Agency Information Collection Activities: Proposed Collection; Comment Request, 26479-26480 [2020-09452]

Download as PDF Federal Register / Vol. 85, No. 86 / Monday, May 4, 2020 / Notices ability of the organization to provide continuing surveyor training. ++ The comparability of TCT’s to our standards and processes, including survey frequency, and the ability to investigate and respond appropriately to complaints against accredited facilities. ++ TCT’s processes and procedures for monitoring a HIT supplier found out of compliance with TCT’s program requirements. ++ TCT’s capacity to report deficiencies to the surveyed supplier and respond to the suppliers’ plan of correction in a timely manner. ++ TCT’s capacity to provide us with electronic data and reports necessary for effective assessment and interpretation of the organization’s survey process. ++ The adequacy of TCT’s staff and other resources, and its financial viability. ++ TCT’s capacity to adequately fund required surveys. ++ TCT’s policies with respect to whether surveys are announced or unannounced, to assure that surveys are unannounced. ++ TCT’s agreement to provide us with a copy of the most current accreditation survey together with any other information related to the survey as we may require (including corrective action plans). • TCT’s agreement or policies for voluntary and involuntary termination of suppliers. • TCT agreement or policies for voluntary and involuntary termination of the HIT AO program. • TCT’s policies and procedures to avoid conflicts of interest, including the appearance of conflicts of interest, involving individuals who conduct surveys or participate in accreditation decisions IV. Collection of Information Requirements This document does not impose information collection and requirements, that is, reporting, recordkeeping or third party disclosure requirements. Consequently, there is no need for review by the Office of Management and Budget under the authority of the Paperwork Reduction Act of 1995 (44 U.S.C. 3501 et seq). jbell on DSKJLSW7X2PROD with NOTICES V. Response to Public Comments Because of the large number of public comments we normally receive on Federal Register documents, we are not able to acknowledge or respond to them individually. We will consider all comments we receive by the date and time specified in the DATES section of this preamble, and, when we proceed with a subsequent document, we will VerDate Sep<11>2014 19:03 May 01, 2020 Jkt 250001 respond to the comments in the preamble to that document. Upon completion of our evaluation, including evaluation of comments received as a result of this notice, we will publish a final notice in the Federal Register announcing the result of our evaluation. The Administrator of the Centers for Medicare & Medicaid Services (CMS), Seema Verma, having reviewed and approved this document, authorizes Evell J. Barco Holland, who is the Federal Register Liaison, to electronically sign this document for purposes of publication in the Federal Register. Dated: April 21, 2020. Evell J. Barco Holland, Federal Register Liaison, Department of Health and Human Services. [FR Doc. 2020–09393 Filed 5–1–20; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier: CMS–10287 and CMS– 10540] Agency Information Collection Activities: Proposed Collection; 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 (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 information technology to minimize the information collection burden. SUMMARY: PO 00000 Frm 00040 Fmt 4703 Sfmt 4703 26479 Comments must be received by July 6, 2020. 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 ll, Room C4–26–05, 7500 Security Boulevard, Baltimore, Maryland 21244–1850. To obtain copies of a supporting statement and any related forms for the proposed collection(s) summarized in this notice, 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: DATES: 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–10287 Medicare Quality of Care Complaint Form CMS–10540 Quality Improvement Strategy Implementation Plan and Progress Report Form 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 E:\FR\FM\04MYN1.SGM 04MYN1 26480 Federal Register / Vol. 85, No. 86 / Monday, May 4, 2020 / Notices jbell on DSKJLSW7X2PROD with NOTICES 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: Revision of a currently approved collection; Title of Information Collection: Medicare Quality of Care Complaint Form; Use: Since 1986, Quality Improvement Organizations (QIO) have been responsible for conducting appropriate reviews of written complaints submitted by beneficiaries about the quality of care they have received. In order to receive these written complaints, each QIO has developed its own unique form on which beneficiaries can submit their complaints. CMS has initiated several efforts aimed at increasing the standardization of all QIO activities, and the development of a single, standardized Medicare Quality of Care Complaint Form beneficiaries can use to submit complaints is a key step towards attaining this increased standardization. The Medicare Quality of Care Complaint Form has been revised to improve its content, in order to provide clarity and support to beneficiaries. Section two of the form was updated to replace the Health Insurance Claim Number (HICN) with the current Medicare Beneficiary Identifier (MBI), a randomly generated number that replaced the SSN-based HICN. The information page of the form was revised to provide clear instruction as to how to complete the form and the implication of not providing certain requested information. Form Number: CMS–10287 (OMB control number: 0938–1102); Frequency: Occasionally; Affected Public: Individuals and Households; Number of Respondents: 4,350; Total Annual Responses: 4,350; Total Annual Hours: 725. (For policy questions regarding this collection contact Peter Ajuonuma at 410–786– 3580.) 