Medicare Program; Revised Civil Money Penalties, Assessments, Exclusions, and Related Appeals Procedures, 44879-44882 [05-15291]
Download as PDF
Federal Register / Vol. 70, No. 149 / Thursday, August 4, 2005 / Proposed Rules
developing the Copyright Office’s
system for online preregistration, it is
not entirely clear whether the system
will be compatible with web browsers
other than Microsoft Internet Explorer
versions 5.1 and higher. Filers of
preregistration applications will be able
to employ these Internet Explorer
browsers successfully. Support for
Netscape 7.2, Firefox 1.0.3, and Mozilla
1.7.7 is planned but will not be
available when preregistration goes into
effect. Present users of these browsers
may experience problems when filing
claims.
In order to ensure that preregistration
can be implemented in a smoothly
functioning and timely manner, the
Office now seeks comments that will
assist it in determining whether any
eligible parties will be prevented from
preregistering a claim due to browser
requirements of the preregistration
system. Therefore, this notice seeks
information whether any potential
preregistration filers would have
difficulties using Internet Explorer
(version 5.1 or higher) to file
preregistration claims, and if so, why.
More generally, in the interest of
achieving support for browsers in the
Office’s preregistration processing
environment, this notice inquires
whether (and why) an eligible party
who anticipates preregistering a claim
on the electronic–only form will not be
able to use Internet Explorer to do so,
or will choose not to preregister if it is
necessary to use Internet Explorer.
The Office requests that responses to
this supplemental notice of inquiry be
made part of the responders’ comments
on the July 22nd Notice of Proposed
Rulemaking. Whether or not
accompanied by comments on the
proposed rule, the response to this
notice of inquiry should be submitted
by the due dates for comment on the
Notice of Proposed Rulemaking, i.e., no
later than August 22, 2005, with reply
comments due no later than September
7, 2005.
Dated: August 1, 2005.
Tanya Sandros,
Associate General Counsel.
[FR Doc. 05–15458 Filed 8–3–05; 8:45 am]
BILLING CODE 1410–30–S
VerDate jul<14>2003
15:17 Aug 03, 2005
Jkt 205001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Part 402
[CMS–6019–P]
RIN 0938–AN48
Medicare Program; Revised Civil
Money Penalties, Assessments,
Exclusions, and Related Appeals
Procedures
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Proposed rule.
AGENCY:
SUMMARY: This proposed rule sets forth
the general requirements and
procedures that would allow certain
entities who are identified for exclusion
from the Medicare program to request
that CMS act on their behalf to
recommend to the Inspector General
that their exclusion from Medicare be
waived because of a hardship that
would result on Medicare beneficiaries.
This proposed rule would implement
section 949 of the Medicare Prescription
Drug, Improvement, and Modernization
Act of 2003 (MMA).
DATES: To be assured consideration,
comments must be received at the
appropriate address, as provided below,
no later than 5 p.m. on October 3, 2005.
ADDRESSES: In commenting, please refer
to file code CMS–6019–P. Because of
staff and resource limitations, we cannot
accept comments by facsimile (FAX)
transmission.
You may submit comments in one of
three ways (no duplicates, please):
1. Electronically. You may submit
electronic comments on specific issues
in this regulation to https://
www.cms.hhs.gov/regulations/
ecomments. (Attachments should be in
Microsoft Word, WordPerfect, or Excel;
however, we prefer Microsoft Word.)
2. By mail. You may mail written
comments (one original and two copies)
to the following address ONLY: Centers
for Medicare & Medicaid Services,
Department of Health and Human
Services, Attention: CMS–6019–P, 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 hand or courier. If you prefer,
you may deliver (by hand or courier)
your written comments (one original
and two copies) before the close of the
comment period to one of the following
addresses. If you intend to deliver your
comments to the Baltimore address,
PO 00000
Frm 00012
Fmt 4702
Sfmt 4702
44879
please call telephone number (410) 786–
9994 in advance to schedule your
arrival with one of our staff members.
Room 445–G, Hubert H. Humphrey
Building, 200 Independence Avenue,
SW., Washington, DC 20201; or 7500
Security Boulevard, Baltimore, MD
21244–1850.
Because access to the interior of the
HHH Building is not readily available to
persons without Federal government
identification, commenters are
encouraged to leave their comments in
the CMS drop slots located in the main
lobby of the building. A stamp-in clock
is available for persons wishing to retain
a proof of filing by stamp in and
retaining an extra copy of the comments
being filed.
Comments mailed to the addresses
indicated as appropriate for hand or
courier delivery may be delayed and
could be considered late.
For information on viewing public
comments, see the beginning of the
SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT: Joel
Cohen, (410) 786–3349.
