Agency Information Collection Activities: Proposed Collection; Comment Request, 64463-64465 [2024-17484]
Download as PDF
Federal Register / Vol. 89, No. 152 / Wednesday, August 7, 2024 / Notices
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
October 7, 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
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–10237 Applications for Part C
Medicare Advantage, 1876 Cost Plans,
and Employer Group Waiver Plans to
Provide Part C Benefits
CMS–R–308 State Children’s Health
Insurance Program and Supporting
Regulations
Under the PRA (44 U.S.C. 3501–
3520), Federal agencies must obtain
VerDate Sep<11>2014
17:07 Aug 06, 2024
Jkt 262001
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 Collections
1. Type of Information Collection
Request: Revision of a currently
approved information collection; Title
of Information Collection: Applications
for Part C Medicare Advantage, 1876
Cost Plans, and Employer Group Waiver
Plans to Provide Part C Benefits; Use:
Collection of this information is
mandated by the Code of Federal
Regulations, MMA, and CMS
regulations at 42 CFR part 422, subpart
K, in ‘‘Application Procedures and
Contracts for Medicare Advantage
Organizations.’’ In addition, the
Medicare Improvement for Patients and
Providers Act of 2008 (MIPPA) further
amended titles XVII and XIX of the
Social Security Act.
This information collection includes
the process for organizations wishing to
provide healthcare services under MA
plans. These organizations must
complete an application annually (if
required), file a bid, and receive final
approval from CMS. The MA
application process has two options for
applicants that include (1) request for
new MA product or (2) request for
expanding the service area of an existing
product. CMS utilizes the application
process as the means to review, assess
and determine if applicants are
compliant with the current
requirements for participation in the
MA program and to make a decision
related to contract award. This
collection process is the only
mechanism for organizations to
complete the required MA application
process. Form Number: CMS–10237
(OMB control number: 0938–0935);
Frequency: Yearly; Affected Public:
Private Sector, Business or other forprofits, Not for-profits and Federal
Government; Number of Respondents:
500; Number of Responses: 500; Total
Annual Hours: 9,173. (For policy
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Fmt 4703
Sfmt 4703
64463
questions regarding this collection
contact Jackie Ford at 410–786–7767 or
Jacqueline.Ford@cms.hhs.gov).
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: State Children’s
Health Insurance Program and
Supporting Regulations; Use: States
must submit title XXI plans and
amendments for approval by the
Secretary. We use the plan and its
subsequent amendments to determine if
the state has met the requirements of
title XXI. Information provided in the
state plan, state plan amendments, and
from the other information we are
collecting will be used by advocacy
groups, beneficiaries, applicants, other
governmental agencies, providers
groups, research organizations, health
care corporations, health care
consultants. States will use the
information collected to assess state
plan performance, health outcomes and
an evaluation of the amount of
substitution of private coverage that
occurs as a result of the subsidies and
the effect of the subsidies on access to
coverage. Form Number: CMS–R–308
(OMB control number: 0938–0841);
Frequency: Yearly, once, and
occasionally; Affected Public: State,
Local, or Tribal Governments; Number
of Respondents: 51; Total Annual
Responses: 16,024,071; Total Annual
Hours: 803,280. (For policy questions
regarding this collection contact Joyce
Jordan at 410–786–3413.)
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–17467 Filed 8–6–24; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–R–48]
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
SUMMARY:
E:\FR\FM\07AUN1.SGM
07AUN1
64464
Federal Register / Vol. 89, No. 152 / Wednesday, August 7, 2024 / Notices
khammond on DSKJM1Z7X2PROD with NOTICES
(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
October 7, 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: lll, 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).
VerDate Sep<11>2014
17:07 Aug 06, 2024
Jkt 262001
CMS–R–48 Hospital Conditions of
Participation (CoPs) and Supporting
Regulations
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 Collections
1. Type of Information Collection
Request: Reinstatement with change of a
previously approved collection; Title of
Information Collection: Hospital
Conditions of Participation (CoPs) and
Supporting Regulations; Use: The
purpose of this package is to request
from the Office of Management and
Budget (OMB) approval of the
reinstatement with change of the
information collection request
associated with OMB control number:
0938–0328.
