Agency Information Collection Activities: Submission for OMB Review; Comment Request, 23679-23680 [2023-08182]
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Federal Register / Vol. 88, No. 74 / Tuesday, April 18, 2023 / Notices
Prevention and the Agency for Toxic
Substances and Disease Registry.
ACTION:
[FR Doc. 2023–08246 Filed 4–14–23; 4:15 pm]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Order of Succession
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: General notice.
AGENCY:
Section C–C, Order of Succession, is
hereby amended as follows:
Delete in its entirety Section C–C,
Order of Succession, and insert the
following:
During the absence or disability of the
Director, CDC, or in the event of a
vacancy in that office, the first official
listed below who is available shall act
as Director, except that during a
planned period of absence, the Director
may specify a different order of
succession:
1. Principal Deputy Director
2. Deputy Director for Program and
Science and CDC Chief Medical
Officer
3. Deputy Director for Global Health
4. Director of the Office of Readiness
and Response
5. Director of the National Center for
Emerging and Zoonotic Infectious
Diseases
6. Director of the National Institute for
Occupational Safety and Health
Robin Bailey,
Chief Operating Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2023–08169 Filed 4–17–23; 8:45 am]
BILLING CODE 4160–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
ddrumheller on DSK120RN23PROD with NOTICES1
Centers for Medicare & Medicaid
Services
[Document Identifiers CMS–10387]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
VerDate Sep<11>2014
18:08 Apr 17, 2023
Jkt 259001
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.
DATES: Comments on the collection(s) of
information must be received by the
OMB desk officer by May 18, 2023.
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
SUMMARY:
Kalwant Smagh,
Director, Strategic Business Initiatives Unit,
Office of the Chief Operating Officer, Centers
for Disease Control and Prevention.
AGENCY:
Notice.
PO 00000
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23679
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: Minimum Data
Set 3.0 Nursing Home and Swing Bed
Prospective Payment System (PPS) For
the collection of data related to the
Patient Driven Payment Model and the
Skilled Nursing Facility Quality
Reporting Program (QRP); Use: We are
requesting to implement to the MDS 3.0
v1.18.11 beginning October 1, 2023 to
October 1, 2026 in order to meet the
requirements of policies finalized in the
Federal Fiscal Year (FY) 2020 Skilled
Nursing Facility (SNF) Prospective
Payment System (PPS) final rule (84 FR
38728). The compliance date for the
finalized policies (10/01/2020) was
delayed due to the COVID–19 public
health emergency (PHE). While there
has been no change in assessment-level
burden since the approval of the MDS
3.0 v1.17.2, there has been a change in
total burden since 2019 when the
package was originally approved due to
a decrease in the number of MDS
assessments completed and a change in
the hourly rate for clinicians completing
the assessment.
We use the MDS 3.0 PPS Item Set to
collect the data used to reimburse
skilled nursing facilities for SNF-level
care furnished to Medicare beneficiaries
and to collect information for quality
measures and standardized patient
assessment data under the SNF QRP.
There have been some revisions to the
assessment tool since the approval of
MDS 3.0 vl.17.2. Form Number: CMS–
10387 (OMB control number: 0938–
1140); Frequency: Yearly; Affected
Public: Private Sector: Business or other
for-profit and not-for-profit institutions;
Number of Respondents: 15,472; Total
Annual Responses: 3,371,993; Total
Annual Hours: 2,866,194. (For policy
questions regarding this collection
contact Heidi Magladry at 410–786–
6034).
E:\FR\FM\18APN1.SGM
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23680
Federal Register / Vol. 88, No. 74 / Tuesday, April 18, 2023 / Notices
Dated: April 13, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2023–08182 Filed 4–17–23; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers CMS–10849]
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
June 20, 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.
