Agency Information Collection Activities: Submission for OMB Review; Comment Request, 78853-78855 [2020-26862]
Download as PDF
Federal Register / Vol. 85, No. 235 / Monday, December 7, 2020 / Notices
william.garrett@gsa.gov. Please cite
Notice of GSA Bulletin FMR B–51.
SUPPLEMENTARY INFORMATION:
B. Annual Reporting Burden
Respondents: 91.
Responses Per Respondent: 2.
Total Annual Responses: 182.
Hours per Response: 5.
Total Burden Hours: 910.
C. Public Comments
A 60-day notice published in the
Federal Register at 85 FR 55678 on
September 9, 2020. There were no
comments.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the GSA Regulatory Secretariat Division,
by calling 202–501–4755 or emailing
GSARegSec@gsa.gov. Please cite OMB
Control No. 3090–0300, Implementation
of Information Technology Security
Provision, in all correspondence.
Jeffrey Koses,
Senior Procurement Executive, Office of
Acquisition Policy, Office of Governmentwide Policy.
[FR Doc. 2020–26817 Filed 12–4–20; 8:45 am]
BILLING CODE 6820–61–P
GENERAL SERVICES
ADMINISTRATION
[Notice–MA–2020–09; Docket No. 2020–
0002; Sequence No. 25]
Notice of GSA Bulletin FMR B–51 and
Supersession of GSA Bulletin FMR B–
27
Office of Government-wide
Policy (OGP), General Services
Administration (GSA).
ACTION: Notice of GSA Bulletin FMR B–
51, Annual Executive Agency Reports
on Exchange/Sale and Personal Property
Furnished to Non-Federal Recipients,
Supersession and Cancellation of GSA
Bulletin FMR B–27.
AGENCY:
GSA is updating guidance on
the Non-Federal Recipients Report and
Exchange/Sale Report. This bulletin
supersedes and cancels GSA Bulletin
FMR B–27, ‘‘Annual Executive Agency
Reports on Excess and Exchange/Sale
Personal Property,’’ issued on July 22,
2010, as this bulletin provides updated
information on the same topic. See the
SUPPLEMENTARY INFORMATION section
below for additional information.
DATES: Applicability Date: December 7,
2020.
FOR FURTHER INFORMATION CONTACT: For
clarification of content, contact Mr.
William Garrett, Director, Personal
Property Policy, Office of Governmentwide Policy, Office of Asset and
Transportation Management, at 202–
368–8163, or by email at
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SUMMARY:
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Background
GSA has Governmentwide oversight
and management responsibilities for the
Exchange/Sale and Non-Federal
Recipient Reports. GSA’s
responsibilities include issuing
appropriate regulations and monitoring
agency adherence to the regulations
through these reports.
On December 20, 2019, GAO publicly
released its report GAO–20–101,
‘‘FEDERAL PROPERTY: Improved
Monitoring, Oversight, and Data Would
Help Understand Effects of Providing
Property to Non-Federal Recipients.’’
The report recommended that ‘‘the GSA
Administrator should direct the Office
of Government-wide Policy to document
in what circumstances excess property
loaned to non-federal recipients should
be reported and what property GSA is
reporting on behalf of agencies, for
example, by updating GSA guidance.’’
To address this recommendation, this
bulletin is being issued to clarify the
requirements to annually submit to GSA
a report on personal property furnished
within the United States to non-Federal
recipients and a report on property
exchanged or sold for replacement
purposes. This bulletin also provides
updated guidance on reporting loans to
non-Federal recipients and clarifies
what property GSA is reporting on
behalf of agencies. This Bulletin
supersedes and cancels GSA Bulletin
FMR B–27. GSA Bulletin FMR B–51 is
available at www.gsa.gov/reference/gsabulletins.
Authority: 40 U.S.C. 503 and 529.
Jessica Salmoiraghi,
Associate Administrator, Office of
Government-wide Policy.
[FR Doc. 2020–26633 Filed 12–4–20; 8:45 am]
BILLING CODE 6820–14–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10265, CMS–
10171 and CMS–P–0015A]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
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78853
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 January 6, 2021.
