Agency Information Collection Activities: Proposed Collection; Comment Request, 7457-7458 [2022-02738]
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Federal Register / Vol. 87, No. 27 / Wednesday, February 9, 2022 / Notices
committee management activities, for both
the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Strategic Business Initiatives Unit,
Office of the Chief Operating Officer, Centers
for Disease Control and Prevention.
[FR Doc. 2022–02648 Filed 2–8–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10545 and
CMS–10520]
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 (the
PRA), Federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
the necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions,
the accuracy of the estimated burden,
ways to enhance the quality, utility, and
clarity of the information to be
collected, and the use of automated
collection techniques or other forms of
information technology to minimize the
information collection burden.
DATES: Comments must be received by
April 11, 2022.
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’’
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SUMMARY:
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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, you may make your request
using one of following:
1. Access CMS’ website address at
website address at https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.
FOR FURTHER INFORMATION CONTACT:
William N. Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10545 Outcome and Assessment
Information Set OASIS–E
CMS–10520 Marketplace Quality
Standards
Under the PRA (44 U.S.C. 3501–
3520), federal agencies must obtain
approval from the Office of Management
and Budget (OMB) for each collection of
information they conduct or sponsor.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
Information Collection
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Outcome and
Assessment Information Set OASIS–E;
Use: This request is for OMB approval
PO 00000
Frm 00036
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7457
to modify the Outcome and Assessment
Information Set (OASIS) that home
health agencies (HHAs) are required to
collect in order to participate in the
Medicare program. The current version
of the OASIS, OASIS–D (0938–1279)
data item set was approved by the Office
of Management and Budget (OMB) on
December 6, 2018 and implemented on
January 1, 2019. We are seeking OMB
approval for the proposed revised
OASIS item set, referred to hereafter as
OASIS–E, scheduled for
implementation on January 1, 2023. The
OASIS–E includes changes pursuant to
the Improving Medicare Post-Acute Care
Transformation Act of 2014 (the
IMPACT Act); and, to accommodate
data element removals to reduce
burden; and improve formatting
throughout the document. Form
Number: CMS–10545 (OMB control
number: 0938–1279); Frequency:
Occasionally; Affected Public: Private
Sector (Business or other for-profit and
Not-for-profit institutions); Number of
Respondents: 11,354; Total Annual
Responses: 18,030,766; Total Annual
Hours: 13,139,904. (For policy questions
regarding this collection contact Joan
Proctor at 410–786–0949).
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Marketplace
Quality Standards; Use: The Patient
Protection and Affordable Care Act
establishes requirements to support the
delivery of quality health care coverage
for health insurance issuers offering
Qualified Health Plans (QHPs) in
Exchanges. Section 1311(c)(3) of the
Patient Protection and Affordable Care
Act directs the Secretary to develop a
system to rate QHPs on the basis of
quality and price and requires
Exchanges to display this quality rating
information on their respective
websites. Section 1311(c)(4) of the
Patient Protection and Affordable Care
Act requires the Secretary to develop an
enrollee satisfaction survey system to
assess enrollee experience with each
QHP (with more than 500 enrollees in
the previous year) offered through an
Exchange. Section 1311(h) requires
QHPs to contract with certain hospitals
that meet specific patient safety and
health care quality standards.
This collection of information is
necessary to provide adequate and
timely health care quality information
for consumers, regulators, and
Exchanges as well as to collect
information to appropriately monitor
and provide a process for a survey
vendor to appeal HHS’ decision to not
approve a QHP Enrollee Survey vendor
application. Form Number: CMS–10520
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Federal Register / Vol. 87, No. 27 / Wednesday, February 9, 2022 / Notices
(OMB control number: 0938–1249);
Frequency: Annually; Affected Public:
Public sector (Individuals and
Households); Private sector (Business or
other for-profits and Not-for-profit
institutions); Number of Respondents:
314; Total Annual Responses: 314; Total
Annual Hours: 384,014. For policy
questions regarding this collection
contact Nidhi Singh Shah at 301–492–
5110.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: February 4, 2022.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
AGENCY:
[FR Doc. 2022–02738 Filed 2–8–22; 8:45 am]
BILLING CODE 4120–01–P
[CMS–9133–N]
It is
possible that an interested party may
need specific information and not be
able to determine from the listed
information whether the issuance or
regulation would fulfill that need.
