Agency Information Collection Activities: Proposed Collection; Comment Request, 15037-15038 [2023-04935]
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Federal Register / Vol. 88, No. 47 / Friday, March 10, 2023 / Notices
the inpatient population it intends to
serve will meet the requirements of the
IPPS exclusion criteria for IRFs. The
completed CMS–437A and 437B forms
are submitted to the State Agency (SA)
no later than 5 months before the date
the IRF unit or hospital would become
subject to Inpatient Rehabilitation
Facility Prospective Payment System
(IRF–PPS). For IRF units and hospitals
already excluded from the IPPS, annual
onsite re-verification surveys by the SA
are no longer required. IRF units and
hospitals must now re-attest to meeting
the exclusion criteria every 3 years
thereafter.
IRF units and hospitals that have
already been excluded need not reapply
for exclusion. These facilities will
automatically be reevaluated yearly to
determine whether they continue to
meet the exclusion criteria. For the triannual re-verification, IRF units and
hospitals will be provided with a copy
of the appropriate CMS–437 worksheet
at least 5-months prior to the beginning
of its cost reporting period, so that the
IRF unit or hospital official may
complete and sign an attestation
statement and complete and return the
appropriate form CMS–437A or CMS–
437B at least 5-months prior to the
beginning of the cost reporting period.
However, Fiscal Intermediaries (FIs)
will continue to verify, on an annual
basis, compliance with the 60 percent
rule (42 CFR 412.29(b)(2)) for IRF units
and hospitals through a sample of
medical records and the SA will verify
the medical director requirement.
The SA will notify the RO at least 60
days prior to the end of the IRF unit’s
or hospital’s cost reporting period of the
status of compliance or non-compliance
with the payment requirements. The
information collected on the 437A and
437B forms, along with other
information submitted by the IRF is
necessary for determining the IRF’s IPPS
exclusion status. We have revised the
CMS–437A and 437B forms so that they
more adequately reflect the regulatory
requirements of § 412.20 to § 412.29.
More specifically, we have updated the
text in the 3rd column of the form,
which tells the facility what actions
must be taken and what information
must be verified to receive IPPS
excluded status. Subsequent to
publication of the 60-day Federal
Register notice (87 FR 48482) and notice
extending the comment period for the
60-day notice (87 FR 61333), the
collection instrument was revised to
correct errors in the guidance and
verification requirements sections of the
forms. Form Number: CMS–437A and
CMS–437B (OMB control number:
0938–0986); Frequency: tri-annually;
VerDate Sep<11>2014
17:45 Mar 09, 2023
Jkt 259001
Affected Public: Private sector (Business
or other for-profits); Number of
Respondents: 497; Total Annual
Responses: 497; Total Annual Hours:
497. (For policy questions regarding this
collection contact Caroline Gallaher at
410–786–8705).
2. Type of Information Collection
Request: New Collection; Title of
Information Collection: Medicare Plan
Performance Warning Information; Use:
The Centers for Medicare & Medicaid
Services (CMS) is seeking approval to
collect information to assist in the
Agency’s response to two reports from
the Department of Health and Human
Services Office of the Inspector General
(OIG) related to how the agency conveys
information on plan performance.
CMS is conducting this research to
respond to OIG’s recommendations
related to sharing additional
information with beneficiaries on plan
performance in a clear and accessible
format, particularly related to
information which may warn or caution
beneficiaries about plan performance
issues. CMS is seeking to learn more
about how beneficiaries, caregivers, and
the intermediaries who assist them use
and understand the information CMS
currently makes (or may make)
available, as well as to assess their
interest in accessing this information.
Form number: CMS–10836 (OMB
control number: 0938–New); Frequency:
Annually; Affected Public: Individuals
and Households; Number of
Respondents: 288; Number of
Responses: 288; Total Burden Hours:
561 (For questions regarding this
collection contact Elizabeth Goldstein at
443 845–6993).
Dated: March 6, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2023–04889 Filed 3–9–23; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers CMS–10834]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
PO 00000
Frm 00068
Fmt 4703
Sfmt 4703
15037
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.
SUMMARY:
Comments must be received by
May 9, 2023.
DATES:
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/PRAListing.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
William N. Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION:
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15038
Federal Register / Vol. 88, No. 47 / Friday, March 10, 2023 / Notices
lotter on DSK11XQN23PROD with NOTICES1
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–10834 Requirement for Electronic
Prescribing for Controlled Substances
(EPCS) for a Covered Part D Drug
Under a Prescription Drug Plan or an
MA–PD Plan
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: Requirement for
Electronic Prescribing for Controlled
Substances (EPCS) for a Covered Part D
Drug Under a Prescription Drug Plan or
an MA–PD Plan; Use: Section 2003 of
the SUPPORT for Patients and
Communities Act of 2018 requires that
prescribing of a Schedule II, III, IV, and
V controlled substance under Medicare
Part D be done electronically in
accordance with an electronic
prescription drug program beginning
January 1, 2021, subject to any
exceptions, which HHS may specify. In
the calendar year (CY) 2021 and 2022
Physician Fee Schedule (PFS) final
rules, CMS finalized the electronic
prescribing for controlled substances
(EPCS) requirements and exceptions at
42 CFR 423.160(a)(5). Compliance for
prescribers not in long-term care
facilities begins in CY 2023. Compliance
for prescribers in long-term care
facilities begins in CY 2025.
