Agency Information Collection Activities: Proposed Collection; Comment Request, 26892-26893 [2024-08011]
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Federal Register / Vol. 89, No. 74 / Tuesday, April 16, 2024 / Notices
advance will not be permitted to enter
the building and will be unable to
attend the meeting. We note that the
public may not enter the CMS building
earlier than 8:15 a.m. E.D.T. (45 minutes
before the convening of the meeting).
Security measures include the
following:
• Presentation of government-issued
photographic identification to the
Federal Protective Service or Guard
Service personnel. Persons without
proper identification may be denied
access to the building.
• Interior and exterior inspection of
vehicles (this includes engine and trunk
inspection) at the entrance to the
grounds. Parking permits and
instructions will be issued after the
vehicle inspection.
• Passing through a metal detector
and inspection of items brought into the
building. We note that all items brought
to CMS, whether personal or for the
purpose of demonstration or to support
a demonstration, are subject to
inspection. We cannot assume
responsibility for coordinating the
receipt, transfer, transport, storage, setup, safety, or timely arrival of any
personal belongings or items used for
demonstration or to support a
demonstration.
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. 3501 et seq.).
The Administrator of CMS, Chiquita
Brooks-LaSure, 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.
khammond on DSKJM1Z7X2PROD with NOTICES
Vanessa Garcia,
Federal Register Liaison, Centers for Medicare
& Medicaid Services.
[FR Doc. 2024–08005 Filed 4–15–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10573]
Agency Information Collection
Activities: Proposed Collection;
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
60 days for public comment on the
proposed action. Interested persons are
invited to send 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
June 17, 2024.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. 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: Document Identifier/OMB
Control Number: ll, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
SUMMARY:
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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:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10573 Reform of Requirements
for Long-Term Care Facilities
Under the 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
requires federal agencies to publish a
60-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.
Information Collection
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Reform of
Requirements for Long-Term Care
Facilities; Use: The purpose of this
package is to request Office of
Management and Budget (OMB)
approval of the collection of information
requirements for the requirements of
participation for Long-Term Care (LTC)
facilities that must be met in order to
participate in the Medicare and
Medicaid Programs. LTC facilities
include skilled nursing facilities (SNFs)
as defined in section 1819(a) of the
Social Security Act in the Medicare
program and nursing facilities (NFs) as
defined in 1919(a) of the Act in the
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16APN1
khammond on DSKJM1Z7X2PROD with NOTICES
Federal Register / Vol. 89, No. 74 / Tuesday, April 16, 2024 / Notices
Medicaid program. SNFs and NFs
provide skilled nursing care and related
services for residents who require
medical or nursing care, or
rehabilitation services for the
rehabilitation of injured, disabled, or
sick persons. In addition, NFs provide
health-related care and services to
individuals who because of their mental
or physical condition require care and
services (above the level of room and
board) which can be made available to
them only through institutional
facilities, and is not primarily for the
care and treatment of mental diseases.
SNFs and NFs must care for their
residents in such a manner and in such
an environment as will promote
maintenance or enhancement of the
quality of life of each resident and must
provide to residents services to attain or
maintain the highest practicable
physical, mental, and psychosocial
well-being of each resident, in
accordance with a written plan of care,
which describes the medical, nursing,
and psychosocial needs of the resident
and how such needs will be met and is
updated periodically.
The primary users of this information
will be State agency surveyors, CMS,
and the LTC facilities for the purposes
of ensuring compliance with Medicare
and Medicaid requirements as well as
ensuring the quality of care provided to
LTC facility residents. The ICs specified
in the regulations may be used as a basis
for determining whether a LTC is
meeting the requirements to participate
in the Medicare program. In addition,
the information collected for purposes
of ensuring compliance may be used to
inform the data provided on CMS’
Nursing Home Compare website and as
such used by the public in considering
nursing home selections for services.
We are revising this information
collection request to include new
requirements proposed at 42 CFR 483.35
and 483.71. The proposed requirements
were discussed in detail in the proposed
rule that published September 6, 2023
(88 FR 61352). The discussion related to
proposed requirements and the
associated information collection
burden begins on page 61391. We are
not making any other revisions to the
information collection request at this
time.