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, you may make your request
using one of following:
1. Access CMS’ website address at
https://www.cms.gov/Regulations-andGuidance/Legislation/Paperwork
ReductionActof1995/PRA-Listing.html.
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.
SUMMARY:
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78854
Federal Register / Vol. 85, No. 235 / Monday, December 7, 2020 / Notices
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 with change of a
currently approved collection; Title of
Information Collection: Mandatory
Insurer Reporting Requirements of
Section 111 of the Medicare, Medicaid
and SCHIP Act of 2007; Use: The
Centers for Medicare & Medicaid
Services (CMS) collects various data
elements from the applicable reporting
entities (see supporting documents) for
purposes of carrying out the mandatory
MSP reporting requirements of Section
111 of the Medicare, Medicaid and
SCHIP Extension Act. This information
is used to ensure that Medicare makes
payment in the proper order and/or
takes necessary recovery actions. 42
U.S.C. 1395y(b)(7)(A)(i)(II) was updated
by the Substance Use-Disorder
Prevention that Promotes Opioid
Recovery and Treatment (SUPPORT) for
Patients and Communities Act. Section
4002 of the SUPPORT Act also applies
to Section 111 that requires Group
Health Plan (GHP) reporting of primary
prescription drug coverage.
MSP is generally divided into ‘‘prepayment’’ and ‘‘post-payment’’
activities. Pre-payment activities are
generally designed to stop mistaken
primary payments in situations where
Medicare should be secondary.
Medicare post-payment activities are
designed to recover mistaken payments
or conditional payments made by
Medicare where there is a contested
liability insurance (including selfinsurance), no-fault insurance, or
workers’ compensation which has
resulted in a settlement, judgment,
award, or other payment. CMS specialty
contractors perform most of the MSP
activity pre-payment.
The information is collected from
applicable reporting entities for the
purpose of coordination of benefits and
the recovery of mistaken and
conditional payments. Section 111
mandates the reporting of information
in the form and manner specified by the
Secretary, DHHS. Data the Secretary
collects is necessary for both prepayment and post-payment
coordination of benefit purposes,
including necessary recovery actions.
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18:32 Dec 04, 2020
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Both GHP and NGHP entities have
had and continue to have the
responsibility for determining when
they are primary to Medicare and to pay
appropriately, even without the
mandatory Section 111 process. Insurers
should always collect the NGHP, GHP
and GHP prescription drug information
that CMS requires in connection with
Section 111 of the MMSEA. Form
Number: CMS–10265 (OMB control
number: 0938–1074); Frequency: Yearly;
Affected Public: Private Sector, Business
or other for-profits; Number of
Respondents: 21,141; Total Annual
Responses: 8,079,697; Total Annual
Hours: 618,060. (For policy questions
regarding this collection contact Richard
Mazur at 410–786–1418.)
2. Type of Information Collection
Request: Revision with change of a
currently approved collection; Title of
Information Collection: Part D
Coordination of Benefits Data; Use:
Sections 1860D–23 and 1860D–24 of the
Act require the Secretary to establish
requirements for prescription drug plans
to promote effective coordination
between Part D plans and SPAPs and
other payers. These Part D Coordination
of Benefits (COB) requirements have
been codified into the Code of Federal
Regulations at 42 CFR 423.464. In
particular, CMS’ requirements relate to
the following elements: (1) Enrollment
file sharing; (2) claims processing and
payment; (3) claims reconciliation
reports; (4) application of the
protections against high out-of-pocket
expenditures by tracking TrOOP
expenditures; and (5) other processes
that the Secretary determines.
This information collection assists
CMS, pharmacists, Part D plans, and
other payers coordinate prescription
drug benefits at the point-of-sale and
track beneficiary True out-of-pocket
(TrOOP) expenditures using the Part D
Transaction Facilitator (PDTF).
The collected information will be
used by Part D plans, other health
insurers or payers, pharmacies and CMS
to coordinate prescription drug benefits
provided to the Medicare beneficiary.
Part D plans share data with each other
and with CMS. The types of data
collected for sharing include enrollment
data, other health insurance
information, TrOOP and Gross drug
spending and supplemental payer data.
