Medicare and Medicaid Programs; Application From The Compliance Team (TCT) for Continued Approval of its Rural Health Clinics Program, 88393-88395 [2023-28111]
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Federal Register / Vol. 88, No. 244 / Thursday, December 21, 2023 / Notices
concert, to retain voting shares of Lakin
Bancshares, Inc., and thereby indirectly
retain voting shares of the KCB Bank,
both of Lakin, Kansas.
Board of Governors of the Federal Reserve
System.
Erin M. Cayce,
Assistant Secretary of the Board.
[FR Doc. 2023–28035 Filed 12–20–23; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–9889–N]
Charter Renewal for Advisory
Committee on Ground Ambulance and
Patient Billing (GAPB)—November 16,
2023
Centers for Medicare &
Medicaid Services (CMS), Department
of Health and Human Services (HHS).
ACTION: Notice.
AGENCY:
The No Surprises Act,
enacted as part of the Consolidated
Appropriations Act, 2021, requires the
Secretary of Health and Human Services
(HHS), the Secretary of Labor, and the
Secretary of the Treasury (the
Secretaries) to establish and convene an
advisory committee for the purpose of
reviewing options to improve the
disclosure of charges and fees for
ground ambulance services, better
inform consumers of insurance options
for such services, and protect consumers
from balance billing (the ‘‘GAPB
Advisory Committee’’ or the
‘‘Committee’’). The Secretaries
established the GAPB Advisory
Committee on November 16, 2021 with
a standard 2-year expiration period
ending November 16, 2023. In
accordance with the Federal Advisory
Committee Act (FACA), HHS is hereby
giving notice that the charter for the
Advisory Committee on Ground
Ambulance and Patient Billing (GAPB)
was renewed effective November 16,
2023.
SUMMARY:
The charter for the Advisory
Committee on GAPB was renewed is
November 16, 2023.
ADDRESSES: Inquiries about the
Committee can be mailed to Center for
Consumer Information & Insurance
Oversight, Centers for Medicare &
Medicaid Services, 7500 Security
Boulevard, Mail Stop WB–22–75,
Baltimore, MD 21244–8016.
FOR FURTHER INFORMATION CONTACT:
khammond on DSKJM1Z7X2PROD with NOTICES
DATES:
VerDate Sep<11>2014
18:15 Dec 20, 2023
Jkt 262001
Shaheen Halim, CMS, by phone (410)
786–0641 or via email at
gapbadvisorycommittee@cms.hhs.gov.
Press inquiries may be submitted by
phone at (202) 690–6145 or via email at
press@cms.hhs.gov.
SUPPLEMENTARY INFORMATION: Section
117(a) of the No Surprises Act, enacted
as part of the Consolidated
Appropriations Act, 2021, div. BB, tit. I,
Public Law 116–260 (Dec. 27, 2020),
requires the Secretaries of Labor, HHS,
and the Treasury to establish and
convene an advisory committee for the
purpose of reviewing options to
improve the disclosure of charges and
fees for ground ambulance services,
better inform consumers of insurance
options for such services, and protect
consumers from balance billing. The
GAPB Advisory Committee is governed
by the provisions of the Federal
Advisory Committee Act (FACA), Public
Law 92–463 (Oct. 6, 1972), as amended,
5 U.S.C. App. 2.
The GAPB Advisory Committee first
convened in 2023. It will make
recommendations with respect to the
disclosure of charges and fees for
ground ambulance services and
insurance coverage, consumer
protection and enforcement authorities
of the Departments of Labor, Health and
Human Services, and the Treasury (the
Departments) and relevant States, and
the prevention of balance billing to
consumers. The recommendations shall
address options, best practices, and
identified standards to prevent
instances of balance billing; steps that
can be taken by State legislatures, State
insurance regulators, State attorneys
general, and other State officials as
appropriate, consistent with current
legal authorities regarding consumer
protection; and legislative options for
Congress to prevent balance billing. The
purpose of renewing the GAPB
Advisory Committee is to provide the
Committee with more time to review
relevant information, review options
and best practices, and consider the
recommendations that it has been
charged with making. A copy of the
charter and other information regarding
the GAPB Advisory Committee’s
activity can be found at: https://
www.cms.gov/medicare/regulationsguidance/advisory-committees/
advisory-committee-ground-ambulanceand-patient-billing-gapb. The
Administrator of CMS, Chiquita BrooksLaSure, having reviewed and approved
this document, authorizes Vanessa
Garcia, who is the Federal Register
Liaison, to electronically sign this
document for purposes of publication in
the Federal Register.
