Information Collection: 10 CFR Part 35, “Medical Use of Byproduct Material”, 8959-8960 [2017-02074]

Download as PDF Federal Register / Vol. 82, No. 20 / Wednesday, February 1, 2017 / Notices FOR FURTHER INFORMATION CONTACT: NUCLEAR REGULATORY COMMISSION [Docket No. 50–333; NRC–2016–0059] Entergy Nuclear Operations, Inc.; James A. FitzPatrick Nuclear Power Plant Nuclear Regulatory Commission. ACTION: License amendment application; withdrawal by applicant. AGENCY: The U.S. Nuclear Regulatory Commission (NRC) has granted the request of Entergy Nuclear Operations, Inc. (Entergy, the licensee), to withdraw its application dated February 4, 2016, for a proposed amendment to Facility Operating License No. DPR–59. The proposed amendment request would have revised the James A. FitzPatrick Nuclear Power Plant (JAF) Emergency Plan to reduce the Emergency Response Organization (ERO) positions that the licensee considers unnecessary to effectively respond to credible accidents following permanent defueling. ADDRESSES: Please refer to Docket ID NRC–2016–0059 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–2016–0059. 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. The ADAMS accession number for each document referenced (if it is available in ADAMS) is provided the first time that it is mentioned in 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. sradovich on DSK3GMQ082PROD with NOTICES SUMMARY: VerDate Sep<11>2014 16:23 Jan 31, 2017 Jkt 241001 James Kim, Office of Nuclear Reactor Regulation, U.S. Nuclear Regulatory Commission, Washington DC 20555– 0001; telephone: 301–415–4125; email: James.Kim@nrc.gov. SUPPLEMENTARY INFORMATION: The NRC has granted the request of Entergy to withdraw its application dated February 4, 2016 (ADAMS Accession No. ML16043A424), for a proposed amendment to Facility Operating License No. DPR–59 for JAF, located in Oswego County, New York. The proposed amendment request would have revised the JAF Emergency Plan to reduce the ERO positions that the licensee considers unnecessary to effectively respond to credible accidents following permanent defueling. The Commission has previously issued a proposed finding that the amendment involves no significant hazards consideration published in the Federal Register on March 29, 2016 (81 FR 17504). However, by letter dated January 13, 2017 (ADAMS Accession No. ML17015A000), the licensee requested to withdraw the proposed amendment. Dated at Rockville, Maryland, this 25th day of January 2017. For the Nuclear Regulatory Commission. James Kim, Project Manager, Special Projects and Process Branch, Division of Operating Reactor Licensing, Office of Nuclear Reactor Regulation. [FR Doc. 2017–02130 Filed 1–31–17; 8:45 am] BILLING CODE 7590–01–P NUCLEAR REGULATORY COMMISSION [NRC–2017–0013] Information Collection: 10 CFR Part 35, ‘‘Medical Use of Byproduct Material’’ Nuclear Regulatory Commission. ACTION: Renewal of existing information collection; request for comment. AGENCY: The U.S. Nuclear Regulatory Commission (NRC) invites public comment on the renewal of Office of Management and Budget (OMB) approval for an existing collection of information. The information collection is entitled, 10 CFR part 35, ‘‘Medical Use of Byproduct Material.’’ DATES: Submit comments by April 3, 2017. Comments received after this date will be considered if it is practical to do so, but the Commission is able to ensure consideration only for comments received on or before this date. SUMMARY: PO 00000 Frm 00051 Fmt 4703 Sfmt 4703 8959 You may submit comments by any of the following methods: • Federal Rulemaking Web site: Go to https://www.regulations.gov and search for Docket ID NRC–2017–0013. 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. • Mail comments to: David Cullison, Office of the Chief Information Officer, Mail Stop: T–5 F53, U.S. Nuclear Regulatory Commission, Washington, DC 20555–0001. For additional direction on obtaining information and submitting comments, see ‘‘Obtaining Information and Submitting Comments’’ in the SUPPLEMENTARY INFORMATION section of this document. FOR FURTHER INFORMATION CONTACT: David Cullison, Office of the Chief Information Officer, U.S. Nuclear Regulatory Commission, Washington, DC 20555–0001; telephone: 301–415– 2084; email: INFOCOLLECTS.Resource@ nrc.gov. SUPPLEMENTARY INFORMATION: ADDRESSES: I. Obtaining Information and Submitting Comments A. Obtaining Information Please refer to Docket ID NRC–20170013 when contacting the NRC about the availability of information for this action. You may obtain publiclyavailable information related to this action by any of the following methods: • Federal Rulemaking Web site: Go to https://www.regulations.gov and search for Docket ID NRC–2017–0013. • 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. The supporting statement is available in ADAMS under Accession No. ML16333A028. • 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. • NRC’s Clearance Officer: A copy of the collection of information and related E:\FR\FM\01FEN1.SGM 01FEN1 8960 Federal Register / Vol. 82, No. 20 / Wednesday, February 1, 2017 / Notices instructions may be obtained without charge by contacting NRC’s Clearance Officer, David Cullison, Office of the Chief Information Officer, U.S. Nuclear Regulatory Commission, Washington, DC 20555–0001; telephone: 301–415– 2084; email: INFOCOLLECTS.Resource@ nrc.gov. sradovich on DSK3GMQ082PROD with NOTICES B. Submitting