Medicare Program; Meeting of the Medicare Evidence Development and Coverage Advisory Committee-August 22, 2018, 27993-27995 [2018-12831]
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Federal Register / Vol. 83, No. 116 / Friday, June 15, 2018 / Notices
accrediting organization requires the
accredited provider entities to meet
requirements that are at least as
stringent as the Medicare conditions.
Our regulations concerning the
reapproval of accrediting organizations
are set forth at § 488.5. The regulations
at § 488.5(e)(2)(i) require accrediting
organizations to reapply for continued
deeming authority every 6 years or
sooner as we determine.
The Community Health Accreditation
Partner’s (CHAP’s) term of approval for
its hospice accreditation program
expires November 20, 2018.
sradovich on DSK3GMQ082PROD with NOTICES
II. Approval of Deeming Organizations
Section 1865(a)(2) of the Act and our
regulations at § 488.5 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 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 CHAP’s
request for continued CMS approval of
its hospice accreditation program. This
notice also solicits public comment on
whether CHAP’s requirements meet or
exceed the Medicare conditions for
participation for hospices.
III. Evaluation of Deeming Authority
Request
CHAP submitted all the necessary
materials to enable us to make a
determination concerning its request for
continued approval of its hospice
accreditation program. This application
was determined to be complete on April
24, 2018. Under section 1865(a)(2) of the
Act and our regulations at § 488.5
(Application and re-application
procedures for national organizations),
our review and evaluation of CHAP will
be conducted in accordance with, but
not necessarily limited to, the following
factors:
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Jkt 244001
• The equivalency of CHAP’s
standards for hospices as compared
with CMS’ hospice conditions of
participation.
• CHAP’s survey process to
determine the following:
++ CHAP’s composition of the survey
team, surveyor qualifications, and the
ability of the organization to provide
continuing surveyor training.
++ CHAP’s processes compared to
those of State agencies, including survey
frequency, and the ability to investigate
and respond appropriately to
complaints against accredited facilities.
++ CHAP’s processes and procedures
for monitoring a hospice found out of
compliance with CHAP’s program
requirements. These monitoring
procedures are used only when CHAP
identifies noncompliance. If
noncompliance is identified through
validation reviews, the State survey
agency monitors corrections as specified
at § 488.9(c).
++ CHAP’s capacity to report
deficiencies to the surveyed facilities
and respond to the facility’s plan of
correction in a timely manner.
++ CHAP’s capacity to provide CMS
with electronic data, and reports
necessary for effective validation and
assessment of the organization’s survey
process.
++ CHAP’s staff adequacy and other
resources, and its financial viability.
++ CHAP’s capacity to adequately
fund required surveys.
++ CHAP’s policies with respect to
whether surveys are announced or
unannounced, to assure that surveys are
unannounced.
++ CHAP’s agreement to provide
CMS 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).
Upon completion of our evaluation,
including evaluation of comments
received as a result of this proposed
notice, we will publish a final notice in
the Federal Register announcing the
result of our evaluation.
III. 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.).
IV. Response to Comments
Because of the large number of public
comments we normally receive on
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27993
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.
Dated: May 29, 2018.
Seema Verma,
Administrator, Centers for Medicare &
Medicaid Services.
[FR Doc. 2018–12840 Filed 6–14–18; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3363–N]
Medicare Program; Meeting of the
Medicare Evidence Development and
Coverage Advisory Committee—
August 22, 2018
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice of meeting.
AGENCY:
This notice announces that a
public meeting of the Medicare
Evidence Development & Coverage
Advisory Committee (MEDCAC)
(‘‘Committee’’) will be held on
Wednesday, August 22, 2018. This
meeting will focus on the state of
evidence on Chimeric Antigen Receptor
(CAR) T-cell therapies that are approved
by the Food and Drug Administration
(FDA). We are seeking the MEDCAC’s
recommendations regarding collection
of patient reported outcomes (PRO) in
cancer clinical studies. The MEDCAC
will specifically focus on appraisal of
evidence-based PRO assessments to
provide information that impacts
patients, their providers, and caregivers
after a CAR T-cell therapy intervention
for the patient’s cancer. This meeting is
open to the public in accordance with
the Federal Advisory Committee Act.