SUPPLEMENTARY INFORMATION:
Submitting Comments: We welcome
comments from the public on all issues
set forth in this rule to assist us in fully
considering issues and developing
policies. You can assist us by
referencing the file code CMS–6019–P
and the specific ‘‘issue identifier’’ that
precedes the section on which you
choose to comment.
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. CMS posts all electronic
comments received before the close of
the comment period on its public
website as soon as possible after they
have been received. Hardcopy
comments received timely will be
available for public inspection as they
are received, generally beginning
approximately 3 weeks after publication
of a document, at the headquarters of
the Centers for Medicare & Medicaid
Services, 7500 Security Boulevard,
Baltimore, Maryland 21244, Monday
through Friday of each week from 8:30
a.m. to 4 p.m. To schedule an
appointment to view public comments,
phone 1–800–743–3951.
This Federal Register document is
also available from the Federal Register
online database through GPO Access, a
service of the U.S. Government Printing
Office. The Web site address is: https://
www.gpoaccess.gov/fr/.
E:\FR\FM\04AUP1.SGM
04AUP1
44880
Federal Register / Vol. 70, No. 149 / Thursday, August 4, 2005 / Proposed Rules
I. Background
[If you choose to comment on issues in this
section, please include the caption
‘‘BACKGROUND’’ at the beginning of your
comments.]
Section 1128A of the Social Security
Act (the Act) authorizes the Secretary of
Health and Human Services to impose
civil money penalties (CMPs),
assessments, and/or exclusion from the
Medicare program for certain health
care facilities, practitioners, suppliers or
other entities under prescribed
circumstances. Exclusion, as defined in
42 CFR 402.3, provides the ultimate
enforcement tool for agencies
attempting to establish compliance with
legal and program standards, and is
used in addition to potential civil,
criminal, and/or administrative
proceedings.
The Congress has significantly
increased both the number and types of
circumstances under which the
Secretary may impose an exclusion of a
provider or an entity from the Medicare
and State health care programs. The
Secretary has delegated the authority for
these provisions to either the Office of
the Inspector General (OIG) or the
Centers for Medicare & Medicaid
Services (CMS). The exclusion
authorities delegated to the OIG address
fraud, misrepresentation, or
falsification, while those delegated to us
address noncompliance with
programmatic or regulatory
requirements. However, the OIG has the
authority to impose an exclusion and to
prosecute cases involving exclusions
that were delegated to us, if CMS and
the OIG jointly determine it to be in the
interest of economy, efficiency, or
effective coordination of activities. The
determination may be made either on a
case-by-case basis, or for all cases
brought under a particular listed
authority.
On December 14, 1998, we published
a final rule (63 FR 68687) delineating
the procedures for pursuing CMPs and
assessments. That final rule added a
new part 402 to title 42, chapter IV of
the Code of Federal Regulations (CFR) to
incorporate our CMP and assessment
authorities. We did not address
exclusions in that final rule, but we did
reserve subpart C to incorporate this
information in the future.
In the December 14, 1998 final rule,
we indicated that our procedures for
imposing the CMPs and assessment
authorities delegated to us were based
on the procedures that the OIG
delineated in 42 CFR part 1003. We also
made the OIG’s hearing and appeal
procedures set forth in 42 CFR part 1005
VerDate jul<14>2003
15:17 Aug 03, 2005
Jkt 205001
effective for the CMP, assessment, and
exclusion authorities delegated to CMS.
On July 23, 2004, we published a
proposed rule in the Federal Register
(69 FR 43956), delineating the
procedures for pursuing exclusions. It is
our intent to respond to the public
comments we received from the July 3,
2004 proposed rule and this rule in a
single final rule.
Section 949 of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA) (Pub.
L. 108–173) amended section
1128(c)(3)(B) of the Act to indicate that,
‘‘Subject to subparagraph (g), in the case
of an exclusion under subsection (a), the
minimum period of exclusion shall not
be less than 5 years, except that, upon
the request of the administrator of a
Federal health care program (as defined
in section 1128B(f)) who determines
that the exclusion would impose a
hardship on individuals entitled to
benefits under Part A of title XVIII or
enrolled under Part B of such title, or
both, the Secretary may, after consulting
with the Inspector General of the
Department of Health and Human
Services, waive the exclusion under
subsection (a)(1), (a)(3), or (a)(4) with
respect to that program in the case of an
individual or entity that is the sole
community physician or sole source of
essential specialized services in the
community.’’ The Conference
Agreement accompanying the MMA
clarifies the intent of the statutory
requirement that a hardship
determination be made before a waiver
is approved.
II. Provisions of the Proposed Rule
[If you choose to comment on issues in this
section, please include the caption
‘‘PROVISIONS OF THE PROPOSED RULE’’
at the beginning of your comments.]
