Submission for OMB Review; 30-Day Comment Request; Data and Specimen Hub (DASH) (Eunice Kennedy Shriver National Institute of Child Health and Human Development), 52481-52483 [2024-13715]
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Federal Register / Vol. 89, No. 121 / Monday, June 24, 2024 / Notices
who plan to view the virtual meeting
and need special assistance or other
reasonable accommodations to view the
meeting, should notify the Contact
Person listed below in advance of the
meeting. The meeting can be accessed
from the NIH Videocast at the following
link: https://videocast.nih.gov/.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute on Alcohol Abuse
and Alcoholism; Notice of Closed
Meeting
Pursuant to section 1009 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
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute on
Alcohol Abuse and Alcoholism Special
Emphasis Panel; NIAAA Member Conflict
Reviews.
Date: July 17, 2024.
Time: 1:00 p.m. to 3:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institute of Health,
National Institute on Alcohol Abuse and
Alcoholism, 6700B Rockledge Drive,
Bethesda, MD 20892 (Virtual Meeting).
Contact Person: Beata Buzas, Ph.D.,
Scientific Review Officer, Extramural Project
Review Branch, Office of Extramural
Activities, National Institute on Alcohol
Abuse and Alcoholism, 6700B Rockledge
Drive, Room 2116, MSC 6902, Bethesda, MD
20892, (301) 443–0800, bbuzas@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.273, Alcohol Research
Programs, National Institutes of Health, HHS)
Dated: June 17, 2024.
David W. Freeman,
Supervisory Program Analyst, Office of
Federal Advisory Committee Policy.
Name of Committee: Frederick National
Laboratory Advisory Committee to the
National Cancer Institute.
Date: July 10, 2024.
Time: 9:30 a.m. to 4:00 p.m.
Agenda: Ongoing and new activities at the
Frederick National Laboratory for Cancer
Research.
Place: National Cancer Institute Shady
Grove, 9609 Medical Center Drive, Rockville,
MD 20850 (Virtual Meeting).
Contact Person: Christopher D. Kane,
Ph.D., Health Science Administrator and
Program Officer, Office of Scientific
Operations, Frederick Office of Scientific
Operations, National Cancer Institute, NIH,
1050 Boyles Street, Building 427, Room 4
Frederick, MD 21702, christopher.kane@
nih.gov.
Any interested person may file written
comments with the committee by forwarding
the statement to the Contact Person listed on
this notice. The statement should include the
name, address, telephone number and when
applicable, the business or professional
affiliation of the interested person.
Information is also available on the
Institute’s/Center’s home page: FNLAC:
https://deainfo.nci.nih.gov/advisory/fac/
fac.htm, where an agenda and any additional
information for the meeting will be posted
when available.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.392, Cancer Construction;
93.393, Cancer Cause and Prevention
Research; 93.394, Cancer Detection and
Diagnosis Research; 93.395, Cancer
Treatment Research; 93.396, Cancer Biology
Research; 93.397, Cancer Centers Support;
93.398, Cancer Research Manpower; 93.399,
Cancer Control, National Institutes of Health,
HHS)
[FR Doc. 2024–13732 Filed 6–21–24; 8:45 am]
Dated: June 17, 2024.
David W. Freeman,
Supervisory Program Analyst, Office of
Federal Advisory Committee Policy.
BILLING CODE 4140–01–P
[FR Doc. 2024–13731 Filed 6–21–24; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institutes of Health
lotter on DSK11XQN23PROD with NOTICES1
National Cancer Institute; Notice of
Meeting
Pursuant to section 1009 of the
Federal Advisory Committee Act, as
amended, notice is hereby given of a
meeting of the Frederick National
Laboratory Advisory Committee to the
National Cancer Institute.
The meeting will be held virtually
and is open to the public. Individuals
VerDate Sep<11>2014
18:55 Jun 21, 2024
Jkt 262001
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:
PO 00000
Notice.
Frm 00049
Fmt 4703
Sfmt 4703
52481
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.
