[Federal Register Volume 64, Number 89 (Monday, May 10, 1999)]
[Notices]
[Pages 25082-25083]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-11673]
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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: Extension.
2. The title of the information collection: 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: 364 (104 registration
certificates from NRC licensees and 260 registration certificates from
Agreement State licensees).
7. The estimated number of annual respondents: 364 (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, 7 minutes per response.
9. An indication of whether section 3507(d), Pub. L. 104-13
applies: N/A.
10. Abstract: Section 31.11 of 10 CFR establishes a general license
authorizing any physician, clinical laboratory,
[[Page 25083]]
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 final supporting statement may be viewed free of
charge at the NRC Public Document Room, 2120 L Street, NW (lower
level), Washington, DC. OMB clearance requests are available at the NRC
worldwide web site (http://www.nrc.gov/NRC/PUBLIC/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 and questions should be directed to the OMB reviewer
listed below by June 9, 1999. Comments received after this date will be
considered if it is practical to do so, but assurance of consideration
cannot be given to comments received after this date.
Erik Godwin, 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 (202) 395-3087.
The NRC Clearance Officer is Brenda Jo. Shelton, 301-415-7233.
Dated at Rockville, MD, this 4th day of May 1999.
For the Nuclear Regulatory Commission.
Brenda Jo. Shelton,
NRC Clearance Officer, Office of the Chief Information Officer.
[FR Doc. 99-11673 Filed 5-7-99; 8:45 am]
BILLING CODE 7590-01-P