Agency Information Collection Activities: Submission to OMB for Review and Approval; Public Comment Request; Applications for and Monitoring of New, One-Time Funding Programs Administered by the Health Resources and Services Administration, 52479-52480 [2024-13713]
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Federal Register / Vol. 89, No. 121 / Monday, June 24, 2024 / Notices
52479
TABLE 2—NEW ENTRIES TO THE LIST OF RECOGNIZED STANDARDS—Continued
Title of standard 1
Recognition No.
Reference No. and date
S. Tissue Engineering
No new entries at this time.
1 All
standard titles in this table conform to the style requirements of the respective organizations.
IV. List of Recognized Standards
FDA maintains the current list of FDA
Recognized Consensus Standards in a
searchable database that may be
accessed at https://
www.accessdata.fda.gov/scripts/cdrh/
cfdocs/cfStandards/search.cfm. Such
standards are those that FDA has
recognized by notice published in the
Federal Register or that FDA has
decided to recognize but for which
recognition is pending (because a
periodic notice has not yet appeared in
the Federal Register). FDA will
announce additional modifications and
revisions to the list of recognized
consensus standards, as needed, in the
Federal Register once a year, or more
often if necessary.
V. Recommendation of Standards for
Recognition by FDA
Any person may recommend
consensus standards as candidates for
recognition under section 514 of the
FD&C Act by submitting such
recommendations, with reasons for the
recommendation, to
CDRHStandardsStaff@fda.hhs.gov. To
be considered, such recommendations
should contain, at a minimum, the
information available at https://
www.fda.gov/medical-devices/deviceadvice-comprehensive-regulatoryassistance/standards-and-conformityassessment-program#process.
Dated: June 18, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024–13777 Filed 6–21–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Submission to OMB for
Review and Approval; Public Comment
Request; Applications for and
Monitoring of New, One-Time Funding
Programs Administered by the Health
Resources and Services
Administration
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
AGENCY:
In compliance with the
Paperwork Reduction Act of 1995,
HRSA submitted an Information
Collection Request (ICR) to the Office of
Management and Budget (OMB) for
review and approval. Comments
submitted during the first public review
of this ICR will be provided to OMB.
OMB will accept further comments from
the public during the review and
approval period. OMB may act on
HRSA’s ICR only after the 30-day
comment period for this notice has
closed.
SUMMARY:
Comments on this ICR should be
received no later than July 24, 2024.
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 Review—Open for
Public Comments’’ or by using the
search function.
FOR FURTHER INFORMATION CONTACT: To
request a copy of the clearance requests
submitted to OMB for review, email
Joella Roland, the HRSA Information
Collection Clearance Officer, at
paperwork@hrsa.gov or call (301) 443–
3983.
SUPPLEMENTARY INFORMATION:
Information Collection Request Title:
Applications for and Monitoring of
New, One-Time Funding Programs
Administered by the Health Resources
DATES:
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
and Services Administration (HRSA)—
OMB Control No. 0906–xxxx–New
Abstract: HRSA is seeking approval
for a generic umbrella clearance to
collect applications for awards for
HRSA-funded programs that provide
one-time funding, including pilot
programs. Should any of these pilot
programs become permanent, HRSA
will seek OMB clearance for these
programs using a mechanism outside of
this generic umbrella clearance. OMB
guidance allows for the use of generic
packages in cases where there may be a
need for a data collection, but the
agency ‘‘cannot determine the details of
the specific individual collections until
a later time.’’ 1 HRSA will only use this
collection for HRSA-funded programs
that provide one-time funding,
including pilot programs. HRSA would
only request OMB approval for
collections under this generic umbrella
collection if the collection is lowburden, uncontroversial, and is a onetime application.
Furthermore, if Congress appropriates
additional funding for such a program
or HRSA plans to use the information
from the applications for policy
decisions not related to funding awards,
HRSA will prepare a standard
information collection request for that
program, which will include the
required 60- and 30-day Federal
Register notices.
