Medicare Program: Medicare Clinical Laboratory Services Competitive Bidding Demonstration Project, 58856-58857 [E7-20499]
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Federal Register / Vol. 72, No. 200 / Wednesday, October 17, 2007 / Notices
and research within the national
centers; shall conduct peer-review of
scientific programs; and monitor the
overall strategic direction and focus of
the national centers. The board, after
conducting its periodic reviews, shall
submit a written description of the
results of the review and its
recommendations to the Director, CDC.
The board shall also perform secondlevel peer review of applications for
grants-in-aid for research and research
training activities, cooperative
agreements, and research contract
proposals relating to the broad areas
within the national centers.
For information, contact Dr. Tom
Savel, Executive Secretary, Centers for
Disease Control and Prevention, of the
Department of Health and Human
Services, 1600 Clifton Road, NE.,
Mailstop E78, Atlanta, Georgia 30333,
telephone 404/498–3081 or fax 404/
498–6570. The Director, Management
Analysis and Services Office, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the CDC and the Agency for Toxic
Substances and Disease Registry.
Dated: October 9, 2007.
Elaine L. Baker,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention (CDC).
[FR Doc. E7–20475 Filed 10–16–07; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–5045–N]
Medicare Program: Medicare Clinical
Laboratory Services Competitive
Bidding Demonstration Project
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
sroberts on PROD1PC70 with NOTICES
AGENCY:
SUMMARY: This notice announces the
first demonstration site for the Medicare
Clinical Laboratory Services
Competitive Bidding Demonstration
project and the date for the Bidder’s
Conference. The Medicare Clinical
Laboratory Competitive Bidding
Demonstration was mandated by the
Congress. Section 302(b) of the
Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 (MMA) (Pub. L. 108–173) requires
the Centers for Medicare & Medicaid
Services (CMS) to conduct a
VerDate Aug<31>2005
19:05 Oct 16, 2007
Jkt 214001
demonstration project on the
application of competitive acquisition
for clinical laboratory services that
would otherwise be paid under the
Medicare Part B fee schedule. The
objective of the demonstration is to
determine whether competitive bidding
can be used to provide Part B clinical
laboratory services at fees below current
Medicare payment rates while
maintaining quality and access to care.
The MMA specifically requires that
the demonstration: (1) Includes tests
paid under the Medicare Part B Clinical
Laboratory Fee Schedule; (2) excludes
entities that have a ‘‘face-to-face
encounter’’ with the patient; (3)
excludes Pap smears and colorectal
cancer screening tests; and, (4) includes
requirements under the Clinical
Laboratory Improvement Amendments
(CLIA) program. An initial Report to the
Congress was submitted April 2006.
Site(S): The fundamental criteria for
selecting demonstration sites require
that each Metropolitan Statistical Area
(MSA) allows for potential Medicare
program savings from the
demonstration, is administratively
feasible, represents the laboratory
market, and will yield demonstration
results that can be generalized to other
MSAs.
The first demonstration site will be
the San Diego-Carlsbad-San Marcos,
California MSA.
A Bidders Conference is planned for
October 31, 2007 in the San DiegoCarlsbad-San Marcos, California MSA.
The demonstration covers tests
provided to beneficiaries enrolled in the
traditional fee-for-service (FFS)
Medicare program who reside in the
area of the demonstration site or
competitive bid area (CBA) during the 3
year demonstration period. Beneficiaries
who travel outside the CBA during the
demonstration period and require
laboratory services will be able to access
services from most laboratories in the
United States. We will not directly pay,
however, for services furnished by a
required bidder that did not bid or bid
and did not win or a non-required
bidder that bid and did not win. (The
terms ‘‘required bidder’’ and ‘‘nonrequired bidder’’ are explained in
section II below.) Laboratories may not
bill beneficiaries for laboratory services
covered under the Medicare program.
FOR FURTHER INFORMATION CONTACT:
Linda Lebovic at (410) 786–3402 or lab_
bid _demo@cms. hhs.gov. Interested
parties can obtain information about the
demonstration project on the CMS Web
site at https://www.cms.hhs.gov/ Demo
ProjectsEvalRpts/ downloads/2004_
Demonstration_ Competitive_ Bidding_
Clinical_ Laboratory_ Services.pdf.
