Agency Information Collection Activities: Proposed Collection; Comment Request, 78048-78050 [2023-25059]
Download as PDF
78048
Federal Register / Vol. 88, No. 218 / Tuesday, November 14, 2023 / Notices
some data elements (e.g., date of birth,
date of diagnosis, county of residence)
could potentially be combined with
other information to identify
individuals. Private information is not
disclosed unless otherwise compelled
by law, and all data are treated in a
secure manner consistent with the
technical, administrative, and
operational controls required by the
Federal Information Security
Management Act of 2002 (FISMA) and
the 2010 National Institute of Standards
and Technology (NIST) Recommended
Security Controls for Federal
Information Systems and Organizations.
Weekly tables of nationally notifiable
diseases are available through CDC
WONDER and www.data.cdc.gov.
Annual summaries of finalized
nationally notifiable disease data are
burden estimates for the one-time
burden for reporting jurisdictions are for
the addition of case notification data for
Cronobacter and Ehrlichiosis, new
notifiable conditions; the addition of
case notification data for Congenital
cytomegalovirus infection and
Toxoplasmosis, new conditions under
standardized surveillance; and the
addition of new disease-specific data
elements for Cronobacter, Hansen’s
Disease (Leprosy) and Leptospirosis.
Because there were fewer diseasespecific data elements added in this
Revision, the total burden hours
decreased from 18,594 to 18,414. CDC
requests OMB approval for an estimated
18,414 annual burden hours from the
257 respondents.
published on CDC WONDER and
www.data.cdc.gov and disease-specific
data are published by individual CDC
programs.
The burden estimates include the
number of hours that the public health
department uses to process and send
case notification data from their
jurisdiction to CDC. Specifically, the
burden estimates include separate
burden hours incurred for automated
and non-automated transmissions,
separate weekly burden hours incurred
for modernizing surveillance systems as
part of CDC’s Data Modernization
Initiative (DMI) implementation,
separate burden hours incurred for
annual data reconciliation and
submission, and separate one-time
burden hours incurred for the addition
of new diseases and data elements. The
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
States
States
States
States
States
.............................
.............................
.............................
.............................
.............................
Territories
Territories
Territories
Territories
Territories
.......................
.......................
.......................
.......................
.......................
Freely
Freely
Freely
Freely
Associated
Associated
Associated
Associated
States
States
States
States
Cities
Cities
Cities
Cities
Cities
..............................
..............................
..............................
..............................
..............................
Total ........................
50
10
50
50
50
52
52
52
1
1
20/60
2
4
75
3
867
1,040
10,400
3,750
150
5
5
5
5
5
52
56
52
1
1
20/60
20/60
4
5
3
87
93
1,040
25
15
3
3
3
3
52
56
1
1
20/60
20/60
5
3
52
56
15
9
2
2
2
2
2
52
52
52
1
1
20/60
2
4
75
3
35
208
416
150
6
..............................................................................
........................
........................
........................
18,414
[FR Doc. 2023–25088 Filed 11–13–23; 8:45 am]
BILLING CODE 4163–18–P
khammond on DSKJM1Z7X2PROD with NOTICES
Total burden
(in hours)
Weekly (Automated) ............................................
Weekly (Non-automated) .....................................
Weekly (DMI Implementation) .............................
Annual ..................................................................
One-time Addition of Diseases and Data Elements.
Weekly (Automated) ............................................
Weekly, Quarterly (Non-automated) ....................
Weekly (DMI Implementation) .............................
Annual ..................................................................
One-time Addition of Diseases and Data Elements.
Weekly (Automated) ............................................
Weekly, Quarterly (Non-automated) ....................
Annual ..................................................................
One-time Addition of Diseases and Data Elements.
Weekly (Automated) ............................................
Weekly (Non-automated) .....................................
Weekly (DMI Implementation) .............................
Annual ..................................................................
One-time Addition of Diseases and Data Elements.
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10552]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
VerDate Sep<11>2014
Average
burden per
response
(in hours)
Number of
responses per
respondent
Number of
respondents
Form name
16:48 Nov 13, 2023
Jkt 262001
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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
SUMMARY:
E:\FR\FM\14NON1.SGM
14NON1
Federal Register / Vol. 88, No. 218 / Tuesday, November 14, 2023 / Notices
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
January 16, 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/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–10552 Implementation of
Medicare Programs;—Medicare
Promoting Interoperability Program
Under the PRA (44 U.S.C. 3501–
3520), Federal agencies must obtain
approval from the Office of Management
VerDate Sep<11>2014
16:48 Nov 13, 2023
Jkt 262001
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: Implementation
of Medicare Programs;—Medicare
Promoting Interoperability Program;
Use: The Centers for Medicare &
Medicaid Services (CMS) is requesting
approval to collect information from
eligible hospitals and critical access
hospitals (CAHs). We have finalized
changes to this program as discussed in
the FY 2024 Inpatient Prospective
Payment System (IPPS)/Long-term Care
Hospital Prospective Payment System
(LTCH PPS) final rule. This is a revision
of the information collection request.
