[Federal Register Volume 79, Number 139 (Monday, July 21, 2014)]
[Notices]
[Pages 42375-42376]
From the Federal Register Online via the Government Printing 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 INFOCOLLECTS.Resource@NRC.GOV.

    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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