Agency Information Collection Activities: Proposed Collection; Comment Request, 78685-78687 [2022-27864]
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Federal Register / Vol. 87, No. 245 / Thursday, December 22, 2022 / Notices
3090–XXXX; Federal Audit
Clearinghouse, in all correspondence
related to this collection. Comments
received generally will be posted
without change to https://
www.regulations.gov, including any
personal and/or business confidential
information provided. To confirm
receipt of your comment(s), please
check www.regulations.gov,
approximately two-to-three days after
submission to verify posting.
FOR FURTHER INFORMATION CONTACT:
Mary Katharine Koch, Senior
Procurement Analyst, Federal
Acquisition Service, GSA, at 202–501–
4755.
SUPPLEMENTARY INFORMATION:
lotter on DSK11XQN23PROD with NOTICES1
A. Purpose
Non-Federal entities (states, local
governments, Indian tribes, institutions
of higher education, and nonprofit
organizations) are required by the Single
Audit Act Amendments of 1996 (31
U.S.C. 7501, et. seq.) (Act) and 2 CFR
part 200, ‘‘Uniform Administrative
Requirements, Cost Principles, and
Audit Requirements for Federal
Awards,’’ (Uniform Guidance) to have
audits conducted of their federal award
expenditures, and to file the resulting
reporting packages (Single Audit
reports) and data collection Form SF–
SAC (Form) with the Federal Audit
Clearinghouse. The Form SF–SAC is
Appendix X to 2 CFR part 200.
The Single Audit process is the
primary method Federal agencies and
pass-through entities use to provide
oversight of Federal awards and reduce
risk of non-compliance and improper
payments. This oversight includes
following up on audit findings and
questioned costs.
The Office of Management and Budget
has historically designated the U.S.
Census Bureau (Census) as the FAC, to
serve as the government-wide repository
of record for Single Audit reports
collected under OMB control number
0607–0518. At the direction of OMB,
GSA will become the new FAC
repository of record, beginning as early
as spring 2023 with collection of Single
Audit reports with fiscal periods ending
in 2023 and later. On approximately
October 1, 2023, GSA will also begin
data collection of 2016–2022 Single
Audit reports currently collected by
Census. All these collections will be
conducted under this PRA clearance
application.
Single Audit reports under this
clearance will be collected
electronically through GSA’s new FAC
internet collection portal at https://
www.fac.gov/.
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18:01 Dec 21, 2022
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There are few proposed changes to the
existing data elements and data
collection method in this clearance.
Planned changes are intended to make
the reporting process easier, improve
data integrity, and ensure compliance
with the GREAT Act. All changes listed
below are intended to take effect for all
audit years collected by GSA, unless
specified otherwise.
The proposed changes include:
• end collection of the DUNS number
• upload the majority of data via
templates rather than graphical user
interface (GUI) in the initial GSA
system, subject to creation of a GUI for
additional data submission options
before expiration of this proposed
clearance (collection items are not
changing, just the means of collection)
• collect auditee’s Unique Entity
Identifier (UEI) for audits with fiscal
periods ending in 2016–2021 (already
approved to be collected for audits with
fiscal periods 2022 and future)
• import the auditee name and
address directly from SAM.gov (when
the auditee’s UEI is entered, their
auditee name and address will be pulled
from SAM.gov into Part I of the Form)
• update terminology, similar to the
following, in order to be in compliance
with the GREAT Act: change ‘‘award’’
to ‘‘federal award’’; ‘‘CFDA’’ to
‘‘Assistance Listing’’; ‘‘sub-award’’ to
‘‘subaward’’; ‘‘sub-recipient’’ to
‘‘subrecipient’’
• clarify on-screen and/or Form
instructions to improve data collection
and accuracy, as part of the creation of
an updated data collection and
dissemination system
B. Annual Reporting Burden
Respondents: 80,000 (40,000 auditees
and 40,000 auditors).
Responses per Respondent: 1.
Total Annual Responses: 80,000
(40,000 auditees and 40,000 auditors).
Hours per Response: 100 hours for
each of the 400 large respondents and
21 hours for each of the 79,600 small
respondents.
Total Burden Hours: 1,711,600.