A 60-day notice published in the
Federal Register on March 22, 2024,
vol. 89, No. 57; pp. 20484–85. There
were no public comments.
Need and Proposed Use of the
Information: HRSA seeks to use an
umbrella generic clearance for HRSAfunded programs that provide one-time
funding, including pilot programs, so
that funding can be awarded
expeditiously. Expeditious awarding of
funding is helpful not only for
administrative ease, but also for cases in
which a pilot program or a program
receiving one-time funding has a
statutory deadline for completion.
Approval of this proposed generic
1 Memorandum for the Heads of Executive
Departments and Agencies and Independent
Regulatory Agencies (July 2016), ‘‘Flexibilities
under the Paperwork Reduction Act for Compliance
with Information Collection Requirements.’’ Pages
4–5.
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52480
Federal Register / Vol. 89, No. 121 / Monday, June 24, 2024 / Notices
umbrella collection would enable HRSA
to collect information from individual
and site applicants and enable HRSA to
make selection determinations for onetime awards in a timely manner.
Information collections under this
umbrella generic collection would be
applications for funding (solely
providing applicants with an
opportunity to demonstrate their
capabilities in accordance with HRSA’s
statement of work or selection criteria
and other related information) and
forms required for monitoring funding
recipients. Following the award, the
awardee may also be required to provide
progress reports or additional
documents.
Likely Respondents: Each fast-track
ICR under this generic umbrella ICR
will specify the manner that
respondents will be enlisted.
Respondents will vary by the specific
program and are determined by each
program’s eligibility, to include but are
not limited to the following: health
providers and other paraprofessionals,
health facilities, accredited health
professions schools or programs, state
and local governments, and other
eligible entities.
Respondents will be recruited by
means of information listed on HRSA’s
website, or advertisements in public
venues. The privacy of any potential or
actual respondents will be preserved to
the extent requested by participants and
as permitted by law.
Once applicants are selected and
awards are made, these awardees will be
respondents for monitoring collections
such as progress reports.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose, or provide the information
requested. This includes the time
needed to review instructions; to
develop, acquire, install, and utilize
technology and systems for the purpose
of collecting, validating, and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information; to search
data sources; to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
HRSA intends to use this generic
umbrella ICR for applications with a
low burden and monitoring awardees.
To estimate the burden for this
collection, HRSA estimated how much
time it would take for a respondent to
complete a two-page application with
typical fields used in current collections
that may fall under this generic
umbrella ICR. HRSA then calculated the
average burden estimate from these ICRs
for the purpose of the estimate for this
ICR. To estimate the burden for
monitoring funding recipients, HRSA
estimated how much time it would take
for funding recipients to complete the
average two-page form used for program
monitoring. The total burden hours over
a 3-year period estimated for this ICR
are summarized in the table below.
TOTAL ESTIMATED BURDEN HOURS OVER 3 YEARS
Estimated
number of
respondents
Instrument name
Estimated
total
responses
Average
burden per
response
(in hours)
Total burden
hours
Program Applications ...........................................................
Program Monitoring .............................................................
5,000
2,500
1.5
1.0
7,500
2,500
1.75
2.00
13,125
5,000
Total ..............................................................................
7,500
........................
10,000
........................
18,125
Maria G. Button,
Director, Executive Secretariat.
applications and/or contract proposals,
the disclosure of which would
constitute a clearly unwarranted
invasion of personal privacy.
[FR Doc. 2024–13713 Filed 6–21–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute on Drug Abuse;
Notice of Closed Meetings
lotter on DSK11XQN23PROD with NOTICES1
Average
number of
responses per
respondent
Pursuant to section 1009 of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meetings.
