30-day notice

khammond on DSKJM1Z7X2PROD with NOTICES

Federal Register / Vol. 87, No. 191 / Tuesday, October 4, 2022 / Notices
Neuropathophysiology of Decision Making
and Chemobrain.
Date: October 26, 2022.
Time: 1:00 p.m. to 7:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Virtual Meeting).
Contact Person: Aleksey Gregory
Kazantsev, Ph.D., Scientific Review Officer,
Center for Scientific Review, National
Institutes of Health, 6701 Rockledge Drive,
Room 5201, Bethesda, MD 20817, (301) 435–
1042, aleksey.kazantsev@nih.gov.
Name of Committee: Endocrinology,
Metabolism, Nutrition and Reproductive
Sciences Integrated Review Group;
Pathophysiology of Obesity and Metabolic
Disease Study Section.
Date: October 27–28, 2022.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Washington Marriott Georgetown,
1221 22nd Street NW, Washington, DC
20037.
Contact Person: Raul Rojas, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 6185,
Bethesda, MD 20892, (301)451–6319, rojasr@
mail.nih.gov.
Name of Committee: Oncology 1—Basic
Translational Integrated Review Group;
Biochemical and Cellular Oncogenesis Study
Section.
Date: October 27–28, 2022.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Embassy Suites at the Chevy Chase
Pavilion, 4300 Military Road NW,
Washington, DC 20015.
Contact Person: Jian Cao, MD, Scientific
Review Officer, Center for Scientific Review,
National Institutes of Health, 6701 Rockledge
Drive, Bethesda, MD 20892, (301) 827–5902,
caojn@csr.nih.gov.
Name of Committee: Cardiovascular and
Respiratory Sciences Integrated Review
Group; Cardiovascular Differentiation and
Development Study Section.
Date: October 27, 2022.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Westin Grand, 2350 M Street NW,
Washington, DC 20037.
Contact Person: Sara Ahlgren, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, RM 4136,
Bethesda, MD 20892, (301) 435–0904,
sara.ahlgren@nih.gov.
Name of Committee: Genes, Genomes, and
Genetics Integrated Review Group;
Prokaryotic Cell and Molecular Biology
Study Section.
Date: October 27–28, 2022.
Time: 8:00 a.m. to 8:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Bethesdan Hotel, Tapestry
Collection by Hilton, 8120 Wisconsin Ave.,
Bethesda, MD 20814.

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Contact Person: Rebecca C Burgess, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Bethesda, MD
20892, (301) 480–8034, rebecca.burgess@
nih.gov.
Name of Committee: Biology of
Development and Aging Integrated Review
Group; Radiation Therapeutics and Biology
Study Section.
Date: October 27–28, 2022.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hyatt Regency Bethesda, 1 Bethesda
Metro Center, Bethesda, MD 20814.
Contact Person: Bo Hong, Ph.D., Scientific
Review Officer, Center for Scientific Review,
National Institutes of Health, 6701 Rockledge
Drive, Room 6194, MSC 7804, Bethesda, MD
20892, 301–996–6208, hongb@csr.nih.gov.
Name of Committee: Infectious Diseases
and Immunology A Integrated Review Group;
Cellular and Molecular Immunology—B
Study Section.
Date: October 27–28, 2022.
Time: 8:00 a.m. to 7:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Residence Inn Bethesda, 7335
Wisconsin Avenue, Bethesda, MD 20814.
Contact Person: Liying Guo, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4198,
MSC 7812, Bethesda, MD 20892, (301) 827–
7728, lguo@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: September 28, 2022.
Victoria E. Townsend,
Program Analyst, Office of Federal Advisory
Committee Policy.

individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Center for
Complementary and Integrative Health
Special Emphasis Panel; NCCIH Training and
Education Review Panel (CT).
Date: November 9–10, 2022.
Time: 10:00 a.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Center for Complementary
and Integrative, Democracy II, 6707
Democracy Blvd., Bethesda, MD 20892
(Virtual Meeting).
Contact Person: Jessica Marie McKlveen,
Ph.D., Scientific Review Officer, Office of
Scientific Review, Division of Extramural
Activities, NCCIH, NIH, 6707 Democracy
Boulevard, Suite 401, Bethesda, MD 20892–
547, jessica.mcklveen@nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.213, Research and Training
in Complementary and Alternative Medicine,
National Institutes of Health, HHS)
Dated: September 28, 2022.
Victoria E. Townsend,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2022–21426 Filed 10–3–22; 8:45 am]
BILLING CODE 4140–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 30-Day
Comment Request; PHS Research
Performance Progress Report and
Other Post-Award Reporting (Office of
the Director)

[FR Doc. 2022–21429 Filed 10–3–22; 8:45 am]

AGENCY:

BILLING CODE 4140–01–P

HHS.
ACTION:

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Center for Complementary &
Integrative Health; Notice of Closed
Meeting
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. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning

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National Institutes of Health,

Notice.

In compliance with the
Paperwork Reduction Act of 1995, the
National Institutes of Health (NIH) has
submitted to the Office of Management
and Budget (OMB) a request for review
and approval of the information
collection listed below.
DATES: Comments regarding this
information collection are best assured
of having their full effect if received
within 30-days of the date of this
publication.
SUMMARY:

Written comments and
recommendations for the proposed
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 30-day Review—Open

ADDRESSES:

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60184

Federal Register / Vol. 87, No. 191 / Tuesday, October 4, 2022 / Notices

for Public Comments’’ or by using the
search function.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, contact: Ms. Mikia P.
Currie, Program Analyst, Office of
Policy for Extramural Research
Administration, 6705 Rockledge Drive,
Suite 803–B, Bethesda, Maryland 20892,
or call non-toll-free number (301) 435–
0941 or email your request, including
your address to:
ProjectClearanceBranch@mail.nih.gov.
SUPPLEMENTARY INFORMATION: This
proposed information collection was
previously published in the Federal
Register on June 8, 2022, pages 34888/
34889 (87 FR 34888) and allowed 60
days for public comment. No public
comments were received. The purpose
of this notice is to allow an additional
30 days for public comment.
The Office of the Director, Office of
Extramural Research (OER), National
Institutes of Health (NIH), may not
conduct or sponsor, and the respondent
is not required to respond to, an
information collection that has been

2023, NIH will require applicants and
recipients to submit and address Data
Management and Sharing (DMS) Plans
within the SF424 Research and Related
(R&R) application and the Research
Performance Progress Report (RPPR) in
accordance with the DMS Policy. The
application and progress report forms
will be updated to align with this
requirement. NIH is also introducing a
new, optional Data Management and
Sharing (DMS) Plan format page that
applicants may use to develop their
DMS Plan. This collection will also
update the PHS 2271 Statement of
Appointment for trainees appointed
institutional training awards to report
on childcare cost support received. This
collection is also updated to remove the
iEdison instrument in accordance with
the transfer of the iEdison system to the
National Institute of Standards and
Technology (NIST) under the
Department of Commerce (DOC). NIST
will maintain OMB clearance under
0693–0090.
OMB approval is requested for three
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are.

extended, revised, or implemented on or
after October 1, 1995, unless it displays
a currently valid OMB control number.
In compliance with Section
3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Institutes of Health (NIH) has submitted
to the Office of Management and Budget
(OMB) a request for review and
approval of the information collection
listed below.
Proposed Collection: Public Health
Service (PHS) Research Performance
Progress Report and Other Post-award
Reporting –0925–0002 expiration date–
09/30/2024, REVISION, Office of the
Director, National Institutes of Health
(NIH).
Need and Use of Information
Collection: This collection under 0925–
0002 expiration date 09/30/2024 is
being revised to update the noncompeting progress report collections
for the implementation of the final
National Institutes of Health (NIH)
Policy for Data Management and
Sharing (DMS Policy) to promote the
management and sharing of scientific
data generated from NIH-funded or
conducted research. Starting in January

