Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: Ryan White HIV/AIDS Program Client-Level Data Reporting System, OMB No. 0906-0039-Revision, 30384-30385 [2024-08610]
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30384
Federal Register / Vol. 89, No. 79 / Tuesday, April 23, 2024 / Notices
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17:48 Apr 22, 2024
Jkt 262001
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Dated: April 18, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024–08656 Filed 4–22–24; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request; Information
Collection Request Title: Ryan White
HIV/AIDS Program Client-Level Data
Reporting System, OMB No. 0906–
0039—Revision
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
AGENCY:
In compliance with the
requirement for opportunity for public
comment on proposed data collection
projects of the Paperwork Reduction Act
of 1995, HRSA announces plans to
submit an Information Collection
Request (ICR), described below, to the
Office of Management and Budget
(OMB). Prior to submitting the ICR to
OMB, HRSA seeks comments from the
public regarding the burden estimate,
below, or any other aspect of the ICR.
DATES: Comments on this ICR should be
received no later than June 24, 2024.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, Room 14N39, 5600 Fishers
Lane, Rockville, Maryland, 20857.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and draft
instruments, email paperwork@hrsa.gov
or call Joella Roland, the HRSA
Information Collection Clearance
Officer, at (301) 443–3983.
SUMMARY:
PO 00000
Frm 00065
Fmt 4703
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When
submitting comments or requesting
information, please include the ICR title
for reference.
Information Collection Request Title:
Ryan White HIV/AIDS Program ClientLevel Data Reporting System, OMB No.
0906–0039—Revision.
Abstract: The Ryan White HIV/AIDS
Program (RWHAP), authorized under
Title XXVI of the Public Health Service
Act, is administered by the HIV/AIDS
Bureau within HRSA. HRSA awards
funding to recipients in areas of the
greatest need to respond effectively to
the HIV epidemic, with an emphasis on
providing life-saving and life-extending
medical care, treatment, and support
services for people with HIV in the
United States.
The RWHAP reporting requirements
include the annual submission of clientlevel data in the Ryan White HIV/AIDS
Program Services Report (RSR). The
RSR is designed to collect information
from grant recipients and their
subawarded service providers, funded
under Parts A, B, C, and D of the
RWHAP statute.
HRSA is requesting a revision of the
current RSR with one proposed update:
SUPPLEMENTARY INFORMATION:
Current Questions
• Within your organization/agency,
identify the number of physicians, nurse
practitioners, or physician assistants
who obtained a Drug Addiction
Treatment Act of 2000 waiver to treat
opioid use disorder with medication
assisted treatment (MAT), [e.g.,
buprenorphine, naltrexone] specifically
approved by the U.S. Food and Drug
Administration.
• How many of the above physicians,
nurse practitioners, or physician
assistants prescribed MAT (e.g.,
buprenorphine, naltrexone) for opioid
use disorders in the reporting period?
Proposed Change to Question in 2024
RSR Form
• How many physicians, nurse
practitioners, or physician assistants in
your organization prescribed
medications for opioid use disorder
(MOUD) [e.g., buprenorphine,
naltrexone] for opioid use disorders
during the reporting period?
Need and Proposed Use of the
Information: The RWHAP statute
specifies HRSA’s responsibilities in
administering grant funds, allocating
funding, assessing HIV care outcomes
(e.g., viral suppression), and serving
particular populations. The RSR collects
data on the characteristics of RWHAPfunded recipients, their contracted
service providers, and the patients or
clients served. The RSR system consists
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Federal Register / Vol. 89, No. 79 / Tuesday, April 23, 2024 / Notices
of two primary components, the
Recipient Report, and the Provider
Report, and a data file containing deidentified client-level data elements.
Data are submitted annually. The
RWHAP statute specifies the importance
of recipient accountability and linking
performance to budget. The RSR is used
to ensure recipient compliance with the
law, including evaluating the
effectiveness of programs, monitoring
recipient and provider performance, and
informing annual reports to Congress.