Comments Please include Docket ID NRC–2017– 0013 in the subject line of your comment submission, in order to ensure that the NRC is able to make your comment submission available to the public in this docket. The NRC cautions you not to include identifying or contact information in comment submissions that you do not want to be publicly disclosed in your comment submission. The NRC will post all comment submissions at https:// www.regulations.gov as well as enter the comment submissions into ADAMS, and the NRC does not routinely edit comment submissions to remove identifying or contact information. If you are requesting or aggregating comments from other persons for submission to the NRC, then you should inform those persons not to include identifying or contact information that they do not want to be publicly disclosed in their comment submission. Your request should state that the NRC does not routinely edit comment submissions to remove such information before making the comment submissions available to the public or entering the comment into ADAMS. II. Background In accordance with the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35), the NRC is requesting public comment on its intention to request the OMB’s approval for the information collection summarized below. 1. The title of the information collection: 10 CFR part 35, ‘‘Medical Use of Byproduct Material.’’ 2. OMB approval number: 3150–0010 3. Type of submission: Extension 4. The form number, if applicable: N/A 5. How often the collection is required or requested: Reports of medical events, doses to an embryo/fetus or nursing child, or leaking source are reportable on occurrence. A specialty board certifying entity desiring to be recognized by the NRC must submit a one-time request for recognition and infrequently revise the information. 6. Who will be required or asked to respond: Physicians and medical institutions holding an NRC license authorizing the administration of VerDate Sep<11>2014 16:23 Jan 31, 2017 Jkt 241001 byproduct material or radiation from this material to humans for medical use. A specialty board certification entity desiring to have its certifying process and board certificate recognized by NRC. 7. The estimated number of annual responses: 276,359 ((NRC: 36,313 + 962 recordkeepers = 37,275) + (Agreement States: 232,925 + 6,157 recordkeepers + 2 specialty certification entity = 239,084)). 8. The estimated number of annual respondents: 7,121(NRC: 962 + Agreement states 6,157+ 2 specialty certification entities). 9. The estimated number of hours needed annually to comply with the information collection requirement or request: 1,073,224 hours (NRC Licensees 145,195 hrs + Agreement States 928,027 hrs + specialty certifying entities 2 hrs). 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. Part 35 contains mandatory requirements that apply to NRC licensees authorized to administer byproduct material or radiation therefrom to humans for medical use. These requirements also provide voluntary provisions for specialty boards to apply to have their certification processes recognized by the NRC so that their board certified individuals can use the certifications as proof of training and experience. III. Specific Requests for Comments The NRC is seeking 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 estimate of the burden of the information collection 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 on respondents be minimized, including the use of automated collection techniques or other forms of information technology? Dated at Rockville, Maryland, this 26th day of January 2017. PO 00000 Frm 00052 Fmt 4703 Sfmt 4703 For the Nuclear Regulatory Commission. David Cullison, NRC Clearance Officer. [FR Doc. 2017–02074 Filed 1–31–17; 8:45 am] BILLING CODE 7590–01–P POSTAL SERVICE Temporary Emergency Committee of the Board of Governors; Sunshine Act Meeting Wednesday, February 8, 2017, at 8:00 a.m. PLACE: Washington, DC. STATUS: Closed. MATTERS TO BE CONSIDERED: DATES AND TIMES: Wednesday, February 8, 2017, at 8:00 a.m. 1. Strategic Issues. 2. Financial Matters. 3. Personnel Matters and Compensation Issues. 4. Executive Session—Discussion of prior agenda items and Temporary Emergency Committee governance. GENERAL COUNSEL CERTIFICATION: The General Counsel of the United States Postal Service has certified that the meeting may be closed under the Government in the Sunshine Act. CONTACT PERSON FOR MORE INFORMATION: Julie S. Moore, Secretary of the Board, U.S. Postal Service, 475 L’Enfant Plaza SW., Washington, DC 20260–1000. Telephone: (202) 268–4800. Julie S. Moore, Secretary. [FR Doc. 2017–02256 Filed 1–30–17; 4:15 pm] BILLING CODE 7710–12–P PRESIDIO TRUST Notice of Public Meeting of Presidio Institute Advisory Council The Presidio Trust. Notice of public meeting of Presidio Institute Advisory Council. AGENCY: ACTION: Pursuant to the Federal Advisory Committee Act, as amended, notice is hereby given that a public meeting of the Presidio Institute Advisory Council (Council) will be held from 1:00 p.m. to 3:00 p.m. on Tuesday, March 7, 2017. The meeting is open to the public, and oral public comment will be received at the meeting. The Council was formed to advise the CEO of the Presidio Trust (Trust) on matters pertaining to the rehabilitation and reuse of Fort Winfield Scott as a new national center focused on service and leadership development. SUMMARY: E:\FR\FM\01FEN1.SGM 01FEN1