DATES:
Meeting Date: The public meeting will
be held on Wednesday, August 22, 2018
from 7:30 a.m. until 4:30 p.m., Eastern
Daylight Time (EDT).
Deadline for Submission of Written
Comments: Written comments must be
received at the address specified in the
ADDRESSES section of this notice by 5:00
p.m., EDT, Monday, July 16, 2018. Once
submitted, all comments are final.
Deadlines for Speaker Registration
and Presentation Materials: The
SUMMARY:
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sradovich on DSK3GMQ082PROD with NOTICES
27994
Federal Register / Vol. 83, No. 116 / Friday, June 15, 2018 / Notices
deadline to register to be a speaker and
to submit PowerPoint presentation
materials and writings that will be used
in support of an oral presentation is 5:00
p.m., EDT on Monday, July 16, 2018.
Speakers may register by phone or via
email by contacting the person listed in
the FOR FURTHER INFORMATION CONTACT
section of this notice. Presentation
materials must be received at the
address specified in the ADDRESSES
section of this notice.
Deadline for All Other Attendees
Registration: Individuals may register
online at https://www.cms.gov/apps/
events/upcoming
events.asp?strOrderBy=1&type=3 or by
phone by contacting the person listed in
the FOR FURTHER INFORMATION CONTACT
section of this notice by 5:00 p.m. EDT,
Wednesday, August 15, 2018.
We will be broadcasting the meeting
live via Webcast at https://www.cms.gov/
live/.
Deadline for Submitting a Request for
Special Accommodations: Persons
attending the meeting who are hearing
or visually impaired, or have a
condition that requires special
assistance or accommodations, are
asked to contact the Executive Secretary
as specified in the FOR FURTHER
INFORMATION CONTACT section of this
notice no later than 5:00 p.m., EDT
Friday, August 3, 2018.
ADDRESSES:
Meeting Location: The meeting will be
held in the main auditorium of the
Centers for Medicare & Medicaid
Services, 7500 Security Boulevard,
Baltimore, MD 21244.
Submission of Presentations and
Comments: Presentation materials and
written comments that will be presented
at the meeting must be submitted via
email to MedCACpresentations@
cms.hhs.gov or by regular mail to the
contact listed in the FOR FURTHER
INFORMATION CONTACT section of this
notice by the date specified in the DATES
section of this notice.
FOR FURTHER INFORMATION CONTACT:
Maria Ellis, Executive Secretary for
MEDCAC, Centers for Medicare &
Medicaid Services, Center for Clinical
Standards and Quality, Coverage and
Analysis Group, S3–02–01, 7500
Security Boulevard, Baltimore, MD
21244 or contact Ms. Ellis by phone
(410–786–0309) or via email at
Maria.Ellis@cms.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
MEDCAC, formerly known as the
Medicare Coverage Advisory Committee
(MCAC), is advisory in nature, with all
final coverage decisions resting with
VerDate Sep<11>2014
17:11 Jun 14, 2018
Jkt 244001
CMS. MEDCAC is used to supplement
CMS’ internal expertise. Accordingly,
the advice rendered by the MEDCAC is
most useful when it results from a
process of full scientific inquiry and
thoughtful discussion, in an open
forum, with careful framing of
recommendations and clear
identification of the basis of those
recommendations. MEDCAC members
are valued for their background,
education, and expertise in a wide
variety of scientific, clinical, and other
related fields. (For more information on
MCAC, see the MEDCAC Charter (https://
www.cms.gov/Regulations-andGuidance/Guidance/FACA/Downloads/
medcaccharter.pdf) and the CMS
Guidance Document, Factors CMS
Considers in Referring Topics to the
MEDCAC (https://www.cms.gov/
medicare-coverage-database/details/
medicare-coverage-documentdetails.aspx?MCDId=10)).
