Agency Information Collection Activities: Proposed Collection; Comment Request, 56754-56756 [2024-15152]
Download as PDF
56754
Federal Register / Vol. 89, No. 132 / Wednesday, July 10, 2024 / Notices
Collection Activities: Proposed
Collection; Comment Request.’’ The
document invited public comments on
four separate information collection
requests notices specific to document
identifiers: CMS–179, CMS–10536,
CMS–R–153 and CMS–10326. Through
the publication of this document, we are
withdrawing each of the aforementioned
notices.
DATES: The comment period associated
with the publication for CMS–179,
CMS–10536, CMS–R–153 and CMS–
10326 on July 2, 2024 (89 FR 54826),
will be null and void upon publication
of this document.
SUPPLEMENTARY INFORMATION: Each of
the aforementioned notices already
published on June 28, 2024 (89 FR
54002) and the comment period
associated with that publication remains
in full effect.
In FR document, 2024–14581,
published on July 2, 2024 (89 FR
54826), we are withdrawing all four of
the notices listed in the Information
Collections section of the document.
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–15097 Filed 7–9–24; 8:45 am]
BILLING CODE 4120–01–P
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–1500/1490S]
Agency Information Collection
Activities: Submission for OMB
Review; 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
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
ddrumheller on DSK120RN23PROD with NOTICES1
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Comments on the collection(s) of
information must be received by the
OMB desk officer by August 9, 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.
DATES:
FOR FURTHER INFORMATION CONTACT:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
SUMMARY:
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.
William Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. The term ‘‘collection of
information’’ is defined in 44 U.S.C.
3502(3) and 5 CFR 1320.3(c) and
includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension or
reinstatement of an existing collection
of information, before submitting the
collection to OMB for approval. To
comply with this requirement, CMS is
publishing this notice that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Health
Insurance Common Claims Form and
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
Supporting Regulations at 42 CFR part
424, subpart C; Use: The CMS–1500 and
the CMS–1490S forms are used to
deliver information to CMS for CMS to
reimburse for provided services.
Medicare Administrative Contractors
use the data collected on the CMS–1500
and the CMS–1490S to determine the
proper amount of reimbursement for
Part B medical and other health services
(as listed in section 1861(s) of the Social
Security Act) provided by physicians
and suppliers to beneficiaries. The
CMS–1500 is submitted by physicians/
suppliers for all Part B Medicare.
Serving as a common claim form, the
CMS–1500 can be used by other thirdparty payers (commercial and nonprofit
health insurers) and other Federal
programs (e.g. TRICARE, RRB, and
Medicaid). Form Number: CMS–1500/
1490S (OMB control number: 0938–
1197); Frequency: Occasionally;
Affected Public: Private Sector: Business
or other for-profit and not-for-profit
institutions; Number of Respondents:
2,507,992; Total Annual Responses:
994,038,623; Total Annual Hours:
17,328,912. (For policy questions
regarding this collection contact Sadaf
Ali-Simpson at 667–414–0004.)
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–15137 Filed 7–9–24; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–222–17, CMS–
10261, and CMS–R–284]
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
SUMMARY:
E:\FR\FM\10JYN1.SGM
10JYN1
Federal Register / Vol. 89, No. 132 / Wednesday, July 10, 2024 / Notices
ddrumheller on DSK120RN23PROD with NOTICES1
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
September 9, 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:
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–222–17 Rural Health Clinic Cost
Report
CMS–10261 Part C Medicare
Advantage Reporting Requirements
CMS–R–284 Transformed—Medicaid
Statistical Information System (T–
MSIS)
VerDate Sep<11>2014
18:33 Jul 09, 2024
Jkt 262001
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: Rural Health
Clinic Cost Report; Use: Under the
authority of sections 1815(a) and
1833(e) of the Social Security Act (42
U.S.C. 1395g), CMS requires that
providers of services participating in the
Medicare program submit information
to determine costs for health care
services rendered to Medicare
beneficiaries. CMS requires that
providers follow reasonable cost
principles under 1861(v)(1)(A) of the
Act when completing the Medicare cost
report. Regulations at 42 CFR 413.20
and 413.24 require that providers
submit acceptable cost reports on an
annual basis and maintain sufficient
financial records and statistical data,
capable of verification by qualified
auditors.
