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