Advisory Committee on the Medical Uses of Isotopes; Renewal, 14134-14135 [2016-05944]

Download as PDF mstockstill on DSK4VPTVN1PROD with NOTICES 14134 Federal Register / Vol. 81, No. 51 / Wednesday, March 16, 2016 / Notices OMB is particularly interested in comments that help the agency to: • Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; • Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information including the validity of the methodology and assumptions used; • Enhance the quality, utility and clarity of the information to be collected; and • Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g. permitting electronic submissions of responses. ADDRESSES: Christopher J. Reich, Senior Advisor, Institute of Museum and Library Services, 1800 M St. NW., 9th Floor, Washington, DC 20036. Mr. Reich can be reached by Telephone: 202–653– 4685, Fax: 202–653–4608, or by email at creich@imls.gov, or by teletype (TTY/ TDD) at 202–653–4614. SUPPLEMENTARY INFORMATION: The Institute of Museum and Library Services is the primary source of federal support for the Nation’s 123,000 libraries and 35,000 museums. The Institute’s mission is to inspire libraries and museums to advance innovation, learning, and civic engagement. The Institute works at the national level and in coordination with state and local organizations to sustain heritage, culture, and knowledge; enhance learning and innovation; and support professional development. IMLS is responsible for identifying national needs for and trends in museum, library, and information services; measuring and reporting on the impact and effectiveness of museum, library and information services throughout the United States, including programs conducted with funds made available by IMLS; identifying, and disseminating information on, the best practices of such programs; and developing plans to improve museum, library, and information services of the United States and strengthen national, State, local, regional, and international communications and cooperative networks (20 U.S.C. 72, 20 U.S.C. 9108). The purpose of this survey is to gauge the effect of the Museum Assessment Program (MAP) on participating museums and the museum field at large. The survey will be used to measure the VerDate Sep<11>2014 19:28 Mar 15, 2016 Jkt 238001 degree to which the program is meeting the needs and building the institutional capacity of individual museums, and its overall impact on the museum field nationwide. Methods will include web surveys and telephone interviews. The web survey will consist of approximately 40 questions that will examine the participating museums’ experience with the MAP program and the subsequent changes in its operations that can be attributed to the program, as well as basic institutional profile information. The web survey will require an average of 60 minutes to complete. The telephone interview guide will be organized into approximately four sections (e.g. institutional changes resulting from MAP participation; funding; professionalization; and future expectations) and is projected to average 30 minutes to complete. Current Actions: This notice proposes clearance of the Museum Assessment Program (MAP) Evaluation. The 60-day notice for the Museum Assessment Program (MAP) Evaluation, was published in the Federal Register on July 10, 2015 (FR vol. 80, No. 152, pgs. 39805–39806). The agency has taken into consideration the one comment that was received under this notice. The web survey will consist of approximately 40 questions that will examine the participating museums’ experience with the MAP program and the subsequent changes in its operations that can be attributed to the program, as well as basic institutional profile information. The web survey will require an average of 60 minutes to complete. The telephone interview guide will be organized into approximately four sections (e.g. institutional changes resulting from MAP participation; funding; professionalization; and future expectations) and is projected to average 30 minutes to complete. Agency: Institute of Museum and Library Services. Title: Museum Assessment Program Evaluation. OMB Number: To Be Determined. Frequency: Anticipated for Every Five Years. Affected Public: The target population is museums that have participated in the Museum Assessment Program during the past eight years, all of which are located in the United States. Number of Respondents: 309. Estimated Average Burden per Response: The burden per respondent is estimated to be an average of 30 minutes for the web survey and one hour for the telephone interview. PO 00000 Frm 00056 Fmt 4703 Sfmt 4703 Estimated Total Annual Burden: 159 hours. Total Annualized Capital/Startup Costs: $7,000. Total Annual Costs: $3,388.29. FOR FURTHER INFORMATION CONTACT: Comments should be sent to Office of Information and Regulatory Affairs, Attn.: OMB Desk Officer for Education, Office of Management and Budget, Room 10235, Washington, DC 20503, (202) 395–7316. Dated: March 10, 2016. Kim A. Miller, Management Analyst. [FR Doc. 2016–05919 Filed 3–15–16; 8:45 am] BILLING CODE 7036–01–P NUCLEAR REGULATORY COMMISSION Advisory Committee on the Medical Uses of Isotopes; Renewal U.S. Nuclear Regulatory Commission. ACTION: Notice. AGENCY: The U.S. Nuclear Regulatory Commission (NRC) has determined that the renewal of the Charter for the Advisory Committee on the Medical Uses of Isotopes for the 2 year period commencing on March 10, 2016, is in the public interest, in connection with duties imposed on the Commission by law. This action is being taken in accordance with the Federal Advisory Committee Act, after consultation with the Committee Management Secretariat, General Services Administration. FOR FURTHER INFORMATION CONTACT: Sophie Holiday, Office of Federal and State Materials and Environmental Management Programs, U.S. Nuclear Regulatory Commission, Washington, DC 20555; Telephone (301) 415–7865; email Sophie.Holiday@nrc.gov. SUPPLEMENTARY INFORMATION: The purpose of the ACMUI is to provide advice to NRC on policy and technical issues that arise in regulating the medical use of byproduct material for diagnosis and therapy. Responsibilities include providing guidance and comments on current and proposed NRC regulations and regulatory guidance concerning medical use; evaluating certain non-routine uses of byproduct material for medical use; and evaluating training and experience of proposed authorized users. The members are involved in preliminary discussions of major issues in determining the need for changes in NRC policy and regulation to ensure the continued safe use of byproduct SUMMARY: E:\FR\FM\16MRN1.SGM 16MRN1 Federal Register / Vol. 81, No. 51 / Wednesday, March 16, 2016 / Notices material. Each member provides technical