This proposed rule would amend part
402, by adding to subpart C, a new
section that establishes the general
requirements and procedures
concerning our authority to request a
waiver of exclusion, for an excluded
person, from Medicare exclusions that
are imposed by the OIG.
Specifically, we are proposing to add
the following provision to subpart C:
• Section 402.308, Waivers of
Exclusions.
This section provides the basis and
purpose for the excluded person to
make a request to us. This subpart also
sets forth the requirements that must be
met by the excluded person in order for
us to make a request to the OIG of a
waiver to the exclusion. The statute
specifies the basis upon which a request
of waiver for an exclusion must be
based, but provides few details
PO 00000
Frm 00013
Fmt 4702
Sfmt 4702
regarding the administrative decisionmaking process.
We will consider any supportive
information submitted by the
respondent. We will not limit nor
suggest what type of information may be
presented. However, while the burden
to present convincing information is left
to the discretion of the respondent, we
will initiate our own validation of the
facts presented. During this analysis, we
may require the person to furnish
additional, specific information, and
authorization to obtain information from
private health insurers, peer review
organizations (including, but not limited
to, Quality Improvement Organizations),
and others as necessary to determine the
validity of the facts provided.
It is our interpretation that unless a
hardship (defined for purposes of
§ 402.308 as something that negatively
affects Medicare beneficiaries and
results from the imposition of an
exclusion, because the excluded person
is the sole community physician or sole
source of essential specialized services
in the Medicare community) is met, no
requests for a waiver of Medicare
exclusion will be considered or
forwarded to the OIG by CMS. Our
decision is not subject to administrative
or judicial review. Furthermore, a
request made by CMS to the OIG does
not automatically grant a waiver. The
final decision is that of the OIG as
defined in § 1001.1801 of the OIG’s
regulations.
III. Collection of Information
Requirements
The collection of information
requirements at 5 CFR part 1320 are
applicable to requirements affecting 10
or more entities. While this proposed
rule contains information collection
requirements, because we believe that
these requirements will affect less than
10 entities, we believe that these
collection requirements are exempt from
OMB for review and approval, as
specified at 5 CFR 1320.3(c)(4).
Consequently, this proposed rule need
not be reviewed by the Office of
Management and Budget under the
authority of the Paperwork Reduction
Act of 1995.
IV. Response to Comments
Because of the large number of items
of correspondence we normally receive
on Federal Register documents
published for comment, 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, if we proceed with
a subsequent document, we will
E:\FR\FM\04AUP1.SGM
04AUP1
Federal Register / Vol. 70, No. 149 / Thursday, August 4, 2005 / Proposed Rules
respond to the major comments in the
preamble to that document.
V. Regulatory Impact Statement
We have examined the impacts of this
proposed rule as required by Executive
Order 12866 (September 1993,
Regulatory Planning and Review), the
Regulatory Flexibility Act (RFA)
(September 19, 1980, Pub. L. 96–354),
Executive Order 13132 (August 4, 1999,
Federalism), and the Unfunded
Mandates Reform Act of 1995 (2 U.S.C.
1532).
Executive Order 12866 directs
agencies taking ‘‘significant regulatory
action’’ to reflect consideration of all
costs and benefits of available regulatory
alternatives and, if regulation is
necessary, to select regulatory
approaches that maximize net benefits
(including potential economic,
environmental, public health and safety
effects, distributive impacts, and
equity). A regulatory impact analysis
(RIA) must be prepared for major rules
with economically significant effects
($100 million or more in any 1 year).
This proposed rule is not a significant
regulatory action as defined by section
3(f) of Executive Order 12866. We
believe that there are no significant
costs associated with this proposed rule
that would impose any mandates on
State, local or tribal governments, or the
private sector that would result in an
expenditure of $100 million in any
given year. Since most program
participants comply with the statutory
and regulatory requirements making
unnecessary the imposition of an
exclusion from Medicare, Medicaid and,
where applicable, other Federal health
care programs, we do not anticipate
more than a de minimis economic
impact as a result of this proposed rule.
Further, any impact that may occur
would only affect those limited few
individuals or entities that engage in
prohibited behavior. We do not
anticipate any savings or costs as a
result of this proposed rule.
The RFA (15 U.S.C. 603(a)), as
modified by the Small Business
Regulatory Enforcement Fairness Act of
1996 (SBREFA) (Pub. L. 104–121),
requires agencies to determine whether
the proposed rule would have a
significant economic impact on a
substantial number of small entities
and, if so, to identify in the notice of
proposed rulemaking any regulatory
options that could mitigate the impact
of the proposed regulation on small
businesses. For purposes of the RFA,
small entities include small businesses,
nonprofit organizations, and small
government jurisdictions. Most
hospitals and most other providers and
VerDate jul<14>2003
15:17 Aug 03, 2005
Jkt 205001
suppliers are small entities, either by
nonprofit status or by having revenues
of $26 million or less annually.
