestic endorsements of unlimited tonnage for those mariners who provide proof of service on the Great Lakes or inland waters. A large portion of the skills and assessments that the STCW Code requires for its endorsements overlaps with the skills and techniques these officers are currently using as deck and engineer officers on the Great Lakes or inland waters. Applicants serving on Great Lakes waters will receive day-for-day credit. Applicants serving on inland waters will be credited 1 day of ocean service for every 2 days of inland service for up to 50 percent of the total required service. The reason for the difference in service credit is based on the fact that Great Lakes service most closely resembles the length, breadth, equipment, and operation of ocean service.</P>
          <HD SOURCE="HD3">4. Medical Examinations and Endorsements</HD>
          <P>The Coast Guard proposes to add provisions regarding the issuance of medical endorsements for mariners to improve maritime safety and provide consistency with the 2010 STCW amendments. Medical endorsements issued to a mariner serving under the authority of an STCW endorsement would be issued for a maximum period of 2 years unless the mariner is under the age of 18, in which case the maximum period of validity would be 1 year, as stipulated in the 2010 amendments to the STCW Convention. Medical endorsements issued to a mariner who is serving as a first-class pilot, or acting as a pilot under § 15.812, would be issued for a maximum period of 1 year consistent with the already implemented requirement for a first-class pilot to complete an annual medical exam. All other mariners would be issued a medical certificate/endorsement valid for a maximum period of 5 years, consistent with the current practice and requirements.</P>
          <P>The Coast Guard proposes to revise the physical requirements for mariners applying for domestic and STCW credentials issued by the Coast Guard. These proposed changes include: annual submission of physical examination results by pilots, removal of some specific tests for color vision, revision of vision standards, revision of hearing standards, and clarification regarding demonstration of physical ability. These changes would provide the Coast Guard some flexibility in the acceptance of other tests, as well as serve as acknowledgement that some of the vision tests are no longer available. They would enable mariners and examining physicians to use a range of effective tests to demonstrate physical competence, rather than limit them to specific tests which may have become outdated or unavailable. They also implement the STCW requirement that mariners seeking an STCW endorsement demonstrate physical ability.</P>
          <P>In particular, the Coast Guard proposes to revise the vision standards for deck personnel with STCW endorsements by expanding the applicability of the vision standards from one eye to both eyes. This proposal would provide consistency with the 2010 amendments to the STCW Convention. Requirements for mariners who suffer from vision loss or lost vision in one eye remain the same. At the time of application for an endorsement, mariners must hold a valid medical certificate or endorsement, or they must submit an application for a medical certificate. Unless provided otherwise, mariners sailing onboard vessels to which STCW applies must hold a valid 2-year medical certificate.</P>
          <HD SOURCE="HD3">5. Ceremonial License</HD>
          <P>The Coast Guard proposes to add a provision for issuance of a ceremonial license, which reflects his or her existing domestic officer endorsements, and is suitable for framing. The addition of this optional license is being proposed in response to numerous requests from the public.</P>
          <HD SOURCE="HD3">6. Quality Standards System (QSS)</HD>
          <P>The Coast Guard proposes to add Quality Standards System (QSS) requirements for Coast Guard-approved courses. A QSS is a set of policies, procedures, processes, and data that help an organization fulfill its objectives. The use of a QSS by training providers helps in the oversight of courses, ensuring that mariners obtain the training that they need. This proposal would provide consistency with the obligation under the STCW Convention for approved training to be part of a QSS. This would also require providers of approved courses and training programs to be compliant with QSS provisions.</P>
          <P>To make it easier for training providers to meet the QSS requirements, the Coast Guard proposes to accept documentation from a National Academic accreditation body or from a national or international quality standard system as meeting one or more of the QSS requirements.</P>

          <P>The Coast Guard also proposes to clarify that Coast Guard-accepted QSS organizations may accept and monitor training on behalf of the Coast Guard. Coast Guard-accepted QSS organizations will need to have processes for reviewing, accepting, and monitoring training that are equal to the Coast Guard's course approval and oversight processes.<PRTPAGE P="45912"/>
          </P>
          <P>Additionally, the Coast Guard proposes to introduce a grandfather provision to ensure that approved courses, programs, and training creditable towards an STCW endorsement approved prior to July 1, 2013 must meet the requirements of this section at the next renewal.</P>
