Medicare and Medicaid Programs; Renewal of Deeming Authority of the Accreditation Association for National Committee for Quality Assurance (NCQA), 51170-51172 [2014-20446]
Download as PDF
mstockstill on DSK4VPTVN1PROD with NOTICES
51170
Federal Register / Vol. 79, No. 166 / Wednesday, August 27, 2014 / Notices
B. Annual Reporting Burden
Supplies:
FAR Clause 52.225–2, Buy American
Certificate (formerly OMB Control No.
9000–0024), requires the offeror to
identify in its proposal supplies that do
not meet the definition of domestic end
product. The Buy American Act no
longer applies to acquisitions of
commercial information technology.
Respondents: 3,480.
Responses per Respondent: 10.
Total Responses: 34,800.
Hours per Response: .25.
Total Burden Hours: 8,700.
FAR Clause 52.225–4, Buy
American—Free Trade Agreements—
Israeli Trade Act Certificate (formerly
OMB Control No. 9000–0130), requires
separate listing of foreign products that
are eligible under a trade agreement,
and listing of all other foreign end
products.
Respondents: 2,550.
Responses per Respondent: 10.
Total Responses: 25,550.
Hours per Response: .25.
Total Burden Hours: 6,375.
FAR Clause 52.225–6, Trade
Agreements Certificate (formerly OMB
Control No. 9000–0025), requires the
offeror to certify that all end products
are either U.S.-made or designated
country end products, except as listed
in paragraph (b) of the provision.
Offerors are not allowed to provide
other than a U.S.-made or designated
country end product, unless the
requirement is waived.
Respondents: 320.
Responses per Respondent: 3.
Total Responses: 960.
Hours per Response: .25.
Total Burden Hours: 240.
Construction provisions and clauses
(formerly OMB Control No. 9000–0141)
provide that an offeror/contractor
requesting to use foreign construction
material due to unreasonable cost of
domestic construction material shall
provide adequate information to permit
evaluation of the request.
—52.225–9, Buy American Act
Construction Materials
—52.225–10, Notice of Buy American
Act Requirements—Construction
Materials
—52.225–11, Buy American Act
Construction Materials—Trade
Agreements
—52.225–12, Notice of Buy American
Act requirements—Construction
Materials under Trade Agreements
—52.225–21, Required Use of American
Iron, Steel and Manufactured Goods—
Buy American Act—Construction
Materials
—52.225–23, Required Use of American
Iron, Steel and Manufactured Goods—
VerDate Mar<15>2010
17:44 Aug 26, 2014
Jkt 232001
Buy American Act—Construction
Materials
Under Trade Agreements
Respondents: 1,000.
Responses per Respondent: 2.
Total Responses: 2,000.
Hours per Response: 2.5.
Total Burden Hours: 5,000.
C. Public Comments
Public comments are particularly
invited on: Whether this collection of
information is necessary for the proper
performance of functions of the FAR,
and whether it will have practical
utility; whether our estimate of the
public burden of this collection of
information is accurate, and based on
valid assumptions and methodology;
ways to enhance the quality, utility, and
clarity of the information to be
collected; and ways in which we can
minimize the burden of the collection of
information on those who are to
respond, through the use of appropriate
technological collection techniques or
other forms of information technology.
Obtaining Copies Of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat Division (MVCB),
1800 F Street NW., Washington, DC
20405, telephone 202–501–4755. Please
cite OMB Control No. 9000–0024, Buy
American Act Certificate, in all
correspondence.
Dated: August 22, 2014.
Edward Loeb,
Acting Director, Federal Acquisition Policy
Division, Office of Government-Wide
Acquisition Policy, Office of Acquisition
Policy, Office of Government-Wide Policy.
[FR Doc. 2014–20364 Filed 8–26–14; 8:45 am]
BILLING CODE 6820–EP–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Interagency Task Force on
Antimicrobial Resistance (ITFAR)
Public Meeting Cancellation
current work and future direction in this
area. This meeting will be rescheduled
at a future date.
