Medicaid and Children's Health Insurance Program (CHIP) Generic Information Collection Activities: Proposed Collection; Comment Request, 1095-1097 [2024-00205]
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khammond on DSKJM1Z7X2PROD with NOTICES
Federal Register / Vol. 89, No. 6 / Tuesday, January 9, 2024 / Notices
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The public portions of the
applications listed below, as well as
other related filings required by the
Board, if any, are available for
immediate inspection at the Federal
Reserve Bank(s) indicated below and at
the offices of the Board of Governors.
This information may also be obtained
on an expedited basis, upon request, by
contacting the appropriate Federal
Reserve Bank and from the Board’s
Freedom of Information Office at
https://www.federalreserve.gov/foia/
request.htm. Interested persons may
express their views in writing on the
standards enumerated in the BHC Act
(12 U.S.C. 1842(c)).
Comments regarding each of these
applications must be received at the
Reserve Bank indicated or the offices of
the Board of Governors, Ann E.
Misback, Secretary of the Board, 20th
Street and Constitution Avenue NW,
Washington, DC 20551–0001, not later
than February 7, 2024.
A. Federal Reserve Bank of Atlanta
(Erien O. Terry, Assistant Vice
President) 1000 Peachtree Street NE,
Atlanta, Georgia 30309; Comments can
also be sent electronically to
Applications.Comments@atl.frb.org]:
1. Eureka Investor Group, Inc.,
Birmingham, Alabama; to become a
bank holding company by acquiring
Eureka Homestead Bancorp, Inc., a
savings and loan holding company, and
thereby indirectly acquire Eureka
Homestead, a savings association
subsidiary, both of Metairie, Louisiana.
In addition, Eureka Homestead Bancorp,
Inc. will convert from a savings and
loan holding company to a bank holding
company in connection with Eureka
Homestead’s conversion from a savings
association to a national bank.
Board of Governors of the Federal
Reserve System.
Michele Taylor Fennell,
Deputy Associate Secretary of the Board.
[FR Doc. 2024–00166 Filed 1–8–24; 8:45 am]
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GOVERNMENT ACCOUNTABILITY
OFFICE
Request for Medicare Payment
Advisory Commission (MedPAC)
Nominations
U.S. Government
Accountability Office.
ACTION: Request for letters of
nomination and resumes.
AGENCY:
The Balanced Budget Act of
1997 established the Medicare Payment
Advisory Commission (MedPAC) and
gave the Comptroller General
responsibility for appointing its
members. The U.S. Government
Accountability Office (GAO) is now
accepting nominations for MedPAC
appointments that will be effective in
May 2024. Nominations should be sent
to the email address listed below.
Acknowledgement of receipt will be
provided within a week of submission.
DATES: Letters of nomination and
resumes should be submitted no later
than February 9, 2024, to ensure
adequate opportunity for review and
consideration of nominees prior to
appointment.
SUMMARY:
Submit letters of
nomination and resumes to
MedPACappointments@gao.gov.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Gregory Giusto at (202) 512–8268 or
giustog@gao.gov if you do not receive an
acknowledgement or need additional
information. For general information,
contact GAO’s Office of Public Affairs at
(202) 512–4800.
Authority: 42 U.S.C. 1395b–6.
Gene L. Dodaro,
Comptroller General of the United States.
[FR Doc. 2024–00181 Filed 1–8–24; 8:45 am]
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1095
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: Disease,
Disability, and Injury Prevention and
Control Special Emphasis Panel (SEP)–
RFA–PS–24–040, Understanding Infant
Feeding Preferences, Practices, and
Outcomes for Mothers and other Parents
with HIV in the United States.
Date: March 28, 2024.
Time: 10 a.m.–5 p.m., EDT.
Place: Videoconference.
Agenda: To review and evaluate grant
applications.
For Further Information Contact:
Seraphine Pitt Barnes, Ph.D., M.P.H.,
C.H.E.S., Scientific Review Officer,
National Center for HIV, Viral Hepatitis,
STD, and TB Prevention, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, Mailstop H24–6,
Atlanta, Georgia 30329–4027.