          <HD SOURCE="HD3">7. Post-Dating of MMCs</HD>
          <P>The Coast Guard proposes to add requirements for an applicant to request post-dating of his or her MMC upon submitting an application. These changes would provide flexibility to the mariner to post-date an MMC for up to 12 months allowing a mariner to start his or her application process early in case a problem arises or he or she has to return to sea. Their application can continue to be processed in their absence. This change will alleviate the situation where a mariner was not getting the benefit of the full 5-year credential.</P>
          <HD SOURCE="HD3">8. New Towing Endorsements</HD>
          <P>The Coast Guard proposes to add three new towing endorsements and the associated requirements to obtain them: Apprentice mate (steersman) of towing vessels (utility), Master of Towing Vessels (Utility), and Master of Towing Vessels (Harbor Assist). These endorsements are being proposed in response to recommendations from the Towing Safety Advisory Committee (TSAC) in its review of the towing vessel NVIC 04-01. TSAC recommended the addition of these three endorsements because some mariners were performing these functions without the proper authority, experience, and in some cases, qualifications.</P>
          <P>The Coast Guard is establishing a towing vessel (utility) progression, including apprentice mate (steersmen) and a Master of Towing Vessels (Utility) endorsement to cover Towing Vessels performing marine repair, construction, and other utility type services where a full, unlimited Master of Towing Vessels endorsement is inappropriate, and where some persons with Assistance Towing endorsements are currently working beyond the authority of their credentials.</P>
          <P>The Master of Towing Vessels (Utility) will authorize service to tow: (1) Barges not used for moving bulk cargo (commodities) for trade; (2) Barges associated with Marine Construction; (3) Dredges; and (4) Pile Drivers.</P>
          <P>The Master of Towing Vessels (Harbor Assist) endorsement authorizes service on towing vessels for escorting ships with limited propulsion or navigating capabilities in restricted waters, and for assisting ships to dock and undock in limited local areas. This endorsement may be added to a Master of Towing Vessels (Limited) endorsement after a period of service and the completion of a specified TOAR.</P>
          <HD SOURCE="HD3">9. Bridge Resource Management (BRM), Leadership and Teamworking Skills, Leadership and Managerial Skills</HD>
          <P>The Coast Guard proposes to change the name of Procedures for Bridge Team Work to Bridge Resource Management (BRM). BRM and leadership and teamworking skills would be required for the operational-level credential only; and leadership and managerial skills would be required for the management-level credential, as provided in the 2010 amendments to the STCW Convention. These requirements would allow for the approval of BRM courses or combined BRM and leadership and managerial skills courses.</P>
          <HD SOURCE="HD3">10. Engine Room Resource Management (ERM), Leadership and Teamworking Skills, Leadership and Managerial Skills</HD>
          <P>The Coast Guard proposes to require Engine room resource management (ERM) training for engineers seeking STCW endorsements. Basic ERM will be required for the operational-level credential, and leadership and managerial skills would be required for the management-level credential in accordance with the 2010 amendments to the STCW Convention. These requirements would allow for the approval of ERM courses or combined ERM and leadership and managerial skills courses.</P>
          <HD SOURCE="HD3">11. Grandfathering and Transitional Provisions</HD>
          <P>The Coast Guard proposes transitional and grandfathering provisions consistent with the 2010 amendments to the STCW Convention. The 2010 amendments to the STCW Convention will enter into force on January 1, 2012. However, STCW Regulation I/15 on transitional provisions, allows requirements to come into effect over a 5-year period in order to avoid disruption to the maritime industry. STCW Regulation I/15 also provides that a Party may continue, until January 1, 2017, to issue certificates (MMC) in accordance with the credentialing rules it has in place before the 2010 amendments come into force (January 1, 2012) only with respect to seafarers who begin their sea service or their approved maritime training before July 1, 2013. Candidates who begin their service or their training on or after July 1, 2013, will be subject to the full application of the revised STCW requirements. The Coast Guard has drafted this SNPRM to allow for this phase-in process. These provisions require any seafarer who holds an STCW endorsement prior to January 1, 2012, to provide evidence of meeting the appropriate standard of competence for the applicable STCW endorsement by January 1, 2017.</P>
          <P>Domestic requirements provided in this proposed rule will be transitioned during a 5-year period (after the effective date of the final rule) to coincide with the renewal of existing domestic endorsements. Individuals seeking an original credential or raise of grade to an existing credential during this period, and who begin training or service before January 1, 2012, need only meet the requirements in place before that date. Those individuals who start training or service on or after January 1, 2012, must meet all provisions described in the final rule.</P>
