National Library of Medicine; Notice of Meeting, 6025-6026 [05-2130]
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Federal Register / Vol. 70, No. 23 / Friday, February 4, 2005 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Notice of Meeting: Secretary’s
Advisory Committee on Genetics,
Health, and Society
Pursuant to Public Law 92–463,
notice is hereby given of the sixth
meeting of the Secretary’s Advisory
Committee on Genetics, Health, and
Society (SACGHS), U.S. Public Health
Service. The meeting will be held from
8:30 a.m. to 5:30 p.m. on February 28,
2005 and 8:30 a.m. to 5 p.m. on March
1, 2005 at the Bethesda North Marriott
Hotel, 5701 Marinelli Road, North
Bethesda, Maryland. The meeting will
be open to the public with attendance
limited to space available. The meeting
will be webcast.
The meeting is expected to include
presentations and deliberations on
several topics, including the following:
a revised draft report with
recommendations about coverage and
reimbursement for genetic technologies
and services; current and proposed
efforts to understand gene-environment
interactions through large population
studies; the Committee’s efforts to
explore stakeholder perspectives on the
need for Federal legislation to prevent
genetic discrimination in health
insurance and employment; the
recommendations of the Advisory
Committee on Heritable Disorders and
Genetic Diseases in Newborns and
Children regarding the provision of
screening, counseling and health care
services for newborns and children
having or at risk for heritable disorders;
and efforts to improve the quality of
laboratory testing for rare diseases. Time
will be provided each day for public
comments.
Under authority of 42 U.S.C. 217a,
Section 222 of the Public Health Service
Act, as amended, the Department of
Health and Human Services established
SACGHS to serve as a public forum for
deliberations on the broad range of
human health and societal issues raised
by the development and use of genetic
technologies and, as warranted, to
provide advice on these issues. The
draft meting agenda and other
information about SACGHS, including
information about access to the webcast,
will be available at the following Web
site: https://www.od.nih.gov/oba/
sacghs.htm.
The Committee would welcome
hearing from anyone wishing to provide
public comment on any issue related to
genetics, health and society. Individuals
who would like to provide public
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comment or who plan to attend the
meeting and need special assistance,
such as sign language interpretation or
other reasonable accommodations,
should notify the SACGHS Executive
Secretary, Ms. Sarah Carr, by telephone
at 301–496–9838 or e-mail at
sc112@nih.gov. The SACGHS office is
located at 6705 Rockledge Drive, Suite
750, Bethesda, MD 20892.
Dated: January 27, 2005.
LaVerne Stringfield,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 05–2128 Filed 2–3–05; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
6025
Contact Person: Dr. Myrlene Staten, Senior
Advisor, Diabetes Translation Research,
Division of Diabetes, Endocrinology and
Metabolic Diseases, NIDDK, NIH, 6707
Democracy Boulevard, Bethesda, MD 20892–
5460. (301) 402–7886.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.847, Diabetes,
Endocrinology and Metabolic Research,
93.848, Digestive Diseases and Nutrition
Research; 98.849, Kidney Diseases, Urology
and Hematology Research, National Institutes
of Health, HHS.)
Dated: January 26, 2005
LaVerne Y. Stringfield,
Director, Office of Federal Advisory
Committee Policy.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
[FR Doc. 05–2131 Filed 2–3–05; 8:45 am]
National Institutes of Health
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National Institute of Diabetes and
Digestive and Kidney Disorders;
Notice of Closed Meeting
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. Appendix 2) notice
is hereby given of the following
meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), title 5 U.S.C.,
as amended. The purpose of this
meeting is to evaluate requests for
preclinical development resources for
potential new therapeutics for type 1
diabetes. The outcome of the evaluation
will be a decision whether NIDDK
should support the request and make
available contract resources for
development of the potential
therapeutic to improve the treatment or
prevent the development of type 1
diabetes and its complications. The
reserach proposals and the discussions
could disclose confidential trade secrets
or commercial property such as
patentable material, and personal
information concerning individuals
associated with the proposed research
projects, the disclosure of which would
constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Type 1 Diabetes—
Rapid Access to Intervention Development
Special Emphasis Panel, National Institute of
Diabetes and Digestive and Kidney Diseases.
Date: February 9, 2005.
Time: 10 a.m.–2 p.m.
Agenda: To evaluate requests for
preclinical development resources for
potential new therapeutics for type 1 diabetes
and its complications.
Place: 6707 Democracy Boulevard,
Bethesda, MD 20892. (Telephone conference
call.)
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National Institutes of Health
National Library of Medicine; Notice of
Meeting
Pursuant to section 10(a) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. Appendix 2), notice
is hereby given of the third meeting of
the Commission on Systemic
Interoperability.