ADDRESSES: 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
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 301–
827–4602, or email your request,
including your address to:
NICHD.DASH@mail.nih.gov. 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 March 14, 2024, page
18650–18652, (Vol. 89 FR 18650–18652)
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 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.
SUMMARY:
E:\FR\FM\24JNN1.SGM
24JNN1
52482
Federal Register / Vol. 89, No. 121 / Monday, June 24, 2024 / Notices
Proposed Collection: Data and
Specimen Hub (DASH)–0925–0744
expiration date 06/30/2024, REVISION,
Eunice Kennedy Shriver National
Institute of Child Health and Human
Development (NICHD), National
Institutes of Health (NIH).
Need and Use of Information
Collection: This is a request to revise the
previously approved submission (OMB
number: 0925–0744) to add the
collection of additional information
from Users who wish to extend their
data access beyond the standard threeyear period, remove a Biospecimen
Annual Report form that is no longer in
use, extend the information collection
in Institutional Certifications to cover
both data and biospecimen submissions,
and implement minor revisions on
previously approved forms, including
additional field options and language
revisions that do not impact the nature
of information being collected or its
associated burden.
DASH has been established by NICHD
as a data sharing mechanism for
biomedical research investigators. It
serves as a centralized resource for
investigators to share and access deidentified study data from studies
funded by NICHD. DASH also serves as
a portal for requesting biospecimens
from select DASH studies.
NICHD also supports other public
archives, data collections, and
resources, such as Data Sharing for
Demographic Research (DSDR), NICHD/
DIPHR Biospecimen Repository Access
and Data Sharing (BRADS), the Down
Syndrome Registry (DS-Connect),
Zebrafish Information Network (ZFIN),
etc. In addition to these NICHD-funded
public archives, many collaborative
studies funded through NICHD are
dispersed across other NIH designated
archives, including the National Heart,
Lung, and Blood Institute (NHLBI)
Biologic Specimen and Data Repository
Information Coordinating Center
(BioLINCC), and other NIH-wide
repositories, such as the Database of
Genotypes and Phenotypes (dbGaP).
In an effort to link these data
resources and increase the visibility of
NICHD-funded studies and data
collections, DASH enables Users to
catalog studies and data collections
required to provide additional
supporting information to ensure proper
use and security of NICHD DASH study
data and biospecimens. For data and/or
biospecimen requests, information is
collected both for initial data and/or
biospecimen access and then
throughout the request duration to
maintain access. This includes research
objectives and analysis plans, research
teams, and institution information, as
well as significant findings details for
annual progress reports or extension
justification for data request renewals.
The information collected throughout
these processes is limited to the
essential data required to ensure the
management of Users in NICHD DASH
is efficient and the sharing of data and
biospecimens among investigators is
effective and aligns with DASH data
sharing policies. The primary uses of
the information collected from Uses by
NICHD will be to:
• Communicate with the Users
regarding data submission, study catalog
submission, external resource catalog
submission, data requests, and
biospecimen requests;
• Monitor data submissions, study
catalog submission, external resource
catalog submission, data requests, and
biospecimen requests;
• Notify interested Users of updates
to data and biospecimens available
through NICHD DASH; and
• Help NICHD understand the use of
NICHD DASH study data and
biospecimens by the research
community.
All the data collected from use of
NICHD DASH are for the purposes of
internal administrative management of
NICHD DASH, with the exception of the
Recipient’s approved use of DASH data
and/or biospecimens, Recipient name
and institution, and significant findings
reporting in the Data Request Annual
Use Report, which may be shared on the
DASH website or in publications
describing the performance and value of
the DASH system for the broader
scientific community.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
433.
stored in other external archives to
facilitate their discovery through DASH.
Users submitting studies or external
resources for cataloging in DASH will
provide descriptive information about
the study required to populate the Study
Overview Page in DASH. This
cataloging process closely mirrors the
existing study data submission process
in DASH; however, no study
documentation or data will be uploaded
to DASH. Requesters will be directed to
the external archive via a URL link to
obtain access to the data stored in the
external archives and resources.