Telephone: (770) 488–6115; Email:
SPittBarnes@cdc.gov.
The Director, Office of Strategic
Business Initiatives, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2024–00214 Filed 1–8–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Centers for Medicare & Medicaid
Services
Notice of Closed Meeting
Pursuant to 5 U.S.C. 1009(d), 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, and the Determination of
the Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, CDC, pursuant to Public Law
92–463. The grant applications and the
discussions could disclose confidential
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[Document Identifiers: CMS–10398 #43, #45,
and #48]
Medicaid and Children’s Health
Insurance Program (CHIP) Generic
Information Collection Activities:
Proposed Collection; Comment
Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
E:\FR\FM\09JAN1.SGM
09JAN1
1096
Federal Register / Vol. 89, No. 6 / Tuesday, January 9, 2024 / Notices
On May 28, 2010, the Office
of Management and Budget (OMB)
issued Paperwork Reduction Act (PRA)
guidance related to the ‘‘generic’’
clearance process. Generally, this is an
expedited process by which agencies
may obtain OMB’s approval of
collection of information requests that
are ‘‘usually voluntary, low-burden, and
uncontroversial collections,’’ do not
raise any substantive or policy issues,
and do not require policy or
methodological review. The process
requires the submission of an
overarching plan that defines the scope
of the individual collections that would
fall under its umbrella. On October 23,
2011, OMB approved our initial request
to use the generic clearance process
under control number 0938–1148
(CMS–10398). It was last approved on
April 26, 2021, via the standard PRA
process which included the publication
of 60- and 30-day Federal Register
notices. The scope of the April 2021
umbrella accounts for Medicaid and
CHIP State plan amendments, waivers,
demonstrations, and reporting. This
Federal Register notice seeks public
comment on one or more of our
collection of information requests that
we believe are generic and fall within
the scope of the umbrella. Interested
persons are invited to submit comments
regarding our burden estimates or any
other aspect of this collection of
information, including: the necessity
and utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of
the estimated burden, ways to enhance
the quality, utility and clarity of the
information to be collected, and the use
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
DATES: Comments must be received by
January 23, 2024.
ADDRESSES: When commenting, please
reference the applicable form number
(CMS–10398 #see below) and the OMB
control number (0938–1148). To be
assured consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
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16:38 Jan 08, 2024
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Division of Regulations Development,
Attention: CMS–10398 (#ll)/OMB
control number: 0938–1148, Room C4–
26–05, 7500 Security Boulevard,
Baltimore, Maryland 21244–1850.
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 N. Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION: Following
is a summary of the use and burden
associated with the subject information
collection(s). More detailed information
can be found in the collection’s
supporting statement and associated
materials (see ADDRESSES).
Generic Information Collections
1. Title of Information Collection:
Certified Community Behavioral Health
Clinic (CCBHC) Cost Report; Type of
Information Collection Request:
Revision of an active collection of
information request; Use: The CCBHC
cost report allows clinics in the
demonstration to calculate Prospective
Payment System (PPS) rates using
clinic-specific cost and visit data
associated with delivery of the nine
statutory services as outlined under the
authorizing Protecting Access to
Medicare Act (PAMA) (Pub. L. 113–93)
at section 223(D) Scope of Services.
Currently CCBHCs use the cost report to
calculate rates based on the existing CC
PPS–1 daily, or CC PPS–2 monthly rate
that do not include separate crisis rate
options. Calculation of the new daily
and monthly special crisis services PPS
rates required CMS to revise the existing
CCBHC cost report to include addition
worksheets to address the new crisis
rate offerings being finalized in the
CCBHC Technical Guide. SCS rates
would be effective beginning January 1,
2024, for any existing states that may be
interested in implementing either CC
PPS–3 or CC PPS–4, and new states
entering the program by July 2024 will
have the option to choose from among
the four PPS rate options made available
under the updated Technical Guide and
CCBHC cost report.
