Agency Information Collection Activities: Proposed Collection; Comment Request, 50453-50455 [2019-20858]
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Federal Register / Vol. 84, No. 186 / Wednesday, September 25, 2019 / Notices
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
Public Health Accreditation Board
(PHAB): Assessment of Processes and
Outcomes—New—Center for State,
Tribal, Local and Territorial Support
(CSTLTS), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) works to protect
America from health, safety and security
50453
running through December 2019, the
Robert Wood Johnson Foundation
(RWJF) and the social science
organization NORC at the University of
Chicago, led evaluation efforts. CDC will
assume support of the evaluation
starting in 2020 and as a result, OMB
approval for data collection is being
sought.
The purpose of this ICR is to support
the collection of information from
participating health departments
through a series of five surveys. The
surveys seek to collect longitudinal data
on each health department throughout
their accreditation process.
The respondent universe will include
STLT health department directors or
designees. All surveys will be
administered electronically; a link to the
survey website will be provided in the
email invitation. The surveys will be
administered on a quarterly basis and
sent to all health departments that reach
each milestone in the accreditation
process (application, recently
accredited, accredited for one year,
approaching reaccreditation, and
reaccreditation). Each health
department will be invited to participate
in each survey once (for a total of five
surveys max per health department).
The total annualized estimated burden
is 100 hours. There are no costs to
respondents except their time.
threats, both foreign, and in the U.S.
CDC strives to fulfill this mission, in
part, by supporting state, tribal, local,
and territorial (STLT) health
departments. One mechanism for
supporting STLT health departments is
through CDC’s support of a national,
voluntary accreditation program.
CDC supports the Public Health
Accreditation Board (PHAB), a nonprofit organization that serves as the
independent accrediting body. PHAB,
with considerable input from national,
state, tribal, and local public health
professionals, developed a consensus
set of standards to assess the capacity of
state, tribal, local, and territorial health
departments. The first health
departments were accredited by PHAB
in early 2013; as of August 2019, a total
of 268 health departments (36 state,
three Tribal and 229 local), as well as
one statewide integrated local public
health department system have been
accredited. Accreditation is granted for
a five-year period and the first several
health departments have successfully
completed the reaccreditation process.
Formal efforts to assess the outcomes of
the accreditation program began in late
2012, and continue to date. Priorities
focus on gathering feedback for program
improvement and documenting program
outcomes to demonstrate impact and
inform decision making about future
program direction. Starting in 2012 and
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
STLT
STLT
STLT
STLT
HD
HD
HD
HD
Directors
Directors
Directors
Directors
or
or
or
or
Designee
Designee
Designee
Designee
.......
.......
.......
.......
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
60
60
60
60
1
1
1
1
20/60
20/60
20/60
20/60
20
20
20
20
STLT HD Directors or Designee .......
Survey 1: Applicants ........................
Survey 2: Recently Accredited HDs
Survey 3: HDs Accredited One Year
Survey 4: HDs Approaching Reaccreditation.
Survey 5: Reaccredited HDs ...........
60
1
20/60
20
Total ...........................................
...........................................................
........................
........................
........................
100
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–20704 Filed 9–24–19; 8:45 am]
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Number of
respondents
Form name
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10062, CMS–
10344 and CMS–588]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
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18:25 Sep 24, 2019
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PO 00000
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The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
SUMMARY:
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50454
Federal Register / Vol. 84, No. 186 / Wednesday, September 25, 2019 / Notices
jbell on DSK3GLQ082PROD with NOTICES
burden estimates or any other aspect of
this collection of information, including
the necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions,
the accuracy of the estimated burden,
ways to enhance the quality, utility, and
clarity of the information to be
collected, and the use of automated
collection techniques or other forms of
information technology to minimize the
information collection burden.
DATES: Comments must be received by
November 25, 2019.
