Medicare Program; Application by The Compliance Team (TCT) for Continued CMS Approval of Its Home Infusion Therapy (HIT) Accreditation Program, 76841-76843 [2024-21410]
Download as PDF
Federal Register / Vol. 89, No. 182 / Thursday, September 19, 2024 / Notices
notice also solicited public comments
regarding whether NABP’s requirements
met or exceeded the Medicare
conditions for participation for HIT. No
comments were received in response to
our proposed notice.
V. Provisions of the Final Notice
lotter on DSK11XQN23PROD with NOTICES1
A. Differences Between NABP’s
Standards and Requirements for
Accreditation and Medicare Conditions
and Survey Requirements
We compared NABP’s HIT
accreditation requirements and survey
process with the Medicare Conditions
for Coverage of 42 CFR part 486, and the
survey and certification process
requirements of part 488. Our review
and evaluation of NABP’s HIT
application, which were conducted as
described in section III of this final
notice, yielded the following areas
where, as of the date of this notice,
NABP has completed revising its
standards and certification processes to
meet the conditions at §§ 486.500 to
486.525.
• Section 486.520(a), to address the
requirement that all patients must be
under the care of an applicable
provider.
• Section 486.520(b), to address the
requirement that the plan of care must
be established by a physician and that
it prescribes the type, amount, and
duration of the home infusion therapy
services that are to be furnished.
• Section 486.520(c), to address the
requirement that the plan of care for
each patient must be periodically
reviewed by the physician.
• Section 486.525(a), to address the
requirement that the HIT supplier must
provide the following services on a 7day a week, 24 hour-a-day basis in
accordance with the plan of care:
++ Section 486.525(a)(1), to provide
professional services, including nursing
services.
++ Section 486.525(a)(2), to address
the requirement for patient training and
education and not otherwise paid for as
durable medical equipment.
++ Section 486.525(a)(3), to address
the requirement of remote monitoring
services for the provision of HIT
services and home infusion drugs.
Section 486.525(b), to address the
requirement that all home infusion
therapy suppliers must provide HIT
services in accordance with nationally
recognized standards of practice, and in
accordance with all applicable state and
federal laws and regulations.
B. Term of Approval
Based on the review and observations
described in section III. of this final
VerDate Sep<11>2014
16:59 Sep 18, 2024
Jkt 262001
notice, we have determined that NABP’s
requirements for HIT meet or exceed our
requirements. Therefore, we approve
NABP as a national accreditation
organization for HITs that request
participation in the Medicare program,
effective September 26, 2024 through
September 26, 2030.
VI. 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. Chapter 35).
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. 2024–21409 Filed 9–18–24; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3462–FN]
Medicare Program; Application by The
Compliance Team (TCT) for Continued
CMS Approval of Its Home Infusion
Therapy (HIT) Accreditation Program
Centers for Medicare &
Medicaid Services (CMS), Health and
Human Services (HHS).
ACTION: Final notice.
AGENCY:
This final notice announces
our decision to approve The
Compliance Team (TCT) for continued
recognition as a national accrediting
organization that accredits suppliers of
home infusion therapy (HIT) services
that wish to participate in the Medicare
or Medicaid programs.
DATES: The approval announced in this
final notice is effective September 28,
2024, through September 28, 2030.
FOR FURTHER INFORMATION CONTACT:
Shannon Freeland, (410) 786–4348.
SUPPLEMENTARY INFORMATION:
SUMMARY:
PO 00000
Frm 00056
Fmt 4703
Sfmt 4703
76841
I. Background
Home infusion therapy (HIT) is a
treatment option for Medicare
beneficiaries with a wide range of acute
and chronic conditions. Section 5012 of
the 21st Century Cures Act (Pub. L. 114–
255, enacted December 13, 2016) added
section 1861(iii) to the Social Security
Act (the Act), establishing a new
Medicare benefit for HIT services.
Section 1861(iii)(1) of the Act defines
‘‘home infusion therapy’’ as professional
services, including nursing services;
training and education not otherwise
covered under the Durable Medical
Equipment (DME) benefit; remote
monitoring; and other monitoring
services. Home infusion therapy must
be furnished by a qualified HIT supplier
and furnished in the individual’s home.
Sections 1861(iii)(A) and (B) of the Act
require that the individual (patient)
must:
• Be under the care of an applicable
provider (that is, physician, nurse
practitioner, or physician assistant); and
• Have a plan of care established and
periodically reviewed by a physician in
coordination with the furnishing of
home infusion drugs under Part B,
which prescribes the type, amount, and
duration of infusion therapy services
that are to be furnished.
