Agency Information Collection Activities: Proposed Collection; Comment Request, 14847-14848 [2024-04302]
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Federal Register / Vol. 89, No. 41 / Thursday, February 29, 2024 / Notices
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.
khammond on DSKJM1Z7X2PROD with NOTICES
Information Collection
1. Type of Information Collection
Request: Extension of a currently
approved information collection; Title
of Information Collection: Generic
Clearance for the Center for Clinical
Standards and Quality IT Product and
Support Teams; Use: The CMS Center
for Clinical Standards and Quality
(CCSQ) is responsible for administering
appropriate information systems so that
the public can submit healthcare-related
information. While beneficiaries
ultimately benefit, the primary users of
CCSQ IT Product and Support Teams
(CIPST) systems are healthcare facility
employees and contractors. They are
responsible for the collection and
submission of appropriate beneficiary
data to CMS to receive merit-based
compensation.
The systems that support CCSQ
programs includes but is not limited to:
End-Stage Renal Disease Quality
Reporting System (EQRS), Enterprise
Shared Services (ESS), HCQIS
ServiceNow (SNOW), Hospital Quality
Reporting (HQR), Quality Improvement
and Evaluation System (iQIES), Quality
Management and Reporting System
(QMARS), and Quality Payment
Program (QPP).
The generic clearance will allow CMS
to gather information to improve
information systems that serve CMS
audiences. CMS will gather this
information using a mixture of
qualitative and quantitative consumer
research strategies (including formative
research studies and methodological
tests). CMS implements human-centered
methods and activities for the
improvement of policies, services, and
products. This collection of information
is necessary to enable CMS to garner
customer and stakeholder feedback in
an efficient, timely manner, in
accordance with our commitment to
improving service delivery.
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As information systems and
technologies are developed or improved
upon, they can be tested and evaluated
for end-user feedback regarding utility,
usability, and desirability. The overall
goal is to apply a human-centered
engagement model to maximize the
extent to which CIPST can gather
ongoing feedback from consumers.
Feedback helps engineers and designers
arrive at better solutions, therefore
minimizing the burden on consumers
and meeting their needs and goals.
The activities under this clearance
involve voluntary engagement with
target CCSQ users to receive design and
research feedback. The respondents will
be voluntary end-users from selfselected customers, as well as
convenience samples. It is our intent
that selected respondents will either
cover a broad range of customers or
include specific characteristics related
to certain products or services. All
collections of information will allow us
to continually refine our processes,
systems, and services for the benefit of
internal and external stakeholders. Form
Number: CMS–10706 (OMB control
number: 0938–1397); Frequency:
Occasionally; Affected Public:
Individuals and Private Sector (Business
or other for-profit and Not-for-profit
institutions); Number of Respondents:
54,750; Total Annual Responses:
54,750; Total Annual Hours: 17,850.
(For policy questions regarding this
collection contact Brandy Barnette at
410–786–6455).
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Cost-Sharing
Reduction Reconciliation Use: Under
established Department of Health and
Human Services (HHS) regulations,
although cost-sharing reduction (CSR)
payments are not being advanced to
qualified health plan (QHP) issuers at
the present time, issuers are still
permitted to submit data that compares
the CSR-eligible enrollment for each
issuer with their actual CSRs provided
by the issuer for covered services for
each eligible enrollee in a benefit year.
HHS will compare this CSR-eligible
enrollment with the actual CSRs
provided by the issuers that participate
in the optional data submission window
to verify the issuer’s reporting of CSRs
provided. This revised collection does
not add any data elements and
continues to make summary plan level
reporting optional.
Based upon CMS’ experience in the
CSR data collection and evaluation
process, CMS is not making any
substantive changes to this information
collection. The only changes are to
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14847
update the number of policies issuers
will report data for, based on the most
recent enrollment numbers in CSR plan
variants as of June 15, 2023. There are
no programmatic changes. The CSR
Issuer Summary Report and Standard
Methodology Template Plan and Policy
Report remain the same. Form Number:
CMS–10526 (OMB control number:
0938–1266); Frequency: Annually;
Affected Public: Private Sector, Business
or other for-profit and not-for-profit
institutions; Number of Respondents:
150; Number of Responses: 150; Total
Annual Hours: 2,362.5. (For policy
questions regarding this collection,
contact Deborah Noymer at 301–448–
3755.)
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–04151 Filed 2–28–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10882]
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.
SUMMARY:
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14848
Federal Register / Vol. 89, No. 41 / Thursday, February 29, 2024 / Notices
Comments must be received by
April 29, 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.
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:
khammond on DSKJM1Z7X2PROD with NOTICES
DATES:
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–10882 The Medicare Advantage
and Prescription Drug Programs: Part
C and Part D Medicare Prescription
Payment Plan Model Documents.
