Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: State Maternal Health Innovation Maternal Health Annual Report, 55950-55951 [2024-14790]
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Federal Register / Vol. 89, No. 130 / Monday, July 8, 2024 / Notices
coverage to their qualified covered
retirees are eligible to receive a 28%
subsidy for allowable drug costs.
CMS has contracted with an outside
vendor to assist in the administration of
the RDS program; this effort is called the
RDS Center. Plan Sponsors will apply
on-line for the retiree drug subsidy by
logging on to the RDS Secure website.
42 CFR 423.844 describes the
requirement for qualified retiree
prescription drug plans who want to
receive the retiree drug subsidy. Once
the Plan Sponsor submits the RDS
application via the RDS Secure website
(and a valid initial retiree list) CMS,
using its contractor, will analyze the
application to determine whether the
Plan Sponsor qualifies for the RDS. To
qualify for the subsidy, the Plan
Sponsor must show that its coverage is
as generous as, or more generous than,
the defined standard coverage under the
Medicare Part D prescription drug
benefit. The information within the
application includes sponsor account
registration information, plan
information, benefit options under the
plan, actuary information and actuarial
attestation. The RDS center has various
checks within each section of the
application. Applications can be denied
if issues cannot be resolved.
Form Number: CMS–10170 (OMB
control number: 0938–0977); Frequency:
Yearly; Affected Public: Private Sector;
Business or other for-profits, and Not-for
Profits; Number of Respondents: 1,245;
Number of Responses: 1,245; Total
Annual Hours: 79,680. (For questions
regarding this collection, contact Ivan
Iveljic at 410–786–3312 or Ivan.iveljic@
cms.hhs.gov.)
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–14825 Filed 7–5–24; 8:45 am]
BILLING CODE 4120–01–P
Information Collection Request Title:
State Maternal Health Innovation
Maternal Health Annual Report, OMB
No. 0906–xxxx–New.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request; Information
Collection Request Title: State
Maternal Health Innovation Maternal
Health Annual Report
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 September 6,
2024.
SUMMARY:
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.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the ICR title
for reference.
ADDRESSES:
Abstract: The State Maternal Health
Innovation (MHI) program is authorized
by 42 U.S.C. 701(a)(2) (title V, sec.
501(a)(2) of the Social Security Act),
which authorizes awards for special
projects of regional and national
significance in maternal and child
health. Special projects of regional and
national significance support HRSA’s
mission to improve the health and wellbeing of America’s mothers, children,
and families. HRSA directly funds states
to implement maternal health
innovation projects. The Maternal
Health Annual Report will be completed
by all grantees who receive funding
under the program.
Need and Proposed Use of the
Information: HRSA will use the
information to monitor grantees’
progress in accessing, analyzing, and
using state-level maternal health data
and to summarize the data focused work
that grantees accomplish.
Likely Respondents: Recipients of the
HRSA State MHI grants.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose, and 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. It also
includes training personnel to be able to
respond to the information collection, to
search data sources, to complete and
review, 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
respondents
khammond on DSKJM1Z7X2PROD with NOTICES
Form name
Number of
responses per
respondent
Total
responses
Average
burden per
response
(in hours)
Total burden
hours
Maternal Health Annual Report (MHAR): Respondents
(Medical and Health Services Managers) ........................
30
1
30
12
360
Total ..............................................................................
30
........................
30
........................
360
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Federal Register / Vol. 89, No. 130 / Monday, July 8, 2024 / Notices
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. 2024–14790 Filed 7–5–24; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the Secretary’s Advisory
Committee on Human Research
Protections
Department of Health and
Human Services, Office of the Secretary,
Office of the Assistant Secretary for
Health.
ACTION: Notice.
AGENCY:
Pursuant to the Federal
Advisory Committee Act, notice is
hereby given that the Secretary’s
Advisory Committee on Human
Research Protections (SACHRP) will
hold a meeting that will be open to the
public. Information about SACHRP, the
full meeting agenda, and instructions for
linking to public access will be posted
on the SACHRP website at https://
www.hhs.gov/ohrp/sachrp-committee/
meetings/.
DATES: The meeting will be held on
Tuesday, July 23, 2024 from 11:00 a.m.
until 4:00 p.m., and Wednesday, July
24, 2024, from 11:00 a.m. until 4:00 p.m.
(times are tentative and subject to
change). The confirmed times and
agenda will be posted on the SACHRP
website as this information becomes
available.
ADDRESSES: This meeting will be held
via webcast. Members of the public may
also attend the meeting via webcast.
Instructions for attending via webcast
will be posted at least one week prior
to the meeting at https://www.hhs.gov/
ohrp/sachrp-committee/meetings/
index.html.
FOR FURTHER INFORMATION CONTACT: Julia
Gorey, J.D., Executive Director,
SACHRP; U.S. Department of Health
and Human Services, 1101 Wootton
Parkway, Suite 200, Rockville,
Maryland 20852; telephone: 240–453–
8141; fax: 240–453–6909; email address:
SACHRP@hhs.gov.
