Medicare and Medicaid Programs; Continued Approval of the American Osteopathic Association/Healthcare Facilities Accreditation Program's (AOA/HFAP's) Ambulatory Surgical Center Accreditation Program, 44414-44416 [2017-20281]
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44414
Federal Register / Vol. 82, No. 183 / Friday, September 22, 2017 / Notices
Dated: September 18, 2017.
Lorin S. Curit,
Director, Federal Acquisition Policy Division,
Office of Government-Wide Acquisition
Policy, Office of Acquisition Policy, Office
of Government-Wide Policy.
[FR Doc. 2017–20169 Filed 9–21–17; 8:45 am]
BILLING CODE 6820–EP–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[Docket No. CDC–2015–0049]
Notice of Availability of a Revised
Environmental Assessment for HHS/
CDC Lawrenceville Campus Proposed
Improvements 2015–2025,
Lawrenceville, Georgia
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of availability and
request for comment.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), within
the Department of Health and Human
Services (HHS), announces the
availability and opportunity for public
review and comment of a revised
Environmental Assessment (EA) for the
HHS/CDC Lawrenceville Campus
Proposed Improvements 2015–2025 on
the HHS/CDC Lawrenceville Campus,
Lawrenceville, Georgia. The revised EA
has been prepared in accordance with
the National Environmental Policy Act
of 1969 (NEPA), as amended (42 U.S.C.
4321 et seq.), the Council on
Environmental Quality (CEQ)
implementing regulations (40 CFR
1500–1508) and the HHS General
Administration Manual (GAM) Part 30
Environmental Procedures, dated
February 25, 2000.
DATES: Written comments must be
received by October 23, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0049 by any of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Comments submitted by mail
should be sent to Stephen Klim, RA,
LEED Green Associate Architect Centers
for Disease Control and Prevention,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
K96, Atlanta, Georgia 30329, Attn:
Docket No. CDC–2015–0049.
Instructions: All submissions received
must include the agency name and
SUMMARY:
VerDate Sep<11>2014
18:11 Sep 21, 2017
Jkt 241001
Docket Number. All relevant comments
received will be posted without change
to https://regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
https://www.regulations.gov.
Hard copies of the revised EA are
available for review at the following
locations:
D Gwinnett County Public Library,
Lawrenceville Branch, 1001
Lawrenceville Hwy, Lawrenceville, GA
30046, Telephone: (770) 978–5154.
D Gwinnett County Public Library,
Five Forks Branch, 2780 Five Forks
Trickum Road, Lawrenceville, GA
30044–5865, Telephone: (770) 978–
5154.
D Gwinnett County Public Library,
Grayson Branch, 700 Grayson Parkway,
Grayson, GA 30017–1208, Telephone:
(770) 978–5154.
FOR FURTHER INFORMATION CONTACT:
Stephen Klim, RA, Office of Safety,
Security, and Asset Management,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
K96, Atlanta, Georgia 30329, Telephone:
(770)488–8009.
SUPPLEMENTARY INFORMATION: On
February 16, 2016 CDC published a
Notice of Availability for the Final
Environmental Assessment (2016 Final
EA) and Finding of No Significant
Impact (FONSI) for the HHS/CDC’s
Lawrenceville Campus Proposed
Improvements 2015–2025 (81 FR 7800).
The proposed improvements identified
in the 2016 Final EA included (1)
building demolition; (2) new building
construction, including an
approximately 12,000 gross square feet
(gsf) Science Support Building, a new
Transshipping and Receiving Area at
approximately 2,500 gsf and two new
Office Support Buildings at
approximately 8,000 gsf and 6,000 gsf;
(3) expansion and relocation of parking
on campus; and (4) the creation of an
additional point of access to the campus
and pedestrian improvements. The 2016
Final EA concluded that no significant
impacts to the human or natural
environment would result and HHS/
CDC issued a FONSI.
