Submission for Office of Management and Budget Review; Healthy Marriage and Responsible Fatherhood Local Evaluation Final Report (New Collection), 97010-97011 [2024-28555]
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lotter on DSK11XQN23PROD with NOTICES1
97010
Federal Register / Vol. 89, No. 235 / Friday, December 6, 2024 / Notices
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.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, please access the CMS PRA
website by copying and pasting the
following web address into your web
browser: https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.
FOR FURTHER INFORMATION CONTACT:
William Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. The term ‘‘collection of
information’’ is defined in 44 U.S.C.
3502(3) and 5 CFR 1320.3(c) and
includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires Federal agencies
to publish a 30-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension or
reinstatement of an existing collection
of information, before submitting the
collection to OMB for approval. To
comply with this requirement, CMS is
publishing this notice that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: Reinstatement without change
of a previously approved collection;
Title of Information Collection: Patient
Access through Application
Programming Interfaces (API); Use: This
final rule is the first phase of policies
centrally focused on advancing
interoperability and patient access to
health information using the authority
available to the Centers for Medicare &
Medicaid Services (CMS). We believe
this is an important step in advancing
interoperability, putting patients at the
center of their health care, and ensuring
they have electronic access to their
health information. We are committed
to working with stakeholders to solve
the issue of interoperability and getting
patients access to information about
their health care, and we are taking an
active approach to move participants in
the health care market toward
interoperability and the secure and
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timely exchange of electronic health
information by adopting policies for the
Medicare and Medicaid programs, the
Children’s Health Insurance Program
(CHIP), and qualified health plan (QHP)
issuers on the individual market
Federally-facilitated Exchanges (FFEs).
For purposes of this rule, references to
QHP issuers on the FFEs excludes
issuers offering only stand-alone dental
plans (SADPs). Likewise, we are also
excluding QHP issuers only offering
QHPs in the Federally-facilitated Small
Business Health Options Program
Exchanges (FF–SHOPs) from the
provisions of this rule. This rule
requires these impacted payers to
maintain and use standards-based APIs
to make certain information available to
enrollees. CMS regulations at 42 CFR
417.414, 417.416, 422.112(a)(1)(i), and
422.114(a)(3)(ii) require that all
Medicare Advantage organizations
(MAOs) offering coordinated care plans,
network-based private fee-for-service
(PFFS) plans, and as well as section
1876 cost organizations, maintain a
network of appropriate providers that is
sufficient to provide adequate access to
covered services to meet the needs of
the population served. To enforce this
requirement, CMS regulations at
§ 422.116 outline network adequacy
criteria which set forth the minimum
number of providers and maximum
travel time and distance from enrollees
to providers, for required provider
specialty types in each county in the
United States and its territories.
Organizations must be in compliance
with the current CMS network adequacy
criteria guidance, which is updated and
published annually on CMS’s website.
This collection of information is
essential to appropriate and timely
compliance monitoring by CMS, in
order to ensure that all active contracts
offering network-based plans maintain
an adequate network.
This notice originally published on
August 22, 2024 (89 FR 67943), but CMS
was delayed in submitting it to OMB.
For that reason, we are republishing this
notice and the associated information
collection request will be submitted
upon to OMB upon publication of this
notice. Form Number: CMS–10767
(OMB control number: 0938–1412);
Frequency: Occasionally; Affected
Public: Private sector; Number of
Respondents: 345; Number of
Responses: 345; Total Annual Hours:
589,950. (For policy questions regarding
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this collection contact Lorraine Doo at
410–786–6597.)
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–28515 Filed 12–5–24; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for Office of Management
and Budget Review; Healthy Marriage
and Responsible Fatherhood Local
Evaluation Final Report (New
Collection)
Office of Planning, Research,
and Evaluation, Administration for
Children and Families, U.S. Department
of Health and Human Services.
AGENCY:
ACTION:
Request for public comments.
The Office of Planning,
Research, and Evaluation (OPRE) in the
Administration for Children and
Families (ACF), U.S. Department of
Health and Human Services is
requesting approval of the Healthy
Marriage and Responsible Fatherhood
(HMRF) Final Report Templates. HMRF
grant programs are required to submit a
final report describing their local
evaluation analyses and findings. This
request includes guidance for grant
recipients in the form of templates.
