Agency Information Collection Activities: Submission for OMB Review; Comment Request, 7974-7976 [2023-02579]
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Federal Register / Vol. 88, No. 25 / Tuesday, February 7, 2023 / Notices
advise the contact listed below as soon
as possible.
ADDRESSES: Direct all PRA comments to
Cathy Williams, FCC, via email to PRA@
fcc.gov and to Cathy.Williams@fcc.gov.
FOR FURTHER INFORMATION CONTACT: For
additional information about the
information collection, contact Cathy
Williams at (202) 418–2918.
SUPPLEMENTARY INFORMATION:
OMB Control Number: 3060–XXXX.
Title: Empowering Broadband
Consumers Through Transparency,
Report and Order and Further Notice of
Proposed Rulemaking, CG Docket No.
22–2, FCC 22–86 (Broadband Label
Order).
Form Number: N/A.
Type of Review: New information
collection.
Respondents: Business or other forprofit entities.
Number of Respondents: 6,010
respondents; 30,050 responses.
Estimated Time per Response: 0.5 (30
minutes) to 9 hours.
Frequency of Response: On-occasion
reporting requirement and
recordkeeping requirement.
Obligation to Respond: Required to
obtain or retain benefits. The statutory
authority for the information collection
requirements is contained in sections
4(i), 4(j), 13, 201(b), 254, 257, 301, 303,
316, and 332 of the Communications
Act of 1934, as amended, 47 U.S.C.
154(i), 154(j), 163, 201(b), 254, 257, 301,
303, 316, 332, section 60504 of the
Infrastructure Investment and Jobs Act,
Public Law 117–58, 135 Stat. 429
(2021), and section 904 of the
Consolidated Appropriations Act, 2021,
Public Law 116–260, 134 Stat. 1182
(2020), as amended.
Total Annual Burden: 117,271 hours.
Total Annual Cost: No cost.
Needs and Uses: This notice and
request for comments seeks to establish
a new information collection as it
pertains to Empowering Broadband
Consumers Through Transparency,
Report and Order and Further Notice of
Proposed Rulemaking, published at 87
FR 76959 (Dec. 16, 2022) (Broadband
Label Order). The information will be
used to implement section 60504(a) of
the Infrastructure Investment and Jobs
Act (Infrastructure Act). The
Infrastructure Act, in relevant part,
directed the Commission ‘‘[n]ot later
than 1 year after the date of enactment
of th[e] Act, to promulgate regulations to
require the display of broadband
consumer labels, as described in the
Public Notice of the Commission issued
on April 4, 2016 (DA 16–357), to
disclose to consumers information
regarding broadband internet access
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service plans.’’ Further, the
Infrastructure Act required that the label
‘‘include information regarding whether
the offered price is an introductory rate
and, if so, the price the consumer will
be required to pay following the
introductory period.’’
On January 27, 2022, the Commission
released a Notice of Proposed
Rulemaking, published at 87 FR 6827
(Feb. 7, 2022), initiating a proceeding to
implement section 60504 of the
Infrastructure Act. Specifically, the
Commission proposed to require that
broadband internet access service
providers (ISPs or providers) display, at
the point of sale, labels that disclose to
consumers certain information about
prices, introductory rates, data
allowances, broadband speeds, and
management practices, among other
things.
On November 14, 2022, the
Commission adopted the Broadband
Label Order requiring ISPs to display a
new broadband label to help consumers
comparison shop among broadband
services, thereby implementing section
60504 of the Infrastructure Act.
Specifically, the Commission required
ISPs to display, at the point of sale, a
broadband consumer label containing
critical information about the provider’s
service offerings, including information
about pricing, introductory rates, data
allowances, performance metrics, and
whether the provider participates in the
Affordable Connectivity Program (ACP).
The Commission required that ISPs
display the label for each stand-alone
broadband internet access service they
currently offer for purchase, and that the
label link to other important
information such as network
management practices, privacy policies,
and other educational materials.
Consistent with the Infrastructure Act,
the label adopted for fixed and mobile
broadband internet access service is
similar to the two voluntary labels the
Commission approved in 2016, with
certain modifications. The label
resembles the well-known nutrition
labels that consumers have come to rely
on when shopping for food products.