Form Number: CMS–10171 (OMB
control number: 0938–0978); Frequency:
Yearly; Affected Public: State, Local, or
Tribal Governments; Number of
Respondents: 63,910; Total Annual
Responses: 770,855,926; Total Annual
Hours: 938,065. (For policy questions
regarding this collection contact Chad
Buskirk at 410–786–1630.)
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3. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Medicare
Current Beneficiary Survey; Use: CMS is
the largest single payer of health care in
the United States. The agency plays a
direct or indirect role in administering
health insurance coverage for more than
120 million people across the Medicare,
Medicaid, CHIP, and Exchange
populations. A critical aim for CMS is
to be an effective steward, major force,
and trustworthy partner in supporting
innovative approaches to improving
quality, accessibility, and affordability
in healthcare. CMS also aims to put
patients first in the delivery of their
health care needs.
The Medicare Current Beneficiary
Survey (MCBS) is the most
comprehensive and complete survey
available on the Medicare population
and is essential in capturing data not
otherwise collected through our
operations. The MCBS is a nationallyrepresentative, longitudinal survey of
Medicare beneficiaries that we sponsor
and is directed by the Office of
Enterprise Data and Analytics (OEDA).
The survey is usually conducted inperson but can also be conducted by
phone. It captures beneficiary
information whether aged or disabled,
living in the community or facility, or
serviced by managed care or fee-forservice. Data produced as part of the
MCBS are enhanced with our
administrative data (e.g., fee-for-service
claims, prescription drug event data,
enrollment, etc.) to provide users with
more accurate and complete estimates of
total health care costs and utilization.
The MCBS has been continuously
fielded for more than 28 years,
encompassing over 1 million interviews
and more than 100,000 survey
participants. Respondents participate in
up to 11 interviews over a four-year
period. This gives a comprehensive
picture of health care costs and
utilization over a period of time.
The MCBS continues to provide
unique insight into the Medicare
program and helps CMS and our
external stakeholders better understand
and evaluate the impact of existing
programs and significant new policy
initiatives. In the past, MCBS data have
been used to assess potential changes to
the Medicare program. For example, the
MCBS was instrumental in supporting
the development and implementation of
the Medicare prescription drug benefit
by providing a means to evaluate
prescription drug costs and out-ofpocket burden for these drugs to
Medicare beneficiaries. Beginning in
2021, this proposed revision to the
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Federal Register / Vol. 85, No. 235 / Monday, December 7, 2020 / Notices
clearance will add a few new measures
to existing questionnaire sections and
will add a new COVID–19
Questionnaire section previously
approved by OMB on August 7, 2020
under Emergency Clearance 0938–1379.
The revisions will result in an increase
in respondent burden due to the
addition of the new items.
Form Number: CMS–P–0015A (OMB:
0938–0568); Frequency: Occasionally;
Affected Public: Business or other forprofits and Not-for-profit institutions;
Number of Respondents: 13,656; Total
Annual Responses: 35,998; Total
Annual Hours: 53,176 (For policy
questions regarding this collection
contact William Long at 410–786–7927.)
Dated: December 2, 2020.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2020–26862 Filed 12–4–20; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10733]
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 (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
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
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
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18:32 Dec 04, 2020
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information technology to minimize the
information collection burden.
DATES: Comments must be received by
February 5, 2021.
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 lllll, 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
https://www.cms.gov/Regulations-andGuidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
2. 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–10733 Data Management Plan
Self-Attestation Questionnaire (DMP
SAQ)
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
PO 00000
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78855
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
Information Collection
1. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Data
Management Plan Self-Attestation
Questionnaire (DMP SAQ); Use: The
Privacy Act of 1974 allows for
discretionary releases of data
maintained in Privacy Act protected
systems of records under § 552a(b)
(Conditions of Disclosure). The mandate
to account for disclosures of data under
the Privacy Act is found at
§ 552a(c)(Accounting of Certain
Disclosures). This section states that
certain information must be maintained
regarding disclosures made by each
agency. This information is: Date,
Nature, Purpose, and Name/Address of
Recipient. Section 552a(e) sets the
overall Agency Requirements that each
agency must meet in order to maintain
records under the Privacy Act. The Data
Use Agreement (DUA) form is needed as
part of the review of each CMS data
request to ensure compliance with the
requirements of the Privacy Act for
disclosures that contain PII.