States and clinics selecting either the
CC PPS–3 or CC PPS–4 crisis rate
methodology will require additional
time to separate costs and visit data for
up to three special crisis services rates.
CCBHCs in states that choose CC PPS–
2 rate methodology will require
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additional time to gather data for special
populations and account for outlier
thresholds.
Because use of this cost report
involves participation in the CCBHC
demonstration program, the information
is expected to be collected annually,
assuming rates are trended forward for
the second year of the program using the
Medicare Economic Index (MEI),
rebased in the third year of the
demonstration and trended forward for
the fourth year of the demonstration
using the MEI. However, if the state
requires CCBHCs to rebase rates for
other years of the demonstration using
CCBHC cost report data, the provider
would be required to complete the cost
report each time the state rebases the
rate. CMS does also require CCBHC
demonstration states to submit cost
reports in trended years although rates
may only reflect changes based on MEI
adjustment for inflationary changes.
Form Number: CMS–10398 #43 (OMB
control number: 0938–1148); Frequency:
Annual; Affected Public: Private Sector
(Businesses or other for profits and Not
for profit institutions) and State, Local,
or Tribal Governments; Number of
Respondents: 60; Total Annual
Responses: 60; Total Annual Hours:
3,389. (For policy questions regarding
this collection contact: Beverly Boston
at 410–786–4186.)
2. Title of Information Collection:
Certified Community Behavioral Health
Clinic (CCBHC) 2024 State Proposal
Demonstration Application; Type of
Information Collection Request:
Revision of an active collection of
information request; Use: Based on
recent extension and expansion of the
CCBHC Demonstration under section
11001 of Bipartisan Safer Communities
Act 1 (BSCA) of 2022, the State Proposal
Demonstration Application is required
to be completed by existing CCBHC
grantee states and submitted to the
Centers for Medicare & Medicaid
Services (CMS) and the Substance
Abuse and Mental Health Services
Administration (SAMHSA) to determine
state readiness and eligibility to be
selected as one of the 10 new states
added to the CCBHC demonstration in
2024 and every two years thereafter per
the BSCA legislation. The awarding of
Planning Grants to states was the first
phase of a two-phase process. Phase II
will consist of participation in the
demonstration. Form Number: CMS–
10398 #45 (OMB control number: 0938–
1148); Frequency: One time and On
occasion; Affected Public: State, Local,
or Tribal Governments; Number of
Respondents: 30; Total Annual
1 Bipartisan
E:\FR\FM\09JAN1.SGM
Safer Communities Act.
09JAN1
Federal Register / Vol. 89, No. 6 / Tuesday, January 9, 2024 / Notices
Responses: 30; Total Annual Hours:
1,790. (For policy questions regarding
this collection contact: Beverly Boston
at 410–786–4186.)
3. Title of Information Collection:
Behavioral Health Clinic Quality Data
Reporting; Type of Information
Collection Request: Revision of an active
collection of information request; Use:
This Information Collection concerns
the Behavioral Health Clinic Quality
Data Reporting Template (hereinafter
‘‘Reporting Template’’ or ‘‘Template’’),
developed in partnership with the
Substance Abuse and Mental Health
Services Administration (SAMHSA) and
the Assistant Secretary for Planning and
Evaluation (ASPE) (collectively, ‘‘the
Agencies’’). The Reporting Template is
designed to collect quality measure data
and to report at the clinic level. The
Agencies developed the Template to
provide states and clinics with a
streamlined and structured tool to
report quality measures data. The
Reporting Template aims to eliminate
the time required for states or clinics to
develop their own reporting templates
for quality measure data reporting and
minimizes inconsistencies in reporting.