In addition to label content, the
Commission adopted requirements for
the label’s format and display location
to ensure consumers can make side-byside comparisons of various service
offerings from an individual provider or
from alternative providers—something
essential for making informed decisions.
Labels must be displayed on providers’
websites and at alternate sales channels
such as retail locations and over the
phone. The label must be accessible for
people with disabilities and for nonEnglish speakers. Labels must also be
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available via a customer’s online
account portal. ISPs shall maintain an
archive of all labels for a period of no
less than two years from the time the
service plan reflected in the label is no
longer available for purchase by a new
subscriber and the provider has
removed the label from its website or
alternate sales channels. In addition,
third parties will be able to easily
analyze information contained in the
labels and help consumers with their
purchase decisions, as providers are
required to make the label content
available in a machine-readable format
on their websites. Finally, the
Commission adopted a label template
that all ISPs are required to display at
the point of sale. This label establishes
the formatting and content of all
requirements adopted in the Broadband
Label Order.
Federal Communications Commission.
Marlene Dortch,
Secretary, Office of the Secretary.
[FR Doc. 2023–02486 Filed 2–6–23; 8:45 am]
BILLING CODE 6712–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers CMS–R–262, CMS–R–
282, CMS–10227, CMS–10609 and CMS–
10731]
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
information, including the necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of
SUMMARY:
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Federal Register / Vol. 88, No. 25 / Tuesday, February 7, 2023 / Notices
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.
Comments on the collection(s) of
information must be received by the
OMB desk officer by March 9, 2023.
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:
William Parham at (410) 786–4669.
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: Revision of a currently
approved collection; Title of
Information Collection: CMS Plan
Benefit Package (PBP) and Formulary
CY 2024; Use: Under the Medicare
Modernization Act (MMA), Medicare
Advantage (MA) and Prescription Drug
Plan (PDP) organizations are required to
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SUPPLEMENTARY INFORMATION:
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Jkt 259001
submit plan benefit packages for all
Medicare beneficiaries residing in their
service area. The plan benefit package
submission consists of the Plan Benefit
Package (PBP) software, formulary file,
and supporting documentation, as
necessary. MA and PDP organizations
use the PBP software to describe their
organization’s plan benefit packages,
including information on premiums,
cost sharing, authorization rules, and
supplemental benefits. They also
generate a formulary to describe their
list of drugs, including information on
prior authorization, step therapy,
tiering, and quantity limits.
CMS requires that MA and PDP
organizations submit a completed PBP
and formulary as part of the annual
bidding process. During this process,
organizations prepare their proposed
plan benefit packages for the upcoming
contract year and submit them to CMS
for review and approval. CMS uses this
data to review and approve the benefit
packages that the plans will offer to
Medicare beneficiaries. This allows
CMS to review the benefit packages in
a consistent way across all submitted
bids during with incredibly tight
timeframes. This data is also used to
populate data on Medicare Plan Finder,
which allows beneficiaries to access and
compare Medicare Advantage and
Prescription Drug plans. Form Number:
CMS–R–262 (OMB control number:
0938–0763); Frequency: Yearly; Affected
Public: Private Sector, Business or other
for-profits, Not-for-profits institutions;
Number of Respondents: 839; Total
Annual Responses: 8,932; Total Annual
Hours: 57,126. (For policy questions
regarding this collection contact Kristy
Holtje, at 410–786–2209.)
2. Type of Information Collection
Request: Extension with no change of a
currently approved collection; Title of
Information Collection: Medicare
Advantage Appeals and Grievance Data
Form; Use: Part 422 of Title 42 of the
Code of Federal Regulations (CFR)
distinguishes between certain
information a Medicare Advantage (MA)
organization must provide to each
enrollee (on an annual basis) and
information that the MA organization
must disclose to any MA eligible
individual (upon request). This
requirement can be found in
§ 1852(c)(2)(C) of the Social Security Act
and in 42 CFR 422.111(c)(3) which
states that MA organizations must
disclose information pertaining to the
number of disputes, and their
disposition in the aggregate, with the
categories of grievances and appeals, to
any individual eligible to elect an MA
organization who requests this
information.
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7975
The appeals and grievance data form
is an OMB approved form for use by
Medicare Advantage organizations to
disclose grievance and appeal data,
upon request, to individuals eligible to
elect an MA organization. By utilizing
the form, MA organizations will meet
the disclosure requirements set forth in
regulations at 42 CFR 422.111(c)(3).
