Agency Information Collection Activities: Submission for OMB Review; Comment Request, 71427-71428 [2019-27926]

Download as PDF Federal Register / Vol. 84, No. 248 / Friday, December 27, 2019 / Notices date for this item. With regard to the memoranda items related to cross jurisdictional activity and derivatives in Schedule E, certain of these items will be calculated in large part consistent with current reporting requirements for the FFIEC 009. Therefore, the revisions to Schedules D and E will become effective for existing FR Y–15 respondents as of the December 31, 2019, report date, as originally proposed. One commenter asked if the Board would require FBOs to complete the proposed memorandum items, including the trading volume memorandum items, with respect to their combined U.S. operations (CUSO), as certain FBOs will begin filing the FR Y–15 based on their CUSO as of June 30, 2020, consistent with the Board’s recent tailoring rule. The Board has finalized the FR Y–15 revisions with the following effective dates for FBOs that will be required to file the FR Y–15 based on their CUSO: • June 30, 2020, report date: Revisions to Schedule E; • December 31, 2020, report date: Revisions to Schedules C and D.8 For the trading volume memorandum items being added to Schedule C, given that the FBO will begin filing the FR Y– 15 based on its CUSO as of June 30, 2020, an FBO would annualize its CUSO trading activity until it were to file four quarters of the FR Y–15. jbell on DSKJLSW7X2PROD with NOTICES Comments on GSIB Surcharge Methodology One commenter requested that prior to incorporating the proposed memoranda items into the GSIB surcharge framework, the Board undertake a holistic review and recalibration of the framework methodology subject to public comment. This commenter also requested that the Board adopt a procedural mechanism to ensure that the GSIB surcharge methodology is periodically reassessed, such as once every three or four years. These comments are beyond the scope of the proposal; however staff notes that any incorporation of these memoranda items into the GSIB surcharge framework would be subject to the rulemaking process and provide opportunity for public feedback. 8 An FBO required to file the FR Y–15 for its CUSO as of December 31, 2020 would look back to collect two quarters of trading volume data (i.e., trading volume information for July 1st–December 31st) and annualize the additional two quarters in Schedule C. VerDate Sep<11>2014 18:44 Dec 26, 2019 Jkt 250001 Board of Governors of the Federal Reserve System, December 19, 2019. Michele Taylor Fennell, Assistant Secretary of the Board. [FR Doc. 2019–27849 Filed 12–26–19; 8:45 am] BILLING CODE 6210–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier CMS–10701, CMS– 10191 and CMS–10142] 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. SUMMARY: Comments on the collection(s) of information must be received by the OMB desk officer by January 27, 2020. 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 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. DATES: PO 00000 Frm 00080 Fmt 4703 Sfmt 4703 71427 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: New collection (Request for a new OMB control number); Title of Information Collection: Medicare Beneficiary Experiences with Care Survey System; Use: The MBECS system is designed to conduct 1–2 surveys per year on priority groups of interest, thereby allowing CMS OMH to respond quickly to the data needs of stakeholders with interests in these underrepresented groups. Data collected through the MBECS system will be used to better understand—and thus serve the needs of—Medicare beneficiaries in minority populations. The core questionnaire will collect information on communication with medical professionals, coordination of health care, experiences getting needed health care, experiences with personal doctors and specialists, and key demographics. Data will be compared to benchmarks from the FFS CAHPS, MA CAHPS, and E:\FR\FM\27DEN1.SGM 27DEN1 jbell on DSKJLSW7X2PROD with NOTICES 71428 Federal Register / Vol. 84, No. 248 / Friday, December 27, 2019 / Notices NAM CAHPS surveys. The populationspecific questionnaire module will collect information about issues most relevant for particular minority groups; population-specific modules will be described in individual information collection requests. These data will be compared to benchmarks from the relevant CAHPS source surveys when available. Collection of these data from people who have been identified through CMS administrative data and administrative flags as part of specific minority populations will also serve as a critical validation step of this method for identifying difficult-to-study populations, thus making it easier to study beneficiaries in these groups in the future. Form Number: CMS–10701 (OMB control number: 0938–NEW); Frequency: Yearly; Affected Public: State, Local, or Tribal Governments; Number of Respondents: 10,000; Total Annual Responses: 10,000; Total Annual Hours: 3,333. (For policy questions regarding this collection contact Luis Perez at 410–786–8557.) 