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, 38251-38252 [E8-15118]
Download as PDF
Federal Register / Vol. 73, No. 129 / Thursday, July 3, 2008 / Notices
NCD is an independent
federal agency and is composed of 15
members appointed by the President, by
and with the advice and consent of the
Senate. NCD provides advice to the
President, Congress, and executive
branch agencies promoting policies,
programs, practices, and procedures that
(A) guarantee equal opportunity for all
individuals with disabilities, regardless
of the nature or severity of the
disability; and (B) to empower
individuals with disabilities to achieve
economic self-sufficiency, independent
living, and inclusion and integration
into all aspects of society.
AGENCY MISSION:
Those needing
reasonable accommodations should
notify NCD immediately.
ACCOMMODATIONS:
In accordance
with E.O. 13166, Improving Access to
Services for Persons with Limited
English Proficiency, those people with
disabilities who are limited English
proficient and seek translation services
for this meeting should notify NCD
immediately.
Dated: June 26, 2008.
Michael C. Collins,
Executive Director.
[FR Doc. 08–1407 Filed 6–30–08; 12:45 pm]
BILLING CODE 6820–MA–P
NATIONAL TRANSPORTATION
SAFETY BOARD
Sunshine Act Meeting; Agenda
9:30 a.m., Tuesday, July
8, 2008
NTSB Conference Center, 429
L’Enfant Plaza, SW., Washington, DC
20594.
PLACE:
STATUS:
The one item is open to the
public.
mstockstill on PROD1PC66 with NOTICES
MATTER TO BE CONSIDERED:
8021 Highway Accident Report—
Motorcoach Override of Elevated Exit
Ramp, Interstate 75, Atlanta, Georgia,
March 2, 2007 (HWY–07–MH–015).
NEWS MEDIA CONTACT: Telephone: (202)
314–6100.
Individuals requesting specific
accommodations should contact
Rochelle Hall at (202) 314–6305 by
Thursday, July 3, 2008.
The public may view the meeting via
a live or archived Webcast by accessing
a link under ‘‘News & Events’’ on the
NTSB home page at https://
www.ntsb.gov.
FOR FURTHER INFORMATION CONTACT:
Vicky D’Onofrio, (202) 314–6410.
VerDate Aug<31>2005
16:46 Jul 02, 2008
Jkt 214001
BILLING CODE 7533–01–P
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
Nuclear Regulatory
Commission.
ACTION: Issuance of Environmental
Assessment and Finding of No
Significant Impact for License
Amendment.
AGENCY:
LANGUAGE TRANSLATION:
TIME AND DATE:
Dated: Monday, June 30, 2008.
Candi R. Bing,
Federal Register Liaison Officer.
[FR Doc. E8–15248 Filed 7–2–08; 8:45 am]
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,
PO 00000
Frm 00080
Fmt 4703
Sfmt 4703
38251
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 halflives 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 XRay Fluorescence Analyzers—Final
Report,’’ Appendix Q, ‘‘Radiation Safety
Survey Topics.’’ These release criteria
are the same as the radionuclidespecific 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
E:\FR\FM\03JYN1.SGM
03JYN1
38252
Federal Register / Vol. 73, No. 129 / Thursday, July 3, 2008 / Notices
Environmental Impact Statement in
Support of Rulemaking on Radiological
Criteria for License Termination of NRCLicensed 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.
mstockstill on PROD1PC66 with NOTICES
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.
VerDate Aug<31>2005
16:46 Jul 02, 2008
Jkt 214001
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.
6. NUREG–1556, Volume 7,
‘‘Program-Specific Guidance About
Academic, Research and Development,
and Other Licenses of Limited Scope
Including Gas Chromatographs and XRay 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.
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.
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]
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 https://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 NRCLicensed Nuclear Facilities’’;
5. NUREG–1757, ‘‘Consolidated
NMSS Decommissioning Guidance.’’
PO 00000
Frm 00081
Fmt 4703
Sfmt 4703
BILLING CODE 7590–01–P
OFFICE OF PERSONNEL
MANAGEMENT
Federal Employees Health Benefits
Program: Medically Underserved Areas
for 2009
Office of Personnel
Management.
ACTION: Notice of Medically
Underserved Areas for 2009.
AGENCY:
SUMMARY: The Office of Personnel
Management (OPM) has completed its
annual determination of the States that
qualify as Medically Underserved Areas
under the Federal Employees Health
Benefits (FEHB) Program for calendar
year 2009. This is necessary to comply
with a provision of the FEHB law that
mandates special consideration for
enrollees of certain FEHB plans who
receive covered health services in States
with critical shortages of primary care
physicians. Accordingly, for calendar
year 2009, the following states are
Medically Underserved Areas under the
FEHB Program: Alabama, Arizona,
Idaho, Illinois, Kentucky, Louisiana,
Mississippi, Missouri, Montana, New
Mexico, North Dakota, South Carolina,
South Dakota, and Wyoming. For the
2009 calendar year the State of Illinois
is being added.
DATES: Effective Date: January 1, 2009.
FOR FURTHER INFORMATION CONTACT:
Ingrid Burford, 202–606–0004.
E:\FR\FM\03JYN1.SGM
03JYN1
Agencies
[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]
=======================================================================
-----------------------------------------------------------------------
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.
-----------------------------------------------------------------------
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 https://
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]
BILLING CODE 7590-01-P