Medicare, Medicaid, and Children's Health Insurance Programs; Provider Enrollment Application Fee Amount for 2011, 16422-16424 [2011-6813]
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jlentini on DSKJ8SOYB1PROD with NOTICES
16422
Federal Register / Vol. 76, No. 56 / Wednesday, March 23, 2011 / Notices
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VerDate Mar<15>2010
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Jkt 223001
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Sandra L. Kusumoto,
Director, Bureau of Certification and
Licensing.
[FR Doc. 2011–6865 Filed 3–22–11; 8:45 am]
BILLING CODE 6730–01–P
PO 00000
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–6029–N]
RIN 0938–AQ99
Medicare, Medicaid, and Children’s
Health Insurance Programs; Provider
Enrollment Application Fee Amount for
2011
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:
This notice announces the
$505 calendar year (CY) 2011
application fee for institutional
providers that are: Initially enrolling in
the Medicare, program; revalidating
their Medicare enrollment; or adding a
new Medicare practice location. These
institutional providers and suppliers are
required to submit the 2011 fee amount
with any enrollment applications
submitted on or after March 25, 2011
and on or before December 31, 2011.
Similarly, beginning March 25, 2011
prospective or re-enrolling Medicaid or
CHIP providers must submit the
applicable application fee unless:
(1) The provider is an individual
physician or nonphysician practitioner;
or (2) the provider is enrolled in Title
XVIII of the Act or another State’s title
XIX or XXI plan and has paid the
application fee to a Medicare contractor
or another State.
DATES: Effective Date: This notice is
effective on March 23, 2011.
FOR FURTHER INFORMATION CONTACT:
Frank Whelan, (410) 786–1302 for
Medicare enrollment issues. Claudia
Simonson, (312) 353–2115 for Medicaid
and CHIP enrollment issues.
SUPPLEMENTARY INFORMATION:
SUMMARY:
I. Background
In the February 2, 2011 Federal
Register (76 FR 5862) we published a
final rule with comment period entitled:
‘‘Medicare, Medicaid, and Children’s
Health Insurance Programs; Additional
Screening Requirements, Application
Fees, Temporary Enrollment Moratoria,
Payment Suspensions and Compliance
Plans for Providers and Suppliers’’. This
final rule with comment finalized,
among other things, provisions related
to the submission of application fees as
part of the Medicare, Medicaid and
Children’s Health Insurance Program
(CHIP) provider enrollment processes.
Specifically, and as stated in 42 CFR
424.514, institutional providers and
suppliers that are: Initially enrolling in
E:\FR\FM\23MRN1.SGM
23MRN1
Federal Register / Vol. 76, No. 56 / Wednesday, March 23, 2011 / Notices
the Medicare program; revalidating their
Medicare enrollment; or adding a new
Medicare practice location, will be
required to submit an application fee
beginning March 25, 2011 with any
enrollment application. We will adjust
the amount of the fee annually for
inflation. Institutional providers are
defined at § 424.502 as—
reminded that they can submit a
hardship exception request in the event
they believe that it is appropriate;
additional information on the hardship
exception is available in the February 2,
2011 final rule with comment period.
The application fee for calendar year
2012 will be published in the Federal
Register later this year.
Any provider or supplier that submits a
paper Medicare enrollment application using
the CMS–855A, CMS–855B (not including
physician and non-physician practitioner
organizations), CMS–855S or associated
Internet-based PECOS enrollment
application.
III. Collection of Information
Requirements
This document does not impose
information collection and
recordkeeping requirements.
Consequently, it need not be reviewed
by the Office of Management and
Budget under the authority of the
Paperwork Reduction Act of 1995
(44 U.S.C. chapter 35). However, it does
reference previously approved
information collections. As stated in
Section I of this notice, the forms CMS–
855(A and B) and the CMS–855(S) are
approved under OMB control numbers
0938–0685 and 0938–1057.
jlentini on DSKJ8SOYB1PROD with NOTICES
Similarly, as stated in 42 CFR 455.460,
beginning March 25, 2011 prospective
or re-enrolling Medicaid or CHIP
providers must submit the applicable
application fee unless: (1) The provider
is an individual physician or
nonphysician practitioner; or (2) the
provider is enrolled in Title XVIII of the
Act or another State’s title XIX or XXI
plan and has paid the application fee to
a Medicare contractor or another State.
The February 2, 2011 final rule with
comment period contains additional
information about the entities that must
submit an application fee, the purpose
of the fee, and the process of obtaining
a hardship exception or a waiver for
Medicaid providers.