Since completion of the 2016 Final
EA and FONSI, HHS/CDC proposed
changes to the Proposed Action. HHS/
CDC has revised the EA to include the
installation of a photovoltaic system
within the northern portion of the
campus. The photovoltaic system would
consist of a 249.9-kilowat (KW) groundmounted solar array covering an area of
approximately 41,750 sf (0.99 acre). The
proposed photovoltaic system would
provide the Lawrenceville Campus with
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a renewable energy source in order to
comply with federal renewable energy
mandates.
The revised EA evaluates the
potential environmental impacts of the
proposed photovoltaic system, along
with the proposed improvements
identified in the 2016 Final EA.
Potential impacts of the No Build and
the Build Alternative are evaluated on
the following resource categories:
Socioeconomics; land use; zoning;
public policy; community facilities;
transportation; air quality; noise;
cultural resources; urban design and
visual resources; natural resources;
utilities; waste; and greenhouse gases
and sustainability.
Dated: September 18, 2017.
Lauren Hoffman,
Acting Executive Secretary, Centers for
Disease Control and Prevention.
[FR Doc. 2017–20104 Filed 9–21–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3343–FN]
Medicare and Medicaid Programs;
Continued Approval of the American
Osteopathic Association/Healthcare
Facilities Accreditation Program’s
(AOA/HFAP’s) Ambulatory Surgical
Center Accreditation Program
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Final notice.
AGENCY:
This final notice announces
our decision to approve the American
Osteopathic Association/Healthcare
Facilities Accreditation Program (AOA/
HFAP) for continued recognition as a
national accrediting organization for
ambulatory surgical centers (ASCs) that
wish to participate in the Medicare or
Medicaid programs.
DATES: This final notice is effective
September 22, 2017 through September
22, 2023.
FOR FURTHER INFORMATION CONTACT:
Monda Shaver, (410) 786–3410, Erin
McCoy, (410) 786–2337, or Patricia
Chmielewski, (410) 786–6899.
SUPPLEMENTARY INFORMATION:
SUMMARY:
I. Background
Under the Medicare program, eligible
beneficiaries may receive covered
services in an ambulatory surgical
center (ASC) provided certain
requirements are met. Sections
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Federal Register / Vol. 82, No. 183 / Friday, September 22, 2017 / Notices
1832(a)(2)(F)(i) of the Social Security
Act (the Act) establishes distinct criteria
for facilities seeking designation as an
ASC. Regulations concerning provider
agreements are at 42 CFR part 489 and
those pertaining to activities relating to
the survey and certification of facilities
are at 42 CFR part 488. The regulations
at 42 CFR part 416, specify the
conditions that an ASC must meet in
order to participate in the Medicare
program, the scope of covered services
and the conditions for Medicare
payment for ASCs.
Generally, to enter into an agreement,
an ASC must first be certified as
complying with the conditions set forth
in Part 416 and recommended to the
Centers of Medicare & Medicaid
Services (CMS) for participation by a
state survey agency. Thereafter, the ASC
is subject to periodic surveys by a state
survey agency to determine whether it
continues to meet these conditions.
However, there is an alternative to
certification surveys by state agencies.
Accreditation by a nationally recognized
Medicare accreditation program
approved by CMS may substitute for
both initial and ongoing state review.
Section 1865(a)(1) of the Act provides
that, if the Secretary of the Department
of Health and Human Services (the
Secretary) finds that accreditation of a
provider entity by an approved national
accrediting organization meets or
exceeds all applicable Medicare
conditions, we may treat the provider
entity as having met those conditions,
that is, we may ‘‘deem’’ the provider
entity to be in compliance.
Accreditation by an accrediting
organization is voluntary and is not
required for Medicare participation.
Part 488, subpart A, implements the
provisions of section 1865 of the Act
and requires that a national accrediting
organization applying for approval of its
Medicare accreditation program must
provide CMS with reasonable assurance
that the accrediting organization
requires its accredited provider entities
to meet requirements that are at least as
stringent as the Medicare conditions.
Our regulations concerning the approval
of accrediting organizations are set forth
at § 488.5.