Individuals and States are not included
in the definition of a small entity. We
believe that any impact as a result of the
proposed rule would be minimal, since,
as mentioned above, the only
individuals or entities affected would be
those limited few who have engaged in
prohibited conduct and were excluded
from the Medicare program by the OIG.
Since the vast majority of program
participants comply with statutory and
regulatory requirements and are not
excluded from the Medicare program,
any aggregate economic impact would
not be significant.
In addition, section 1102(b) of the Act
requires us to prepare a regulatory
impact analysis if a rule may have a
significant impact on the operations of
a substantial number of small rural
hospitals. This analysis must conform to
the provisions of section 603 of the
RFA. For purposes of section 1102(b) of
the Act, we define a small rural hospital
as a hospital that is located outside of
a Metropolitan Statistical Area and has
fewer than 100 beds. We do not believe
a regulatory impact analysis is required
here because, for the reasons stated
above concerning our obligations under
the RFA and SBREFA, this proposed
rule would not have a significant impact
on the operations of a substantial
number of small rural hospitals.
Section 202 of the Unfunded
Mandates Reform Act of 1995 also
requires that agencies assess anticipated
costs and benefits before issuing any
rule that may result in expenditure in
any 1 year by State, local, or tribal
governments, in the aggregate, or by the
private sector, of $110 million. We
believe that there are no significant
costs associated with this technical rule
that would impose any mandates on
State, local, or tribal governments, or the
private sector that would result in an
expenditure of $110 million in any
given year.
As was previously mentioned, since
the majority of program participants
comply with statutory and regulatory
requirements and are not excluded from
the Medicare program, any aggregate
economic impact would not be
significant.
Executive Order 13132 establishes
certain requirements that an agency
must meet when it publishes a proposed
rule (and subsequent final rule) that
imposes substantial direct requirement
costs on State and local governments,
preempts State law, or otherwise has
Federalism implications. We have
determined that this proposed rule
would not significantly affect the rights,
PO 00000
Frm 00014
Fmt 4702
Sfmt 4702
44881
roles, or responsibilities of the States.
This rule would not impose substantial
direct requirement costs on State or
local governments, preempt State law,
or otherwise implicate Federalism.
In accordance with the provisions of
Executive Order 12866, the Office of
Management and Budget reviewed this
regulation.
List of Subjects in 42 CFR Part 402
Administrative practice and
procedure, Health facilities, Health
professions, Medicaid, Medicare,
Penalties.
For the reasons stated in the
preamble, the Centers for Medicare &
Medicaid Services proposes to amend
42 CFR chapter IV as set forth below:
PART 402—CIVIL MONEY PENALTIES,
ASSESSMENTS, AND EXCLUSIONS
Subpart C—Exclusions
1. The authority citation for part 402
continues to read as follows:
Authority: Secs. 1102 and 1871 of the
Social Security Act (42 U.S.C. 1302 and
1395hh).
2. Part 402, subpart C is amended by
adding § 402.308 to read as follows:
§ 402.308
Waivers of exclusions.
(a) Basis. Section 1128(c)(3)(B) of the
Act specifies that in the case of an
exclusion from participation in the
Medicare program based upon section
1128(a)(1), (a)(3), or (a)(4) of the Act, the
individual may request that CMS
present, on his or her behalf, a request
to the OIG for a waiver of the exclusion.
(b) Definition. For purposes of this
part:
(1) Excluded person has the same
meaning as a ‘‘person’’ as defined in
§ 402.3 who meets for the purposes of
this subpart, the definition of the term
‘‘exclusion’’ in § 402.3.
(2) Hardship for purposes of this
section means something that negatively
affects Medicare beneficiaries and
results from the imposition of an
exclusion, because the excluded person
is the sole community physician or sole
source of essential specialized services
in the Medicare community.
(c) General rule. If CMS determines
that a hardship as defined in paragraph
(b)(2) of this section results from
exclusion of an affected person from the
Medicare program, CMS may consider
and may make a recommendation to the
Inspector General for waiver of the
Medicare exclusion.
(d) Submission and content of a
waiver of exclusion request. An
excluded person must submit a request
for waiver of exclusion in writing to
CMS that includes the following:
E:\FR\FM\04AUP1.SGM
04AUP1
44882
Federal Register / Vol. 70, No. 149 / Thursday, August 4, 2005 / Proposed Rules
(1) A copy of the exclusion notice
from the OIG.
(2) A statement requesting that CMS
present a waiver of exclusion request to
the OIG on his or her behalf.
