Agency Information Collection Activities: Proposed Collection; Comment Request, 39339 [E8-15569]
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Federal Register / Vol. 73, No. 132 / Wednesday, July 9, 2008 / Notices
Further information about this
meeting can be obtained from Michael
P. McDonald, Advisory Committee
Management Officer, National
Endowment for the Humanities, 1100
Pennsylvania Avenue, NW.,
Washington, DC 20506, or by calling
(202) 606–8322, TDD (202) 606–8282.
Advance notice of any special needs or
accommodations is appreciated.
Michael P. McDonald,
Advisory Committee, Management Officer.
[FR Doc. E8–15597 Filed 7–8–08; 8:45 am]
BILLING CODE 7536–01–P
NUCLEAR REGULATORY
COMMISSION
[Docket No. NRC–2008–0368]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
U.S. Nuclear Regulatory
Commission (NRC).
ACTION: Notice of pending NRC action to
submit an information collection
request to the Office of Management and
Budget (OMB) and solicitation of public
comment.
jlentini on PROD1PC65 with NOTICES
AGENCY:
SUMMARY: The NRC is preparing a
submittal to OMB for review of
continued approval of information
collections under the provisions of the
Paperwork Reduction Act of 1995 (44
U.S.C. Chapter 35).
Information pertaining to the
requirement to be submitted:
1. The title of the information
collection: Registration Certificate InVitro. Testing with Byproduct Material
under General License.
2. Current OMB approval number:
3150–0038.
3. How often the collection is
required: There is a one-time submittal
of information to receive a validated
copy of NRC Form 483 with an assigned
registration number. In addition, any
changes in the information reported on
NRC Form 483 must be reported in
writing to the Commission within 30
days after the effective date of such
change.
4. Who is required or asked to report:
Any physician, veterinarian in the
practice of veterinary medicine, clinical
laboratory or hospital which desires a
general license to receive, acquire,
possess, transfer, or use specified units
of byproduct material in certain in vitro
clinical or laboratory tests.
5. The number of annual respondents:
85.
6. The number of hours needed
annually to complete the requirement or
VerDate Aug<31>2005
16:15 Jul 08, 2008
Jkt 214001
request: 12.4 hours (Record keeping:
1.13 hours + Reporting: 2 hours NRC
licensees and 9.3 hours Agreement State
licensees).
7. Abstract: Section 31.11 of 10 CFR
establishes a general license authorizing
any physician, clinical laboratory,
veterinarian in the practice of veterinary
medicine, or hospital to possess certain
small quantities of byproduct material
for in vitro clinical or laboratory tests
not involving the internal or external
administration of the byproduct
material or the radiation there from to
human beings or animals. Possession of
byproduct material under 10 CFR 31.11
is not authorized until the physician,
clinical laboratory, veterinarian in the
practice of veterinary medicine, or
hospital has filed NRC Form 483 and
received from the Commission a
validated copy of NRC Form 483 with
a registration number.
Submit, by September 8, 2008,
comments that address the following
questions:
1. Is the proposed collection of
information necessary for the NRC to
properly perform its functions? Does the
information have practical utility?
2. Is the burden estimate accurate?
3. Is there a way to enhance the
quality, utility, and clarity of the
information to be collected?
4. How can the burden of the
information collection be minimized,
including the use of automated
collection techniques or other forms of
information technology?
A copy of the draft supporting
statement may be viewed free of charge
at the NRC Public Document Room, One
White Flint North, 11555 Rockville
Pike, Room O–1 F21, Rockville, MD
20852. OMB clearance requests are
available at the NRC worldwide Web
site: https://www.nrc.gov/public-involve/
doc-comment/omb/. The
document will be available on the NRC
home page site for 60 days after the
signature date of this notice. Comments
submitted in writing or in electronic
form will be made available for public
inspection. Because your comments will
not be edited to remove any identifying
or contact information, the NRC
cautions you against including any
information in your submission that you
do not want to be publicly disclosed.
Comments submitted should reference
Docket No. NRC–2008–0368. You may
submit your comments by any of the
following methods. Electronic
comments: Go to https://
www.regulations.gov and search for
Docket No. NRC–2008–0368. Mail
comments to NRC Clearance Officer,
Margaret A. Janney (T–5 F52), U.S.
Nuclear Regulatory Commission,
PO 00000
Frm 00062
Fmt 4703
Sfmt 4703
39339
Washington, DC 20555–0001. Questions
about the information collection
requirements may be directed to the
NRC Clearance Officer, Margaret A.
Janney (T–5 F52), U.S. Nuclear
Regulatory Commission, Washington,
DC 20555–0001, by telephone at 301–
415–7245, or by e-mail to
INFOCOLLECTS.Resource@NRC.GOV.
Dated at Rockville, Maryland, this 30th day
of June 2008.
For the Nuclear Regulatory Commission.
Gregory Trussell,
Acting NRC Clearance Officer, Office of
Information Services.