II. Provisions of the Notice
The application fee amount for the
period on or after March 25, 2011 and
on or before December 31, 2011 will be
$505. This figure was calculated in
accordance with the following:
• Section 1866(j)(2)(C)(i)(I) of the
Social Security Act (the Act) established
a $500 application fee for providers and
suppliers in calendar year (CY) 2010.
• In 42 CFR 424.514(d)(2) of our
regulations, and consistent with
section1866(j)(2)(C)(i)(II) of the Act, we
stated that for CY 2011 and for
subsequent years, the fee will be
adjusted by the percentage change in the
consumer price index (CPI) for all urban
consumers (all items; United States city
average) for the 12-month period ending
with June of the previous year.
• As stated in the Regulatory Impact
Analysis section of the February 2, 2011
final rule with comment period
(76 FR 5955) the CPI–U increase for the
12-month period ending with June of
the previous year is1.0 percent, based
on data obtained from the Bureau of
Labor Statistics. This results in an
application fee for the CY 2011 of $505
(or, $500 × 1.01).
We will provide additional
information to institutional providers on
how the application fee can be
submitted. Institutional providers are
VerDate Mar<15>2010
16:46 Mar 22, 2011
Jkt 223001
IV. Regulatory Impact Statement
We have examined the impact of this
notice as required by Executive Order
12866 on Regulatory Planning and
Review (September 30, 1993), Executive
Order 13563 on Improving Regulation
and Regulatory Review (February 2,
2011), the Regulatory Flexibility Act
(RFA) (September 19, 1980, Pub. L. 96–
354), section 1102(b) of the Social
Security Act, section 202 of the
Unfunded Mandates Reform Act of 1995
(March 22, 1995; Pub. L. 104–4),
Executive Order 13132 on Federalism
(August 4, 1999) and the Congressional
Review Act (5 U.S.C. 804(2)). Executive
Orders 12866 and 13563 direct agencies
to assess 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).
In the regulatory impact analysis
section of the February 2, 2011
published final rule with comment
(76 FR 5862), we estimated the total
costs for institutional providers and
suppliers in application fees for each
CYs from 2011 through 2015. For
2011—and based on an application fee
of $505—we projected in Tables 11 and
12 (76 FR 5955 through 5956) a total
cost of $46,160,030 for Medicare
providers and suppliers (or 91,406
providers and suppliers × $505). For
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16423
Medicaid providers, the estimated total
cost for 2011—as indicated in Tables 13
and 14 (76 FR 5957)—was $9,519,755
(or 18,851 providers × $505).
We are retaining these estimates for
purposes of this notice. Thus, we project
the total cost in application fees for
Medicare and Medicaid providers and
suppliers in CY 2011 to be $55,679,785.
This notice does not reach the
economic threshold and thus is not
considered a major rule.
The RFA requires agencies to analyze
options for regulatory relief of small
entities. For purposes of the RFA, small
entities include small businesses,
nonprofit organizations, and small
governmental jurisdictions. Most
hospitals and most other providers and
suppliers are small entities, either by
nonprofit status or by having revenues
of $7.0 million to $34.5 million in any
1 year. Individuals and States are not
included in the definition of a small
entity. We are not preparing an analysis
for the RFA because we have
determined, and the Secretary certifies,
that this notice will not have a
significant economic impact on a
substantial number of small entities.
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 604 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 for
Medicare payment regulations and has
fewer than 100 beds. We are not
preparing an analysis for section 1102(b)
of the Act because we have determined,
and the Secretary certifies, that this
notice will 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 whose mandates require spending
in any 1 year of $100 million in 1995
dollars, updated annually for inflation.
In 2011, that threshold is approximately
$136 million. This notice will have no
consequential effect on State, local, or
Tribal governments or on the private
sector.
Executive Order 13132 establishes
certain requirements that an agency
must meet when it promulgates 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.
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16424
Federal Register / Vol. 76, No. 56 / Wednesday, March 23, 2011 / Notices
Since this regulation does not impose
any costs on State or local governments,
the requirements of Executive Order
13132 are not applicable.
In accordance with the provisions of
Executive Order 12866, this notice was
not reviewed by the Office of
Management and Budget.
(Catalog of Federal Domestic Assistance
Program No. 93.778, Medical Assistance
Program and Catalog of Federal Domestic
Assistance Program No. 93.773, Medicare—
Hospital Insurance; and Program No. 93.774,
Medicare—Supplementary Medical
Insurance Program)
Dated: March 16, 2011.