Section 1861(iii)(3)(D)(i)(III) of the Act
requires that a qualified HIT supplier be
accredited by an accrediting
organization (AO) designated by the
Secretary in accordance with section
1834(u)(5) of the Act.
Section 1834(u)(5)(A) of the Act
identifies factors for designating HIT
AOs and for reviewing and modifying
the list of designated HIT AOs. These
statutory factors are as follows:
• The ability of the accrediting
organization to conduct timely reviews
of HIT accreditation applications.
• The ability of the accrediting
organization to take into account the
capacities HIT suppliers located in a
rural area (as defined in section
1886(d)(2)(D) of the Act).
• Whether the accrediting
organization has established reasonable
fees to be charged to HIT suppliers
applying for accreditation.
• Such other factors as the Secretary
determines appropriate.
Section 1834(u)(5)(B) of the Act
requires the Secretary to designate AOs
to accredit HIT suppliers furnishing HIT
not later than January 1, 2021. Section
1861(iii)(3)(D)(i)(III) of the Act requires
a ‘‘qualified home infusion therapy
supplier’’ to be accredited by a CMSapproved AO, pursuant to section
1834(u)(5) of the Act.
The current term of approval for The
Compliance Team (TCT) HIT
E:\FR\FM\19SEN1.SGM
19SEN1
76842
Federal Register / Vol. 89, No. 182 / Thursday, September 19, 2024 / Notices
accreditation program expires
September 28, 2024.
II. Approval of Deeming Organization
Section 1834(u)(5) of the Act and
§ 488.1010 require that our findings
concerning review and approval of a
national accrediting organization’s
requirements consider, among other
factors, the applying accrediting
organization’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 CMS with the
necessary data.
Our rules at 42 CFR 488.1020(a)
require that we publish, after 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. Pursuant to our rules
at 42 CFR 488.1010(d), we have 210
days from the receipt of a complete
application to publish notice of
approval or denial of the application.
lotter on DSK11XQN23PROD with NOTICES1
III. Provisions of the Proposed Notice
In the April 29, 2024, Federal
Register (89 FR 33354), we published a
proposed notice announcing TCT’s
request for continued recognition as a
national accrediting organization for
suppliers providing HIT services that
wish to participate in the Medicare or
Medicaid programs. In that proposed
notice, we detailed our evaluation
criteria. Under section 1834(u)(5) the
Act and in our regulations at § 488.1010,
we conducted a review of TCT’s
Medicare HIT accreditation application
in accordance with the criteria specified
by our regulations, which include, but
are not limited to, the following:
• An administrative review of TCT’s:
++ Corporate policies;
++ Financial and human resources
available to accomplish the proposed
surveys;
++ Procedures for training,
monitoring, and evaluation of its HIT
surveyors;
++ Ability to investigate and respond
appropriately to complaints against
accredited HITs; and
++ Survey review and decisionmaking process for accreditation.
• The equivalency of TCT’s standards
for HIT as compared with CMS’ HIT
conditions for participation.
• TCT’s survey process to determine
the following:
VerDate Sep<11>2014
16:59 Sep 18, 2024
Jkt 262001
++ The composition of the survey
team, surveyor qualifications, and the
ability of the organization to provide
continuing surveyor training;
++ The comparability of TCT’s to
CMS’ standards and processes,
including survey frequency, and the
ability to investigate and respond
appropriately to complaints against
accredited facilities;
++ TCT’s processes and procedures
for monitoring a HIT supplier found out
of compliance with TCT’s program
requirements;
++ TCT’s capacity to report
deficiencies to the surveyed HIT
facilities and respond to the facility’s
evidence of standards compliance in a
timely manner;
++ TCT’s capacity to provide CMS
with electronic data and reports
necessary for effective assessment and
interpretation of the organization’s
survey process;
++ TCT’s capacity to adequately fund
required surveys;
++ TCT’s policies with respect to
whether surveys are announced or
unannounced, to ensure that surveys are
unannounced; and
++ TCT’s agreement to provide CMS
with a copy of the most current
accreditation survey together with any
other information related to the survey
as CMS may require (including
corrective action plans or TCT’s
evidence of standards compliance).
• The adequacy of TCT’s staff and
other resources, and its financial
viability.
• TCT’s agreement or policies for
voluntary and involuntary termination
of suppliers.
