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Federal Register / Vol. 91, No. 172 / Tuesday, September 8, 2026 / Notices
Group; Cancer Cell Biology Study
Section.
Date: October 5–6, 2026.
Time: 9:30 a.m. to 6:30 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Alyssa Diane Gregory,
Ph.D., Scientific Review Officer, Center
for Scientific Review, National Institutes
of Health, 6701 Rockledge Drive,
Bethesda, MD 20892, (301) 480–4906
[email protected].
Name of Committee: Center for
Scientific Review Special Emphasis
Panel; RFA Panel: BRAIN Initiative on
Technology Integration and
Dissemination.
Date: October 6, 2026.
Time: 9:30 a.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Shilpakala Ketha,
Ph.D., Scientific Review Officer, Center
for Scientific Review, National Institutes
of Health, 6701 Rockledge Dr., Bethesda,
MD 20892, (301) 496–0221,
[email protected].
Name of Committee: Biobehavioral
and Behavioral Processes Integrated
Review Group; Language and
Communication Study Section.
Date: October 7–8, 2026.
Time: 9:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Natalie S. Dailey,
Ph.D., Scientific Review Officer, Center
for Scientific Review, National Institutes
of Health, 6701 Rockledge Drive,
Bethesda, MD 20892, (301) 827–4451
[email protected].
Name of Committee: Bioengineering
Sciences & Technologies Integrated
Review Group; Modeling and Analysis
of Biological Systems Study Section.
Date: October 7–8, 2026.
Time: 9:30 a.m. to 6:30 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Zarana Patel, Ph.D.,
MPH Scientific Review Officer, Center
for Scientific Review, National Institutes

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of Health, 6701 Rockledge Drive,
Bethesda, MD 20892, (301) 496–9295,
[email protected].
Name of Committee: Center for
Scientific Review Special Emphasis
Panel; PAR: Clinical and Data
Coordinating Centers for Clinical Trials.
Date: October 8, 2026.
Time: 9:00 a.m. to 6:30 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Prashant Sharma,
Ph.D., Scientific Review Officer, Center
for Scientific Review National Institutes
of Health, 6701 Rockledge Drive,
Bethesda, MD 20892, (240) 961–8570
[email protected].
Name of Committee: Cardiovascular
and Respiratory Sciences Integrated
Review Group; Pulmonary Vascular
Disease and Physiology Study Section.
Date: October 8–9, 2026.
Time: 9:00 a.m. to 7:00 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Bradley Nuss, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room
4142, MSC7814, Bethesda, MD 20892,
301–451–8754, [email protected].
Name of Committee: Center for
Scientific Review Special Emphasis
Panel; Optimization of the Health
Services Workforce.
Date: October 8–9, 2026.
Time: 9:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Anna L. Riley, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room
3114, MSC 7759, Bethesda, MD 20892,
(301) 435–2889, [email protected].
Name of Committee: Center for
Scientific Review Special Emphasis
Panel; PAR Panel: Innovative Research
in Cancer Nanotechnology.
Date: October 8–9, 2026.
Time: 9:15 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.

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Meeting Format: Virtual Meeting.
Contact Person: Mirela Milescu,
Ph.D., Scientific Review Officer, Center
for Scientific Review, National Institutes
of Health, 6701 Rockledge Drive,
Bethesda, MD 20892, mirela.milescu@
nih.gov.
Name of Committee: Center for
Scientific Review Special Emphasis
Panel; Societal and Ethical Issues in
Research.
Date: October 9, 2026.
Time: 10:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Rochelle Francine
Hentges, Ph.D., Scientific Review
Officer, Center for Scientific Review,
National Institutes of Health, 6701
Rockledge Drive, Room 1000C,
Bethesda, MD 20892, (301) 402–8720,
[email protected].
(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 2, 2026.
Bruce A. George,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2026–18193 Filed 9–4–26; 8:45 am]
BILLING CODE 4167–05–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 30-Day
Comment Request Data and Specimen
Hub (DASH) (Eunice Kennedy Shriver
National Institute of Child Health and
Human Development)
AGENCY: National Institutes of Health,

HHS.
ACTION: Notice.
SUMMARY: 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 by
October 8, 2026.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent

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Federal Register / Vol. 91, No. 172 / Tuesday, September 8, 2026 / Notices

