U.S. Nuclear Regulatory Commission (NRC).
Notice of the OMB review of information collection and solicitation of public comment.
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: 10 CFR Part 35 Medical Use of Byproduct Material.
3. The form number if applicable: N/A.
4. 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.
5. Who will be 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.
6. An estimate of the number of annual responses: 259,332 (53,346 responses from NRC Licenses + 1,862 recordkeepers and 197,235 responses from Agreement States + 6,889 recordkeepers) .
7. An estimate of the number of annual respondents: 8,751 (1,862 for NRC Licenses and 6,889 for Agreement States).
8. An estimate of the total number of hours needed annually to complete the requirement or request: 987,764 hours (251,200 for NRC Licenses and 736,564 for Agreement States).
9. An indication of whether Section 3507(d), Public Law 104-13 applies: N/A.
10. 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.
A copy of the final 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, Maryland 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 should be directed to the OMB reviewer listed below by September 6, 2007. 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. Nathan Frey, Desk Officer, Office of Information and Regulatory Affairs (3150-0010), NEOB-10202, Office of Management and Budget, Washington, DC 20503.
Comments can also be e-mailed to Nathan_Frey@omb.eop.gov or submitted by telephone at (202) 395-4650.
The NRC Clearance Officer is Margaret A. Janney, 301-415-7245.Start Signature
Dated at Rockville, Maryland, this 1st day of August, 2007.
For the Nuclear Regulatory Commission.
Acting NRC Clearance Officer, Office of Information Services.
[FR Doc. E7-15301 Filed 8-6-07; 8:45 am]
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