II. Meeting Topic and Format
This notice announces the
Wednesday, August 22, 2018, public
meeting of the Committee. This meeting
will focus on the state of evidence on
CAR–T cell therapies that are approved
by the FDA. We are seeking the
MEDCAC’s recommendations regarding
collection of PRO in cancer clinical
studies. The MEDCAC will specifically
focus on appraisal of evidence-based
PRO assessments to provide information
that impacts patients, their providers,
and caregivers after a CAR T-cell
therapy intervention for the patient’s
cancer. Background information about
this topic, including panel materials, is
available at https://www.cms.gov/
medicare-coverage-database/indexes/
medcac-meetings-index.aspx?bc=
BAAAAAAAAAAA&. We will no longer
be providing paper copies of the
handouts for the meeting. Electronic
copies of all the meeting materials will
be on the CMS website no later than 2
business days before the meeting. We
encourage the participation of
organizations with expertise in the
appraisal of the state of evidence for
patient reported outcomes, development
of patient reported health outcome
measures, and use of patient reported
health outcome assessments in cancer
clinical trials. This meeting is open to
the public. The Committee will hear
oral presentations from the public for
approximately 45 minutes. Time
allotted for each presentation may be
limited. If the number of registrants
requesting to speak is greater than can
be reasonably accommodated during the
scheduled open public hearing session,
we may conduct a lottery to determine
the speakers for the scheduled open
PO 00000
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Fmt 4703
Sfmt 4703
public hearing session. The contact
person will notify interested persons
regarding their request to speak by July
23, 2018. Your comments should focus
on issues specific to the list of topics
that we have proposed to the
Committee. The list of research topics to
be discussed at the meeting will be
available on the following website prior
to the meeting: https://www.cms.gov/
medicare-coverage-database/indexes/
medcac-meetings-index.aspx?bc=
BAAAAAAAAAAA&. We require that
you declare at the meeting whether you
have any financial involvement with
manufacturers (or their competitors) of
any items or services being discussed.
Speakers presenting at the MEDCAC
meeting should include a full disclosure
slide as their second slide in their
presentation for financial interests (for
example, type of financial association—
consultant, research support, advisory
board, and an indication of level, such
as minor association <$10,000 or major
association >$10,000) as well as
intellectual conflicts of interest (for
example, involvement in a federal or
nonfederal advisory committee that has
discussed the issue) that may pertain in
any way to the subject of this meeting.
If you are representing an organization,
we require that you also disclose
conflict of interest information for that
organization. If you do not have a
PowerPoint presentation, you will need
to present the full disclosure
information requested previously at the
beginning of your statement to the
Committee.
The Committee will deliberate openly
on the topics under consideration.
Interested persons may observe the
deliberations, but the Committee will
not hear further comments during this
time except at the request of the
chairperson. The Committee will also
allow a 15-minute unscheduled open
public session for any attendee to
address issues specific to the topics
under consideration. At the conclusion
of the day, the members will vote and
the Committee will make its
recommendation(s) to CMS.
III. Registration Instructions
CMS’ Coverage and Analysis Group is
coordinating meeting registration. While
there is no registration fee, individuals
must register to attend. You may register
online at https://www.cms.gov/apps/
events/upcoming
events.asp?strOrderBy=1&type=3 or by
phone by contacting the person listed in
the FOR FURTHER INFORMATION CONTACT
section of this notice by the deadline
listed in the DATES section of this notice.
Please provide your full name (as it
appears on your state-issued driver’s
E:\FR\FM\15JNN1.SGM
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Federal Register / Vol. 83, No. 116 / Friday, June 15, 2018 / Notices
sradovich on DSK3GMQ082PROD with NOTICES
license), address, organization,
telephone number(s), fax number, and
email address. You will receive a
registration confirmation with
instructions for your arrival at the CMS
complex or you will be notified that the
seating capacity has been reached.
meeting. The public may not enter the
building earlier than 45 minutes prior to the
convening of the meeting.
