Agency Information Collection Activities: Submission for OMB Review; Comment Request, 57901-57903 [2024-15581]
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Federal Register / Vol. 89, No. 136 / Tuesday, July 16, 2024 / Notices
our regulations, which include, but are
not limited to the following:
• An onsite administrative review of
DNV’s: (1) Corporate policies; (2)
financial and human resources available
to accomplish the proposed surveys; (3)
procedures for training, monitoring, and
evaluation of its psychiatric hospital
surveyors; (4) ability to investigate and
respond appropriately to complaints
against accredited psychiatric hospitals;
and (5) survey review and decisionmaking process for accreditation.
• The comparison of DNV’s Medicare
psychiatric hospital accreditation
program standards to our current
Medicare hospitals Conditions of
Participation (CoPs) and psychiatric
hospital special CoPs.
• A documentation review of DNV’s
psychiatric hospital survey process to
do the following:
++ Determine the composition of the
survey team, surveyor qualifications,
and DNV’s ability to provide continuing
surveyor training.
++ Compare DNV’s processes to those
we require of State Survey Agencies,
including periodic re-survey and the
ability to investigate and respond
appropriately to complaints against
accredited psychiatric hospitals.
++ Evaluate DNV’s procedures for
monitoring psychiatric hospitals it has
found to be out of compliance with
DNV’s program requirements. (This
pertains only to monitoring procedures
when DNV identifies non-compliance. If
noncompliance is identified by a State
Survey Agency through a validation
survey, the State Survey Agency
monitors corrections as specified at
§ 488.9(c)(1)).
++ Assess DNV’s ability to report
deficiencies to the surveyed hospital
and respond to the psychiatric
hospital’s plan of correction in a timely
manner.
++ Establish DNV’s ability to provide
CMS with electronic data and reports
necessary for effective validation and
assessment of the organization’s survey
process.
++ Determine the adequacy of DNV’s
staff and other resources.
++ Confirm DNV’s ability to provide
adequate funding for performing
required surveys.
++ Confirm DNV’s policies with
respect to surveys being unannounced.
++ DNV’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.
++ Obtain DNV’s agreement to
provide CMS with a copy of the most
current accreditation survey together
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with any other information related to
the survey as we may require, including
corrective action plans.
++ As authorized under 488.8(h),
CMS reserves the right to conduct onsite
observations of accrediting organization
operations at any time as part of the
ongoing review and continuing
oversight of an AO’s performance.
In accordance with section
1865(a)(3)(A) of the Act, the February 6,
2024, proposed notice also solicited
public comments regarding whether
DNV’s requirements met or exceeded
the Medicare CoPs for psychiatric
hospitals. No comments were received
in response to our proposed notice.
IV. Provisions of the Final Notice
A. Differences Between DNV’s
Standards and Requirements for
Accreditation and Medicare Conditions
and Survey Requirements
We compared DNV’s psychiatric
hospital accreditation program
requirements and survey process with
the Medicare CoPs at 42 CFR part 482
subpart E, and the survey and
certification process requirements of
parts 488 and 489. Our review and
evaluation of DNV’s psychiatric hospital
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, DNV
has completed revising its standards
and certification processes in order to
meet the requirements at:
• Section 482.41(c)(2), to address the
requirements regarding the Health Care
Facilities Code waiver allowance.
• Section 488.5(4)(ii), to address the
requirements to include the requirement
for Life Safety Specialist to have
training or experience in the Health
Care Facilities Code.
B. Term of Approval
Based on our review and observations
described in section III of this final
notice, we have determined that DNV’s
psychiatric hospital accreditation
program requirements meet or exceed
our requirements, and its survey
processes are also comparable.
Therefore, we approve DNV as a
national accreditation organization for
psychiatric hospitals that request
participation in the Medicare program,
effective July 30, 2024 through July 30,
2028.
V. Collection of Information
Requirements
This document does not impose
information collection requirements,
that is, reporting, recordkeeping, or
third-party disclosure requirements.
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57901
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 the Centers for
Medicare & Medicaid Services (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.
Vanessa Garcia,
Federal Register Liaison, Centers for Medicare
& Medicaid Services.
[FR Doc. 2024–15519 Filed 7–15–24; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–P–0015A,
CMS–10316, and CMS–10054]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
AGENCY:
ACTION:
Notice.