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Information collection forms

Number of
responses per
respondent

Average
burden per
response
(in hours)

Total annual
burden hours

khammond on DSKJM1Z7X2PROD with NOTICES

REPORTING
PHS 416–7 ......................................................................................................
PHS 6031–1 ....................................................................................................
PHS 568 ..........................................................................................................
PHS 2271 ........................................................................................................
PHS 2590 ........................................................................................................
RPPR – ............................................................................................................
Core Data ........................................................................................................
Biosketch (Part of RPPR) ................................................................................
Data Tables (Part of RPPR) ............................................................................
Trainee Diversity Report (Part of RPPR) ........................................................
PHS Human Subjects and Clinical Trial Information (Part of RPPR, includes
inclusion enrollment report) ..........................................................................
Publication Reporting .......................................................................................
Final RPPR—Core Data ..................................................................................
Data Tables (Part of Final RPPR) ...................................................................
Trainee Diversity Report (Part of Final RPPR) ...............................................
PHS Human Subjects and Clinical Trial Information (Part of Final RPPR, includes inclusion/enrollment) .........................................................................
PHS 3734 ........................................................................................................
Data Management and Sharing Plan (Part of RPPR) .....................................
Data Management and Sharing Plan (Part of Final RPPR) ............................

12,580
1,778
11,180
22,035
243

1
1
1
1
1

30/60
20/60
5/60
15/60
18

6,290
593
932
5,509
4,374

32,098
2,544
758
480

1
1
1
1

8
2
4
15/60

256,784
5,088
3,032
120

6,420
97,023
18,000
758
480

1
3
1
1
1

4
5/60
10
4
15/60

25,680
24,256
180,000
3,032
120

3,600
479
15,649
8,621

1
1
1
1

4
30/60
2
2

14,400
240
31,298
17,242

Reporting Burden Total ............................................................................

........................

........................

........................

578,990

RECORDKEEPING
SBIR/STTR Life Cycle Certification .................................................................

1,500

1

15/60

375

Total ..........................................................................................................

236,226

430,272

........................

579,365

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Federal Register / Vol. 87, No. 191 / Tuesday, October 4, 2022 / Notices
Dated: September 27, 2022.
Tara A. Schwetz,
Acting Principal Deputy Director, National
Institutes of Health.
[FR Doc. 2022–21547 Filed 10–3–22; 8:45 am]
BILLING CODE 4140–01–P

DEPARTMENT OF HOMELAND
SECURITY
U.S. Customs and Border Protection
[1651–0077]

Customs-Trade Partnership Against
Terrorism (CTPAT) and CTPAT Trade
Compliance Program
U.S. Customs and Border
Protection (CBP), Department of
Homeland Security.
ACTION: 30-Day notice and request for
comments; revision of an existing
collection of information.
AGENCY:

The Department of Homeland
Security, U.S. Customs and Border
Protection will be submitting the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995 (PRA). The
information collection is published in
the Federal Register to obtain comments
from the public and affected agencies.
DATES: Comments are encouraged and
must be submitted no later than
November 3, 2022 to be assured of
consideration.
ADDRESSES: Written comments and/or
suggestions regarding the item(s)
contained in this notice 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 30-day Review—Open
for Public Comments’’ or by using the
search function.
FOR FURTHER INFORMATION CONTACT:
Requests for additional PRA information
should be directed to Seth Renkema,
Chief, Economic Impact Analysis
Branch, U.S. Customs and Border
Protection, Office of Trade, Regulations
and Rulings, 90 K Street NE, 10th Floor,
Washington, DC 20229–1177, telephone
number 202–325–0056 or via email
CBP_PRA@cbp.dhs.gov. Please note that
the contact information provided here is
solely for questions regarding this
notice. Individuals seeking information
about other CBP programs should
contact the CBP National Customer
Service Center at 877–227–5511, (TTY)
1–800–877–8339, or CBP website at
https://www.cbp.gov/.

