Medicare and Medicaid Programs: National Dialysis Accreditation Commission (NDAC) for Approval of its End Stage Renal Disease (ESRD) Facility Accreditation Program, 38697-38699 [2018-16871]
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Federal Register / Vol. 83, No. 152 / Tuesday, August 7, 2018 / Notices
program enables CMS to compare its
data to SSA data to confirm an
applicant’s or other relevant
individual’s identity, citizenship, status
as deceased or imprisoned, and Title II
disability benefit quarters of coverage
(QC) and monthly and annual income.
The data is used by CMS to authenticate
identity, determine eligibility, and
determine the amount of an advance
payment of the premium tax credit
(APTC) or cost sharing reduction (CSR).
CATEGORIES OF INDIVIDUALS:
The categories of individuals whose
information is involved in the matching
program are consumers who apply for
any of the following eligibility
determinations, and other relevant
individuals (e.g., an applicant’s
household members) who have
eligibility to enroll in a qualified health
plan through an exchange established
under the ACA, eligibility for insurance
affordability programs and certificates of
exemption, and subsequent eligibility
redeterminations and renewals,
including appeal determinations.
daltland on DSKBBV9HB2PROD with NOTICES
CATEGORIES OF RECORDS:
The categories of records used in the
matching program are identity,
citizenship, birth, death, disability
coverage and income, and
imprisonment status records. The data
elements are as follows:
1. For each applicant and for relevant
individuals, CMS will submit a request
file to SSA that contains the following
mandatory specified data elements in a
fixed record format: Last name, first
name, date of birth, social security
number (SSN), and citizenship
indicator.
2. For each applicant, SSA will
provide CMS with a response file in a
fixed record format. Depending on CMS’
request, SSA’s response may include the
following data elements: Last name, first
name, date of birth, death indicator,
disability indicator, prisoner
information, Title II (annual and
monthly) income information, and
confirmation of attestations of
citizenship status and SSN. SSA may
also provide QC data when CMS
requests it.
3. For relevant individuals, CMS will
request a limited amount of SSA
information. Based on CMS’ request,
SSA will verify a relevant individual’s
SSN with a death indicator and may
provide a relevant individual’s QC data
or Title II (annual and monthly) income
information. CMS will not request
citizenship or immigration status data
for a relevant individual.
4. For renewals and redeterminations,
CMS will request and SSA will verify
VerDate Sep<11>2014
16:54 Aug 06, 2018
Jkt 244001
SSN with a death indicator, disclose
Title II income information, and provide
the disability indicator.
5. For self-reported redeterminations,
CMS will provide SSA with the
following: Updated or new information
reported by the enrollee or enrolled
individual, last name, first name, date of
birth, and SSN. Depending on CMS’
request, SSA’s response will include
each of the following data elements that
are relevant and responsive to CMS’
request: Last name, first name, date of
birth, death indicator, disability
indicator, prisoner information, Title II
(annual and monthly) income
information, and confirmation of new
attestations of citizenship status,
verification of SSN, and QC data.
6. For individuals seeking an
exemption, CMS will provide last name,
first name, date of birth, citizenship
indicator, and SSN to SSA. SSA will
provide CMS with a response including:
Last name, first name, date of birth,
confirmation of attestations of
citizenship status, verification of SSN,
death indicator, disability indicator,
prisoner information, and Title II
(annual and monthly) income
information.
SYSTEM(S) OF RECORDS:
The records used in this matching
program are disclosed from the
following systems of records, as
authorized by routine uses published in
the System of Records Notices (SORNs)
cited below:
CMS System of Records:
b The CMS SOR that supports this
matching program is the ‘‘CMS Health
Insurance Exchanges System (HIX)’’,
CMS System No. 09–70–0560, last
published in full at 78 FR 63211
(October 23, 2013), as amended at 83 FR
6591 (February 14, 2018).