II. Application Approval Process
Section 1865(a)(3)(A) of the Act
provides a statutory timetable to ensure
that our review of applications for CMS
approval of an accreditation program is
conducted in a timely manner. The Act
provides us 210 days after the date of
receipt of a complete application, with
any documentation necessary to make
the determination, to complete our
survey activities and application
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18:11 Sep 21, 2017
Jkt 241001
process. Within 60 days after receiving
a complete application, we must
publish a notice in the Federal Register
that identifies the national accrediting
body making the request, describes the
request, and provides no less than a 30day public comment period. At the end
of the 210-day period, we must publish
a notice in the Federal Register
approving or denying the application.
III. Provisions of the Proposed Notice
On June 13, 2017, we published a
proposed notice (82 FR 27067) in the
Federal Register, announcing AOA/
HFAP’s request for continued approval
of its Medicare ASC accreditation
program. In the proposed notice, we
detailed our evaluation criteria. Under
section 1865(a)(2) of the Act and in our
regulations at § 488.5, we conducted a
review of AOA/HFAP’s Medicare ASC
accreditation renewal application in
accordance with the criteria specified by
our regulations, which include, but are
not limited to the following:
• An onsite administrative review of
AOA/HFAP’s: (1) Corporate policies; (2)
financial and human resources available
to accomplish the proposed surveys; (3)
procedures for training, monitoring and
evaluation of its ASC surveyors; (4)
ability to investigate and respond
appropriately to complaints against
accredited ASCs; and (5) survey review
and decision-making process for
accreditation.
• The comparison of AOA/HFAP’s
Medicare ASC accreditation program
standards to our current Medicare ASC
condition of coverage (CfC’s).
• A documentation review of ASC’s
survey process to:
++ Determine the composition of the
survey team, surveyor qualifications,
and AOA/HFAP’s ability to provide
continuing surveyor training.
++ Compare AOA/HFAP’s processes
to those we require of state survey
agencies, including periodic resurvey
and the ability to investigate and
respond appropriately to complaints
against accredited ASCs.
++ Evaluate AOA/HFAP’s procedures
for monitoring ASCs found to be out of
compliance with AOA/HFAP’s program
requirements. (This pertains only to
monitoring procedures when AOA/
HFAP identifies non-compliance. If
noncompliance is identified by a state
survey agency through a validation
survey, the state survey agency monitors
corrections as specified at § 488.9(c).)
++ Assess AOA/HFAP’s ability to
report deficiencies to the surveyed ASC
and respond to the ASCs plan of
correction in a timely manner.
++ Establish AOA/HFAP’s ability to
provide CMS with electronic data and
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44415
reports necessary for effective validation
and assessment of the organization’s
survey process.
++ Determine the adequacy of AOA/
HFAP’s staff and other resources.
++ Confirm AOA/HFAP’s ability to
provide adequate funding for
performing required surveys.
++ Confirm AOA/HFAP’s policies
with respect to surveys being
unannounced.
++ Obtain AOA/HFAP’s agreement to
provide CMS with a copy of the most
current accreditation survey, along with
any other information related to the
survey as we may require, including
corrective action plans.
In accordance with section
1865(a)(3)(A) of the Act, the June 13,
2017 proposed notice also solicited
public comments regarding whether
AOA/HFAP’s requirements met or
exceeded the Medicare CfCs for ASCs.
We received 2 comments in response to
our proposed notice. All of the
comments received expressed
unanimous support for AOA/HFAP’s
ASC accreditation program.
IV. Provisions of the Final Notice
A. Differences Between AOA/HFAP’s
Standards and Requirements for
Accreditation and Medicare Conditions
and Survey Requirements
We compared AOA/HFAP’s ASC
accreditation program requirements and
survey process with the Medicare CfCs
at 42 CFR part 416, and the survey and
certification process requirements of
Parts 488 and 489. Our review and
evaluation of AOA/HFAP’s ASC
application, which were conducted as
described in section III of this final
notice, yielded the following areas
where, as of the date of this notice,
AOA/HFAP has revised its standards
and certification processes in order to
meet the requirements at:
• Section 416.2, to ensure its
standards appropriately reference
§ 416.2 and Part 416 subparts B and C.