Agencies

[Federal Register Volume 82, Number 20 (Wednesday, February 1, 2017)]
[Notices]
[Pages 8959-8960]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-02074]


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NUCLEAR REGULATORY COMMISSION

[NRC-2017-0013]


Information Collection: 10 CFR Part 35, ``Medical Use of 
Byproduct Material''

AGENCY: Nuclear Regulatory Commission.

ACTION: Renewal of existing information collection; request for 
comment.

-----------------------------------------------------------------------

SUMMARY: The U.S. Nuclear Regulatory Commission (NRC) invites public 
comment on the renewal of Office of Management and Budget (OMB) 
approval for an existing collection of information. The information 
collection is entitled, 10 CFR part 35, ``Medical Use of Byproduct 
Material.''

DATES: Submit comments by April 3, 2017. Comments received after this 
date will be considered if it is practical to do so, but the Commission 
is able to ensure consideration only for comments received on or before 
this date.

ADDRESSES: You may submit comments by any of the following methods:
     Federal Rulemaking Web site: Go to https://www.regulations.gov and search for Docket ID NRC-2017-0013. 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.
     Mail comments to: David Cullison, Office of the Chief 
Information Officer, Mail Stop: T-5 F53, U.S. Nuclear Regulatory 
Commission, Washington, DC 20555-0001.
    For additional direction on obtaining information and submitting 
comments, see ``Obtaining Information and Submitting Comments'' in the 
SUPPLEMENTARY INFORMATION section of this document.

FOR FURTHER INFORMATION CONTACT: David Cullison, Office of the Chief 
Information Officer, U.S. Nuclear Regulatory Commission, Washington, DC 
20555-0001; telephone: 301-415-2084; email: 
INFOCOLLECTS.Resource@nrc.gov.