CMS requires Form CMS–222–17 to
determine an RHC’s reasonable costs
incurred in furnishing medical services
to Medicare beneficiaries and
reimbursement due to or from an RHC.
Each RHC submits the cost report to its
contractor for a reimbursement
determination. Section 1874A of the Act
describes the functions of the
contractor.
CMS regulations at 42 CFR
413.24(f)(4)(ii) requires that each RHC
submit an annual cost report to their
contractor in American Standard Code
for Information Interchange (ASCII)
electronic cost report (ECR) format.
RHCs submit the ECR file to contractors
using a compact disk (CD), flash drive,
or the CMS approved Medicare Cost
Report E-filing (MCREF) portal, [URL:
https://mcref.cms.gov]. Form Number:
CMS–222–17 (OMB control number:
PO 00000
Frm 00041
Fmt 4703
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56755
0938–0107); Frequency: Yearly; Affected
Public: Private Sector, State, Local, or
Tribal Governments, Federal
Government, Business or other forprofits, Not-for-profits institutions;
Number of Respondents: 2,101; Total
Annual Responses: 2,101; Total Annual
Hours: 115,555. (For policy questions
regarding this collection contact LuAnn
Piccione at (410) 786–5423).
2. Type of Information Collection
Request: Revision with of a currently
approved collection; Title of
Information Collection: Part C Medicare
Advantage Reporting Requirements;
Use: The Centers for Medicare and
Medicaid Services (CMS) established
reporting requirements for Medicare
Advantage Organizations (MAOs) under
the authority described in 42 CFR
422.516(a). Each MAO must have an
effective procedure to develop, compile,
evaluate, and report to CMS, to its
enrollees, and to the general public at
the times and in the manner that CMS
requires. At the same time, each MAO
must, in accordance with 42 CFR
422.516(a), safeguard the confidentiality
of the provider-patient relationship.
Health plans can use this information
to measure and benchmark their
performance. CMS receives inquiries
from the industry and other interested
stakeholders about the beneficiary use
of available benefits, including
supplemental benefits, grievance and
appeals rates, cost, and other factors
pertaining to use of government funds,
as well the performance of MA plans.
Form Number: CMS–10261 (OMB
control number: 0938–1054); Frequency:
Yearly; Affected Public: Business or
other for-profits; Number of
Respondents: 743; Total Annual
Responses: 6,687; Total Annual Hours:
187,979. (For policy questions regarding
this collection contact Lucia Patrone at
410–786–8621).
3. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Transformed—
Medicaid Statistical Information System
(T–MSIS); Use: The data reported in T–
MSIS are used by Federal, State, and
local officials, as well as by private
researchers and corporations to monitor
past and projected future trends in the
Medicaid program. The data provide the
only national level information
available on enrollees, beneficiaries, and
expenditures. It also provides the only
national level information available on
Medicaid utilization. The information is
the basis for analyses and for cost
savings estimates for the Department’s
cost sharing legislative initiatives to
Congress. The collected data are also
crucial to our actuarial forecasts. Form
E:\FR\FM\10JYN1.SGM
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56756
Federal Register / Vol. 89, No. 132 / Wednesday, July 10, 2024 / Notices
Number: CMS–R–284 (OMB control
number: 0938–0345); Frequency:
Quarterly and monthly; Affected Public:
State, Local, or Tribal Governments;
Number of Respondents: 54; Total
Annual Responses: 648; Total Annual
Hours: 7,290. (For policy questions
regarding this collection contact Connie
Gibson at 410–786–0755.)