C. Public Comments
Public comments are particularly
invited on whether this collection of
information is necessary; whether it will
have practical utility; whether our
estimate of the public burden of this
collection of information is accurate,
and based on valid assumptions and
methodology; ways to enhance the
quality, utility, and clarity of the
information to be collected; and ways in
which we can minimize the burden of
the collection of information on those
who are to respond, through the use of
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78685
appropriate technological collection
techniques or other forms of information
technology.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the Regulatory Secretariat Division by
calling 202–501–4755 or emailing
GSARegSec@gsa.gov. Please cite OMB
Control No. 3090–XXXX, Federal Audit
Clearinghouse, in all correspondence.
Beth Anne Killoran,
Deputy Chief Information Officer.
[FR Doc. 2022–27893 Filed 12–21–22; 8:45 am]
BILLING CODE 6820–EP–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10823 and CMS–
588]
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
(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
February 21, 2023.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
SUMMARY:
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Federal Register / Vol. 87, No. 245 / Thursday, December 22, 2022 / Notices
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:
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–10823 End-stage Renal Disease
(ESRD) Quality Incentive Program
(QIP): Study of Quality and Patient
Experience
CMS–588 Electronic Funds Transfer
(EFT) Authorization Agreement
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
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18:01 Dec 21, 2022
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requirement, CMS is publishing this
notice.
Information Collection
1. Type of Information Collection
Request: New Collection (Request for
new OMB control number); Title of
Information Collection: End-stage Renal
Disease (ESRD) Quality Incentive
Program (QIP): Study of Quality and
Patient Experience; Use: The Centers for
Medicare & Medicaid Services (CMS)
oversees the quality of care provided by
dialysis facilities by administering the
Quality Incentive Program (QIP). As part
of the evaluation of this program, CMS
seeks to gain a deeper understanding of
emerging trends observed across the
dialysis landscape by conducting
qualitative data collection and analysis.
These primary qualitative data
collection activities seek to answer the
following research questions related to
dialysis quality, access to care, health
equity, and quality of life:
1. What aspects of patient dialysis
care do patients report as a priority?
2. How, if at all, do dialysis facilities
evaluate the quality of care they
provide?
3. What strategies do providers and
dialysis facilities use to improve access
to care for underserved populations?
4. What do patients, providers, and
stakeholder organizations believe
contributes to high quality of life for
patients with ESRD? Do perceptions
vary by respondent type or respondent
characteristics?
5. How do dialysis facilities measure
patient satisfaction and quality of life?
6. How do dialysis providers and
stakeholder organizations think quality
of life for dialysis patients has changed
over time? What was the impetus for
that change?
We are requesting to collect
information through indepth interviews
with stakeholders of the CMS end-stage
renal disease (ESRD) Quality Incentive
Program (QIP). The interviews will
collect data from individuals with
ESRD, dialysis facility administrators,
dialysis social workers, transplant
center administrators, corporate
representatives from dialysis
organizations, and patient advocacy
organizations.
This data collection seeks to answer
several research questions specific to
health outcomes for dialysis patients, as
measured by the QIP, that are not
available through current literature or
secondary data collection. In
preparation for this study, the
evaluation team conducted a scan of
peer-reviewed literature and document
review of previous ESRD QIP
monitoring and evaluation reports and
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policy documents describing CMS
priorities. Based on the results from this
scan, the study team identified
persistent knowledge gaps and
opportunities for primary data
collection. Drawing on high-quality
data, empirical rigor, and knowledge of
nonprogrammatic factors, the evaluation
will benefit CMS by providing datadriven findings and recommendations
to improve patient care, reduce health
disparities, and promote health equity.
This primary data collection will
allow CMS to more comprehensively
understand the data being compiled and
analyzed quantitatively and will
provide more context related to dialysis
quality, quality of life of individuals
with ESRD, access to dialysis care, and
the patient experience, which are
current CMS priorities. Form Number:
CMS–10823 (OMB control number:
0938–NEW); Frequency: Once; Affected
Public: Private Sector (Business or other
for-profits, Not-for-Profit Institutions),
Individuals and Households; Number of
Respondents: 1,945; Total Annual
Responses: 1,945; Total Annual Hours:
604. (For policy questions regarding this
collection contact Christopher King at
(410) 786–6972).
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Electronic
Funds Transfer Authorization
Agreement; Use: Section 1815(a) of the
Social Security Act provides the
authority for the Secretary of Health and
Human Services to pay providers/
suppliers of Medicare services at such
time or times as the Secretary
determines appropriate (but no less
frequently than monthly). Under
Medicare, CMS, acting for the Secretary,
contracts with Fiscal Intermediaries and
Carriers to pay claims submitted by
providers/suppliers who furnish
services to Medicare beneficiaries.