• Section 416.25, to ensure its
standards to require facilities meet the
definition at § 416.2.
• Section 416.41(b)(3)(i), to ensure its
standards appropriately reference
§ 416.41(b)(2).
• Section 416.41(b)(3)(ii), to ensure
its standards appropriately reference
§ 416.41(b)(2).
• Section 416.42(b)(2), to ensure its
standards appropriately reference
§ 416.42(c)
• Section 416.49(b)(2), to ensure
standards appropriately reference
§ 416.49(c).
• Section 416.50(a), to ensure its
standards appropriately reference
§ 416.50.
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Federal Register / Vol. 82, No. 183 / Friday, September 22, 2017 / Notices
• Section 416.50(b), to ensure its
standards appropriately reference Part
420.
• Section 488.5(a)(4)(ii), to ensure
AOA/HFAP’s surveyors review the
minimum number of medical records as
specified by CMS and AOA/HFAP
policy.
• Section 488.5(a)(4)(iv), to ensure
each that all observations of noncompliance are documented in the
survey report.
• Section 488.5(a)(7) through (9), to
ensure AOA/HFAP complies with its
policy and criteria for surveyor
qualifications, education and evaluation
system to monitor the performance of
surveyors and teams.
• Section 488.26(b), to ensure AOA/
HFAP cites findings of observed noncompliance at the appropriate level
(condition versus standard level).
B. Term of Approval
Based on our review and observations
described in section III of this final
notice, we approve AOA/HFAP as a
national accreditation organization for
ASCs that request participation in the
Medicare program, effective September
22, 2017 through September 22, 2023.
V. Collection of Information
Requirements
This document does not impose
information collection 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.).
Dated: September 14, 2017.
Seema Verma,
Administrator, Centers for Medicare &
Medicaid Services.
[FR Doc. 2017–20281 Filed 9–21–17; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers CMS–R–185, CMS–
718–721, CMS–10123/–10124, CMS–10142,
and CMS–R–262]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
VerDate Sep<11>2014
18:11 Sep 21, 2017
Jkt 241001
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
November 21, 2017.
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’ Web site address at
https://www.cms.hhs.gov/Paperwork
ReductionActof1995.
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 Parham at (410) 786–4669.
SUMMARY:
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Frm 00041
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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–R–185 Granting and Withdrawal
of Deeming Authority to Private
Nonprofit Accreditation
Organizations and CLIA Exemption
under State Laboratory Programs
CMS–718–721 Business Proposal
Forms for Quality Improvement
Organizations (QIOs)
CMS–10123/–10124 Fast Track
Appeals Notices: NOMNC/DENC
CMS–10142 Bid Pricing Tool (BPT) for
Medicare Advantage (MA) Plans and
Prescription Drug Plans (PDP)
CMS–R–262 Contract Year 2019 Plan
Benefit Package (PBP) Software and
Formulary Submission
Under the PRA (44 U.S.C. 3501–
3520), federal agencies must obtain
approval from the Office of Management
and Budget (OMB) for each collection of
information they conduct or sponsor.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
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: Extension of currently
approved collection; Title of
Information Collection: Granting and
Withdrawal of Deeming Authority to
Private Nonprofit Accreditation
Organizations and CLIA Exemption
Under State Laboratory Programs; Use:
The information required is necessary to
determine whether a private
accreditation organization/State
licensure program standards and
accreditation/licensure process is at
least equal to or more stringent than
those of the Clinical Laboratory
Improvement Amendments of 1988
(CLIA). If an accreditation organization
is approved, the laboratories that it
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Agencies
[Federal Register Volume 82, Number 183 (Friday, September 22, 2017)]
[Notices]
[Pages 44414-44416]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-20281]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-3343-FN]
Medicare and Medicaid Programs; Continued Approval of the
American Osteopathic Association/Healthcare Facilities Accreditation
Program's (AOA/HFAP's) Ambulatory Surgical Center Accreditation Program
AGENCY: Centers for Medicare & Medicaid Services, HHS.
ACTION: Final notice.