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–15152 Filed 7–9–24; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2024–N–2930]
Genetic Metabolic Diseases Advisory
Committee; Notice of Meeting;
Establishment of a Public Docket;
Request for Comments—New Drug
Application 214927, for Arimoclomol
AGENCY:
Food and Drug Administration,
HHS.
Notice; establishment of a
public docket; request for comments.
ACTION:
The Food and Drug
Administration (FDA) announces a
forthcoming public advisory committee
meeting of the Genetic Metabolic
Diseases Advisory Committee (the
Committee). The general function of the
Committee is to provide advice and
recommendations to FDA on regulatory
issues. The meeting will be open to the
public. FDA is establishing a docket for
public comment on this document.
DATES: The meeting will be held on
August 2, 2024, from 9 a.m. to 6 p.m.
Eastern Time.
ADDRESSES: FDA and invited
participants may attend the meeting at
the FDA White Oak Campus, 10903
New Hampshire Ave., Bldg. 31
Conference Center, the Great Room
(Rm.1503), Silver Spring, MD 20993–
0002. The public will have the option to
participate via an online
teleconferencing and/or video
conferencing platform, and the advisory
committee meeting will be heard,
viewed, captioned, and recorded
through an online teleconferencing and/
or video conferencing platform.
Answers to commonly asked
questions about FDA advisory
committee meetings, including
information regarding special
accommodations due to a disability,
visitor parking, and transportation may
ddrumheller on DSK120RN23PROD with NOTICES1
SUMMARY:
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be accessed at: https://www.fda.gov/
AdvisoryCommittees/
AboutAdvisoryCommittees/
ucm408555.htm.
FDA is establishing a docket for
public comment on this meeting. The
docket number is FDA–2024–N–2930.
The docket will close on August 1,
2024. Please note that late, untimely
filed comments will not be considered.
The https://www.regulations.gov
electronic filing system will accept
comments until 11:59 p.m. Eastern Time
at the end of August 1, 2024. Comments
received by mail/hand delivery/courier
(for written/paper submissions) will be
considered timely if they are received
on or before that date.
Comments received on or before July
25, 2024, will be provided to the
Committee. Comments received after
that date will be taken into
consideration by FDA. In the event that
the meeting is cancelled, FDA will
continue to evaluate any relevant
applications or information, and
consider any comments submitted to the
docket, as appropriate.
You may submit comments as
follows:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2024–N–2930 for ‘‘Genetic Metabolic
Diseases Advisory Committee; Notice of
Meeting; Establishment of a Public
Docket; Request for Comments—
Arimoclomol.’’ Received comments,
those filed in a timely manner (see
ADDRESSES), will be placed in the docket
and, except for those submitted as
‘‘Confidential Submissions,’’ publicly
viewable at https://www.regulations.gov
or at the Dockets Management Staff
between 9 a.m. and 4 p.m., Monday
through Friday, 240–402–7500.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ FDA
will review this copy, including the
claimed confidential information, in its
consideration of comments. The second
copy, which will have the claimed
confidential information redacted/
blacked out, will be available for public
viewing and posted on https://
www.regulations.gov. Submit both
copies to the Dockets Management Staff.
If you do not wish your name and
contact information be made publicly
available, you can provide this
information on the cover sheet and not
in the body of your comments and you
must identify the information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://
www.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.pdf.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Dockets Management
E:\FR\FM\10JYN1.SGM
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Agencies
[Federal Register Volume 89, Number 132 (Wednesday, July 10, 2024)]
[Notices]
[Pages 56754-56756]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-15152]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-222-17, CMS-10261, and CMS-R-284]
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
[[Page 56755]]
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 September 9, 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-222-17 Rural Health Clinic Cost Report
CMS-10261 Part C Medicare Advantage Reporting Requirements
CMS-R-284 Transformed--Medicaid Statistical Information System (T-MSIS)
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: Rural Health
Clinic Cost Report; Use: Under the authority of sections 1815(a) and
1833(e) of the Social Security Act (42 U.S.C. 1395g), CMS requires that
providers of services participating in the Medicare program submit
information to determine costs for health care services rendered to
Medicare beneficiaries. CMS requires that providers follow reasonable
cost principles under 1861(v)(1)(A) of the Act when completing the
Medicare cost report. Regulations at 42 CFR 413.20 and 413.24 require
that providers submit acceptable cost reports on an annual basis and
maintain sufficient financial records and statistical data, capable of
verification by qualified auditors.