Furthermore, the Reporting Template,
with its accompanying instructions,
support an innovative approach to
improve behavioral health, a key focus
of health care reform. Form Number:
CMS–10398 (#48) (OMB control
number: 0938–1148); Frequency:
Annual; Affected Public: Private Sector
(Businesses or other for profits and Not
for profit institutions) and State, Local,
or Tribal Governments; Number of
Respondents: 429; Total Annual
Responses: 1,009; Total Annual Hours:
6,814. (For policy questions regarding
this collection contact: Beverly Boston
at 410–786–4186.)
Dated: January 4, 2024.
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–00205 Filed 1–8–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
khammond on DSKJM1Z7X2PROD with NOTICES
Food and Drug Administration
[Docket No. FDA–2020–N–0026]
Issuance of Priority Review Voucher;
Rare Pediatric Disease Product
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
16:38 Jan 08, 2024
FOR FURTHER INFORMATION CONTACT:
Myrna Hanna, Center for Biologics
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 71, Rm. 7301,
Silver Spring, MD 20993–0002, 240–
402–7911.
FDA is
announcing the issuance of a priority
review voucher to the sponsor of an
approved rare pediatric disease product
application. Under section 529 of the
FD&C Act (21 U.S.C. 360ff), FDA will
award priority review vouchers to
sponsors of approved rare pediatric
disease product applications that meet
certain criteria. FDA has determined
that CASGEVY (exagamglogene
autotemcel), manufactured by Vertex
Pharmaceuticals, Inc., meets the criteria
for a priority review voucher.
CASGEVY (exagamglogene
autotemcel) is indicated for treatment of
sickle cell disease in patients 12 years
of age and older with recurrent vasoocclusive crises.
For further information about the Rare
Pediatric Disease Priority Review
Voucher Program and for a link to the
full text of section 529 of the FD&C Act,
go to https://www.fda.gov/industry/
developing-products-rare-diseasesconditions/rare-pediatric-disease-rpddesignation-and-voucher-programs. For
further information about CASGEVY
(exagamglogene autotemcel), go to the
Center for Biologics Evaluation and
Research’s Approved Cellular and Gene
Therapy Products website at https://
www.fda.gov/vaccines-blood-biologics/
cellular-gene-therapy-products/
approved-cellular-and-gene-therapyproducts.
SUPPLEMENTARY INFORMATION:
Dated: January 4, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024–00263 Filed 1–8–24; 8:45 am]
Notice.
VerDate Sep<11>2014
The Food and Drug
Administration (FDA) is announcing the
issuance of a priority review voucher to
the sponsor of a rare pediatric disease
product application. The Federal Food,
Drug, and Cosmetic Act (FD&C Act)
authorizes FDA to award priority review
vouchers to sponsors of approved rare
pediatric disease product applications
that meet certain criteria. FDA is
required to publish notice of the award
of the priority review voucher. FDA has
determined that CASGEVY
(exagamglogene autotemcel),
manufactured by Vertex
Pharmaceuticals, Inc., meets the criteria
for a priority review voucher.
SUMMARY:
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1097
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2014–N–0987]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Generic Clearance
for the Collection of Qualitative Data
on Tobacco Products and
Communications
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
announcing an opportunity for public
comment on the proposed collection of
certain information by the Agency.
Under the Paperwork Reduction Act of
1995 (PRA), Federal Agencies are
required to publish notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information, and
to allow 60 days for public comment in
response to the notice. This notice
solicits comments on the collection of
qualitative data on tobacco products and
communications.
DATES: Either electronic or written
comments on the collection of
information must be submitted by
March 11, 2024.
ADDRESSES: You may submit comments
as follows. Please note that late,
untimely filed comments will not be
considered. The https://
www.regulations.gov electronic filing
system will accept comments until
11:59 p.m. Eastern Time at the end of
March 11, 2024. Comments received by
mail/hand delivery/courier (for written/
paper submissions) will be considered
timely if they are received on or before
that date.