Donald M. Berwick,
Administrator, Centers for Medicare &
Medicaid Services.
[FR Doc. 2011–6813 Filed 3–22–11; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–D–0277]
Draft Guidance for Industry:
Compliance With Regulations
Restricting the Sale and Distribution of
Cigarettes and Smokeless Tobacco To
Protect Children and Adolescents;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing the
availability of a revised draft guidance
for industry entitled ‘‘Draft Guidance for
Industry: Compliance With Regulations
Restricting the Sale and Distribution of
Cigarettes and Smokeless Tobacco to
Protect Children and Adolescents.’’ This
revised draft guidance replaces the
original draft guidance published in the
Federal Register of June 9, 2010 (75 FR
32791). The original draft guidance was
revised to remove potential ambiguities
and to address several issues not
included in the original draft guidance.
This revised draft guidance is intended
to help small entities comply with the
final rule entitled ‘‘Regulations
Restricting the Sale and Distribution of
Cigarettes and Smokeless Tobacco to
Protect Children and Adolescents.’’
DATES: Although you can comment on
any guidance at any time (see 21 CFR
10.115(g)(5)), to ensure that the Agency
considers your comment on this draft
guidance before it begins work on the
final version of the guidance, submit
either electronic or written comments
on the draft guidance by May 23, 2011.
jlentini on DSKJ8SOYB1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
16:46 Mar 22, 2011
Jkt 223001
The draft guidance for
industry entitled ‘‘Draft Guidance for
Industry: Compliance with Regulations
Restricting the Sale and Distribution of
Cigarettes and Smokeless Tobacco to
Protect Children and Adolescents’’ is
available on the Internet at https://
www.fda.gov/TobaccoProducts/
GuidanceComplianceRegulatory
Information/default.htm, or a paper
copy may be ordered free of charge by
calling 1–877–287–1373.
Submit electronic comments to
https://www.regulations.gov. Submit
written comments to the Division of
Dockets Management (HFA–305), Food
and Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
Identify comments with the docket
number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Office of Compliance and Enforcement,
Center for Tobacco Products, Food and
Drug Administration, 9200 Corporate
Blvd., Rockville, MD 20850–3229, 877–
287–1373, ctpcompliance@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
I. Background
The Family Smoking Prevention and
Tobacco Control Act (Tobacco Control
Act) (Pub. L. 111–31; 123 Stat. 1776)
was enacted on June 22, 2009, amending
the Federal Food, Drug, and Cosmetic
Act and providing FDA with the
authority to regulate tobacco products.
Section 102 of the Tobacco Control Act
requires FDA to publish final
regulations regarding cigarettes and
smokeless tobacco, which are identical
in their provisions to the regulations
issued by FDA on August 28, 1996 (61
FR 44396), with certain specified
exceptions. In the Federal Register of
March 19, 2010 (75 FR 13225), FDA
published a final rule entitled
‘‘Regulations Restricting the Sale and
Distribution of Cigarettes and Smokeless
Tobacco to Protect Children and
Adolescents.’’ The final regulations
apply to manufacturers, distributors,
and retailers who make, distribute, or
sell cigarettes or smokeless tobacco
products.
As of June 22, 2010, these Federal
regulations, among other things,
prohibit retailers from selling cigarettes,
cigarette tobacco, or smokeless tobacco
to persons under the age of 18, and
require retailers to verify the age of all
customers under the age of 27 by
checking a photographic identification
that includes the bearer’s date of birth.
FDA announced the publication of the
original draft guidance document on
June 9, 2010 (75 FR 32791). This revised
draft guidance replaces the original draft
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guidance. The original draft guidance
was revised to remove potential
ambiguities and to address several
issues not included in the original draft
guidance. This revised draft guidance is
intended to help small entities comply
with the final rule entitled ‘‘Regulations
Restricting the Sale and Distribution of
Cigarettes and Smokeless Tobacco to
Protect Children and Adolescents’’
published on March 19, 2010. FDA is
soliciting comments on the revised draft
guidance document which replaces the
original draft guidance document. FDA
may amend the guidance document
periodically as a result of comments
received.
II. Significance of Guidance
FDA is issuing this draft guidance
document consistent with FDA’s good
guidance practices regulation (21 CFR
10.115). The draft guidance, when
finalized, will represent the Agency’s
current thinking on ‘‘Compliance with
Regulations Restricting the Sale and
Distribution of Cigarettes and Smokeless
Tobacco to Protect Children and
Adolescents.’’ It does not create or
confer any rights for or on any person
and does not operate to bind FDA or the
public. An alternative approach may be
used if such approach satisfies the
requirements of the applicable statute
and regulations.