2. Type of Information Collection Request: Revision with change of a currently approved collection; Title of Information Collection: Medicare Parts C and D Program Audit Protocols and Data Requests; Use: Under the Medicare Prescription Drug, Improvement, and Modernization Act of 2003 and implementing regulations at 42 CFR parts 422 and 423, Medicare Part D plan sponsors and Medicare Advantage organizations are required to comply with all Medicare Parts C and D program requirements. CMS’ annual audit plan ensures that we evaluate sponsoring organizations’ compliance with these requirements. CMS program audits focus on high-risk areas that have the greatest potential for beneficiary harm. As such, CMS has developed several audit protocols that are included within the program area data request documents and that are posted to the CMS website each year for use by sponsoring organizations to prepare for their audit. As part of a robust audit process, CMS also requires sponsoring organizations who have been audited and found to have deficiencies to undergo a validation audit to ensure correction. The validation audit utilizes the same audit protocols, but only tests the elements where deficiencies were found, as opposed to re-administering the entire audit. Currently CMS utilizes the following 5 protocols to audit sponsoring organization performance: Part D Formulary and Benefit Administration (FA); Part D Coverage Determinations, Appeals, and Grievances (CDAG); Part C VerDate Sep<11>2014 18:44 Dec 26, 2019 Jkt 250001 Organization Determinations, Appeals, and Grievances (ODAG); Special Needs Model of Care (SNP–MOC) (only administered on organizations who operate SNPs); and, Compliance Program Effectiveness (CPE). The data collected is detailed in each of these protocols and the exact fields are located in the record layouts, at the end of each protocol. In addition, this collection request includes a pre-audit issue summary, three CPE questionnaires, one CPE organizational structure presentation template, one FA impact analysis template, two CDAG impact analysis templates, four ODAG impact analysis templates, three SNP– MOC impact analysis templates, and a SNP–MOC questionnaire. The information gathered during this audit will be used by the Medicare Parts C and D Oversight and Enforcement Group (MOEG) within the Center for Medicare (CM) and CMS Regional Offices to assess sponsoring organizations’ compliance with Medicare program requirements. If outliers or other data anomalies are detected, Regional Offices will work in collaboration with MOEG and other divisions within CMS for follow-up and resolution. Additionally, MA and Part D organizations will receive the audit results and will be required to implement corrective action to correct any identified deficiencies. Form Number: CMS–10191 (OMB control number: 0938–1000); Frequency: Yearly; Affected Public: State, Local, or Tribal Governments; Number of Respondents: 201; Total Annual Responses: 207; Total Annual Hours: 39,456. (For policy questions regarding this collection contact Brenda Hudson at 443–743– 9299.) 3. Type of Information Collection Request: Revision with change of a currently approved collection; Title of Information Collection: Bid Pricing Tool (BPT) for Medicare Advantage (MA) Plans and Prescription Drug Plans (PDP); Use: Under the Medicare Prescription Drug, Improvement, and Modernization Act of 2003 (MMA), and implementing regulations at 42 CFR, Medicare Advantage organizations (MAOs) and Prescription Drug Plans (PDPs) are required to submit an actuarial pricing ‘‘bid’’ for each plan offered to Medicare beneficiaries for approval by the Centers for Medicare & Medicaid Services (CMS). Medicare Advantage organizations (MAO) and Prescription Drug Plans (PDP) are required to submit an actuarial pricing ‘‘bid’’ for each plan offered to Medicare beneficiaries for approval by CMS. The MAOs and PDPs use the Bid Pricing Tool (BPT) software PO 00000 Frm 00081 Fmt 4703 Sfmt 4703 to develop their actuarial pricing bid. The competitive bidding process defined by the ‘‘The Medicare Prescription Drug, Improvement, and Modernization Act’’ (MMA) applies to both the MA and Part D programs. It is an annual process that encompasses the release of the MA rate book in April, the bid’s that plans submit to CMS in June, and the release of the Part D and RPPO benchmarks, which typically occurs in August. Form Number: CMS–10142 (OMB control number: 0938–0944); Frequency: Yearly; Affected Public: State, Local, or Tribal Governments; Number of Respondents: 555; Total Annual Responses: 4995; Total Annual Hours: 149,850. (For policy questions regarding this collection contact Rachel Shevland at 410–786–3026.) Dated: December 20, 2019. William N. Parham, III, Director, Paperwork Reduction Staff, Office of Strategic Operations and Regulatory Affairs. [FR Doc. 2019–27926 Filed 12–26–19; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families [CFDA Numbers: 93.581, 93.587, 93.612] Notice for Public Comment on Administration for Native Americans’ Program Policies and Procedures Administration for Native Americans (ANA), Administration for Children and Families (ACF), Department of Health and Human Services (HHS). ACTION: Notice for public comment. AGENCY: Pursuant to Section 814 of the Native American Programs Act of 1974 (NAPA), as amended, the ANA is required to provide members of the public an opportunity to comment on proposed changes in interpretive rules and general statements of policy and to give notice of the proposed changes no less than 30 days before such changes become effective. In accordance with notice requirements of NAPA, ANA herein describes proposed interpretive rules and general statements of policy that relate to ANA’s funding opportunities in Fiscal Year (FY) 2020. Changes to FY 2020 Funding Opportunity Announcements (FOAs) will be based on the following previously published programs: Environmental Regulatory Enhancement (ERE), HHS–2018–ACF–ANA–NR–1344; Native American Language Preservation SUMMARY: E:\FR\FM\27DEN1.SGM 27DEN1