The American Recovery and
Reinvestment Act of 2009 (Recovery
Act) (Pub. L. 111–5) was enacted on
February 17, 2009. Title IV of Division
B of the Recovery Act amended Titles
XVIII and XIX of the Social Security Act
(the Act) by establishing incentive
payments to eligible professionals (EPs),
eligible hospitals and CAHs, and
Medicare Advantage (MA) organizations
participating in the Medicare and
Medicaid programs that adopt and
successfully demonstrate meaningful
use of certified EHR technology
(CEHRT). These Recovery Act
provisions, together with Title XIII of
Division A of the Recovery Act, may be
cited as the ‘‘Health Information
Technology for Economic and Clinical
Health Act’’ or the ‘‘HITECH Act.’’
The HITECH Act created incentive
programs for EPs, eligible hospitals
including CAHs, and MA organizations
in the Medicare Fee-for-Service (FFS),
and Medicaid programs that
successfully demonstrated meaningful
use of CEHRT. In their first payment
year, Medicaid EPs, eligible hospitals
including MA organizations and CAHs
could adopt, implement, or upgrade to
certified EHR technology. It also
PO 00000
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Fmt 4703
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78049
allowed for negative payment
adjustments in the Medicare FFS and
MA programs starting in 2015 for EPs,
eligible hospitals including MA
organizations and CAHs participating in
Medicare that are not meaningful users
of CEHRT. The Medicaid Promoting
Interoperability Program did not
authorize negative payment
adjustments, but its participants were
eligible for incentive payments until
December 31, 2021, when the program
ended.
In CY 2017, we began collecting data
from eligible hospitals and CAHs to
determine the application of the
Medicare payment adjustments. This
information collection was also used to
make incentive payments to eligible
hospitals in Puerto Rico from 2016
through 2021. At this time, Medicare
eligible professionals no longer reported
to the EHR Incentive Program, as they
began reporting under the Merit-based
Incentive Payment System’s (MIPS)
Promoting Interoperability Performance
Category. In 2019, the EHR Incentives
Program for eligible hospitals and CAHs
was subsequently renamed the Medicare
Promoting Interoperability Program. In
subsequent years, we have focused on
balancing reporting burden for eligible
hospitals and CAHs while also
implementing changes designed to
incentivize the advanced use of CEHRT
to support health information exchange,
interoperability, advanced quality
measurement, and maximizing clinical
effectiveness and efficiencies.
In the FY 2024 IPPS/LTCH PPS final
rule, we finalized the following policy
changes for eligible hospitals and CAHs
that attest to CMS under the Medicare
Promoting Interoperability Program.
None of the policies we finalized will
affect the information collection burden:
(i) to adopt three electronic clinical
quality measures (eCQMs) beginning
with the CY 2025 reporting period: (1)
Hospital Harm—Pressure Injury eCQM;
(2) Hospital Harm—Acute Kidney Injury
eCQM; and (3) Excessive Radiation Dose
or Inadequate Image Quality for
Diagnostic Computed Tomography
(CMT) in Adults eCQM; (ii) to modify
the Safety Assurance Factors for EHR
Resilience (SAFER) Guides measure to
require eligible hospitals and CAHs to
submit a ‘‘yes’’ attestation to fulfill the
measure beginning with the EHR
reporting period in CY 2024; and (iii) to
establish an EHR reporting period of a
minimum of any continuous 180-day
period in CY 2025. Form Number:
CMS–10552 (OMB control number:
0938–1278); Frequency: Annually;
Affected Public: State, Local or Private
Government; Business and for-profit
and Not-for-profit; Number of
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78050
Federal Register / Vol. 88, No. 218 / Tuesday, November 14, 2023 / Notices
Respondents: 4,500; Total Annual
Responses: 4,500; Total Annual Hours:
29,625. (For policy questions regarding
this collection, contact Jessica Warren at
410–786–7519.)
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: November 8, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
National Rural Health Information
Clearinghouse Program
Health Resources and Services
Administration
FOR FURTHER INFORMATION CONTACT:
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Announcing Funding
Supplement for National Rural Health
Information Clearinghouse Program
recipient.
