[Federal Register Volume 73, Number 129 (Thursday, July 3, 2008)]
[Notices]
[Pages 38251-38252]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-15118]
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NUCLEAR REGULATORY COMMISSION
[Docket No. 030-33820]
Notice of Availability of Environmental Assessment and Finding of
No Significant Impact for Amendment of Byproduct Materials License No.
13-26640-01, for Unrestricted Release of a Facility in Evansville, IN
AGENCY: Nuclear Regulatory Commission.
ACTION: Issuance of Environmental Assessment and Finding of No
Significant Impact for License Amendment.
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FOR FURTHER INFORMATION CONTACT: Peter J. Lee, PhD, CHP, Health
Physicist, Decommissioning Branch, Division of Nuclear Materials
Safety, Region III, U.S. Nuclear Regulatory Commission, 2443
Warrenville Road, Lisle, Illinois 60532; telephone: (630) 829-9870; fax
number: (630) 515-1259; or by e-mail at Peter.Lee@nrc.gov.
SUPPLEMENTARY INFORMATION:
I. Introduction
The U.S. Nuclear Regulatory Commission (NRC) is proposing to amend
Byproduct Materials License No. 13-26640-01. The license is held by the
Covance Clinical Research Unit, Inc. (the Licensee), now located at 617
Oakley Street, Evansville, Indiana. Issuance of the amendment would
authorize release of the Licensee's facility, located at 800 St. Mary's
Drive, Evansville, Indiana (the Facility) for unrestricted use. The
Licensee requested this action in NRC FORM 313 dated February 1, 2008.
The NRC has prepared an Environmental Assessment (EA) in support of
this proposed action in accordance with the requirements of Title 10,
Code of Federal Regulations (CFR), Part 51 (10 CFR Part 51). Based on
the EA, the NRC has concluded that a Finding of No Significant Impact
(FONSI) is appropriate with respect to the proposed action. The
amendment will be issued to the Licensee following the publication of
this FONSI and EA in the Federal Register.
II. Environmental Assessment
Identification of Proposed Action
The proposed action would approve the Licensee's February 1, 2008
request, resulting in release of the Facility for unrestricted use.
License No. 13-26640-01 was issued on August 16, 1995, pursuant to 10
CFR Part 35, and has been amended periodically since that time. The
license authorizes the use of by-product materials (carbon-14 and
hydrogen-3) in human research studies.
Need for the Proposed Action
The Licensee has ceased conducting licensed activities at the
Facility and seeks the unrestricted use of its Facility.
Environmental Impacts of the Proposed Action
The historical review of licensed activities conducted at the
Facility shows that such activities involved use of the following
radionuclides with half-lives greater than 120 days: hydrogen-3 and
carbon-14, and that use of these materials at the Facility ceased in
early January 2008. Prior to performing the final status survey, the
Licensee conducted decontamination activities, as necessary, in the
areas of the Facility affected by these radionuclides.
The Licensee completed final status surveys at the Facility on
January 22, 2008. The final status survey report was attached to the
Licensee's amendment request dated February 1, 2008. The Licensee
elected to demonstrate compliance with the radiological criteria for
unrestricted release as specified in 10 CFR 20.1402 using release
criteria for building surfaces based on NUREG-1556, Volume 7,
``Program-Specific Guidance About Academic, Research and Development,
and Other Licenses of Limited Scope Including Gas Chromatographs and X-
Ray Fluorescence Analyzers--Final Report,'' Appendix Q, ``Radiation
Safety Survey Topics.'' These release criteria are the same as the
radionuclide-specific dose-based release criteria, described in NUREG-
1757, ``Consolidated NMSS Decommissioning Guidance,'' Volume 2. These
values provide acceptable levels of surface contamination to
demonstrate compliance with the NRC requirements in Subpart E of 10 CFR
Part 20 for unrestricted release. The Licensee's final status survey
results were below these values and are in compliance with the As Low
As Reasonably Achievable (ALARA) requirement of 10 CFR 20.1402. The NRC
thus finds that the Licensee's final status survey results are
acceptable.
Based on its review, the staff has determined that the affected
environment and any environmental impacts associated with the proposed
action are bounded by the impacts evaluated by the ``Generic
[[Page 38252]]
Environmental Impact Statement in Support of Rulemaking on Radiological
Criteria for License Termination of NRC-Licensed Nuclear Facilities,''
(NUREG-1496) Volumes 1-3 (ML042310492, ML042320379, and ML042330385).