DATES: The public meeting cancelled by
this notice was to be held at the Ronald
Reagan Building and International
Trade Center in Washington, DC, on
Thursday, September 4, 2014, from 1:00
p.m. to 5:00 p.m.
FOR FURTHER INFORMATION CONTACT:
Stephanie Gumbis, Office of
Antimicrobial Resistance, National
Center for Emerging and Zoonotic
Infectious Diseases, Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., Mailstop A–28, Atlanta, GA
30329; Telephone 404–639–4000; Email
ITFAR@cdc.gov.
Dated: August 22, 2014.
Ron A. Otten,
Acting Deputy Associate Director for Science,
Centers for Disease Control and Prevention.
[FR Doc. 2014–20393 Filed 8–26–14; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–4132–FN]
Medicare and Medicaid Programs;
Renewal of Deeming Authority of the
Accreditation Association for National
Committee for Quality Assurance
(NCQA)
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Final notice.
AGENCY:
This final notice announces
our decision to renew the Medicare
Advantage ‘‘deeming authority’’ of the
National Committee for Quality
Assurance (NCQA) for a period of 6
years. This new term of approval would
begin October 19, 2014 and end October
18, 2020.
DATES: This final notice is effective
October 19, 2014 through October 18,
2020.
SUMMARY:
FOR FURTHER INFORMATION CONTACT:
Jennifer Bates, 410–786–6258 or
Milonda Mitchell, 410–786–1644.
SUPPLEMENTARY INFORMATION:
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Cancellation of public meeting.
I. Background
The meeting of the
Interagency Task Force on
Antimicrobial Resistance (ITFAR) is
cancelled. The purpose of the meeting
was to communicate the strategic
direction of ITFAR in the fight against
antimicrobial resistance, centering on
Under the Medicare program, eligible
beneficiaries may receive covered
services through a Medicare Advantage
(MA) organization that contracts with
the Centers for Medicare & Medicaid
Services (CMS). The regulations
specifying the Medicare requirements
AGENCY:
SUMMARY:
PO 00000
Frm 00033
Fmt 4703
Sfmt 4703
E:\FR\FM\27AUN1.SGM
27AUN1
mstockstill on DSK4VPTVN1PROD with NOTICES
Federal Register / Vol. 79, No. 166 / Wednesday, August 27, 2014 / Notices
that must be met for a Medicare
Advantage Organization (MAO) to enter
into a contract with CMS are located at
42 CFR part 422. These regulations
implement Part C of Title XVIII of the
Social Security Act (the Act), which
specifies the services that an MAO must
provide and the requirements that the
organization must meet to offer an MA
contractor. Other relevant sections of
the Act are Parts A and B of Title XVIII
and Part A of Title XI pertaining to the
provision of services by Medicarecertified providers and suppliers. Under
§ 422.400, one significant prerequisite
for an entity to be an MA organization
is that the organization be licensed by
the state as a risk bearing organization,
unless a waiver is authorized for a
provider-sponsored organization
pursuant to § 422.370. In addition,
MAOs and MA plans must meet
requirements related to access to
services, antidiscrimination,
confidentiality and accuracy of
beneficiary records, provider
participation, advance directives, and
quality assurance programs.
As a method of assuring compliance
with certain Medicare requirements, an
MA organization may choose to become
accredited by a CMS approved
accrediting organization (AO). In
addition to their CMS-recognized
deemed status accreditation program,
approved AOs offer other accreditation
programs that are not recognized by
CMS. For Medicare participation
purposes, the MA organization may be
‘‘deemed’’ compliant in one or more of
six requirements set forth in section
1852(e)(4)(B) of the Act and
§ 422.156(b). For an AO to be able to
‘‘deem’’ an MA plan as compliant with
these MA requirements, the AO must
demonstrate that it meets the
requirements outlined in § 422.157,
including demonstrating that its
standards are at least as stringent as
Medicare requirements with respect to
the standards in the deemable area.
