Information Collection; Reporting Purchases From Sources Outside the United States, 77614-77615 [2022-27430]
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77614
Federal Register / Vol. 87, No. 242 / Monday, December 19, 2022 / Notices
with the following Federal Acquisition
Regulation (FAR) requirements:
FAR 52.212–5, Contract Terms and
Conditions Required to Implement
Statutes or Executive Orders—
Commercial Products and Commercial
Services. Paragraph (d) of this clause
requires contractors to make available at
its offices at all reasonable times the
records, materials, and other evidence
for examination, audit, or reproduction
by the Comptroller General of the
United States, or an authorized
representative. As used in this clause,
records include books, documents,
accounting procedures and practices,
and other data, regardless of type and
regardless of form.
FAR 52.214–26, Audit and Records—
Sealed Bidding. This clause requires
contractors required to submit certified
cost or pricing data in connection with
the pricing of a modification under a
contract to make all records available to
the contracting officer, or its authorized
representative, including computations
and projections related to the proposal
for the modification; the discussions
conducted on the proposal(s), including
those related to negotiating; pricing of
the modification; or performance of the
modification. This clause requires
contractors to make all records available
to the Comptroller General of the United
States, or an authorized representative,
in the case of pricing a modification.
This clause allows the Comptroller
General to interview any current
employee regarding such transactions.
FAR 52.215–2, Audit and Records—
Negotiation. This clause requires
contractors to maintain records for costreimbursement, incentive, time-andmaterials, labor-hour, or price
redeterminable contracts, or any
combination of these, for contracting
officers, or an authorized representative,
to examine and audit all records and
other evidence sufficient to reflect
properly all costs claimed to have been
incurred or anticipated to be incurred
directly or indirectly in performance of
a contract. The right of examination
includes inspection at all reasonable
times of contractor’s plants, or parts of
them, engaged in performing the
pertinent contract. Contractors required
to submit certified cost or pricing data
in connection with a pricing action
under a contract must make all records
available to the contracting officer, or its
authorized representative, including
computations and projections related to
the proposal for the contract,
subcontract, or modification; the
discussions conducted on the
proposal(s), including those related to
negotiating; pricing of the contract,
subcontract, or modification; or
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19:38 Dec 16, 2022
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performance of the contract, subcontract
or modification. Also, this clause
requires contractors to make all records
available to the Comptroller General of
the United States, or an authorized
representative, to examine any of the
contractor’s directly pertinent records
involving transactions under the
pertinent contract or subcontract. This
clause allows the Comptroller General
to interview any current employee
regarding such transactions.
The information must be retained so
that audits necessary for contract
surveillance, verification of contract
pricing, and reimbursement of
contractor costs can be performed. This
information collection does not require
contractors to create or maintain any
record that the contractor does not
maintain in its ordinary course of
business.
C. Annual Burden
Respondents: 19,033.
Total Annual Responses: 93,578.
Total Burden Hours: 93,578.
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. 9000–0034, Examination of
Records by Comptroller General and
Contract Audit, in all correspondence.
Janet Fry,
Director, Federal Acquisition Policy Division,
Office of Governmentwide Acquisition Policy,
Office of Acquisition Policy, Office of
Governmentwide Policy.
[FR Doc. 2022–27433 Filed 12–16–22; 8:45 am]
BILLING CODE 6820–EP–P
DEPARTMENT OF DEFENSE
GENERAL SERVICES
ADMINISTRATION
NATIONAL AERONAUTICS AND
SPACE ADMINISTRATION
[OMB Control No. 9000–0161; Docket No.
2022–0053; Sequence No. 23]
Information Collection; Reporting
Purchases From Sources Outside the
United States
(OMB) regulations, DoD, GSA, and
NASA invite the public to comment on
an extension concerning reporting
purchases from sources outside the
United States. DoD, GSA, and NASA
invite comments on: whether the
proposed collection of information is
necessary for the proper performance of
the functions of Federal Government
acquisitions, including whether the
information will have practical utility;
the accuracy of the estimate of the
burden of the proposed information
collection; ways to enhance the quality,
utility, and clarity of the information to
be collected; and ways to minimize the
burden of the information collection on
respondents, including the use of
automated collection techniques or
other forms of information technology.
OMB has approved this information
collection for use through May 31, 2023.
DoD, GSA, and NASA propose that
OMB extend its approval for use for
three additional years beyond the
current expiration date.
DATES: DoD, GSA, and NASA will
consider all comments received by
February 17, 2023.
ADDRESSES: DoD, GSA, and NASA
invite interested persons to submit
comments on this collection through
https://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. If there are difficulties
submitting comments, contact the GSA
Regulatory Secretariat Division at 202–
501–4755 or GSARegSec@gsa.gov.