Consequently, we are providing contact
persons to answer general questions
concerning each of the addenda
published in this notice.
FOR FURTHER INFORMATION CONTACT:
Medicare and Medicaid Programs;
Quarterly Listing of Program
Issuances—October through
December 2021
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
This quarterly notice lists
CMS manual instructions, substantive
and interpretive regulations, and other
SUMMARY:
Addenda
Contact
I CMS Manual Instructions ..............................
II Regulation Documents Published in the
Federal Register.
III CMS Rulings ...............................................
IV Medicare National Coverage Determinations.
V FDA-Approved Category B IDEs .................
VI Collections of Information ...........................
VII Medicare –Approved Carotid Stent Facilities.
VIII American College of Cardiology-National
Cardiovascular Data Registry Sites.
IX Medicare’s Active Coverage-Related Guidance Documents.
X One-time Notices Regarding National Coverage Provisions.
XI National Oncologic Positron Emission Tomography Registry Sites.
XII Medicare-Approved Ventricular Assist Device (Destination Therapy) Facilities.
XIII Medicare-Approved Lung Volume Reduction Surgery Facilities.
XIV Medicare-Approved Bariatric Surgery Facilities.
XV Fluorodeoxyglucose Positron Emission
Tomography for Dementia Trials.
All Other Information .........................................
Ismael Torres ...................................................
Terri Plumb .......................................................
(410) 786–1864
(410) 786–4481
Tiffany Lafferty ..................................................
Wanda Belle, MPA ...........................................
(410)786–7548
(410) 786–7491
John Manlove ...................................................
William Parham ................................................
Sarah Fulton, MHS ...........................................
(410) 786–6877
(410) 786–4669
(410) 786–2749
Sarah Fulton, MHS ...........................................
(410) 786–2749
JoAnna Baldwin, MS ........................................
(410) 786–7205
JoAnna Baldwin, MS ........................................
(410) 786–7205
David Dolan, MBA ............................................
(410) 786–3365
David Dolan, MBA ............................................
(410) 786–3365
Sarah Fulton, MHS ...........................................
(410) 786–2749
Sarah Fulton, MHS ...........................................
(410) 786–2749
David Dolan, MBA ............................................
(410) 786–3365
Annette Brewer .................................................
(410) 786–6580
SUPPLEMENTARY INFORMATION:
Association of Insurance Commissioners
(NAIC), health insurers, and other
stakeholders. To implement the various
statutes on which the programs are
based, we issue regulations under the
authority granted to the Secretary of the
Department of Health and Human
Services under sections 1102, 1871,
1902, and related provisions of the
Social Security Act (the Act) and Public
Health Service Act. We also issue
various manuals, memoranda, and
statements necessary to administer and
oversee the programs efficiently.
Section 1871(c) of the Act requires
that we publish a list of all Medicare
manual instructions, interpretive rules,
statements of policy, and guidelines of
general applicability not issued as
regulations at least every 3 months in
the Federal Register.
I. Background
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Centers for Medicare & Medicaid
Services
Federal Register notices that were
published from July through September
2021, relating to the Medicare and
Medicaid programs and other programs
administered by CMS.
The Centers for Medicare & Medicaid
Services (CMS) is responsible for
administering the Medicare and
Medicaid programs and coordination
and oversight of private health
insurance. Administration and oversight
of these programs involves the
following: (1) Furnishing information to
Medicare and Medicaid beneficiaries,
health care providers, and the public;
and (2) maintaining effective
communications with CMS regional
offices, state governments, state
Medicaid agencies, state survey
agencies, various providers of health
care, all Medicare contractors that
process claims and pay bills, National
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Phone No.
II. Format for the Quarterly Issuance
Notices
This quarterly notice provides only
the specific updates that have occurred
in the 3-month period along with a
hyperlink to the full listing that is
available on the CMS website or the
appropriate data registries that are used
as our resources. This is the most
current up-to-date information and will
be available earlier than we publish our
quarterly notice. We believe the website
list provides more timely access for
beneficiaries, providers, and suppliers.