          <HD SOURCE="HD3">12. Tankerman Endorsements</HD>
          <P>The Coast Guard proposes to add new STCW endorsements for basic and advanced tankerman for oil and chemical, and for basic and advanced tankerman for liquefied gas tanker cargo operations, as required by the 2010 amendments to the STCW Convention. The Coast Guard proposes to use the domestic requirements for the tankerman endorsements as the means to qualify for an STCW tankerman endorsement. Candidates for an STCW endorsement will only need to complete the appropriate assessments of competence in accordance with the appropriate table of competence in the STCW Code.</P>
          <P>The Coast Guard proposes to include an STCW endorsement equivalent to the tankerman-PIC (barge).</P>
          <P>All of these changes are being proposed to ensure compliance with the 2010 amendments.</P>
          <P>The Coast Guard proposes to clarify and update the list of subjects that the tanker courses must cover by including tables of topics for each tanker course.</P>
          <HD SOURCE="HD3">13. Lifeboatman and Proficiency in Survival Craft Endorsements</HD>

          <P>In response to comments we received objecting to the use of the term “survivalman”, the Coast Guard has withdrawn its proposed use and substitutes, in its place, the term “lifeboatman-limited” for the domestic endorsement. Regarding the STCW endorsement, the Coast Guard is proposing to use the term proficiency in survival craft and rescue boats other than lifeboats and fast rescue boats—limited (PSC—limited), to ensure consistency with the STCW Convention.<PRTPAGE P="45913"/>
          </P>
          <P>To ensure consistency and clarity, the Coast Guard is proposing to separate the domestic requirements for lifeboatman endorsements (found in §§ 12.407 and 12.409) from the STCW Code requirements for proficiency in survival craft endorsements (found in §§ 12.613 and 12.615). Persons who meet the requirements for a domestic lifeboatman (lifeboatman or lifeboatman-limited) endorsement will be deemed to meet the requirements for an STCW endorsement for proficiency in survival craft (PSC or PSC-limited).</P>
          <P>Mariners holding an STCW endorsement will be required to prove that they have maintained the standard of competence every 5 years, in accordance with the 2010 amendments to the STCW Convention. This may be accomplished through a combination of drills and onboard training and experience, with shore-side assessments. The Coast Guard is proposing to accept proof of sea service, specifically one year in the last 5 years, as proof of meeting the requirements for those components of the competence table that can be performed through drills and/or training on board vessels. For those components that cannot be performed onboard a ship, shore-side assessments must be successfully demonstrated.</P>
          <HD SOURCE="HD3">14. Basic Safety Training (BST) and Advanced Firefighting</HD>
          <P>The Coast Guard proposes to amend the BST and advanced firefighting requirements to require that mariners prove they have maintained the standard of competence every 5 years, in accordance with the 2010 amendments to the STCW Convention and Code. This may be accomplished through a combination of drills and onboard training and experience, with shore-side assessments. The Coast Guard is proposing to retain the existing arrangement of acceptance of sea service, specifically one year in the last 5 years, as proof of meeting the requirements only for those components of the competence table that can be performed through drills and/or training on board vessels. For those components that cannot be performed onboard a ship, shore-side assessments must be successfully demonstrated.</P>
          <HD SOURCE="HD3">15. Recognition of Certificates Issued by Other Parties to the STCW Convention</HD>
          <P>The Coast Guard proposes to establish requirements and procedures for the recognition and endorsement of officer certificates of competence issued by other Parties signatory to the STCW Convention in accordance with the existing laws of the United States.</P>
          <P>46 U.S.C. 8103(b)(3)(A) waives the citizenship requirements (except for master) for offshore supply vessels (OSVs) operating from a foreign port. To ensure compliance with the STCW Convention, in the limited cases of OSVs, the U.S. needs to recognize seafarer competence certificates from other countries that have ratified the STCW Convention and are known to issue STCW certificates.</P>
          <HD SOURCE="HD3">16. Work Hours and Rest Periods</HD>
          <P>In accordance with the 2010 amendments to the STCW Convention and Code, the Coast Guard proposes to amend the work and rest hours requirements as follows: (1) Expand the application for hours of work and rest periods for mariners to include all personnel with designated safety, prevention of pollution, and security duties onboard any vessel; (2) change the weekly rest hours requirements from 70 hours to 77 hours; (3) require the recording of hours of rest; and (4) include flexibility from the rest hours requirements in exceptional circumstances.</P>