All visitors must be escorted in areas other
than the lower and first floor levels in the
Central Building.
IV. Security, Building, and Parking
Guidelines
This meeting will be held in a federal
government building; therefore, federal
security measures are applicable. The
Real ID Act, enacted in 2005, establishes
minimum standards for the issuance of
state-issued driver’s licenses and
identification (ID) cards. It prohibits
Federal agencies from accepting an
official driver’s license or ID card from
a state unless the Department of
Homeland Security determines that the
state meets these standards. Beginning
October 2015, photo IDs (such as a valid
driver’s license) issued by a state or
territory not in compliance with the
Real ID Act will not be accepted as
identification to enter Federal buildings.
Visitors from these states/territories will
need to provide alternative proof of
identification (such as a valid passport)
to gain entrance into CMS buildings.
The current list of states from which a
Federal agency may accept driver’s
licenses for an official purpose is found
at https://www.dhs.gov/real-idenforcement-brief. We recommend that
confirmed registrants arrive reasonably
early, but no earlier than 45 minutes
prior to the start of the meeting, to allow
additional time to clear security.
Security measures include the
following:
• Presentation of government-issued
photographic identification to the
Federal Protective Service or Guard
Service personnel.
• Inspection of vehicle’s interior and
exterior (this includes engine and trunk
inspection) at the entrance to the
grounds. Parking permits and
instructions will be issued after the
vehicle inspection.
• Inspection, via metal detector or
other applicable means, of all persons
entering the building. We note that all
items brought into CMS, whether
personal or for the purpose of
presentation or to support a
presentation, are subject to inspection.
We cannot assume responsibility for
coordinating the receipt, transfer,
transport, storage, set-up, safety, or
timely arrival of any personal
belongings or items used for
presentation or to support a
presentation.
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).
Note: Individuals who are not registered in
advance will not be permitted to enter the
building and will be unable to attend the
VerDate Sep<11>2014
17:11 Jun 14, 2018
Jkt 244001
V. Collection of Information
Authority: 5 U.S.C. App. 2, section 10(a).
Dated: June 4, 2018.
Kate Goodrich,
Director, Center for Clinical Standards and
Quality, Chief Medical Officer, Centers for
Medicare & Medicaid Services.
[FR Doc. 2018–12831 Filed 6–14–18; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Submission for OMB
Review; Public Comment Request;
State Councils on Developmental
Disabilities—Annual Program
Performance Report (PPR) (OMB
Control Number—0985–0033)
Administration on Intellectual
and Developmental Disabilities (AIDD),
Administration for Community Living
(ACL), U.S. Department of Health and
Human Services (HHS).
ACTION: Notice.
AGENCY:
The Administration for
Community Living is announcing that
the proposed collection of information
listed above has been submitted to the
Office of Management and Budget
(OMB) for review and clearance as
required under section 506(c)(2)(A) of
the Paperwork Reduction Act of 1995.
This 30-day notice collects comments
on the information collection
requirements related to the State
Councils on Developmental
Disabilities—Annual Program
Performance Report (PPR) [Proposed
Extension with Changes of a Currently
Approved Collection (ICR Rev)].
DATES: Submit written comments on the
collection of information by July 16,
2018.
SUMMARY:
Submit written comments
on the collection of information by:
ADDRESSES:
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Frm 00047
Fmt 4703
Sfmt 4703
27995
(a) Email to: OIRA_submission@
omb.eop.gov, Attn: OMB Desk Officer
for ACL;
(b) fax to 202.395.5806, Attn: OMB
Desk Officer for ACL; or
(c) by mail to the Office of
Information and Regulatory Affairs,
OMB, New Executive Office Bldg., 725
17th St. NW, Rm. 10235, Washington,
DC 20503, Attn: OMB Desk Officer for
ACL.