Form Number: CMS–R–282 (OMB
control number: 0938–0778); Frequency:
Yearly; Affected Public: State, Local, or
Tribal Governments; Number of
Respondents: 949; Total Annual
Responses: 63,740; Total Annual Hours:
5,964. (For policy questions regarding
this collection contact Sabrina
Edmonston at 410–786–3209.)
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: PACE State Plan
Amendment Preprint; Use: If a state
elects to offer PACE as an optional
Medicaid benefit, it must complete a
state plan amendment preprint packet
described as ‘‘Enclosures 3, 4, 5, 6, and
7.’’ CMS will review the information
provided in order to determine if the
state has properly elected to cover PACE
services as a state plan option. In the
event that the state changes something
in the state plan, only the affected page
must be updated. Form Number: CMS–
10227 (OMB control number: 0938–
1027); Frequency: Once and
occasionally; Affected Public: State,
Local, or Tribal Governments; Number
of Respondents: 7; Total Annual
Responses: 2; Total Annual Hours: 140.
(For policy questions regarding this
collection contact Angela Cimino at
410–786–2638.)
4. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Medicaid
Program Face-to-Face Requirements for
Home Health Services and Supporting
Regulations; Use: Physicians (or for
medical equipment, authorized nonphysician practitioners (NPPs)
including nurse practitioners, clinical
nurse specialists and physician
assistants) must document that there
was a face-to-face encounter with the
Medicaid beneficiary prior to the
physician making a certification that
home health services are required. The
burden associated with this requirement
is the time and effort to complete this
documentation. The burden also
includes writing, typing, or dictating the
face-to-face documentation and signing/
dating the documentation.
Section 3708 of the Coronavirus Aid,
Relief, and Economic Security (CARES)
Act permits nurse practitioners (NPs),
clinical nurse specialists (CNSs), and
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physician assistants (PAs) to certify the
need for home health services and to
order services in the Medicare and
Medicaid programs. As such, under
CMS–5531–IFC, CMS amended 42 CFR
440.70 to remove the requirement that
the NPPs have to communicate the
clinical finding of the face-to-face
encounter to the ordering physician.
With expanding authority to order home
health services, the CARES Act also
provided that such practitioners are
now capable of independently
performing the face-to-face encounter
for the patient for whom they are the
ordering practitioner, in accordance
with state law. Form Number: CMS–
10609 (OMB control number: 0938–
1319); Frequency: Occasionally;
Affected Public: Private sector (business
or other for-profits); Number of
Respondents: 381,148; Total Annual
Responses: 1,143,443; Total Annual
Hours: 190,955. (For policy questions
regarding this collection contact
Alexandra Eitel at 410–786–0790.)
5. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Generic
Clearance for CMS and Medicare
Administrative Contractor (MAC)
Generic Customer Experience; Use: The
Centers for Medicare & Medicaid
Services (CMS) is requesting approval to
collect generic feedback from
respondents including, but not limited
to Medicare providers, Medicare
suppliers, provider or supplier staff,
billers, credentialing agencies,
researchers, clearinghouses, consultants,
and attorneys. These surveys will give
us insights into customers’ perceptions
and opinions and will be used to
improve customer experiences and
communications materials; however, the
results will not be generalized to the
population of study.
Improving agency programs requires
ongoing systemic review of service
delivery and program operations
compared to defined standards. We’ll
use multiple methods to collect,
analyze, and interpret information from
this generic clearance to find the
strengths and weaknesses of our current
services. We’ll use this feedback to
inform process improvements or
maintain service quality offered to
providers and stakeholders. Form
Number: CMS–10731 (OMB control
number: 0938–New); Frequency:
Occasionally; Affected Public: Private
sector (business or other for-profits);
Number of Respondents: 997,100; Total
Annual Responses: 997,100; Total
Annual Hours: 50,000. (For policy
questions regarding this collection
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18:52 Feb 06, 2023
Jkt 259001
contact Alyssa Schaub-Rimel at 410–
786–4660.)
Dated: February 2, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory.
[FR Doc. 2023–02579 Filed 2–6–23; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers CMS–10704, CMS–
10387, CMS–10846, CMS–R–246 and CMS–
10316]
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
April 10, 2023.
