[Federal Register Volume 73, Number 132 (Wednesday, July 9, 2008)]
[Notices]
[Page 39339]
From the Federal Register Online via the Government Publishing 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.

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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: 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-2008-0368. 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-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 [email protected].

    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]
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