Disease, Disability, and Injury Prevention and Control Special Emphasis Panel: State-Based Occupational Safety and Health Surveillance and Occupational Health and Safety Research, Request for Application (RFA) PAR-04-106; and Occupational Health and Safety Research, RFA PAR-04-038, 51623-51624 [E6-14418]
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jlentini on PROD1PC65 with NOTICES
Federal Register / Vol. 71, No. 168 / Wednesday, August 30, 2006 / Notices
reasonably necessary to obtain
significant efficiencies through the joint
arrangement.
A ‘‘qualified clinically-integrated joint
arrangement,’’ on the other hand, need
not involve any sharing of financial risk.
Instead, as defined in the proposed
order, physician participants must
participate in active and ongoing
programs to evaluate and modify their
clinical practice patterns in order to
control costs and ensure the quality of
services provided, and the arrangement
must create a high degree of
interdependence and cooperation
among physicians. As with qualified
risk-sharing arrangements, any
agreement concerning price or other
terms of dealing must be reasonably
necessary to achieve the efficiency goals
of the joint arrangement.
Paragraph III, for three years, requires
New Century and Prime Care to notify
the Commission before entering into any
arrangement to act as an agent on behalf
of any physicians, with payors regarding
contracts. Paragraph III also sets out the
information necessary to make the
notification complete.
Paragraph IV, for three years, requires
the Proposed Respondents to notify the
Commission before participating in
contracting with health plans on behalf
of a qualified risk-sharing joint
arrangement, or a qualified clinicallyintegrated joint arrangement. The
contracting discussions that trigger the
notice provision may be either among
physicians, or between New Century or
Prime Care and health plans. Paragraph
IV also sets out the information
necessary to satisfy the notification
requirement.
Paragraph V provides that, for three
years, the New Century and Prime Care
officials named in the proposed
complaint and order may not: (1)
Negotiate or act as an agent on behalf of
any physician or medical group practice
that participates or has participated in
either New Century or Prime Care; or (2)
advise any physician or medical group
practice that participates in or has
participated in either New Century or
Prime Care on contracts, offers, contract
terms, conditions, or requirements for
dealing with any payors. Exempted from
Paragraph V’s prohibition are the
officials’ participation in: (1) Certain
qualified risk-sharing joint
arrangements; (2) certain qualified
clinically-integrated joint arrangements;
and (3) activities that solely involve
physicians in a medical group practice
in which the official participates.
For three years, Paragraph VI requires
both New Century and Prime Care,
respectively, to distribute the complaint
and order: (1) To all physicians who
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have participated in the IPAs, who
currently participate in the IPAs, or who
express interest in participating in the
IPAs; and (2) to payors that have
negotiated contracts with the IPAs, or
that contract with the IPAs in the future.
Paragraphs VII, VIII, IX, and X of the
proposed order impose various
obligations on the Proposed
Respondents to report or provide access
to information to the Commission to
facilitate the monitoring of compliance
with the order. Paragraph XI provides
that the proposed order will expire in 20
years.
By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. E6–14360 Filed 8–29–06; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Advisory Committee on Childhood
Lead Poisoning Prevention (ACCLPP)
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC), National
Center for Environmental Health
(NCEH) announces the following
committee meeting.
Name: Advisory Committee on
Childhood Lead Poisoning Prevention
(ACCLPP).
Times and Dates: October 17, 2006,
8:30 a.m.–5 p.m., October 18, 2006, 8:30
a.m.–12:30 p.m.
Place: Hilton St. Louis at the Ballpark,
One South Broadway, St. Louis, MO
63102, Telephone: 314 421–1776 or Toll
free 1–877–845–7354.
Status: Open to the public, limited
only by the space available. The meeting
room accommodates approximately 75
people.
Purpose: The Committee provides
advice and guidance to the Secretary;
the Assistant Secretary for Health; and
the Director, CDC, regarding new
scientific knowledge and technological
developments and their practical
implications for childhood lead
poisoning prevention efforts. The
committee also reviews and reports
regularly on childhood lead poisoning
prevention practices and recommends
improvements in national childhood
lead poisoning prevention efforts.
Matters To Be Discussed: Update on
the Lead and Pregnancy Workgroup
activities, update on the clinical
implications of blood lead levels (BLL)
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51623
less than 10 and discussions of
laboratory capacity to analyze BLL <2
µg/dL. Agenda items are subject to
change as priorities dictate.
Opportunities will be provided during
the meeting for oral comments.