[FR Doc. E8–15569 Filed 7–8–08; 8:45 am]
BILLING CODE 7590–01–P
NUCLEAR REGULATORY
COMMISSION
South Carolina Electric and Gas
Company (SCE&G) and the South
Carolina Public Service Authority
(Santee Cooper); Notice of Receipt and
Availability of Application for a
Combined License
On March 27, 2008, South Carolina
Electric and Gas Company (SCE&G)
acting as itself and agent for the South
Carolina Public Service Authority also
known as Santee Cooper filed with the
U.S. Nuclear Regulatory Commission
(NRC, the Commission) pursuant to
Section 103 of the Atomic Energy Act
and Title 10 of the Code of Federal
Regulations (10 CFR) part 52, ‘‘Licenses,
Certifications, and Approvals for
Nuclear Power Plants,’’ an application
for a combined license (COL) for two
AP1000 nuclear power plants at the
existing Virgil C. Summer Nuclear Site
(VCSNS) located in Fairfield County,
South Carolina. The reactors are to be
identified as VCSNS Units 2 and 3.
An applicant may seek a COL in
accordance with Subpart C of 10 CFR
part 52. The information submitted by
the applicant includes certain
administrative information such as
financial qualifications submitted
pursuant to 10 CFR 52.77, as well as
technical information submitted
pursuant to 10 CFR 52.79. The applicant
also requested exemptions from certain
requirements of Section IV.A.2.
Appendix D to 10 CFR part 52 and 10
CFR 52.79(a)(44) as documented in part
7 of the application.
Subsequent Federal Register notices
will address the acceptability of the
tendered COL application for docketing
and provisions for participation of the
public in the COL review process.
A copy of the application is available
for public inspection at the
Commission’s Public Document Room
E:\FR\FM\09JYN1.SGM
09JYN1
Agencies
[Federal Register Volume 73, Number 132 (Wednesday, July 9, 2008)]
[Notices]
[Page 39339]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-15569]
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NUCLEAR REGULATORY COMMISSION
[Docket No. NRC-2008-0368]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: U.S. Nuclear Regulatory Commission (NRC).
ACTION: Notice of pending NRC action to submit an information
collection request to the Office of Management and Budget (OMB) and
solicitation of public comment.
-----------------------------------------------------------------------
SUMMARY: The NRC is preparing a submittal to OMB for review of
continued approval of information collections under the provisions of
the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35).
Information pertaining to the requirement to be submitted:
1. The title of the information collection: Registration
Certificate In-Vitro. Testing with Byproduct Material under General
License.
2. Current OMB approval number: 3150-0038.
3. How often the collection is required: There is a one-time
submittal of information to receive a validated copy of NRC Form 483
with an assigned registration number. In addition, any changes in the
information reported on NRC Form 483 must be reported in writing to the
Commission within 30 days after the effective date of such change.
4. Who is required or asked to report: Any physician, veterinarian
in the practice of veterinary medicine, clinical laboratory or hospital
which desires a general license to receive, acquire, possess, transfer,
or use specified units of byproduct material in certain in vitro
clinical or laboratory tests.
5. The number of annual respondents: 85.
6. The number of hours needed annually to complete the requirement
or request: 12.4 hours (Record keeping: 1.13 hours + Reporting: 2 hours
NRC licensees and 9.3 hours Agreement State licensees).
7. Abstract: Section 31.11 of 10 CFR establishes a general license
authorizing any physician, clinical laboratory, veterinarian in the
practice of veterinary medicine, or hospital to possess certain small
quantities of byproduct material for in vitro clinical or laboratory
tests not involving the internal or external administration of the
byproduct material or the radiation there from to human beings or
animals. Possession of byproduct material under 10 CFR 31.11 is not
authorized until the physician, clinical laboratory, veterinarian in
the practice of veterinary medicine, or hospital has filed NRC Form 483
and received from the Commission a validated copy of NRC Form 483 with
a registration number.
Submit, by September 8, 2008, comments that address the following
questions:
1. Is the proposed collection of information necessary for the NRC
to properly perform its functions? Does the information have practical
utility?
2. Is the burden estimate accurate?
3. Is there a way to enhance the quality, utility, and clarity of
the information to be collected?
4. How can the burden of the information collection be minimized,
including the use of automated collection techniques or other forms of
information technology?
A copy of the draft supporting statement may be viewed free of
charge at the NRC Public Document Room, One White Flint North, 11555
Rockville Pike, Room O-1 F21, Rockville, MD 20852. OMB clearance
requests are available at the NRC worldwide Web site: https://
www.nrc.gov/public-involve/doc-comment/omb/. The document
will be available on the NRC home page site for 60 days after the
signature date of this notice. Comments submitted in writing or in
electronic form will be made available for public inspection. Because
your comments will not be edited to remove any identifying or contact
information, the NRC cautions you against including any information in
your submission that you do not want to be publicly disclosed. Comments
submitted should reference Docket No. NRC-2008-0368. You may submit
your comments by any of the following methods. Electronic comments: Go
to https://www.regulations.gov and search for Docket No. NRC-2008-0368.
Mail comments to NRC Clearance Officer, Margaret A. Janney (T-5 F52),
U.S. Nuclear Regulatory Commission, Washington, DC 20555-0001.
Questions about the information collection requirements may be directed
to the NRC Clearance Officer, Margaret A. Janney (T-5 F52), U.S.
Nuclear Regulatory Commission, Washington, DC 20555-0001, by telephone
at 301-415-7245, or by e-mail to INFOCOLLECTS.Resource@NRC.GOV.
Dated at Rockville, Maryland, this 30th day of June 2008.
For the Nuclear Regulatory Commission.
Gregory Trussell,
Acting NRC Clearance Officer, Office of Information Services.
[FR Doc. E8-15569 Filed 7-8-08; 8:45 am]
BILLING CODE 7590-01-P