Agencies

[Federal Register Volume 84, Number 248 (Friday, December 27, 2019)]
[Notices]
[Pages 71427-71428]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-27926]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare & Medicaid Services

[Document Identifier CMS-10701, CMS-10191 and CMS-10142]


Agency Information Collection Activities: Submission for OMB 
Review; 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 (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 27, 2020.

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 
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: 
[email protected].
    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.
    1. Email your request, including your address, phone number, OMB 
number, and CMS document identifier, to [email protected].
    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: New collection (Request 
for a new OMB control number); Title of Information Collection: 
Medicare Beneficiary Experiences with Care Survey System; Use: The 
MBECS system is designed to conduct 1-2 surveys per year on priority 
groups of interest, thereby allowing CMS OMH to respond quickly to the 
data needs of stakeholders with interests in these underrepresented 
groups. Data collected through the MBECS system will be used to better 
understand--and thus serve the needs of--Medicare beneficiaries in 
minority populations. The core questionnaire will collect information 
on communication with medical professionals, coordination of health 
care, experiences getting needed health care, experiences with personal 
doctors and specialists, and key demographics. Data will be compared to 
benchmarks from the FFS CAHPS, MA CAHPS, and

[[Page 71428]]

NAM CAHPS surveys. The population-specific questionnaire module will 
collect information about issues most relevant for particular minority 
groups; population-specific modules will be described in individual 
information collection requests. These data will be compared to 
benchmarks from the relevant CAHPS source surveys when available.
    Collection of these data from people who have been identified 
through CMS administrative data and administrative flags as part of 
specific minority populations will also serve as a critical validation 
step of this method for identifying difficult-to-study populations, 
thus making it easier to study beneficiaries in these groups in the 
future. Form Number: CMS-10701 (OMB control number: 0938-NEW); 
Frequency: Yearly; Affected Public: State, Local, or Tribal 
Governments; Number of Respondents: 10,000; Total Annual Responses: 
10,000; Total Annual Hours: 3,333. (For policy questions regarding this 
collection contact Luis Perez at 410-786-8557.)
    2. Type of Information Collection Request: Revision with change of 
a currently approved collection; Title of Information Collection: 
Medicare Parts C and D Program Audit Protocols and Data Requests; Use: 
Under the Medicare Prescription Drug, Improvement, and Modernization 
Act of 2003 and implementing regulations at 42 CFR parts 422 and 423, 
Medicare Part D plan sponsors and Medicare Advantage organizations are 
required to comply with all Medicare Parts C and D program 
requirements. CMS' annual audit plan ensures that we evaluate 
sponsoring organizations' compliance with these requirements. CMS 
program audits focus on high-risk areas that have the greatest 
potential for beneficiary harm. As such, CMS has developed several 
audit protocols that are included within the program area data request 
documents and that are posted to the CMS website each year for use by 
sponsoring organizations to prepare for their audit. As part of a 
robust audit process, CMS also requires sponsoring organizations who 
have been audited and found to have deficiencies to undergo a 
