[Federal Register Volume 81, Number 132 (Monday, July 11, 2016)]
[Notices]
[Pages 44875-44876]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-16349]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2009-N-0221; FDA-2012-N-0559; FDA-2015-N-3287; FDA-
2015-N-3815; FDA-2007-D-0429; FDA-2012-N-0447; FDA-2011-D-0597; FDA-
2011-D-0164; FDA-2013-N-0013; FDA-2011-N-0146; FDA-2014-N-1533; FDA-
2011-N-0921; FDA-2015-N-2163]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approvals
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is publishing a list of
information collections that have been approved by the Office of
Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations,
Food and Drug Administration, Three White Flint North 10A63, 11601
Landsdown St., North Bethesda, MD 20852, [email protected].
SUPPLEMENTARY INFORMATION: The following is a list of FDA information
collections recently approved by OMB under section 3507 of the
Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control
number and expiration date of OMB approval for each information
collection are shown in table 1. Copies of the supporting statements
for the information collections are available on the Internet at http://www.reginfo.gov/public/do/PRAMain. 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.
Table 1--List of Information Collections Approved by OMB
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OMB control Date approval
Title of collection No. expires
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Food Labeling: Notification Procedures 0910-0331 6/30/2019
for Statements on Dietary Supplements..
PHS Guideline on Infectious Disease 0910-0456 6/30/2019
Issues in Xenotransplantation..........
MDUFMA Small Business Qualification 0910-0508 6/30/2019
Certification..........................
Electronic Submission of Medical Device 0910-0625 6/30/2019
Registration and Listing...............
Guidance for Industry on Q & A Regarding 0910-0641 6/30/2019
Labeling of Nonprescription Human Drug
Products Marketed Without an Approved
Application as Required by the Dietary
Supplement & Nonprescription Drug
Consumer Protection Act................
Antimicrobial Animal Drug Distribution 0910-0659 6/30/2019
Reports and Recordkeeping..............
Guidance for Industry on Oversight of 0910-0733 6/30/2019
Clinical Investigations: A Risk-Based
Approach to Monitoring.................
Guidance for Industry on Safety Labeling 0910-0734 6/30/2019
Changes; Implementation of the Federal
Food, Drug, and Cosmetic Act...........
Accreditation of Third Party 0910-0750 6/30/2019
Certification Bodies to Conduct Food
Safety Audits and Issue Certifications.
Sanitary Transportation of Human and 0910-0773 6/30/2019
Animal Food............................
National Panel of Tobacco Consumer 0910-0815 6/30/2019
Studies................................
Standards for the Growing, Harvesting, 0910-0816 6/30/2019
Packaging, and Holding of Produce for
Human Consumption......................
Hearing, Aging, and Direct-to-Consumer 0910-0818 6/30/2019
Television Advertisements..............
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Dated: July 6, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016-16349 Filed 7-8-16; 8:45 am]
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