Submission for OMB Review; Protecting Life in Global Health Assistance, 83086-83087 [2020-28152]

Download as PDF 83086 Federal Register / Vol. 85, No. 245 / Monday, December 21, 2020 / Notices ADMINISTRATIVE, TECHNICAL, AND PHYSICAL SAFEGUARDS: staff engaged in processing or making determinations on the requests. ROUTINE USES OF RECORDS MAINTAINED IN THE SYSTEM, INCLUDING CATEGORIES OF USERS AND PURPOSES OF SUCH USES: General routine uses C, D, G, I, and J apply to this system. These general routine uses are located at https:// www.federalreserve.gov/files/SORNpage-general-routine-uses-of-boardsystems-of-records.pdf and are published in the Federal Register at 83 FR 43872 at 43873–74 (August 28, 2018). In addition, records may also be disclosed to: 1. A federal or state government agency, foreign government, institution, firm, or organization having a substantial interest in the determination of the request or for the purpose of consulting with that entity as to the propriety of access to the record in order to complete the processing of the request; 2. The National Archives and Records Administration, Office of Government Information Services (OGIS), to the extent necessary to fulfill its responsibilities in 5 U.S.C. 552(h), to review administrative agency policies, procedures and compliance with the FOIA and to facilitate OGIS’ offering of mediation services to resolve disputes between persons making FOIA requests and administrative agencies; and 3. The news media and the public, unless it is determined that release of specific information in the context of a particular case would constitute an unwarranted invasion of personal privacy. POLICIES AND PRACTICES FOR STORAGE OF RECORDS: Electronic records are stored on a secure server. POLICIES AND PRACTICES FOR RETRIEVAL OF RECORDS: Records can be retrieved by the name of the requester, tracking number assigned to the request, subject matter of the request, or any other field of information that is collected. POLICIES AND PRACTICES FOR RETENTION AND DISPOSAL OF RECORDS: The Board retains the records for the designated retention period, which ranges from six years after final agency action or three years after final adjudication by the courts, whichever is later, but longer retention is authorized if required for business use. Requests submitted in paper form are scanned as electronic records and the paper copies of the request are disposed in accordance with applicable procedures. VerDate Sep<11>2014 22:33 Dec 18, 2020 Jkt 253001 The system has the ability to track individual user actions within the system. The audit and accountability controls are based on NIST and Board standards, which are based on applicable laws and regulations. The controls assist in detecting security violations and performance or other issues in the system. Access to the system is restricted to authorized users within the Board who require access for official business purposes. Users are classified into different roles and common access and usage rights are established for each role. User roles are used to delineate between the different types of access requirements such that users are restricted to data that is required in the performance of their duties. Periodic assessments and reviews are conducted to determine whether users still require access, have the appropriate role, and whether there have been any unauthorized changes. RECORD ACCESS PROCEDURES: The Privacy Act allows individuals the right to access records maintained about them in a Board system of records. Your request for access must: (1) Contain a statement that it is made pursuant to the Privacy Act of 1974; (2) provide either the name of the Board system of records expected to contain the record requested or a concise description of the system of records; (3) provide the information necessary to verify your identity; and (4) provide any other information that may assist in the rapid identification of the record you seek. Current or former Board employees may make a request for access by contacting the Board office that maintains the record. The Board handles all Privacy Act requests as both a Privacy Act request and as a Freedom of Information Act request. The Board does not charge fees to a requestor seeking to access or amend his/her Privacy Act