The meeting will be open to the
public, with attendance limited to space
available. Individuals who plan to
attend and need special assistance, such
as sign language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the meeting.
The mission of the Commission on
Systemic Interoperability is to submit a
report to the Secretary of Health and
Human Services and to Congress on a
comprehensive strategy for the adoption
and implementation of health care
information technology standards that
includes a timeline and prioritization
for such adoption and implementation.
In developing that strategy, the
Commission will consider: (1) The costs
and benefits of the standards, both
financial impact and quality
improvement; (2) the current demand
on industry resources to implement the
Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 and other electronic standards,
including HIPAA standards; and (3) the
most cost-effective and efficient means
for industry to implement the standards.
Name of Committee: Commission on
Systemic Interoperability.
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Federal Register / Vol. 70, No. 23 / Friday, February 4, 2005 / Notices
Date: March 15, 2005.
Time: 8 a.m. to 4 p.m.
Agenda: Healthcare Information
Technology Standards.
Place: Hubert H. Humphrey Building,
Room 800, 200 Independence Avenue,
Washington, DC 20201.
Contact Person: Ms. Dana Haza, Director,
Commission on Systemic Interoperability,
National Library of Medicine, National
Institutes of Health, Building 38, Room 2N21,
Bethesda, MD 20894. (301) 594–7520.
Any interested person may file written
comments with the committee by forwarding
the statement to the Contact Person listed on
this notice. The comments should include
the name, address, telephone number and,
when applicable, the business or professional
affiliation of the interested person.
In the interest of security, HHS has
procedures for entrance into the building by
non-government employees. Persons without
a government I.D. will need to show a photo
I.D. at the security desk upon entering the
building.
Dated: January 28, 2005.
Anna Snouffer,
Deputy Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 05–2130 Filed 2–3–05; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Prospective Grant of Exclusive
License: Use of 3-deazaneplanocin A
and Cyclopentenyl Cytosine for the
Development of the Topical Treatment
of Basal Cell Carcinoma and Resistant
Herpes Simplex Virus Infections
National Institutes of Health,
Public Health Service, HHS.
ACTION: Notice.
AGENCY:
SUMMARY: This is notice, in accordance
with 35 U.S.C. 209(c)(1) and 37 CFR
404.7(a)(1)(i), that the National
Institutes of Health (NIH), Department
of Health and Human Services, is
contemplating the grant of a an
exclusive license to practice the
invention embodied in:
(1) U.S. Patent No. 4,968,690, issued
Nov. 6, 1990, entitled ‘‘3DEAZANEPLANOCIN A AND METHOD
OF PREPARATION’’ (E–493–1985/0–
US–02) (Inventors: Victor E. Marquez,
John S. Driscoll, Mu–III Lim,
Christopher K Tseng, Alberto Haces and
Robert Glazer) (NCI), a continuation of
prior application 867,583, filed May 27,
1986, now abandoned.
(2) U.S. Patent No. 4,975,434, issued
Dec. 4, 1990, entitled ‘‘ANTIVIRAL
AND ANTICANCER CYCLOPENTENYL
CYTOSINE’’ (E–493–1985/1–US–01)
(Inventors: Victor E. Marquez, John S.
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Driscoll, Mu–III Lim, Christopher K
Tseng, Alberto Haces and Robert Glazer)
(NCI), a continuation of prior
application 867,583, filed May 27, 1986,
now abandoned to GRX
Pharmaceuticals (hereafter GRX), having
a place of business in Marlboro, New
Jersey. The patent rights in these
inventions have been assigned to the
United States of America.
DATES: Only written comments and/or
application for a license, which are
received by the NIH Office of
Technology Transfer on or before April
5, 2005, will be considered.
ADDRESSES: Requests for a copy of the
patent application, inquiries, comments
and other materials relating to the
contemplated license should be directed
to: Sally Hu, Ph.D., M.B.A., Office of
Technology Transfer, National Institutes
of Health, 6011 Executive Boulevard,
Suite 325, Rockville, MD 20852–3804; email: hus@od.nih.gov; telephone: (301)
435–5606; Facsimile: (301) 402–0220.
SUPPLEMENTARY INFORMATION: The
technology described in E–493–1985/0–
US–02 relates to antiviral and cancer
chemotherapy and, more particularly, to
the compound 3-deazaneplanocin A and
related compounds and a method of
preparation thereof, as well as the
methods of preparation of a great variety
of unsaturated (cyclopentenyl)
carbocyclic nucleosides.
The technology described in E–493–
1985/1–US–01 relates to antiviral and
cancer chemotherapy and, more
particularly, to cyclopentenyl
pyrimidines which can be used for
antiviral and cancer chemotherapy, as
well as to methods of preparation of
these compounds.
