[Federal Register Volume 72, Number 85 (Thursday, May 3, 2007)]
[Notices]
[Pages 24626-24627]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E7-8439]


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NUCLEAR REGULATORY COMMISSION


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.

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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: 10 CFR Part 35, 
``Medical Use of Byproduct Material''.
    2. Current OMB approval number: 3150-0010.
    3. How often the collection is required: Reports of medical events, 
doses to an embryo/fetus or nursing child, or leaking sources are 
reportable on occurrence. A certifying entity desiring to be recognized 
by the NRC must submit a one-time request for recognition.
    4. Who is required or asked to report: Physicians and medical 
institutions holding an NRC license authorizing the administration of 
byproduct material or radiation therefrom to humans for medical use.
    5. The number of annual respondents: 8,751.
    6. The number of hours needed annually to complete the requirement 
or request: 987,764 hours.
    7. Abstract: 10 CFR Part 35, ``Medical Use of Byproduct Material,'' 
contains NRC's requirements and provisions for the medical use of 
byproduct material and for issuance of specific licenses authorizing 
the medical use of this material. These requirements and provisions 
provide for the radiation safety of workers, the general public, 
patients, and human research subjects. 10 CFR Part 35 contains 
mandatory requirements that apply to NRC licensees authorized to 
administer byproduct material or radiation therefrom to humans for 
medical use. The information in the required reports and records is 
used by the NRC to ensure that public health and safety is protected, 
and that the possession and use of byproduct material is in compliance 
with the license and regulatory requirements.
    Submit, by July 2, 2007, 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 and questions about the information collection requirement 
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 Internet electronic mail to 
[email protected].


[[Page 24627]]


    Dated at Rockville, Maryland, this 26th day of April, 2007.

    For the Nuclear Regulatory Commission.
Margaret A. Janney,
NRC Clearance Officer, Office of Information Services.
 [FR Doc. E7-8439 Filed 5-2-07; 8:45 am]
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