Nuclear Regulatory Commission September 12, 2011 – Federal Register Recent Federal Regulation Documents
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Impacts of Compatibility Changes in General License Regulations
The U.S. Nuclear Regulatory Commission (NRC or the Commission) plans to hold public meetings on September 20, 2011, in Lisle, Illinois, and on September 22, 2011, in Mansfield, Massachusetts, to solicit information on impacts to manufacturers and distributors and end-users of generally licensed devices from revising the compatibility categories of Title 10 of the Code of Federal Regulations (10 CFR) 31.5 and 31.6 from ``B'' to ``C.'' In addition to providing information on impacts at the public meetings, information on the issues raised in this document may be submitted to the NRC at any time through the end of the comment period.
Advisory Committee on the Medical Uses of Isotopes; Meeting Notice
NRC will convene a meeting of the Advisory Committee on the Medical Uses of Isotopes (ACMUI) on September 22-23, 2011. A sample of agenda items to be discussed during the public session includes: (1) A discussion on the reporting structure and methods of ACMUI and Advisory Committee on Reactor Safeguards best practices; (2) an update on the status of a Commission paper on data collection regarding patient release; (3) a discussion on electronic signatures for documents that are required to be signed in accordance with U.S. Nuclear Regulatory Commission (NRC) regulations; (4) a discussion on strontium breakthrough with rubidium-82 generators from a U.S. Food and Drug Administration perspective; (5) a discussion on strontium breakthrough with rubidium-82 generators from an NRC perspective; (6) a discussion on ACMUI's 2008 recommended revisions to the medical event abnormal occurrence language; (7) a discussion on medical-related events; (8) a summary from the outcomes of the NRC Medical Related Rulemaking Workshops; (9) a discussion on possible changes to the permanent implant brachytherapy subcommittee report; (10) and the status of 10 CFR part 35 rulemaking. A copy of the agenda will be available at https://www.nrc.gov/reading-rm/doc-collections/acmui/agenda or by e- mailing Ms. Sophie Holiday at the contact information below. Purpose: Discuss issues related to 10 CFR part 35 Medical Use of Byproduct Material. Date and Time for Closed Session: September 22, 2011, from 8 a.m. to 12 p.m. This session will be closed so that ACMUI members can enroll for and activate new badges and undergo NRC training. Date and Time for Open Sessions: September 22, 2011, from 1:30 p.m. to 5 p.m. and September 23, 2011, from 8 a.m. to 4 p.m. Address for Public Meeting: U.S. Nuclear Regulatory Commission, Two White Flint North Building, Room T2-B3, 11545 Rockville Pike, Rockville, Maryland 20852. Public Participation: Any member of the public who wishes to participate in the meeting in person or via phone should contact Ms. Holiday using the information below. The meeting will also be webcast live: https://www.nrc.gov/public-involve/public- meetings/webcast-live.html. Contact Information: Sophie J. Holiday, e-mail: sophie.holiday@nrc.gov, telephone: (301) 415-7865.
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