PO 00000
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88393
Dated: December 18, 2023.
Vanessa Garcia,
Federal Register Liaison, Centers for Medicare
& Medicaid Services.
[FR Doc. 2023–28128 Filed 12–20–23; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3455–PN]
Medicare and Medicaid Programs;
Application From The Compliance
Team (TCT) for Continued Approval of
its Rural Health Clinics Program
Centers for Medicare &
Medicaid Services (CMS), Department
of Health and Human Services (HHS).
ACTION: Notice with request for
comment.
AGENCY:
This proposed notice
acknowledges the receipt of an
application from the Compliance Team
(TCT) for continued recognition as a
national accrediting organization (AO)
for Rural Health Clinics (RHCs) that
wish to participate in the Medicare or
Medicaid programs. The statute requires
that within 60 days of receipt of an
organization’s complete application, the
Centers for Medicare & Medicaid
Services (CMS) publish a notice that
identifies the national accrediting body
making the request, describes the nature
of the request, and provides at least a
30-day public comment period.
DATES: To be assured consideration,
comments must be received at one of
the addresses provided below, by
January 22, 2024.
ADDRESSES: In commenting, refer to file
code CMS–3455–PN.
Comments, including mass comment
submissions, must be submitted in one
of the following three ways (please
choose only one of the ways listed):
1. Electronically. You may submit
electronic comments on this regulation
to https://www.regulations.gov. Follow
the ‘‘Submit a comment’’ instructions.
2. By regular mail. You may mail
written comments to the following
address ONLY: Centers for Medicare &
Medicaid Services, Department of
Health and Human Services, Attention:
CMS–3455–PN, P.O. Box 8013,
Baltimore, MD 21244–8013.
Please allow sufficient time for mailed
comments to be received before the
close of the comment period.
3. By express or overnight mail. You
may send written comments to the
following address ONLY: Centers for
SUMMARY:
E:\FR\FM\21DEN1.SGM
21DEN1
88394
Federal Register / Vol. 88, No. 244 / Thursday, December 21, 2023 / Notices
Medicare & Medicaid Services,
Department of Health and Human
Services, Attention: CMS–3455–PN,
Mail Stop C4–26–05, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
For information on viewing public
comments, see the beginning of the
SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT:
Joy Webb (410) 786–1667.
Shonte Carter (410) 786–3532.
SUPPLEMENTARY INFORMATION:
Inspection of Public Comments: All
comments received before the close of
the comment period are available for
viewing by the public, including any
personally identifiable or confidential
business information that is included in
a comment. We post all comments
received before the close of the
comment period on the following
website as soon as possible after they
have been received: https://
www.regulations.gov. Follow the search
instructions on that website to view
public comments. We will not post on
Regulations.gov public comments that
make threats to individuals or
institutions or suggest that the
individual will take actions to harm the
individual. We continue to encourage
individuals not to submit duplicative
comments. We will post acceptable
comments from multiple unique
commenters even if the content is
identical or nearly identical to other
comments.
khammond on DSKJM1Z7X2PROD with NOTICES
I. Background
Under the Medicare program, eligible
beneficiaries may receive covered
services from a Medicare-participating
Rural Health Clinic (RHC), provided
certain requirements are met. Sections
1861(aa)(1) and (2) and 1905(l)(1) of the
Social Security Act (the Act) establish
distinct criteria for an entity seeking
designation as an RHC. Regulations
concerning provider agreements are at
42 CFR part 489, and those pertaining
to activities relating to the survey and
certification of facilities and other
entities are at 42 CFR part 488. The
regulations at 42 CFR part 491 specify
the conditions that a RHC must meet to
participate in the Medicare program.