validation audit to ensure correction. The validation audit utilizes 
the same audit protocols, but only tests the elements where 
deficiencies were found, as opposed to re-administering the entire 
audit.
    Currently CMS utilizes the following 5 protocols to audit 
sponsoring organization performance: Part D Formulary and Benefit 
Administration (FA); Part D Coverage Determinations, Appeals, and 
Grievances (CDAG); Part C Organization Determinations, Appeals, and 
Grievances (ODAG); Special Needs Model of Care (SNP-MOC) (only 
administered on organizations who operate SNPs); and, Compliance 
Program Effectiveness (CPE). The data collected is detailed in each of 
these protocols and the exact fields are located in the record layouts, 
at the end of each protocol. In addition, this collection request 
includes a pre-audit issue summary, three CPE questionnaires, one CPE 
organizational structure presentation template, one FA impact analysis 
template, two CDAG impact analysis templates, four ODAG impact analysis 
templates, three SNP-MOC impact analysis templates, and a SNP-MOC 
questionnaire.
    The information gathered during this audit will be used by the 
Medicare Parts C and D Oversight and Enforcement Group (MOEG) within 
the Center for Medicare (CM) and CMS Regional Offices to assess 
sponsoring organizations' compliance with Medicare program 
requirements. If outliers or other data anomalies are detected, 
Regional Offices will work in collaboration with MOEG and other 
divisions within CMS for follow-up and resolution. Additionally, MA and 
Part D organizations will receive the audit results and will be 
required to implement corrective action to correct any identified 
deficiencies. Form Number: CMS-10191 (OMB control number: 0938-1000); 
Frequency: Yearly; Affected Public: State, Local, or Tribal 
Governments; Number of Respondents: 201; Total Annual Responses: 207; 
Total Annual Hours: 39,456. (For policy questions regarding this 
collection contact Brenda Hudson at 443-743-9299.)
    3. Type of Information Collection Request: Revision with change of 
a currently approved collection; Title of Information Collection: Bid 
Pricing Tool (BPT) for Medicare Advantage (MA) Plans and Prescription 
Drug Plans (PDP); Use: Under the Medicare Prescription Drug, 
Improvement, and Modernization Act of 2003 (MMA), and implementing 
regulations at 42 CFR, Medicare Advantage organizations (MAOs) and 
Prescription Drug Plans (PDPs) are required to submit an actuarial 
pricing ``bid'' for each plan offered to Medicare beneficiaries for 
approval by the Centers for Medicare & Medicaid Services (CMS).
    Medicare Advantage organizations (MAO) and Prescription Drug Plans 
(PDP) are required to submit an actuarial pricing ``bid'' for each plan 
offered to Medicare beneficiaries for approval by CMS. The MAOs and 
PDPs use the Bid Pricing Tool (BPT) software to develop their actuarial 
pricing bid. The competitive bidding process defined by the ``The 
Medicare Prescription Drug, Improvement, and Modernization Act'' (MMA) 
applies to both the MA and Part D programs. It is an annual process 
that encompasses the release of the MA rate book in April, the bid's 
that plans submit to CMS in June, and the release of the Part D and 
RPPO benchmarks, which typically occurs in August. Form Number: CMS-
10142 (OMB control number: 0938-0944); Frequency: Yearly; Affected 
Public: State, Local, or Tribal Governments; Number of Respondents: 
555; Total Annual Responses: 4995; Total Annual Hours: 149,850. (For 
policy questions regarding this collection contact Rachel Shevland at 
410-786-3026.)

    Dated: December 20, 2019.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and 
Regulatory Affairs.
[FR Doc. 2019-27926 Filed 12-26-19; 8:45 am]
 BILLING CODE 4120-01-P


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