Information collected through the RSR
is critical for HRSA, state and local
grant recipients, and individual
providers to assess the status of existing
HIV-related service delivery systems,
monitor trends in service utilization,
evaluate the impact of data reporting,
and identify areas of greatest need.
Likely Respondents: RWHAP grant
recipients, as well as their subawarded
service providers, funded under
RWHAP Parts A, B, C, and D.
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
Total
responses
Average
burden per
response
(in hours)
Total
burden
hours
Recipient Report ...................................................................................................
Provider Report .....................................................................................................
Client Report .........................................................................................................
595
2,063
1,532
1
1
1
595
2,063
1,532
11
13
113
6,545
26,819
173,116
Total ...............................................................................................................
4,190
........................
4,190
........................
206,480
HRSA specifically requests comments
on: (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.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2024–08610 Filed 4–22–24; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Eunice Kennedy Shriver National
Institute of Child Health & Human
Development; Notice of Closed
Meeting
ddrumheller on DSK120RN23PROD with NOTICES1
Number of
responses per
respondent
Number of
respondents
Form name
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. The total annual burden
hours estimated for this ICR are
summarized in the table below.
Total Estimated Annualized Burden
Hours:
Pursuant to section 1009 of the
Federal Advisory Committee Act, as
amended, notice is hereby given of a
meeting of the Board of Scientific
Counselors Eunice Kennedy Shriver
National Institute of Child Health and
Human Development.
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
VerDate Sep<11>2014
19:24 Apr 22, 2024
Jkt 262001
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: Eunice Kennedy
Shriver National Institute of Child Health and
Human Development Initial Review Group;
Reproduction, Andrology, and Gynecology
Study Section.
Date: June 20, 2024.
Time: 9:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Eunice Kennedy Shriver National
Institute of Child Health and Human
Development, National Institutes of Health,
10 Center Drive, Room 10D39, Bethesda, MD
20892 (Virtual Meeting).
Contact Person: Jagpreet Singh Nanda,
Ph.D., Scientific Review Branch, Eunice
Kennedy Shriver National Institute of Child
Health and Human Development, National
Institute of Health, 6710B Rockledge Drive,
Room 2125D, Bethesda, MD 20892, (301)
451–4454, jagpreet.nanda@nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.864, Population Research;
93.865, Research for Mothers and Children;
93.929, Center for Medical Rehabilitation
Research; 93.209, Contraception and
Infertility Loan Repayment Program, National
Institutes of Health, HHS)
Dated: April 18, 2024.
Lauren A. Fleck,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2024–08632 Filed 4–22–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Allergy and
Infectious Diseases; 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 of
Allergy and Infectious Diseases Special
Emphasis Panel; NIAID Investigator Initiated
Program Project Applications (P01 Clinical
Trial Not Allowed).
Date: May 21, 2024.
Time: 10:00 a.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institute of Allergy and
Infectious Diseases, National Institutes of
Health, 5601 Fishers Lane, MSC 9834,
Rockville, MD 20852 (Video Assisted
Meeting).
Contact Person: Rekha Dhanwani, Ph.D.,
Scientific Review Program, Scientific Review
Program, Division of Extramural Activities,
National Institute of Allergy and Infectious
E:\FR\FM\23APN1.SGM
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Agencies
[Federal Register Volume 89, Number 79 (Tuesday, April 23, 2024)]
[Notices]
[Pages 30384-30385]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-08610]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Public Comment Request; Information Collection Request Title: Ryan
White HIV/AIDS Program Client-Level Data Reporting System, OMB No.
0906-0039--Revision
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement for opportunity for public
comment on proposed data collection projects of the Paperwork Reduction
Act of 1995, HRSA announces plans to submit an Information Collection
Request (ICR), described below, to the Office of Management and Budget
(OMB). Prior to submitting the ICR to OMB, HRSA seeks comments from the
public regarding the burden estimate, below, or any other aspect of the
ICR.