(3) A statement that he or she is the
sole community physician or sole
source of essential specialized services
in the community.
(4) Documentation to support the
statement in paragraph (d)(3) of this
section.
(e) Processing of waiver of exclusion
requests. CMS processes a request for a
waiver of exclusion as follows:
(1) Notifies the submitter that the
waiver of exclusion request has been
received.
(2) Reviews and validates all
submitted documents.
VerDate jul<14>2003
15:17 Aug 03, 2005
Jkt 205001
(3) During its analysis, CMS may
require additional, specific information,
and authorization to obtain information
from private health insurers, peer
review organizations (including, but not
limited to, Quality Improvement
Organizations), and others as necessary
to determine validity.
(4) Makes a determination regarding
whether or not to submit the waiver of
exclusion request to the OIG based on
review and validation of the submitted
documents.
(5) If CMS elects to submit the waiver
of exclusion request to the OIG, CMS
copies the excluded person on the
request.
(6) If CMS denies the request, then
CMS notifies the excluded person of the
decision and specifies the reason(s) for
the decision.
PO 00000
Frm 00015
Fmt 4702
Sfmt 4702
(f) Administrative or judicial review.
A determination rendered under
paragraph (e)(3) of this section is not
subject to administrative or judicial
review.
(Catalog of Federal Domestic Assistance
Program No. 93.773, Medicare—Hospital
Insurance; and Program No. 93.774,
Medicare—Supplementary Medical
Insurance Program)
Dated: April 8, 2005.
Mark B. McClellan,
Administrator, Centers for Medicare &
Medicaid Services.
Dated: April 15, 2005.
Michael O. Leavitt,
Secretary.
[FR Doc. 05–15291 Filed 8–3–05; 8:45 am]
BILLING CODE 4120–01–P
E:\FR\FM\04AUP1.SGM
04AUP1
Agencies
[Federal Register Volume 70, Number 149 (Thursday, August 4, 2005)]
[Proposed Rules]
[Pages 44879-44882]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-15291]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
42 CFR Part 402
[CMS-6019-P]
RIN 0938-AN48
Medicare Program; Revised Civil Money Penalties, Assessments,
Exclusions, and Related Appeals Procedures
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: This proposed rule sets forth the general requirements and
procedures that would allow certain entities who are identified for
exclusion from the Medicare program to request that CMS act on their
behalf to recommend to the Inspector General that their exclusion from
Medicare be waived because of a hardship that would result on Medicare
beneficiaries. This proposed rule would implement section 949 of the
Medicare Prescription Drug, Improvement, and Modernization Act of 2003
(MMA).
DATES: To be assured consideration, comments must be received at the
appropriate address, as provided below, no later than 5 p.m. on October
3, 2005.
ADDRESSES: In commenting, please refer to file code CMS-6019-P. Because
of staff and resource limitations, we cannot accept comments by
facsimile (FAX) transmission.
You may submit comments in one of three ways (no duplicates,
please):
1. Electronically. You may submit electronic comments on specific
issues in this regulation to https://www.cms.hhs.gov/regulations/
ecomments. (Attachments should be in Microsoft Word, WordPerfect, or
Excel; however, we prefer Microsoft Word.)
2. By mail. You may mail written comments (one original and two
copies) to the following address ONLY: Centers for Medicare & Medicaid
Services, Department of Health and Human Services, Attention: CMS-6019-
P, 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 hand or courier. If you prefer, you may deliver (by hand or
courier) your written comments (one original and two copies) before the
close of the comment period to one of the following addresses. If you
intend to deliver your comments to the Baltimore address, please call
telephone number (410) 786-9994 in advance to schedule your arrival
with one of our staff members. Room 445-G, Hubert H. Humphrey Building,
200 Independence Avenue, SW., Washington, DC 20201; or 7500 Security
Boulevard, Baltimore, MD 21244-1850.
Because access to the interior of the HHH Building is not readily
available to persons without Federal government identification,
commenters are encouraged to leave their comments in the CMS drop slots
located in the main lobby of the building. A stamp-in clock is
available for persons wishing to retain a proof of filing by stamp in
and retaining an extra copy of the comments being filed.
Comments mailed to the addresses indicated as appropriate for hand
or courier delivery may be delayed and could be considered late.
For information on viewing public comments, see the beginning of
the SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT: Joel Cohen, (410) 786-3349.
SUPPLEMENTARY INFORMATION:
Submitting Comments: We welcome comments from the public on all
issues set forth in this rule to assist us in fully considering issues
and developing policies. You can assist us by referencing the file code
CMS-6019-P and the specific ``issue identifier'' that precedes the
section on which you choose to comment.