Therefore, for example, MA
organizations that are licensed as health
maintenance organizations (HMOs) or
preferred provider organizations (PPOs)
and are accredited by an approved
accrediting organization may receive, at
the MA organization’s request, deemed
status for CMS requirements in the
following six MA areas: Quality
Improvement, Antidiscrimination,
Access to Services, Confidentiality and
Accuracy of Enrollee Records,
Information on Advanced Directives,
and Provider Participation Rules. (See
§ 422.156(b).) Organizations that apply
for MA deeming authority are generally
recognized by the health care industry
VerDate Mar<15>2010
17:44 Aug 26, 2014
Jkt 232001
as entities that accredit HMOs and
PPOs. As specified at § 422.157(b)(2)(ii),
the term for which an AO may be
approved by CMS may not exceed 6
years. For continuing approval, the AO
must renew its application with CMS.
The National Committee for Quality
Assurance (NCQA) was approved as an
accrediting organization for MA
deeming of HMOs on October 19, 2010,
and that term will expire on October 18,
2014. On January 30, 2014, NCQA
submitted an application to renew its
deeming authority. On that same date,
NCQA submitted materials requested
from CMS which included updates and/
or changes to items listed in § 422.158(a)
that are prerequisites for receiving
deeming program approval by CMS, and
which were furnished to CMS by NCQA
as a part of its renewal applications for
HMOs and PPOs.
II. Deeming Applications Approval
Process
Section 1852(e)(4)(c) of the Act
provides a statutory timetable to ensure
that our review of deeming applications
is conducted in a timely manner. The
Act provides us with 210 calendar days
after the date of receipt of an application
to complete our survey activities and
application review process. In
accordance with our policy for
providers and suppliers, within 60 days
of receiving a completed application, we
must publish a notice in the Federal
Register that identifies the national
accreditation body making the request,
describes the request, and provides no
less than a 30-day public comment
period. At the end of the 210-day
period, we must publish an approval or
denial of the application.
III. Proposed Notice
In the March 25, 2014, Federal
Register (79 FR 16338), we published a
proposed notice announcing NCQA’s
request for continued CMS approval of
its deeming authority for MA HMOs and
PPOs. In the proposed notice, we
detailed our evaluation criteria. Under
section 1852(e)(4) of the Act and our
regulations at § 422.158 (Federal review
of accrediting organizations), we
conducted a review of NCQA’s
application in accordance with the
criteria specified by our regulations,
which include, but are not limited to the
following:
• The types of MA plans that it would
review as part of its accreditation
process.
• A detailed comparison of the AO’s
accreditation requirements and
standards with the Medicare
requirements (for example, a crosswalk).
PO 00000
Frm 00034
Fmt 4703
Sfmt 4703
51171
• Detailed information about the
organization’s survey process, including
the following—
++ Frequency of surveys and whether
surveys are announced or unannounced.
++ Copies of survey forms, and
guidelines and instructions to
surveyors.
++ Descriptions of—
— The survey review process and the
accreditation status decision making
process;
— The procedures used to notify
accredited MA organizations of
deficiencies and to monitor the
correction of those deficiencies; and
— The procedures used to enforce
compliance with accreditation
requirements.
• Detailed information about the
individuals who perform surveys for the
accreditation organization, including
the following—
++ The size and composition of
accreditation survey teams for each type
of plan reviewed as part of the
accreditation process;
++ The education and experience
requirements surveyors must meet;
++ The content and frequency of the
in-service training provided to survey
personnel;
++ The evaluation systems used to
monitor the performance of individual
surveyors and survey teams; and
++ The organization’s policies and
practice with respect to the
participation, in surveys or in the
accreditation decision process by an
individual who is professionally or
financially affiliated with the entity
being surveyed.
• A description of the organization’s
data management and analysis system
with respect to its surveys and
accreditation decisions, including the
kinds of reports, tables, and other
displays generated by that system.