          <HD SOURCE="HD3">17. Certification for Vessel Personnel With Security Duties and Security Awareness</HD>
          <P>The Coast Guard is proposing that, after July 1, 2012, all personnel with designated security duties must hold a valid endorsement as vessel personnel with designated security duties or a certificate of course completion from an appropriate Coast Guard-accepted course meeting the requirements of 33 CFR 104.220. This requirement is consistent with the STCW 2010 amendments to ensure that all personnel hold a certificate of proficiency.</P>
          <P>The Coast Guard also is proposing that, after July 1, 2012, all other vessel personnel, including contractors, whether part-time, full-time, temporary, or permanent, must hold a valid endorsement in security awareness, or a certificate of course completion from an appropriate Coast Guard-accepted course meeting the requirements of 33 CFR 104.225. This requirement is consistent with the 2010 STCW amendments to ensure that personnel hold a certificate of proficiency.</P>
          <P>The training requirements for vessel personnel with designated security duties and for security awareness in compliance with the 2010 amendments to the STCW Convention and Code will be part of a separate rulemaking.</P>
          <HD SOURCE="HD2">C. Thirty Months of Training for Officer in Charge of an Engineering Watch (OICEW)/Designated Duty Engineer (DDE) Candidates</HD>
          <P>The November 17, 2009, NPRM proposed to include a requirement for an OICEW or DDE candidate to complete approved education and training of at least 30 months in accordance with Regulation III/1 of the 1995 amendments to the STCW requirements. The 2010 amendments deleted this requirement from regulation; therefore, this SNPRM does not include this provision.</P>
          <HD SOURCE="HD2">D. Table of Proposed Changes</HD>
          <P>The following table provides a more detailed summary of significant changes proposed in this SNPRM. The table includes the changes noted in the brief summary of the significant changes listed in part B above, “Differences between this SNPRM and the Coast Guard's current regulations”.</P>
          <GPOTABLE CDEF="xs80,r48,r100,r100" COLS="4" OPTS="L2,tp0,i1">
            <TTITLE/>
            <BOXHD>
              <CHED H="1">Current cite</CHED>
              <CHED H="1">Cite under proposed rule</CHED>
              <CHED H="1">Summary of proposed changes</CHED>
              <CHED H="1">Explanation of and reasons for proposed changes</CHED>
            </BOXHD>
            <ROW>
              <ENT I="01">§ 10.107</ENT>
              <ENT>N/A</ENT>
              <ENT>Removes definition of<E T="03">Competent Person</E>
              </ENT>
              <ENT>Moved relevant information into part 13 to ensure consistency, because “competent person” deals with tankerman endorsements.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 10.107</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Revises the definition for<E T="03">Coast Guard-accepted</E>
              </ENT>
              <ENT>The definition is being revised to provide clarification on the instances where something may be approved by the Coast Guard for use in meeting a particular requirement.</ENT>
            </ROW>
            <ROW>
              <PRTPAGE P="45914"/>
              <ENT I="01">§ 10.107</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Revises definition of<E T="03">Day</E>
              </ENT>
              <ENT>References authorization by the U.S. Code and the two-watch system, in accordance with part 15. Adds clarification on service on MODUs.<LI>This will link the definition to the U.S. Code and provide further clarification within the regulations.</LI>
              </ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 10.107</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Revises definition of<E T="03">Designated examiner</E>
              </ENT>
              <ENT>The definition was revised to ensure that a DE applies to the Towing Officer Assessment Record only, as DE previously applied to all qualification processes.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 10.107</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Revises the definition of<E T="03">Near-coastal</E>
              </ENT>
              <ENT>Amends to include exceptions for operator of uninspected passenger vessels (OUPVs) in order to formalize a pre-existing exception for OUPVs.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 10.109</ENT>
              <ENT>§ 10.109</ENT>
              <ENT>Revises list of endorsements</ENT>
              <ENT>Adds new endorsements in accordance with parts 11 and 12 to ensure that the lists of endorsements are consistent throughout the regulations.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 10.209, 10.231</ENT>
              <ENT>§ 10.209, 10.231</ENT>
              <ENT>Adds required documentation for medical examinations</ENT>
              <ENT>Adds a medical certificate issued by the Coast Guard.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>This serves as documentary proof of passing the medical examination.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 10.215</ENT>
              <ENT>Part 10, subpart C</ENT>