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: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, contact: Rebecca F. Rosen,
Ph.D., Director of the Office of Data
Science and Sharing, Eunice Kennedy
Shriver National Institute of Child
Health and Human Development
(NICHD), National Institutes of Health,
6710B Rockledge Drive, Bethesda, MD
20817, call non-toll-free number 240–
447–7723, or email your request,
including your address to:
[email protected]. Formal
requests for additional plans and
instruments must be requested in
writing.
SUPPLEMENTARY INFORMATION: This

proposed information collection was
previously published in the Federal
Register on May 27, 2026, pages 31471–
31473, (Vol. 91 FR 31471) and allowed
60 days for public comment. One
request for information was received for
the data collection plan and tools to be
provided. This was sent to the requester
on June 29, 2026. There were no public
comments. The purpose of this notice is
to allow an additional 30 days for public
comment.
The Eunice Kennedy Shriver National
Institute of Child Health and Human
Development (NICHD), National
Institutes of Health, may not conduct or
sponsor, and the respondent is not
required to respond to, an information
collection that has been 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: Data and
Specimen Hub (DASH) 0925–0744

expiration date 07/31/2027, REVISION,
Eunice Kennedy Shriver National
Institute of Child Health and Human
Development (NICHD), National
Institutes of Health (NIH).
Need and Use of Information
Collection: NICHD DASH was
established by NICHD as a data sharing
mechanism for clinical and population
health research studies. It serves as a
centralized resource for investigators to
share and access de-identified study
data funded by NICHD. DASH also
serves as a portal for requesting
biospecimens from select DASH studies.
NICHD is in the process of migrating
DASH data to a new instance of the
Biomedical Research Informatics
Computing System (BRICS) platform
operated by the NIH Center for
Information Technology (CIT). This
requires changes to the existing Office of
Management and Budget (OMB)approved DASH forms to align with the
BRICS platform structure and to
incorporate new NIH Requirements for
Controlled-Access Data Repositories
(CADRs) from the Required Security and
Operational Standards for NIH
Controlled-Access Data Repositories
(NIH CADR Guidebook), hereinafter
referred to as ‘‘NOT–OD–25–159’’
(https://www.grants.nih.gov/grants/
guide/notice-files/NOT-OD-25159.html).
Six (6) NICHD DASH information
collection forms have been updated and
three (3) forms have been removed. No
(0) forms have been added.
Information collected from Users
wishing to create an account will be
sufficient to identify them as unique
Users in the NICHD DASH system and
to comply with user access
requirements in NOT–OD–25–159.
Users submitting or requesting data and/
or biospecimens will be required to
provide information to ensure proper
use and secure handling of NICHD
DASH study data and biospecimens, in
alignment with the standard data
submission and access processes and
security standards and practices in
NOT–OD–25–159. Users submitting
data will be required to provide an
institutional attestation that the data
and biospecimen catalog being
submitted are appropriate for sharing in
NICHD DASH, following the standard

language in NOT–OD–25–159. Users
with approved data and biospecimen
requests will be required to submit an
annual progress or closeout report to
provide data and/or biospecimen usage
information and comply with data
access process and security standards in
NOT–OD–25–159 and biospecimen
access terms. The information collected
from Users who register in NICHD
DASH and submit or request data and/
or biospecimens will be used to monitor
submissions and requests, oversee
Users’ experiences with DASH, notify
interested recipients of updates to study
data or biospecimen catalogs available
through NICHD DASH, and maintain
User and NICHD DASH compliance
with NOT–OD–25–159.
The potential for public benefit to be
achieved through sharing study data
and/or biospecimens through DASH for
secondary analysis is significant. NICHD
DASH supports NICHD’s mission to
lead research and training to understand
human development, improve
reproductive health, enhance the lives
of children and adolescents, and
optimize abilities for all. Study data and
biospecimen sharing and reuse
promotes testing of new hypotheses
from data and biospecimens already
collected, facilitate trans-disciplinary
collaboration, accelerate scientific
findings, and enable NICHD to
maximize the return on its investments
in research.
This revised information collection
package is being submitted to OMB to
revise NICHD DASH clearance for use of
the forms indicated in the Table
(Estimated Annualized Burden Hours)
below. OMB approval is requested for 3
years. There are no costs to respondents
other than their time.
The total User burden increased from
2024 to 2026 as a result of: (a)
Additional attestation information and
data collection required to comply with
NOT–OD–25–159, and (b) NICHD DASH
supporting a significant increase in User
numbers due to NIH-wide data sharing
expectations under the NIH DMS Policy.
The estimated annualized burden is
1,361 hours. See details in the Table
below.
Estimated Annualized Burden Hours

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ANNUAL BURDEN HOURS ESTIMATE
Form name

Number of
respondents

Number of
responses per
respondent

1,500
100
100

1
1
1

User Registration .............................................................................................
Data and Biospecimen Catalog Submission ...................................................
Institutional Certification Template ..................................................................