2. Type of Information Collection Request: Revision; Title of Information Collection: Quality Improvement Strategy Implementation Plan and Progress Report Form; Use: Section 1311(c)(1)(E) of the Affordable Care Act requires qualified health plans (QHPs) offered through an Exchange must implement a quality improvement strategy (QIS) as described in section VerDate Sep<11>2014 19:03 May 01, 2020 Jkt 250001 1311(g)(1). Section 1311(g)(3) of the Affordable Care Act specifies the guidelines under Section 1311(g)(2) shall require the periodic reporting to the applicable Exchange the activities that a qualified health plan has conducted to implement a strategy which is described as a payment structure providing increased reimbursement or other incentives for improving health outcomes of plan enrollees, implementing activities to prevent hospital readmissions, improving patient safety and reducing medical errors, promoting wellness and health, and/or implementing activities to reduce health and health care disparities. CMS has created a separation of the QIS form into a separate Implementation Plan, Progress Report and Modification Summary which is intended to decrease overall burden on issuers. With these separate forms, issuers would no longer need to complete and resubmit an Implementation Plan every year (which is currently the process). Issuers would only submit the Implementation Plan form in the first year of a QIS, and then issuers would submit the Progress Report form in each subsequent year (with the Modification Summary Supplement as necessary). This adjustment will eliminate the need for issuers to enter and submit unchanged data, and allow them to focus their time on reporting new progress achieved for the QIS. The QIS form will allow: (1) The Department of Health & Human Services (HHS) to evaluate the compliance and adequacy of QHP issuers’ quality improvement efforts, as required by Section 1311(c) of the Affordable Care Act, and (2) HHS will use the issuers’ validated information to evaluate the issuers’ quality improvement strategies for compliance with the requirements of Section 1311(g) of the Affordable Care Act. Form Number: CMS–10540 (OMB Control Number: 0938–1286) Frequency: Monthly, Annual; Affected Public: Private Sector; Number of Respondents: 250; Number of Responses: 250; Total Annual Hours: 11,000. (For policy questions regarding this collection, contact Nidhi Singh-Shah at 301–492– 5110.) Dated: April 29, 2020. William N. Parham, III, Director,Paperwork Reduction Staff, Office of Strategic Operations and Regulatory Affairs. [FR Doc. 2020–09452 Filed 5–1–20; 8:45 am] BILLING CODE 4120–01–P PO 00000 Frm 00041 Fmt 4703 Sfmt 4703 DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [CMS–1743–N] Medicare Program; Meeting Announcement for the Medicare Advisory Panel on Clinical Diagnostic Laboratory Tests Centers for Medicare & Medicaid Services (CMS), HHS. ACTION: Notice of meeting. AGENCY: This notice announces the virtual public meeting dates for the Medicare Advisory Panel on Clinical Diagnostic Laboratory Tests (the Panel) on Wednesday, July 29, 2020 and Thursday, July 30, 2020. The purpose of the Panel is to advise the Secretary of the Department of Health and Human Services and the Administrator of the Centers for Medicare & Medicaid Services on issues related to clinical diagnostic laboratory tests. DATES: Meeting Dates: The virtual meeting of the Panel is scheduled for Wednesday, July 29, 2020 from 8:30 a.m. to 5:00 p.m., Eastern Daylight Time (E.D.T.) and Thursday, July 30, 2020, from 8:30 a.m. to 5:00 p.m., E.D.T. The Panel is also expected to virtually participate in the Clinical Laboratory Fee Schedule (CLFS) Annual Public Meeting for Calendar Year (CY) 2021 on June 22, 2020 in order to gather information and ask questions to presenters. Notice of the CLFS Annual Public Meeting for CY 2021 is published elsewhere in this issue of the Federal Register. Deadline Date for Registration: All stand-by speakers for the Panel meeting must register electronically to our Clinical Diagnostic Laboratory Test (CDLT) Panel dedicated email box, CDLTPanel@cms.hhs.gov. Registration is not required for non-speakers. The public may view this meeting via webinar, or listen-only via teleconference. Webinar and Teleconference Meeting Information: Teleconference dial-in instructions, and related webinar details will be posted on the meeting agenda, which will be available on the CMS website approximately 2 weeks prior to the meeting at https://www.cms.gov/ Regulations-and-Guidance/Guidance/ FACA/AdvisoryPanelonClinical DiagnosticLaboratoryTests.html. A preliminary agenda is described in section II of this notice. ADDRESSES: Due to the current COVID– 19 public health emergency, the Panel SUMMARY: E:\FR\FM\04MYN1.SGM 04MYN1

Agencies

[Federal Register Volume 85, Number 86 (Monday, May 4, 2020)]
[Notices]
[Pages 26479-26480]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-09452]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare & Medicaid Services

[Document Identifier: CMS-10287 and CMS-10540]


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 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 July 6, 2020.