              <ENT>Transfer medical requirements to a new subpart. Revises the physical requirements for mariners applying for a Coast Guard-issued credential These changes include: annual submission of physicals by pilots, revision of vision standard, revision of hearing standard, clarification regarding demonstration of physical ability</ENT>
              <ENT>Provides the Coast Guard some flexibility in the acceptance of other tests.<LI>The requirement to demonstrate physical ability provides information required for those mariners serving on vessels to which STCW applies.</LI>
              </ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 10.215</ENT>
              <ENT>§ 10.301</ENT>
              <ENT>Revises medical certificate validity period</ENT>
              <ENT>Adds issuance of the new medical certificates with the following period of validity:</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT O="oi2">(1) 2 years for STCW-endorsed mariners, unless the mariner is under the age of 18, in which case the maximum period of validity would be 1 year;</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT O="oi2">(2) 1 year for a mariner who is serving as a first-class pilot, or acting as a pilot under § 15.812; and</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT O="oi2">(3) 5 years for all other mariners, consistent with the current practice and requirements.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 10.215</ENT>
              <ENT>§ 10.305</ENT>
              <ENT>Vision requirements</ENT>
              <ENT>The 2010 amendments have expanded the applicability of vision standards from one eye to both eyes for deck personnel with STCW endorsements.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 10.217</ENT>
              <ENT>§ 10.217</ENT>
              <ENT>Removes reference to temporary permits.</ENT>
              <ENT>Temporary permits are no longer issued.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>Formalizes long-standing Coast Guard practice.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 10.219</ENT>
              <ENT>§ 10.219</ENT>
              <ENT>Amends the manner in which user fees may be paid to credit card or electronic payment only</ENT>
              <ENT>This change would eliminate the ability of a mariner to pay by cash and by attaching a check or money order to their application package.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>This would update fee payment practices by permitting electronic payment of fees.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§§ 10.227, 10.231</ENT>
              <ENT>§§ 10.227, 10.231</ENT>
              <ENT>Revises renewal requirements for credentials</ENT>
              <ENT>Removes the requirement to submit an old, original credential in an application for renewal.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>This would permit mariners to retain their previous credentials.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 10.303</ENT>
              <ENT>§ 10.410</ENT>
              <ENT>Removed QSS requirements from § 10.303 and moved them into a new § 10.410</ENT>
              <ENT>Adds QSS information into a new section and adds requirement for training providers to develop a QSS.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>This reflects the STCW requirement to use a QSS.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>
                <E T="03">Adds a grandfather provision to ensure that approved courses, programs, and training creditable towards an STCW endorsement approved prior to July 1, 2013 must meet the requirements of this section at the next renewal.</E>
              </ENT>
            </ROW>
            <ROW>
              <PRTPAGE P="45915"/>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds the definition of<E T="03">Boundary line</E>
              </ENT>
              <ENT>Adding the definition will assist applicants in understanding the limits of the STCW Convention.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds definition of<E T="03">Ceremonial license</E>
              </ENT>
              <ENT>Provides mariners an MMC endorsement suitable for framing.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>This is in response to mariner demand for a ceremonial license.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds the definition of a<E T="03">Coast Guard-accepted quality standards system (QSS) organization</E>
              </ENT>
              <ENT>Adds definition regarding those organizations that may conduct QSS activities in regard to training, consistent with STCW requirements.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds definition of<E T="03">Coastwise Voyage</E>
              </ENT>
              <ENT>This is being done to add clarity to the boundaries of these types of voyages.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds definition of<E T="03">Deck department</E>
              </ENT>
              <ENT>To clarify the functions of this department.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds definition of<E T="03">Designated medical examiner</E>
              </ENT>
              <ENT>To clarify who can give medical examinations to mariners, establishing a network of medical examiners who have demonstrated an understanding of mariner fitness.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds the definition of<E T="03">Domestic voyage</E>
              </ENT>