The meetings 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/or contract proposals and the
discussions could disclose confidential
trade secrets or commercial property
such as patentable material, and
personal information concerning
individuals associated with the grant
VerDate Sep<11>2014
18:55 Jun 21, 2024
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Name of Committee: National Institute on
Drug Abuse Special Emphasis Panel; GMP
Synthesis of Bulk Drug Testing.
Date: July 18, 2024.
Time: 2:00 p.m. to 4:00 p.m.
Agenda: To review and evaluate contract
proposals.
Place: National Institute of Health,
National Institute on Drug Abuse, 301 North
Stonestreet Avenue, Bethesda, MD 20892
(Virtual Meeting).
Contact Person: Meysam Yazdankhah,
Ph.D., Scientific Review Officer, Scientific
Review Branch, National Institute on Drug
Abuse, NIH, 301 North Stonestreet Avenue,
MSC 6021, Bethesda, MD 20892, (301) 402–
6965 meysam.yazdankhah@nih.gov.
Name of Committee: National Institute on
Drug Abuse Special Emphasis Panel; NIDA–
L Conflict SEP.
Date: July 23, 2024.
Time: 2:00 p.m. to 3:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institute of Health,
National Institute on Drug Abuse, 301 North
PO 00000
Frm 00048
Fmt 4703
Sfmt 9990
Stonestreet Avenue, Bethesda, MD 20892
(Virtual Meeting).
Contact Person: Sudhirkumar U.
Yanpallewar, M.D., Scientific Review Officer,
Scientific Review Branch, National Institute
on Drug Abuse, NIH, 301 North Stonestreet
Avenue, MSC 6021, Bethesda, MD 20892,
(301) 443–4577, sudhirkumar.yanpallewar@
nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.277, Drug Abuse Scientist
Development Award for Clinicians, Scientist
Development Awards, and Research Scientist
Awards; 93.278, Drug Abuse National
Research Service Awards for Research
Training; 93.279, Drug Abuse and Addiction
Research Programs, National Institutes of
Health, HHS)
Dated: June 17, 2024.
Lauren A. Fleck,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2024–13709 Filed 6–21–24; 8:45 am]
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Agencies
[Federal Register Volume 89, Number 121 (Monday, June 24, 2024)]
[Notices]
[Pages 52479-52480]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-13713]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Submission to OMB for
Review and Approval; Public Comment Request; Applications for and
Monitoring of New, One-Time Funding Programs Administered by the Health
Resources and Services Administration
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the Paperwork Reduction Act of 1995, HRSA
submitted an Information Collection Request (ICR) to the Office of
Management and Budget (OMB) for review and approval. Comments submitted
during the first public review of this ICR will be provided to OMB. OMB
will accept further comments from the public during the review and
approval period. OMB may act on HRSA's ICR only after the 30-day
comment period for this notice has closed.
DATES: Comments on this ICR should be received no later than July 24,
2024.
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 Review--Open for
Public Comments'' or by using the search function.
FOR FURTHER INFORMATION CONTACT: To request a copy of the clearance
requests submitted to OMB for review, email Joella Roland, the HRSA
Information Collection Clearance Officer, at [email protected] or call
(301) 443-3983.
SUPPLEMENTARY INFORMATION:
Information Collection Request Title: Applications for and
Monitoring of New, One-Time Funding Programs Administered by the Health
Resources and Services Administration (HRSA)--OMB Control No. 0906-
xxxx-New
Abstract: HRSA is seeking approval for a generic umbrella clearance
to collect applications for awards for HRSA-funded programs that
provide one-time funding, including pilot programs. Should any of these
pilot programs become permanent, HRSA will seek OMB clearance for these
programs using a mechanism outside of this generic umbrella clearance.
OMB guidance allows for the use of generic packages in cases where
there may be a need for a data collection, but the agency ``cannot
determine the details of the specific individual collections until a
later time.'' \1\ HRSA will only use this collection for HRSA-funded
programs that provide one-time funding, including pilot programs. HRSA
would only request OMB approval for collections under this generic
umbrella collection if the collection is low-burden, uncontroversial,
and is a one-time application.
