[Federal Register Volume 79, Number 139 (Monday, July 21, 2014)]
[Notices]
[Pages 42375-42376]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2014-16990]
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NUCLEAR REGULATORY COMMISSION
[Docket No. NRC-2014-0155]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Nuclear Regulatory Commission.
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 of byproduct material in certain in vitro
clinical or laboratory tests.
5. The number of annual respondents: 8 respondents.
6. The number of hours needed annually to complete the requirement
or request: 1.18 hours (1.07 hours reporting + 0.11 hour
recordkeeping).
7. Abstract: Section 31.11 of Title 10 of the Code of Federal
Regulations (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 test not
involving the internal or external administration of the byproduct
material or the radiation therefrom 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 19, 2014, 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. The OMB clearance requests
are available at
[[Page 42376]]
the NRC's Web site: http://www.nrc.gov/public-involve/doc-comment/omb/.
The document will be available on the NRC's 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-2014-0155. 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-2014-0155. Mail
comments to the Acting NRC Clearance Officer, Brenda Miles (T-5 F44),
U.S. Nuclear Regulatory Commission, Washington, DC 20555-0001.
Questions about the information collection requirements may be
directed to the Acting NRC Clearance Officer, Brenda Miles (T-5 F44),
U.S. Nuclear Regulatory Commission, Washington, DC 20555-0001,
telephone: 301-415-7884, or by email to [email protected].
Dated at Rockville, Maryland, this 15th day of July 2014.
For the Nuclear Regulatory Commission.
Brenda Miles,
Acting NRC Clearance Officer, Office of Information Services.
[FR Doc. 2014-16990 Filed 7-18-14; 8:45 am]
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