              <ENT>To clarify that domestic service does not include entering foreign waters.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>This will assist those operating small passenger vessels in waters close to or adjacent to foreign waters in determining whether the operator would be required to hold an STCW endorsement.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds definition of<E T="03">Dual-mode integrated tug barge</E>
              </ENT>
              <ENT>To clarify what is included in the operations and configuration of this type of ITB.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds definition of<E T="03">Engine department</E>
              </ENT>
              <ENT>To clarify the functions of this department.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds definition of<E T="03">Gross register tons (GRT)</E>
              </ENT>
              <ENT>Provides definition for term used in the proposed rule and establishes an abbreviation for the use of this term throughout this subchapter.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>This will help the mariner to readily distinguish between GRT and gross tonnage.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds the definition of<E T="03">Gross tonnage (GT)</E>
              </ENT>
              <ENT>This will provide consistency with the STCW Convention and simplify the regulations by establishing an abbreviation for use throughout this subchapter.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds definition of<E T="03">Integrated tug barge</E>
              </ENT>
              <ENT>To specify and make clear the features and capabilities of this type of tug barge combination.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds the definition of<E T="03">Kilowatt (kW)</E>
              </ENT>
              <ENT>To provide clarity and consistency, as the term is used in conjunction with the implementation of the STCW Convention and STCW Code.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds the definition of<E T="03">Management level</E>
              </ENT>
              <ENT>To explain that master, chief mate, chief engineer and first assistant engineer (second engineer officer) are considered management level under the STCW Convention.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>

              <ENT>Adds definition of Officer in Charge of a Navigational Watch (<E T="03">OICEW</E>)</ENT>
              <ENT>To clarify that this endorsement is at the operational level.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>

              <ENT>Adds definition of Officer in Charge of an Engineering Watch (<E T="03">OICEW</E>)</ENT>
              <ENT>To clarify that this endorsement is at the operational level.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds the definition of<E T="03">Operational level</E>
              </ENT>
              <ENT>Provides that officer endorsements other than management level are considered operational level under the STCW Convention.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>This will provide consistency with STCW.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds the definition of Periodically unattended engine room</ENT>
              <ENT>Provides clarity in the application of the service requirements for engineers.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds the definition of<E T="03">Propulsion power</E>
              </ENT>
              <ENT>To provide consistency with the use of the term “propulsion power” in STCW and to encompass methods of measurement, such as horsepower (HP) and kilowatts (kW).</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds definition of<E T="03">Push-mode ITBs</E>
              </ENT>
              <ENT>To specify what is included in the configuration of this tug barge unit.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds definition of<E T="03">Qualified Assessor</E>
              </ENT>
              <ENT>To clarify the qualifications for this type of evaluator.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds the definition of<E T="03">Quality standard system (QSS)</E>
              </ENT>
              <ENT>To ensure conformity with STCW requirements for use of a QSS and provide clarification of what is intended by this term when used in this subchapter.</ENT>
            </ROW>
            <ROW>
              <PRTPAGE P="45916"/>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds definition of<E T="03">Seagoing service</E>
              </ENT>
              <ENT>Clarify for the mariner what is included in this type of service, including Great Lakes and inland service.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>This is in response to public comments specifically requesting credit for all waters.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds the definition of<E T="03">Seagoing vessel</E>
              </ENT>
              <ENT>To ensure the definition captures all vessels to which STCW Convention and Code apply.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>There is no commercial vessels restriction, as appears in the current 46 CFR 15.1101 definition, because that would have excluded vessels such as yachts and government-owned vessels, which are required to be operated by mariners holding an STCW endorsement.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds definition of<E T="03">Lifeboatman-Limited</E>