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, you may make your request
using one of following:
1. Access CMS’ website address at
website address at https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
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–10062 Collection of Diagnostic
Data in the Abbreviated RAPS Format
from Medicare Advantage
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18:25 Sep 24, 2019
Jkt 247001
Organizations for Risk Adjusted
Payments
CMS–10344 Elimination of CostSharing for full benefit dual-eligible
Individuals Receiving Home and
Community-Based Services
CMS–588 Electronic Funds Transfer
Authorization Agreement
Under the PRA (44 U.S.C. 3501–
3520), federal agencies must obtain
approval from the Office of Management
and Budget (OMB) for each collection of
information they conduct or sponsor.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
Information Collection
1. Type of Information Collection
Request: Extension without change of a
currently approved collection; Title of
Information Collection: Collection of
Diagnostic Data in the Abbreviated
RAPS Format from Medicare Advantage
Organizations for Risk Adjusted
Payments; Use: The 1997 BBA and later
legislation required CMS to adjust perbeneficiary payments with a risk
adjustment methodology using
diagnoses to measure relative risk due to
health status instead of just
demographic characteristics such as age,
sex, and Medicaid eligibility. The
purpose of risk adjustment is to pay
plan sponsors accurately based on the
health status and diagnoses of their
Medicare enrollees. Risk adjustment
using diagnoses provides more accurate
payments for Medicare Advantage
Organizations (MAO), with higher
payments for enrollees at risk for being
sicker, and lower payments for enrollees
predicted to be healthier.
The BBA constituted the first
legislative mandate for health status risk
adjustment. Section 1853 (a)(3) of the
Social Security Act as enacted by
Section 4001 of Subtitle A of the BBA
required the Secretary to implement a
risk adjustment methodology that
accounted for variations in per capita
costs based on health status and other
demographic factors for payment to
Medicare+Choice (now MA)
organizations. The new methodology
PO 00000
Frm 00084
Fmt 4703
Sfmt 4703
was to be effective no later than January
1, 2000. The BBA also required that
M+C organizations submit data for use
in developing risk adjusted payments.
Risk adjustment allows CMS to pay
plans for the health risk of the
beneficiaries they enroll, instead of
paying an identical an average amount
for each enrollee Medicare beneficiaries.
By risk adjusting plan payments, CMS is
able to make appropriate and accurate
payments for enrollees with differences
in expected costs. Risk adjustment is
used to adjust bidding and payment
based on the health status and
demographic characteristics of an
enrollee. Risk scores measure individual
beneficiaries’ relative risk and the risk
scores are used to adjust payments for
each beneficiary’s expected
expenditures. By risk adjusting plan
bids, CMS is able to also use
standardized bids as base payments to
plans.
CMS’ fundamental goal for the
abbreviate format RAPS data is to
require collection of the minimum data
necessary for accurate risk-adjusted
payment. We believe that diagnostic
data provide the most reliable approach
to measuring health status, as required
by statute. In the absence of these data,
we would not be able to accurately
determine the beneficiary’s health (risk)
status. Form Number: CMS–10062
(OMB control number: 0938–0878);
Frequency: Quarterly; Affected Public:
State, Local, or Tribal Governments;
Number of Respondents: 761; Total
Annual Responses: 46,610,448; Total
Annual Hours: 33,484. (For policy
questions regarding this collection
contact Michael P. Massimini at 410–
786–1566.)
2. Type of Information Collection
Request: Extension without change of a
currently approved collection; Title of
Information Collection: Elimination of
Cost-Sharing for full benefit dualeligible Individuals Receiving Home
and Community-Based Services; Use:
Each month CMS deems individuals
automatically eligible for the full
subsidy, based on data from State
Medicaid Agencies and the Social
Security Administration (SSA). The
SSA sends a monthly file of
Supplementary Security Income-eligible
beneficiaries to CMS. Similarly, the
State Medicaid agencies submit
Medicare Modernization Act files to
CMS that identify full subsidy
beneficiaries. CMS deems the
beneficiaries as having full subsidy and
auto-assigns these beneficiaries to bench
mark Part D plans. Part D plans receive
premium amounts based on the monthly
assessments.