III. Comments
The draft guidance is being
distributed for comment purposes only
and is not intended for implementation
at this time. Interested persons may
submit to the Division of Dockets
Management (see ADDRESSES) either
electronic or written comments
regarding this document. It is only
necessary to send one set of comments.
It is no longer necessary to send two
copies of mailed comments. Identify
comments with the docket number
found in brackets in the heading of this
document. Received comments may be
seen in the Division of Dockets
Management between 9 a.m. and 4 p.m.,
Monday through Friday.
IV. Electronic Access
Persons with access to the Internet
may obtain the document at either
https://www.fda.gov/TobaccoProducts/
GuidanceComplianceRegulatory
Information/default.htm or https://
www.regulations.gov.
Dated: March 17, 2011.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2011–6794 Filed 3–22–11; 8:45 am]
BILLING CODE P
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Agencies
[Federal Register Volume 76, Number 56 (Wednesday, March 23, 2011)]
[Notices]
[Pages 16422-16424]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-6813]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-6029-N]
RIN 0938-AQ99
Medicare, Medicaid, and Children's Health Insurance Programs;
Provider Enrollment Application Fee Amount for 2011
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the $505 calendar year (CY) 2011
application fee for institutional providers that are: Initially
enrolling in the Medicare, program; revalidating their Medicare
enrollment; or adding a new Medicare practice location. These
institutional providers and suppliers are required to submit the 2011
fee amount with any enrollment applications submitted on or after March
25, 2011 and on or before December 31, 2011. Similarly, beginning March
25, 2011 prospective or re-enrolling Medicaid or CHIP providers must
submit the applicable application fee unless: (1) The provider is an
individual physician or nonphysician practitioner; or (2) the provider
is enrolled in Title XVIII of the Act or another State's title XIX or
XXI plan and has paid the application fee to a Medicare contractor or
another State.
DATES: Effective Date: This notice is effective on March 23, 2011.
FOR FURTHER INFORMATION CONTACT: Frank Whelan, (410) 786-1302 for
Medicare enrollment issues. Claudia Simonson, (312) 353-2115 for
Medicaid and CHIP enrollment issues.
SUPPLEMENTARY INFORMATION:
I. Background
In the February 2, 2011 Federal Register (76 FR 5862) we published
a final rule with comment period entitled: ``Medicare, Medicaid, and
Children's Health Insurance Programs; Additional Screening
Requirements, Application Fees, Temporary Enrollment Moratoria, Payment
Suspensions and Compliance Plans for Providers and Suppliers''. This
final rule with comment finalized, among other things, provisions
related to the submission of application fees as part of the Medicare,
Medicaid and Children's Health Insurance Program (CHIP) provider
enrollment processes. Specifically, and as stated in 42 CFR 424.514,
institutional providers and suppliers that are: Initially enrolling in
[[Page 16423]]
the Medicare program; revalidating their Medicare enrollment; or adding
a new Medicare practice location, will be required to submit an
application fee beginning March 25, 2011 with any enrollment
application. We will adjust the amount of the fee annually for
inflation. Institutional providers are defined at Sec. 424.502 as--
Any provider or supplier that submits a paper Medicare
enrollment application using the CMS-855A, CMS-855B (not including
physician and non-physician practitioner organizations), CMS-855S or
associated Internet-based PECOS enrollment application.
Similarly, as stated in 42 CFR 455.460, beginning March 25, 2011
prospective or re-enrolling Medicaid or CHIP providers must submit the
applicable application fee unless: (1) The provider is an individual
physician or nonphysician practitioner; or (2) the provider is enrolled
in Title XVIII of the Act or another State's title XIX or XXI plan and
has paid the application fee to a Medicare contractor or another State.
The February 2, 2011 final rule with comment period contains
additional information about the entities that must submit an
application fee, the purpose of the fee, and the process of obtaining a
hardship exception or a waiver for Medicaid providers.
II. Provisions of the Notice
The application fee amount for the period on or after March 25,
2011 and on or before December 31, 2011 will be $505. This figure was
calculated in accordance with the following:
Section 1866(j)(2)(C)(i)(I) of the Social Security Act
(the Act) established a $500 application fee for providers and
suppliers in calendar year (CY) 2010.
In 42 CFR 424.514(d)(2) of our regulations, and consistent
with section1866(j)(2)(C)(i)(II) of the Act, we stated that for CY 2011
and for subsequent years, the fee will be adjusted by the percentage
change in the consumer price index (CPI) for all urban consumers (all
items; United States city average) for the 12-month period ending with
June of the previous year.