SSA Systems of Records:
b Master Files of SSN Holders and
SSN Applications, 60–0058, 75 FR
82121 (Dec. 29, 2010), as amended at 78
FR 40542 (July 5, 2013), and 79 FR 8780
(Feb. 13, 2014);
b Prisoner Update Processing System
(PUPS), 60–0269, 64 FR 11076 (Mar. 8,
1999), as amended at 72 FR 69723 (Dec.
10, 2007) and 78 FR 40542 (July 5,
2013);
b Master Beneficiary Record, 60–
0090, 71 FR 1826 (Jan. 1, 2006), as
amended at 72 FR 69723 (Dec. 10, 2007)
and 78 FR 40542 (July 5, 2013); and
b Earnings Recording and SelfEmployment Income System, 60–0059,
71 FR 1819 (Jan. 11, 2006), as amended
at 78 FR 40542 (July 5, 2013).
[FR Doc. 2018–16821 Filed 8–6–18; 8:45 am]
BILLING CODE 4120–03–P
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38697
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3366–PN]
Medicare and Medicaid Programs:
National Dialysis Accreditation
Commission (NDAC) for Approval of
its End Stage Renal Disease (ESRD)
Facility Accreditation Program
Centers for Medicare and
Medicaid Services (CMS), HHS.
ACTION: Notice with request for
comment.
AGENCY:
This proposed notice
acknowledges the receipt of an
application from the National Dialysis
Accreditation Commission (NDAC) for
recognition as a national accrediting
organization (AO) for End Stage Renal
Disease (ESRD) Facilities that wish to
participate in the Medicare or Medicaid
programs.
DATES: To be assured consideration,
comments must be received at one of
the addresses provided below, no later
than 5 p.m. on September 6, 2018.
ADDRESSES: In commenting, refer to file
code CMS–3366–PN. Because of staff
and resource limitations, we cannot
accept comments by facsimile (FAX)
transmission.
Comments, including mass comment
submissions, must be submitted in one
of the following three ways (please
choose only one of the ways listed):
1. Electronically. You may submit
electronic comments on this regulation
to https://www.regulations.gov. Follow
the ‘‘Submit a comment’’ instructions.
2. By regular mail. You may mail
written comments to the following
address ONLY: Centers for Medicare &
Medicaid Services, Department of
Health and Human Services, Attention:
CMS–3366–PN, P.O. Box 8010,
Baltimore, MD 21244–8010.
Please allow sufficient time for mailed
comments to be received before the
close of the comment period.
3. By express or overnight mail. You
may send written comments to the
following address ONLY: Centers for
Medicare & Medicaid Services,
Department of Health and Human
Services, Attention: CMS–3366–PN,
Mail Stop C4–26–05, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
For information on viewing public
comments, see the beginning of the
SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT: Tara
Lemons, (410) 786–3030, Monda
Shaver, (410) 786–3410, or Marie
Vasbinder, (410) 786–8665.
SUMMARY:
E:\FR\FM\07AUN1.SGM
07AUN1
38698
Federal Register / Vol. 83, No. 152 / Tuesday, August 7, 2018 / Notices
SUPPLEMENTARY INFORMATION:
daltland on DSKBBV9HB2PROD with NOTICES
Inspection of Public Comments: All
comments received before the close of
the comment period are available for
viewing by the public, including any
personally identifiable or confidential
business information that is included in
a comment. We post all comments
received before the close of the
comment period on the following
website as soon as possible after they
have been received: https://
www.regulations.gov. Follow the search
instructions on that website to view
public comments.
I. Background
Under the Medicare program, eligible
beneficiaries may receive covered
services from an end-stage renal disease
(ESRD) facility provided the facility
meets the requirements established by
the Secretary of the Department of
Health and Human Services (Secretary).
Section 1881(b) of the Social Security
Act (the Act) establishes distinct
requirements for facilities seeking
designation as an ESRD facility under
Medicare. Regulations concerning
provider agreements and supplier
approval are at 42 CFR part 489 and
those pertaining to activities relating to
the survey, certification, and
enforcement procedures of suppliers
which include ESRD facilities are at 42
CFR part 488. The regulations at 42 CFR
part 494 subparts A through D
implement section 1881(b) of the Act,
which specify the conditions that an
ESRD facility must meet in order to
participate in the Medicare program and
the conditions for Medicare payment for
ESRD facilities.