assistance in his/her specific area(s) of expertise, particularly with respect to emerging technologies. Members also provide guidance as to NRC’s role in relation to the responsibilities of other Federal agencies as well as of various professional organizations and boards. Members of this Committee have demonstrated professional qualifications and expertise in both scientific and non-scientific disciplines including nuclear medicine; nuclear cardiology; radiation therapy; medical physics; nuclear pharmacy; State medical regulation; patient’s rights and care; health care administration; and Food and Drug Administration regulation. Dated at Rockville, Maryland, this 10th day of March 2016. For the Nuclear Regulatory Commission. Andrew L. Bates, Federal Advisory Committee Management Officer. [FR Doc. 2016–05944 Filed 3–15–16; 8:45 am] BILLING CODE 7590–01–P NUCLEAR REGULATORY COMMISSION [Docket Nos. 50–010, 50–237, 50–249, and 72–37; NRC–2016–0046] Exelon Generation Company, LLC; Dresden Nuclear Power Station, Units 1, 2, and 3; Independent Spent Fuel Storage Installation Nuclear Regulatory Commission. ACTION: Exemption; issuance. AGENCY: The U.S. Nuclear Regulatory Commission (NRC) is issuing an exemption from certain requirements regarding the storage of a thoria rod canister in response to a request submitted by Exelon Generation Company, LLC (EGC) on January 29, 2015, for its general license to operate an independent spent fuel storage installation (ISFSI) at the Dresden Nuclear Power Station (DNPS). This exemption would permit EGC to load and store the DNPS Unit 1 thoria rod canister containing 18 DNPS Unit 1 thoria rods in a Holtec International, Inc., HI–STORM 100 multi-purpose canister (MPC)-68M using Certificate of Compliance (CoC) No. 1014, Amendment No. 8, Rev. 1.1 mstockstill on DSK4VPTVN1PROD with NOTICES SUMMARY: 1 The licensee’s application referred to Amendment 8; since that time, Amendment 8 has been revised. (On February 16, 2016, Amendment 8, Rev. 1 to CoC 1014 became effective.) The revision does not impact the exemption request that VerDate Sep<11>2014 18:11 Mar 15, 2016 Jkt 238001 14135 March 16, 2016. Please refer to Docket ID NRC–2016–0046 when contacting the NRC about the availability of information regarding this document. You may obtain publicly-available information related to this document using any of the following methods: • Federal Rulemaking Web site: Go to https://www.regulations.gov and search for Docket ID NRC–2016–0046. Address questions about NRC dockets to Carol Gallagher; telephone: 301–415–3463; email: Carol.Gallagher@nrc.gov. For technical questions, contact the individual listed in the FOR FURTHER INFORMATION CONTACT section of this document. • NRC’s Agencywide Documents Access and Management System (ADAMS): You may obtain publiclyavailable documents online in the ADAMS Public Documents collection at https://www.nrc.gov/reading-rm/ adams.html. To begin the search, select ‘‘ADAMS Public Documents’’ and then select ‘‘Begin Web-based ADAMS Search.’’ For problems with ADAMS, please contact the NRC’s Public Document Room (PDR) reference staff at 1–800–397–4209, 301–415–4737, or by email to pdr.resource@nrc.gov. For the convenience of the reader, the ADAMS accession numbers are provided in a table in the ‘‘Availability of Documents’’ section of this document. • NRC’s PDR: You may examine and purchase copies of public documents at the NRC’s PDR, Room O1–F21, One White Flint North, 11555 Rockville Pike, Rockville, Maryland 20852. FOR FURTHER INFORMATION CONTACT: Bernard White, Office of Nuclear Material Safety and Safeguards, U.S. Nuclear Regulatory Commission, Washington DC 20555–0001; telephone: 301–415–6577; email: Bernard.White@ nrc.gov. an ISFSI at power reactor sites to persons authorized to possess or operate nuclear power reactors under 10 CFR part 50. EGC is currently authorized to store spent fuel at the DNPS ISFSI under the 10 CFR part 72 general license provisions. The DNPS ISFSI is currently loading and storing spent fuel in Holtec HI–STORM 100 storage casks, approved by the NRC under CoC No. 1014. SUPPLEMENTARY INFORMATION: A. Authorized by Law This exemption would permit the applicant to load and store the DNPS Unit 1 thoria rod canister containing 18 DNPS Unit 1 thoria rods in the HI– STORM 100 MPC–68M CoC 1014, Amendment No. 8, Rev. 1, which otherwise would not permit the storage of thoria rods. The provisions from which the NRC is granting the exemption require the licensee to comply with the terms, conditions, and specifications of the CoCs for the approved cask model it uses. Section 72.7 allows the Commission to grant exemptions from the requirements of 10 CFR part 72 if the exemption is authorized by law, will not endanger life or property or the common defense DATES: ADDRESSES: I. Background Dresden Unit 1 produced power commercially from 1960 to October 31, 1978. The plant shut down in October 1978 and is currently in SAFSTOR. The decommissioning plan was approved in September 1993. No significant dismantlement activities are underway. Isolation of Units 1, 2, and 3 is complete. Consistent with subpart K of part 72 of title 10 of the Code of Federal Regulations (10 CFR), a general license is issued for the storage of spent fuel in is the subject of this exemption because none of the changes in the revision revised the thoria contents or the physical characteristics of the storage cask. PO 00000 Frm 00057 Fmt 4703 Sfmt 4703 II. Request/Action By letter dated January 29, 2015, as supplemented on June 8, 2015, EGC submitted a request for an exemption from 10 CFR 72.212(b)(3) and the portion of 10 CFR 72.212(b)(11) that requires compliance with the terms, conditions, and specifications of CoC No. 1014, Amendment No. 8, for the Holtec HI–STORM 100 with the MPC– 68M, to the extent necessary for EGC to load and store one DNPS Unit 1 thoria rod canister containing 18 DNPS Unit 1 thoria rods. Upon review, the NRC added the following requirements for the proposed action pursuant to its authority under 10 CFR 72.7: 10 CFR 72.212(a)(2), which limits storage of spent fuel in casks approved under part 72; 72.212(b)(5)(i), which states a ‘‘cask, once loaded with spent fuel . . . will conform to the terms, conditions and specifications of a CoC or an amended CoC listed in § 72.214’’; and 10 CFR 72.214, ‘‘List of approved spent fuel storage casks.’’ III. Discussion Pursuant to 10 CFR 72.7, the Commission may, upon application by any interested person or upon its own initiative, grant such exemptions from the requirements of the regulations of 10 CFR part 72 as it determines are authorized by law and will not endanger life or property or the common defense and security, and are otherwise in the public interest. E:\FR\FM\16MRN1.SGM 16MRN1