The information collection
requirements described herein are
needed to implement the Medicare and
Medicaid Conditions of Participation
(CoPs) for a total of 5,132 facilities that
includes: 4,994 accredited and nonaccredited hospitals and 138 Critical
Access Hospitals (CAHs) with Distinct
Part Units (DPUs); specifically, 119
CAHs with psychiatric DPUs and 19
CAHs with rehabilitation DPUs. The
information collection requirements for
the 1,245 CAHs without DPUs (1,383
total CAHs less 138 CAHs with DPUs)
are covered under OMB control number:
0938–1043 (CMS–10239).
As previous stated, this notice is
related to a reinstatement of the
information collection request that
expired on 11/30/2017. The previous
iteration of this OMB control number
0938–0328 (approved November 14,
2014) had a burden of 14,424,655
annual hours. For this requested
reinstatement, with changes, the
adjusted annual hourly burden for
industry is 3,566,521 hours at an annual
cost of $310,989,894. The decrease in
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Frm 00064
Fmt 4703
Sfmt 4703
burden hours is primarily due to the fact
that many of the information collections
that were previously required as CoPs
by CMS are now customary and usual
industry practice and would take place
in the absence of the Medicare and
Medicaid programs. In addition, where
possible, CMS reduced the burden of
CoPs with prior information collections.
For example, the burden for individual
hospitals that are part of a multihospital system was reduced by
allowing a multi-hospital system, which
represent approximately 70% of
hospitals today, to develop a unified
Quality Assessment and Performance
Improvement (QAPI) program rather
than requiring each hospital in the
system to maintain separate programs
and reporting requirements.
This reinstatement also reflects a
change in how the annual burden costs
for information collection requirements
for Hospital CoPs are calculated. In
prior submissions, the fully loaded wage
estimates applied only an additional
33% to the hourly wage to account for
fringe benefits. This reinstatement
applies an additional 100% to the
median hourly wage to reflect the costs
more accurately to hospitals for
compliance with the current CoPs.
Additional changes reflected in this
reinstatement are some of the
information collections were placed on
participating hospitals as CoPs during
the recent COVID–19 Public Health
Emergency (PHE), specifically regarding
collecting and reporting data on
incidents and hospital management of
infection diseases. The burden of many
of these information collections were
accounted for in other OMB
submissions, such as the ‘‘Unified
Hospital Data Surveillance System (U.S.
Healthcare COVID–19 Collection’’ (OMB
control number 0990–0478), and some
of these collections ended or were
revised after HHS declared the end of
the COVID–19 PHE in April 2024. As a
result, this reinstatement does not
include information collection
requirements that have expired, and
only includes the annual burden and
costs to participating hospitals and
CAHs with DPUs for information
collections that have remained as CoPs
after the COVID–19 PHE ended. In
addition, in anticipation of an upcoming
final rule titled ‘‘Medicare and Medicaid
Programs and the Children’s Health
Insurance Program; Hospital Inpatient
Prospective Payment Systems for Acute
Care Hospitals and the Long-Term Care
Hospital Prospective Payment System
and Policy Changes and Fiscal Year
2025 Rates; Quality Programs
Requirements; and Other Policy
Changes,’’ this package includes burden
E:\FR\FM\07AUN1.SGM
07AUN1
Federal Register / Vol. 89, No. 152 / Wednesday, August 7, 2024 / Notices
estimates for additional information
collection requirements that CMS is
adding as CoPs in the interest of public
health and ensuring resiliency in the
U.S. health care system. The
aforementioned final rule, CMS–1808–F
(RIN 0938–AV34), is currently on public
display at the Office of the Federal
Register and scheduled for publication
on August 28, 2024.
Finally, this reinstatement
incorporates additional information
collection requirements associated with
a number of new CoPs for hospitals and
CAHs regarding obstetrical services
which are outlined in detail in the July
2024 proposed rule titled ‘‘Medicare
and Medicaid Programs: Hospital
Outpatient Prospective Payment and
Ambulatory Surgical Center Payment
Systems; Quality Reporting Programs,
Including the Hospital Inpatient Quality
Reporting Program; Health and Safety
Standards for Obstetrical Services in
Hospitals and Critical Access Hospitals;
Prior Authorization; Requests for
Information; Medicaid and CHIP
Continuous Eligibility; Medicaid Clinic
Services Four Walls Exceptions;
Individuals Currently or Formerly in
Custody of Penal Authorities; Revision
to Medicare Special Enrollment Period
for Formerly Incarcerated Individuals;
and All-Inclusive Rate Add-On Payment
for High-Cost Drugs Provided by Indian
Health Service and Tribal Facilities’’ (89
FR 59186). Form Number: CMS–R–48
(OMB control number: 0938–0328);
Frequency: Yearly; Affected Public:
Private Sector (Business or other forprofit); Number of Respondents: 4,664;
Total Annual Responses: 2,647,647;
Total Annual Hours: 3,566,521 (For
policy questions regarding this
collection contact Claudia Molinar at
410–786–8445).
