Agency Information Collection Activities: Proposed Collection; Comment Request, 54002-54004 [2024-14338]
Download as PDF
54002
Federal Register / Vol. 89, No. 125 / Friday, June 28, 2024 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Type of respondent
Type of data collection instrument
Intermediary or end users (e.g., employers, workers, manufactures,
labor/professional
associations,
policymakers).
Total ...........................................
1
1
1
1
20/60
5/60
25
3,333
54
Interview or focus group guide ........
650
1
1
650
...........................................................
........................
........................
........................
6,069
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention
[FR Doc. 2024–14289 Filed 6–27–24; 8:45 am]
Advisory Committee on Breast Cancer
in Young Women; Notice of Charter
Renewal
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of charter renewal.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), within
the Department of Health and Human
Services (HHS), announces the renewal
of the charter of the Advisory
Committee on Breast Cancer in Young
Women (ACBCYW).
FOR FURTHER INFORMATION CONTACT:
Kimberly E. Smith, M.B.A., M.H.A.,
Designated Federal Officer, Advisory
Committee on Breast Cancer in Young
Women, Centers for Disease Control and
Prevention, Department of Health and
Human Services, 4770 Buford Highway
NE, Mailstop S107–4, Atlanta, Georgia
30341–3717. Telephone: (404) 498–
0073; Email: KESmith@cdc.gov.
SUPPLEMENTARY INFORMATION: CDC is
providing notice under 5 U.S.C. 1001–
1014 of the renewal of the charter of the
Advisory Committee on Breast Cancer
in Young Women, Centers for Disease
Control and Prevention, Department of
Health and Human Services. This
charter has been renewed for a two-year
period through June 17, 2026.
The Director, Office of Strategic
Business Initiatives, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
SUMMARY:
Jkt 262001
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, Centers for Disease Control and
Prevention.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
khammond on DSKJM1Z7X2PROD with NOTICES
Total burden
hours
25
10,000
650
[FR Doc. 2024–14309 Filed 6–27–24; 8:45 am]
19:25 Jun 27, 2024
Average
burden per
response
(in hours)
Interview or focus group guide ........
Survey instrument (pre and post) ....
Informed consent form .....................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
VerDate Sep<11>2014
Number of
responses per
respondent
Number of
respondents
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–179, CMS–
10536, CMS–R–153 and CMS–10326]
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,
SUMMARY:
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Fmt 4703
Sfmt 4703
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
August 27, 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:
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
E:\FR\FM\28JNN1.SGM
28JNN1
Federal Register / Vol. 89, No. 125 / Friday, June 28, 2024 / Notices
and associated materials (see
ADDRESSES).
CMS–179 Medicaid State Plan Base
Plan Pages
CMS–10536 Medicaid Eligibility
and Enrollment (EE) Implementation
Advanced Planning Document (IAPD)
Template
CMS–R–153 Medicaid Drug Use
Review (DUR) Program
CMS–10326 Electronic Submission
of Medicare Graduate Medical
Education (GME)
Affiliation Agreements
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.
khammond on DSKJM1Z7X2PROD with NOTICES
Information Collections
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Medicaid State
Plan Base Plan Pages; Use: State
Medicaid agencies complete the plan
pages while we review the information
to determine if the state has met all of
the requirements of the provisions the
states choose to implement. If the
requirements are met, we will approve
the amendments to the state’s Medicaid
plan giving the state the authority to
implement the flexibilities. For a state to
receive Medicaid Title XIX funding,
there must be an approved Title XIX
state plan. Form Number: CMS–179
(OMB control number 0938–0193);
Frequency: Occasionally; Affected
Public: State, Local, and Tribal
Governments; Number of Respondents:
56; Total Annual Responses: 1,120;
Total Annual Hours: 22,400. (For policy
questions regarding this collection
contact Gary Knight at 304–347–5723.)
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Medicaid
VerDate Sep<11>2014
19:25 Jun 27, 2024
Jkt 262001
Eligibility and Enrollment (EE)
Implementation Advanced Planning
Document (IAPD) Template; Use: To
assess the appropriateness of states’
requests for enhanced federal financial
participation for expenditures related to
Medicaid eligibility determination
systems, we will review the submitted
information and documentation to make
an approval determination for the
advanced planning document. Form
Number: CMS–10536 (OMB control
number: 0938–1268); Frequency: Yearly,
once, and occasionally; Affected Public:
State, Local, or Tribal Governments;
Number of Respondents: 56; Total
Annual Responses: 168; Total Annual
Hours: 2,688. (For policy questions
regarding this collection contact Loren
Palestino at 410–786–8842.)
3. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Medicaid Drug
Use Review (DUR) Program; Use: States
must provide for a review of drug
therapy before each prescription is filled
or delivered to a Medicaid patient. This
review includes screening for potential
drug therapy problems due to
therapeutic duplication, drug-disease
contraindications, drug-drug
interactions, incorrect drug dosage or
duration of drug treatment, drug-allergy
interactions, and clinical abuse/misuse.
Pharmacists must make a reasonable
effort to obtain, record, and maintain
Medicaid patient profiles. These profiles
must reflect at least the patient’s name,
address, telephone number, date of
birth/age, gender, history, e.g., allergies,
drug reactions, list of medications, and
pharmacist’s comments relevant to the
individual’s drug therapy. The State
must conduct retrospective drug use
review which provides for the ongoing
periodic examination of claims data and
other records in order to identify
patterns of fraud, abuse, inappropriate
or medically unnecessary care. Patterns
or trends of drug therapy problems are
identified and reviewed to determine
the need for intervention activity with
pharmacists and/or physicians. States
may conduct interventions via
telephone, correspondence, or face-toface contact. The states and managed
care organizations (MCOs) are provided
the reporting instrument (a survey) by
CMS, and by responding to the survey,
the states generate annual reports which
are submitted to CMS for the purposes
of monitoring compliance and
evaluating the progress of states’ DUR
programs. The survey and the annual
recordkeeping and reporting
requirements under the pertinent
regulations, are completed by
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Fmt 4703
Sfmt 4703
54003
pharmacists employed by, or contracted
with the various state Medicaid
programs and their MCOs. The annual
reports submitted by states are reviewed
and results are compiled by CMS in a
format intended to provide information,
comparisons and trends related to
states’ experiences with DUR. The states
benefit from the information and may
enhance their programs each year based
on state reported innovative practices
that are compiled by CMS from the
annual reports. A comparison/summary
of the data from the annual reports is
published on Medicaid.gov annually,
and serves as a resource for
stakeholders, including but not limited
to states, manufacturers, researchers,
congress, CMS, the Office of Inspector
General, non-governmental payers and
clinicians on the topic of DUR in state
Medicaid programs. Form Number:
CMS–R–153 (OMB control number:
0938–0659); Frequency: Yearly,
quarterly, and occasionally; Affected
Public: State, Local, or Tribal
Governments; Number of Respondents:
52; Total Annual Responses: 676; Total
Annual Hours: 41,860. (For policy
questions regarding this collection
contact Mike Forman at 410–786–2666.)
4. Type of Information Collection
Request: Reinstatement without change
of a currently approved collection; Title
of Information Collection: Electronic
Submission of Medicare Graduate
Medical Education (GME) Affiliation
Agreements; Use: Existing regulations at
§ 413.75(b) permit hospitals that share
residents to elect to form a Medicare
GME affiliated group if they are in the
same or contiguous urban or rural areas,
if they are under common ownership, or
if they are jointly listed as program
sponsors or major participating
institutions in the same program by the
accrediting agency. The purpose of a
Medicare GME affiliated group is to
provide flexibility to hospitals in
structuring rotations under an aggregate
full time equivalent (FTE) resident cap
when they share residents. The existing
regulations at § 413.79(f)(1) specify that
each hospital in a Medicare GME
affiliated group must submit a Medicare
GME affiliation agreement (as defined
under § 413.75(b)) to the Medicare
Administrative Contractor (MAC)
servicing the hospital and send a copy
to the Centers for Medicare and
Medicaid Services’ (CMS) Central
Office, no later than July 1 of the
residency program year during which
the Medicare GME affiliation agreement
will be in effect.
CMS will use the information
contained in electronic affiliation
agreements as documentation of the
existence of Medicare GME affiliations,
E:\FR\FM\28JNN1.SGM
28JNN1
54004
Federal Register / Vol. 89, No. 125 / Friday, June 28, 2024 / Notices
and to verify that the affiliations being
formed by teaching hospitals for the
purposes of sharing their Medicare GME
FTE cap slots are valid according to
CMS regulations. CMS will also use
these affiliation agreements as reference
materials when potential issues
involving specific affiliations arise.
While we have used hard copies of
affiliation agreements for those same
purposes in the past, we implemented
this electronic submission process in
order to expedite and ease the process
of retrieving, analyzing and evaluating
affiliation agreements. Form Number:
CMS–10326 (OMB control number:
0938–1111); Frequency: Annually;
Affected Public: Private Sector, Business
or other for profits, Not for profit
institutions; Number of Respondents:
125; Total Annual Responses: 125; Total
Annual Hours: 166. (For policy
questions regarding this collection
contact Shevi Marciano at 410–786–
2874.)