Under CMS’ payment policy, Medicare
providers/suppliers have the option of
receiving payments electronically. The
collection and verification of this
information via Form CMS–588 protects
our beneficiaries from illegitimate
health care providers/suppliers. These
procedures also protect the Medicare
Trust Funds against fraud. Form
Number: CMS–588 (OMB control
number: 0938–0626); Frequency:
Occasionally; Affected Public: Business
or other for-profit and Not-for-profit
institutions; Number of Respondents:
115,833; Total Annual Responses:
115,833; Total Annual Hours: 57,917.
(For policy questions regarding this
collection contact Frank Whelan at (410)
786–1302.
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Federal Register / Vol. 87, No. 245 / Thursday, December 22, 2022 / Notices
Dated: December 19, 2022.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2022–27864 Filed 12–21–22; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for Office of Management
and Budget Review; Case Studies of
Child Care and Development Fund
Lead Agencies’ Consumer Education
Strategies (New Collection)
Office of Planning, Research,
and Evaluation, Administration for
Children and Families, U.S. Department
of Health and Human Services.
ACTION: Request for public comments.
AGENCY:
The Administration for
Children and Families (ACF) within the
U.S. Department of Health and Human
Services (HHS) is proposing to collect
qualitative data to examine innovative
and promising consumer education
strategies that Child Care and
Development Fund (CCDF) Lead
Agencies are using to help families
SUMMARY:
search for and select child care and
early education (CCEE). This
information collection aims to present
an internally valid description of the
experiences of up to six, purposively
selected case study sites, not to promote
statistical generalization to different
sites or service populations.
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.
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. You can also obtain
copies of the proposed collection of
information by emailing
OPREinfocollection@acf.hhs.gov.
Identify all requests by the title of the
information collection.
SUPPLEMENTARY INFORMATION:
Description: The Consumer Education
and Parental Choice in Early Care and
Education project is proposing to
conduct qualitative case studies to
examine consumer education strategies
in up to six sites. Sites will be selected
based on a scan of innovative or
promising strategies being used to help
parents looking for and selecting CCEE.
In each site, we will conduct
interviews with CCDF administrators
and agency staff, consumer education
services staff, and other key informants
to collect information on select
consumer education strategies and
implementation successes and
challenges. We will conduct focus
groups with parents of young children
to gather information about their
experiences looking for CCEE.
The study will collect information
about (a) the selected consumer
education strategies; (b) implementation
successes and challenges; and (c)
parents’ experiences looking for CCEE,
including the resources they used and
their awareness of and perspectives on
state/local consumer education
resources.
Respondents: State, Territory, and
Tribal CCDF program administrators
and agency staff, consumer education
services staff, key informants who
interact with parents and provide a
state/local perspective, and parents/
guardians of children under age 6.
ANNUAL BURDEN ESTIMATES
Number of
respondents
(total over
request
period)
Instrument
Interview Guide for State, Tribal, and Territory CCDF Administrators ............
Interview Guide for Consumer Education Services Staff ................................
Key Informant Interview Guide ........................................................................
Parent Focus Group Facilitator’s Guide ..........................................................
Focus Group Brief Questionnaire ....................................................................
Estimated Total Annual Burden
Hours: 248.
Authority: Child Care and
Development Block Grant (CCDBG) Act
of 1990, as amended (42 U.S.C. 9857 et
seq.)
Mary B. Jones,
ACF/OPRE Certifying Officer.
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[FR Doc. 2022–27808 Filed 12–21–22; 8:45 am]
BILLING CODE 4184–23–P
12
30
18
120
120
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2016–N–0736]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Tracking Network
for PETNet, LivestockNet, and
SampleNet
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
SUMMARY:
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18:01 Dec 21, 2022
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Number of
responses per
respondent
(total over
request
period)
1
1
1
1
1
Avg. burden
per response
(in hours)
1
1
.75
1.5
.1
Total/annual
burden
(in hours)
12
30
14
180
12
announcing an opportunity for public
comment on the proposed collection of
certain information by the Agency.
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 of an
existing collection of information, and
to allow 60 days for public comment in
response to the notice. This notice
solicits comments on our use of a
tracking network to collect and share
safety information about animal food
from Federal, State, and Territorial
Agencies.
E:\FR\FM\22DEN1.SGM
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]]>Agencies
[Federal Register Volume 87, Number 245 (Thursday, December 22, 2022)]
[Notices]
[Pages 78685-78687]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-27864]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10823 and CMS-588]
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 (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 February 21, 2023.