FOR FURTHER INFORMATION CONTACT: Sara
Newell-Perez at (202) 795–7413 or
Sara.Newell-Perez@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, ACL
has submitted the following proposed
collection of information to OMB for
review and clearance. The proposed
data collection represents a revision of
a currently approved information
collection (ICR-Rev). This collection is
necessary for the proper performance
and function of the agency. On an
annual basis, Councils are required to
submit a Program Performance Report
(PPR) to describe the extent to which
annual progress is being achieved on the
5-year State plan goals. The PPR will be
used by (1) the Council as a planning
document to track progress made in
meeting state plan goals; (2) the
citizenry of the State as a mechanism for
monitoring progress and activities on
the plans of the Council; and (3) the
Department as a stewardship tool for
ensuring compliance with the
Developmental Disabilities Assistance
and Bill of Rights Act of 2000 and for
monitoring and providing technical
assistance (e.g., during site visits), and
support for management decision
making.
Comments in Response to the 60-Day
Federal Register Notice
A notice was published in the Federal
Register on October 4, 2017 (Vol. 82,
Number 191; pp. 46246–46247). Two
comments were received. The first was
a comment about ACL and policies
around deinstitutionalization. The
second comment requested that
Councils have more transparency and
make their PPRs available to the public
via their websites. ACL appreciates and
understands these comments. Although
ACL recognizes that these comments
might provide useful information for the
program, it is not required to meet the
statutory requirements for this program.
No change is proposed.
The proposed template may be found
on the ACL website at https://
www.acl.gov/about-acl/public-input.
Estimated Program Burden
ACL estimates the burden of this
collection of information as follows: The
E:\FR\FM\15JNN1.SGM
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Agencies
[Federal Register Volume 83, Number 116 (Friday, June 15, 2018)]
[Notices]
[Pages 27993-27995]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-12831]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-3363-N]
Medicare Program; Meeting of the Medicare Evidence Development
and Coverage Advisory Committee--August 22, 2018
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Notice of meeting.
-----------------------------------------------------------------------
SUMMARY: This notice announces that a public meeting of the Medicare
Evidence Development & Coverage Advisory Committee (MEDCAC)
(``Committee'') will be held on Wednesday, August 22, 2018. This
meeting will focus on the state of evidence on Chimeric Antigen
Receptor (CAR) T-cell therapies that are approved by the Food and Drug
Administration (FDA). We are seeking the MEDCAC's recommendations
regarding collection of patient reported outcomes (PRO) in cancer
clinical studies. The MEDCAC will specifically focus on appraisal of
evidence-based PRO assessments to provide information that impacts
patients, their providers, and caregivers after a CAR T-cell therapy
intervention for the patient's cancer. This meeting is open to the
public in accordance with the Federal Advisory Committee Act.
DATES:
Meeting Date: The public meeting will be held on Wednesday, August
22, 2018 from 7:30 a.m. until 4:30 p.m., Eastern Daylight Time (EDT).
Deadline for Submission of Written Comments: Written comments must
be received at the address specified in the ADDRESSES section of this
notice by 5:00 p.m., EDT, Monday, July 16, 2018. Once submitted, all
comments are final.
Deadlines for Speaker Registration and Presentation Materials: The
[[Page 27994]]
deadline to register to be a speaker and to submit PowerPoint
presentation materials and writings that will be used in support of an
oral presentation is 5:00 p.m., EDT on Monday, July 16, 2018. Speakers
may register by phone or via email by contacting the person listed in
the FOR FURTHER INFORMATION CONTACT section of this notice.
Presentation materials must be received at the address specified in the
ADDRESSES section of this notice.
Deadline for All Other Attendees Registration: Individuals may
register online at https://www.cms.gov/apps/events/upcomingevents.asp?strOrderBy=1&type=3 or by phone by contacting the
person listed in the FOR FURTHER INFORMATION CONTACT section of this
notice by 5:00 p.m. EDT, Wednesday, August 15, 2018.
We will be broadcasting the meeting live via Webcast at https://www.cms.gov/live/.