• TCT’s agreement or policies for
voluntary and involuntary termination
of the HIT AO program.
• 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.
IV. Analysis of and Responses to Public
Comments on the Proposed Notice
In accordance with section 1834(u)(5)
of the Act, the April 29, 2024, proposed
notice also solicited public comments
regarding whether TCT’s requirements
met or exceeded the Medicare
conditions for participation for HIT. No
comments were received in response to
our proposed notice.
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
V. Provisions of the Final Notice
A. Differences Between TCT’s Standards
and Requirements for Accreditation and
Medicare Conditions and Survey
Requirements
We compared TCT’s HIT accreditation
requirements and survey process with
the Medicare Conditions for Coverage of
42 CFR part 486, and the survey and
certification process requirements of
part 488. Our review and evaluation of
TCT’s HIT application, which were
conducted as described in section III of
this final notice, yielded the following
areas where, as of the date of this notice,
TCT has completed revising its
standards and certification processes to
meet the conditions at §§ 486.500 to
486.525.
• Section 486.520(a), to address the
requirement of all patients must be
under the care of an applicable
provider.
• Section 486.520(b), to address the
requirement that the plan of care must
be established by a physician and that
it prescribes the type, amount, and
duration of the home infusion therapy
services that are to be furnished.
• Section 486.520(c), to address the
requirement that the plan of care for
each patient must be periodically
reviewed by the physician.
• Section 486.525(a), to address the
requirement that the HIT supplier must
provide the following services on a 7day a week, 24 hour-a-day basis in
accordance with the plan of care:
++ Section 486.525(a)(1), to provide
professional services, including nursing
services.
++ Section 486.525(a)(2), to address
the requirement for patient training and
education and not otherwise paid for as
durable medical equipment.
++ Section 486.525(a)(3), to address
the requirement of remote monitoring
services for the provision of HIT
services and home infusion drugs.
• Section 486.525(b), to address the
requirement that all home infusion
therapy suppliers must provide HIT
services in accordance with nationally
recognized standards of practice, and in
accordance with all applicable state and
federal laws and regulations.
B. Term of Approval
Based on the review and observations
described in section III. of this final
notice, we have determined that TCT’s
requirements for HIT meet or exceed our
requirements. Therefore, we approve
TCT as a national accreditation
organization for HITs that request
participation in the Medicare program,
effective September 28, 2024 through
September 28, 2030.
E:\FR\FM\19SEN1.SGM
19SEN1
Federal Register / Vol. 89, No. 182 / Thursday, September 19, 2024 / Notices
VI. 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. Chapter 35).
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. 2024–21410 Filed 9–18–24; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. 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 or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate 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
lotter on DSK11XQN23PROD with NOTICES1
16:59 Sep 18, 2024
Jkt 262001
William Parham at (410) 786–4669.
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: Revision of a currently
approved collection; Title of
Information Collection: Section 1915(c)
Home and Community-Based Services
Waivers and Supporting Regulations;
Use: We use this report to compare
actual data to the approved waiver
estimates. In conjunction with the
waiver compliance review reports, the
information provided will be compared
to that in the Medicaid Statistical
SUPPLEMENTARY INFORMATION:
[Document Identifiers: CMS–372(S) and
CMS–R–284]
VerDate Sep<11>2014
Comments on the collection(s) of
information must be received by the
OMB desk officer by October 21, 2024.
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.
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
DATES:
FOR FURTHER INFORMATION CONTACT:
Centers for Medicare & Medicaid
Services
SUMMARY:
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
PO 00000
Frm 00058
Fmt 4703
Sfmt 9990
76843
Information System (MSIS) (CMS–R–
284; OMB control number: 0938–0345)
report and FFP claimed on a State’s
Quarterly Expenditure Report (CMS–64;
OMB control number: 0938–1265), to
determine whether to continue the
State’s home and community-based
services waiver. States’ estimates of cost
and utilization for renewal purposes are
based upon the data compiled in the
CMS–372(S) reports. Form Number:
CMS–372(S) (OMB control number:
0938–0272); Frequency: Yearly; Affected
Public: State, Local, or Tribal
Governments; Number of Respondents:
47; Total Annual Responses: 259; Total
Annual Hours: 11,396. (For policy
questions regarding this collection
contact George Failla at 410–786–7561.)