DATES: Comments on this ICR should be received no later than June 24,
2024.
ADDRESSES: Submit your comments to [email protected] or mail the HRSA
Information Collection Clearance Officer, Room 14N39, 5600 Fishers
Lane, Rockville, Maryland, 20857.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the data collection plans and
draft instruments, email [email protected] or call Joella Roland, the
HRSA Information Collection Clearance Officer, at (301) 443-3983.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the ICR title for reference.
Information Collection Request Title: Ryan White HIV/AIDS Program
Client-Level Data Reporting System, OMB No. 0906-0039--Revision.
Abstract: The Ryan White HIV/AIDS Program (RWHAP), authorized under
Title XXVI of the Public Health Service Act, is administered by the
HIV/AIDS Bureau within HRSA. HRSA awards funding to recipients in areas
of the greatest need to respond effectively to the HIV epidemic, with
an emphasis on providing life-saving and life-extending medical care,
treatment, and support services for people with HIV in the United
States.
The RWHAP reporting requirements include the annual submission of
client-level data in the Ryan White HIV/AIDS Program Services Report
(RSR). The RSR is designed to collect information from grant recipients
and their subawarded service providers, funded under Parts A, B, C, and
D of the RWHAP statute.
HRSA is requesting a revision of the current RSR with one proposed
update:
Current Questions
Within your organization/agency, identify the number of
physicians, nurse practitioners, or physician assistants who obtained a
Drug Addiction Treatment Act of 2000 waiver to treat opioid use
disorder with medication assisted treatment (MAT), [e.g.,
buprenorphine, naltrexone] specifically approved by the U.S. Food and
Drug Administration.
How many of the above physicians, nurse practitioners, or
physician assistants prescribed MAT (e.g., buprenorphine, naltrexone)
for opioid use disorders in the reporting period?
Proposed Change to Question in 2024 RSR Form
How many physicians, nurse practitioners, or physician
assistants in your organization prescribed medications for opioid use
disorder (MOUD) [e.g., buprenorphine, naltrexone] for opioid use
disorders during the reporting period?
Need and Proposed Use of the Information: The RWHAP statute
specifies HRSA's responsibilities in administering grant funds,
allocating funding, assessing HIV care outcomes (e.g., viral
suppression), and serving particular populations. The RSR collects data
on the characteristics of RWHAP-funded recipients, their contracted
service providers, and the patients or clients served. The RSR system
consists
[[Page 30385]]
of two primary components, the Recipient Report, and the Provider
Report, and a data file containing de-identified client-level data
elements. Data are submitted annually. The RWHAP statute specifies the
importance of recipient accountability and linking performance to
budget. The RSR is used to ensure recipient compliance with the law,
including evaluating the effectiveness of programs, monitoring
recipient and provider performance, and informing annual reports to
Congress. Information collected through the RSR is critical for HRSA,
state and local grant recipients, and individual providers to assess
the status of existing HIV-related service delivery systems, monitor
trends in service utilization, evaluate the impact of data reporting,
and identify areas of greatest need.
Likely Respondents: RWHAP grant recipients, as well as their
subawarded service providers, funded under RWHAP Parts A, B, C, and D.
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. The total annual burden hours estimated for
this ICR are summarized in the table below.
Total Estimated Annualized Burden Hours:
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Form name Number of responses per Total per response Total burden
respondents respondent responses (in hours) hours
----------------------------------------------------------------------------------------------------------------
Recipient Report................ 595 1 595 11 6,545
Provider Report................. 2,063 1 2,063 13 26,819
Client Report................... 1,532 1 1,532 113 173,116
-------------------------------------------------------------------------------
Total....................... 4,190 .............. 4,190 .............. 206,480
----------------------------------------------------------------------------------------------------------------
HRSA specifically requests comments on: (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.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2024-08610 Filed 4-22-24; 8:45 am]
BILLING CODE 4165-15-P