Instructions: All items submitted
must cite OMB Control No. 9000–0161,
Reporting Purchases from Sources
Outside the United States. Comments
received generally will be posted
without change to https://
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.
FOR FURTHER INFORMATION CONTACT:
Zenaida Delgado, Procurement Analyst,
at telephone 202–969–7207, or
zenaida.delgado@gsa.gov.
SUPPLEMENTARY INFORMATION:
Department of Defense (DOD),
General Services Administration (GSA),
and National Aeronautics and Space
Administration (NASA).
ACTION: Notice and request for
comments.
A. OMB Control Number, Title, and
Any Associated Form(s)
9000–0161, Reporting Purchases from
Sources Outside the United States.
In accordance with the
Paperwork Reduction Act of 1995, and
the Office of Management and Budget
B. Need and Uses
This clearance covers the information
that offerors must submit to comply
AGENCY:
SUMMARY:
PO 00000
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Federal Register / Vol. 87, No. 242 / Monday, December 19, 2022 / Notices
with the FAR provision 52.225–18,
Place of Manufacture. This provision
requires offerors of manufactured end
products to indicate in response to a
solicitation, by checking a box, whether
the place of manufacture of the end
products it expects to provide is
predominantly manufactured in the
United States or outside the United
States. Contracting officers use the
information as the basis for entry into
the Federal Procurement Data System
for further data on the rationale for
purchasing foreign manufactured items.
The data is necessary for analysis of the
application of the Buy American statute
and the trade agreements.
C. Annual Burden
Respondents: 50,106.
Total Annual Responses: 2,600,361.
Total Burden Hours: 26,004.
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. 9000–0161, Reporting
Purchases from Sources Outside the
United States, in all correspondence.
Janet Fry,
Director, Federal Acquisition Policy Division,
Office of Governmentwide Acquisition Policy,
Office of Acquisition Policy, Office of
Governmentwide Policy.
Kalwant Smagh,
Director, Strategic Business Initiatives Unit,
Office of the Chief Operating Officer, Centers
for Disease Control and Prevention.
[FR Doc. 2022–27430 Filed 12–16–22; 8:45 am]
[FR Doc. 2022–27454 Filed 12–16–22; 8:45 am]
BILLING CODE 6820–EP–P
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
Centers for Disease Control and
Prevention
[CMS–3429–FN]
Notice of Closed Meeting
tkelley on DSK125TN23PROD with NOTICE
unwarranted invasion of personal
privacy.
Name of Committee: Disease,
Disability, and Injury Prevention and
Control Special Emphasis Panel (SEP)—
RFA–OH–22–002, NIOSH Centers for
Agricultural Safety and Health.
Date: March 7, 2023.
Time: 11:00 a.m.–6:00 p.m., EST.
Place: Video-Assisted Meeting.
Agenda: To review and evaluate grant
applications.
For Further Information Contact:
Marilyn Ridenour, B.S.N., M.P.H.,
Scientific Review Officer, Office of
Extramural Programs, National Institute
for Occupational Safety and Health,
CDC, 1095 Willowdale Road,
Morgantown, West Virginia, 26505;
Telephone: (304) 285–5879; Email:
MRidenour@cdc.gov.
The Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), title 5 U.S.C.,
as amended, and the Determination of
the Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, CDC, pursuant to
Public Law 92–463. The grant
applications and the discussions could
disclose confidential trade secrets or
commercial property such as patentable
material, and personal information
concerning individuals associated with
the grant applications, the disclosure of
which would constitute a clearly
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Jkt 259001
Medicare and Medicaid Programs:
Application From the Center for
Improvement in Healthcare Quality for
Continued Approval of Its Hospital
Accreditation Program
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:
This notice announces our
decision to approve the Center for
Improvement in Healthcare Quality
(CIHQ) for continued recognition as a
national accrediting organization for
hospitals that wish to participate in the
Medicare or Medicaid programs.
DATES: The decision announced in this
notice is applicable January 1, 2023
through January 1, 2028.
FOR FURTHER INFORMATION CONTACT:
SUMMARY:
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77615
Erin Imhoff, (410) 786–2337.
Caecilia Blondiaux, (410) 786–2190.
SUPPLEMENTARY INFORMATION:
I. Background
Under the Medicare program, eligible
beneficiaries may receive covered
services from a hospital, provided
certain requirements are met. Section
1861(e) of the Social Security Act (the
Act) establishes statutory authority for
the Secretary of the Department of
Health and Human Services (Secretary)
to set distinct criteria for facilities
seeking designation as a hospital.
Regulations concerning provider
agreements are at 42 CFR part 489 and
those pertaining to activities relating to
the survey and certification of facilities
are at 42 CFR part 488. The regulations
at 42 CFR part 482 specify the minimum
conditions of participation that a
hospital must meet to participate in the
Medicare program.