Generally, to enter into a Medicare
agreement, an ESRD facility must first
be certified by a State survey agency as
complying with the conditions or
requirements set forth in part 494
subparts A through D of our Medicare
regulations. Thereafter, the ESRD
facility is subject to regular surveys by
a State survey agency to determine
whether it continues to meet these
requirements.
Section 1865(a)(1) of the Act provides
that, if a provider entity demonstrates
through accreditation by a Centers for
Medicare & Medicaid Services (CMS)
approved national accrediting
organization (AO) that all applicable
Medicare conditions are met or
exceeded, we may deem those provider
entities as having met the requirements.
Section 1865(a)(1) of the Act had
historically prohibited dialysis facilities
from participating in Medicare via a
CMS-approved accreditation program;
however, section 50403 of the
Bipartisan Budget Act of 2018 amended
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16:54 Aug 06, 2018
Jkt 244001
section 1865(a) of the Act to include
renal dialysis facilities as provider
entities allowed to participate in
Medicare through a CMS-approved
accreditation program. Accreditation by
an AO is voluntary and is not required
for Medicare participation.
If an AO is recognized by the
Secretary as having standards for
accreditation that meet or exceed
Medicare requirements, any provider
entity accredited by the national
accrediting body’s approved program
may be deemed to meet the Medicare
conditions. An AO applying for
approval of its accreditation program
under part 488, subpart A, must provide
CMS with reasonable assurance that the
AO requires the accredited provider
entities to meet requirements that are at
least as stringent as the Medicare
conditions. Our regulations concerning
the approval of AOs are set forth at
§ 488.5.
II. Provisions of the Proposed Notice
A. Approval of Deeming Organizations
Section 1865(a)(2) of the Act and our
regulations at § 488.5 require that our
findings concerning review and
approval of an AO’s requirements
consider, among other factors, the
applying AO’s requirements for
accreditation; survey procedures;
resources for conducting required
surveys; capacity to furnish information
for use in enforcement activities;
monitoring procedures for provider
entities found not in compliance with
the conditions or requirements; and
ability to provide CMS with the
necessary data for validation.
Section 1865(a)(3)(A) of the Act
further requires that we publish, within
60 days of receipt of an organization’s
complete application, a notice
identifying the national accrediting
body making the request, describing the
nature of the request, and providing at
least a 30-day public comment period.
We have 210 days from the receipt of a
complete application to publish notice
of approval or denial of the application.
The purpose of this proposed notice
is to inform the public of National
Dialysis Accreditation Commission’s
(NDAC) request for CMS-approval of its
ESRD facility accreditation program.
This notice also solicits public comment
on whether NDAC’s requirements meet
or exceed the Medicare conditions for
coverage (CfCs) for ESRD facilities.
This is the first application from a
national accreditation body seeking
approval of an accreditation program for
ESRD facilities.
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Frm 00022
Fmt 4703
Sfmt 4703
B. Evaluation of Deeming Authority
Request
NDAC submitted all the necessary
materials to enable us to make a
determination concerning its request for
CMS-approval of its ESRD facility
accreditation program. This application
was determined to be complete on June
8, 2018. Under section 1865(a)(2) of the
Act and our regulations at § 488.5, our
review and evaluation of NDAC will be
conducted in accordance with, but not
necessarily limited to, the following
factors:
• The equivalency of NDAC’s
standards for ESRD facilities as
compared with Medicare’s CfCs for
ESRD facilities.
• NDAC’s survey process to
determine the following:
++ The composition of the survey
team, surveyor qualifications, and the
ability of the organization to provide
continuing surveyor training.
++ The comparability of NDAC’s
processes to those of State agencies,
including survey frequency, and the
ability to investigate and respond
appropriately to complaints against
accredited facilities.