Information will inform technical
assistance to support grantees in
developing and submitting the final
reports to ACF to fulfill a grant
requirement.
SUMMARY:
Comments due January 6, 2025.
OMB must decide about the collection
of information between 30 and 60 days
after publication of this document in the
Federal Register. Therefore, a comment
is best assured of having its full effect
if OMB receives it within 30 days of
publication.
DATES:
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. You can also obtain
copies of the proposed collection of
information by emailing
OPREinfocollection@acf.hhs.gov.
ADDRESSES:
E:\FR\FM\06DEN1.SGM
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97011
Federal Register / Vol. 89, No. 235 / Friday, December 6, 2024 / Notices
Identify all requests by the title of the
information collection.
SUPPLEMENTARY INFORMATION:
Description: Since 2005, Congress has
authorized dedicated funding for
discretionary awards from ACF’s Office
of Family Assistance to support HMRF
programs. Per the 2020 HMRF Notice of
Funding Opportunities issued by ACF,
HMRF grant recipients that are carrying
out local evaluations are required to
submit a final evaluation report to ACF
at the end of their grant. The final
reports must document the research
questions, measures, study design,
planned and actual implementation of
the program, analytic methods for their
evaluation, and evaluation findings.
OPRE is conducting the HMRF Local
Evaluation Technical Assistance (LETA)
projects, jointly referred to as the
HMRF–LETA projects, to support
federally funded programs in evaluating
their healthy relationship and family
stability services to adult couples, adult
individuals, fathers, and youth. As part
of the HMRF–LETA project, grant
recipients receive technical assistance to
support planning and executing a local
evaluation and analyzing and reporting
local evaluation findings.
The purpose of the current
information collection request is to
provide standardized report templates
and table shells to grant recipients to
document their evaluation’s analysis
and findings. A structured final report
template will facilitate grant recipients’
efficient and consistent reporting of
evaluation findings in their final
reports. The completed draft reports
will be reviewed by the HMRF–LETA
teams to determine whether the analysis
and reports meet standards set by ACF,
and to develop recommendations for
grant recipients to improve the analysis
and reports before final submission to
ACF. Grant recipients will finalize and
submit their final reports to ACF, as
required. This request includes the time
to develop and submit the reports.
Respondents: The respondents are
HMRF grant recipients conducting a
local evaluation. There are currently 79
grant recipients conducting local
evaluations: 50 evaluations using
descriptive designs (‘‘descriptive
evaluations’’) and 29 evaluations using
impact designs (‘‘impact evaluations’’).
ANNUAL BURDEN ESTIMATES
Number of
respondents
(total over
request period)
Instrument
Descriptive Evaluation Final Report Template ....................................
Impact Evaluation Final Report Template ...........................................
Impact Evaluation Final Report Table Shells ......................................
Estimated Total Annual Burden
Hours: 3,160.
Authority: 42 U.S.C. 603(a)(2).
Mary C. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2024–28555 Filed 12–5–24; 8:45 am]
BILLING CODE 4184–73–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2024–D–2033]
Expedited Program for Serious
Conditions—Accelerated Approval of
Drugs and Biologics; Draft Guidance
for Industry; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of a draft
guidance for industry entitled
‘‘Expedited Program for Serious
Conditions—Accelerated Approval of
Drugs and Biologics.’’ Accelerated
approval is one of FDA’s expedited
programs intended to facilitate and
expedite development and review of
certain drugs and biological products for
serious or life-threatening conditions.
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SUMMARY:
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18:02 Dec 05, 2024
Jkt 265001
Number of
responses per
respondent
(total over
request period)
50
29
29
This guidance provides information on
FDA’s policies and procedures for the
accelerated approval program, including
discussions of which products may be
candidates for accelerated approval, the
standards for granting accelerated
approval, and the procedures for
withdrawing accelerated approval.
When finalized, this draft guidance will
replace the accelerated approval-related
content in the final guidance for
industry entitled ‘‘Expedited Programs
for Serious Conditions—Drugs and
Biologics’’ issued on May 30, 2014 (the
2014 final guidance). Additional
programs to expedite product
development are covered in the 2014
final guidance as well as other
guidances.