Deadline for Submitting a Request for Special Accommodations:
Persons attending the meeting who are hearing or visually impaired, or
have a condition that requires special assistance or accommodations,
are asked to contact the Executive Secretary as specified in the FOR
FURTHER INFORMATION CONTACT section of this notice no later than 5:00
p.m., EDT Friday, August 3, 2018.
ADDRESSES:
Meeting Location: The meeting will be held in the main auditorium
of the Centers for Medicare & Medicaid Services, 7500 Security
Boulevard, Baltimore, MD 21244.
Submission of Presentations and Comments: Presentation materials
and written comments that will be presented at the meeting must be
submitted via email to [email protected] or by regular
mail to the contact listed in the FOR FURTHER INFORMATION CONTACT
section of this notice by the date specified in the DATES section of
this notice.
FOR FURTHER INFORMATION CONTACT: Maria Ellis, Executive Secretary for
MEDCAC, Centers for Medicare & Medicaid Services, Center for Clinical
Standards and Quality, Coverage and Analysis Group, S3-02-01, 7500
Security Boulevard, Baltimore, MD 21244 or contact Ms. Ellis by phone
(410-786-0309) or via email at [email protected].
SUPPLEMENTARY INFORMATION:
I. Background
MEDCAC, formerly known as the Medicare Coverage Advisory Committee
(MCAC), is advisory in nature, with all final coverage decisions
resting with CMS. MEDCAC is used to supplement CMS' internal expertise.
Accordingly, the advice rendered by the MEDCAC is most useful when it
results from a process of full scientific inquiry and thoughtful
discussion, in an open forum, with careful framing of recommendations
and clear identification of the basis of those recommendations. MEDCAC
members are valued for their background, education, and expertise in a
wide variety of scientific, clinical, and other related fields. (For
more information on MCAC, see the MEDCAC Charter (https://www.cms.gov/Regulations-and-Guidance/Guidance/FACA/Downloads/medcaccharter.pdf) and
the CMS Guidance Document, Factors CMS Considers in Referring Topics to
the MEDCAC (https://www.cms.gov/medicare-coverage-database/details/medicare-coverage-document-details.aspx?MCDId=10)).
II. Meeting Topic and Format
This notice announces the Wednesday, August 22, 2018, public
meeting of the Committee. This meeting will focus on the state of
evidence on CAR-T cell therapies that are approved by the FDA. We are
seeking the MEDCAC's recommendations regarding collection of PRO in
cancer clinical studies. The MEDCAC will specifically focus on
appraisal of evidence-based PRO assessments to provide information that
impacts patients, their providers, and caregivers after a CAR T-cell
therapy intervention for the patient's cancer. Background information
about this topic, including panel materials, is available at https://www.cms.gov/medicare-coverage-database/indexes/medcac-meetings-index.aspx?bc=BAAAAAAAAAAA&. We will no longer be providing paper
copies of the handouts for the meeting. Electronic copies of all the
meeting materials will be on the CMS website no later than 2 business
days before the meeting. We encourage the participation of
organizations with expertise in the appraisal of the state of evidence
for patient reported outcomes, development of patient reported health
outcome measures, and use of patient reported health outcome
assessments in cancer clinical trials. This meeting is open to the
public. The Committee will hear oral presentations from the public for
approximately 45 minutes. Time allotted for each presentation may be
limited. If the number of registrants requesting to speak is greater
than can be reasonably accommodated during the scheduled open public
hearing session, we may conduct a lottery to determine the speakers for
the scheduled open public hearing session. The contact person will
notify interested persons regarding their request to speak by July 23,
2018. Your comments should focus on issues specific to the list of
topics that we have proposed to the Committee. The list of research
topics to be discussed at the meeting will be available on the
following website prior to the meeting: https://www.cms.gov/medicare-coverage-database/indexes/medcac-meetings-index.aspx?bc=BAAAAAAAAAAA&.
