[Federal Register Volume 88, Number 72 (Friday, April 14, 2023)]
[Notices]
[Pages 23084-23085]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-07913]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-1797-N]
Medicare Program; Meeting Announcement for the Medicare Advisory
Panel on Clinical Diagnostic Laboratory Tests
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Notice.
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SUMMARY: This notice announces the public meeting dates for the
Medicare Advisory Panel on Clinical Diagnostic Laboratory Tests (the
Panel) on Wednesday, July 19, 2023 and Thursday, July 20, 2023. 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 virtual meeting of the Panel is scheduled for
Wednesday, July 19, 2023 from 9:00 a.m. to 5:00 p.m., Eastern Daylight
Time (E.D.T.) and Thursday, July 20, 2023, from 9:00 a.m. to 5:00 p.m.,
E.D.T. The Panel is also expected to virtually participate in the
Clinical Laboratory Fee Schedule (CLFS) Annual Public Meeting for
Calendar Year (CY) 2024 on Thursday June 22, 2023 in order to gather
information and ask questions to presenters. Notice of the CLFS Annual
Public Meeting for CY 2024 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, [email protected] by June 1, 2023. Registration is not
required for non-speakers. The public may view this meeting via
webinar, or listen-only via teleconference.
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/
AdvisoryPanelonClinicalDiagnosticLaboratoryTests.html. A preliminary
agenda is described in section II of this notice.
ADDRESSES: The Panel meeting will be held virtually and will not occur
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,
[email protected]; 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 Medicare & Medicaid Services
(CMS), on the following:
The establishment of payment rates under section 1834A of
the Act for new clinical diagnostic laboratory tests, including whether
to use ``crosswalking'' or ``gapfilling'' processes to determine
payment for a specific new test.
The factors used in determining coverage and payment
processes for new clinical diagnostic laboratory tests.
Other aspects of the payment system under section 1834A of
the Act.
A notice announcing the establishment of the Panel and soliciting
nominations for members was published in the October 27, 2014 Federal
Register (79 FR 63919 through 63920). In the August 7, 2015 Federal
Register (80 FR 47491), we announced membership appointments to the
Panel along with the first public meeting date for the Panel, which was
held on August 26, 2015. Subsequent meetings of the Panel and
membership appointments were also announced in the Federal Register.
II. Agenda
The Agenda for the July 19 and July 20, 2023 Panel meeting will
provide for discussion and comment on the following topics as
designated in the Panel's charter:
Calendar Year (CY) 2024 Clinical Laboratory Fee Schedule
(CLFS) new and reconsidered test codes, which will be posted on the CMS
website at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/ClinicalLabFeeSched/Laboratory_Public_Meetings.html.
Other CY 2024 CLFS issues designated in the Panel's
charter and further described on our Agenda.
A detailed Agenda will be posted approximately 2 weeks before the
meeting, on the CMS website at https://www.cms.gov/Regulations-and-
Guidance/Guidance/FACA/
AdvisoryPanelonClinicalDiagnosticLaboratoryTests.html. The Panel will
make recommendations to the Secretary and the Administrator of CMS
regarding crosswalking and gapfilling for new and reconsidered
laboratory tests discussed during the CLFS Annual Public Meeting for CY
2024. The Panel will also provide input on other CY 2024 CLFS issues
that are designated in the Panel's charter and specified on the meeting
agenda.
III. Meeting Participation
This meeting is open to the public. Stand-by speakers may
participate in the meeting via teleconference and webinar. A stand-by
speaker is an individual who will speak on behalf of a company or
organization if the Panel has any questions during the meeting about
technical information described in the public comments or presentation
previously submitted or presented by the organization or company at the
recent CLFS Annual Public Meeting for CY 2023 on June 22, 2023. The
public may also view or listen-only to the meeting via teleconference
and webinar.
IV. Registration Instructions for Stand-by Speakers
Beginning May 1, 2023 and ending June 27, 2023 at 5:00 p.m. E.D.T.,
registration to serve as a stand-by speaker may be completed by sending
an email to the following resource box [email protected]. The
subject of the email should state ``Stand-by Speaker Registration for
CDLT Panel Meeting.'' In the email, all of the
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following information must be submitted when registering:
Stand-by Speaker name.
Organization or company name.
Email addresses that will be used by the speaker in order
to connect to the virtual meeting.
New or Reconsidered Code (s) for which the company or
organization you are representing submitted a comment or presentation.
Registration details may not be revised once they are submitted. If
registration details require changes, a new registration entry must be
submitted by the date specified in the DATES section of this notice.
Additionally, registration information must reflect individual- level
content and not reflect an organization entry. Also, each individual
may only register one person at a time. That is, one individual may not
register multiple individuals at the same time.
After registering, a confirmation email will be sent upon receipt
of the registration. The email will provide information to the speaker
in preparation for the meeting. Registration is only required for
stand-by speakers and must be submitted by the deadline specified in
the DATES section of this notice. Note: No registration is required for
participants who plan to view the Panel meeting via webinar or listen
via teleconference.
V. Panel Recommendations and Discussions
The Panel's recommendations will be posted approximately 2 weeks
after the meeting on the CMS website at https://www.cms.gov/Regulations-and-Guidance/Guidance/FACA/
AdvisoryPanelonClinicalDiagnosticLaboratoryTests.html.
VI. Special Accommodations
Individuals viewing or listening to the meeting who are hearing or
visually impaired and have special requirements, or a condition that
requires special assistance, should send an email to the resource box
([email protected]). The deadline for submitting this request is
listed in the DATES section of this notice.
VII. Copies of the Charter
The Secretary's Charter for the Medicare Advisory Panel on CDLT's
is available on the CMS website at http://cms.gov/Regulations-and-Guidance/Guidance/FACA/AdvisoryPanelonClinicalDiagnosticLaboratoryTests.html or you may obtain
a copy of the charter by submitting a request to the contact listed in
the FOR FURTHER INFORMATION CONTACT section of this notice.
VIII. 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 Evell J. Barco Holland, who is
the Federal Register Liaison, to electronically sign this document for
purposes of publication in the Federal Register.
Dated: April 11, 2023.
Evell J. Barco Holland,
Federal Register Liaison, Centers for Medicare & Medicaid Services.
[FR Doc. 2023-07913 Filed 4-13-23; 8:45 am]
BILLING CODE 4120-01-P