SUMMARY:
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,
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
E:\FR\FM\09JAN1.SGM
09JAN1
Agencies
[Federal Register Volume 89, Number 6 (Tuesday, January 9, 2024)]
[Notices]
[Pages 1095-1097]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-00205]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-10398 #43, #45, and #48]
Medicaid and Children's Health Insurance Program (CHIP) Generic
Information Collection Activities: Proposed Collection; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
[[Page 1096]]
SUMMARY: On May 28, 2010, the Office of Management and Budget (OMB)
issued Paperwork Reduction Act (PRA) guidance related to the
``generic'' clearance process. Generally, this is an expedited process
by which agencies may obtain OMB's approval of collection of
information requests that are ``usually voluntary, low-burden, and
uncontroversial collections,'' do not raise any substantive or policy
issues, and do not require policy or methodological review. The process
requires the submission of an overarching plan that defines the scope
of the individual collections that would fall under its umbrella. On
October 23, 2011, OMB approved our initial request to use the generic
clearance process under control number 0938-1148 (CMS-10398). It was
last approved on April 26, 2021, via the standard PRA process which
included the publication of 60- and 30-day Federal Register notices.
The scope of the April 2021 umbrella accounts for Medicaid and CHIP
State plan amendments, waivers, demonstrations, and reporting. This
Federal Register notice seeks public comment on one or more of our
collection of information requests that we believe are generic and fall
within the scope of the umbrella. Interested persons are invited to
submit comments regarding our burden estimates or any other aspect of
this collection of information, including: the necessity and utility of
the proposed information collection for the proper performance of the
agency's functions, the accuracy of the estimated burden, ways to
enhance the quality, utility and clarity of the information to be
collected, and the use of automated collection techniques or other
forms of information technology to minimize the information collection
burden.
DATES: Comments must be received by January 23, 2024.
ADDRESSES: When commenting, please reference the applicable form number
(CMS-10398 #see below) and the OMB control number (0938-1148). To be
assured consideration, comments and recommendations must be submitted
in any one of the following ways:
1. Electronically. You may send your comments electronically to
https://www.regulations.gov. Follow the instructions for ``Comment or
Submission'' or ``More Search Options'' to find the information
collection document(s) that are accepting comments.
2. By regular mail. You may mail written comments to the following
address: CMS, Office of Strategic Operations and Regulatory Affairs,
Division of Regulations Development, Attention: CMS-10398 (#__)/OMB
control number: 0938-1148, Room C4-26-05, 7500 Security Boulevard,
Baltimore, Maryland 21244-1850.
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 N. Parham at (410) 786-4669.
SUPPLEMENTARY INFORMATION: Following is a summary of the use and burden
associated with the subject information collection(s). More detailed
information can be found in the collection's supporting statement and
associated materials (see ADDRESSES).
Generic Information Collections
1. Title of Information Collection: Certified Community Behavioral
Health Clinic (CCBHC) Cost Report; Type of Information Collection
Request: Revision of an active collection of information request; Use:
The CCBHC cost report allows clinics in the demonstration to calculate
Prospective Payment System (PPS) rates using clinic-specific cost and
visit data associated with delivery of the nine statutory services as
outlined under the authorizing Protecting Access to Medicare Act (PAMA)
(Pub. L. 113-93) at section 223(D) Scope of Services. Currently CCBHCs
use the cost report to calculate rates based on the existing CC PPS-1
daily, or CC PPS-2 monthly rate that do not include separate crisis
rate options. Calculation of the new daily and monthly special crisis
services PPS rates required CMS to revise the existing CCBHC cost
report to include addition worksheets to address the new crisis rate
offerings being finalized in the CCBHC Technical Guide. SCS rates would
be effective beginning January 1, 2024, for any existing states that
may be interested in implementing either CC PPS-3 or CC PPS-4, and new
states entering the program by July 2024 will have the option to choose
from among the four PPS rate options made available under the updated
Technical Guide and CCBHC cost report.
States and clinics selecting either the CC PPS-3 or CC PPS-4 crisis
rate methodology will require additional time to separate costs and
visit data for up to three special crisis services rates. CCBHCs in
states that choose CC PPS-2 rate methodology will require additional
time to gather data for special populations and account for outlier
thresholds.