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
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
SUMMARY:
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57902
Federal Register / Vol. 89, No. 136 / Tuesday, July 16, 2024 / Notices
Comments on the collection(s) of
information must be received by the
OMB desk officer by August 15, 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.
FOR FURTHER INFORMATION CONTACT:
William Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION: 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: Medicare
Current Beneficiary Survey (MCBS);
Use: CMS is the largest single payer of
health care in the United States. The
agency plays a direct or indirect role in
administering health insurance coverage
for more than 120 million people across
the Medicare, Medicaid, CHIP, and
Exchange populations. A critical aim for
CMS is to be an effective steward, major
force, and trustworthy partner in
supporting innovative approaches to
improving quality, accessibility, and
affordability in healthcare. CMS also
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DATES:
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aims to put patients first in the delivery
of their health care needs.
The MCBS is the most comprehensive
and complete survey available on the
Medicare population and is essential in
capturing information not otherwise
collected through operational or
administrative data on the Medicare
program. The MCBS is a nationallyrepresentative, longitudinal survey of
Medicare beneficiaries that is sponsored
by CMS and is directed by the Office of
Enterprise Data and Analytics (OEDA).
MCBS data collection includes both inperson and phone interviewing. The
survey captures beneficiary information
whether aged or disabled, living in the
community or facility, or serviced by
managed care or fee-for-service. Data
produced as part of the MCBS are
enhanced with administrative data (e.g.,
fee-for-service claims, prescription drug
event data, enrollment, etc.) to provide
users with more accurate and complete
estimates of total health care costs and
utilization. The MCBS has been
continuously fielded for more than 30
years, encompassing over 1.2 million
interviews and more than 140,000
survey participants. Respondents
participate in up to 11 interviews over
a four-year period. The MCBS provides
a holistic view of Medicare
beneficiaries’ social and medical risk
factors and rich information on the
relationship between these risk factors,
healthcare utilization, and health
outcomes—at a point in time and over
time.
The MCBS continues to provide
unique insight into the Medicare
program and helps CMS and its external
stakeholders better understand and
evaluate the impact of existing programs
and significant new policy initiatives. In
the past, MCBS data have been used to
assess potential changes to the Medicare
program. For example, the MCBS was
instrumental in supporting the
development and implementation of the
Medicare prescription drug benefit by
providing a means to evaluate
prescription drug costs and out-ofpocket burden for these drugs to
Medicare beneficiaries. Beginning in
2025, this proposed revision would add
new measures to the questionnaire and
remove a few items that are no longer
relevant for administration. The
revisions would result in a net increase
in respondent burden. Form Number:
CMS–P–0015A (OMB control number:
0938–0568); Frequency: Occasionally;
Affected Public: Business or other forprofits and Not-for-profits institutions;
Number of Respondents: 35,015; Total
Annual Responses: 35,015; Total
Annual Hours: 35,344. (For policy
questions regarding this collection
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contact: William Long at 410–786–
7927.)
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Implementation
of the Medicare Prescription Drug Plan
(PDP) and Medicare Advantage (MA)
Plan Disenrollment Reasons Survey;
Use: Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 (MMA) provides a requirement to
collect and report performance data for
Part D prescription drug plans. Section
1860D–4 (Information to Facilitate
Enrollment) of the MMA requires CMS
to conduct consumer satisfaction
surveys regarding the PDP and MA
contracts. Plan disenrollment is
generally believed to be a broad
indicator of beneficiary dissatisfaction
with some aspect of plan services, such
as access to care, customer service, cost
of the plan, services, benefits provided,
or quality of care.
This data collection complements the
enrollee beneficiary experience data
collected through the Medicare
Consumer Assessment of Healthcare
Providers and Systems (Medicare
CAHPS) survey by providing
information on the reasons for
disenrollment from a Medicare
Advantage (with or without prescription
drug coverage) or Prescription Drug
Plan.
The Disenrollment Survey results are
an important source of information for
CMS to monitor contract performance
and identify potential problems (e.g.,
plans providing incorrect information to
beneficiaries or creating access
problems). CMS uses the results to
monitor the quality of service that
Medicare beneficiaries get from
contracted plans and their providers
and to understand beneficiaries’
expectations relative to provided
benefits and services for MA and PDPs.
Form Number: CMS–10316 (OMB
control number: 0938–1113); Frequency:
Yearly; Affected Public: Individuals and
households; Number of Respondents:
36,050; Total Annual Responses:
36,050; Total Annual Hours: 6,730. (For
policy questions regarding this
collection contact Beth Simon at 415–
744–3780.)
