[Federal Register Volume 61, Number 21 (Wednesday, January 31, 1996)]
[Notices]
[Pages 3495-3496]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-1866]
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NUCLEAR REGULATORY COMMISSION
Documents Containing Reporting or Recordkeeping Requirements:
Notice of Pending Submittal to the Office of Management and Budget
(OMB) for Review
AGENCY: Nuclear Regulatory Commission (NRC).
ACTION: Notice of pending NRC action to submit an information
collection request to 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: 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
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
[[Page 3496]]
of byproduct material in certain in vitro clinical or laboratory tests.
5. The number of annual respondents: 104 NRC licensees and 260
Agreement State licensees.
6. The number of hours needed annually to complete the requirement
or request: 42 hours or approximately 7 minutes per NRC or Agreement
State licensee.
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 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 April 1, 1996, 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, 2120 L Street, NW, (Lower
Level), Washington, DC. Members of the public who are in the
Washington, DC, area can access this document via modem on the Public
Document Room Bulletin Board (NRC's Advanced 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.
Comments and questions may be directed to the NRC Clearance
Officer, Brenda Jo. Shelton, U.S. Nuclear Regulatory Commission, T-6
F33, Washington, DC, 20555-0001, or by telephone at (301) 415-7233, or
by Internet electronic mail at [email protected].
Dated at Rockville, MD., this 25th day of January, 1996.
For the Nuclear Regulatory Commission.
Gerald F. Cranford,
Designated Senior, Official for Information Resources Management.
[FR Doc. 96-1866 Filed 1-30-96; 8:45 am]
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