++ NDAC’s processes and procedures
for monitoring an ESRD facility found
out of compliance with NDAC’s
program requirements. These
monitoring procedures are used only
when NDAC identifies noncompliance.
If noncompliance is identified through
validation reviews or complaint
surveys, the State survey agency
monitors corrections as specified at
§ 488.9(c)(1).
++ NDAC’s capacity to report
deficiencies to the surveyed facilities
and respond to the facility’s plan of
correction in a timely manner.
++ NDAC’s capacity to provide CMS
with electronic data and reports
necessary for effective validation and
assessment of the organization’s survey
process.
++ The adequacy of NDAC’s staff and
other resources, and its financial
viability.
++ NDAC’s capacity to adequately
fund required surveys.
++ NDAC’s policies with respect to
whether surveys are announced or
unannounced, to assure that surveys are
unannounced.
++ NDAC’s agreement to provide
CMS with a copy of the most current
accreditation survey together with any
other information related to the survey
as CMS may require (including
corrective action plans).
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07AUN1
Federal Register / Vol. 83, No. 152 / Tuesday, August 7, 2018 / Notices
III. 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.).
IV. 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
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.
Dated: July 27, 2018.
Seema Verma,
Administrator, Centers for Medicare &
Medicaid Services.
[FR Doc. 2018–16871 Filed 8–6–18; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2018–D–2382]
Opioid Use Disorder: Endpoints for
Demonstrating Effectiveness of Drugs
for Medication-Assisted Treatment;
Draft Guidance for Industry;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of a draft
guidance for industry entitled ‘‘Opioid
Use Disorder: Endpoints for
Demonstrating Effectiveness of Drugs for
Medication-Assisted Treatment.’’ This
guidance addresses the clinical
endpoints acceptable to demonstrate
effectiveness of drugs for medicationassisted treatment of opioid use
disorder. FDA is also requesting
comments on when the use of placebo
or active controls is most appropriate in
clinical trials for such drugs.
daltland on DSKBBV9HB2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
16:54 Aug 06, 2018
Jkt 244001
Submit either electronic or
written comments on the draft guidance
by October 9, 2018 to ensure that the
Agency considers your comment on this
draft guidance before it begins work on
the final version of the guidance.
ADDRESSES: You may submit comments
on any guidance at any time as follows:
DATES:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2018–D–2382 for ‘‘Opioid Use Disorder:
Endpoints for Demonstrating
Effectiveness of Drugs for MedicationAssisted Treatment.’’ Received
comments will be placed in the docket
and, except for those submitted as
‘‘Confidential Submissions,’’ publicly
viewable at https://www.regulations.gov
or at the Dockets Management Staff
between 9 a.m. and 4 p.m., Monday
through Friday.
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38699
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on
https://www.regulations.gov. Submit
both copies to the Dockets Management
Staff. If you do not wish your name and
contact information to be made publicly
available, you can provide this
information on the cover sheet and not
in the body of your comments and you
must identify this information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://www.gpo.gov/
fdsys/pkg/FR-2015-09-18/pdf/201523389.pdf.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Dockets Management
Staff, 5630 Fishers Lane, Rm. 1061,
Rockville, MD 20852.
You may submit comments on any
guidance at any time (see 21 CFR
10.115(g)(5)).
Submit written requests for single
copies of the draft guidance to the
Division of Drug Information, Center for
Drug Evaluation and Research, Food
and Drug Administration, 10001 New
Hampshire Ave., Hillandale Building,
4th Floor, Silver Spring, MD 20993–
0002. Send one self-addressed adhesive
label to assist that office in processing
your requests. See the SUPPLEMENTARY
INFORMATION section for electronic
access to the draft guidance document.