Depending on the time available and the
number of requests, it may be necessary
to limit the time of each presenter.
For Further Information Contact:
Claudine Johnson, Clerk, (Contractor)
Lead Poisoning Prevention Branch,
Division of Environmental Emergency
Health Services, NCEH, CDC, 4770
Buford Hwy., NE., Mailstop F–40,
Atlanta, GA 30341, telephone 770 488–
3629,fax 770 488–3635.
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 CDC
and the Agency for Toxic Substances
and Disease Registry.
Dated: August 22, 2006.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E6–14441 Filed 8–29–06; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel: State-Based
Occupational Safety and Health
Surveillance and Occupational Health
and Safety Research, Request for
Application (RFA) PAR–04–106; and
Occupational Health and Safety
Research, RFA PAR–04–038
Correction: This notice was published
in the Federal Register on August 17,
2006, Volume 71, Number 159, page
47498. The meeting has been changed to
reflect an additional Request for
Applications.
Title: State-Based Occupational Safety
and Health Surveillance and
Occupational Health and Safety
Research, RFA PAR–04–106; and
Occupational Health and Safety
Research, RFA PAR–04–038.
Contact Person for More Information:
M. Chris Langub, Scientific Review
Administrator, National Institute for
Occupational Safety and Health, Centers
for Disease Control and Prevention,
1600 Clifton Road NE, MS E–74,
E:\FR\FM\30AUN1.SGM
30AUN1
51624
Federal Register / Vol. 71, No. 168 / Wednesday, August 30, 2006 / Notices
Atlanta, GA 30333, Telephone
404.639.2543.
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 CDC
and the Agency for Toxic Substances
and Disease Registry.
Dated: August 21, 2006.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E6–14418 Filed 8–29–06; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Savannah River Site Dose
Reconstruction Project
The Centers for Disease Control
and Prevention (CDC) and the Agency
for Toxic Substances and Disease
Registry (ATSDR).
ACTION: CDC and ATSDR announce the
following meeting.
jlentini on PROD1PC65 with NOTICES
AGENCY:
Name: Public Meeting to Present
Final Report of the Savannah River Site
Dose Reconstruction Project.
Time and Date: 6 p.m.–8 p.m.,
(Eastern Time), Tuesday, September 19,
2006.
Place: University of South Carolina/
Aiken, Conference Center/Business and
Education Building, Room 122, 471
University Parkway, Parking Lot ‘‘C’’,
Aiken, South Carolina 29801.
Status: Open to the public, limited
only by the space available. The meeting
room accommodates approximately 50
people.
Background: Under a Memorandum
of Understanding (MOU) signed in
December 1990 with DOE, and replaced
by MOUs signed in 1996 and 2000, the
Department of Health and Human
Services (HHS) was given the
responsibility and resources for
conducting analytic epidemiologic
investigations of residents of
communities in the vicinity of DOE
facilities, workers at DOE facilities, and
other persons potentially exposed to
radiation or to potential hazards from
non-nuclear energy production use.
HHS delegated program responsibility
to CDC.
In addition, a memo was signed in
October 1990 and renewed in November
1992, 1996, and in 2000, between
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16:39 Aug 29, 2006
Jkt 208001
ATSDR and DOE. The MOU delineates
the responsibilities and procedures for
ATSDR’s public health activities at DOE
sites required under sections 104, 105,
107, and 120 of the Comprehensive
Environmental Response,
Compensation, and Liability Act
(CERCLA or ‘‘Superfund’’). These
activities include health consultations
and public health assessments at DOE
sites listed on, or proposed for, the
Superfund National Priorities List and
at sites that are the subject of petitions
from the public; and other healthrelated activities such as epidemiologic
studies, health surveillance, exposure
and disease registries, health education,
substance-specific applied research,
emergency response, and preparation of
toxicological profiles.
Purpose: CDC will present the Final
Report of the Savannah River Site Dose
Reconstruction Project to area
stakeholders and provide a forum for
community interaction. This meeting
will also serve as a vehicle for members
of the public to express concerns to
CDC.
Matters To Be Discussed: The
National Center for Environmental
Health (NCEH) will make a presentation
of the Final Report of the Savannah
River Site Dose Reconstruction Project.
There will be time for public questions
and comments. Agenda items are
subject to change as priorities dictate.
Contact Person For Additional
Information: Phillip R. Green, Public
Health Advisor, Radiation Studies
Branch, Division of Environmental
Hazards and Health Effects, NCEH, CDC,
1600 Clifton Road, NE., (MS–E39),
Atlanta, GA 30333, telephone 404/498–
1717, fax 404/498–1811, or e-mail
address: prg1@cdc.gov
Dated: August 23, 2006.