SUPPLEMENTARY INFORMATION:

I. Obtaining Information and Submitting Comments

A. Obtaining Information

    Please refer to Docket ID NRC-2017- 0013 when contacting the NRC 
about the availability of information for this action. You may obtain 
publicly-available information related to this action by any of the 
following methods:
     Federal Rulemaking Web site: Go to https://www.regulations.gov and search for Docket ID NRC-2017-0013.
     NRC's Agencywide Documents Access and Management System 
(ADAMS): You may obtain publicly-available 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. The 
supporting statement is available in ADAMS under Accession No. 
ML16333A028.
     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.
     NRC's Clearance Officer: A copy of the collection of 
information and related

[[Page 8960]]

instructions may be obtained without charge by contacting NRC's 
Clearance Officer, David Cullison, Office of the Chief Information 
Officer, U.S. Nuclear Regulatory Commission, Washington, DC 20555-0001; 
telephone: 301-415-2084; email: INFOCOLLECTS.Resource@nrc.gov.

B. Submitting Comments

    Please include Docket ID NRC-2017-0013 in the subject line of your 
comment submission, in order to ensure that the NRC is able to make 
your comment submission available to the public in this docket.
    The NRC cautions you not to include identifying or contact 
information in comment submissions that you do not want to be publicly 
disclosed in your comment submission. The NRC will post all comment 
submissions at https://www.regulations.gov as well as enter the comment 
submissions into ADAMS, and the NRC does not routinely edit comment 
submissions to remove identifying or contact information.
    If you are requesting or aggregating comments from other persons 
for submission to the NRC, then you should inform those persons not to 
include identifying or contact information that they do not want to be 
publicly disclosed in their comment submission. Your request should 
state that the NRC does not routinely edit comment submissions to 
remove such information before making the comment submissions available 
to the public or entering the comment into ADAMS.

II. Background

    In accordance with the Paperwork Reduction Act of 1995 (44 U.S.C. 
Chapter 35), the NRC is requesting public comment on its intention to 
request the OMB's approval for the information collection summarized 
below.
    1. The title of the information collection: 10 CFR part 35, 
``Medical Use of Byproduct Material.''
    2. OMB approval number: 3150-0010
    3. Type of submission: Extension
    4. The form number, if applicable: N/A
    5. How often the collection is required or requested: Reports of 
medical events, doses to an embryo/fetus or nursing child, or leaking 
source are reportable on occurrence. A specialty board certifying 
entity desiring to be recognized by the NRC must submit a one-time 
request for recognition and infrequently revise the information.
    6. Who will be required or asked to respond: Physicians and medical 
institutions holding an NRC license authorizing the administration of 
byproduct material or radiation from this material to humans for 
medical use. A specialty board certification entity desiring to have 
its certifying process and board certificate recognized by NRC.
    7. The estimated number of annual responses: 276,359 ((NRC: 36,313 
+ 962 recordkeepers = 37,275) + (Agreement States: 232,925 + 6,157 
recordkeepers + 2 specialty certification entity = 239,084)).
    8. The estimated number of annual respondents: 7,121(NRC: 962 + 
Agreement states 6,157+ 2 specialty certification entities).
    9. The estimated number of hours needed annually to comply with the 
information collection requirement or request: 1,073,224 hours (NRC 
Licensees 145,195 hrs + Agreement States 928,027 hrs + specialty 
certifying entities 2 hrs).
    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. Part 35 contains 
mandatory requirements that apply to NRC licensees authorized to 
administer byproduct material or radiation therefrom to humans for 
medical use. These requirements also provide voluntary provisions for 
specialty boards to apply to have their certification processes 
recognized by the NRC so that their board certified individuals can use 
the certifications as proof of training and experience.

III. Specific Requests for Comments

    The NRC is seeking 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 estimate of the burden of the information collection 
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 on respondents 
be minimized, including the use of automated collection techniques or 
other forms of information technology?

    Dated at Rockville, Maryland, this 26th day of January 2017.

    For the Nuclear Regulatory Commission.
David Cullison,
NRC Clearance Officer.
[FR Doc. 2017-02074 Filed 1-31-17; 8:45 am]
BILLING CODE 7590-01-P
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