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–17484 Filed 8–2–24; 4:15 pm]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
khammond on DSKJM1Z7X2PROD with NOTICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10874 and CMS–
R–285]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
AGENCY:
VerDate Sep<11>2014
17:07 Aug 06, 2024
Jkt 262001
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.
DATES: Comments on the collection(s) of
information must be received by the
OMB desk officer by September 6, 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
SUMMARY:
PO 00000
Frm 00065
Fmt 4703
Sfmt 4703
64465
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: New collection (Request for a
new OMB control number); Title of
Information Collection: Part D Drug
Management Program (DMP); Use:
Section 1860D–4(c)(5)(A) of the Social
Security Act requires that Part D
sponsors have a DMP for beneficiaries at
risk of abuse or misuse of frequently
abused drugs (FADs). The information
in this collection of information request
is necessary for sponsor conformance
with DMP requirements at § 423.153(f),
including communicating with
prescribers and pharmacies, informing
beneficiaries that they have been
identified as a PARB or ARB, and
informing beneficiaries and CMS
whether a beneficiary’s access to FADs
will be restricted to a selected prescriber
and/or network pharmacy(ies) and/or
through a beneficiary-specific point-ofsale claim edit. Part D sponsors will use
the standardized and model documents
to communicate with providers,
enrollees, and other sponsors.
Specifically, Part D sponsors may use
the Model Part D Drug Management
Program Prescriber Inquiry Letter to
inform providers that their patient’s
pattern of use or history of use of FADs
is potentially unsafe and has prompted
a case management review under the
plan’s DMP. Part D sponsors must use
the standardized Initial Notice and
Second Notice, or Alternate Second
Notice, to inform enrollees, following
identification by CMS’s OMS and
subsequent case management, whether
the beneficiaries have been identified as
being potentially at risk or at risk for
abuse or misuse of FADs. Part D
sponsors may use the Model Part D Drug
Management Program Sponsor
Information Transfer Memorandum to
communicate to a gaining sponsor the
enrollee’s history of misuse or abuse of
FADs; Form Number: CMS–10874 (OMB
control number: 0938–1465); Frequency:
Yearly and once; Affected Public:
Private sector; Number of Respondents:
319; Number of Responses: 62,248;
Total Annual Hours: 152,585. (For
policy questions regarding this
E:\FR\FM\07AUN1.SGM
07AUN1
Agencies
[Federal Register Volume 89, Number 152 (Wednesday, August 7, 2024)]
[Notices]
[Pages 64463-64465]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-17484]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-R-48]
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
[[Page 64464]]
(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 October 7, 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-R-48 Hospital Conditions of Participation (CoPs) and Supporting
Regulations
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 Collections
1. Type of Information Collection Request: Reinstatement with
change of a previously approved collection; Title of Information
Collection: Hospital Conditions of Participation (CoPs) and Supporting
Regulations; Use: The purpose of this package is to request from the
Office of Management and Budget (OMB) approval of the reinstatement
with change of the information collection request associated with OMB
control number: 0938-0328.
The information collection requirements described herein are needed
to implement the Medicare and Medicaid Conditions of Participation
(CoPs) for a total of 5,132 facilities that includes: 4,994 accredited
and non-accredited hospitals and 138 Critical Access Hospitals (CAHs)
with Distinct Part Units (DPUs); specifically, 119 CAHs with
psychiatric DPUs and 19 CAHs with rehabilitation DPUs. The information
collection requirements for the 1,245 CAHs without DPUs (1,383 total
CAHs less 138 CAHs with DPUs) are covered under OMB control number:
0938-1043 (CMS-10239).