Generally, to enter into an agreement,
a RHC must first be certified by a State
survey agency as complying with the
conditions or requirements set forth in
part 491 of our regulations. Thereafter,
the RHC is subject to regular surveys by
a State survey agency to determine
whether it continues to meet these
requirements.
However, there is an alternative to
surveys by State agencies. Section
1865(a)(1) of the Act provides that if a
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18:15 Dec 20, 2023
Jkt 262001
provider entity demonstrates through
accreditation by a Center for Medicare &
Medicaid Services (CMS) approved
national accrediting organization (AO)
that all applicable Medicare conditions
are met or exceeded, we will deem those
provider entities as having met the
requirements. Accreditation by an AO is
voluntary and is not required for
Medicare participation.
If an AO is recognized by the
Secretary of Health and Human Services
(the Secretary) as having standards for
accreditation that meet or exceed
Medicare requirements, any provider
entity accredited by the national
accrediting body’s approved program
would be deemed to meet the Medicare
conditions. A national AO applying for
approval of its accreditation program
under 42 CFR part 488, subpart A must
provide CMS with reasonable assurance
that the AO requires the accredited
provider entities to meet requirements
that are at least as stringent as the
Medicare conditions. Our regulations
concerning the approval of AO are set
forth at § 488.4 and 488.5. The
regulations at § 488.5(e)(2)(i) require
AOs to reapply for continued approval
of their accreditation program every 6
years or sooner as determined by CMS.
The Compliance Team’s (TCT’s) term
of approval for their RHC accreditation
program expires July 17, 2024.
II. Approval of Deeming Organization
Section 1865(a)(2) of the Act and our
regulations at § 488.5 require that our
findings concerning review and
approval of a national AO’s
requirements consider, among other
factors, the applying AO’s requirements
for accreditation; survey procedures;
resources for conducting required
surveys; capacity to furnish information
for use in enforcement activities;
monitoring procedures for provider
entities found not in compliance with
the conditions or requirements; and
ability to provide us with the necessary
data for validation.
Section 1865(a)(3)(A) of the Act
further requires that we publish, within
60 days of receipt of an organization’s
complete application, a notice
identifying the national accrediting
body making the request, describing the
nature of the request, and providing at
least a 30-day public comment period.
We have 210 days from the receipt of a
complete application to publish notice
of approval or denial of the application.
The purpose of this proposed notice
is to inform the public of TCT’s request
for continued approval for its RHC
accreditation program. This notice also
solicits public comment on whether
TCT’s requirements meet or exceed the
PO 00000
Frm 00035
Fmt 4703
Sfmt 4703
Medicare conditions for certification
(CfCs) for RHCs.
III. Evaluation of Deeming Authority
Request
TCT submitted all the necessary
materials to enable us to make a
determination concerning its request for
continued approval of its RHC
accreditation program. This application
was determined to be complete on
October 25, 2023. Under section
1865(a)(2) of the Act and our regulations
at § 488.5 (Application and reapplication procedures for national
accrediting organizations), our review
and evaluation of TCT will be
conducted in accordance with, but not
necessarily limited to, the following
factors:
• The equivalency of TCT’s standards
for RHCs as compared with CMS’ RHC
CfCs.
• TCT’s survey process to determine
the following:
++ The composition of the survey
team, surveyor qualifications, and the
ability of the organization to provide
continuing surveyor training.
++ The comparability of TCT’s
processes to those of State agencies,
including survey frequency, and the
ability to investigate and respond
appropriately to complaints against
accredited RHCs.
++ TCT’s processes and procedures
for monitoring RHCs found out of
compliance with TCT’s program
requirements. These monitoring
procedures are used only when TCT
identifies noncompliance. If
noncompliance is identified through
validation reviews or complaint
surveys, the State survey agency
monitors corrections as specified at
§ 488.9(c).
++ TCT’s capacity to report
deficiencies to the surveyed RHCs and
respond to the RHC’s plan of correction
in a timely manner.
++ TCT’s capacity to provide us with
electronic data and reports necessary for
effective validation and assessment of
the organization’s survey process.
++ The adequacy of TCT’s staff and
other resources, and its financial
viability.
++ TCT’s capacity to adequately fund
required surveys.
++ TCT’s policies with respect to
whether surveys are announced or
unannounced, to assure that surveys are
unannounced.