• A description of the organization’s
procedures for responding to and
investigating complaints against
accredited organizations, including
policies and procedures regarding
coordination of these activities with
appropriate licensing bodies and
ombudsmen programs.
• A description of the organization’s
policies and procedures with respect to
the withholding or removal of
accreditation for failure to meet the
accreditation organization’s standards or
requirements, and other actions the
organization takes in response to
noncompliance with its standards and
requirements.
• A description of all types (for
example, full, partial) and categories (for
example, provisional, conditional,
temporary) of accreditation offered by
E:\FR\FM\27AUN1.SGM
27AUN1
51172
Federal Register / Vol. 79, No. 166 / Wednesday, August 27, 2014 / Notices
the organization, the duration of each
type and category of accreditation and a
statement identifying the types and
categories that would serve as a basis for
accreditation if CMS approves the
accreditation organization.
• A list of all currently accredited MA
organizations and the type, category,
and expiration date of the accreditation
held by each of them.
• A list of all full and partial
accreditation surveys scheduled to be
performed by the accreditation
organization.
• The name and address of each
person with an ownership or control
interest in the accreditation
organization.
• CMS’s analysis of NCQA’s past
performance in the deeming program
and the results of recent deeming
validation reviews, or look-behind
audits conducted as part of continuing
federal oversight of the deeming
program under § 422.157(d).
In accordance with section
1865(a)(3)(A) of the Act, the March 25,
2014 proposed notice (79 FR 16338) also
solicited public comments regarding
whether NCQA’s requirements met or
exceeded the Medicare conditions of
participation as an accrediting
organization for MA HMOs and PPOs.
We received no public comments in
response to our proposed notice.
IV. Provisions of the Final Notice
A. Differences Between NCQA’s
Standards and Requirements for
Accreditation and Medicare’s
Conditions and Survey Requirements
mstockstill on DSK4VPTVN1PROD with NOTICES
We compared the standards and
survey process contained in NCQA’s
application with the Medicare
conditions for accreditation. Our review
and evaluation of NCQA’s application
for continued CMS-approval were
conducted as described in section III of
this final notice, and yielded the
following:
• To meet the requirements at
§ 422.158(a)(1), NCQA provided CMS
with documentation listing its types of
MA plans that it would review as part
of its accreditation process. In addition,
AO provided clarification and
documentation to demonstrate how it
distinguishes its CMS-recognized
deemed status accreditation program
from its other accreditation programs
that are not recognized by CMS.
• AO revised its ‘‘Grounds of
Revocation’’ policy to meet the
requirements at § 422.158(a)(3)(iii)(C) by
revising its requirements to include
non-compliance with ‘‘State, Federal, or
other duly authorized regulatory or
judicial action restricts or limits the
organization’s operations.’’
• To comply with the requirements at
§ 422.158(a)(6), AO revised its processes
for responding to and investigating
complaints against accredited
organizations by requiring the reporting
of any serious problems identified with
an MA plan to the designated CMS MA
deeming representative.
B. Term of Approval
Based on the review and observations
described in section III of this final
notice, we have determined that
NCQA’s accreditation program
requirements continue to meet or
exceed our requirements. Therefore, we
renew NCQA as a national accreditation
organization with deeming authority for
MA HMOs and PPOs, effective October
19, 2014 through October 18, 2020.
V. Collection of Information
Requirements
This document does not impose any
new or revised information collection or
recordkeeping requirements.
Consequently, it need not be reviewed
by the Office of Management and
Budget under the authority of the
Paperwork Reduction Act of 1995.
Dated: August 15, 2014.
Marilyn Tavenner,
Administrator, Centers for Medicare &
Medicaid Services.
[FR Doc. 2014–20446 Filed 8–26–14; 8:45 am]
BILLING CODE 4120–01–P
Total number
of respondents
Instrument
Implementation Survey Interview Topic Guide: State-level
Respondents ....................................................................