              </ENT>
              <ENT>To provide for a new endorsement for persons serving in a position similar to Lifeboatman but on a vessel without a lifeboat.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.107</ENT>
              <ENT>Adds the definition of<E T="03">Training program</E>
              </ENT>
              <ENT>To provide clarity regarding what is encompassed within training programs.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.205(b)(i)</ENT>
              <ENT>Adds grandfathering provision for existing STCW endorsements</ENT>
              <ENT>Clarifies that this proposed rule does not require a mariner to meet newly proposed requirements in order to retain a credential already held.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>This will provide mariners with time to meet new requirements, while still being able to serve on those credentials already held.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.205(i)</ENT>
              <ENT>Adds provision regarding Document of Continuity</ENT>
              <ENT>To explain the process of replacing a Document of Continuity with an MMC.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.209</ENT>
              <ENT>Adds ceremonial license</ENT>
              <ENT>Allows mariners to request a ceremonial license when renewing his or her credential.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.405</ENT>
              <ENT>Adds requirements for qualification as a qualified assessor or designated examiner</ENT>
              <ENT>To ensure that qualified individuals conduct evaluations of mariners in conformity with the STCW Convention. See Section A-I/6 of the STCW Code.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.409</ENT>
              <ENT>Adds requirements for approval as a Coast Guard-accepted QSS organization</ENT>
              <ENT>Requires organizations wishing to accept and monitor training to submit application for approval. Coast Guard-accepted QSS organizations will be audited once every five years.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>This is to ensure compliance with STCW and to provide oversight of these organizations.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.411</ENT>
              <ENT>Adds simulator performance standards</ENT>
              <ENT>To provide consistency with existing requirements and Section A-I/12 of the STCW Code.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">N/A</ENT>
              <ENT>§ 10.412</ENT>
              <ENT>Adds distance and e-learning</ENT>
              <ENT>Adds a provision that will allow mariners to complete certain approved training via distance or e-learning courses.</ENT>
            </ROW>
            <ROW>
              <ENT I="22"/>
              <ENT O="xl"/>
              <ENT O="xl"/>
              <ENT>This will allow more options for obtaining training.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§§ 11.201, 11.205</ENT>
              <ENT>§ 11.201</ENT>
              <ENT>Re-organizes and consolidates all general requirements applicable to all domestic and STCW officer endorsements</ENT>
              <ENT>Consolidates all endorsement requirements from the various sections (including §§ 11.201, 11.205) into a general section with sub-titles to allow for easy reference.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 11.202</ENT>
              <ENT>§ 15.817</ENT>
              <ENT>Moves section for GMDSS competency<LI>Requires that all deck officers serving on vessels equipped with Global Maritime Distress and Safety System (GMDSS) provide an endorsement for GMDSS</LI>
              </ENT>
              <ENT>This re-organizes the regulations to make them easier to access and follow.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 11.202</ENT>
              <ENT>§ 15.816</ENT>
              <ENT>Moves section for ARPA competency<LI>Requires that all deck officers serving on vessels equipped with ARPA prove competency</LI>
              </ENT>
              <ENT>This re-organizes the regulations to make them easier to access and follow.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 11.202, 11.205</ENT>
              <ENT>§ 11.301</ENT>
              <ENT>Re-organizes and consolidates all requirements applicable to all STCW officer endorsements</ENT>
              <ENT>Consolidates all endorsement requirements from various sections (including §§ 11.202 and 11.205) into a general section with sub-titles to allow for easy reference.</ENT>
            </ROW>
            <ROW>
              <ENT I="01">§ 11.202(c)</ENT>
              <ENT>§§ 11.305 to 11.321</ENT>
              <ENT>Moves the requirement for automatic radar plotting aid (ARPA) from the general section</ENT>
              <ENT>To place the requirement in the appropriate operational-level and management-level certificate.</ENT>
            </ROW>
            <ROW>
              <PRTPAGE P="45917"/>
              <ENT I="01">§ 11.202(d)</ENT>
              <ENT>§§ 11.305 to 11.321</ENT>
              <ENT>Moves the requirement for the training and assessment on Global Maritime Distress and Safety System (GMDSS) from the general section</ENT>
              <ENT>Incorporates the GMDSS requirement with the requirement for the appropriate operational-level and manage