The potential for public benefit to be
achieved through sharing study data
and/or biospecimen inventories through
DASH for secondary analysis is
significant. Additionally, the ability to
centralize information regarding where
to find, and how to access, studies, and
data collections funded by NICHD
stored across various public archives
(i.e., cataloged studies and data
collections) further helps to promote
information discovery and reuse of data.
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 will
promote 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.
Anyone can access NICHD DASH to
browse and view descriptive
information about the studies and data
collections without creating an account.
Users who wish to submit studies or
request data (stored in DASH) and/or
biospecimens (stored in NICHD
contracted Biorepository) must register
for an account. Users who wish to
submit a study catalog and/or external
resource catalog must also register for an
account.
Information will be collected from
those wishing to create an account,
sufficient to identify them as unique
Users. Those submitting or requesting
data and/or biospecimens will be
lotter on DSK11XQN23PROD with NOTICES1
ESTIMATED ANNUALIZED BURDEN HOURS
Annual burden hours estimate
Number of
respondents
Form name
User Registration .............................................................................................
VerDate Sep<11>2014
18:55 Jun 21, 2024
Jkt 262001
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
900
E:\FR\FM\24JNN1.SGM
1
24JNN1
Average
burden per
response
(in hours)
5/60
Total annual
burden hour
75
52483
Federal Register / Vol. 89, No. 121 / Monday, June 24, 2024 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Annual burden hours estimate
Number of
respondents
Form name
Average
burden per
response
(in hours)
Total annual
burden hour
Data and Biospecimen Catalog Submission ...................................................
Institutional Certification Template ..................................................................
Data Request ...................................................................................................
Biospecimen Request ......................................................................................
Data Request Annual Progress Report ...........................................................
Study Catalog Submission ..............................................................................
External Resource Catalog Submission ..........................................................
Data Request Renewal ....................................................................................
36
36
150
4
240
2
4
42
1
1
1
1
1
1
1
1
2
5/60
1
1
30/60
30/60
15/60
10/60
72
3
150
4
120
1
1
7
Total ..........................................................................................................
1,414
1,414
........................
433
Dated: June 17, 2024.
Jennifer M. Guimond,
Project Clearance Liaison, Eunice Kennedy
Shriver National Institute of Child Health and
Human Development, National Institutes of
Health.
[FR Doc. 2024–13715 Filed 6–21–24; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Agency Information Collection
Activities: Proposed Collection;
Comment Request
lotter on DSK11XQN23PROD with NOTICES1
Number of
responses per
respondent
In compliance with Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 concerning
opportunity for public comment on
proposed collections of information, the
Substance Abuse and Mental Health
Services Administration (SAMHSA)
will publish periodic summaries of
proposed projects. To request more
information on the proposed project or
to obtain a copy of the information
collection plans, call the SAMHSA
Reports Clearance Officer at (240) 276–
0166.
Comments are invited on: (a) whether
the proposed collections of information
are necessary for the proper
performance of the functions of the
agency, including whether the
information shall have practical utility;
(b) the accuracy of the agency’s estimate
of the burden of the proposed collection
of information; (c) ways to enhance the
quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
VerDate Sep<11>2014
18:55 Jun 21, 2024
Jkt 262001
Project: State Opioid Response (SOR)/
Tribal Opioid Response (TOR) Program
Instrument (OMB No. 0930–0384)—
Revision
SAMHSA is requesting approval to
modify its existing SOR/TOR Program
Instrument by (1) broadening language
from ‘naloxone’ to ‘naloxone and other
opioid overdose reversal medications’
due to the availability of new FDAapproved non-naloxone overdose
reversal medications; (2) broadening
language from ‘fentanyl test strips’ to
‘drug checking technologies as directed
by SAMHSA’ due to the availability of
new drug checking technology,
including test strips for other emerging
substances; (3) reducing the number of
questions from 12 to 10 by combining
four questions with similar themes into
two questions for clarity; (4) removing
question 12 because it is comprised of
more than one question with several
different ideas, making it unsuited for
this instrument; and (5) adding one
question at the request of Office of
National Drug Control Policy
(ONDCP)to collect information on
Congressionally mandated and
programmatic activities and comply
with reporting requirements. The
program-level information is collected
quarterly and entered and stored in
SAMHSA’s Performance Accountability
and Reporting System, which is a realtime, performance management system
that captures information on SAMHSA
funded substance use and substance use
disorder prevention, harm reduction,
treatment, and recovery support
services, and mental health services
delivered in the United States.