AGENCY:
[FR Doc. 2023–25059 Filed 11–13–23; 8:45 am]
BILLING CODE 4120–01–P
Program recipient to develop toolkits
and other resources that address
strategies to promote rural community
health.
HRSA provided supplemental
award funds to the National Rural
Health Information Clearinghouse
SUMMARY:
Sarah Scott, Federal Office of Rural
Health Policy, HRSA, at sscott2@
hrsa.gov and (301) 287–2619.
SUPPLEMENTARY INFORMATION:
Intended Recipient of the Award: The
University of North Dakota.
Amount of Non-Competitive Award:
One award for $485,000.
Project Period: June 1, 2023, to May
31, 2024.
CFDA Number: 93.223.
Award Instrument: Supplement.
Authority: Social Security Act 711(b)
(42 U.S.C. 912(b)).
TABLE 1—RECIPIENTS AND AWARD AMOUNTS
Grant No.
Award recipient name
City, State
U56RH05539 ...........................................
University of North Dakota ......................
Grand Forks, ND .....................................
Justification: This funding will
provide a one-time supplement to the
University of North Dakota via the
National Rural Health Information
Clearinghouse Program. This
supplement will allow the University of
North Dakota to build on past and
ongoing projects supported by HRSA to
improve health care in rural areas by
serving as a primary resource for
information, opportunities, and tools
related to rural health. The supplement
will allow the University of North
Dakota to create new toolkits and
resources on important topics related to
rural community health. This builds
upon the planned work within the
scope of its existing award.
Carole Johnson,
Administrator.
[FR Doc. 2023–25068 Filed 11–13–23; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
khammond on DSKJM1Z7X2PROD with NOTICES
Health Resources and Services
Administration
National Vaccine Injury Compensation
Program; List of Petitions Received
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services (HHS).
ACTION: Notice.
AGENCY:
HRSA is publishing this
notice of petitions received under the
SUMMARY:
VerDate Sep<11>2014
16:48 Nov 13, 2023
Jkt 262001
National Vaccine Injury Compensation
Program (the Program), as required by
the Public Health Service (PHS) Act, as
amended. While the Secretary of HHS is
named as the respondent in all
proceedings brought by the filing of
petitions for compensation under the
Program, the United States Court of
Federal Claims is charged by statute
with responsibility for considering and
acting upon the petitions.
FOR FURTHER INFORMATION CONTACT: For
information about requirements for
filing petitions, and the Program in
general, contact Lisa L. Reyes, Clerk of
Court, United States Court of Federal
Claims, 717 Madison Place NW,
Washington, DC 20005, (202) 357–6400.
For information on HRSA’s role in the
Program, contact the Director, National
Vaccine Injury Compensation Program,
5600 Fishers Lane, Room 08N146B,
Rockville, Maryland 20857; (301) 443–
6593, or visit our website at: https://
www.hrsa.gov/vaccinecompensation/
index.html.
SUPPLEMENTARY INFORMATION: The
Program provides a system of no-fault
compensation for certain individuals
who have been injured by specified
childhood vaccines. Subtitle 2 of title
XXI of the PHS Act, 42 U.S.C. 300aa–
10 et seq., provides that those seeking
compensation are to file a petition with
the United States Court of Federal
Claims and to serve a copy of the
petition to the Secretary of HHS, who is
named as the respondent in each
proceeding. The Secretary has delegated
this responsibility under the Program to
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Frm 00103
Fmt 4703
Sfmt 4703
Supplemental
award amount
$485,000
HRSA. The Court is directed by statute
to appoint special masters who take
evidence, conduct hearings as
appropriate, and make initial decisions
as to eligibility for, and amount of,
compensation.
A petition may be filed with respect
to injuries, disabilities, illnesses,
conditions, and deaths resulting from
vaccines described in the Vaccine Injury
Table (the Table) set forth at 42 CFR
100.3. This Table lists for each covered
childhood vaccine the conditions that
may lead to compensation and, for each
condition, the time period for
occurrence of the first symptom or
manifestation of onset or of significant
aggravation after vaccine
administration. Compensation may also
be awarded for conditions not listed in
the Table and for conditions that are
manifested outside the time periods
specified in the Table, but only if the
petitioner shows that the condition was
caused by one of the listed vaccines.