PO 00000
Frm 00053
Fmt 4703
Sfmt 4703
SUPPLEMENTARY INFORMATION:
I. Background
Section 302(b) of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA) (Pub.
L. 108–173) amends section 1847(e) of
the Social Security Act (the Act) (42
U.S.C. 1395w–3) —‘‘Competitive
Acquisition of Certain Items and
Services,’’ to include a demonstration
project for clinical laboratory services.
The statute requires the Secretary of
Health and Human Services to conduct
a demonstration project on the
application of competitive acquisition
for payment of clinical laboratory
services that would otherwise be made
under Medicare Part B Clinical
Laboratory Fee Schedule.
II. Provisions of the Notice
Under section 1847(e) of the Act, Pap
smears and colorectal cancer screening
tests are excluded from this
demonstration. Requirements under
CLIA as mandated in section 353 of the
Public Health Service Act apply. The
aggregate amounts to be paid to
contractors in a competitive acquisition
area are expected to be less than the
aggregate amounts that would otherwise
be paid under the laboratory fee
schedule. The payment basis
determined for each competitive
acquisition area will be substituted for
payment under the existing Medicare
Part B Clinical Laboratory Fee Schedule.
The demonstration period is 3 years for
each demonstration site or ‘‘competitive
bid area’’ (CBA). The competitively set
demonstration fee schedule will be used
to pay for laboratory services in the CBA
for the duration of the 3-year
demonstration period. Multiple winners
are expected in each CBA.
Required bidders are defined as those
organizations that will supply, or expect
to supply, at least $100,000 annually in
demonstration tests to Medicare
beneficiaries residing in the CBA during
any year of the demonstration. Required
bidders that bid and win will be paid
under one demonstration fee schedule
for services provided to beneficiaries
residing in the CBA for the duration of
the demonstration.
Non-required bidders are defined as
laboratories that are not exempt from
the demonstration, but have the option
of participating in the bidding process.
Non-required bidders that do not bid as
well as those that bid and win, will be
paid under the demonstration fee
schedule for the duration of the
demonstration. These laboratories will
be paid under the same fee schedule as
the winning required bidders. Nonrequired bidders that choose to bid and
E:\FR\FM\17OCN1.SGM
17OCN1
sroberts on PROD1PC70 with NOTICES
Federal Register / Vol. 72, No. 200 / Wednesday, October 17, 2007 / Notices
do not win will not receive payment for
services provided to beneficiaries
residing in the CBA for the duration of
the demonstration period.
A non-required bidder is:
• A small business laboratory, which
we are defining as one that will supply
less than $100,000 annually in
demonstration tests to Medicare FFS
beneficiaries residing in the CBA during
each year of the demonstration. These
laboratories may choose to be a
‘‘passive’’ laboratory. A passive-small
business laboratory will have a $100,000
ceiling on annual payment from
Medicare for demonstration tests for the
duration of the demonstration.
• A laboratory that exclusively serves
beneficiaries entitled to Medicare
because they have end-stage renal
disease (ESRD) residing in the CBA may
choose to be a ‘‘passive’’ laboratory
under the demonstration. A passiveESRD laboratory may continue to
provide services to ESRD beneficiaries
residing in the CBA and receive
payment from Medicare for
demonstration tests paid under the
competitively set Part B Clinical
Laboratory Fee Schedule (demonstration
fee schedule) for the duration of the
demonstration.
• A laboratory that exclusively serves
beneficiaries residing in nursing homes
or receiving home health services in the
CBA may choose to be a ‘‘passive’’
laboratory under the demonstration. A
passive-nursing home laboratory may
continue to provide services to
beneficiaries residing in nursing homes
or receiving home health services in the
CBA and receive payment from
Medicare for demonstration tests paid
under the demonstration fee schedule
for the duration of the demonstration.