++ TCT’s policies and procedures to
avoid conflicts of interest, including the
appearance of conflicts of interest,
involving individuals who conduct
surveys or participate in accreditation
decisions.
E:\FR\FM\21DEN1.SGM
21DEN1
Federal Register / Vol. 88, No. 244 / Thursday, December 21, 2023 / Notices
++ TCT’s agreement to provide us
with a copy of the most current
accreditation survey together with any
other information related to the survey
as we may require (including corrective
action plans).
IV. Collection of Information
Requirements
This document does not impose
information collection requirements,
that is, reporting, recordkeeping or
third-party disclosure requirements.
Consequently, there is no need for
review by the Office of Management and
Budget under the authority of the
Paperwork Reduction Act of 1995 (44
U.S.C. 3501 et seq.).
V. Response to Comments
Because of the large number of public
comments we normally receive on
Federal Register documents, we are not
able to acknowledge or respond to them
individually. We will consider all
comments we receive by the date and
time specified in the ‘‘DATES’’ section
of this preamble, and when we proceed
with a subsequent document, we will
respond to the comments in the
preamble to that document.
The Administrator of the Centers for
Medicare & Medicaid Services (CMS),
Chiquita Brooks-LaSure, having
reviewed and approved this document,
authorizes Trenesha Fultz-Mimms, who
is the Federal Register Liaison, to
electronically sign this document for
purposes of publication in the Federal
Register.
Trenesha Fultz-Mimms,
Federal Register Liaison, Centers for Medicare
& Medicaid Services.
[FR Doc. 2023–28111 Filed 12–20–23; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2016–D–2565]
khammond on DSKJM1Z7X2PROD with NOTICES
510(k) Third Party Review Program and
Third Party Emergency Use
Authorization (EUA) Review; Draft
Guidance for Industry, Food and Drug
Administration Staff, and Third Party
Review Organizations; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of the draft
guidance entitled ‘‘510(k) Third Party
Review Program and Third Party
SUMMARY:
VerDate Sep<11>2014
18:15 Dec 20, 2023
Jkt 262001
Emergency Use Authorization (EUA)
Review.’’ This draft guidance provides
FDA’s current thinking regarding the
510(k) Third Party (3P510k) Review
Program and review of Emergency Use
Authorizations (EUA) requests by a
third party review organizations
(3PEUA review). The 3P510k Review
Program and 3PEUA review create an
alternative process for manufacturers to
seek review of 510(k) submissions and
EUA requests to assist FDA in reviewing
in a timely manner. This draft guidance
is not final nor is it for implementation
at this time.
DATES: Submit either electronic or
written comments on the draft guidance
by February 20, 2024 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:
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
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
well as any attachments, except for
PO 00000
Frm 00036
Fmt 4703
Sfmt 4703
88395
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2016–D–2565 for ‘‘510(k) Third Party
Review Program and Third Party
Emergency Use Authorization (EUA)
Review.’’ Received comments will be
placed in the docket and, except for
those submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
Dockets Management Staff between 9
a.m. and 4 p.m., Monday through
Friday, 240–402–7500.
• Confidential Submissions—To
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information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on
https://www.regulations.gov. Submit
both copies to the Dockets Management
Staff. If you do not wish your name and
contact information to be made publicly
available, you can provide this
information on the cover sheet and not
in the body of your comments and you
must identify this information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://
www.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.pdf.
Docket: For access to the docket to
read background documents or the
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received, go to https://
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docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
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You may submit comments on any
guidance at any time (see 21 CFR
10.115(g)(5)).
An electronic copy of the guidance
document is available for download
from the internet. See the
E:\FR\FM\21DEN1.SGM
21DEN1
Agencies
[Federal Register Volume 88, Number 244 (Thursday, December 21, 2023)]
[Notices]
[Pages 88393-88395]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-28111]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-3455-PN]
Medicare and Medicaid Programs; Application From The Compliance
Team (TCT) for Continued Approval of its Rural Health Clinics Program
AGENCY: Centers for Medicare & Medicaid Services (CMS), Department of
Health and Human Services (HHS).
ACTION: Notice with request for comment.
