96-10348. Agency Information Collection Activities: Submission for OMB Review; Comment Request

[Federal Register Volume 61, Number 82 (Friday, April 26, 1996)]
[Notices]
[Page 18630]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-10348]



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NUCLEAR REGULATORY COMMISSION

Agency Information Collection Activities: Submission for OMB 
Review; Comment Request

AGENCY: Nuclear Regulatory Commission (NRC).

ACTION: Notice of the OMB review of information collection and 
solicitation of public comment.

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SUMMARY: The NRC has recently submitted to OMB for review the following 
proposal for the collection of information under the provisions of the 
Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35). The NRC hereby 
informs potential respondents that an agency may not conduct or 
sponsor, and that a person is not required to respond to, a collection 
of information unless it displays a currently valid OMB control number.
    1. Type of submission, new, revision, or extension: Revision.
    2. The title of the information collection: NRC Form 483, 
``Registration Certificate--In Vitro Testing with Byproduct Material 
under General License.''
    3. The form number if applicable: NRC Form 483.
    4. 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.
    5. Who will be 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.
    6. An estimate of the number of responses: 104 registration 
certificates from NRC licensees and 260 registration certificates from 
Agreement State licensees.
    7. The estimated number of annual respondents: 104 NRC licensees 
and 260 Agreement State licensees.
    8. An estimate of the total number of hours needed annually to 
complete the requirement or request: 42 hours or approximately 7 
minutes per NRC or Agreement State licensee.
    9. An indication of whether Section 3507(d), Public Law 104-13 
applies: Not applicable.
    10. 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 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.
    A copy of the submittal may be viewed free of charge at the NRC 
Public Document Room, 2120 L Street, NW, (Lower Level), Washington, DC. 
Members of the public who are in the Washington, DC, area can access 
the submittal via modem on the Public Document Room Bulletin Board 
(NRC's Advance Copy Document Library) NRC subsystem at FedWorld, 703-
321-3339. Members of the public who are located outside of the 
Washington, DC, area can dial FedWorld, 1-800-303-9672, or use the 
FedWorld Internet address: fedworld.gov (Telnet). The document will be 
available on the bulletin board for 30 days after the signature date of 
this notice. If assistance is needed in accessing the document, please 
contact the FedWorld help desk at 703-487-4608. Additional assistance 
in locating the document is available from the NRC Public Document 
Room, nationally at 1-800-397-4209, or within the Washington, DC, area 
at 202-634-3273.
    Comments and questions should be directed to the OMB reviewer by 
May 28, 1996.

Peter Francis, Office of Information and Regulatory Affairs (3150-
0038), NEOB-10202, Office of Management and Budget, Washington, DC 
20503

    Comments can also be submitted by telephone at [phone].
    The NRC Clearance Officer is Brenda Jo. Shelton, [phone].

    Dated at Rockville, Maryland, this 18th day of April 1996.

    For the Nuclear Regulatory Commission.
Gerald F. Cranford,
Designated Senior Official for Information Resources Management.
[FR Doc. 96-10348 Filed 4-25-96; 8:45 am]
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