Implementation Survey Interview Topic Guide: Providerlevel Respondents ............................................................
VerDate Mar<15>2010
17:44 Aug 26, 2014
Jkt 232001
PO 00000
Frm 00035
Annual
number of
respondents
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Personal Responsibility
Education Program (PREP) MultiComponent Evaluation—Data Collection
Related to the Design and
Implementation Study.
OMB No.: 0970–0398.
Description: The Office of Data
Analysis, Research, and Evaluation
(HHS/ACF/ACYF/ODARE) in the
Administration for Children, Youth and
Families (ACYF) and the Office of
Planning, Research, and Evaluation
(HHS/ACF/OPRE) in the Administration
for Children and Families (ACF)
propose a data collection activity as part
of the Personal Responsibility Education
Program (PREP) Multi-Component
Evaluation.
The goals of the PREP MultiComponent Evaluation are to document
how PREP programs are designed and
implemented in the field, collect
performance measure data for PREP
programs, and assess the effectiveness of
selected PREP-funded programs.
The PREP Multi-Component
Evaluation contains three components:
The ‘‘Design and Implementation
Study,’’ the ‘‘Performance Analysis
Study,’’ and the ‘‘Impact and In-Depth
Implementation Study.’’ This notice is
specific to data collection activities for
the implementation portion of the
Design and Implementation Study.
The goals of this portion of the study
are to document how States and subawardees actually implemented their
PREP programs, given their program
designs. In order to meet this goal, both
State PREP Administrators and a
selection of sub-awardee program
providers will be interviewed. The
interviews will be used to understand
important aspects of implementation,
such as training, technical assistance
and program fidelity monitoring.
Respondents: State grantee staff; State
training and technical assistance staff;
State program evaluator staff program
providers.
Number of
responses per
respondent
Average
burden hours
per response
Total annual
burden hours
16
1
1
6
16
Fmt 4703
6
6
1
1
6
Sfmt 4703
E:\FR\FM\27AUN1.SGM
27AUN1
Agencies
[Federal Register Volume 79, Number 166 (Wednesday, August 27, 2014)]
[Notices]
[Pages 51170-51172]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-20446]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-4132-FN]
Medicare and Medicaid Programs; Renewal of Deeming Authority of
the Accreditation Association for National Committee for Quality
Assurance (NCQA)
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Final notice.
-----------------------------------------------------------------------
SUMMARY: This final notice announces our decision to renew the Medicare
Advantage ``deeming authority'' of the National Committee for Quality
Assurance (NCQA) for a period of 6 years. This new term of approval
would begin October 19, 2014 and end October 18, 2020.
DATES: This final notice is effective October 19, 2014 through October
18, 2020.
FOR FURTHER INFORMATION CONTACT: Jennifer Bates, 410-786-6258 or
Milonda Mitchell, 410-786-1644.
SUPPLEMENTARY INFORMATION:
I. Background
Under the Medicare program, eligible beneficiaries may receive
covered services through a Medicare Advantage (MA) organization that
contracts with the Centers for Medicare & Medicaid Services (CMS). The
regulations specifying the Medicare requirements
[[Page 51171]]
that must be met for a Medicare Advantage Organization (MAO) to enter
into a contract with CMS are located at 42 CFR part 422. These
regulations implement Part C of Title XVIII of the Social Security Act
(the Act), which specifies the services that an MAO must provide and
the requirements that the organization must meet to offer an MA
contractor. Other relevant sections of the Act are Parts A and B of
Title XVIII and Part A of Title XI pertaining to the provision of
services by Medicare-certified providers and suppliers. Under Sec.
422.400, one significant prerequisite for an entity to be an MA
organization is that the organization be licensed by the state as a
risk bearing organization, unless a waiver is authorized for a
provider-sponsored organization pursuant to Sec. 422.370. In addition,
MAOs and MA plans must meet requirements related to access to services,
antidiscrimination, confidentiality and accuracy of beneficiary
records, provider participation, advance directives, and quality
assurance programs.