The DUA legally binds the user to the
Agreement’s terms. The user must agree
to all the terms and sign off on them
prior to the release or access to data files
containing protected health information,
and individual identifiers. The DMP
SAQ is a technical, evidence-based
questionnaire that DUA users must
complete as part of the data request
packet. The DMP SAQ will enable CMS
to evaluate researcher data systems to
ensure that CMS data are adequately
secured and appropriately protected, as
per the Privacy Act and the HIPAA
Privacy Rule. The DMP SAQ also allows
CMS to measure compliance through
the implementation of security and
privacy controls as outlined in the
National Institute of Standards and
Technology (NIST) Special Publication
800–53 and the Centers for Medicare &
Medicaid Services (CMS) Information
Security and Acceptable Risk
Safeguards (ARS). The second
component of the DMP SAQ is to
provide ongoing oversight. All
organizations will be subject to routine
audits of the environments used to store
and process CMS data, as described in
their organizational-level DMP SAQ.
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Agencies
[Federal Register Volume 85, Number 235 (Monday, December 7, 2020)]
[Notices]
[Pages 78853-78855]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-26862]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10265, CMS-10171 and CMS-P-0015A]
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 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 January 6, 2021.
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, you may make
your request using one of following:
1. Access CMS' website address at https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.html.
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.
[[Page 78854]]
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 with change of
a currently approved collection; Title of Information Collection:
Mandatory Insurer Reporting Requirements of Section 111 of the
Medicare, Medicaid and SCHIP Act of 2007; Use: The Centers for Medicare
& Medicaid Services (CMS) collects various data elements from the
applicable reporting entities (see supporting documents) for purposes
of carrying out the mandatory MSP reporting requirements of Section 111
of the Medicare, Medicaid and SCHIP Extension Act. This information is
used to ensure that Medicare makes payment in the proper order and/or
takes necessary recovery actions. 42 U.S.C. 1395y(b)(7)(A)(i)(II) was
updated by the Substance Use-Disorder Prevention that Promotes Opioid
Recovery and Treatment (SUPPORT) for Patients and Communities Act.
Section 4002 of the SUPPORT Act also applies to Section 111 that
requires Group Health Plan (GHP) reporting of primary prescription drug
coverage.
MSP is generally divided into ``pre-payment'' and ``post-payment''
activities. Pre-payment activities are generally designed to stop
mistaken primary payments in situations where Medicare should be
secondary. Medicare post-payment activities are designed to recover
mistaken payments or conditional payments made by Medicare where there
is a contested liability insurance (including self-insurance), no-fault
insurance, or workers' compensation which has resulted in a settlement,
judgment, award, or other payment. CMS specialty contractors perform
most of the MSP activity pre-payment.
The information is collected from applicable reporting entities for
the purpose of coordination of benefits and the recovery of mistaken
and conditional payments. Section 111 mandates the reporting of
information in the form and manner specified by the Secretary, DHHS.
Data the Secretary collects is necessary for both pre-payment and post-
payment coordination of benefit purposes, including necessary recovery
actions.
Both GHP and NGHP entities have had and continue to have the
responsibility for determining when they are primary to Medicare and to
pay appropriately, even without the mandatory Section 111 process.
Insurers should always collect the NGHP, GHP and GHP prescription drug
information that CMS requires in connection with Section 111 of the
MMSEA. Form Number: CMS-10265 (OMB control number: 0938-1074);
Frequency: Yearly; Affected Public: Private Sector, Business or other
for-profits; Number of Respondents: 21,141; Total Annual Responses:
8,079,697; Total Annual Hours: 618,060. (For policy questions regarding
this collection contact Richard Mazur at 410-786-1418.)