The staff finds there were no significant environmental impacts from
the use of radioactive material at the Facility. The NRC staff reviewed
available docket file records and the survey results to identify any
non-radiological hazards that may have impacted the environment
surrounding the Facility. No such hazards or impacts to the environment
were identified. The NRC has identified no other radiological or non-
radiological activities in the area that could result in cumulative
environmental impacts.
The NRC staff finds that issuance of the proposed amendment is in
compliance with 10 CFR Part 20. Based on its review, the staff
considered the impact of the residual radioactivity at the Facility and
concluded that the proposed action will not have a significant effect
on the quality of the human environment.
Environmental Impacts of the Alternatives to the Proposed Action
Due to the largely administrative nature of the proposed action,
its environmental impacts are small. Therefore, the only alternative
the staff considered is the no-action alternative, under which the
staff would leave things as they are by simply denying the amendment
request. This no-action alternative is not feasible because it
conflicts with 10 CFR 30.36(d), requiring that decommissioning of
byproduct material facilities be completed and approved by the NRC
after licensed activities cease. The NRC's analysis of the Licensee's
final status survey data confirmed that the Facility meets the
requirements of 10 CFR 20.1402 for unrestricted release. Additionally,
denying the amendment request would result in no change in current
environmental impacts. The environmental impacts of the proposed action
and the no-action alternative are, therefore, similar; and the no-
action alternative is accordingly not further considered.
Conclusion
The NRC staff has concluded that the proposed action is consistent
with the NRC's unrestricted release criteria specified in 10 CFR
20.1402. Because the proposed action will not significantly impact the
quality of the human environment, the NRC staff concludes that the
proposed action is the preferred alternative.
Agencies and Persons Consulted
NRC provided a draft of this Environmental Assessment to the
Indiana Emergency Response Program for review on March 24, 2008. By
response dated May 12, 2008, the State agreed with the conclusions of
the EA, and provided no comments.
The NRC staff has determined that the proposed action is of a
procedural nature, and will not affect listed species or critical
habitat. Therefore, no further consultation is required under section 7
of the Endangered Species Act. The NRC staff has also determined that
the proposed action is not the type of activity that has the potential
to cause effects on historic properties. Therefore, no further
consultation is required under section 106 of the National Historic
Preservation Act.
III. Finding of No Significant Impact
The NRC staff has prepared this EA in support of the proposed
action. On the basis of this EA, the NRC finds that there are no
significant environmental impacts from the proposed action, and that
preparation of an environmental impact statement is not warranted.
Accordingly, the NRC has determined that a Finding of No Significant
Impact is appropriate.
IV. Further Information
Documents related to this action, including the application for
license amendment and supporting documentation, are available
electronically at the NRC's Electronic Reading Room at http://
www.nrc.gov/reading-rm/adams.html. From this site, you can access the
NRC's Agencywide Document Access and Management System (ADAMS), which
provides text and image files of NRC's public documents. The documents
related to this action are listed below, along with their ADAMS
accession numbers.
1. Mary L. Westrick, Covance Clinical Research Unit Inc., NRC Form
313 dated February 1, 2008 (ADAMS Accession No. ML080810513);
2. Title 10 Code of Federal Regulations, Part 20, Subpart E,
``Radiological Criteria for License Termination'';
3. Title 10 Code of Federal Regulations, Part 51, ``Environmental
Protection Regulations for Domestic Licensing and Related Regulatory
Functions'';
4. NUREG-1496, ``Generic Environmental Impact Statement in Support
of Rulemaking on Radiological Criteria for License Termination of NRC-
Licensed Nuclear Facilities'';
5. NUREG-1757, ``Consolidated NMSS Decommissioning Guidance.''
6. NUREG-1556, Volume 7, ``Program-Specific Guidance About
Academic, Research and Development, and Other Licenses of Limited Scope
Including Gas Chromatographs and X-Ray Fluorescence Analyzers--Final
Report,'' Appendix Q, ``Radiation Safety Survey Topics.''
If you do not have access to ADAMS, or if there are problems in
accessing the documents located in ADAMS, contact the NRC Public
Document Room (PDR) Reference staff at 1-800-397-4209, 301-415-4737, or
by e-mail to pdr@nrc.gov. These documents may also be viewed
electronically on the public computers located at the NRC's PDR, O 1
F21, One White Flint North, 11555 Rockville Pike, Rockville, MD 20852.
The PDR reproduction contractor will copy documents for a fee.
Dated at Lisle, Illinois, this 23rd day of June 2008.
For the Nuclear Regulatory Commission.
Christine A. Lipa,
Chief, Decommissioning Branch, Division of Nuclear Materials Safety,
Region III.
[FR Doc. E8-15118 Filed 7-2-08; 8:45 am]
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