-----------------------------------------------------------------------
SUMMARY: This proposed notice acknowledges the receipt of an
application from the Compliance Team (TCT) for continued recognition as
a national accrediting organization (AO) for Rural Health Clinics
(RHCs) that wish to participate in the Medicare or Medicaid programs.
The statute requires that within 60 days of receipt of an
organization's complete application, the Centers for Medicare &
Medicaid Services (CMS) publish a notice that identifies the national
accrediting body making the request, describes the nature of the
request, and provides at least a 30-day public comment period.
DATES: To be assured consideration, comments must be received at one of
the addresses provided below, by January 22, 2024.
ADDRESSES: In commenting, refer to file code CMS-3455-PN.
Comments, including mass comment submissions, must be submitted in
one of the following three ways (please choose only one of the ways
listed):
1. Electronically. You may submit electronic comments on this
regulation to https://www.regulations.gov. Follow the ``Submit a
comment'' instructions.
2. By regular mail. You may mail written comments to the following
address ONLY: Centers for Medicare & Medicaid Services, Department of
Health and Human Services, Attention: CMS-3455-PN, P.O. Box 8013,
Baltimore, MD 21244-8013.
Please allow sufficient time for mailed comments to be received
before the close of the comment period.
3. By express or overnight mail. You may send written comments to
the following address ONLY: Centers for
[[Page 88394]]
Medicare & Medicaid Services, Department of Health and Human Services,
Attention: CMS-3455-PN, Mail Stop C4-26-05, 7500 Security Boulevard,
Baltimore, MD 21244-1850.
For information on viewing public comments, see the beginning of
the SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT:
Joy Webb (410) 786-1667.
Shonte Carter (410) 786-3532.
SUPPLEMENTARY INFORMATION:
Inspection of Public Comments: All comments received before the
close of the comment period are available for viewing by the public,
including any personally identifiable or confidential business
information that is included in a comment. We post all comments
received before the close of the comment period on the following
website as soon as possible after they have been received: https://www.regulations.gov. Follow the search instructions on that website to
view public comments. We will not post on Regulations.gov public
comments that make threats to individuals or institutions or suggest
that the individual will take actions to harm the individual. We
continue to encourage individuals not to submit duplicative comments.
We will post acceptable comments from multiple unique commenters even
if the content is identical or nearly identical to other comments.
I. Background
Under the Medicare program, eligible beneficiaries may receive
covered services from a Medicare-participating Rural Health Clinic
(RHC), provided certain requirements are met. Sections 1861(aa)(1) and
(2) and 1905(l)(1) of the Social Security Act (the Act) establish
distinct criteria for an entity seeking designation as an RHC.
Regulations concerning provider agreements are at 42 CFR part 489, and
those pertaining to activities relating to the survey and certification
of facilities and other entities are at 42 CFR part 488. The
regulations at 42 CFR part 491 specify the conditions that a RHC must
meet to participate in the Medicare program.
Generally, to enter into an agreement, a RHC must first be
certified by a State survey agency as complying with the conditions or
requirements set forth in part 491 of our regulations. Thereafter, the
RHC is subject to regular surveys by a State survey agency to determine
whether it continues to meet these requirements.
However, there is an alternative to surveys by State agencies.
Section 1865(a)(1) of the Act provides that if a provider entity
demonstrates through accreditation by a Center for Medicare & Medicaid
Services (CMS) approved national accrediting organization (AO) that all
applicable Medicare conditions are met or exceeded, we will deem those
provider entities as having met the requirements. Accreditation by an
AO is voluntary and is not required for Medicare participation.
If an AO is recognized by the Secretary of Health and Human
Services (the Secretary) as having standards for accreditation that
meet or exceed Medicare requirements, any provider entity accredited by
the national accrediting body's approved program would be deemed to
meet the Medicare conditions. A national AO applying for approval of
its accreditation program under 42 CFR part 488, subpart A must provide
CMS with reasonable assurance that the AO requires the accredited
provider entities to meet requirements that are at least as stringent
as the Medicare conditions. Our regulations concerning the approval of
AO are set forth at Sec. 488.4 and 488.5. The regulations at Sec.