records. You may submit your Privacy Act request to the— Secretary of the Board, Board of Governors of the Federal Reserve System, 20th Street and Constitution Avenue NW, Washington DC 20551. You may also submit your Privacy Act request electronically through the Board’s FOIA ‘‘Electronic Request Form’’ located here: https:// www.federalreserve.gov/secure/forms/ efoiaform.aspx. CONTESTING RECORD PROCEDURES: The Privacy Act allows individuals to seek amendment of information that is erroneous, irrelevant, untimely, or PO 00000 Frm 00060 Fmt 4703 Sfmt 4703 incomplete and is maintained in a system of records that pertains to them. To request an amendment to your record, you should clearly mark the request as a ‘‘Privacy Act Amendment Request.’’ You have the burden of proof for demonstrating the appropriateness of the requested amendment and you must provide relevant and convincing evidence in support of your request. Your request for amendment must: (1) Provide the name of the specific Board system of records containing the record you seek to amend; (2) identify the specific portion of the record you seek to amend; (3) describe the nature of and reasons for each requested amendment; (4) explain why you believe the record is not accurate, relevant, timely, or complete; and (5) unless you have already done so in a related Privacy Act request for access or amendment, provide the necessary information to verify your identity. NOTIFICATION PROCEDURES: Same as ‘‘Access procedures’’ above. You may also follow this procedure in order to request an accounting of previous disclosures of records pertaining to you as provided for by 5 U.S.C. 552a(c). EXEMPTIONS PROMULGATED FOR THE SYSTEM: No exemptions are claimed for this system. HISTORY: This SORN was previously published in the Federal Register at 84 FR 71421 (December 27, 2019) and 73 FR 24984 at 25002 (May 6, 2008). The SORN was also amended to incorporate two new routine uses required by OMB at 83 FR 43872 (August 28, 2018). Board of Governors of the Federal Reserve System. Ann Misback, Secretary of the Board. [FR Doc. 2020–27990 Filed 12–18–20; 8:45 am] BILLING CODE P DEPARTMENT OF DEFENSE GENERAL SERVICES ADMINISTRATION NATIONAL AERONAUTICS AND SPACE ADMINISTRATION [OMB Control No. 9000–0200; Docket No. 2020–0053; Sequence No. 19] Submission for OMB Review; Protecting Life in Global Health Assistance Department of Defense (DOD), General Services Administration (GSA), AGENCY: E:\FR\FM\21DEN1.SGM 21DEN1 Federal Register / Vol. 85, No. 245 / Monday, December 21, 2020 / Notices and National Aeronautics and Space Administration (NASA). ACTION: Notice. Under the provisions of the Paperwork Reduction Act, the Regulatory Secretariat Division has submitted to the Office of Management and Budget (OMB) a request to review and approve a new information collection requirement regarding documents, records, reports, and processes associated with determining compliance with FAR part 25, Protecting Life in Global Health Assistance. SUMMARY: Submit comments on or before January 20, 2021. ADDRESSES: Written comments and recommendations for this information collection should be sent within 30 days of publication of this notice to www.reginfo.gov/public/do/PRAMain. Find this particular information collection by selecting ‘‘Currently under Review—Open for Public Comments’’ or by using the search function. Additionally submit a copy to GSA through http://www.regulations.gov and follow the instructions on the site. This website provides the ability to type short comments directly into the comment field or attach a file for lengthier comments. Instructions: All items submitted must cite OMB Control No. 9000–0200, Protecting Life in Global Health Assistance. Comments received generally will be posted without change to http://www.regulations.gov, including any personal and/or business confidential information provided. To confirm receipt of your comment(s), please check www.regulations.gov, approximately two to three days after submission to verify posting. If there are difficulties submitting comments, contact the GSA Regulatory Secretariat Division at 202–501–4755 or GSARegSec@gsa.gov. FOR FURTHER INFORMATION CONTACT: Email FARPolicy@gsa.gov or call 202– 969–4075. SUPPLEMENTARY INFORMATION: DATES: A. OMB Control Number, Title, and