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Transformed—
Medicaid Statistical Information System
(T–MSIS); Use: The data reported in T–
MSIS are used by Federal, State, and
local officials, as well as by private
researchers and corporations to monitor
past and projected future trends in the
Medicaid program. The data provide the
only national level information
available on enrollees, beneficiaries, and
expenditures. It also provides the only
national level information available on
Medicaid utilization. The information is
the basis for analyses and for cost
savings estimates for the Department’s
cost sharing legislative initiatives to
Congress. The collected data are also
crucial to our actuarial forecasts. Form
Number: CMS–R–284 (OMB control
number: 0938–0345); Frequency:
Quarterly and monthly; Affected Public:
State, Local, or Tribal Governments;
Number of Respondents: 54; Total
Annual Responses: 648; Total Annual
Hours: 7,290. (For policy questions
regarding this collection contact Connie
Gibson at 410–786–0755.)
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–21444 Filed 9–18–24; 8:45 am]
BILLING CODE 4120–01–P
E:\FR\FM\19SEN1.SGM
19SEN1
Agencies
[Federal Register Volume 89, Number 182 (Thursday, September 19, 2024)]
[Notices]
[Pages 76841-76843]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-21410]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-3462-FN]
Medicare Program; Application by The Compliance Team (TCT) for
Continued CMS Approval of Its Home Infusion Therapy (HIT) Accreditation
Program
AGENCY: Centers for Medicare & Medicaid Services (CMS), Health and
Human Services (HHS).
ACTION: Final notice.
-----------------------------------------------------------------------
SUMMARY: This final notice announces our decision to approve The
Compliance Team (TCT) for continued recognition as a national
accrediting organization that accredits suppliers of home infusion
therapy (HIT) services that wish to participate in the Medicare or
Medicaid programs.
DATES: The approval announced in this final notice is effective
September 28, 2024, through September 28, 2030.
FOR FURTHER INFORMATION CONTACT: Shannon Freeland, (410) 786-4348.
SUPPLEMENTARY INFORMATION:
I. Background
Home infusion therapy (HIT) is a treatment option for Medicare
beneficiaries with a wide range of acute and chronic conditions.
Section 5012 of the 21st Century Cures Act (Pub. L. 114-255, enacted
December 13, 2016) added section 1861(iii) to the Social Security Act
(the Act), establishing a new Medicare benefit for HIT services.
Section 1861(iii)(1) of the Act defines ``home infusion therapy'' as
professional services, including nursing services; training and
education not otherwise covered under the Durable Medical Equipment
(DME) benefit; remote monitoring; and other monitoring services. Home
infusion therapy must be furnished by a qualified HIT supplier and
furnished in the individual's home. Sections 1861(iii)(A) and (B) of
the Act require that the individual (patient) must:
Be under the care of an applicable provider (that is,
physician, nurse practitioner, or physician assistant); and
Have a plan of care established and periodically reviewed
by a physician in coordination with the furnishing of home infusion
drugs under Part B, which prescribes the type, amount, and duration of
infusion therapy services that are to be furnished.
Section 1861(iii)(3)(D)(i)(III) of the Act requires that a
qualified HIT supplier be accredited by an accrediting organization
(AO) designated by the Secretary in accordance with section 1834(u)(5)
of the Act.
Section 1834(u)(5)(A) of the Act identifies factors for designating
HIT AOs and for reviewing and modifying the list of designated HIT AOs.
These statutory factors are as follows:
The ability of the accrediting organization to conduct
timely reviews of HIT accreditation applications.
The ability of the accrediting organization to take into
account the capacities HIT suppliers located in a rural area (as
defined in section 1886(d)(2)(D) of the Act).
Whether the accrediting organization has established
reasonable fees to be charged to HIT suppliers applying for
accreditation.
Such other factors as the Secretary determines
appropriate.
Section 1834(u)(5)(B) of the Act requires the Secretary to
designate AOs to accredit HIT suppliers furnishing HIT not later than
January 1, 2021. Section 1861(iii)(3)(D)(i)(III) of the Act requires a
``qualified home infusion therapy supplier'' to be accredited by a CMS-
approved AO, pursuant to section 1834(u)(5) of the Act.
The current term of approval for The Compliance Team (TCT) HIT
[[Page 76842]]
accreditation program expires September 28, 2024.
II. Approval of Deeming Organization
Section 1834(u)(5) of the Act and Sec. 488.1010 require that our
findings concerning review and approval of a national accrediting
organization's requirements consider, among other factors, the applying
accrediting organization'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 CMS with the
necessary data.
Our rules at 42 CFR 488.1020(a) require that we publish, after
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.