FOR FURTHER INFORMATION CONTACT:
Silvana Borges, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 22, Rm. 3200,
E:\FR\FM\07AUN1.SGM
07AUN1
Agencies
[Federal Register Volume 83, Number 152 (Tuesday, August 7, 2018)]
[Notices]
[Pages 38697-38699]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-16871]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-3366-PN]
Medicare and Medicaid Programs: National Dialysis Accreditation
Commission (NDAC) for Approval of its End Stage Renal Disease (ESRD)
Facility Accreditation Program
AGENCY: Centers for Medicare and Medicaid Services (CMS), HHS.
ACTION: Notice with request for comment.
-----------------------------------------------------------------------
SUMMARY: This proposed notice acknowledges the receipt of an
application from the National Dialysis Accreditation Commission (NDAC)
for recognition as a national accrediting organization (AO) for End
Stage Renal Disease (ESRD) Facilities that wish to participate in the
Medicare or Medicaid programs.
DATES: To be assured consideration, comments must be received at one of
the addresses provided below, no later than 5 p.m. on September 6,
2018.
ADDRESSES: In commenting, refer to file code CMS-3366-PN. Because of
staff and resource limitations, we cannot accept comments by facsimile
(FAX) transmission.
Comments, including mass comment submissions, must be submitted in
one of the following three ways (please choose only one of the ways
listed):
1. Electronically. You may submit electronic comments on this
regulation to https://www.regulations.gov. Follow the ``Submit a
comment'' instructions.
2. By regular mail. You may mail written comments to the following
address ONLY: Centers for Medicare & Medicaid Services, Department of
Health and Human Services, Attention: CMS-3366-PN, P.O. Box 8010,
Baltimore, MD 21244-8010.
Please allow sufficient time for mailed comments to be received
before the close of the comment period.
3. By express or overnight mail. You may send written comments to
the following address ONLY: Centers for Medicare & Medicaid Services,
Department of Health and Human Services, Attention: CMS-3366-PN, Mail
Stop C4-26-05, 7500 Security Boulevard, Baltimore, MD 21244-1850.
For information on viewing public comments, see the beginning of
the SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT: Tara Lemons, (410) 786-3030, Monda
Shaver, (410) 786-3410, or Marie Vasbinder, (410) 786-8665.
[[Page 38698]]
SUPPLEMENTARY INFORMATION:
Inspection of Public Comments: All comments received before the
close of the comment period are available for viewing by the public,
including any personally identifiable or confidential business
information that is included in a comment. We post all comments
received before the close of the comment period on the following
website as soon as possible after they have been received: https://www.regulations.gov. Follow the search instructions on that website to
view public comments.
I. Background
Under the Medicare program, eligible beneficiaries may receive
covered services from an end-stage renal disease (ESRD) facility
provided the facility meets the requirements established by the
Secretary of the Department of Health and Human Services (Secretary).
Section 1881(b) of the Social Security Act (the Act) establishes
distinct requirements for facilities seeking designation as an ESRD
facility under Medicare. Regulations concerning provider agreements and
supplier approval are at 42 CFR part 489 and those pertaining to
activities relating to the survey, certification, and enforcement
procedures of suppliers which include ESRD facilities are at 42 CFR
part 488. The regulations at 42 CFR part 494 subparts A through D
implement section 1881(b) of the Act, which specify the conditions that
an ESRD facility must meet in order to participate in the Medicare
program and the conditions for Medicare payment for ESRD facilities.
Generally, to enter into a Medicare agreement, an ESRD facility
must first be certified by a State survey agency as complying with the
conditions or requirements set forth in part 494 subparts A through D
of our Medicare regulations. Thereafter, the ESRD facility is subject
to regular surveys by a State survey agency to determine whether it
continues to meet these requirements.
Section 1865(a)(1) of the Act provides that, if a provider entity
demonstrates through accreditation by a Centers for Medicare & Medicaid
Services (CMS) approved national accrediting organization (AO) that all
applicable Medicare conditions are met or exceeded, we may deem those
provider entities as having met the requirements. Section 1865(a)(1) of
the Act had historically prohibited dialysis facilities from
participating in Medicare via a CMS-approved accreditation program;
however, section 50403 of the Bipartisan Budget Act of 2018 amended
section 1865(a) of the Act to include renal dialysis facilities as
provider entities allowed to participate in Medicare through a CMS-
approved accreditation program. Accreditation by an AO is voluntary and
is not required for Medicare participation.