We require that you declare at the meeting whether you have any
financial involvement with manufacturers (or their competitors) of any
items or services being discussed. Speakers presenting at the MEDCAC
meeting should include a full disclosure slide as their second slide in
their presentation for financial interests (for example, type of
financial association--consultant, research support, advisory board,
and an indication of level, such as minor association <$10,000 or major
association >$10,000) as well as intellectual conflicts of interest
(for example, involvement in a federal or nonfederal advisory committee
that has discussed the issue) that may pertain in any way to the
subject of this meeting. If you are representing an organization, we
require that you also disclose conflict of interest information for
that organization. If you do not have a PowerPoint presentation, you
will need to present the full disclosure information requested
previously at the beginning of your statement to the Committee.
The Committee will deliberate openly on the topics under
consideration. Interested persons may observe the deliberations, but
the Committee will not hear further comments during this time except at
the request of the chairperson. The Committee will also allow a 15-
minute unscheduled open public session for any attendee to address
issues specific to the topics under consideration. At the conclusion of
the day, the members will vote and the Committee will make its
recommendation(s) to CMS.
III. Registration Instructions
CMS' Coverage and Analysis Group is coordinating meeting
registration. While there is no registration fee, individuals must
register to attend. You may register online at https://www.cms.gov/apps/events/upcomingevents.asp?strOrderBy=1&type=3 or by phone by contacting
the person listed in the FOR FURTHER INFORMATION CONTACT section of
this notice by the deadline listed in the DATES section of this notice.
Please provide your full name (as it appears on your state-issued
driver's
[[Page 27995]]
license), address, organization, telephone number(s), fax number, and
email address. You will receive a registration confirmation with
instructions for your arrival at the CMS complex or you will be
notified that the seating capacity has been reached.
IV. Security, Building, and Parking Guidelines
This meeting will be held in a federal government building;
therefore, federal security measures are applicable. The Real ID Act,
enacted in 2005, establishes minimum standards for the issuance of
state-issued driver's licenses and identification (ID) cards. It
prohibits Federal agencies from accepting an official driver's license
or ID card from a state unless the Department of Homeland Security
determines that the state meets these standards. Beginning October
2015, photo IDs (such as a valid driver's license) issued by a state or
territory not in compliance with the Real ID Act will not be accepted
as identification to enter Federal buildings. Visitors from these
states/territories will need to provide alternative proof of
identification (such as a valid passport) to gain entrance into CMS
buildings. The current list of states from which a Federal agency may
accept driver's licenses for an official purpose is found at https://www.dhs.gov/real-id-enforcement-brief. We recommend that confirmed
registrants arrive reasonably early, but no earlier than 45 minutes
prior to the start of the meeting, to allow additional time to clear
security. Security measures include the following:
Presentation of government-issued photographic
identification to the Federal Protective Service or Guard Service
personnel.
Inspection of vehicle's interior and exterior (this
includes engine and trunk inspection) at the entrance to the grounds.
Parking permits and instructions will be issued after the vehicle
inspection.
Inspection, via metal detector or other applicable means,
of all persons entering the building. We note that all items brought
into CMS, whether personal or for the purpose of presentation or to
support a presentation, are subject to inspection. We cannot assume
responsibility for coordinating the receipt, transfer, transport,
storage, set-up, safety, or timely arrival of any personal belongings
or items used for presentation or to support a presentation.
Note: Individuals who are not registered in advance will not be
permitted to enter the building and will be unable to attend the
meeting. The public may not enter the building earlier than 45
minutes prior to the convening of the meeting.
All visitors must be escorted in areas other than the lower and
first floor levels in the Central Building.
V. Collection of Information
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).
Authority: 5 U.S.C. App. 2, section 10(a).
Dated: June 4, 2018.
Kate Goodrich,
Director, Center for Clinical Standards and Quality, Chief Medical
Officer, Centers for Medicare & Medicaid Services.
[FR Doc. 2018-12831 Filed 6-14-18; 8:45 am]
BILLING CODE 4120-01-P