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-10287 Medicare Quality of Care Complaint Form
CMS-10540 Quality Improvement Strategy Implementation Plan and Progress 
Report Form

    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

[[Page 26480]]

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: Revision of a currently 
approved collection; Title of Information Collection: Medicare Quality 
of Care Complaint Form; Use: Since 1986, Quality Improvement 
Organizations (QIO) have been responsible for conducting appropriate 
reviews of written complaints submitted by beneficiaries about the 
quality of care they have received. In order to receive these written 
complaints, each QIO has developed its own unique form on which 
beneficiaries can submit their complaints. CMS has initiated several 
efforts aimed at increasing the standardization of all QIO activities, 
and the development of a single, standardized Medicare Quality of Care 
Complaint Form beneficiaries can use to submit complaints is a key step 
towards attaining this increased standardization. The Medicare Quality 
of Care Complaint Form has been revised to improve its content, in 
order to provide clarity and support to beneficiaries. Section two of 
the form was updated to replace the Health Insurance Claim Number 
(HICN) with the current Medicare Beneficiary Identifier (MBI), a 
randomly generated number that replaced the SSN-based HICN. The 
information page of the form was revised to provide clear instruction 
as to how to complete the form and the implication of not providing 
certain requested information. Form Number: CMS-10287 (OMB control 
number: 0938-1102); Frequency: Occasionally; Affected Public: 
Individuals and Households; Number of Respondents: 4,350; Total Annual 
Responses: 4,350; Total Annual Hours: 725. (For policy questions 
regarding this collection contact Peter Ajuonuma at 410-786-3580.)
    2. Type of Information Collection Request: Revision; Title of 
Information Collection: Quality Improvement Strategy Implementation 
Plan and Progress Report Form; Use: Section 1311(c)(1)(E) of the 
Affordable Care Act requires qualified health plans (QHPs) offered 
through an Exchange must implement a quality improvement strategy (QIS) 
as described in section 1311(g)(1). Section 1311(g)(3) of the 
Affordable Care Act specifies the guidelines under Section 1311(g)(2) 
shall require the periodic reporting to the applicable Exchange the 
activities that a qualified health plan has conducted to implement a 
strategy which is described as a payment structure providing increased 
reimbursement or other incentives for improving health outcomes of plan 
enrollees, implementing activities to prevent hospital readmissions, 
improving patient safety and reducing medical errors, promoting 
wellness and health, and/or implementing activities to reduce health 
and health care disparities. CMS has created a separation of the QIS 
form into a separate Implementation Plan, Progress Report and 
Modification Summary which is intended to decrease overall burden on 
issuers. With these separate forms, issuers would no longer need to 
complete and resubmit an Implementation Plan every year (which is 
currently the process). Issuers would only submit the Implementation 
Plan form in the first year of a QIS, and then issuers would submit the 
Progress Report form in each subsequent year (with the Modification 
Summary Supplement as necessary). This adjustment will eliminate the 
need for issuers to enter and submit unchanged data, and allow them to 
focus their time on reporting new progress achieved for the QIS.
    The QIS form will allow: (1) The Department of Health & Human 
Services (HHS) to evaluate the compliance and adequacy of QHP issuers' 
quality improvement efforts, as required by Section 1311(c) of the 
Affordable Care Act, and (2) HHS will use the issuers' validated 
information to evaluate the issuers' quality improvement strategies for 
compliance with the requirements of Section 1311(g) of the Affordable 
Care Act. Form Number: CMS-10540 (OMB Control Number: 0938-1286) 
Frequency: Monthly, Annual; Affected Public: Private Sector; Number of 
Respondents: 250; Number of Responses: 250; Total Annual Hours: 11,000. 
(For policy questions regarding this collection, contact Nidhi Singh-
Shah at 301-492-5110.)

    Dated: April 29, 2020.
William N. Parham, III,
Director,Paperwork Reduction Staff, Office of Strategic Operations and 
Regulatory Affairs.
[FR Doc. 2020-09452 Filed 5-1-20; 8:45 am]
BILLING CODE 4120-01-P


This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.