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 khammond on DSKJM1Z7X2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 18:32 Dec 04, 2020 Jkt 253001 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: PO 00000 Frm 00033 Fmt 4703 Sfmt 4703 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: E:\FR\FM\07DEN1.SGM 07DEN1 khammond on DSKJM1Z7X2PROD with NOTICES 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. VerDate Sep<11>2014 18:32 Dec 04, 2020 Jkt 253001 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.) PO 00000 Frm 00034 Fmt 4703 Sfmt 4703 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 E:\FR\FM\07DEN1.SGM 07DEN1 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: VerDate Sep<11>2014 18:32 Dec 04, 2020 Jkt 253001 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 Frm 00035 Fmt 4703 Sfmt 4703 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. E:\FR\FM\07DEN1.SGM 07DEN1

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

[[Page 78855]]

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
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