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. CMS posts all electronic
comments received before the close of the comment period on its public
website as soon as possible after they have been received. Hardcopy
comments received timely will be available for public inspection as
they are received, generally beginning approximately 3 weeks after
publication of a document, at the headquarters of the Centers for
Medicare & Medicaid Services, 7500 Security Boulevard, Baltimore,
Maryland 21244, Monday through Friday of each week from 8:30 a.m. to 4
p.m. To schedule an appointment to view public comments, phone 1-800-
743-3951.
This Federal Register document is also available from the Federal
Register online database through GPO Access, a service of the U.S.
Government Printing Office. The Web site address is: https://
www.gpoaccess.gov/fr/.
[[Page 44880]]
I. Background
[If you choose to comment on issues in this section, please include
the caption ``BACKGROUND'' at the beginning of your comments.]
Section 1128A of the Social Security Act (the Act) authorizes the
Secretary of Health and Human Services to impose civil money penalties
(CMPs), assessments, and/or exclusion from the Medicare program for
certain health care facilities, practitioners, suppliers or other
entities under prescribed circumstances. Exclusion, as defined in 42
CFR 402.3, provides the ultimate enforcement tool for agencies
attempting to establish compliance with legal and program standards,
and is used in addition to potential civil, criminal, and/or
administrative proceedings.
The Congress has significantly increased both the number and types
of circumstances under which the Secretary may impose an exclusion of a
provider or an entity from the Medicare and State health care programs.
The Secretary has delegated the authority for these provisions to
either the Office of the Inspector General (OIG) or the Centers for
Medicare & Medicaid Services (CMS). The exclusion authorities delegated
to the OIG address fraud, misrepresentation, or falsification, while
those delegated to us address noncompliance with programmatic or
regulatory requirements. However, the OIG has the authority to impose
an exclusion and to prosecute cases involving exclusions that were
delegated to us, if CMS and the OIG jointly determine it to be in the
interest of economy, efficiency, or effective coordination of
activities. The determination may be made either on a case-by-case
basis, or for all cases brought under a particular listed authority.
On December 14, 1998, we published a final rule (63 FR 68687)
delineating the procedures for pursuing CMPs and assessments. That
final rule added a new part 402 to title 42, chapter IV of the Code of
Federal Regulations (CFR) to incorporate our CMP and assessment
authorities. We did not address exclusions in that final rule, but we
did reserve subpart C to incorporate this information in the future.
In the December 14, 1998 final rule, we indicated that our
procedures for imposing the CMPs and assessment authorities delegated
to us were based on the procedures that the OIG delineated in 42 CFR
part 1003. We also made the OIG's hearing and appeal procedures set
forth in 42 CFR part 1005 effective for the CMP, assessment, and
exclusion authorities delegated to CMS.
On July 23, 2004, we published a proposed rule in the Federal
Register (69 FR 43956), delineating the procedures for pursuing
exclusions. It is our intent to respond to the public comments we
received from the July 3, 2004 proposed rule and this rule in a single
final rule.
Section 949 of the Medicare Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA) (Pub. L. 108-173) amended section
1128(c)(3)(B) of the Act to indicate that, ``Subject to subparagraph
(g), in the case of an exclusion under subsection (a), the minimum
period of exclusion shall not be less than 5 years, except that, upon
the request of the administrator of a Federal health care program (as
defined in section 1128B(f)) who determines that the exclusion would
impose a hardship on individuals entitled to benefits under Part A of
title XVIII or enrolled under Part B of such title, or both, the
Secretary may, after consulting with the Inspector General of the
Department of Health and Human Services, waive the exclusion under
subsection (a)(1), (a)(3), or (a)(4) with respect to that program in
the case of an individual or entity that is the sole community
physician or sole source of essential specialized services in the
community.'' The Conference Agreement accompanying the MMA clarifies
the intent of the statutory requirement that a hardship determination
be made before a waiver is approved.
II. Provisions of the Proposed Rule
[If you choose to comment on issues in this section, please
include the caption ``PROVISIONS OF THE PROPOSED RULE'' at the
beginning of your comments.]
This proposed rule would amend part 402, by adding to subpart C, a
new section that establishes the general requirements and procedures
concerning our authority to request a waiver of exclusion, for an
excluded person, from Medicare exclusions that are imposed by the OIG.
Specifically, we are proposing to add the following provision to
subpart C:
Section 402.308, Waivers of Exclusions.
This section provides the basis and purpose for the excluded person
to make a request to us. This subpart also sets forth the requirements
that must be met by the excluded person in order for us to make a
request to the OIG of a waiver to the exclusion. The statute specifies
the basis upon which a request of waiver for an exclusion must be
based, but provides few details regarding the administrative decision-
making process.
