Agency Information Collection Request; 60-Day Public Comment Request, 658 [2024-31615]
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[FR Doc. 2024–31614 Filed 1–3–25; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: OS–0990–0481]
Agency Information Collection
Request; 60-Day Public Comment
Request
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
In compliance with the
requirement of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, is publishing the
following summary of a proposed
collection for public comment.
SUMMARY:
Comments on the ICR must be
received on or before March 7, 2025.
ADDRESSES: Submit your comments to
Sherrette.Funn@hhs.gov or by calling
(202) 264–0041 and PRA@HHS.GOV
FOR FURTHER INFORMATION CONTACT:
When submitting comments or
requesting information, please include
the document identifier 0990–0481–60D
and project title for reference, to
Sherrette A. Funn, email:
Sherrette.Funn@hhs.gov, PRA@
HHS.GOV or call (202) 264–0041 the
Reports Clearance Officer.
SUPPLEMENTARY INFORMATION: Interested
persons are invited to send comments
regarding this burden estimate or any
other aspect of this collection of
information, including any of the
following subjects: (1) The necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions; (2) the accuracy
of the estimated burden; (3) ways to
enhance the quality, utility, and clarity
of the information to be collected; and
(4) the use of automated collection
techniques or other forms of information
technology to minimize the information
collection burden.
Title of the Collection: For HHS/
OASH Consultation Process,
Institutional Review Board (IRB)
Records.
DATES:
Type of Collection: Renewal, 3-year
extension without change.
OMB No.: 0990–0481
Abstract: The Office of the Assistant
Secretary for Health (OASH), Office for
Human Research Protections (OHRP) is
requesting a 3-year extension without
change to the currently approved
information collection request, For
OASH/HHS Consultation Process,
Institutional Review Board (IRB)
Records, OMB No. 0990–0481. The
purpose of the collection is for OHRP to
receive IRB records when an IRB or an
institution requests an HHS
consultation process for proposed
research that is not otherwise
approvable by an IRB involving,
respectively: (1) pregnant women,
human fetuses and neonates; (2)
prisoners; or, (3) children, as subjects.
The information that must be submitted
to OHRP by an IRB or institution
includes the research protocol, consent
form, parental permission and child
assent forms (if relevant), and other
relevant IRB records (e.g., IRB minutes).
The Office of the Assistant Secretary for
Health, on behalf of the Secretary of
HHS, may determine that such research
can be conducted or supported by HHS
after consulting with experts and
meeting other procedural requirements.
Likely Respondents: IRBs.
ANNUALIZED BURDEN HOUR TABLE
subpart B, § 46. 207 ............................................................
subpart C, § 46.306 (iii) and (iv) ..........................................
subpart D, § 46.407 .............................................................
IRBs ...............
IRBs ...............
IRBs ...............
3
3
4
1
1
1
1
1
1
3
3
4
Total ..............................................................................
........................
........................
........................
........................
10
[FR Doc. 2024–31615 Filed 1–3–25; 8:45 am]
BILLING CODE 4150–31–P
khammond on DSK9W7S144PROD with NOTICES
DEPARTMENT OF HOMELAND
SECURITY
U.S. Customs and Border Protection
Implementation of the Commonwealth
of the Northern Mariana Islands (CNMI)
Economic Vitality & Security Travel
Authorization Program (EVS–TAP)
U.S. Customs and Border
Protection, DHS.
AGENCY:
VerDate Sep<11>2014
19:04 Jan 03, 2025
Jkt 265001
ACTION:
Number of
respondents
Total
burden
hours
Respondent
type
Vivianna P. Cowl,
Paperwork Reduction Act Reports Clearance
Officer, Health and Human Services, Office
of the Secretary.
Number of
respondents
Average
burden per
response
(in hours)
45 CFR part 46—HHS consultation process provision
General notice.
This document announces the
implementation of the Commonwealth
of the Northern Mariana Islands (CNMI)
Economic Vitality & Security Travel
Authorization Program (EVS–TAP). The
CNMI EVS–TAP is a restricted subprogram of the Guam-CNMI Visa Waiver
Program and allows prescreened
nationals of the People’s Republic of
China to travel to the CNMI without a
visa under specified conditions. In
accordance with Department of
Homeland Security regulations, DHS
will begin implementation of the CNMI
EVS–TAP requirements 45 days after
publication of this notification of
implementation in the Federal Register.