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SUMMARY:
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Under the
authority of 42 U.S.C. 217a, section 222
of the Public Health Service Act, as
amended, SACHRP was established to
provide expert advice and
recommendations to the Secretary of
Health and Human Services, through
the Assistant Secretary for Health, on
issues and topics pertaining to or
associated with the protection of human
research subjects.
The Subpart A Subcommittee (SAS)
was established by SACHRP in October
2006 and is charged with developing
recommendations for consideration by
SACHRP regarding the application of
subpart A of 45 CFR part 46 in the
current research environment.
The Subcommittee on Harmonization
(SOH) was established by SACHRP at its
July 2009 meeting and charged with
identifying and prioritizing areas in
which regulations and/or guidelines for
human subjects research adopted by
various agencies or offices within HHS
would benefit from harmonization,
consistency, clarity, simplification and/
or coordination.
The SACHRP meeting will open to the
public at 11:00 a.m., on Tuesday, July
23, 2024, followed by opening remarks
from Julie Kaneshiro, Acting Director of
OHRP and Dr. Douglas Diekema,
SACHRP Chair. The meeting will begin
with a discussion of the draft
recommendation, Ethical and
Regulatory Considerations for the
Inclusion of LGBTQI+ Populations in
HHS Human Subjects Research. This
topic is a continuation of the discussion
and speaker panel presented at the
October 2023 SACHRP. This will be
followed by discussion of
Considerations for Uninformative
Research. OHRP will also provide an
update on planned changes to the
structure and operation of SACHRP’s
subcommittees. The first day will
adjourn at approximately 4:00 p.m. The
second day of the meeting, July 24, will
begin at 11:00 with a continued
discussion of the previous day’s topics.
Other topics may be added; for the full
and updated meeting agenda, see https://
www.dhhs.gov/ohrp/sachrp-committee/
meetings/. The meeting will
adjourn by 4:00 p.m., July 24, 2024.
Time will be allotted for public
comment on both days of the meeting.
SACHRP materials will be publicly
posted at https://www.regulations.gov/,
docket # HHS–OASH–2024–0008. The
public may submit written public
comment in advance to SACHRP@
hhs.gov no later than midnight July
19th, 2024, ET. Written comments will
be shared with SACHRP members and
may read aloud during the meeting.
Comments which are read aloud are
SUPPLEMENTARY INFORMATION:
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55951
limited to three minutes each. Public
comment must be relevant to topics
currently being addressed by the
SACHRP.
Dated: July 2, 2024.
Yvonne Lau,
Acting Director, Office for Human Research
Protections.
[FR Doc. 2024–14865 Filed 7–5–24; 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 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
Drug Abuse Special Emphasis Panel; NIDA–
K Alternate SEP.
Date: August 1, 2024.
Time: 12:00 p.m. to 12:45 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institute of Health,
National Institute on Drug Abuse, 301 North
Stonestreet Avenue, Bethesda, MD 20892.
Contact Person: Marisa Srivareerat, Ph.D.,
Scientific Review Officer, Scientific Review
Branch, Office of Extramural Policy, National
Institute on Drug Abuse, NIH, 301 North
Stonestreet Avenue, MSC 6021, Bethesda,
MD 20892, (301) 435–1258,
marisa.srivareerat@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: July 2, 2024.
Lauren A. Fleck,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2024–14870 Filed 7–5–24; 8:45 am]
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]]>Agencies
[Federal Register Volume 89, Number 130 (Monday, July 8, 2024)]
[Notices]
[Pages 55950-55951]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-14790]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Public Comment Request; Information Collection Request Title: State
Maternal Health Innovation Maternal Health Annual Report
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 September
6, 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: State Maternal Health
Innovation Maternal Health Annual Report, OMB No. 0906-xxxx-New.
Abstract: The State Maternal Health Innovation (MHI) program is
authorized by 42 U.S.C. 701(a)(2) (title V, sec. 501(a)(2) of the
Social Security Act), which authorizes awards for special projects of
regional and national significance in maternal and child health.
Special projects of regional and national significance support HRSA's
mission to improve the health and well-being of America's mothers,
children, and families. HRSA directly funds states to implement
maternal health innovation projects. The Maternal Health Annual Report
will be completed by all grantees who receive funding under the
program.
Need and Proposed Use of the Information: HRSA will use the
information to monitor grantees' progress in accessing, analyzing, and
using state-level maternal health data and to summarize the data
focused work that grantees accomplish.
Likely Respondents: Recipients of the HRSA State MHI grants.
Burden Statement: Burden in this context means the time expended by
persons to generate, maintain, retain, disclose, and 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. It also includes training personnel to be able
to respond to the information collection, to search data sources, to
complete and review, 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
----------------------------------------------------------------------------------------------------------------
Maternal Health Annual Report 30 1 30 12 360
(MHAR): Respondents (Medical
and Health Services Managers)..
-------------------------------------------------------------------------------
Total....................... 30 .............. 30 .............. 360
----------------------------------------------------------------------------------------------------------------
[[Page 55951]]
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. 2024-14790 Filed 7-5-24; 8:45 am]
BILLING CODE 4165-15-P