We will consider any supportive information submitted by the
respondent. We will not limit nor suggest what type of information may
be presented. However, while the burden to present convincing
information is left to the discretion of the respondent, we will
initiate our own validation of the facts presented. During this
analysis, we may require the person to furnish additional, specific
information, and authorization to obtain information from private
health insurers, peer review organizations (including, but not limited
to, Quality Improvement Organizations), and others as necessary to
determine the validity of the facts provided.
It is our interpretation that unless a hardship (defined for
purposes of Sec. 402.308 as something that negatively affects Medicare
beneficiaries and results from the imposition of an exclusion, because
the excluded person is the sole community physician or sole source of
essential specialized services in the Medicare community) is met, no
requests for a waiver of Medicare exclusion will be considered or
forwarded to the OIG by CMS. Our decision is not subject to
administrative or judicial review. Furthermore, a request made by CMS
to the OIG does not automatically grant a waiver. The final decision is
that of the OIG as defined in Sec. 1001.1801 of the OIG's regulations.
III. Collection of Information Requirements
The collection of information requirements at 5 CFR part 1320 are
applicable to requirements affecting 10 or more entities. While this
proposed rule contains information collection requirements, because we
believe that these requirements will affect less than 10 entities, we
believe that these collection requirements are exempt from OMB for
review and approval, as specified at 5 CFR 1320.3(c)(4). Consequently,
this proposed rule need not be reviewed by the Office of Management and
Budget under the authority of the Paperwork Reduction Act of 1995.
IV. Response to Comments
Because of the large number of items of correspondence we normally
receive on Federal Register documents published for comment, 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, if we proceed with a subsequent
document, we will
[[Page 44881]]
respond to the major comments in the preamble to that document.
V. Regulatory Impact Statement
We have examined the impacts of this proposed rule as required by
Executive Order 12866 (September 1993, Regulatory Planning and Review),
the Regulatory Flexibility Act (RFA) (September 19, 1980, Pub. L. 96-
354), Executive Order 13132 (August 4, 1999, Federalism), and the
Unfunded Mandates Reform Act of 1995 (2 U.S.C. 1532).
Executive Order 12866 directs agencies taking ``significant
regulatory action'' to reflect consideration of all costs and benefits
of available regulatory alternatives and, if regulation is necessary,
to select regulatory approaches that maximize net benefits (including
potential economic, environmental, public health and safety effects,
distributive impacts, and equity). A regulatory impact analysis (RIA)
must be prepared for major rules with economically significant effects
($100 million or more in any 1 year). This proposed rule is not a
significant regulatory action as defined by section 3(f) of Executive
Order 12866. We believe that there are no significant costs associated
with this proposed rule that would impose any mandates on State, local
or tribal governments, or the private sector that would result in an
expenditure of $100 million in any given year. Since most program
participants comply with the statutory and regulatory requirements
making unnecessary the imposition of an exclusion from Medicare,
Medicaid and, where applicable, other Federal health care programs, we
do not anticipate more than a de minimis economic impact as a result of
this proposed rule. Further, any impact that may occur would only
affect those limited few individuals or entities that engage in
prohibited behavior. We do not anticipate any savings or costs as a
result of this proposed rule.
The RFA (15 U.S.C. 603(a)), as modified by the Small Business
Regulatory Enforcement Fairness Act of 1996 (SBREFA) (Pub. L. 104-121),
requires agencies to determine whether the proposed rule would have a
significant economic impact on a substantial number of small entities
and, if so, to identify in the notice of proposed rulemaking any
regulatory options that could mitigate the impact of the proposed
regulation on small businesses. For purposes of the RFA, small entities
include small businesses, nonprofit organizations, and small government
jurisdictions. Most hospitals and most other providers and suppliers
are small entities, either by nonprofit status or by having revenues of
$26 million or less annually. Individuals and States are not included
in the definition of a small entity. We believe that any impact as a
result of the proposed rule would be minimal, since, as mentioned
above, the only individuals or entities affected would be those limited
few who have engaged in prohibited conduct and were excluded from the
Medicare program by the OIG. Since the vast majority of program
participants comply with statutory and regulatory requirements and are
not excluded from the Medicare program, any aggregate economic impact
would not be significant.
In addition, section 1102(b) of the Act requires us to prepare a
regulatory impact analysis if a rule may have a significant impact on
the operations of a substantial number of small rural hospitals. This
analysis must conform to the provisions of section 603 of the RFA. For
purposes of section 1102(b) of the Act, we define a small rural
hospital as a hospital that is located outside of a Metropolitan
Statistical Area and has fewer than 100 beds. We do not believe a
regulatory impact analysis is required here because, for the reasons
stated above concerning our obligations under the RFA and SBREFA, this
proposed rule would not have a significant impact on the operations of
a substantial number of small rural hospitals.