Any Associated Form(s): 9000–0200, Protecting Life in Global Health. B. Needs and Uses The Secretary of State approved on May 9, 2017, a plan to implement the manner in which U.S. Government Departments and Agencies will apply the provisions of the ‘‘Mexico City Policy,’’ which was reinstated in the January 23, 2017 Presidential Memorandum, to foreign VerDate Sep<11>2014 00:23 Dec 19, 2020 Jkt 253001 nongovernmental organizations (NGOs) that receive U.S. funding for global health assistance; this included the extension of the policy to Federal contracts. This clearance covers the information contractors must keep and make available to the Government to comply with the requirements of FAR clause 52.225–XX. a. 52.225–XX(c)(2)(i) requires foreign prime contractors to allow authorized Government representatives to inspect documents and materials maintained or prepared by the Contractor in the usual course of its operations that describe the health activities implemented by the Contractor. b. 52.225–XX(j)(1)(ii)(A) requires foreign subcontractors to allow authorized Government representatives to inspect documents and materials maintained or prepared by the subcontractor in the usual course of its operations that describe the health activities of the subcontractor. c. 52.225–XX(e) requires the Contractor to provide the Contracting Officer a request for consent to subcontract if the contract includes the clause at FAR 52.244–2, Subcontracts. d. 52.225–XX(g)(2) requires the Contractor to provide the Contracting Officer the results of a subcontractor review when the Government has reason to believe that a foreign subcontractor may have violated the requirements of this clause. e. 52.225–XX(j)(2) and (j)(3) requires the Contractor to review the foreign subcontractor’s health program to determine if a violation has occurred, and to consult with the Contracting Officer prior to terminating the subcontract or determining other corrective action is warranted. C. Annual Burden Respondents: 253. Total Annual Responses: 1,089. Total Burden Hours: 38,992. D. Public Comment A 60-day proposed rule was published within the proposed FAR rule (2018–002, Protecting Life in Global Health) in the Federal Register at 85 FR 56549, on September 14, 2020. Some comments regarding the Paperwork Reduction Burden were received; however, it did not change the estimate of the burden. Comment: The proposed rule provided an estimate of the public reporting burden for required information collection of nearly 39,000 total response burden hours. Please provide the assumptions and methodology used in calculating this estimate. PO 00000 Frm 00061 Fmt 4703 Sfmt 4703 83087 Response: Requesters may obtain a copy of the supporting statement from GSA. Obtaining Copies: Requesters may obtain a copy of the information collection documents from the GSA Regulatory Secretariat Division, by calling 202–501–4755 or emailing GSARegSec@gsa.gov. Please cite OMB Control No. 9000–0200, Protecting Life in Global Health. William F. Clark, Director,Office of Governmentwide Acquisition Policy,Office of Acquisition Policy,Office of Governmentwide Policy. [FR Doc. 2020–28152 Filed 12–18–20; 8:45 am] BILLING CODE 6820–EP–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day-21–21AC; Docket No. CDC–2020– 0110] Proposed Data Collection Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice with comment period. AGENCY: The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies the opportunity to comment on a proposed and/or continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information collection project titled The GAIN (Greater Access and Impact with NAT) Study: Improving HIV Diagnosis, Linkage to Care, and Prevention Services with HIV Point-ofCare Nucleic Acid Tests (NATs). GAIN is an implementation study to compare a point-of-care nucleic acid HIV test (HIV RNA POC NAT) to standard labbased HIV testing. DATES: CDC must receive written comments on or before February 19, 2021. ADDRESSES: You may submit comments, identified by Docket No. CDC–2020– 0110 by any of the following methods: • Federal eRulemaking Portal: Regulations.gov. Follow the instructions for submitting comments. • Mail: Jeffrey M. Zirger, Information Collection Review Office, Centers for SUMMARY: E:\FR\FM\21DEN1.SGM 21DEN1