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25SEN1
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Federal Register / Vol. 84, No. 186 / Wednesday, September 25, 2019 / Notices
State MMA Phase Down (SPD)
exchange enables CMS to implement the
Medicare Prescription Drug,
Improvement, and Modernization Act,
also called the Medicare Modernization
Act (MMA), which was enacted into law
in 2003. This data exchange allows the
State Medicaid Agency (SMA) to
identify Medicare beneficiaries with
coverage under the Medicaid program.
The SMAs also identify other lowincome Medicare beneficiaries who
have applied for the Part D Low-Income
Subsidy (LIS). As a result of the
identification of these two groups of
beneficiaries, CMS auto-assigns and/or
facilitates enrollment of the appropriate
beneficiaries into Part D plans.
Section 1860 D–14 of the Social
Security Act sets forth requirements for
premium and cost-sharing subsidies for
low-income beneficiaries enrolled in
Medicare Part D. Based on this statute,
42 CFR 423.771, provides guidance
concerning limitations for payments
made by and on behalf of low-income
Medicare beneficiaries who enroll in
Part D plans. 42 CFR 423.771 (b)
establishes requirements for
determining a beneficiary’s eligibility
for full subsidy under the Part D
program. Regulations set forth in
423.780 and 423.782 outline premium
and cost sharing subsidies to which full
subsidy eligible are entitled under the
Part D program. Form Number: CMS–
10344 (OMB control number: 0938–
1127); Frequency: Monthly; Affected
Public: State, Local, or Tribal
Governments; Number of Respondents:
51; Total Annual Responses: 612; Total
Annual Hours: 612. (For policy
questions regarding this collection
contact Roland Horrea at 410–786–
0668.)
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Electronic
Funds Transfer Authorization
Agreement; Use: Section 1815(a) of the
Social Security Act provides the
authority for the Secretary of Health and
Human Services to pay providers/
suppliers of Medicare services at such
time or times as the Secretary
determines appropriate (but no less
frequently than monthly). Under
Medicare, CMS, acting for the Secretary,
contracts with Fiscal Intermediaries and
Carriers to pay claims submitted by
providers/suppliers who furnish
services to Medicare beneficiaries.
Under CMS’ payment policy, Medicare
providers/suppliers have the option of
receiving payments electronically. Form
Number: CMS–588 (OMB control
number: 0938–0626); Frequency: On
occasion; Affected Public: Business or
VerDate Sep<11>2014
18:25 Sep 24, 2019
Jkt 247001
other for-profit and Not-for-profit
institutions; Number of Respondents:
100,000; Total Annual Responses:
100,000; Total Annual Hours: 100,000.
For questions regarding this collection
contact Kim McPhillips at 410–786–
5374.
Dated: September 20, 2019.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2019–20858 Filed 9–24–19; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10595]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid 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
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 October 25, 2019.
ADDRESSES: When commenting on the
proposed information collections,
please reference the document identifier
or OMB control number. To be assured
consideration, comments and
recommendations must be received by
SUMMARY:
PO 00000
Frm 00085
Fmt 4703
Sfmt 4703
50455
the OMB desk officer via one of the
following transmissions: OMB, Office of
Information and Regulatory Affairs,
Attention: CMS Desk Officer, Fax
Number: (202) 395–5806 OR Email:
OIRA_submission@omb.eop.gov.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ website address at
website address at https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
1. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
2. Call the Reports Clearance Office at
(410) 786–1326.