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–14338 Filed 6–27–24; 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; Refugee Support
Services (RSS) and RSS Set Aside
Sub-Agency List (Office of
Management and Budget #0970–0556)
Office of Refugee Resettlement,
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) Office of
Refugee Resettlement (ORR) is
requesting a 3-year extension of the
Refugee Support Services (RSS) and
RSS Set Aside Sub-Agency List (Office
of Management and Budget #0970–
0556). ORR is not proposing any
changes to the form.
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
SUMMARY:
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. You can also obtain
copies of the proposed collection of
information by emailing infocollection@
acf.hhs.gov. Identify all emailed
requests by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: The RSS and RSS Set
Aside Sub-Agency List requests grantees
to provide the agency name, city, state,
website, and funding amount for each
contracted sub-grantee.
The information will be used for
national resource mapping pertaining to
ORR RSS funding at the local level.
Improved communication and the
knowledge of all local providers is
important to ORR’s overall oversight of
the program. In addition to RSS formula
funding to states and state replacement
agencies who then issue sub-awards to
local providers, ORR also awards
discretionary grants that directly fund
local refugee service providers. This
report will continue to provide ORR a
complete picture of the availability all
ORR resources to assist newly arrived
refugees at the local level increasing our
ability to identify gaps or target areas of
need.
Respondents: State agencies and
replacement designees under 45 CFR
400.301(c) administering or supervising
the administration of programs.
ANNUAL BURDEN ESTIMATES
Instrument
Total
number of
respondents
Annual
number of
responses per
respondent
Average
burden hours
per response
Annual
burden hours
RSS and RSS Set Aside Sub-grantee List .....................................................
59
1
2
118
Authority: Refugee Act of 1980
[Immigration and Nationality Act, title
IV, chapter 2, section 412 (e)] and 45
CFR 400.28.
Mary C. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2024–14165 Filed 6–27–24; 8:45 am]
khammond on DSKJM1Z7X2PROD with NOTICES
BILLING CODE 4184–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for Office of Management
and Budget (OMB) Review; Community
Services Block Grant (CSBG) Annual
Progress Report (OMB No. 0970–0492)
Office of Community Services,
Administration for Children and
Families, U.S. Department of Health and
Human Services.
ACTION: Request for public comments.
AGENCY:
The Office of Community
Services (OCS), Administration for
Children and Families (ACF) requests
SUMMARY:
VerDate Sep<11>2014
19:25 Jun 27, 2024
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Fmt 4703
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an extension with minor changes to the
currently approved Community Services
Block Grant (CSBG) Annual Progress
Report, (OMB #0970–0492, expiration 6/
30/2024) and is submitting the Tribal
Annual Report and Tribal Short Form,
as well as removing supplemental
funding reports that are no longer in
use. Plans for further revisions to this
report are also discussed below.
Comments due July 29, 2024.
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.
DATES:
E:\FR\FM\28JNN1.SGM
28JNN1
Agencies
[Federal Register Volume 89, Number 125 (Friday, June 28, 2024)]
[Notices]
[Pages 54002-54004]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-14338]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-179, CMS-10536, CMS-R-153 and CMS-10326]
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 August 27, 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
[[Page 54003]]
and associated materials (see ADDRESSES).
CMS-179 Medicaid State Plan Base Plan Pages
CMS-10536 Medicaid Eligibility and Enrollment (EE) Implementation
Advanced Planning Document (IAPD) Template
CMS-R-153 Medicaid Drug Use Review (DUR) Program
CMS-10326 Electronic Submission of Medicare Graduate Medical
Education (GME)
Affiliation Agreements
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: Extension of a currently
approved collection; Title of Information Collection: Medicaid State
Plan Base Plan Pages; Use: State Medicaid agencies complete the plan
pages while we review the information to determine if the state has met
all of the requirements of the provisions the states choose to
implement. If the requirements are met, we will approve the amendments
to the state's Medicaid plan giving the state the authority to
implement the flexibilities. For a state to receive Medicaid Title XIX
funding, there must be an approved Title XIX state plan. Form Number:
CMS-179 (OMB control number 0938-0193); Frequency: Occasionally;
Affected Public: State, Local, and Tribal Governments; Number of
Respondents: 56; Total Annual Responses: 1,120; Total Annual Hours:
22,400. (For policy questions regarding this collection contact Gary
Knight at 304-347-5723.)
2. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Medicaid
Eligibility and Enrollment (EE) Implementation Advanced Planning
Document (IAPD) Template; Use: To assess the appropriateness of states'
requests for enhanced federal financial participation for expenditures
related to Medicaid eligibility determination systems, we will review
the submitted information and documentation to make an approval
determination for the advanced planning document. Form Number: CMS-
10536 (OMB control number: 0938-1268); Frequency: Yearly, once, and
occasionally; Affected Public: State, Local, or Tribal Governments;
Number of Respondents: 56; Total Annual Responses: 168; Total Annual
Hours: 2,688. (For policy questions regarding this collection contact
Loren Palestino at 410-786-8842.)
3. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Medicaid Drug Use
Review (DUR) Program; Use: States must provide for a review of drug
therapy before each prescription is filled or delivered to a Medicaid
patient. This review includes screening for potential drug therapy
problems due to therapeutic duplication, drug-disease
contraindications, drug-drug interactions, incorrect drug dosage or
duration of drug treatment, drug-allergy interactions, and clinical
abuse/misuse. Pharmacists must make a reasonable effort to obtain,
record, and maintain Medicaid patient profiles. These profiles must
reflect at least the patient's name, address, telephone number, date of
birth/age, gender, history, e.g., allergies, drug reactions, list of
medications, and pharmacist's comments relevant to the individual's
drug therapy. The State must conduct retrospective drug use review
which provides for the ongoing periodic examination of claims data and
other records in order to identify patterns of fraud, abuse,
inappropriate or medically unnecessary care. Patterns or trends of drug
therapy problems are identified and reviewed to determine the need for
intervention activity with pharmacists and/or physicians. States may
conduct interventions via telephone, correspondence, or face-to-face
contact. The states and managed care organizations (MCOs) are provided
the reporting instrument (a survey) by CMS, and by responding to the
survey, the states generate annual reports which are submitted to CMS
for the purposes of monitoring compliance and evaluating the progress
of states' DUR programs. The survey and the annual recordkeeping and
reporting requirements under the pertinent regulations, are completed
by pharmacists employed by, or contracted with the various state
Medicaid programs and their MCOs. The annual reports submitted by
states are reviewed and results are compiled by CMS in a format
intended to provide information, comparisons and trends related to
states' experiences with DUR. The states benefit from the information
and may enhance their programs each year based on state reported
innovative practices that are compiled by CMS from the annual reports.
A comparison/summary of the data from the annual reports is published
on Medicaid.gov annually, and serves as a resource for stakeholders,
including but not limited to states, manufacturers, researchers,
congress, CMS, the Office of Inspector General, non-governmental payers
and clinicians on the topic of DUR in state Medicaid programs. Form
Number: CMS-R-153 (OMB control number: 0938-0659); Frequency: Yearly,
quarterly, and occasionally; Affected Public: State, Local, or Tribal
Governments; Number of Respondents: 52; Total Annual Responses: 676;
Total Annual Hours: 41,860. (For policy questions regarding this
collection contact Mike Forman at 410-786-2666.)
4. Type of Information Collection Request: Reinstatement without
change of a currently approved collection; Title of Information
Collection: Electronic Submission of Medicare Graduate Medical
Education (GME) Affiliation Agreements; Use: Existing regulations at
Sec. 413.75(b) permit hospitals that share residents to elect to form
a Medicare GME affiliated group if they are in the same or contiguous
urban or rural areas, if they are under common ownership, or if they
are jointly listed as program sponsors or major participating
institutions in the same program by the accrediting agency. The purpose
of a Medicare GME affiliated group is to provide flexibility to
hospitals in structuring rotations under an aggregate full time
equivalent (FTE) resident cap when they share residents. The existing
regulations at Sec. 413.79(f)(1) specify that each hospital in a
Medicare GME affiliated group must submit a Medicare GME affiliation
agreement (as defined under Sec. 413.75(b)) to the Medicare
Administrative Contractor (MAC) servicing the hospital and send a copy
to the Centers for Medicare and Medicaid Services' (CMS) Central
Office, no later than July 1 of the residency program year during which
the Medicare GME affiliation agreement will be in effect.
CMS will use the information contained in electronic affiliation
agreements as documentation of the existence of Medicare GME
affiliations,
[[Page 54004]]
and to verify that the affiliations being formed by teaching hospitals
for the purposes of sharing their Medicare GME FTE cap slots are valid
according to CMS regulations. CMS will also use these affiliation
agreements as reference materials when potential issues involving
specific affiliations arise. While we have used hard copies of
affiliation agreements for those same purposes in the past, we
implemented this electronic submission process in order to expedite and
ease the process of retrieving, analyzing and evaluating affiliation
agreements. Form Number: CMS-10326 (OMB control number: 0938-1111);
Frequency: Annually; Affected Public: Private Sector, Business or other
for profits, Not for profit institutions; Number of Respondents: 125;
Total Annual Responses: 125; Total Annual Hours: 166. (For policy
questions regarding this collection contact Shevi Marciano at 410-786-
2874.)
William N. Parham, III,
Director, Division of Information Collections and Regulatory Impacts,
Office of Strategic Operations and Regulatory Affairs.
[FR Doc. 2024-14338 Filed 6-27-24; 8:45 am]
BILLING CODE 4120-01-P