James D. Seligman,
Chief Information Officer, Centers for Disease
Control and Prevention (CDC).
[FR Doc. E6–14424 Filed 8–29–06; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Prospective Grant of Exclusive
License: Prophylactic Use of
Pneumococcal Surface Adhesin A
Protein as a Vaccine
Office of Technology Transfer;
Centers for Disease Control and
Prevention (CDC); Department of Health
and Human Services.
AGENCY:
PO 00000
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ACTION:
Notice.
SUMMARY: This is a notice in accordance
with 35 U.S.C. 209(e) and 37 CFR
404.7(a)(1)(i) that the Centers for Disease
Control and Prevention (CDC),
Technology Transfer Office, Department
of Health and Human Services (DHHS),
is contemplating the grant of a
worldwide, limited field of use,
exclusive license to practice the
inventions embodied in the patent and
patent applications referred to below to
Intercell, having a place of business in
Vienna, Austria. The patent rights in
these inventions have been assigned to
the government of the United States of
America. The patent and patent
applications to the licensed are: U.S.
Patent No. 5,422,427 entitled
‘‘Pneumococcal Fimbrial Protein A,’’
issued 06.06.95.
U.S. Patent No. 6,312,944 entitled
‘‘Pneumococcal Fimbrial Protein A,’’
issued 11.06.01.
U.S. Patent No. 5,854,416 entitled
‘‘Streptococcus pneumoniae 37-kDa
Surface Adhesin A Protein and
Nucleic Acids Coding Therefore,’’
issued 12.29.98 (CDC Ref: E–157–91/
4).
U.S. Patent No. 6,217,884 entitled
‘‘Streptococcus pneumoniae 37-kDa
Surface Adhesin A Protein,’’ issued
04.17.01.
U.S. Patent No. 6,773,880 entitled
‘‘Streptococcus pneumoniae 37-kDa
Surface Adhesin A Protein,’’ issued
06.05.03.
The prospective exclusive license will
be royalty-bearing and will comply with
the terms and conditions of 35 U.S.C.
209 and 37 CFR 404.7.
ADDRESSES: Requests for a copy of these
patent applications, inquiries,
comments, and other materials relating
to the contemplated license should be
directed to Thomas E. O’Toole, MPH,
Chief Licensing Officer, Technology
Transfer Office, Centers for Disease
Control and Prevention (CDC), 4770
Buford Highway, Mailstop K–79,
Atlanta, GA 30341, telephone: (770)
488–8600; facsimile: (770) 488–8615.
Applications for a license filed in
response to this notice will be treated as
objections to the grant of the
contemplated license. Only written
comments and/or applications for a
license which are received by CDC
within thirty days of this notice will be
considered. Comments and objections
submitted in response to this notice will
not be made available for public
inspection, and, to the extent permitted
by law, will not be released under the
Freedom of Information Act, 5 U.S.C.
552. A signed Confidential Disclosure
E:\FR\FM\30AUN1.SGM
30AUN1
Agencies
[Federal Register Volume 71, Number 168 (Wednesday, August 30, 2006)]
[Notices]
[Pages 51623-51624]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-14418]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Disease, Disability, and Injury Prevention and Control Special
Emphasis Panel: State-Based Occupational Safety and Health Surveillance
and Occupational Health and Safety Research, Request for Application
(RFA) PAR-04-106; and Occupational Health and Safety Research, RFA PAR-
04-038
Correction: This notice was published in the Federal Register on
August 17, 2006, Volume 71, Number 159, page 47498. The meeting has
been changed to reflect an additional Request for Applications.
Title: State-Based Occupational Safety and Health Surveillance and
Occupational Health and Safety Research, RFA PAR-04-106; and
Occupational Health and Safety Research, RFA PAR-04-038.
Contact Person for More Information: M. Chris Langub, Scientific
Review Administrator, National Institute for Occupational Safety and
Health, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS E-74,
[[Page 51624]]
Atlanta, GA 30333, Telephone 404.639.2543.
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 CDC and the Agency for Toxic Substances and Disease Registry.
Dated: August 21, 2006.
Alvin Hall,
Director, Management Analysis and Services Office, Centers for Disease
Control and Prevention.
[FR Doc. E6-14418 Filed 8-29-06; 8:45 am]
BILLING CODE 4163-18-P