EPCS requirements do not require
prescribers or pharmacies to submit
additional data to CMS; however, CMS
did finalize one exception that requires
VerDate Sep<11>2014
17:45 Mar 09, 2023
Jkt 259001
data collection. The EPCS exception, at
§ 423.160(a)(5)(iv), requires a prescriber
to apply for a waiver if the prescriber is
unable to conduct EPCS due to
circumstances beyond the prescriber’s
control. This collection of information is
necessary to provide adequate and
timely exception from the EPCS
requirements if the prescriber is unable
to conduct EPCS due to circumstances
beyond the prescriber’s control. Form
Number: CMS–10834 (OMB control
number: 0938–NEW); Frequency:
Annually; Affected Public: Private
Sector (Business or other for-profits,
Not-for-Profit Institutions), and Public
sector (State, Local or Tribal
Governments); Number of Respondents:
100; Total Annual Responses: 100; Total
Annual Hours: 17. (For policy questions
regarding this collection contact Mei
Zhang at (410) 786–7837).
Dated: March 7, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2023–04935 Filed 3–9–23; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review; National
Communication System for Runaway
and Homeless Youth, Currently
Operated by the National Runaway
Safeline (NRS) Data Collection (New
Collection)
Family and Youth Services
Bureau, Administration for Children
and Families, HHS.
ACTION: Request for public comment.
AGENCY:
The Family and Youth
Services Bureau’s (FYSB) Runaway and
Homeless Youth Division has a
legislative requirement to fund a
National Communication System, which
is currently operated by the National
Runaway Safeline (NRS). The NRS
provides information, referral services,
crisis intervention, and prevention
resources to vulnerable youth at risk of
running away and/or becoming
homeless and their families or legal
guardians at no cost. When necessary,
the NRS refers runaway and homeless
youth to shelters, counseling, medical
assistance, and other vital services. The
NRS collects information from all
contacts with youth and adults
connecting with the NRS (i.e., parents,
family members, legal guardians, service
SUMMARY:
PO 00000
Frm 00069
Fmt 4703
Sfmt 4703
providers) on a voluntary basis to
inform crisis services and develop an
annual report on the information
collected during calls, chats, emails, and
forum posts from young people who
reached out to the NRS’s crisis services.
DATES: Comments due within 30 days of
publication. OMB must make a decision
about the collection of information
between 30 and 60 days after
publication of this document in the
Federal Register. Therefore, a comment
is best assured of having its full effect
if OMB receives it within 30 days of
publication.
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. You can also obtain
copies of the proposed collection of
information by emailing infocollection@
acf.hhs.gov. Identify all emailed
requests by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: The NRS is required to
have a system for collecting and
analyzing data to report on calls, emails,
chat, texts, and online messages
received as well as other information,
such as prevention resources, referrals,
demographics, and visitors to the NRS
website. The NRS must submit monthly
and semi-annual reports that include
the following:
• Number of calls received, answered,
and missed.
• Number of chats, emails, and texts
received; number of chats, emails, and
texts answered; and number of chats,
emails, and texts that were missed and
did not receive a response, in which the
users are youth in crisis, runaway
youth, and youth experiencing
homelessness.
• Number of parents, legal guardians,
and service providers contacting the
NRS and the type of resources,
interventions, and technical support/
assistance requested and provided.
• Number and type of prevention
materials disseminated to communities,
especially to underserved populations.
• Number and type of unique visitors
to the NRS’ website.
• Information on referrals provided
and where youth were referred for
services.
• Information on the callers’ or users’
demographics and where they were
located when contacting the NRS.
ADDRESSES:
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Agencies
[Federal Register Volume 88, Number 47 (Friday, March 10, 2023)]
[Notices]
[Pages 15037-15038]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-04935]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers CMS-10834]
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 May 9, 2023.
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:
[[Page 15038]]
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-10834 Requirement for Electronic Prescribing for Controlled
Substances (EPCS) for a Covered Part D Drug Under a Prescription Drug
Plan or an MA-PD Plan
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:
Requirement for Electronic Prescribing for Controlled Substances (EPCS)
for a Covered Part D Drug Under a Prescription Drug Plan or an MA-PD
Plan; Use: Section 2003 of the SUPPORT for Patients and Communities Act
of 2018 requires that prescribing of a Schedule II, III, IV, and V
controlled substance under Medicare Part D be done electronically in
accordance with an electronic prescription drug program beginning
January 1, 2021, subject to any exceptions, which HHS may specify. In
the calendar year (CY) 2021 and 2022 Physician Fee Schedule (PFS) final
rules, CMS finalized the electronic prescribing for controlled
substances (EPCS) requirements and exceptions at 42 CFR 423.160(a)(5).
Compliance for prescribers not in long-term care facilities begins in
CY 2023. Compliance for prescribers in long-term care facilities begins
in CY 2025.
EPCS requirements do not require prescribers or pharmacies to
submit additional data to CMS; however, CMS did finalize one exception
that requires data collection. The EPCS exception, at Sec.
423.160(a)(5)(iv), requires a prescriber to apply for a waiver if the
prescriber is unable to conduct EPCS due to circumstances beyond the
prescriber's control. This collection of information is necessary to
provide adequate and timely exception from the EPCS requirements if the
prescriber is unable to conduct EPCS due to circumstances beyond the
prescriber's control. Form Number: CMS-10834 (OMB control number: 0938-
NEW); Frequency: Annually; Affected Public: Private Sector (Business or
other for-profits, Not-for-Profit Institutions), and Public sector
(State, Local or Tribal Governments); Number of Respondents: 100; Total
Annual Responses: 100; Total Annual Hours: 17. (For policy questions
regarding this collection contact Mei Zhang at (410) 786-7837).
Dated: March 7, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2023-04935 Filed 3-9-23; 8:45 am]
BILLING CODE 4120-01-P