Section 2112(b)(2) of the PHS Act, 42
U.S.C. 300aa–12(b)(2), requires that
‘‘[w]ithin 30 days after the Secretary
receives service of any petition filed
under section 2111 the Secretary shall
publish notice of such petition in the
Federal Register.’’ Set forth below is a
list of petitions received by HRSA on
September 1, 2023, through September
30, 2023. This list provides the name of
the petitioner, city, and state of
vaccination (if unknown then the city
and state of the person or attorney filing
the claim), and case number. In cases
where the Court has redacted the name
E:\FR\FM\14NON1.SGM
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Agencies
[Federal Register Volume 88, Number 218 (Tuesday, November 14, 2023)]
[Notices]
[Pages 78048-78050]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-25059]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10552]
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
[[Page 78049]]
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 January 16, 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-10552 Implementation of Medicare Programs;--Medicare Promoting
Interoperability Program
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: Implementation of
Medicare Programs;--Medicare Promoting Interoperability Program; Use:
The Centers for Medicare & Medicaid Services (CMS) is requesting
approval to collect information from eligible hospitals and critical
access hospitals (CAHs). We have finalized changes to this program as
discussed in the FY 2024 Inpatient Prospective Payment System (IPPS)/
Long-term Care Hospital Prospective Payment System (LTCH PPS) final
rule. This is a revision of the information collection request.
The American Recovery and Reinvestment Act of 2009 (Recovery Act)
(Pub. L. 111-5) was enacted on February 17, 2009. Title IV of Division
B of the Recovery Act amended Titles XVIII and XIX of the Social
Security Act (the Act) by establishing incentive payments to eligible
professionals (EPs), eligible hospitals and CAHs, and Medicare
Advantage (MA) organizations participating in the Medicare and Medicaid
programs that adopt and successfully demonstrate meaningful use of
certified EHR technology (CEHRT). These Recovery Act provisions,
together with Title XIII of Division A of the Recovery Act, may be
cited as the ``Health Information Technology for Economic and Clinical
Health Act'' or the ``HITECH Act.''
The HITECH Act created incentive programs for EPs, eligible
hospitals including CAHs, and MA organizations in the Medicare Fee-for-
Service (FFS), and Medicaid programs that successfully demonstrated
meaningful use of CEHRT. In their first payment year, Medicaid EPs,
eligible hospitals including MA organizations and CAHs could adopt,
implement, or upgrade to certified EHR technology. It also allowed for
negative payment adjustments in the Medicare FFS and MA programs
starting in 2015 for EPs, eligible hospitals including MA organizations
and CAHs participating in Medicare that are not meaningful users of
CEHRT. The Medicaid Promoting Interoperability Program did not
authorize negative payment adjustments, but its participants were
eligible for incentive payments until December 31, 2021, when the
program ended.
In CY 2017, we began collecting data from eligible hospitals and
CAHs to determine the application of the Medicare payment adjustments.
This information collection was also used to make incentive payments to
eligible hospitals in Puerto Rico from 2016 through 2021. At this time,
Medicare eligible professionals no longer reported to the EHR Incentive
Program, as they began reporting under the Merit-based Incentive
Payment System's (MIPS) Promoting Interoperability Performance
Category. In 2019, the EHR Incentives Program for eligible hospitals
and CAHs was subsequently renamed the Medicare Promoting
Interoperability Program. In subsequent years, we have focused on
balancing reporting burden for eligible hospitals and CAHs while also
implementing changes designed to incentivize the advanced use of CEHRT
to support health information exchange, interoperability, advanced
quality measurement, and maximizing clinical effectiveness and
efficiencies.
In the FY 2024 IPPS/LTCH PPS final rule, we finalized the following
policy changes for eligible hospitals and CAHs that attest to CMS under
the Medicare Promoting Interoperability Program. None of the policies
we finalized will affect the information collection burden: (i) to
adopt three electronic clinical quality measures (eCQMs) beginning with
the CY 2025 reporting period: (1) Hospital Harm--Pressure Injury eCQM;
(2) Hospital Harm--Acute Kidney Injury eCQM; and (3) Excessive
Radiation Dose or Inadequate Image Quality for Diagnostic Computed
Tomography (CMT) in Adults eCQM; (ii) to modify the Safety Assurance
Factors for EHR Resilience (SAFER) Guides measure to require eligible
hospitals and CAHs to submit a ``yes'' attestation to fulfill the
measure beginning with the EHR reporting period in CY 2024; and (iii)
to establish an EHR reporting period of a minimum of any continuous
180-day period in CY 2025. Form Number: CMS-10552 (OMB control number:
0938-1278); Frequency: Annually; Affected Public: State, Local or
Private Government; Business and for-profit and Not-for-profit; Number
of
[[Page 78050]]
Respondents: 4,500; Total Annual Responses: 4,500; Total Annual Hours:
29,625. (For policy questions regarding this collection, contact
Jessica Warren at 410-786-7519.)
Dated: November 8, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2023-25059 Filed 11-13-23; 8:45 am]
BILLING CODE 4120-01-P