khammond on DSKJM1Z7X2PROD with NOTICES

SUMMARY:

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CBP
invites the general public and other
Federal agencies to comment on the
proposed and/or continuing information
collections pursuant to the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501
et seq.). This proposed information
collection was previously published in
the Federal Register (87 FR 12473) on
March 04, 2022, allowing for a 60-day
comment period. This notice allows for
an additional 30 days for public
comments. This process is conducted in
accordance with 5 CFR 1320.8. Written
comments and suggestions from the
public and affected agencies should
address one or more of the following
four points: (1) 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; (2) 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; (3)
suggestions to enhance the quality,
utility, and clarity of the information to
be collected; and (4) suggestions to
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 submission of responses. The
comments that are submitted will be
summarized and included in the request
for approval. All comments will become
a matter of public record.

SUPPLEMENTARY INFORMATION:

Overview of This Information
Collection
Title: Customs-Trade Partnership
Against Terrorism (CTPAT) and CTPAT
Trade Compliance Program.
OMB Number: 1651–0077.
Form Number: N/A.
Current Actions: Revision of an
existing information collection.
Type of Review: Revision.
Affected Public: Businesses.
Abstract: The CTPAT Program
comprises of two different program
divisions, CTPAT Security and CTPAT
Trade Compliance. The CTPAT Security
program is designed to safeguard the
world’s trade industry from terrorists
and smugglers by prescreening its
participants. The CTPAT Security
program applies to United States and
nonresident Canadian importers, United
States exporters, customs brokers,
consolidators, ports and terminal
operators, carriers of cargo in air, sea
and land, third party logistics providers,
Mexican long haul highway carriers,

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60185

and Canadian and Mexican
manufacturers. The Trade Compliance
program division is only available for
U.S. and nonresident Canadian
importers.
The CTPAT Program application
requests an applicant’s contact and
business information, including the
number of company employees, the
number of years in business, and a list
of company officers. CBP is adding the
following data elements for all CTPAT
partners to improve the screening of
companies. This will ensure that CBP is
confident that companies in the
program are low risk:
• Date of Birth (DOB)
• Country of Birth
• Country of Citizenship
• Travel Document number (e.g., visa or
passport number)
• Immigration status information (e.g.,
Alien Registration Number,
Naturalization number)
• Driver’s license information (e.g., state
and country of issuance, number, date
of issuance/expiration)
• Social Security Number
• Trusted Traveler membership type
and number (e.g., FAST/NEXUS/
SENTRI/Global Entry ID)
• Registro Federal de Contribuventes
(RFC) Persona Fisica (needed for
Mexican Foreign Manufacturers,
Highway Carriers, and Long-Haul
Carriers Only)
This collection of information is
authorized by the SAFE Port Act (Pub.
L. 109–347).
The CTPAT Trade Compliance
program is an optional component of
the CTPAT program and adds trade
compliance aspects to the supply chain
security aspects of the CTPAT Security
program. The CTPAT Security program
is a prerequisite to applying to the
CTPAT Trade Compliance program.
Current CTPAT importers are given the
opportunity to receive additional
benefits in exchange for a commitment
to assume responsibility for monitoring
their own compliance by applying to the
CTPAT Trade Compliance program.
After a company has completed the
security aspects of the CTPAT Security
program and is in good standing, it may
opt to apply to the CTPAT Trade
Compliance component. The CTPAT
Trade Compliance program strengthens
security by leveraging the CTPAT
supply chain requirements, identifying
low-risk trade entities for supply chain
security, and increasing the overall
efficiency of trade by segmenting risk
and processing by account.
The CTPAT Trade Compliance
program is open to U.S. and nonresident Canadian importers that have

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