-----------------------------------------------------------------------
SUMMARY: This final notice announces our decision to approve the
American Osteopathic Association/Healthcare Facilities Accreditation
Program (AOA/HFAP) for continued recognition as a national accrediting
organization for ambulatory surgical centers (ASCs) that wish to
participate in the Medicare or Medicaid programs.
DATES: This final notice is effective September 22, 2017 through
September 22, 2023.
FOR FURTHER INFORMATION CONTACT: Monda Shaver, (410) 786-3410, Erin
McCoy, (410) 786-2337, or Patricia Chmielewski, (410) 786-6899.
SUPPLEMENTARY INFORMATION:
I. Background
Under the Medicare program, eligible beneficiaries may receive
covered services in an ambulatory surgical center (ASC) provided
certain requirements are met. Sections
[[Page 44415]]
1832(a)(2)(F)(i) of the Social Security Act (the Act) establishes
distinct criteria for facilities seeking designation as an ASC.
Regulations concerning provider agreements are at 42 CFR part 489 and
those pertaining to activities relating to the survey and certification
of facilities are at 42 CFR part 488. The regulations at 42 CFR part
416, specify the conditions that an ASC must meet in order to
participate in the Medicare program, the scope of covered services and
the conditions for Medicare payment for ASCs.
Generally, to enter into an agreement, an ASC must first be
certified as complying with the conditions set forth in Part 416 and
recommended to the Centers of Medicare & Medicaid Services (CMS) for
participation by a state survey agency. Thereafter, the ASC is subject
to periodic surveys by a state survey agency to determine whether it
continues to meet these conditions. However, there is an alternative to
certification surveys by state agencies. Accreditation by a nationally
recognized Medicare accreditation program approved by CMS may
substitute for both initial and ongoing state review.
Section 1865(a)(1) of the Act provides that, if the Secretary of
the Department of Health and Human Services (the Secretary) finds that
accreditation of a provider entity by an approved national accrediting
organization meets or exceeds all applicable Medicare conditions, we
may treat the provider entity as having met those conditions, that is,
we may ``deem'' the provider entity to be in compliance. Accreditation
by an accrediting organization is voluntary and is not required for
Medicare participation.
Part 488, subpart A, implements the provisions of section 1865 of
the Act and requires that a national accrediting organization applying
for approval of its Medicare accreditation program must provide CMS
with reasonable assurance that the accrediting organization requires
its accredited provider entities to meet requirements that are at least
as stringent as the Medicare conditions. Our regulations concerning the
approval of accrediting organizations are set forth at Sec. 488.5.
II. Application Approval Process
Section 1865(a)(3)(A) of the Act provides a statutory timetable to
ensure that our review of applications for CMS approval of an
accreditation program is conducted in a timely manner. The Act provides
us 210 days after the date of receipt of a complete application, with
any documentation necessary to make the determination, to complete our
survey activities and application process. Within 60 days after
receiving a complete application, we must publish a notice in the
Federal Register that identifies the national accrediting 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 a notice in the Federal Register approving or denying the
application.
III. Provisions of the Proposed Notice
On June 13, 2017, we published a proposed notice (82 FR 27067) in
the Federal Register, announcing AOA/HFAP's request for continued
approval of its Medicare ASC accreditation program. In the proposed
notice, we detailed our evaluation criteria. Under section 1865(a)(2)
of the Act and in our regulations at Sec. 488.5, we conducted a review
of AOA/HFAP's Medicare ASC accreditation renewal application in
accordance with the criteria specified by our regulations, which
include, but are not limited to the following:
An onsite administrative review of AOA/HFAP's: (1)
Corporate policies; (2) financial and human resources available to
accomplish the proposed surveys; (3) procedures for training,
monitoring and evaluation of its ASC surveyors; (4) ability to
investigate and respond appropriately to complaints against accredited
ASCs; and (5) survey review and decision-making process for
accreditation.
The comparison of AOA/HFAP's Medicare ASC accreditation
program standards to our current Medicare ASC condition of coverage
(CfC's).
A documentation review of ASC's survey process to:
++ Determine the composition of the survey team, surveyor
qualifications, and AOA/HFAP's ability to provide continuing surveyor
training.