CMS requires Form CMS-222-17 to determine an RHC's reasonable costs
incurred in furnishing medical services to Medicare beneficiaries and
reimbursement due to or from an RHC. Each RHC submits the cost report
to its contractor for a reimbursement determination. Section 1874A of
the Act describes the functions of the contractor.
CMS regulations at 42 CFR 413.24(f)(4)(ii) requires that each RHC
submit an annual cost report to their contractor in American Standard
Code for Information Interchange (ASCII) electronic cost report (ECR)
format. RHCs submit the ECR file to contractors using a compact disk
(CD), flash drive, or the CMS approved Medicare Cost Report E-filing
(MCREF) portal, [URL: https://mcref.cms.gov]. Form Number: CMS-222-17
(OMB control number: 0938-0107); Frequency: Yearly; Affected Public:
Private Sector, State, Local, or Tribal Governments, Federal
Government, Business or other for-profits, Not-for-profits
institutions; Number of Respondents: 2,101; Total Annual Responses:
2,101; Total Annual Hours: 115,555. (For policy questions regarding
this collection contact LuAnn Piccione at (410) 786-5423).
2. Type of Information Collection Request: Revision with of a
currently approved collection; Title of Information Collection: Part C
Medicare Advantage Reporting Requirements; Use: The Centers for
Medicare and Medicaid Services (CMS) established reporting requirements
for Medicare Advantage Organizations (MAOs) under the authority
described in 42 CFR 422.516(a). Each MAO must have an effective
procedure to develop, compile, evaluate, and report to CMS, to its
enrollees, and to the general public at the times and in the manner
that CMS requires. At the same time, each MAO must, in accordance with
42 CFR 422.516(a), safeguard the confidentiality of the provider-
patient relationship.
Health plans can use this information to measure and benchmark
their performance. CMS receives inquiries from the industry and other
interested stakeholders about the beneficiary use of available
benefits, including supplemental benefits, grievance and appeals rates,
cost, and other factors pertaining to use of government funds, as well
the performance of MA plans. Form Number: CMS-10261 (OMB control
number: 0938-1054); Frequency: Yearly; Affected Public: Business or
other for-profits; Number of Respondents: 743; Total Annual Responses:
6,687; Total Annual Hours: 187,979. (For policy questions regarding
this collection contact Lucia Patrone at 410-786-8621).
3. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Transformed--
Medicaid Statistical Information System (T-MSIS); Use: The data
reported in T-MSIS are used by Federal, State, and local officials, as
well as by private researchers and corporations to monitor past and
projected future trends in the Medicaid program. The data provide the
only national level information available on enrollees, beneficiaries,
and expenditures. It also provides the only national level information
available on Medicaid utilization. The information is the basis for
analyses and for cost savings estimates for the Department's cost
sharing legislative initiatives to Congress. The collected data are
also crucial to our actuarial forecasts. Form
[[Page 56756]]
Number: CMS-R-284 (OMB control number: 0938-0345); Frequency: Quarterly
and monthly; Affected Public: State, Local, or Tribal Governments;
Number of Respondents: 54; Total Annual Responses: 648; Total Annual
Hours: 7,290. (For policy questions regarding this collection contact
Connie Gibson at 410-786-0755.)
William N. Parham, III,
Director, Division of Information Collections and Regulatory Impacts,
Office of Strategic Operations and Regulatory Affairs.
[FR Doc. 2024-15152 Filed 7-9-24; 8:45 am]
BILLING CODE 4120-01-P