2. Type of Information Collection Request: Revision with change of
a currently approved collection; Title of Information Collection: Part
D Coordination of Benefits Data; Use: Sections 1860D-23 and 1860D-24 of
the Act require the Secretary to establish requirements for
prescription drug plans to promote effective coordination between Part
D plans and SPAPs and other payers. These Part D Coordination of
Benefits (COB) requirements have been codified into the Code of Federal
Regulations at 42 CFR 423.464. In particular, CMS' requirements relate
to the following elements: (1) Enrollment file sharing; (2) claims
processing and payment; (3) claims reconciliation reports; (4)
application of the protections against high out-of-pocket expenditures
by tracking TrOOP expenditures; and (5) other processes that the
Secretary determines.
This information collection assists CMS, pharmacists, Part D plans,
and other payers coordinate prescription drug benefits at the point-of-
sale and track beneficiary True out-of-pocket (TrOOP) expenditures
using the Part D Transaction Facilitator (PDTF).
The collected information will be used by Part D plans, other
health insurers or payers, pharmacies and CMS to coordinate
prescription drug benefits provided to the Medicare beneficiary. Part D
plans share data with each other and with CMS. The types of data
collected for sharing include enrollment data, other health insurance
information, TrOOP and Gross drug spending and supplemental payer data.
Form Number: CMS-10171 (OMB control number: 0938-0978); Frequency:
Yearly; Affected Public: State, Local, or Tribal Governments; Number of
Respondents: 63,910; Total Annual Responses: 770,855,926; Total Annual
Hours: 938,065. (For policy questions regarding this collection contact
Chad Buskirk at 410-786-1630.)
3. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Medicare Current
Beneficiary Survey; Use: CMS is the largest single payer of health care
in the United States. The agency plays a direct or indirect role in
administering health insurance coverage for more than 120 million
people across the Medicare, Medicaid, CHIP, and Exchange populations. A
critical aim for CMS is to be an effective steward, major force, and
trustworthy partner in supporting innovative approaches to improving
quality, accessibility, and affordability in healthcare. CMS also aims
to put patients first in the delivery of their health care needs.
The Medicare Current Beneficiary Survey (MCBS) is the most
comprehensive and complete survey available on the Medicare population
and is essential in capturing data not otherwise collected through our
operations. The MCBS is a nationally-representative, longitudinal
survey of Medicare beneficiaries that we sponsor and is directed by the
Office of Enterprise Data and Analytics (OEDA). The survey is usually
conducted in-person but can also be conducted by phone. It captures
beneficiary information whether aged or disabled, living in the
community or facility, or serviced by managed care or fee-for-service.
Data produced as part of the MCBS are enhanced with our administrative
data (e.g., fee-for-service claims, prescription drug event data,
enrollment, etc.) to provide users with more accurate and complete
estimates of total health care costs and utilization. The MCBS has been
continuously fielded for more than 28 years, encompassing over 1
million interviews and more than 100,000 survey participants.
Respondents participate in up to 11 interviews over a four-year period.
This gives a comprehensive picture of health care costs and utilization
over a period of time.
The MCBS continues to provide unique insight into the Medicare
program and helps CMS and our external stakeholders better understand
and evaluate the impact of existing programs and significant new policy
initiatives. In the past, MCBS data have been used to assess potential
changes to the Medicare program. For example, the MCBS was instrumental
in supporting the development and implementation of the Medicare
prescription drug benefit by providing a means to evaluate prescription
drug costs and out-of-pocket burden for these drugs to Medicare
beneficiaries. Beginning in 2021, this proposed revision to the
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clearance will add a few new measures to existing questionnaire
sections and will add a new COVID-19 Questionnaire section previously
approved by OMB on August 7, 2020 under Emergency Clearance 0938-1379.
The revisions will result in an increase in respondent burden due to
the addition of the new items.
Form Number: CMS-P-0015A (OMB: 0938-0568); Frequency: Occasionally;
Affected Public: Business or other for-profits and Not-for-profit
institutions; Number of Respondents: 13,656; Total Annual Responses:
35,998; Total Annual Hours: 53,176 (For policy questions regarding this
collection contact William Long at 410-786-7927.)
Dated: December 2, 2020.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2020-26862 Filed 12-4-20; 8:45 am]
BILLING CODE 4120-01-P