As a method of assuring compliance with certain Medicare
requirements, an MA organization may choose to become accredited by a
CMS approved accrediting organization (AO). In addition to their CMS-
recognized deemed status accreditation program, approved AOs offer
other accreditation programs that are not recognized by CMS. For
Medicare participation purposes, the MA organization may be ``deemed''
compliant in one or more of six requirements set forth in section
1852(e)(4)(B) of the Act and Sec. 422.156(b). For an AO to be able to
``deem'' an MA plan as compliant with these MA requirements, the AO
must demonstrate that it meets the requirements outlined in Sec.
422.157, including demonstrating that its standards are at least as
stringent as Medicare requirements with respect to the standards in the
deemable area. Therefore, for example, MA organizations that are
licensed as health maintenance organizations (HMOs) or preferred
provider organizations (PPOs) and are accredited by an approved
accrediting organization may receive, at the MA organization's request,
deemed status for CMS requirements in the following six MA areas:
Quality Improvement, Antidiscrimination, Access to Services,
Confidentiality and Accuracy of Enrollee Records, Information on
Advanced Directives, and Provider Participation Rules. (See Sec.
422.156(b).) Organizations that apply for MA deeming authority are
generally recognized by the health care industry as entities that
accredit HMOs and PPOs. As specified at Sec. 422.157(b)(2)(ii), the
term for which an AO may be approved by CMS may not exceed 6 years. For
continuing approval, the AO must renew its application with CMS.
The National Committee for Quality Assurance (NCQA) was approved as
an accrediting organization for MA deeming of HMOs on October 19, 2010,
and that term will expire on October 18, 2014. On January 30, 2014,
NCQA submitted an application to renew its deeming authority. On that
same date, NCQA submitted materials requested from CMS which included
updates and/or changes to items listed in Sec. 422.158(a) that are
prerequisites for receiving deeming program approval by CMS, and which
were furnished to CMS by NCQA as a part of its renewal applications for
HMOs and PPOs.
II. Deeming Applications Approval Process
Section 1852(e)(4)(c) of the Act provides a statutory timetable to
ensure that our review of deeming applications is conducted in a timely
manner. The Act provides us with 210 calendar days after the date of
receipt of an application to complete our survey activities and
application review process. In accordance with our policy for providers
and suppliers, within 60 days of receiving a completed application, we
must publish a notice in the Federal Register that identifies the
national accreditation body making the request, describes the request,
and provides no less than a 30-day public comment period. At the end of
the 210-day period, we must publish an approval or denial of the
application.
III. Proposed Notice
In the March 25, 2014, Federal Register (79 FR 16338), we published
a proposed notice announcing NCQA's request for continued CMS approval
of its deeming authority for MA HMOs and PPOs. In the proposed notice,
we detailed our evaluation criteria. Under section 1852(e)(4) of the
Act and our regulations at Sec. 422.158 (Federal review of accrediting
organizations), we conducted a review of NCQA's application in
accordance with the criteria specified by our regulations, which
include, but are not limited to the following:
The types of MA plans that it would review as part of its
accreditation process.
A detailed comparison of the AO's accreditation
requirements and standards with the Medicare requirements (for example,
a crosswalk).
Detailed information about the organization's survey
process, including the following--
++ Frequency of surveys and whether surveys are announced or
unannounced.
++ Copies of survey forms, and guidelines and instructions to
surveyors.
++ Descriptions of--
-- The survey review process and the accreditation status decision
making process;
-- The procedures used to notify accredited MA organizations of
deficiencies and to monitor the correction of those deficiencies; and
-- The procedures used to enforce compliance with accreditation
requirements.
