[Federal Register Volume 70, Number 113 (Tuesday, June 14, 2005)]
[Pages 34505-34506]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E5-3064]



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 OMB and solicitation of public comment.


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

[[Page 34506]]

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 estimated number of annual respondents: 364 (104 NRC 
licensees and 260 Agreement State licensees).
    6. The number of hours needed annually to complete the requirement 
or request: 42 hours (12 hours NRC licensees and 30 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 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 August 15, 2005, comments that address the following 
    1. Is the proposed collection of information necessary for the NRC 
to properly perform its functions? Does the information have practical 
    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 and questions about the information collection 
requirements may be directed to the NRC Clearance Officer, Brenda Jo. 
Shelton, U.S. Nuclear Regulatory Commission, T-5 F53, Washington, DC 
20555-0001, by telephone at 301-415-7233, or by Internet electronic 
mail to [email protected].

    Dated at Rockville, Maryland, this 8th day of June 2005.

    For the Nuclear Regulatory Commission.
Brenda Jo. Shelton,
NRC Clearance Officer, Office of Information Services.
[FR Doc. E5-3064 Filed 6-13-05; 8:45 am]