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. The prospective
exclusive license may be granted unless,
within 60 days from the date of this
published Notice, NIH receives written
evidence and argument that establishes
that the grant of the license would not
be consistent with the requirements of
35 U.S.C. 209 and 37 CFR 404.7.
The field of use may be limited to the
development of the topical treatment of
basal cell carcinoma and resistant
herpes simplex virus infections.
Properly filed competing applications
for a license filed in response to this
notice will be treated as objections to
the contemplated license. 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.
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Dated: January 21, 2005.
Mark L. Rohrbaugh,
Director, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. 05–2126 Filed 2–3–05; 8:45 am]
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DEPARTMENT OF HOMELAND
SECURITY
Construction and Operation of the
National Biodefense Analysis and
Countermeasures Center (NBACC)
Facility by the Department of
Homeland Security at Fort Detrick,
Maryland: Record of Decision
Science and Technology
Directorate, Department of Homeland
Security.
AGENCY:
ACTION:
Notice.
SUMMARY: In keeping with the purposes
of the National Environmental Policy
Act (NEPA), the Department of
Homeland Security (DHS), in
cooperation with the United States
Army Garrison, Fort Detrick, decided on
January 26, 2005, after completion of the
Final Environmental Impact Statement
(FEIS) and a thorough consideration of
public comments, to implement the
Preferred Alternative in the FEIS. This
action involves the construction and
operation of the National Biodefense
Analysis and Countermeasures Center
Facility by DHS on a site adjacent to
existing U.S. Army Medical Research
Institute of Infectious Diseases facilities
at Fort Detrick, Maryland. The notice of
availability of the Draft Environmental
Impact Statement is at 69 FR 56075 and
the notice of intent to prepare an
Environmental Impact Statement is at
69 FR 31830.
Copies of the Final EIS and
this Record of Decision may be obtained
by calling or mailing a request to: Dr.
Kevin Anderson, Department of
Homeland Security, 7435 New
Technology Way, Suite A, Frederick,
Maryland, 21703, by telephone (301)
846–2156, fax (301) 682–3662 or e-mail
kevin.anderson@dhs.gov. The Final EIS
and this Record of Decision are
available at https://
www.detrick.army.mil/.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Questions regarding the Final EIS or this
Record of Decision can be submitted by
calling or mailing them to Dr. Kevin
Anderson at the above phone number or
address.
SUPPLEMENTARY INFORMATION:
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Agencies
[Federal Register Volume 70, Number 23 (Friday, February 4, 2005)]
[Notices]
[Pages 6025-6026]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-2130]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
National Library of Medicine; Notice of Meeting
Pursuant to section 10(a) of the Federal Advisory Committee Act, as
amended (5 U.S.C. Appendix 2), notice is hereby given of the third
meeting of the Commission on Systemic Interoperability.
The meeting will be open to the public, with attendance limited to
space available. Individuals who plan to attend and need special
assistance, such as sign language interpretation or other reasonable
accommodations, should notify the Contact Person listed below in
advance of the meeting.
The mission of the Commission on Systemic Interoperability is to
submit a report to the Secretary of Health and Human Services and to
Congress on a comprehensive strategy for the adoption and
implementation of health care information technology standards that
includes a timeline and prioritization for such adoption and
implementation. In developing that strategy, the Commission will
consider: (1) The costs and benefits of the standards, both financial
impact and quality improvement; (2) the current demand on industry
resources to implement the Medicare Prescription Drug, Improvement, and
Modernization Act of 2003 and other electronic standards, including
HIPAA standards; and (3) the most cost-effective and efficient means
for industry to implement the standards.
Name of Committee: Commission on Systemic Interoperability.
[[Page 6026]]
Date: March 15, 2005.
Time: 8 a.m. to 4 p.m.
Agenda: Healthcare Information Technology Standards.
Place: Hubert H. Humphrey Building, Room 800, 200 Independence
Avenue, Washington, DC 20201.
Contact Person: Ms. Dana Haza, Director, Commission on Systemic
Interoperability, National Library of Medicine, National Institutes
of Health, Building 38, Room 2N21, Bethesda, MD 20894. (301) 594-
7520.
Any interested person may file written comments with the
committee by forwarding the statement to the Contact Person listed
on this notice. The comments should include the name, address,
telephone number and, when applicable, the business or professional
affiliation of the interested person.
In the interest of security, HHS has procedures for entrance
into the building by non-government employees. Persons without a
government I.D. will need to show a photo I.D. at the security desk
upon entering the building.
Dated: January 28, 2005.
Anna Snouffer,
Deputy Director, Office of Federal Advisory Committee Policy.
[FR Doc. 05-2130 Filed 2-3-05; 8:45 am]
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