As stated in the Regulatory Impact Analysis section of the
February 2, 2011 final rule with comment period (76 FR 5955) the CPI-U
increase for the 12-month period ending with June of the previous year
is1.0 percent, based on data obtained from the Bureau of Labor
Statistics. This results in an application fee for the CY 2011 of $505
(or, $500 x 1.01).
We will provide additional information to institutional providers
on how the application fee can be submitted. Institutional providers
are reminded that they can submit a hardship exception request in the
event they believe that it is appropriate; additional information on
the hardship exception is available in the February 2, 2011 final rule
with comment period.
The application fee for calendar year 2012 will be published in the
Federal Register later this year.
III. Collection of Information Requirements
This document does not impose information collection and
recordkeeping requirements. Consequently, it need not be reviewed by
the Office of Management and Budget under the authority of the
Paperwork Reduction Act of 1995 (44 U.S.C. chapter 35). However, it
does reference previously approved information collections. As stated
in Section I of this notice, the forms CMS-855(A and B) and the CMS-
855(S) are approved under OMB control numbers 0938-0685 and 0938-1057.
IV. Regulatory Impact Statement
We have examined the impact of this notice as required by Executive
Order 12866 on Regulatory Planning and Review (September 30, 1993),
Executive Order 13563 on Improving Regulation and Regulatory Review
(February 2, 2011), the Regulatory Flexibility Act (RFA) (September 19,
1980, Pub. L. 96-354), section 1102(b) of the Social Security Act,
section 202 of the Unfunded Mandates Reform Act of 1995 (March 22,
1995; Pub. L. 104-4), Executive Order 13132 on Federalism (August 4,
1999) and the Congressional Review Act (5 U.S.C. 804(2)). Executive
Orders 12866 and 13563 direct agencies to assess 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).
In the regulatory impact analysis section of the February 2, 2011
published final rule with comment (76 FR 5862), we estimated the total
costs for institutional providers and suppliers in application fees for
each CYs from 2011 through 2015. For 2011--and based on an application
fee of $505--we projected in Tables 11 and 12 (76 FR 5955 through 5956)
a total cost of $46,160,030 for Medicare providers and suppliers (or
91,406 providers and suppliers x $505). For Medicaid providers, the
estimated total cost for 2011--as indicated in Tables 13 and 14 (76 FR
5957)--was $9,519,755 (or 18,851 providers x $505).
We are retaining these estimates for purposes of this notice. Thus,
we project the total cost in application fees for Medicare and Medicaid
providers and suppliers in CY 2011 to be $55,679,785.
This notice does not reach the economic threshold and thus is not
considered a major rule.
The RFA requires agencies to analyze options for regulatory relief
of small entities. For purposes of the RFA, small entities include
small businesses, nonprofit organizations, and small governmental
jurisdictions. Most hospitals and most other providers and suppliers
are small entities, either by nonprofit status or by having revenues of
$7.0 million to $34.5 million in any 1 year. Individuals and States are
not included in the definition of a small entity. We are not preparing
an analysis for the RFA because we have determined, and the Secretary
certifies, that this notice will not have a significant economic impact
on a substantial number of small entities.
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 604 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 for Medicare payment regulations and has fewer than
100 beds. We are not preparing an analysis for section 1102(b) of the
Act because we have determined, and the Secretary certifies, that this
notice will 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 whose mandates require spending in any 1 year of $100
million in 1995 dollars, updated annually for inflation. In 2011, that
threshold is approximately $136 million. This notice will have no
consequential effect on State, local, or Tribal governments or on the
private sector.
Executive Order 13132 establishes certain requirements that an
agency must meet when it promulgates 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.
[[Page 16424]]
Since this regulation does not impose any costs on State or local
governments, the requirements of Executive Order 13132 are not
applicable.
In accordance with the provisions of Executive Order 12866, this
notice was not reviewed by the Office of Management and Budget.
(Catalog of Federal Domestic Assistance Program No. 93.778, Medical
Assistance Program and Catalog of Federal Domestic Assistance
Program No. 93.773, Medicare--Hospital Insurance; and Program No.
93.774, Medicare--Supplementary Medical Insurance Program)
Dated: March 16, 2011.
Donald M. Berwick,
Administrator, Centers for Medicare & Medicaid Services.
[FR Doc. 2011-6813 Filed 3-22-11; 8:45 am]
BILLING CODE 4120-01-P