ddrumheller on DSK120RN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
18:08 Apr 17, 2023
Jkt 259001
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:
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–10849 Drug Price Negotiation
Process under Sections 11001 and
11002 of the Inflation Reduction Act
(IRA)
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: Drug Price
Negotiation Process under Sections
11001 and 11002 of the Inflation
Reduction Act (IRA); Use: Under the
authority in sections 11001 and 11002
of the Inflation Reduction Act of 2022
PO 00000
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(Pub. L. 117–169), the Centers for
Medicare & Medicaid Services (CMS) is
implementing the Medicare Drug Price
Negotiation Program (the ‘‘Negotiation
Program’’), codified in sections 1191
through 1198 of the Social Security Act
(‘‘the Act’’). The Act establishes the
Negotiation Program to negotiate a
maximum fair price (‘‘MFP’’) with
manufacturers, defined at section
1191(c)(3) of the Act, for certain high
expenditure, single source drugs
covered under Medicare Part B and Part
D (‘‘selected drugs’’). For the first year
of the Negotiation Program, CMS will
select up to ten Part D high expenditure,
single source drugs for negotiation,
which will be published September 1,
2023. The MFPs that are negotiated for
these drugs will apply beginning in
initial price applicability year 2026. The
negotiation period for initial price
applicability year 2026 begins October
1, 2023, or on the date when the
manufacturer of a selected drug enters
into a Medicare Drug Price Negotiation
Program Agreement with CMS if that
date is prior to October 1, 2023.
The statute provides that, after
receiving CMS’ written initial offer, the
Primary Manufacturer may, in
accordance with section 1194(b)(2)(C) of
the Act, submit an optional written
counteroffer (if CMS’ written initial
offer is not accepted by the Primary
Manufacturer) that must be submitted
no later than 30 days after the date of
receipt of the written initial offer. If the
Primary Manufacturer chooses to
develop and submit a written
counteroffer to CMS’ written initial offer
during the drug price negotiation
process for initial price applicability
year 2026, the Primary Manufacturer
must submit the Counteroffer Form.
Form Number: CMS–10849 (OMB
control number: 0938-New); Frequency:
Once; Affected Public: Private Sector
and Business or other for-profits;
Number of Respondents: 10; Total
Annual Responses: 10; Total Annual
Hours: 793. For policy questions
regarding this collection contact Lara
Strawbridge at (410) 786–6880.
Dated: April 13, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2023–08181 Filed 4–17–23; 8:45 am]
BILLING CODE P
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]]>Agencies
[Federal Register Volume 88, Number 74 (Tuesday, April 18, 2023)]
[Notices]
[Pages 23679-23680]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-08182]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers CMS-10387]
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.
DATES: Comments on the collection(s) of information must be received by
the OMB desk officer by May 18, 2023.
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: Minimum Data Set
3.0 Nursing Home and Swing Bed Prospective Payment System (PPS) For the
collection of data related to the Patient Driven Payment Model and the
Skilled Nursing Facility Quality Reporting Program (QRP); Use: We are
requesting to implement to the MDS 3.0 v1.18.11 beginning October 1,
2023 to October 1, 2026 in order to meet the requirements of policies
finalized in the Federal Fiscal Year (FY) 2020 Skilled Nursing Facility
(SNF) Prospective Payment System (PPS) final rule (84 FR 38728). The
compliance date for the finalized policies (10/01/2020) was delayed due
to the COVID-19 public health emergency (PHE). While there has been no
change in assessment-level burden since the approval of the MDS 3.0
v1.17.2, there has been a change in total burden since 2019 when the
package was originally approved due to a decrease in the number of MDS
assessments completed and a change in the hourly rate for clinicians
completing the assessment.
We use the MDS 3.0 PPS Item Set to collect the data used to
reimburse skilled nursing facilities for SNF-level care furnished to
Medicare beneficiaries and to collect information for quality measures
and standardized patient assessment data under the SNF QRP. There have
been some revisions to the assessment tool since the approval of MDS
3.0 vl.17.2. Form Number: CMS-10387 (OMB control number: 0938-1140);
Frequency: Yearly; Affected Public: Private Sector: Business or other
for-profit and not-for-profit institutions; Number of Respondents:
15,472; Total Annual Responses: 3,371,993; Total Annual Hours:
2,866,194. (For policy questions regarding this collection contact
Heidi Magladry at 410-786-6034).
[[Page 23680]]
Dated: April 13, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2023-08182 Filed 4-17-23; 8:45 am]
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