++ Compare AOA/HFAP's processes to those we require of state survey
agencies, including periodic resurvey and the ability to investigate
and respond appropriately to complaints against accredited ASCs.
++ Evaluate AOA/HFAP's procedures for monitoring ASCs found to be
out of compliance with AOA/HFAP's program requirements. (This pertains
only to monitoring procedures when AOA/HFAP identifies non-compliance.
If noncompliance is identified by a state survey agency through a
validation survey, the state survey agency monitors corrections as
specified at Sec. 488.9(c).)
++ Assess AOA/HFAP's ability to report deficiencies to the surveyed
ASC and respond to the ASCs plan of correction in a timely manner.
++ Establish AOA/HFAP's ability to provide CMS with electronic data
and reports necessary for effective validation and assessment of the
organization's survey process.
++ Determine the adequacy of AOA/HFAP's staff and other resources.
++ Confirm AOA/HFAP's ability to provide adequate funding for
performing required surveys.
++ Confirm AOA/HFAP's policies with respect to surveys being
unannounced.
++ Obtain AOA/HFAP's agreement to provide CMS with a copy of the
most current accreditation survey, along with any other information
related to the survey as we may require, including corrective action
plans.
In accordance with section 1865(a)(3)(A) of the Act, the June 13,
2017 proposed notice also solicited public comments regarding whether
AOA/HFAP's requirements met or exceeded the Medicare CfCs for ASCs. We
received 2 comments in response to our proposed notice. All of the
comments received expressed unanimous support for AOA/HFAP's ASC
accreditation program.
IV. Provisions of the Final Notice
A. Differences Between AOA/HFAP's Standards and Requirements for
Accreditation and Medicare Conditions and Survey Requirements
We compared AOA/HFAP's ASC accreditation program requirements and
survey process with the Medicare CfCs at 42 CFR part 416, and the
survey and certification process requirements of Parts 488 and 489. Our
review and evaluation of AOA/HFAP's ASC application, which were
conducted as described in section III of this final notice, yielded the
following areas where, as of the date of this notice, AOA/HFAP has
revised its standards and certification processes in order to meet the
requirements at:
Section 416.2, to ensure its standards appropriately
reference Sec. 416.2 and Part 416 subparts B and C.
Section 416.25, to ensure its standards to require
facilities meet the definition at Sec. 416.2.
Section 416.41(b)(3)(i), to ensure its standards
appropriately reference Sec. 416.41(b)(2).
Section 416.41(b)(3)(ii), to ensure its standards
appropriately reference Sec. 416.41(b)(2).
Section 416.42(b)(2), to ensure its standards
appropriately reference Sec. 416.42(c)
Section 416.49(b)(2), to ensure standards appropriately
reference Sec. 416.49(c).
Section 416.50(a), to ensure its standards appropriately
reference Sec. 416.50.
[[Page 44416]]
Section 416.50(b), to ensure its standards appropriately
reference Part 420.
Section 488.5(a)(4)(ii), to ensure AOA/HFAP's surveyors
review the minimum number of medical records as specified by CMS and
AOA/HFAP policy.
Section 488.5(a)(4)(iv), to ensure each that all
observations of non-compliance are documented in the survey report.
Section 488.5(a)(7) through (9), to ensure AOA/HFAP
complies with its policy and criteria for surveyor qualifications,
education and evaluation system to monitor the performance of surveyors
and teams.
Section 488.26(b), to ensure AOA/HFAP cites findings of
observed non-compliance at the appropriate level (condition versus
standard level).
B. Term of Approval
Based on our review and observations described in section III of
this final notice, we approve AOA/HFAP as a national accreditation
organization for ASCs that request participation in the Medicare
program, effective September 22, 2017 through September 22, 2023.
V. Collection of Information Requirements
This document does not impose information collection 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.).
Dated: September 14, 2017.
Seema Verma,
Administrator, Centers for Medicare & Medicaid Services.
[FR Doc. 2017-20281 Filed 9-21-17; 8:45 am]
BILLING CODE 4120-01-P