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: New
Technology Services for Ambulatory
Payment Classifications Under
Outpatient Prospective Payment
System; Use: In the April 7, 2000 (65 FR
18434) final rule with comment period
(HCFA–1005–FC, RIN 0938–AI56) first
implementing the hospital outpatient
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khammond on DSKJM1Z7X2PROD with NOTICES
Federal Register / Vol. 89, No. 136 / Tuesday, July 16, 2024 / Notices
prospective payment system (OPPS), we
created a set of New Technology
ambulatory payment classifications
(APCs) to pay for certain new
technology services under the OPPS.
These APCs are intended to pay for new
technology services that were not
covered by the transitional pass-through
payments provisions authorized by the
Balanced Budget Refinement Act
(BBRA) of 1999.
Since implementation of the OPPS on
August 1, 2000, transitional passthrough payments have been made to
hospitals for certain drugs, biologicals,
and medical devices. These are
temporary additional payments required
by section 1833(t)(6) of the Social
Security Act which was added by
section 201(b) of the BBRA. The law
required the Secretary to make these
additional payments to hospitals for at
least 2 but no more than 3 years.
In the April 7, 2000 final rule with
comment period, we specified an
application process and the information
that must be supplied for us to consider
a request for payment under the New
Technology APCs (65 FR 18478). We
posted the application process on our
website at www.cms.hhs.gov. Services
were only considered eligible for
assignment to a New Technology APC if
we listed them in one of a number of
lists published in Medicare Program
Memoranda, which are posted to our
website (https://www.cms.gov/
medicare/regulations-guidance/
transmittals/cms-program-memoranda).
We established a quarterly application
process by which interested parties
could submit applications to us for
particular services. We assign new
services to the New Technology APCs
that we determine cannot be placed
appropriately in clinical APCs. Under
our current policy, we retain services in
a New Technology APC until we gain
sufficient information about actual
hospital costs incurred to furnish a new
technology service. Form Number:
CMS–10054 (OMB control number:
0938–0860); Frequency: Once; Affected
Public: Private sector, Business or other
for-profit; Number of Respondents: 25;
Number of Responses: 25; Total Annual
Hours: 400. (For policy questions
regarding this collection contact Josh
Mcfeeters at 410–786–9732.)
William N. Parham III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–15581 Filed 7–15–24; 8:45 am]
BILLING CODE 4120–01–P
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Announcing the Intent To Award a
Single-Source Supplement for the
National Paralysis Resource Center
(PRC)
Administration for Community
Living, HHS.
ACTION: Notice.
AGENCY:
The Administration for
Community Living (ACL) announces the
intent to award a single-source
supplement to the current cooperative
agreement held by the Christopher and
Dana Reeve Foundation. The National
Paralysis Resource Center (NPRC) is
operated by the Christopher and Dana
Reeve Foundation and offers important
programmatic opportunities for persons
with disabilities and older adults. The
NPRC provides comprehensive
information for people living with
spinal cord injury, paralysis, and
mobility-related disabilities and their
families. Resources include information
and referral by phone and email in
multiple languages; a peer and family
support mentoring program; a military
and veterans’ program; multicultural
outreach services; multiple quality of
life grants; and a national website. The
administrative supplement for FY 2024
will be in the amount of $1,300,000,
bringing the total award for FY 2024 to
$10,000,000.
DATES: The supplement award will be
issued to extend the project period to
August 1, 2024, through June 30, 2025.
FOR FURTHER INFORMATION CONTACT: For
further information or comments
regarding this program supplement,
contact Elizabeth Leef, U.S. Department
of Health and Human Services,
Administration for Community Living,
Administration on Disabilities, Office of
Disability Services Innovations;
telephone (202) 475–2482; email
elizabeth.leef@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: The
purpose of the supplemental funding is
to support the expansion the National
Paralysis Resource Center to improve
the health and quality of life of
individuals living with paralysis and
their families by raising awareness of
and facilitating access to a broad range
of services relevant to individuals with
paralysis. With the additional funding,
the NPRC will work to expand the
National Resource and Information
Center; increase the health and quality
of life of Americans with disabilities
living with paralysis; increase support
and resources to people with paralysis,
SUMMARY:
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57903
their families and caregivers; expand
collaboration with federal agencies and
other national organizations that have a
vested interested in the paralysis
community; and strengthen
performance measures.