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’’
SUMMARY:
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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–10704 Health Reimbursement
Arrangements and Other AccountBased Group Health Plans
CMS–10387 Minimum Data Set 3.0
Nursing Home and Swing Bed
Prospective Payment System (PPS)
For the collection of data related to
the Patient Driven Payment Model
and the Skilled Nursing Facility
Quality Reporting Program (QRP)
CMS–10846 Medicare Part D
Manufacturer Discount Program
Agreement
CMS–R–246 Medicare Advantage,
Medicare Part D, and Medicare FeeFor-Service Consumer Assessment of
Healthcare Providers and Systems
(CAHPS) Survey
CMS–10316 Implementation of the
Medicare Prescription Drug Plan
(PDP) and Medicare Advantage (MA)
Plan Disenrollment Reasons Survey
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
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Agencies
[Federal Register Volume 88, Number 25 (Tuesday, February 7, 2023)]
[Notices]
[Pages 7974-7976]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-02579]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers CMS-R-262, CMS-R-282, CMS-10227, CMS-10609 and
CMS-10731]
Agency Information Collection Activities: Submission for OMB
Review; 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 a second opportunity
for public comment on the notice. Interested persons are invited to
send comments regarding the burden estimate or any other aspect of this
collection of information, including the necessity and utility of the
proposed information collection for the proper performance of the
agency's functions, the accuracy of
[[Page 7975]]
the estimated burden, ways to enhance the quality, utility, and clarity
of the information to be collected, and the use of automated collection
techniques or other forms of information technology to minimize the
information collection burden.
DATES: Comments on the collection(s) of information must be received by
the OMB desk officer by March 9, 2023.
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/PRA-Listing.
FOR FURTHER INFORMATION CONTACT: William Parham at (410) 786-4669.
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. The term ``collection of
information'' is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and
includes agency requests or requirements that members of the public
submit reports, keep records, or provide information to a third party.
Section 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: Revision of a currently
approved collection; Title of Information Collection: CMS Plan Benefit
Package (PBP) and Formulary CY 2024; Use: Under the Medicare
Modernization Act (MMA), Medicare Advantage (MA) and Prescription Drug
Plan (PDP) organizations are required to submit plan benefit packages
for all Medicare beneficiaries residing in their service area. The plan
benefit package submission consists of the Plan Benefit Package (PBP)
software, formulary file, and supporting documentation, as necessary.
MA and PDP organizations use the PBP software to describe their
organization's plan benefit packages, including information on
premiums, cost sharing, authorization rules, and supplemental benefits.
They also generate a formulary to describe their list of drugs,
including information on prior authorization, step therapy, tiering,
and quantity limits.
CMS requires that MA and PDP organizations submit a completed PBP
and formulary as part of the annual bidding process. During this
process, organizations prepare their proposed plan benefit packages for
the upcoming contract year and submit them to CMS for review and
approval. CMS uses this data to review and approve the benefit packages
that the plans will offer to Medicare beneficiaries. This allows CMS to
review the benefit packages in a consistent way across all submitted
bids during with incredibly tight timeframes. This data is also used to
populate data on Medicare Plan Finder, which allows beneficiaries to
access and compare Medicare Advantage and Prescription Drug plans. Form
Number: CMS-R-262 (OMB control number: 0938-0763); Frequency: Yearly;
Affected Public: Private Sector, Business or other for-profits, Not-
for-profits institutions; Number of Respondents: 839; Total Annual
Responses: 8,932; Total Annual Hours: 57,126. (For policy questions
regarding this collection contact Kristy Holtje, at 410-786-2209.)
2. Type of Information Collection Request: Extension with no change
of a currently approved collection; Title of Information Collection:
Medicare Advantage Appeals and Grievance Data Form; Use: Part 422 of
Title 42 of the Code of Federal Regulations (CFR) distinguishes between
certain information a Medicare Advantage (MA) organization must provide
to each enrollee (on an annual basis) and information that the MA
organization must disclose to any MA eligible individual (upon
request). This requirement can be found in Sec. 1852(c)(2)(C) of the
Social Security Act and in 42 CFR 422.111(c)(3) which states that MA
organizations must disclose information pertaining to the number of
disputes, and their disposition in the aggregate, with the categories
of grievances and appeals, to any individual eligible to elect an MA
organization who requests this information.