As previous stated, this notice is related to a reinstatement of
the information collection request that expired on 11/30/2017. The
previous iteration of this OMB control number 0938-0328 (approved
November 14, 2014) had a burden of 14,424,655 annual hours. For this
requested reinstatement, with changes, the adjusted annual hourly
burden for industry is 3,566,521 hours at an annual cost of
$310,989,894. The decrease in burden hours is primarily due to the fact
that many of the information collections that were previously required
as CoPs by CMS are now customary and usual industry practice and would
take place in the absence of the Medicare and Medicaid programs. In
addition, where possible, CMS reduced the burden of CoPs with prior
information collections. For example, the burden for individual
hospitals that are part of a multi-hospital system was reduced by
allowing a multi-hospital system, which represent approximately 70% of
hospitals today, to develop a unified Quality Assessment and
Performance Improvement (QAPI) program rather than requiring each
hospital in the system to maintain separate programs and reporting
requirements.
This reinstatement also reflects a change in how the annual burden
costs for information collection requirements for Hospital CoPs are
calculated. In prior submissions, the fully loaded wage estimates
applied only an additional 33% to the hourly wage to account for fringe
benefits. This reinstatement applies an additional 100% to the median
hourly wage to reflect the costs more accurately to hospitals for
compliance with the current CoPs.
Additional changes reflected in this reinstatement are some of the
information collections were placed on participating hospitals as CoPs
during the recent COVID-19 Public Health Emergency (PHE), specifically
regarding collecting and reporting data on incidents and hospital
management of infection diseases. The burden of many of these
information collections were accounted for in other OMB submissions,
such as the ``Unified Hospital Data Surveillance System (U.S.
Healthcare COVID-19 Collection'' (OMB control number 0990-0478), and
some of these collections ended or were revised after HHS declared the
end of the COVID-19 PHE in April 2024. As a result, this reinstatement
does not include information collection requirements that have expired,
and only includes the annual burden and costs to participating
hospitals and CAHs with DPUs for information collections that have
remained as CoPs after the COVID-19 PHE ended. In addition, in
anticipation of an upcoming final rule titled ``Medicare and Medicaid
Programs and the Children's Health Insurance Program; Hospital
Inpatient Prospective Payment Systems for Acute Care Hospitals and the
Long-Term Care Hospital Prospective Payment System and Policy Changes
and Fiscal Year 2025 Rates; Quality Programs Requirements; and Other
Policy Changes,'' this package includes burden
[[Page 64465]]
estimates for additional information collection requirements that CMS
is adding as CoPs in the interest of public health and ensuring
resiliency in the U.S. health care system. The aforementioned final
rule, CMS-1808-F (RIN 0938-AV34), is currently on public display at the
Office of the Federal Register and scheduled for publication on August
28, 2024.
Finally, this reinstatement incorporates additional information
collection requirements associated with a number of new CoPs for
hospitals and CAHs regarding obstetrical services which are outlined in
detail in the July 2024 proposed rule titled ``Medicare and Medicaid
Programs: Hospital Outpatient Prospective Payment and Ambulatory
Surgical Center Payment Systems; Quality Reporting Programs, Including
the Hospital Inpatient Quality Reporting Program; Health and Safety
Standards for Obstetrical Services in Hospitals and Critical Access
Hospitals; Prior Authorization; Requests for Information; Medicaid and
CHIP Continuous Eligibility; Medicaid Clinic Services Four Walls
Exceptions; Individuals Currently or Formerly in Custody of Penal
Authorities; Revision to Medicare Special Enrollment Period for
Formerly Incarcerated Individuals; and All-Inclusive Rate Add-On
Payment for High-Cost Drugs Provided by Indian Health Service and
Tribal Facilities'' (89 FR 59186). Form Number: CMS-R-48 (OMB control
number: 0938-0328); Frequency: Yearly; Affected Public: Private Sector
(Business or other for-profit); Number of Respondents: 4,664; Total
Annual Responses: 2,647,647; Total Annual Hours: 3,566,521 (For policy
questions regarding this collection contact Claudia Molinar at 410-786-
8445).
William N. Parham, III,
Director, Division of Information Collections and Regulatory Impacts,
Office of Strategic Operations and Regulatory Affairs.
[FR Doc. 2024-17484 Filed 8-2-24; 4:15 pm]
BILLING CODE 4120-01-P