This notice announces a ‘‘Bidder’s
Conference’’ to be held in the San
Diego-Carlsbad-San Marcos, California
MSA on October 31, 2007 for potential
bidders to learn about the
demonstration rules and ask questions
about the bidding process. A Bidder’s
Package provides information about the
demonstration project and is available
to the public on the CMS project Web
site. There will be a single bidding
competition covering demonstration
tests for each CBA. Bidders will be
required to submit a bid price for each
Health Care Procedure Coding System
(HCPCS) code in the demonstration test
menu. Bidding laboratories will be
asked to identify demonstration tests
that they do not perform, and will be
asked to explain their plans for
responding to requests for
demonstration tests that they do not
perform in house (for example,
subcontracting and referrals). As part of
VerDate Aug<31>2005
19:05 Oct 16, 2007
Jkt 214001
their bid, laboratories will provide
information on ownership, location of
affiliated laboratories and specimen
collection sites, CLIA certification,
laboratory finances, and quality.
III. Collection of Information
Requirements
This information collection
requirement is subject to the Paperwork
Reduction Act of 1995 (PRA). The
collection is currently approved under
OMB control number 0938–1008
entitled ‘‘Medicare Clinical Laboratory
Services Competitive Bidding
Demonstration Project Application
Form’’ with a current expiration date of
January 31, 2009.
Authority: Section 302(b) of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA).
(Catalog of Federal Domestic Assistance
Program No. 93.773 Medicare—Hospital
Insurance Program; and No. 93.774,
Medicare—Supplementary Medical
Insurance Program)
Dated: October 4, 2007.
Kerry Weems,
Acting Administrator, Centers for Medicare
& Medicaid Services.
[FR Doc. E7–20499 Filed 10–16–07; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions;
Availability for Licensing
National Institutes of Health,
Public Health Service, HHS.
AGENCY:
ACTION:
Notice.
SUMMARY: The inventions listed below
are owned by an agency of the U.S.
Government and are available for
licensing in the U.S. in accordance with
35 U.S.C. 207 to achieve expeditious
commercialization of results of
federally-funded research and
development. Foreign patent
applications are filed on selected
inventions to extend market coverage
for companies and may also be available
for licensing.
ADDRESSES: Licensing information and
copies of the U.S. patent applications
listed below may be obtained by writing
to the indicated licensing contact at the
Office of Technology Transfer, National
Institutes of Health, 6011 Executive
Boulevard, Suite 325, Rockville,
Maryland 20852–3804; telephone: 301/
496–7057; fax: 301/402–0220. A signed
Confidential Disclosure Agreement will
PO 00000
Frm 00054
Fmt 4703
Sfmt 4703
58857
be required to receive copies of the
patent applications.
Novel Roles of a DNA Repair Protein,
DNA-PKcs, in Obesity, Neurological
Function, and Aging
Description of Technology: The
catalytic subunit of the DNA-dependent
protein kinase complex (DNA-PKcs) has
been shown to be important in DNA
repair and VDJ recombination in
lymphocytes. The inventors have
discovered that DNA-PKcs also plays
novel, important roles in energy
regulation and neurological function.
The inventors observed that mature
DNA-PKcs-deficient mice (also known
as SCID mice) have a lower proportion
of fat, resist obesity, and have
significantly greater physical endurance
than wild-type control mice,
particularly with increasing age. The
inventors also observed that DNA-PKcsdeficient mice have better memory and
less anxiety. One potential explanation
for this is that they express higher levels
of brain-derived neurotrophic factor
(BDNF), which is associated with
neurogenesis, memory formation and
suppression of anxiety and depression.
Moreover, DNA-PKcs-deficient cells
produce less oxidative stress. Thus,
inhibition of DNA-PKcs may have
unexpected utility in the treatment of a
wide range of diseases and conditions.
The invention discloses methods of
inhibiting DNA-PKcs activity to
decrease adiposity, improve physical
endurance and increase insulin
sensitivity and the number of
mitochondria. Also claimed are
methods directed to improved
neurological function, such as methods
for protection from neurodegenerative
disease, improving memory and
learning ability, and for reducing
depression and anxiety. Additionally,
the invention discloses methods for
reducing inflammation and for treating
heart disease.
Applications:
Development of therapeutics targeting
obesity, insulin-resistant diabetes, and
age-related loss of physical endurance.
Development of therapeutics to treat
neurological disorders such as
depression and memory loss.
Market:
Obesity is a large and growing
therapeutic market; over thirty percent
of Americans are obese, and over sixty
percent are overweight.