SUMMARY:
PO 00000
Frm 00076
Fmt 4703
Sfmt 4703
Implementation of the CNMI
EVS–TAP requirements will begin as of
February 20, 2024.
FOR FURTHER INFORMATION CONTACT:
Neyda Yejo, Office of Field Operations,
U.S. Customs and Border Protection,
(202) 344–2373, or via email at
Neyda.I.Yejo@cbp.dhs.gov.
SUPPLEMENTARY INFORMATION:
DATES:
Background
On January 18, 2024, the Department
of Homeland Security (DHS), through
U.S. Customs and Border Protection
(CBP), published an interim final rule
(IFR) in the Federal Register (89 FR
3299) with an effective date of
September 30, 2024. The IFR,
promulgated in consultation with the
Secretary of the Interior and the
E:\FR\FM\06JAN1.SGM
06JAN1
Agencies
[Federal Register Volume 90, Number 3 (Monday, January 6, 2025)]
[Notices]
[Page 658]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-31615]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Document Identifier: OS-0990-0481]
Agency Information Collection Request; 60-Day Public Comment
Request
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement of the Paperwork Reduction
Act of 1995, the Office of the Secretary (OS), Department of Health and
Human Services, is publishing the following summary of a proposed
collection for public comment.
DATES: Comments on the ICR must be received on or before March 7, 2025.
ADDRESSES: Submit your comments to [email protected] or by calling
(202) 264-0041 and [email protected]
FOR FURTHER INFORMATION CONTACT: When submitting comments or requesting
information, please include the document identifier 0990-0481-60D and
project title for reference, to Sherrette A. Funn, email:
[email protected], [email protected] or call (202) 264-0041 the Reports
Clearance Officer.
SUPPLEMENTARY INFORMATION: Interested persons are invited to send
comments regarding this burden estimate or any other aspect of this
collection of information, including any of the following subjects: (1)
The necessity and utility of the proposed information collection for
the proper performance of the agency's functions; (2) the accuracy of
the estimated burden; (3) ways to enhance the quality, utility, and
clarity of the information to be collected; and (4) the use of
automated collection techniques or other forms of information
technology to minimize the information collection burden.
Title of the Collection: For HHS/OASH Consultation Process,
Institutional Review Board (IRB) Records.
Type of Collection: Renewal, 3-year extension without change.
OMB No.: 0990-0481
Abstract: The Office of the Assistant Secretary for Health (OASH),
Office for Human Research Protections (OHRP) is requesting a 3-year
extension without change to the currently approved information
collection request, For OASH/HHS Consultation Process, Institutional
Review Board (IRB) Records, OMB No. 0990-0481. The purpose of the
collection is for OHRP to receive IRB records when an IRB or an
institution requests an HHS consultation process for proposed research
that is not otherwise approvable by an IRB involving, respectively: (1)
pregnant women, human fetuses and neonates; (2) prisoners; or, (3)
children, as subjects. The information that must be submitted to OHRP
by an IRB or institution includes the research protocol, consent form,
parental permission and child assent forms (if relevant), and other
relevant IRB records (e.g., IRB minutes). The Office of the Assistant
Secretary for Health, on behalf of the Secretary of HHS, may determine
that such research can be conducted or supported by HHS after
consulting with experts and meeting other procedural requirements.
Likely Respondents: IRBs.
Annualized Burden Hour Table
----------------------------------------------------------------------------------------------------------------
Average
45 CFR part 46--HHS Number of Number of burden per Total burden
consultation process Respondent type respondents respondents response (in hours
provision hours)
----------------------------------------------------------------------------------------------------------------
subpart B, Sec. 46. 207... IRBs.............. 3 1 1 3
subpart C, Sec. 46.306 IRBs.............. 3 1 1 3
(iii) and (iv).
subpart D, Sec. 46.407.... IRBs.............. 4 1 1 4
---------------------------------------------------------------
Total................... .................. .............. .............. .............. 10
----------------------------------------------------------------------------------------------------------------
Vivianna P. Cowl,
Paperwork Reduction Act Reports Clearance Officer, Health and Human
Services, Office of the Secretary.
[FR Doc. 2024-31615 Filed 1-3-25; 8:45 am]
BILLING CODE 4150-31-P