Agencies

NUCLEAR REGULATORY COMMISSION

[Federal Register Volume 81, Number 51 (Wednesday, March 16, 2016)]
[Notices]
[Pages 14134-14135]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-05944]


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NUCLEAR REGULATORY COMMISSION


Advisory Committee on the Medical Uses of Isotopes; Renewal

AGENCY: U.S. Nuclear Regulatory Commission.

ACTION: Notice.

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SUMMARY: The U.S. Nuclear Regulatory Commission (NRC) has determined 
that the renewal of the Charter for the Advisory Committee on the 
Medical Uses of Isotopes for the 2 year period commencing on March 10, 
2016, is in the public interest, in connection with duties imposed on 
the Commission by law. This action is being taken in accordance with 
the Federal Advisory Committee Act, after consultation with the 
Committee Management Secretariat, General Services Administration.

FOR FURTHER INFORMATION CONTACT: Sophie Holiday, Office of Federal and 
State Materials and Environmental Management Programs, U.S. Nuclear 
Regulatory Commission, Washington, DC 20555; Telephone (301) 415-7865; 
email Sophie.Holiday@nrc.gov.

SUPPLEMENTARY INFORMATION: The purpose of the ACMUI is to provide 
advice to NRC on policy and technical issues that arise in regulating 
the medical use of byproduct material for diagnosis and therapy. 
Responsibilities include providing guidance and comments on current and 
proposed NRC regulations and regulatory guidance concerning medical 
use; evaluating certain non-routine uses of byproduct material for 
medical use; and evaluating training and experience of proposed 
authorized users. The members are involved in preliminary discussions 
of major issues in determining the need for changes in NRC policy and 
regulation to ensure the continued safe use of byproduct

[[Page 14135]]

material. Each member provides technical assistance in his/her specific 
area(s) of expertise, particularly with respect to emerging 
technologies. Members also provide guidance as to NRC's role in 
relation to the responsibilities of other Federal agencies as well as 
of various professional organizations and boards.
    Members of this Committee have demonstrated professional 
qualifications and expertise in both scientific and non-scientific 
disciplines including nuclear medicine; nuclear cardiology; radiation 
therapy; medical physics; nuclear pharmacy; State medical regulation; 
patient's rights and care; health care administration; and Food and 
Drug Administration regulation.

    Dated at Rockville, Maryland, this 10th day of March 2016.

    For the Nuclear Regulatory Commission.
Andrew L. Bates,
Federal Advisory Committee Management Officer.
[FR Doc. 2016-05944 Filed 3-15-16; 8:45 am]
 BILLING CODE 7590-01-P

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