Form Number: CMS–10573 (OMB
control number: 0938–1363); Frequency:
Occasionally; Affected Public: Private
Sector: Business or other for-profit and
not-for-profit institutions; Number of
Respondents: 15,600; Total Annual
Responses: 18,687,318 Total Annual
Hours: 30,309,662. (For policy questions
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regarding this collection contact Diane
Corning at 410–786–8486.)
William N. Parham, III
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–08011 Filed 4–15–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–1824–N]
Medicare Program; Meeting
Announcement for the Medicare
Advisory Panel on Clinical Diagnostic
Laboratory Tests, July 25–26, 2024
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:
This notice announces the
public meeting dates for the Medicare
Advisory Panel on Clinical Diagnostic
Laboratory Tests (the Panel) on
Thursday, July 25, 2024 and Friday, July
26, 2024. The purpose of the Panel is to
advise the Secretary of the Department
of Health and Human Services and the
Administrator of the Centers for
Medicare & Medicaid Services on issues
related to clinical diagnostic laboratory
tests.
DATES:
Meeting Dates: The hybrid (in-person
and virtual) meeting of the Panel is
scheduled for Thursday, July 25, 2024
from 10:00 a.m. to 4:00 p.m., Eastern
Daylight Time (E.D.T.) and Friday, July
26, 2024, from 10:00 a.m. to 4:00 p.m.,
E.D.T. The Panel is also expected to
participate virtually in the Clinical
Laboratory Fee Schedule (CLFS) Annual
Public Meeting for Calendar Year (CY)
2025 on Tuesday, June 25, 2024, to
gather information and ask questions to
presenters. Notice of the CLFS Annual
Public Meeting for CY 2025 is published
elsewhere in this issue of the Federal
Register.
Deadline for Meeting Registration: All
stand-by speakers for the Panel meeting
must register electronically to our CDLT
Panel dedicated email box, CDLTPanel@
cms.hhs.gov by June 1, 2024.
In-Person Attendance: If attending the
meeting in person at the CMS
Headquarters, registration is required
and must be completed by May 30,
2025. For more information on how to
register as an in-person attendee, see the
‘‘Registration Instructions’’ (section IV
of this notice).
SUMMARY:
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26893
Virtual Attendee Only: The public
may also view this meeting via webinar
or listen-only via teleconference. If
attending the meeting via webinar, or
listen-only via teleconference,
registration is not required for nonspeakers.
Webinar and Teleconference Meeting
Information: Teleconference dial-in
instructions, and related webinar details
will be posted on the meeting agenda,
which will be available on the CMS
website approximately 2 weeks prior to
the meeting at https://www.cms.gov/
Regulations-and-Guidance/Guidance/
FACA/AdvisoryPanelonClinical
DiagnosticLaboratoryTests.html. A
preliminary agenda is described in
section II of this notice.
ADDRESSES: The Panel meeting will be
held virtually and in-person at the
campus of the Centers for Medicare &
Medicaid Services (CMS), Central
Building, 7500 Security Boulevard,
Baltimore, Maryland 21244–1850.
FOR FURTHER INFORMATION CONTACT: The
CLFS Policy Team via email,
CDLTPanel@cms.hhs.gov; or Rasheeda
Arthur, (410) 786–3434. The CMS Press
Office, for press inquiries, (202) 690–
6145.
SUPPLEMENTARY INFORMATION:
I. Background
The Medicare Advisory Panel on
Clinical Diagnostic Laboratory Tests
(CDLTs) (the Panel) is authorized by
section 1834A(f)(1) of the Social
Security Act (the Act) (42 U.S.C.
1395m–1), as established by section
216(a) of the Protecting Access to
Medicare Act of 2014 (PAMA) (Pub. L.
113–93), enacted on April 1, 2014. The
Panel is subject to the Federal Advisory
Committee Act (FACA), as amended (5
U.S.C. appendix 2), which sets forth
standards for the formation and use of
advisory panels.
