[Federal Register Volume 76, Number 163 (Tuesday, August 23, 2011)]
[Notices]
[Pages 52698-52699]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2011-21433]
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NUCLEAR REGULATORY COMMISSION
[Docket No. NRC-2011-0181]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: 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.
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SUMMARY: The NRC invites public comment about our intention to request
the OMB's approval for renewal of an existing information collection
that is summarized below. We are required to publish this notice in the
Federal Register 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: NRC Form 483,
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
NRC 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
[[Page 52699]]
of byproduct material in certain in vitro clinical or laboratory tests.
5. The number of annual respondents: 87 (7 NRC licensees + 80
Agreement State licensees).
6. The number of hours needed annually to complete the requirement
or request: 12.87 hours (1 hour for NRC licensees + 10.7 hours for
Agreement State licensees + 1.17 hours recordkeeping).
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 October 24, 2011, 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?
The public may examine and have copied for a fee publicly available
documents, including the draft supporting statement, at the NRC's
Public Document Room, Room O-1F21, One White Flint North, 11555
Rockville Pike, Rockville, Maryland 20852. OMB clearance requests are
available at the NRC Web site: http://www.nrc.gov/public-involve/doc-comment/omb/index.html. 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-
2011-0181. You may submit your comments by any of the following
methods: Electronic comments: Go to http://www.regulations.gov and
search for Docket No. NRC-2011-0181. Mail comments to NRC Clearance
Officer, Tremaine Donnell (T-5 F53), U.S. Nuclear Regulatory
Commission, Washington, DC 20555-0001. Direct questions about the
information collection requirements to the NRC Clearance Officer,
Tremaine Donnell (T-5 F53), U.S. Nuclear Regulatory Commission,
Washington, DC 20555-0001, by telephone at 301-415-6258, or by e-mail
to [email protected].
Dated at Rockville, Maryland, this 17th day of August, 2011.
For the Nuclear Regulatory Commission.
Tremaine Donnell,
NRC Clearance Officer, Office of Information Services.
[FR Doc. 2011-21433 Filed 8-22-11; 8:45 am]
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