---------------------------------------------------------------------------
\1\ Memorandum for the Heads of Executive Departments and
Agencies and Independent Regulatory Agencies (July 2016),
``Flexibilities under the Paperwork Reduction Act for Compliance
with Information Collection Requirements.'' Pages 4-5.
---------------------------------------------------------------------------
Furthermore, if Congress appropriates additional funding for such a
program or HRSA plans to use the information from the applications for
policy decisions not related to funding awards, HRSA will prepare a
standard information collection request for that program, which will
include the required 60- and 30-day Federal Register notices.
A 60-day notice published in the Federal Register on March 22,
2024, vol. 89, No. 57; pp. 20484-85. There were no public comments.
Need and Proposed Use of the Information: HRSA seeks to use an
umbrella generic clearance for HRSA-funded programs that provide one-
time funding, including pilot programs, so that funding can be awarded
expeditiously. Expeditious awarding of funding is helpful not only for
administrative ease, but also for cases in which a pilot program or a
program receiving one-time funding has a statutory deadline for
completion. Approval of this proposed generic
[[Page 52480]]
umbrella collection would enable HRSA to collect information from
individual and site applicants and enable HRSA to make selection
determinations for one-time awards in a timely manner.
Information collections under this umbrella generic collection
would be applications for funding (solely providing applicants with an
opportunity to demonstrate their capabilities in accordance with HRSA's
statement of work or selection criteria and other related information)
and forms required for monitoring funding recipients. Following the
award, the awardee may also be required to provide progress reports or
additional documents.
Likely Respondents: Each fast-track ICR under this generic umbrella
ICR will specify the manner that respondents will be enlisted.
Respondents will vary by the specific program and are determined by
each program's eligibility, to include but are not limited to the
following: health providers and other paraprofessionals, health
facilities, accredited health professions schools or programs, state
and local governments, and other eligible entities.
Respondents will be recruited by means of information listed on
HRSA's website, or advertisements in public venues. The privacy of any
potential or actual respondents will be preserved to the extent
requested by participants and as permitted by law.
Once applicants are selected and awards are made, these awardees
will be respondents for monitoring collections such as progress
reports.
Burden Statement: Burden in this context means the time expended by
persons to generate, maintain, retain, disclose, or provide the
information requested. This includes the time needed to review
instructions; to develop, acquire, install, and utilize technology and
systems for the purpose of collecting, validating, and verifying
information, processing and maintaining information, and disclosing and
providing information; to train personnel and to be able to respond to
a collection of information; to search data sources; to complete and
review the collection of information; and to transmit or otherwise
disclose the information.
HRSA intends to use this generic umbrella ICR for applications with
a low burden and monitoring awardees. To estimate the burden for this
collection, HRSA estimated how much time it would take for a respondent
to complete a two-page application with typical fields used in current
collections that may fall under this generic umbrella ICR. HRSA then
calculated the average burden estimate from these ICRs for the purpose
of the estimate for this ICR. To estimate the burden for monitoring
funding recipients, HRSA estimated how much time it would take for
funding recipients to complete the average two-page form used for
program monitoring. The total burden hours over a 3-year period
estimated for this ICR are summarized in the table below.
Total Estimated Burden Hours Over 3 Years
----------------------------------------------------------------------------------------------------------------
Estimated Average number Estimated Average burden
Instrument name number of of responses total per response Total burden
respondents per respondent responses (in hours) hours
----------------------------------------------------------------------------------------------------------------
Program Applications............ 5,000 1.5 7,500 1.75 13,125
Program Monitoring.............. 2,500 1.0 2,500 2.00 5,000
-------------------------------------------------------------------------------
Total....................... 7,500 .............. 10,000 .............. 18,125
----------------------------------------------------------------------------------------------------------------
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2024-13713 Filed 6-21-24; 8:45 am]
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