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
VerDate Sep<11>2014
16:39 Feb 28, 2024
Jkt 262001
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Information Collection
Proposed Information Collection
Activity; Generic Clearance for the
Comprehensive Child Welfare
Information System (CCWIS) Technical
Assistance and Review Process (Office
of Management and Budget #: 0970–
0568)
1. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: The Medicare
Advantage and Prescription Drug
Programs: Part C and Part D Medicare
Prescription Payment Plan Model
Documents; Use: Sections 1860D–
2(b)(2)(E)(v)(II)–(IV) of the Act state the
requirements for Part D sponsors and
MA organizations in implementing the
program, which include the processes
for outreach to enrollees identified as
likely to benefit, election, and
termination. Subsection II states that
any Part D enrollee may elect into the
program prior to (aa) or during (bb) the
plan year. Subsection III details that
PDP sponsors and MA organizations
must have a mechanism in place to
inform enrollees that they are likely to
benefit from electing into the program at
the point of sale (POS). Subsection
IV(aa) states that plans must terminate
a beneficiary’s participation in the
program when the beneficiary fails to
pay the amounts owed under this
program.
CMS has developed the six materials
in the attached package as model
notices in order to provide standardized
and consistent language for potential
and active program participants,
regardless of which Part D plan they
may be enrolled in. CMS will require
Part D plans to disseminate these
notices, as appropriate, to Part D
enrollees to fulfill the requirements of
the Sections 1860D–2(b)(2)(E)(v)(II)–(IV)
of the Act. Form Number: CMS–10882
(OMB control number: 0938–New);
Frequency: Yearly; Affected Public:
Private, Federal Government, Business
or other for profits, Not-for-profits
institutions; Number of Respondents:
1,065; Total Annual Responses: 3,195;
Total Annual Hours: 127,800. (For
policy questions regarding this
collection contact Michael Brown at
(872) 287–1370 or michael.brown3@
cms.hhs.gov.)
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–04302 Filed 2–28–24; 8:45 am]
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Administration for Children and
Families
Children’s Bureau,
Administration for Children and
Families, U.S. Department of Health and
Human Services.
ACTION: Request for public comments.
AGENCY:
The Children’s Bureau (CB),
Administration for Children and
Families (ACF), U.S. Department of
Health and Human Services (HHS) is
requesting a 3-year extension of the
Generic Clearance for the
Comprehensive Child Welfare
Information System (CCWIS) Technical
Assistance (TA) and Review Process,
(OMB #0970–0568, expiration 4/30/
2024) and all approved information
collections under this generic. There are
no changes requested to the terms of the
umbrella generic or to the currently
approved information collections.
DATES: Comments due within 60 days of
publication. In compliance with the
requirements of the Paperwork
Reduction Act of 1995, ACF is soliciting
public comment on the specific aspects
of the information collection described
above.
ADDRESSES: You can obtain copies of the
proposed collection of information and
submit comments by emailing info
collection@acf.hhs.gov. Identify all
requests by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: The CCWIS Technical
Assistance and Review information
collection includes two components.
The CCWIS Assessment Review
(CAR) Process.
TA tools for title IV–E agencies to selfassess their conformity to CCWIS
project and design requirements at 45
CFR 1355.52–3; The CCWIS
requirements at 45 CFR 1355.55 require
the review, assessment, and inspection
of the planning, design, development,
installation, operation, and maintenance
of each CCWIS project on a continuing
basis. The Advance Planning Document
(APD) regulations at 45 CFR 95.621
require periodic reviews of state and
local agency methods and practices to
ensure information systems, including
CCWIS, are utilized for purposes
SUMMARY:
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Agencies
[Federal Register Volume 89, Number 41 (Thursday, February 29, 2024)]
[Notices]
[Pages 14847-14848]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-04302]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10882]
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.
[[Page 14848]]
DATES: Comments must be received by April 29, 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-10882 The Medicare Advantage and Prescription Drug Programs: Part C
and Part D Medicare Prescription Payment Plan Model Documents.
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: New collection (Request
for a new OMB control number); Title of Information Collection: The
Medicare Advantage and Prescription Drug Programs: Part C and Part D
Medicare Prescription Payment Plan Model Documents; Use: Sections
1860D-2(b)(2)(E)(v)(II)-(IV) of the Act state the requirements for Part
D sponsors and MA organizations in implementing the program, which
include the processes for outreach to enrollees identified as likely to
benefit, election, and termination. Subsection II states that any Part
D enrollee may elect into the program prior to (aa) or during (bb) the
plan year. Subsection III details that PDP sponsors and MA
organizations must have a mechanism in place to inform enrollees that
they are likely to benefit from electing into the program at the point
of sale (POS). Subsection IV(aa) states that plans must terminate a
beneficiary's participation in the program when the beneficiary fails
to pay the amounts owed under this program.
CMS has developed the six materials in the attached package as
model notices in order to provide standardized and consistent language
for potential and active program participants, regardless of which Part
D plan they may be enrolled in. CMS will require Part D plans to
disseminate these notices, as appropriate, to Part D enrollees to
fulfill the requirements of the Sections 1860D-2(b)(2)(E)(v)(II)-(IV)
of the Act. Form Number: CMS-10882 (OMB control number: 0938-New);
Frequency: Yearly; Affected Public: Private, Federal Government,
Business or other for profits, Not-for-profits institutions; Number of
Respondents: 1,065; Total Annual Responses: 3,195; Total Annual Hours:
127,800. (For policy questions regarding this collection contact
Michael Brown at (872) 287-1370 or [email protected].)
William N. Parham, III,
Director, Division of Information Collections and Regulatory Impacts,
Office of Strategic Operations and Regulatory Affairs.
[FR Doc. 2024-04302 Filed 2-28-24; 8:45 am]
BILLING CODE 4120-01-P