The appeals and grievance data form is an OMB approved form for use
by Medicare Advantage organizations to disclose grievance and appeal
data, upon request, to individuals eligible to elect an MA
organization. By utilizing the form, MA organizations will meet the
disclosure requirements set forth in regulations at 42 CFR
422.111(c)(3). Form Number: CMS-R-282 (OMB control number: 0938-0778);
Frequency: Yearly; Affected Public: State, Local, or Tribal
Governments; Number of Respondents: 949; Total Annual Responses:
63,740; Total Annual Hours: 5,964. (For policy questions regarding this
collection contact Sabrina Edmonston at 410-786-3209.)
3. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: PACE State Plan
Amendment Preprint; Use: If a state elects to offer PACE as an optional
Medicaid benefit, it must complete a state plan amendment preprint
packet described as ``Enclosures 3, 4, 5, 6, and 7.'' CMS will review
the information provided in order to determine if the state has
properly elected to cover PACE services as a state plan option. In the
event that the state changes something in the state plan, only the
affected page must be updated. Form Number: CMS-10227 (OMB control
number: 0938-1027); Frequency: Once and occasionally; Affected Public:
State, Local, or Tribal Governments; Number of Respondents: 7; Total
Annual Responses: 2; Total Annual Hours: 140. (For policy questions
regarding this collection contact Angela Cimino at 410-786-2638.)
4. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Medicaid Program
Face-to-Face Requirements for Home Health Services and Supporting
Regulations; Use: Physicians (or for medical equipment, authorized non-
physician practitioners (NPPs) including nurse practitioners, clinical
nurse specialists and physician assistants) must document that there
was a face-to-face encounter with the Medicaid beneficiary prior to the
physician making a certification that home health services are
required. The burden associated with this requirement is the time and
effort to complete this documentation. The burden also includes
writing, typing, or dictating the face-to-face documentation and
signing/dating the documentation.
Section 3708 of the Coronavirus Aid, Relief, and Economic Security
(CARES) Act permits nurse practitioners (NPs), clinical nurse
specialists (CNSs), and
[[Page 7976]]
physician assistants (PAs) to certify the need for home health services
and to order services in the Medicare and Medicaid programs. As such,
under CMS-5531-IFC, CMS amended 42 CFR 440.70 to remove the requirement
that the NPPs have to communicate the clinical finding of the face-to-
face encounter to the ordering physician. With expanding authority to
order home health services, the CARES Act also provided that such
practitioners are now capable of independently performing the face-to-
face encounter for the patient for whom they are the ordering
practitioner, in accordance with state law. Form Number: CMS-10609 (OMB
control number: 0938-1319); Frequency: Occasionally; Affected Public:
Private sector (business or other for-profits); Number of Respondents:
381,148; Total Annual Responses: 1,143,443; Total Annual Hours:
190,955. (For policy questions regarding this collection contact
Alexandra Eitel at 410-786-0790.)
5. Type of Information Collection Request: New collection (Request
for a new OMB control number); Title of Information Collection: Generic
Clearance for CMS and Medicare Administrative Contractor (MAC) Generic
Customer Experience; Use: The Centers for Medicare & Medicaid Services
(CMS) is requesting approval to collect generic feedback from
respondents including, but not limited to Medicare providers, Medicare
suppliers, provider or supplier staff, billers, credentialing agencies,
researchers, clearinghouses, consultants, and attorneys. These surveys
will give us insights into customers' perceptions and opinions and will
be used to improve customer experiences and communications materials;
however, the results will not be generalized to the population of
study.
Improving agency programs requires ongoing systemic review of
service delivery and program operations compared to defined standards.
We'll use multiple methods to collect, analyze, and interpret
information from this generic clearance to find the strengths and
weaknesses of our current services. We'll use this feedback to inform
process improvements or maintain service quality offered to providers
and stakeholders. Form Number: CMS-10731 (OMB control number: 0938-
New); Frequency: Occasionally; Affected Public: Private sector
(business or other for-profits); Number of Respondents: 997,100; Total
Annual Responses: 997,100; Total Annual Hours: 50,000. (For policy
questions regarding this collection contact Alyssa Schaub-Rimel at 410-
786-4660.)
Dated: February 2, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory.
[FR Doc. 2023-02579 Filed 2-6-23; 8:45 am]
BILLING CODE 4120-01-P