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Average
burden per
response
(in hours)
5/60
2
5/60

Total annual
burden hour
125
200
8

57159

Federal Register / Vol. 91, No. 172 / Tuesday, September 8, 2026 / Notices
ANNUAL BURDEN HOURS ESTIMATE—Continued
Number of
responses per
respondent

Data Access Request (New Request) .............................................................
Data Access Request (Renewal) .....................................................................
Biospecimen Access Request (New Request) ................................................
Biospecimen Access Request (Renewal) ........................................................
Annual Progress Report/Closeout Report (Data & Biospecimen Access) ......

500
380
60
3
606

1
1
1
1
1

1
10/60
1
10/60
40/60

500
63
60
1
404

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

3,249

3,249

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

1,361

Dated: September 2, 2026.
Jennifer M. Guimond,
Project Clearance Liaison, Eunice Kennedy
Shriver National Institute of Child Health and
Human Development, National Institutes of
Health.
[FR Doc. 2026–18191 Filed 9–4–26; 8:45 am]

DEPARTMENT OF THE INTERIOR
Geological Survey
[Docket No. USGS–2026–0331;
GR26ZS00MD86700; OMB Control Number
1028–0140]

Agency Information Collection
Activities; Terrestrial Analogs Survey
Submission to the Office of
Management and Budget for Review
and Approval; Terrestrial Analogs
Survey

BILLING CODE 4140–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health

AGENCY: U.S. Geological Survey,

Center for Scientific Review; Amended
Notice of Meeting

Interior.
ACTION: Notice of information collection;

request for comment.
Notice is hereby given of a change in
the meeting of the Center for Scientific
Review Special Emphasis Panel,
October 15, 2026, 09:30 a.m. to October
16, 2026, 09:00 p.m., National Institutes
of Health, Rockledge II, 6701 Rockledge
Drive, Bethesda, MD, 20892 which was
published in the Federal Register on
August 31, 2026, 91 FR 55890 Doc No.
2026–17687.
This meeting is being amended to
change the meeting to 1-day ending on
October 15, 2026. The meeting is closed
to the public.
Dated: September 2, 2026.
Bruce A. George,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2026–18215 Filed 9–4–26; 8:45 am]
BILLING CODE 4167–05–P

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Average
burden per
response
(in hours)

Number of
respondents

Form name

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SUMMARY: In accordance with the

Paperwork Reduction Act of 1995
(PRA), the U.S. Geological Survey
(USGS) is proposing to renew an
information collection with revisions.
DATES: Interested persons are invited to
submit comments on or before October
8, 2026.
ADDRESSES: You may submit comments
by one of the following methods:
D Internet: https://
www.regulations.gov. Search for and
submit comments on Docket No. USGS–
2026–0331.
D U.S. Mail: USGS, Information
Collections Clearance Officer, 12201
Sunrise Valley Drive, MS 159, Reston,
VA 20192.
FOR FURTHER INFORMATION CONTACT: To
request additional information about
this information collection request
(ICR), contact Amber Gullikson by email
at [email protected] or by phone at
928–556–7009. Individuals in the
United States who are deaf, deafblind,
hard of hearing, or have a speech
disability may dial 711 (TTY, TDD, or
TeleBraille) to access
telecommunications relay services.
Individuals outside the United States
should use the relay services offered
within their country to make
international calls to the point-ofcontact in the United States. You may

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Total annual
burden hour

also view the ICR at http://
www.reginfo.gov/public/do/PRAMain.
SUPPLEMENTARY INFORMATION: In
accordance with the PRA (44 U.S.C.
3501 et seq.) and 5 CFR 1320.8(d)(1), we
provide the public and other Federal
agencies with an opportunity to
comment on new, proposed, revised,
and continuing collections of
information. This helps us assess the
impact of our information collection
requirements and minimize the public’s
reporting burden. It also helps the
public understand our information
collection requirements and provide the
requested data in the desired format.
A Federal Register notice with a 60day public comment period soliciting
comments on this collection of
information was published on
Thursday, July 2, 2026 (91 FR 40553).
No comments were received.
As part of our continuing effort to
reduce paperwork and respondent
burdens, we are again soliciting
comments from the public and other
Federal agencies on the proposed ICR
that is described below. We are
especially interested in public
comments addressing the following:
(1) Whether or not the 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 our estimate of the
burden for this collection of
information, including the validity of
the methodology and assumptions used.
(3) Ways to enhance the quality,
utility, and clarity of the information to
be collected; and
(4) How might the agency minimize
the burden of the collection of
information on those who are to
respond, including using appropriate
automated, electronic, mechanical, or
other technological collection
techniques or other forms of information
technology, e.g., permitting electronic
submission of response.
Comments that you submit in
response to this notice are a matter of
public record. Before including your

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