Pursuant to our rules at 42 CFR 488.1010(d), we have 210 days from the
receipt of a complete application to publish notice of approval or
denial of the application.
III. Provisions of the Proposed Notice
In the April 29, 2024, Federal Register (89 FR 33354), we published
a proposed notice announcing TCT's request for continued recognition as
a national accrediting organization for suppliers providing HIT
services that wish to participate in the Medicare or Medicaid programs.
In that proposed notice, we detailed our evaluation criteria. Under
section 1834(u)(5) the Act and in our regulations at Sec. 488.1010, we
conducted a review of TCT's Medicare HIT accreditation application in
accordance with the criteria specified by our regulations, which
include, but are not limited to, the following:
An administrative review of TCT's:
++ Corporate policies;
++ Financial and human resources available to accomplish the
proposed surveys;
++ Procedures for training, monitoring, and evaluation of its HIT
surveyors;
++ Ability to investigate and respond appropriately to complaints
against accredited HITs; and
++ Survey review and decision-making process for accreditation.
The equivalency of TCT's standards for HIT as compared
with CMS' HIT conditions for participation.
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 to CMS' standards and processes,
including survey frequency, and the ability to investigate and respond
appropriately to complaints against accredited facilities;
++ TCT's processes and procedures for monitoring a HIT supplier
found out of compliance with TCT's program requirements;
++ TCT's capacity to report deficiencies to the surveyed HIT
facilities and respond to the facility's evidence of standards
compliance in a timely manner;
++ TCT's capacity to provide CMS with electronic data and reports
necessary for effective assessment and interpretation of the
organization's survey process;
++ TCT's capacity to adequately fund required surveys;
++ TCT's policies with respect to whether surveys are announced or
unannounced, to ensure that surveys are unannounced; and
++ TCT's agreement to provide CMS with a copy of the most current
accreditation survey together with any other information related to the
survey as CMS may require (including corrective action plans or TCT's
evidence of standards compliance).
The adequacy of TCT's staff and other resources, and its
financial viability.
TCT's agreement or policies for voluntary and involuntary
termination of suppliers.
TCT's agreement or policies for voluntary and involuntary
termination of the HIT AO program.
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.
IV. Analysis of and Responses to Public Comments on the Proposed Notice
In accordance with section 1834(u)(5) of the Act, the April 29,
2024, proposed notice also solicited public comments regarding whether
TCT's requirements met or exceeded the Medicare conditions for
participation for HIT. No comments were received in response to our
proposed notice.
V. Provisions of the Final Notice
A. Differences Between TCT's Standards and Requirements for
Accreditation and Medicare Conditions and Survey Requirements
We compared TCT's HIT accreditation requirements and survey process
with the Medicare Conditions for Coverage of 42 CFR part 486, and the
survey and certification process requirements of part 488. Our review
and evaluation of TCT's HIT application, which were conducted as
described in section III of this final notice, yielded the following
areas where, as of the date of this notice, TCT has completed revising
its standards and certification processes to meet the conditions at
Sec. Sec. 486.500 to 486.525.
Section 486.520(a), to address the requirement of all
patients must be under the care of an applicable provider.
Section 486.520(b), to address the requirement that the
plan of care must be established by a physician and that it prescribes
the type, amount, and duration of the home infusion therapy services
that are to be furnished.
Section 486.520(c), to address the requirement that the
plan of care for each patient must be periodically reviewed by the
physician.
Section 486.525(a), to address the requirement that the
HIT supplier must provide the following services on a 7-day a week, 24
hour-a-day basis in accordance with the plan of care:
++ Section 486.525(a)(1), to provide professional services,
including nursing services.
++ Section 486.525(a)(2), to address the requirement for patient
training and education and not otherwise paid for as durable medical
equipment.
++ Section 486.525(a)(3), to address the requirement of remote
monitoring services for the provision of HIT services and home infusion
drugs.
Section 486.525(b), to address the requirement that all
home infusion therapy suppliers must provide HIT services in accordance
with nationally recognized standards of practice, and in accordance
with all applicable state and federal laws and regulations.
B. Term of Approval
Based on the review and observations described in section III. of
this final notice, we have determined that TCT's requirements for HIT
meet or exceed our requirements. Therefore, we approve TCT as a
national accreditation organization for HITs that request participation
in the Medicare program, effective September 28, 2024 through September
28, 2030.
[[Page 76843]]
VI. 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. Chapter 35).
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. 2024-21410 Filed 9-18-24; 8:45 am]
BILLING CODE 4120-01-P