488.5(e)(2)(i) require AOs to reapply for continued approval of their
accreditation program every 6 years or sooner as determined by CMS.
The Compliance Team's (TCT's) term of approval for their RHC
accreditation program expires July 17, 2024.
II. Approval of Deeming Organization
Section 1865(a)(2) of the Act and our regulations at Sec. 488.5
require that our findings concerning review and approval of a national
AO's requirements consider, among other factors, the applying AO's
requirements for accreditation; survey procedures; resources for
conducting required surveys; capacity to furnish information for use in
enforcement activities; monitoring procedures for provider entities
found not in compliance with the conditions or requirements; and
ability to provide us with the necessary data for validation.
Section 1865(a)(3)(A) of the Act further requires that we publish,
within 60 days of receipt of an organization's complete application, a
notice identifying the national accrediting body making the request,
describing the nature of the request, and providing at least a 30-day
public comment period. We have 210 days from the receipt of a complete
application to publish notice of approval or denial of the application.
The purpose of this proposed notice is to inform the public of
TCT's request for continued approval for its RHC accreditation program.
This notice also solicits public comment on whether TCT's requirements
meet or exceed the Medicare conditions for certification (CfCs) for
RHCs.
III. Evaluation of Deeming Authority Request
TCT submitted all the necessary materials to enable us to make a
determination concerning its request for continued approval of its RHC
accreditation program. This application was determined to be complete
on October 25, 2023. Under section 1865(a)(2) of the Act and our
regulations at Sec. 488.5 (Application and re-application procedures
for national accrediting organizations), our review and evaluation of
TCT will be conducted in accordance with, but not necessarily limited
to, the following factors:
The equivalency of TCT's standards for RHCs as compared
with CMS' RHC CfCs.
TCT's survey process to determine the following:
++ The composition of the survey team, surveyor qualifications, and
the ability of the organization to provide continuing surveyor
training.
++ The comparability of TCT's processes to those of State agencies,
including survey frequency, and the ability to investigate and respond
appropriately to complaints against accredited RHCs.
++ TCT's processes and procedures for monitoring RHCs found out of
compliance with TCT's program requirements. These monitoring procedures
are used only when TCT identifies noncompliance. If noncompliance is
identified through validation reviews or complaint surveys, the State
survey agency monitors corrections as specified at Sec. 488.9(c).
++ TCT's capacity to report deficiencies to the surveyed RHCs and
respond to the RHC's plan of correction in a timely manner.
++ TCT's capacity to provide us with electronic data and reports
necessary for effective validation and assessment of the organization's
survey process.
++ The adequacy of TCT's staff and other resources, and its
financial viability.
++ TCT's capacity to adequately fund required surveys.
++ TCT's policies with respect to whether surveys are announced or
unannounced, to assure that surveys are unannounced.
++ TCT's policies and procedures to avoid conflicts of interest,
including the appearance of conflicts of interest, involving
individuals who conduct surveys or participate in accreditation
decisions.
[[Page 88395]]
++ TCT's agreement to provide us with a copy of the most current
accreditation survey together with any other information related to the
survey as we may require (including corrective action plans).
IV. Collection of Information Requirements
This document does not impose information collection requirements,
that is, reporting, recordkeeping or third-party disclosure
requirements. Consequently, there is no need for review by the Office
of Management and Budget under the authority of the Paperwork Reduction
Act of 1995 (44 U.S.C. 3501 et seq.).
V. Response to Comments
Because of the large number of public comments we normally receive
on Federal Register documents, we are not able to acknowledge or
respond to them individually. We will consider all comments we receive
by the date and time specified in the ``DATES'' section of this
preamble, and when we proceed with a subsequent document, we will
respond to the comments in the preamble to that document.
The Administrator of the Centers for Medicare & Medicaid Services
(CMS), Chiquita Brooks-LaSure, having reviewed and approved this
document, authorizes Trenesha Fultz-Mimms, who is the Federal Register
Liaison, to electronically sign this document for purposes of
publication in the Federal Register.
Trenesha Fultz-Mimms,
Federal Register Liaison, Centers for Medicare & Medicaid Services.
[FR Doc. 2023-28111 Filed 12-20-23; 8:45 am]
BILLING CODE 4120-01-P