Generally, to enter into an agreement,
a hospital must first be certified by a
state survey agency (SA) as complying
with the conditions or requirements set
forth in part 482 of our regulations.
Thereafter, the hospital is subject to
regular surveys by a SA to determine
whether it continues to meet these
requirements.
Section 1865(a)(1) of the Act provides
that, if a provider entity demonstrates
through accreditation by a Centers for
Medicare & Medicaid Services (CMS)
approved national accrediting
organization (AO) that all applicable
Medicare requirements are met or
exceeded, we will deem those provider
entities as having met such
requirements. Accreditation by an AO is
voluntary and is not required for
Medicare participation.
If an AO is recognized by the
Secretary of the Department of Health
and Human Services (the Secretary) as
having standards for accreditation that
meet or exceed Medicare requirements,
any provider entity accredited by the
national accrediting body’s approved
program would be deemed to meet the
Medicare requirements. A national AO
applying for approval of its
accreditation program under part 488,
subpart A, must provide CMS with
reasonable assurance that the AO
requires the accredited provider entities
to meet requirements that are at least as
stringent as the Medicare requirements.
Our regulations concerning the approval
of AOs are set forth at §§ 488.4, 488.5
and 488.5(e)(2)(i). The regulations at
§ 488.5(e)(2)(i) require AOs to reapply
for continued approval of its
accreditation program every 6 years or
sooner, as determined by CMS.
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Agencies
[Federal Register Volume 87, Number 242 (Monday, December 19, 2022)]
[Notices]
[Pages 77614-77615]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-27430]
-----------------------------------------------------------------------
DEPARTMENT OF DEFENSE
GENERAL SERVICES ADMINISTRATION
NATIONAL AERONAUTICS AND SPACE ADMINISTRATION
[OMB Control No. 9000-0161; Docket No. 2022-0053; Sequence No. 23]
Information Collection; Reporting Purchases From Sources Outside
the United States
AGENCY: Department of Defense (DOD), General Services Administration
(GSA), and National Aeronautics and Space Administration (NASA).
ACTION: Notice and request for comments.
-----------------------------------------------------------------------
SUMMARY: In accordance with the Paperwork Reduction Act of 1995, and
the Office of Management and Budget (OMB) regulations, DoD, GSA, and
NASA invite the public to comment on an extension concerning reporting
purchases from sources outside the United States. DoD, GSA, and NASA
invite comments on: whether the proposed collection of information is
necessary for the proper performance of the functions of Federal
Government acquisitions, including whether the information will have
practical utility; the accuracy of the estimate of the burden of the
proposed information collection; ways to enhance the quality, utility,
and clarity of the information to be collected; and ways to minimize
the burden of the information collection on respondents, including the
use of automated collection techniques or other forms of information
technology. OMB has approved this information collection for use
through May 31, 2023. DoD, GSA, and NASA propose that OMB extend its
approval for use for three additional years beyond the current
expiration date.
DATES: DoD, GSA, and NASA will consider all comments received by
February 17, 2023.
ADDRESSES: DoD, GSA, and NASA invite interested persons to submit
comments on this collection through https://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. If there are difficulties submitting comments,
contact the GSA Regulatory Secretariat Division at 202-501-4755 or
[email protected].
Instructions: All items submitted must cite OMB Control No. 9000-
0161, Reporting Purchases from Sources Outside the United States.
Comments received generally will be posted without change to https://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.
FOR FURTHER INFORMATION CONTACT: Zenaida Delgado, Procurement Analyst,
at telephone 202-969-7207, or [email protected].
SUPPLEMENTARY INFORMATION:
A. OMB Control Number, Title, and Any Associated Form(s)
9000-0161, Reporting Purchases from Sources Outside the United
States.
B. Need and Uses
This clearance covers the information that offerors must submit to
comply
[[Page 77615]]
with the FAR provision 52.225-18, Place of Manufacture. This provision
requires offerors of manufactured end products to indicate in response
to a solicitation, by checking a box, whether the place of manufacture
of the end products it expects to provide is predominantly manufactured
in the United States or outside the United States. Contracting officers
use the information as the basis for entry into the Federal Procurement
Data System for further data on the rationale for purchasing foreign
manufactured items. The data is necessary for analysis of the
application of the Buy American statute and the trade agreements.
C. Annual Burden
Respondents: 50,106.
Total Annual Responses: 2,600,361.
Total Burden Hours: 26,004.
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. 9000-0161, Reporting Purchases from Sources Outside the
United States, in all correspondence.
Janet Fry,
Director, Federal Acquisition Policy Division, Office of Governmentwide
Acquisition Policy, Office of Acquisition Policy, Office of
Governmentwide Policy.
[FR Doc. 2022-27430 Filed 12-16-22; 8:45 am]
BILLING CODE 6820-EP-P