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: Extension without change of a
currently approved collection; Title of
Information Collection: QHP Issuers
Data Collection for Notices for Plan or
Display Errors Special Enrollment
Periods; Use: The Patient Protection and
Affordable Care Act (Pub. L. 111–148)
and Health Care and Education
Reconciliation Act of 2010 (Pub. L. 111–
152), collectively referred to as the
PPACA, established new competitive
private health insurance markets called
Marketplaces, or Exchanges, which gave
millions of Americans and small
businesses access to qualified health
plans (QHPs), including stand-alone
dental plans (SADPs)— private health
E:\FR\FM\25SEN1.SGM
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Agencies
[Federal Register Volume 84, Number 186 (Wednesday, September 25, 2019)]
[Notices]
[Pages 50453-50455]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-20858]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10062, CMS-10344 and CMS-588]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. Under the Paperwork Reduction
Act of 1995 (the PRA), federal agencies are required to publish notice
in the Federal Register concerning each proposed collection of
information (including each proposed extension or reinstatement of an
existing collection of information) and to allow 60 days for public
comment on the proposed action. Interested persons are invited to send
comments regarding our
[[Page 50454]]
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 November 25, 2019.
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, you may make
your request using one of following:
1. Access CMS' website address at website address at https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.html.
2. Email your request, including your address, phone number, OMB
number, and CMS document identifier, to [email protected].
3. Call the Reports Clearance Office at (410) 786-1326.
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-10062 Collection of Diagnostic Data in the Abbreviated RAPS Format
from Medicare Advantage Organizations for Risk Adjusted Payments
CMS-10344 Elimination of Cost-Sharing for full benefit dual-eligible
Individuals Receiving Home and Community-Based Services
CMS-588 Electronic Funds Transfer Authorization Agreement
Under the PRA (44 U.S.C. 3501-3520), federal agencies must obtain
approval from the Office of Management and Budget (OMB) for each
collection of information they conduct or sponsor. The term
``collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests or requirements that members of
the public submit reports, keep records, or provide information to a
third party. Section 3506(c)(2)(A) of the PRA requires federal agencies
to publish a 60-day notice in the Federal Register concerning each
proposed collection of information, including each proposed extension
or reinstatement of an existing collection of information, before
submitting the collection to OMB for approval. To comply with this
requirement, CMS is publishing this notice.
Information Collection
1. Type of Information Collection Request: Extension without change
of a currently approved collection; Title of Information Collection:
Collection of Diagnostic Data in the Abbreviated RAPS Format from
Medicare Advantage Organizations for Risk Adjusted Payments; Use: The
1997 BBA and later legislation required CMS to adjust per-beneficiary
payments with a risk adjustment methodology using diagnoses to measure
relative risk due to health status instead of just demographic
characteristics such as age, sex, and Medicaid eligibility. The purpose
of risk adjustment is to pay plan sponsors accurately based on the
health status and diagnoses of their Medicare enrollees. Risk
adjustment using diagnoses provides more accurate payments for Medicare
Advantage Organizations (MAO), with higher payments for enrollees at
risk for being sicker, and lower payments for enrollees predicted to be
healthier.
The BBA constituted the first legislative mandate for health status
risk adjustment. Section 1853 (a)(3) of the Social Security Act as
enacted by Section 4001 of Subtitle A of the BBA required the Secretary
to implement a risk adjustment methodology that accounted for
variations in per capita costs based on health status and other
demographic factors for payment to Medicare+Choice (now MA)
organizations. The new methodology was to be effective no later than
January 1, 2000. The BBA also required that M+C organizations submit
data for use in developing risk adjusted payments.
Risk adjustment allows CMS to pay plans for the health risk of the
beneficiaries they enroll, instead of paying an identical an average
amount for each enrollee Medicare beneficiaries. By risk adjusting plan
payments, CMS is able to make appropriate and accurate payments for
enrollees with differences in expected costs. Risk adjustment is used
to adjust bidding and payment based on the health status and
demographic characteristics of an enrollee. Risk scores measure
individual beneficiaries' relative risk and the risk scores are used to
adjust payments for each beneficiary's expected expenditures. By risk
adjusting plan bids, CMS is able to also use standardized bids as base
payments to plans.