ADDRESSES: When commenting, please reference the document identifier or
OMB control number. To be assured consideration, comments and
[[Page 78686]]
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-10823 End-stage Renal Disease (ESRD) Quality Incentive Program
(QIP): Study of Quality and Patient Experience
CMS-588 Electronic Funds Transfer (EFT) Authorization Agreement
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 new OMB control number); Title of Information Collection: End-stage
Renal Disease (ESRD) Quality Incentive Program (QIP): Study of Quality
and Patient Experience; Use: The Centers for Medicare & Medicaid
Services (CMS) oversees the quality of care provided by dialysis
facilities by administering the Quality Incentive Program (QIP). As
part of the evaluation of this program, CMS seeks to gain a deeper
understanding of emerging trends observed across the dialysis landscape
by conducting qualitative data collection and analysis. These primary
qualitative data collection activities seek to answer the following
research questions related to dialysis quality, access to care, health
equity, and quality of life:
1. What aspects of patient dialysis care do patients report as a
priority?
2. How, if at all, do dialysis facilities evaluate the quality of
care they provide?
3. What strategies do providers and dialysis facilities use to
improve access to care for underserved populations?
4. What do patients, providers, and stakeholder organizations
believe contributes to high quality of life for patients with ESRD? Do
perceptions vary by respondent type or respondent characteristics?
5. How do dialysis facilities measure patient satisfaction and
quality of life?
6. How do dialysis providers and stakeholder organizations think
quality of life for dialysis patients has changed over time? What was
the impetus for that change?
We are requesting to collect information through indepth interviews
with stakeholders of the CMS end-stage renal disease (ESRD) Quality
Incentive Program (QIP). The interviews will collect data from
individuals with ESRD, dialysis facility administrators, dialysis
social workers, transplant center administrators, corporate
representatives from dialysis organizations, and patient advocacy
organizations.
This data collection seeks to answer several research questions
specific to health outcomes for dialysis patients, as measured by the
QIP, that are not available through current literature or secondary
data collection. In preparation for this study, the evaluation team
conducted a scan of peer-reviewed literature and document review of
previous ESRD QIP monitoring and evaluation reports and policy
documents describing CMS priorities. Based on the results from this
scan, the study team identified persistent knowledge gaps and
opportunities for primary data collection. Drawing on high-quality
data, empirical rigor, and knowledge of nonprogrammatic factors, the
evaluation will benefit CMS by providing data-driven findings and
recommendations to improve patient care, reduce health disparities, and
promote health equity.
This primary data collection will allow CMS to more comprehensively
understand the data being compiled and analyzed quantitatively and will
provide more context related to dialysis quality, quality of life of
individuals with ESRD, access to dialysis care, and the patient
experience, which are current CMS priorities. Form Number: CMS-10823
(OMB control number: 0938-NEW); Frequency: Once; Affected Public:
Private Sector (Business or other for-profits, Not-for-Profit
Institutions), Individuals and Households; Number of Respondents:
1,945; Total Annual Responses: 1,945; Total Annual Hours: 604. (For
policy questions regarding this collection contact Christopher King at
(410) 786-6972).
2. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Electronic Funds
Transfer Authorization Agreement; Use: Section 1815(a) of the Social
Security Act provides the authority for the Secretary of Health and
Human Services to pay providers/suppliers of Medicare services at such
time or times as the Secretary determines appropriate (but no less
frequently than monthly). Under Medicare, CMS, acting for the
Secretary, contracts with Fiscal Intermediaries and Carriers to pay
claims submitted by providers/suppliers who furnish services to
Medicare beneficiaries. Under CMS' payment policy, Medicare providers/
suppliers have the option of receiving payments electronically. The
collection and verification of this information via Form CMS-588
protects our beneficiaries from illegitimate health care providers/
suppliers. These procedures also protect the Medicare Trust Funds
against fraud. Form Number: CMS-588 (OMB control number: 0938-0626);
Frequency: Occasionally; Affected Public: Business or other for-profit
and Not-for-profit institutions; Number of Respondents: 115,833; Total
Annual Responses: 115,833; Total Annual Hours: 57,917. (For policy
questions regarding this collection contact Frank Whelan at (410) 786-
1302.
[[Page 78687]]
Dated: December 19, 2022.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2022-27864 Filed 12-21-22; 8:45 am]
BILLING CODE 4120-01-P