Submit either electronic or
written comments on the draft guidance
by February 4, 2025. to ensure that the
Agency considers your comment on this
draft guidance before it begins work on
the final version of the guidance.
ADDRESSES: You may submit comments
on any guidance at any time as follows:
DATES:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
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Avg. burden
per response
(in hours)
1
1
1
40
30
10
Total/annual
burden
(in hours)
2,000
870
290
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
E:\FR\FM\06DEN1.SGM
06DEN1
Agencies
[Federal Register Volume 89, Number 235 (Friday, December 6, 2024)]
[Notices]
[Pages 97010-97011]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-28555]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for Office of Management and Budget Review; Healthy
Marriage and Responsible Fatherhood Local Evaluation Final Report (New
Collection)
AGENCY: Office of Planning, Research, and Evaluation, Administration
for Children and Families, U.S. Department of Health and Human
Services.
ACTION: Request for public comments.
-----------------------------------------------------------------------
SUMMARY: The Office of Planning, Research, and Evaluation (OPRE) in the
Administration for Children and Families (ACF), U.S. Department of
Health and Human Services is requesting approval of the Healthy
Marriage and Responsible Fatherhood (HMRF) Final Report Templates. HMRF
grant programs are required to submit a final report describing their
local evaluation analyses and findings. This request includes guidance
for grant recipients in the form of templates. Information will inform
technical assistance to support grantees in developing and submitting
the final reports to ACF to fulfill a grant requirement.
DATES: Comments due January 6, 2025. OMB must decide about the
collection of information between 30 and 60 days after publication of
this document in the Federal Register. Therefore, a comment is best
assured of having its full effect if OMB receives it within 30 days of
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. You can
also obtain copies of the proposed collection of information by
emailing [email protected].
[[Page 97011]]
Identify all requests by the title of the information collection.
SUPPLEMENTARY INFORMATION:
Description: Since 2005, Congress has authorized dedicated funding
for discretionary awards from ACF's Office of Family Assistance to
support HMRF programs. Per the 2020 HMRF Notice of Funding
Opportunities issued by ACF, HMRF grant recipients that are carrying
out local evaluations are required to submit a final evaluation report
to ACF at the end of their grant. The final reports must document the
research questions, measures, study design, planned and actual
implementation of the program, analytic methods for their evaluation,
and evaluation findings.
OPRE is conducting the HMRF Local Evaluation Technical Assistance
(LETA) projects, jointly referred to as the HMRF-LETA projects, to
support federally funded programs in evaluating their healthy
relationship and family stability services to adult couples, adult
individuals, fathers, and youth. As part of the HMRF-LETA project,
grant recipients receive technical assistance to support planning and
executing a local evaluation and analyzing and reporting local
evaluation findings.
The purpose of the current information collection request is to
provide standardized report templates and table shells to grant
recipients to document their evaluation's analysis and findings. A
structured final report template will facilitate grant recipients'
efficient and consistent reporting of evaluation findings in their
final reports. The completed draft reports will be reviewed by the
HMRF-LETA teams to determine whether the analysis and reports meet
standards set by ACF, and to develop recommendations for grant
recipients to improve the analysis and reports before final submission
to ACF. Grant recipients will finalize and submit their final reports
to ACF, as required. This request includes the time to develop and
submit the reports.
Respondents: The respondents are HMRF grant recipients conducting a
local evaluation. There are currently 79 grant recipients conducting
local evaluations: 50 evaluations using descriptive designs
(``descriptive evaluations'') and 29 evaluations using impact designs
(``impact evaluations'').
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of
Number of responses per Avg. burden Total/annual
Instrument respondents respondent (total per response burden (in
(total over over request (in hours) hours)
request period) period)
----------------------------------------------------------------------------------------------------------------
Descriptive Evaluation Final Report 50 1 40 2,000
Template.................................
Impact Evaluation Final Report Template... 29 1 30 870
Impact Evaluation Final Report Table 29 1 10 290
Shells...................................
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 3,160.
Authority: 42 U.S.C. 603(a)(2).
Mary C. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2024-28555 Filed 12-5-24; 8:45 am]
BILLING CODE 4184-73-P