If an AO is recognized by the Secretary as having standards for
accreditation that meet or exceed Medicare requirements, any provider
entity accredited by the national accrediting body's approved program
may be deemed to meet the Medicare conditions. An AO applying for
approval of its accreditation program under part 488, subpart A, must
provide CMS with reasonable assurance that the AO requires the
accredited provider entities to meet requirements that are at least as
stringent as the Medicare conditions. Our regulations concerning the
approval of AOs are set forth at Sec. 488.5.
II. Provisions of the Proposed Notice
A. Approval of Deeming Organizations
Section 1865(a)(2) of the Act and our regulations at Sec. 488.5
require that our findings concerning review and approval of an AO's
requirements consider, among other factors, the applying AO's
requirements for accreditation; survey procedures; resources for
conducting required surveys; capacity to furnish information for use in
enforcement activities; monitoring procedures for provider entities
found not in compliance with the conditions or requirements; and
ability to provide CMS with the necessary data for validation.
Section 1865(a)(3)(A) of the Act further requires that we publish,
within 60 days of receipt of an organization's complete application, a
notice identifying the national accrediting body making the request,
describing the nature of the request, and providing at least a 30-day
public comment period. We have 210 days from the receipt of a complete
application to publish notice of approval or denial of the application.
The purpose of this proposed notice is to inform the public of
National Dialysis Accreditation Commission's (NDAC) request for CMS-
approval of its ESRD facility accreditation program. This notice also
solicits public comment on whether NDAC's requirements meet or exceed
the Medicare conditions for coverage (CfCs) for ESRD facilities.
This is the first application from a national accreditation body
seeking approval of an accreditation program for ESRD facilities.
B. Evaluation of Deeming Authority Request
NDAC submitted all the necessary materials to enable us to make a
determination concerning its request for CMS-approval of its ESRD
facility accreditation program. This application was determined to be
complete on June 8, 2018. Under section 1865(a)(2) of the Act and our
regulations at Sec. 488.5, our review and evaluation of NDAC will be
conducted in accordance with, but not necessarily limited to, the
following factors:
The equivalency of NDAC's standards for ESRD facilities as
compared with Medicare's CfCs for ESRD facilities.
NDAC's survey process to determine the following:
++ The composition of the survey team, surveyor qualifications, and
the ability of the organization to provide continuing surveyor
training.
++ The comparability of NDAC's processes to those of State
agencies, including survey frequency, and the ability to investigate
and respond appropriately to complaints against accredited facilities.
++ NDAC's processes and procedures for monitoring an ESRD facility
found out of compliance with NDAC's program requirements. These
monitoring procedures are used only when NDAC identifies noncompliance.
If noncompliance is identified through validation reviews or complaint
surveys, the State survey agency monitors corrections as specified at
Sec. 488.9(c)(1).
++ NDAC's capacity to report deficiencies to the surveyed
facilities and respond to the facility's plan of correction in a timely
manner.
++ NDAC's capacity to provide CMS with electronic data and reports
necessary for effective validation and assessment of the organization's
survey process.
++ The adequacy of NDAC's staff and other resources, and its
financial viability.
++ NDAC's capacity to adequately fund required surveys.
++ NDAC's policies with respect to whether surveys are announced or
unannounced, to assure that surveys are unannounced.
++ NDAC's agreement to provide CMS with a copy of the most current
accreditation survey together with any other information related to the
survey as CMS may require (including corrective action plans).
[[Page 38699]]
III. 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.).
IV. 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 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.
Dated: July 27, 2018.
Seema Verma,
Administrator, Centers for Medicare & Medicaid Services.
[FR Doc. 2018-16871 Filed 8-6-18; 8:45 am]
BILLING CODE 4120-01-P