We also believe the website offers a
more convenient tool for the public to
find the full list of qualified providers
E:\FR\FM\09FEN1.SGM
09FEN1
Agencies
[Federal Register Volume 87, Number 27 (Wednesday, February 9, 2022)]
[Notices]
[Pages 7457-7458]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-02738]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-10545 and CMS-10520]
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 (the PRA), Federal agencies are required to publish notice
in the Federal Register concerning each proposed collection of
information (including each proposed extension or reinstatement of an
existing collection of information) and to allow 60 days for public
comment on the proposed action. Interested persons are invited to send
comments regarding our burden estimates or any other aspect of this
collection of information, including the necessity and utility of the
proposed information collection for the proper performance of the
agency's functions, the accuracy of the estimated burden, ways to
enhance the quality, utility, and clarity of the information to be
collected, and the use of automated collection techniques or other
forms of information technology to minimize the information collection
burden.
DATES: Comments must be received by April 11, 2022.
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, you may make
your request using one of following:
1. Access CMS' website address at website address at 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-10545 Outcome and Assessment Information Set OASIS-E
CMS-10520 Marketplace Quality Standards
Under the PRA (44 U.S.C. 3501-3520), federal agencies must obtain
approval from the Office of Management and Budget (OMB) for each
collection of information they conduct or sponsor. The term
``collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests or requirements that members of
the public submit reports, keep records, or provide information to a
third party. Section 3506(c)(2)(A) of the PRA requires federal agencies
to publish a 60-day notice in the Federal Register concerning each
proposed collection of information, including each proposed extension
or reinstatement of an existing collection of information, before
submitting the collection to OMB for approval. To comply with this
requirement, CMS is publishing this notice.
Information Collection
1. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Outcome and
Assessment Information Set OASIS-E; Use: This request is for OMB
approval to modify the Outcome and Assessment Information Set (OASIS)
that home health agencies (HHAs) are required to collect in order to
participate in the Medicare program. The current version of the OASIS,
OASIS-D (0938-1279) data item set was approved by the Office of
Management and Budget (OMB) on December 6, 2018 and implemented on
January 1, 2019. We are seeking OMB approval for the proposed revised
OASIS item set, referred to hereafter as OASIS-E, scheduled for
implementation on January 1, 2023. The OASIS-E includes changes
pursuant to the Improving Medicare Post-Acute Care Transformation Act
of 2014 (the IMPACT Act); and, to accommodate data element removals to
reduce burden; and improve formatting throughout the document. Form
Number: CMS-10545 (OMB control number: 0938-1279); Frequency:
Occasionally; Affected Public: Private Sector (Business or other for-
profit and Not-for-profit institutions); Number of Respondents: 11,354;
Total Annual Responses: 18,030,766; Total Annual Hours: 13,139,904.
(For policy questions regarding this collection contact Joan Proctor at
410-786-0949).
2. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Marketplace
Quality Standards; Use: The Patient Protection and Affordable Care Act
establishes requirements to support the delivery of quality health care
coverage for health insurance issuers offering Qualified Health Plans
(QHPs) in Exchanges. Section 1311(c)(3) of the Patient Protection and
Affordable Care Act directs the Secretary to develop a system to rate
QHPs on the basis of quality and price and requires Exchanges to
display this quality rating information on their respective websites.
Section 1311(c)(4) of the Patient Protection and Affordable Care Act
requires the Secretary to develop an enrollee satisfaction survey
system to assess enrollee experience with each QHP (with more than 500
enrollees in the previous year) offered through an Exchange. Section
1311(h) requires QHPs to contract with certain hospitals that meet
specific patient safety and health care quality standards.
This collection of information is necessary to provide adequate and
timely health care quality information for consumers, regulators, and
Exchanges as well as to collect information to appropriately monitor
and provide a process for a survey vendor to appeal HHS' decision to
not approve a QHP Enrollee Survey vendor application. Form Number: CMS-
10520
[[Page 7458]]
(OMB control number: 0938-1249); Frequency: Annually; Affected Public:
Public sector (Individuals and Households); Private sector (Business or
other for-profits and Not-for-profit institutions); Number of
Respondents: 314; Total Annual Responses: 314; Total Annual Hours:
384,014. For policy questions regarding this collection contact Nidhi
Singh Shah at 301-492-5110.
Dated: February 4, 2022.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2022-02738 Filed 2-8-22; 8:45 am]
BILLING CODE 4120-01-P