CMS' fundamental goal for the abbreviate format RAPS data is to
require collection of the minimum data necessary for accurate risk-
adjusted payment. We believe that diagnostic data provide the most
reliable approach to measuring health status, as required by statute.
In the absence of these data, we would not be able to accurately
determine the beneficiary's health (risk) status. Form Number: CMS-
10062 (OMB control number: 0938-0878); Frequency: Quarterly; Affected
Public: State, Local, or Tribal Governments; Number of Respondents:
761; Total Annual Responses: 46,610,448; Total Annual Hours: 33,484.
(For policy questions regarding this collection contact Michael P.
Massimini at 410-786-1566.)
2. Type of Information Collection Request: Extension without change
of a currently approved collection; Title of Information Collection:
Elimination of Cost-Sharing for full benefit dual-eligible Individuals
Receiving Home and Community-Based Services; Use: Each month CMS deems
individuals automatically eligible for the full subsidy, based on data
from State Medicaid Agencies and the Social Security Administration
(SSA). The SSA sends a monthly file of Supplementary Security Income-
eligible beneficiaries to CMS. Similarly, the State Medicaid agencies
submit Medicare Modernization Act files to CMS that identify full
subsidy beneficiaries. CMS deems the beneficiaries as having full
subsidy and auto-assigns these beneficiaries to bench mark Part D
plans. Part D plans receive premium amounts based on the monthly
assessments.
[[Page 50455]]
State MMA Phase Down (SPD) exchange enables CMS to implement the
Medicare Prescription Drug, Improvement, and Modernization Act, also
called the Medicare Modernization Act (MMA), which was enacted into law
in 2003. This data exchange allows the State Medicaid Agency (SMA) to
identify Medicare beneficiaries with coverage under the Medicaid
program. The SMAs also identify other low-income Medicare beneficiaries
who have applied for the Part D Low-Income Subsidy (LIS). As a result
of the identification of these two groups of beneficiaries, CMS auto-
assigns and/or facilitates enrollment of the appropriate beneficiaries
into Part D plans.
Section 1860 D-14 of the Social Security Act sets forth
requirements for premium and cost-sharing subsidies for low-income
beneficiaries enrolled in Medicare Part D. Based on this statute, 42
CFR 423.771, provides guidance concerning limitations for payments made
by and on behalf of low-income Medicare beneficiaries who enroll in
Part D plans. 42 CFR 423.771 (b) establishes requirements for
determining a beneficiary's eligibility for full subsidy under the Part
D program. Regulations set forth in 423.780 and 423.782 outline premium
and cost sharing subsidies to which full subsidy eligible are entitled
under the Part D program. Form Number: CMS-10344 (OMB control number:
0938-1127); Frequency: Monthly; Affected Public: State, Local, or
Tribal Governments; Number of Respondents: 51; Total Annual Responses:
612; Total Annual Hours: 612. (For policy questions regarding this
collection contact Roland Horrea at 410-786-0668.)
3. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Electronic Funds
Transfer Authorization Agreement; Use: Section 1815(a) of the Social
Security Act provides the authority for the Secretary of Health and
Human Services to pay providers/suppliers of Medicare services at such
time or times as the Secretary determines appropriate (but no less
frequently than monthly). Under Medicare, CMS, acting for the
Secretary, contracts with Fiscal Intermediaries and Carriers to pay
claims submitted by providers/suppliers who furnish services to
Medicare beneficiaries. Under CMS' payment policy, Medicare providers/
suppliers have the option of receiving payments electronically. Form
Number: CMS-588 (OMB control number: 0938-0626); Frequency: On
occasion; Affected Public: Business or other for-profit and Not-for-
profit institutions; Number of Respondents: 100,000; Total Annual
Responses: 100,000; Total Annual Hours: 100,000. For questions
regarding this collection contact Kim McPhillips at 410-786-5374.
Dated: September 20, 2019.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2019-20858 Filed 9-24-19; 8:45 am]
BILLING CODE 4120-01-P