Section 1834A(f)(1) of the Act directs
the Secretary of the Department of
Health and Human Services (the
Secretary) to consult with an expert
outside advisory panel established by
the Secretary, composed of an
appropriate selection of individuals
with expertise in issues related to
clinical diagnostic laboratory tests,
which may include the development,
validation, performance, and
application of such tests. Such
individuals may include molecular
pathologists, researchers, and
individuals with expertise in laboratory
science or health economics.
The Panel will provide input and
recommendations to the Secretary and
the Administrator of the Centers for
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Agencies
[Federal Register Volume 89, Number 74 (Tuesday, April 16, 2024)]
[Notices]
[Pages 26892-26893]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-08011]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-10573]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: 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 60 days for public comment on
the proposed action. Interested persons are invited to send 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 June 17, 2024.
ADDRESSES: When commenting, please reference the document identifier or
OMB control number. 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: Document Identifier/OMB
Control Number: __, 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/PRA-Listing.
FOR FURTHER INFORMATION CONTACT: William N. Parham at (410) 786-4669.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the use and burden associated
with the following information collections. More detailed information
can be found in each collection's supporting statement and associated
materials (see ADDRESSES).
CMS-10573 Reform of Requirements for Long-Term Care Facilities
Under the 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 requires federal agencies
to publish a 60-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.
Information Collection
1. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Reform of
Requirements for Long-Term Care Facilities; Use: The purpose of this
package is to request Office of Management and Budget (OMB) approval of
the collection of information requirements for the requirements of
participation for Long-Term Care (LTC) facilities that must be met in
order to participate in the Medicare and Medicaid Programs. LTC
facilities include skilled nursing facilities (SNFs) as defined in
section 1819(a) of the Social Security Act in the Medicare program and
nursing facilities (NFs) as defined in 1919(a) of the Act in the
[[Page 26893]]
Medicaid program. SNFs and NFs provide skilled nursing care and related
services for residents who require medical or nursing care, or
rehabilitation services for the rehabilitation of injured, disabled, or
sick persons. In addition, NFs provide health-related care and services
to individuals who because of their mental or physical condition
require care and services (above the level of room and board) which can
be made available to them only through institutional facilities, and is
not primarily for the care and treatment of mental diseases. SNFs and
NFs must care for their residents in such a manner and in such an
environment as will promote maintenance or enhancement of the quality
of life of each resident and must provide to residents services to
attain or maintain the highest practicable physical, mental, and
psychosocial well-being of each resident, in accordance with a written
plan of care, which describes the medical, nursing, and psychosocial
needs of the resident and how such needs will be met and is updated
periodically.
The primary users of this information will be State agency
surveyors, CMS, and the LTC facilities for the purposes of ensuring
compliance with Medicare and Medicaid requirements as well as ensuring
the quality of care provided to LTC facility residents. The ICs
specified in the regulations may be used as a basis for determining
whether a LTC is meeting the requirements to participate in the
Medicare program. In addition, the information collected for purposes
of ensuring compliance may be used to inform the data provided on CMS'
Nursing Home Compare website and as such used by the public in
considering nursing home selections for services.
We are revising this information collection request to include new
requirements proposed at 42 CFR 483.35 and 483.71. The proposed
requirements were discussed in detail in the proposed rule that
published September 6, 2023 (88 FR 61352). The discussion related to
proposed requirements and the associated information collection burden
begins on page 61391. We are not making any other revisions to the
information collection request at this time.
Form Number: CMS-10573 (OMB control number: 0938-1363); Frequency:
Occasionally; Affected Public: Private Sector: Business or other for-
profit and not-for-profit institutions; Number of Respondents: 15,600;
Total Annual Responses: 18,687,318 Total Annual Hours: 30,309,662. (For
policy questions regarding this collection contact Diane Corning at
410-786-8486.)
William N. Parham, III
Director, Division of Information Collections and Regulatory Impacts,
Office of Strategic Operations and Regulatory Affairs.
[FR Doc. 2024-08011 Filed 4-15-24; 8:45 am]
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