Agencies

[Federal Register Volume 85, Number 245 (Monday, December 21, 2020)]
[Notices]
[Pages 83086-83087]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-28152]


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DEPARTMENT OF DEFENSE

GENERAL SERVICES ADMINISTRATION

NATIONAL AERONAUTICS AND SPACE ADMINISTRATION

[OMB Control No. 9000-0200; Docket No. 2020-0053; Sequence No. 19]


Submission for OMB Review; Protecting Life in Global Health 
Assistance

AGENCY: Department of Defense (DOD), General Services Administration 
(GSA),

[[Page 83087]]

and National Aeronautics and Space Administration (NASA).

ACTION: Notice.

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

SUMMARY: Under the provisions of the Paperwork Reduction Act, the 
Regulatory Secretariat Division has submitted to the Office of 
Management and Budget (OMB) a request to review and approve a new 
information collection requirement regarding documents, records, 
reports, and processes associated with determining compliance with FAR 
part 25, Protecting Life in Global Health Assistance.

DATES: Submit comments on or before January 20, 2021.

ADDRESSES: Written comments and recommendations for this information 
collection should be sent within 30 days of publication of this notice 
to www.reginfo.gov/public/do/PRAMain. Find this particular information 
collection by selecting ``Currently under Review--Open for Public 
Comments'' or by using the search function.
    Additionally submit a copy to GSA through http://www.regulations.gov and follow the instructions on the site. This 
website provides the ability to type short comments directly into the 
comment field or attach a file for lengthier comments.
    Instructions: All items submitted must cite OMB Control No. 9000-
0200, Protecting Life in Global Health Assistance. Comments received 
generally will be posted without change to http://www.regulations.gov, 
including any personal and/or business confidential information 
provided. To confirm receipt of your comment(s), please check 
www.regulations.gov, approximately two to three days after submission 
to verify posting. If there are difficulties submitting comments, 
contact the GSA Regulatory Secretariat Division at 202-501-4755 or 
[email protected].

FOR FURTHER INFORMATION CONTACT: Email [email protected] or call 202-
969-4075.

SUPPLEMENTARY INFORMATION:

A. OMB Control Number, Title, and Any Associated Form(s): 9000-0200, 
Protecting Life in Global Health.

B. Needs and Uses

    The Secretary of State approved on May 9, 2017, a plan to implement 
the manner in which U.S. Government Departments and Agencies will apply 
the provisions of the ``Mexico City Policy,'' which was reinstated in 
the January 23, 2017 Presidential Memorandum, to foreign 
nongovernmental organizations (NGOs) that receive U.S. funding for 
global health assistance; this included the extension of the policy to 
Federal contracts. This clearance covers the information contractors 
must keep and make available to the Government to comply with the 
requirements of FAR clause 52.225-XX.
    a. 52.225-XX(c)(2)(i) requires foreign prime contractors to allow 
authorized Government representatives to inspect documents and 
materials maintained or prepared by the Contractor in the usual course 
of its operations that describe the health activities implemented by 
the Contractor.
    b. 52.225-XX(j)(1)(ii)(A) requires foreign subcontractors to allow 
authorized Government representatives to inspect documents and 
materials maintained or prepared by the subcontractor in the usual 
course of its operations that describe the health activities of the 
subcontractor.
    c. 52.225-XX(e) requires the Contractor to provide the Contracting 
Officer a request for consent to subcontract if the contract includes 
the clause at FAR 52.244-2, Subcontracts.
    d. 52.225-XX(g)(2) requires the Contractor to provide the 
Contracting Officer the results of a subcontractor review when the 
Government has reason to believe that a foreign subcontractor may have 
violated the requirements of this clause.
    e. 52.225-XX(j)(2) and (j)(3) requires the Contractor to review the 
foreign subcontractor's health program to determine if a violation has 
occurred, and to consult with the Contracting Officer prior to 
terminating the subcontract or determining other corrective action is 
warranted.

C. Annual Burden

    Respondents: 253.
    Total Annual Responses: 1,089.
    Total Burden Hours: 38,992.

D. Public Comment

    A 60-day proposed rule was published within the proposed FAR rule 
(2018-002, Protecting Life in Global Health) in the Federal Register at 
85 FR 56549, on September 14, 2020. Some comments regarding the 
Paperwork Reduction Burden were received; however, it did not change 
the estimate of the burden.
    Comment: The proposed rule provided an estimate of the public 
reporting burden for required information collection of nearly 39,000 
total response burden hours. Please provide the assumptions and 
methodology used in calculating this estimate.
    Response: Requesters may obtain a copy of the supporting statement 
from GSA.
    Obtaining Copies: Requesters may obtain a copy of the information 
collection documents from the GSA Regulatory Secretariat Division, by 
calling 202-501-4755 or emailing [email protected]. Please cite OMB 
Control No. 9000-0200, Protecting Life in Global Health.

William F. Clark,
Director,Office of Governmentwide Acquisition Policy,Office of 
Acquisition Policy,Office of Governmentwide Policy.
[FR Doc. 2020-28152 Filed 12-18-20; 8:45 am]
BILLING CODE 6820-EP-P