Because use of this cost report involves participation in the CCBHC
demonstration program, the information is expected to be collected
annually, assuming rates are trended forward for the second year of the
program using the Medicare Economic Index (MEI), rebased in the third
year of the demonstration and trended forward for the fourth year of
the demonstration using the MEI. However, if the state requires CCBHCs
to rebase rates for other years of the demonstration using CCBHC cost
report data, the provider would be required to complete the cost report
each time the state rebases the rate. CMS does also require CCBHC
demonstration states to submit cost reports in trended years although
rates may only reflect changes based on MEI adjustment for inflationary
changes. Form Number: CMS-10398 #43 (OMB control number: 0938-1148);
Frequency: Annual; Affected Public: Private Sector (Businesses or other
for profits and Not for profit institutions) and State, Local, or
Tribal Governments; Number of Respondents: 60; Total Annual Responses:
60; Total Annual Hours: 3,389. (For policy questions regarding this
collection contact: Beverly Boston at 410-786-4186.)
2. Title of Information Collection: Certified Community Behavioral
Health Clinic (CCBHC) 2024 State Proposal Demonstration Application;
Type of Information Collection Request: Revision of an active
collection of information request; Use: Based on recent extension and
expansion of the CCBHC Demonstration under section 11001 of Bipartisan
Safer Communities Act \1\ (BSCA) of 2022, the State Proposal
Demonstration Application is required to be completed by existing CCBHC
grantee states and submitted to the Centers for Medicare & Medicaid
Services (CMS) and the Substance Abuse and Mental Health Services
Administration (SAMHSA) to determine state readiness and eligibility to
be selected as one of the 10 new states added to the CCBHC
demonstration in 2024 and every two years thereafter per the BSCA
legislation. The awarding of Planning Grants to states was the first
phase of a two-phase process. Phase II will consist of participation in
the demonstration. Form Number: CMS-10398 #45 (OMB control number:
0938-1148); Frequency: One time and On occasion; Affected Public:
State, Local, or Tribal Governments; Number of Respondents: 30; Total
Annual
[[Page 1097]]
Responses: 30; Total Annual Hours: 1,790. (For policy questions
regarding this collection contact: Beverly Boston at 410-786-4186.)
---------------------------------------------------------------------------
\1\ Bipartisan Safer Communities Act.
---------------------------------------------------------------------------
3. Title of Information Collection: Behavioral Health Clinic
Quality Data Reporting; Type of Information Collection Request:
Revision of an active collection of information request; Use: This
Information Collection concerns the Behavioral Health Clinic Quality
Data Reporting Template (hereinafter ``Reporting Template'' or
``Template''), developed in partnership with the Substance Abuse and
Mental Health Services Administration (SAMHSA) and the Assistant
Secretary for Planning and Evaluation (ASPE) (collectively, ``the
Agencies''). The Reporting Template is designed to collect quality
measure data and to report at the clinic level. The Agencies developed
the Template to provide states and clinics with a streamlined and
structured tool to report quality measures data. The Reporting Template
aims to eliminate the time required for states or clinics to develop
their own reporting templates for quality measure data reporting and
minimizes inconsistencies in reporting. Furthermore, the Reporting
Template, with its accompanying instructions, support an innovative
approach to improve behavioral health, a key focus of health care
reform. Form Number: CMS-10398 (#48) (OMB control number: 0938-1148);
Frequency: Annual; Affected Public: Private Sector (Businesses or other
for profits and Not for profit institutions) and State, Local, or
Tribal Governments; Number of Respondents: 429; Total Annual Responses:
1,009; Total Annual Hours: 6,814. (For policy questions regarding this
collection contact: Beverly Boston at 410-786-4186.)
Dated: January 4, 2024.
William N. Parham, III,
Director, Division of Information Collections and Regulatory Impacts,
Office of Strategic Operations and Regulatory Affairs.
[FR Doc. 2024-00205 Filed 1-8-24; 8:45 am]
BILLING CODE 4120-01-P