Continued approval of this information
collection will allow SAMHSA to
continue to meet Government
Performance and Results Modernization
Act (GPRA) of 2010 reporting
requirements that quantify the effects
PO 00000
Frm 00051
Fmt 4703
Sfmt 4703
and accomplishments of its
discretionary grant programs.
The SOR/TOR programs are
authorized under the Consolidated
Appropriations Act, 2023, Division H,
Title II [Pub. L. 117–328], and section
1003 of the 21st Century Cures Act [Pub.
L. 114–255] (42 U.S.C. 290ee–3a), as
amended. SOR/TOR programs aim to
address the opioid crisis by increasing
access to FDA-approved medications for
the treatment of opioid use disorder
(MOUD), and support the continuum of
prevention, harm reduction, treatment,
and recovery support services for opioid
use disorder (OUD) and other
concurrent substance use disorders. The
SOR program also supports the
continuum of care for stimulant misuse
and use disorders, including for cocaine
and methamphetamine.
SAMHSA is proposing to revise the
SOR/TOR Program Instrument data
collection instrument (OMB No. 0930–
0384), to collect information on
Congressionally mandated and
programmatic activities and comply
with reporting requirements.
SAMHSA developed the SOR/TOR
Program Instrument to collect minimum
data on naloxone purchase and
distribution, but the SOR/TOR programs
are unique in that they have prevention,
education, and harm reduction
requirements. SOR/TOR grantees are
required to engage in the following
prevention and education activities: (1)
train peers, first responders, and other
key community sectors on recognition
of opioid overdose and appropriate use
of the opioid overdose antidote
naloxone; (2) develop evidence-based
community prevention efforts such as
strategic messaging on the consequences
of opioid and stimulant misuse; (3)
implement school-based prevention
programs and outreach; and (4)
purchase and distribute opioid overdose
antidote reversal naloxone based on the
E:\FR\FM\24JNN1.SGM
24JNN1
]]>Agencies
[Federal Register Volume 89, Number 121 (Monday, June 24, 2024)]
[Notices]
[Pages 52481-52483]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-13715]
-----------------------------------------------------------------------
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 within 30 days of the date of
this publication.
ADDRESSES: 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 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 301-827-4602, 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 March 14, 2024, page
18650-18652, (Vol. 89 FR 18650-18652) 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 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.
[[Page 52482]]
Proposed Collection: Data and Specimen Hub (DASH)-0925-0744
expiration date 06/30/2024, REVISION, Eunice Kennedy Shriver National
Institute of Child Health and Human Development (NICHD), National
Institutes of Health (NIH).
Need and Use of Information Collection: This is a request to revise
the previously approved submission (OMB number: 0925-0744) to add the
collection of additional information from Users who wish to extend
their data access beyond the standard three-year period, remove a
Biospecimen Annual Report form that is no longer in use, extend the
information collection in Institutional Certifications to cover both
data and biospecimen submissions, and implement minor revisions on
previously approved forms, including additional field options and
language revisions that do not impact the nature of information being
collected or its associated burden.
DASH has been established by NICHD as a data sharing mechanism for
biomedical research investigators. It serves as a centralized resource
for investigators to share and access de-identified study data from
studies funded by NICHD. DASH also serves as a portal for requesting
biospecimens from select DASH studies.
NICHD also supports other public archives, data collections, and
resources, such as Data Sharing for Demographic Research (DSDR), NICHD/
DIPHR Biospecimen Repository Access and Data Sharing (BRADS), the Down
Syndrome Registry (DS-Connect), Zebrafish Information Network (ZFIN),
etc. In addition to these NICHD-funded public archives, many
collaborative studies funded through NICHD are dispersed across other
NIH designated archives, including the National Heart, Lung, and Blood
Institute (NHLBI) Biologic Specimen and Data Repository Information
Coordinating Center (BioLINCC), and other NIH-wide repositories, such
as the Database of Genotypes and Phenotypes (dbGaP).