Similarly, the market for therapeutics
directed to insulin-resistant, or Type 2,
diabetes is rapidly expanding; the
market for such drugs is expected to top
$12 billion in 2012.
Loss of endurance and muscle mass is
common in the elderly; the average
E:\FR\FM\17OCN1.SGM
17OCN1
Agencies
[Federal Register Volume 72, Number 200 (Wednesday, October 17, 2007)]
[Notices]
[Pages 58856-58857]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-20499]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-5045-N]
Medicare Program: Medicare Clinical Laboratory Services
Competitive Bidding Demonstration Project
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the first demonstration site for the
Medicare Clinical Laboratory Services Competitive Bidding Demonstration
project and the date for the Bidder's Conference. The Medicare Clinical
Laboratory Competitive Bidding Demonstration was mandated by the
Congress. Section 302(b) of the Medicare Prescription Drug,
Improvement, and Modernization Act of 2003 (MMA) (Pub. L. 108-173)
requires the Centers for Medicare & Medicaid Services (CMS) to conduct
a demonstration project on the application of competitive acquisition
for clinical laboratory services that would otherwise be paid under the
Medicare Part B fee schedule. The objective of the demonstration is to
determine whether competitive bidding can be used to provide Part B
clinical laboratory services at fees below current Medicare payment
rates while maintaining quality and access to care.
The MMA specifically requires that the demonstration: (1) Includes
tests paid under the Medicare Part B Clinical Laboratory Fee Schedule;
(2) excludes entities that have a ``face-to-face encounter'' with the
patient; (3) excludes Pap smears and colorectal cancer screening tests;
and, (4) includes requirements under the Clinical Laboratory
Improvement Amendments (CLIA) program. An initial Report to the
Congress was submitted April 2006.
Site(S): The fundamental criteria for selecting demonstration sites
require that each Metropolitan Statistical Area (MSA) allows for
potential Medicare program savings from the demonstration, is
administratively feasible, represents the laboratory market, and will
yield demonstration results that can be generalized to other MSAs.
The first demonstration site will be the San Diego-Carlsbad-San
Marcos, California MSA.
A Bidders Conference is planned for October 31, 2007 in the San
Diego-Carlsbad-San Marcos, California MSA.
The demonstration covers tests provided to beneficiaries enrolled
in the traditional fee-for-service (FFS) Medicare program who reside in
the area of the demonstration site or competitive bid area (CBA) during
the 3 year demonstration period. Beneficiaries who travel outside the
CBA during the demonstration period and require laboratory services
will be able to access services from most laboratories in the United
States. We will not directly pay, however, for services furnished by a
required bidder that did not bid or bid and did not win or a non-
required bidder that bid and did not win. (The terms ``required
bidder'' and ``non-required bidder'' are explained in section II
below.) Laboratories may not bill beneficiaries for laboratory services
covered under the Medicare program.
FOR FURTHER INFORMATION CONTACT: Linda Lebovic at (410) 786-3402 or
lab-- bid _demo@cms.hhs.gov. Interested parties can obtain
information about the demonstration project on the CMS Web site at
https://www.cms.hhs.gov/DemoProjectsEvalRpts/downloads/2004_
Demonstration_Competitive_Bidding_Clinical_Laboratory_
Services.pdf.
SUPPLEMENTARY INFORMATION:
I. Background
Section 302(b) of the Medicare Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA) (Pub. L. 108-173) amends section
1847(e) of the Social Security Act (the Act) (42 U.S.C. 1395w-3) --
``Competitive Acquisition of Certain Items and Services,'' to include a
demonstration project for clinical laboratory services. The statute
requires the Secretary of Health and Human Services to conduct a
demonstration project on the application of competitive acquisition for
payment of clinical laboratory services that would otherwise be made
under Medicare Part B Clinical Laboratory Fee Schedule.