Detailed information about the individuals who perform
surveys for the accreditation organization, including the following--
++ The size and composition of accreditation survey teams for each
type of plan reviewed as part of the accreditation process;
++ The education and experience requirements surveyors must meet;
++ The content and frequency of the in-service training provided to
survey personnel;
++ The evaluation systems used to monitor the performance of
individual surveyors and survey teams; and
++ The organization's policies and practice with respect to the
participation, in surveys or in the accreditation decision process by
an individual who is professionally or financially affiliated with the
entity being surveyed.
A description of the organization's data management and
analysis system with respect to its surveys and accreditation
decisions, including the kinds of reports, tables, and other displays
generated by that system.
A description of the organization's procedures for
responding to and investigating complaints against accredited
organizations, including policies and procedures regarding coordination
of these activities with appropriate licensing bodies and ombudsmen
programs.
A description of the organization's policies and
procedures with respect to the withholding or removal of accreditation
for failure to meet the accreditation organization's standards or
requirements, and other actions the organization takes in response to
noncompliance with its standards and requirements.
A description of all types (for example, full, partial)
and categories (for example, provisional, conditional, temporary) of
accreditation offered by
[[Page 51172]]
the organization, the duration of each type and category of
accreditation and a statement identifying the types and categories that
would serve as a basis for accreditation if CMS approves the
accreditation organization.
A list of all currently accredited MA organizations and
the type, category, and expiration date of the accreditation held by
each of them.
A list of all full and partial accreditation surveys
scheduled to be performed by the accreditation organization.
The name and address of each person with an ownership or
control interest in the accreditation organization.
CMS's analysis of NCQA's past performance in the deeming
program and the results of recent deeming validation reviews, or look-
behind audits conducted as part of continuing federal oversight of the
deeming program under Sec. 422.157(d).
In accordance with section 1865(a)(3)(A) of the Act, the March 25,
2014 proposed notice (79 FR 16338) also solicited public comments
regarding whether NCQA's requirements met or exceeded the Medicare
conditions of participation as an accrediting organization for MA HMOs
and PPOs. We received no public comments in response to our proposed
notice.
IV. Provisions of the Final Notice
A. Differences Between NCQA's Standards and Requirements for
Accreditation and Medicare's Conditions and Survey Requirements
We compared the standards and survey process contained in NCQA's
application with the Medicare conditions for accreditation. Our review
and evaluation of NCQA's application for continued CMS-approval were
conducted as described in section III of this final notice, and yielded
the following:
To meet the requirements at Sec. 422.158(a)(1), NCQA
provided CMS with documentation listing its types of MA plans that it
would review as part of its accreditation process. In addition, AO
provided clarification and documentation to demonstrate how it
distinguishes its CMS-recognized deemed status accreditation program
from its other accreditation programs that are not recognized by CMS.
AO revised its ``Grounds of Revocation'' policy to meet
the requirements at Sec. 422.158(a)(3)(iii)(C) by revising its
requirements to include non-compliance with ``State, Federal, or other
duly authorized regulatory or judicial action restricts or limits the
organization's operations.''
To comply with the requirements at Sec. 422.158(a)(6), AO
revised its processes for responding to and investigating complaints
against accredited organizations by requiring the reporting of any
serious problems identified with an MA plan to the designated CMS MA
deeming representative.
B. Term of Approval
Based on the review and observations described in section III of
this final notice, we have determined that NCQA's accreditation program
requirements continue to meet or exceed our requirements. Therefore, we
renew NCQA as a national accreditation organization with deeming
authority for MA HMOs and PPOs, effective October 19, 2014 through
October 18, 2020.
V. Collection of Information Requirements
This document does not impose any new or revised information
collection or recordkeeping requirements. Consequently, it need not be
reviewed by the Office of Management and Budget under the authority of
the Paperwork Reduction Act of 1995.
Dated: August 15, 2014.
Marilyn Tavenner,
Administrator, Centers for Medicare & Medicaid Services.
[FR Doc. 2014-20446 Filed 8-26-14; 8:45 am]
BILLING CODE 4120-01-P