Program Name: National Paralysis
Resource Center.
Recipient: Christopher and Dana
Reeve Foundation.
Period of Performance: The
supplement award will be issued for the
current project period, July 1, 2024,
through June 30, 2025.
Award Amount: $1,300,000.
Award Type: Cooperative Agreement.
Basis for Award: The Christopher and
Dana Reeve Foundation is currently
funded to carry out the National
Paralysis Resource Center (NPRC) for
the period of July 1, 2024, through June
30, 2025. As a result of the 2024 budget,
Congress appropriated additional funds
for the expansion of the NPRC. It would
be unnecessarily time consuming and
disruptive to the NPRC project and the
beneficiaries being served for the ACL to
establish a new grantee at this time
when critical services are presently
being provided in an efficient manner.
Statutory Authority: This program is
authorized under Section 317 of the
Public Health Service Act (42 U.S.C.
247(b–4)); Consolidated and Further
Continuing Appropriations Act, 2016,
Public Law 114–113 (Dec. 18, 2015).
Dated: July 10, 2024.
Alison Barkoff,
Principal Deputy Administrator for the
Administration for Community Living,
performing the delegable duties of the
Administrator and the Assistant Secretary for
Aging.
[FR Doc. 2024–15611 Filed 7–15–24; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2024–N–2888]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Substantial
Equivalence Reports for Tobacco
Products
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA, Agency, or we) is
announcing an opportunity for public
comment on the proposed collection of
certain information by the Agency.
Under the Paperwork Reduction Act of
SUMMARY:
E:\FR\FM\16JYN1.SGM
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Agencies
[Federal Register Volume 89, Number 136 (Tuesday, July 16, 2024)]
[Notices]
[Pages 57901-57903]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-15581]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-P-0015A, CMS-10316, and CMS-10054]
Agency Information Collection Activities: Submission for OMB
Review; 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 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 of automated collection techniques or other
forms of information technology to minimize the information collection
burden.
[[Page 57902]]
DATES: Comments on the collection(s) of information must be received by
the OMB desk officer by August 15, 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/PRA-Listing.
FOR FURTHER INFORMATION CONTACT: William Parham at (410) 786-4669.
SUPPLEMENTARY INFORMATION: 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: Medicare Current
Beneficiary Survey (MCBS); Use: CMS is the largest single payer of
health care in the United States. The agency plays a direct or indirect
role in administering health insurance coverage for more than 120
million people across the Medicare, Medicaid, CHIP, and Exchange
populations. A critical aim for CMS is to be an effective steward,
major force, and trustworthy partner in supporting innovative
approaches to improving quality, accessibility, and affordability in
healthcare. CMS also aims to put patients first in the delivery of
their health care needs.
The MCBS is the most comprehensive and complete survey available on
the Medicare population and is essential in capturing information not
otherwise collected through operational or administrative data on the
Medicare program. The MCBS is a nationally-representative, longitudinal
survey of Medicare beneficiaries that is sponsored by CMS and is
directed by the Office of Enterprise Data and Analytics (OEDA). MCBS
data collection includes both in-person and phone interviewing. The
survey captures beneficiary information whether aged or disabled,
living in the community or facility, or serviced by managed care or
fee-for-service. Data produced as part of the MCBS are enhanced with
administrative data (e.g., fee-for-service claims, prescription drug
event data, enrollment, etc.) to provide users with more accurate and
complete estimates of total health care costs and utilization. The MCBS
has been continuously fielded for more than 30 years, encompassing over
1.2 million interviews and more than 140,000 survey participants.
Respondents participate in up to 11 interviews over a four-year period.
The MCBS provides a holistic view of Medicare beneficiaries' social and
medical risk factors and rich information on the relationship between
these risk factors, healthcare utilization, and health outcomes--at a
point in time and over time.
The MCBS continues to provide unique insight into the Medicare
program and helps CMS and its external stakeholders better understand
and evaluate the impact of existing programs and significant new policy
initiatives. In the past, MCBS data have been used to assess potential
changes to the Medicare program. For example, the MCBS was instrumental
in supporting the development and implementation of the Medicare
prescription drug benefit by providing a means to evaluate prescription
drug costs and out-of-pocket burden for these drugs to Medicare
beneficiaries. Beginning in 2025, this proposed revision would add new
measures to the questionnaire and remove a few items that are no longer
relevant for administration. The revisions would result in a net
increase in respondent burden. Form Number: CMS-P-0015A (OMB control
number: 0938-0568); Frequency: Occasionally; Affected Public: Business
or other for-profits and Not-for-profits institutions; Number of
Respondents: 35,015; Total Annual Responses: 35,015; Total Annual
Hours: 35,344. (For policy questions regarding this collection contact:
William Long at 410-786-7927.)
2. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Implementation of
the Medicare Prescription Drug Plan (PDP) and Medicare Advantage (MA)
Plan Disenrollment Reasons Survey; Use: Medicare Prescription Drug,
Improvement, and Modernization Act of 2003 (MMA) provides a requirement
to collect and report performance data for Part D prescription drug
plans. Section 1860D-4 (Information to Facilitate Enrollment) of the
MMA requires CMS to conduct consumer satisfaction surveys regarding the
PDP and MA contracts. Plan disenrollment is generally believed to be a
broad indicator of beneficiary dissatisfaction with some aspect of plan
services, such as access to care, customer service, cost of the plan,
services, benefits provided, or quality of care.
This data collection complements the enrollee beneficiary
experience data collected through the Medicare Consumer Assessment of
Healthcare Providers and Systems (Medicare CAHPS) survey by providing
information on the reasons for disenrollment from a Medicare Advantage
(with or without prescription drug coverage) or Prescription Drug Plan.
The Disenrollment Survey results are an important source of
information for CMS to monitor contract performance and identify
potential problems (e.g., plans providing incorrect information to
beneficiaries or creating access problems). CMS uses the results to
monitor the quality of service that Medicare beneficiaries get from
contracted plans and their providers and to understand beneficiaries'
expectations relative to provided benefits and services for MA and
PDPs. Form Number: CMS-10316 (OMB control number: 0938-1113);
Frequency: Yearly; Affected Public: Individuals and households; Number
of Respondents: 36,050; Total Annual Responses: 36,050; Total Annual
Hours: 6,730. (For policy questions regarding this collection contact
Beth Simon at 415-744-3780.)
3. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: New Technology
Services for Ambulatory Payment Classifications Under Outpatient
Prospective Payment System; Use: In the April 7, 2000 (65 FR 18434)
final rule with comment period (HCFA-1005-FC, RIN 0938-AI56) first
implementing the hospital outpatient
[[Page 57903]]
prospective payment system (OPPS), we created a set of New Technology
ambulatory payment classifications (APCs) to pay for certain new
technology services under the OPPS. These APCs are intended to pay for
new technology services that were not covered by the transitional pass-
through payments provisions authorized by the Balanced Budget
Refinement Act (BBRA) of 1999.
Since implementation of the OPPS on August 1, 2000, transitional
pass-through payments have been made to hospitals for certain drugs,
biologicals, and medical devices. These are temporary additional
payments required by section 1833(t)(6) of the Social Security Act
which was added by section 201(b) of the BBRA. The law required the
Secretary to make these additional payments to hospitals for at least 2
but no more than 3 years.
In the April 7, 2000 final rule with comment period, we specified
an application process and the information that must be supplied for us
to consider a request for payment under the New Technology APCs (65 FR
18478). We posted the application process on our website at
www.cms.hhs.gov. Services were only considered eligible for assignment
to a New Technology APC if we listed them in one of a number of lists
published in Medicare Program Memoranda, which are posted to our
website (https://www.cms.gov/medicare/regulations-guidance/transmittals/cms-program-memoranda). We established a quarterly
application process by which interested parties could submit
applications to us for particular services. We assign new services to
the New Technology APCs that we determine cannot be placed
appropriately in clinical APCs. Under our current policy, we retain
services in a New Technology APC until we gain sufficient information
about actual hospital costs incurred to furnish a new technology
service. Form Number: CMS-10054 (OMB control number: 0938-0860);
Frequency: Once; Affected Public: Private sector, Business or other
for-profit; Number of Respondents: 25; Number of Responses: 25; Total
Annual Hours: 400. (For policy questions regarding this collection
contact Josh Mcfeeters at 410-786-9732.)
William N. Parham III,
Director, Division of Information Collections and Regulatory Impacts,
Office of Strategic Operations and Regulatory Affairs.
[FR Doc. 2024-15581 Filed 7-15-24; 8:45 am]
BILLING CODE 4120-01-P