II. Provisions of the Notice
Under section 1847(e) of the Act, Pap smears and colorectal cancer
screening tests are excluded from this demonstration. Requirements
under CLIA as mandated in section 353 of the Public Health Service Act
apply. The aggregate amounts to be paid to contractors in a competitive
acquisition area are expected to be less than the aggregate amounts
that would otherwise be paid under the laboratory fee schedule. The
payment basis determined for each competitive acquisition area will be
substituted for payment under the existing Medicare Part B Clinical
Laboratory Fee Schedule. The demonstration period is 3 years for each
demonstration site or ``competitive bid area'' (CBA). The competitively
set demonstration fee schedule will be used to pay for laboratory
services in the CBA for the duration of the 3-year demonstration
period. Multiple winners are expected in each CBA.
Required bidders are defined as those organizations that will
supply, or expect to supply, at least $100,000 annually in
demonstration tests to Medicare beneficiaries residing in the CBA
during any year of the demonstration. Required bidders that bid and win
will be paid under one demonstration fee schedule for services provided
to beneficiaries residing in the CBA for the duration of the
demonstration.
Non-required bidders are defined as laboratories that are not
exempt from the demonstration, but have the option of participating in
the bidding process. Non-required bidders that do not bid as well as
those that bid and win, will be paid under the demonstration fee
schedule for the duration of the demonstration. These laboratories will
be paid under the same fee schedule as the winning required bidders.
Non-required bidders that choose to bid and
[[Page 58857]]
do not win will not receive payment for services provided to
beneficiaries residing in the CBA for the duration of the demonstration
period.
A non-required bidder is:
A small business laboratory, which we are defining as one
that will supply less than $100,000 annually in demonstration tests to
Medicare FFS beneficiaries residing in the CBA during each year of the
demonstration. These laboratories may choose to be a ``passive''
laboratory. A passive-small business laboratory will have a $100,000
ceiling on annual payment from Medicare for demonstration tests for the
duration of the demonstration.
A laboratory that exclusively serves beneficiaries
entitled to Medicare because they have end-stage renal disease (ESRD)
residing in the CBA may choose to be a ``passive'' laboratory under the
demonstration. A passive-ESRD laboratory may continue to provide
services to ESRD beneficiaries residing in the CBA and receive payment
from Medicare for demonstration tests paid under the competitively set
Part B Clinical Laboratory Fee Schedule (demonstration fee schedule)
for the duration of the demonstration.
A laboratory that exclusively serves beneficiaries
residing in nursing homes or receiving home health services in the CBA
may choose to be a ``passive'' laboratory under the demonstration. A
passive-nursing home laboratory may continue to provide services to
beneficiaries residing in nursing homes or receiving home health
services in the CBA and receive payment from Medicare for demonstration
tests paid under the demonstration fee schedule for the duration of the
demonstration.
This notice announces a ``Bidder's Conference'' to be held in the
San Diego-Carlsbad-San Marcos, California MSA on October 31, 2007 for
potential bidders to learn about the demonstration rules and ask
questions about the bidding process. A Bidder's Package provides
information about the demonstration project and is available to the
public on the CMS project Web site. There will be a single bidding
competition covering demonstration tests for each CBA. Bidders will be
required to submit a bid price for each Health Care Procedure Coding
System (HCPCS) code in the demonstration test menu. Bidding
laboratories will be asked to identify demonstration tests that they do
not perform, and will be asked to explain their plans for responding to
requests for demonstration tests that they do not perform in house (for
example, subcontracting and referrals). As part of their bid,
laboratories will provide information on ownership, location of
affiliated laboratories and specimen collection sites, CLIA
certification, laboratory finances, and quality.
III. Collection of Information Requirements
This information collection requirement is subject to the Paperwork
Reduction Act of 1995 (PRA). The collection is currently approved under
OMB control number 0938-1008 entitled ``Medicare Clinical Laboratory
Services Competitive Bidding Demonstration Project Application Form''
with a current expiration date of January 31, 2009.
Authority: Section 302(b) of the Medicare Prescription Drug,
Improvement, and Modernization Act of 2003 (MMA).
(Catalog of Federal Domestic Assistance Program No. 93.773
Medicare--Hospital Insurance Program; and No. 93.774, Medicare--
Supplementary Medical Insurance Program)
Dated: October 4, 2007.
Kerry Weems,
Acting Administrator, Centers for Medicare & Medicaid Services.
[FR Doc. E7-20499 Filed 10-16-07; 8:45 am]
BILLING CODE 4120-01-P