In an effort to link these data resources and increase the
visibility of NICHD-funded studies and data collections, DASH enables
Users to catalog studies and data collections stored in other external
archives to facilitate their discovery through DASH. Users submitting
studies or external resources for cataloging in DASH will provide
descriptive information about the study required to populate the Study
Overview Page in DASH. This cataloging process closely mirrors the
existing study data submission process in DASH; however, no study
documentation or data will be uploaded to DASH. Requesters will be
directed to the external archive via a URL link to obtain access to the
data stored in the external archives and resources.
The potential for public benefit to be achieved through sharing
study data and/or biospecimen inventories through DASH for secondary
analysis is significant. Additionally, the ability to centralize
information regarding where to find, and how to access, studies, and
data collections funded by NICHD stored across various public archives
(i.e., cataloged studies and data collections) further helps to promote
information discovery and reuse of data. 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 will promote 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.
Anyone can access NICHD DASH to browse and view descriptive
information about the studies and data collections without creating an
account. Users who wish to submit studies or request data (stored in
DASH) and/or biospecimens (stored in NICHD contracted Biorepository)
must register for an account. Users who wish to submit a study catalog
and/or external resource catalog must also register for an account.
Information will be collected from those wishing to create an
account, sufficient to identify them as unique Users. Those submitting
or requesting data and/or biospecimens will be required to provide
additional supporting information to ensure proper use and security of
NICHD DASH study data and biospecimens. For data and/or biospecimen
requests, information is collected both for initial data and/or
biospecimen access and then throughout the request duration to maintain
access. This includes research objectives and analysis plans, research
teams, and institution information, as well as significant findings
details for annual progress reports or extension justification for data
request renewals. The information collected throughout these processes
is limited to the essential data required to ensure the management of
Users in NICHD DASH is efficient and the sharing of data and
biospecimens among investigators is effective and aligns with DASH data
sharing policies. The primary uses of the information collected from
Uses by NICHD will be to:
Communicate with the Users regarding data submission,
study catalog submission, external resource catalog submission, data
requests, and biospecimen requests;
Monitor data submissions, study catalog submission,
external resource catalog submission, data requests, and biospecimen
requests;
Notify interested Users of updates to data and
biospecimens available through NICHD DASH; and
Help NICHD understand the use of NICHD DASH study data and
biospecimens by the research community.
All the data collected from use of NICHD DASH are for the purposes
of internal administrative management of NICHD DASH, with the exception
of the Recipient's approved use of DASH data and/or biospecimens,
Recipient name and institution, and significant findings reporting in
the Data Request Annual Use Report, which may be shared on the DASH
website or in publications describing the performance and value of the
DASH system for the broader scientific community.
OMB approval is requested for 3 years. There are no costs to
respondents other than their time. The total estimated annualized
burden hours are 433.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Annual burden hours estimate
-----------------------------------------------------------------------------------------------------------------
Number of Average burden
Form name Number of responses per per response Total annual
respondents respondent (in hours) burden hour
----------------------------------------------------------------------------------------------------------------
User Registration............................... 900 1 5/60 75
[[Page 52483]]
Data and Biospecimen Catalog Submission......... 36 1 2 72
Institutional Certification Template............ 36 1 5/60 3
Data Request.................................... 150 1 1 150
Biospecimen Request............................. 4 1 1 4
Data Request Annual Progress Report............. 240 1 30/60 120
Study Catalog Submission........................ 2 1 30/60 1
External Resource Catalog Submission............ 4 1 15/60 1
Data Request Renewal............................ 42 1 10/60 7
---------------------------------------------------------------
Total....................................... 1,414 1,414 .............. 433
----------------------------------------------------------------------------------------------------------------
Dated: June 17, 2024.
Jennifer M. Guimond,
Project Clearance Liaison, Eunice Kennedy Shriver National Institute of
Child Health and Human Development, National Institutes of Health.
[FR Doc. 2024-13715 Filed 6-21-24; 8:45 am]
BILLING CODE 4140-01-P