Section 202 of the Unfunded Mandates Reform Act of 1995 also
requires that agencies assess anticipated costs and benefits before
issuing any rule that may result in expenditure in any 1 year by State,
local, or tribal governments, in the aggregate, or by the private
sector, of $110 million. We believe that there are no significant costs
associated with this technical rule that would impose any mandates on
State, local, or tribal governments, or the private sector that would
result in an expenditure of $110 million in any given year.
As was previously mentioned, since the majority of program
participants comply with statutory and regulatory requirements and are
not excluded from the Medicare program, any aggregate economic impact
would not be significant.
Executive Order 13132 establishes certain requirements that an
agency must meet when it publishes a proposed rule (and subsequent
final rule) that imposes substantial direct requirement costs on State
and local governments, preempts State law, or otherwise has Federalism
implications. We have determined that this proposed rule would not
significantly affect the rights, roles, or responsibilities of the
States. This rule would not impose substantial direct requirement costs
on State or local governments, preempt State law, or otherwise
implicate Federalism.
In accordance with the provisions of Executive Order 12866, the
Office of Management and Budget reviewed this regulation.
List of Subjects in 42 CFR Part 402
Administrative practice and procedure, Health facilities, Health
professions, Medicaid, Medicare, Penalties.
For the reasons stated in the preamble, the Centers for Medicare &
Medicaid Services proposes to amend 42 CFR chapter IV as set forth
below:
PART 402--CIVIL MONEY PENALTIES, ASSESSMENTS, AND EXCLUSIONS
Subpart C--Exclusions
1. The authority citation for part 402 continues to read as
follows:
Authority: Secs. 1102 and 1871 of the Social Security Act (42
U.S.C. 1302 and 1395hh).
2. Part 402, subpart C is amended by adding Sec. 402.308 to read
as follows:
Sec. 402.308 Waivers of exclusions.
(a) Basis. Section 1128(c)(3)(B) of the Act specifies that in the
case of an exclusion from participation in the Medicare program based
upon section 1128(a)(1), (a)(3), or (a)(4) of the Act, the individual
may request that CMS present, on his or her behalf, a request to the
OIG for a waiver of the exclusion.
(b) Definition. For purposes of this part:
(1) Excluded person has the same meaning as a ``person'' as defined
in Sec. 402.3 who meets for the purposes of this subpart, the
definition of the term ``exclusion'' in Sec. 402.3.
(2) Hardship for purposes of this section means something that
negatively affects Medicare beneficiaries and results from the
imposition of an exclusion, because the excluded person is the sole
community physician or sole source of essential specialized services in
the Medicare community.
(c) General rule. If CMS determines that a hardship as defined in
paragraph (b)(2) of this section results from exclusion of an affected
person from the Medicare program, CMS may consider and may make a
recommendation to the Inspector General for waiver of the Medicare
exclusion.
(d) Submission and content of a waiver of exclusion request. An
excluded person must submit a request for waiver of exclusion in
writing to CMS that includes the following:
[[Page 44882]]
(1) A copy of the exclusion notice from the OIG.
(2) A statement requesting that CMS present a waiver of exclusion
request to the OIG on his or her behalf.
(3) A statement that he or she is the sole community physician or
sole source of essential specialized services in the community.
(4) Documentation to support the statement in paragraph (d)(3) of
this section.
(e) Processing of waiver of exclusion requests. CMS processes a
request for a waiver of exclusion as follows:
(1) Notifies the submitter that the waiver of exclusion request has
been received.
(2) Reviews and validates all submitted documents.
(3) During its analysis, CMS may require additional, specific
information, and authorization to obtain information from private
health insurers, peer review organizations (including, but not limited
to, Quality Improvement Organizations), and others as necessary to
determine validity.
(4) Makes a determination regarding whether or not to submit the
waiver of exclusion request to the OIG based on review and validation
of the submitted documents.
(5) If CMS elects to submit the waiver of exclusion request to the
OIG, CMS copies the excluded person on the request.
(6) If CMS denies the request, then CMS notifies the excluded
person of the decision and specifies the reason(s) for the decision.
(f) Administrative or judicial review. A determination rendered
under paragraph (e)(3) of this section is not subject to administrative
or judicial review.
(Catalog of Federal Domestic Assistance Program No. 93.773,
Medicare--Hospital Insurance; and Program No. 93.774, Medicare--
Supplementary Medical Insurance Program)
Dated: April 8, 2005.
Mark B. McClellan,
Administrator, Centers for Medicare & Medicaid Services.
Dated: April 15, 2005.
Michael O. Leavitt,
Secretary.
[FR Doc. 05-15291 Filed 8-3-05; 8:45 am]
BILLING CODE 4120-01-P