President's Committee for People With Intellectual Disabilities: Notice of Meeting, 13406 [E6-3642]
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13406
Federal Register / Vol. 71, No. 50 / Wednesday, March 15, 2006 / Notices
document in the Federal Register.
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comments and recomendations for the
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be sent directly to the following: Office
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ACF, E-mail address:
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Dated: March 8, 2006.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 06–2453 Filed 3–14–06; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
President’s Committee for People With
Intellectual Disabilities: Notice of
Meeting
AGENCY: President’s Committee for
People with Intellectual Disabilities
(PCPID), Administration for Children
and Families, HHS.
ACTION: Notice of meeting.
The meeting will be held on
Friday, March 24, 2006, from 3 p.m. to
5 p.m. Eastern Daylight Savings Time.
The full committee meeting of PCPID
will be conducted by telephone
conference call and will be open to the
public. Anyone interested in
participating in the conference call
should advise Ericka Alston at 202–
619–0634, no later than March 17, 2006.
ADDRESSES: The conference call may be
accessed by dialing, U.S. toll-free 1–
888–395–6878, and the passcode
‘‘March 2006’’ on the date and time
indicated.
SUMMARY: Pursuant to Section 10(a) of
the Federal Advisory Committee Act as
amended (5 U.S.C. Appendix 2) notice
is hereby given that the President’s
Committee for People with Intellectual
Disabilities will hold its first quarterly
meeting of 2006 by telephone
conference call. The conference call will
be open to the public to listen, with callins limited to the number of telephone
lines available. Individuals who plan to
call in and need special assistance, such
as TTY, assistive listening devices, or
materials in alternative format, should
inform Ericka Alston, Executive
Assistant, PCPID, Telephone—202–619–
0634, Fax—202–205–9519, E-mail:
ealston@acf.hhs.gov, no later than
March 10, 2006. Efforts will be made to
meet special requests received after that
sroberts on PROD1PC70 with NOTICES
DATES:
VerDate Aug<31>2005
17:27 Mar 14, 2006
Jkt 208001
date, but availability of special needs
accommodations to respond to these
requests cannot be guaranteed.
AGENDA: Committee members will be
briefed on the outcome of the March 22,
2006 Roundtable on Personal and
Economic Freedom for People with
Intellectual Disabilities: An Exploration
of Asset Development for People with
Intellectual Disabilities that will be
jointly sponsored by PCPID, the
Administration for Children and
Families’ Office of Community Services,
and the U.S. Department of Health and
Human Services’ Office of the Assistant
Secretary for Planning and Evaluation
(ASPE).
FOR FURTHER INFORMATION CONTACT:
Sally Atwater, Executive Director,
President’s Committee for People with
Intellectual Disabilities, Aerospace
Center Office Building, Suite 701, 901 D
Street, SW., Washington, DC 20447,
Telephone—202–619–0634, Fax—202–
205–9519, E-mail: satwater@acf.hhs.gov.
SUPPLEMENTARY INFORMATION: PCPID
acts in an advisory capacity to the
President and the Secretary of Health
and Human Services on a broad range
of topics relating to programs, services
and supports for persons with
intellectual disabilities. The Committee,
by Executive Order, is responsible for
evaluating the adequacy of current
practices in programs, services and
supports for persons with intellectual
disabilities, and for reviewing legislative
proposals that impact the quality of life
experienced by citizens with
intellectual disabilities and their
families.
Dated: March 1, 2006.
Sally Atwater,
Executive Director, President’s Committee for
People with Intellectual Disabilities.
[FR Doc. E6–3642 Filed 3–14–06; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2005E–0256]
Determination of Regulatory Review
Period for Purposes of Patent
Extension; OVIDREL
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) has determined
the regulatory review period for
OVIDREL and is publishing this notice
of that determination as required by
PO 00000
Frm 00075
Fmt 4703
Sfmt 4703
law. FDA has made the determination
because of the submission of an
application to the Director of Patents
and Trademarks, Department of
Commerce, for the extension of a patent
which claims that human drug product.
ADDRESSES: Submit written comments
and petitions to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. Submit
electronic comments to https://
www.fda.gov/dockets/ecomments.
FOR FURTHER INFORMATION CONTACT:
Claudia V. Grillo, Office of Regulatory
Policy (HFD–013), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 240–453–6681.
SUPPLEMENTARY INFORMATION: The Drug
Price Competition and Patent Term
Restoration Act of 1984 (Public Law 98–
417) and the Generic Animal Drug and
Patent Term Restoration Act (Public
Law 100–670) generally provide that a
patent may be extended for a period of
up to 5 years so long as the patented
item (human drug product, animal drug
product, medical device, food additive,
or color additive) was subject to
regulatory review by FDA before the
item was marketed. Under these acts, a
product’s regulatory review period
forms the basis for determining the
amount of extension an applicant may
receive.
A regulatory review period consists of
two periods of time: A testing phase and
an approval phase. For human drug
products, the testing phase begins when
the exemption to permit the clinical
investigations of the drug becomes
effective and runs until the approval
phase begins. The approval phase starts
with the initial submission of an
application to market the human drug
product and continues until FDA grants
permission to market the drug product.
Although only a portion of a regulatory
review period may count toward the
actual amount of extension that the
Director of Patents and Trademarks may
award (for example, half the testing
phase must be subtracted, as well as any
time that may have occurred before the
patent was issued), FDA’s determination
of the length of a regulatory review
period for a human drug product will
include all of the testing phase and
approval phase as specified in 35 U.S.C.
156(g)(1)(B).
FDA recently approved for marketing
the human drug product OVIDREL
(choriogonadotropin alfa for injection).
OVIDREL is indicated for the induction
of final follicular maturation and early
luteinization in infertile women who
have undergone pituitary
desensitization and who have been
E:\FR\FM\15MRN1.SGM
15MRN1
]]>Agencies
[Federal Register Volume 71, Number 50 (Wednesday, March 15, 2006)]
[Notices]
[Page 13406]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-3642]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
President's Committee for People With Intellectual Disabilities:
Notice of Meeting
AGENCY: President's Committee for People with Intellectual Disabilities
(PCPID), Administration for Children and Families, HHS.
ACTION: Notice of meeting.
-----------------------------------------------------------------------
DATES: The meeting will be held on Friday, March 24, 2006, from 3 p.m.
to 5 p.m. Eastern Daylight Savings Time. The full committee meeting of
PCPID will be conducted by telephone conference call and will be open
to the public. Anyone interested in participating in the conference
call should advise Ericka Alston at 202-619-0634, no later than March
17, 2006.
ADDRESSES: The conference call may be accessed by dialing, U.S. toll-
free 1-888-395-6878, and the passcode ``March 2006'' on the date and
time indicated.
SUMMARY: Pursuant to Section 10(a) of the Federal Advisory Committee
Act as amended (5 U.S.C. Appendix 2) notice is hereby given that the
President's Committee for People with Intellectual Disabilities will
hold its first quarterly meeting of 2006 by telephone conference call.
The conference call will be open to the public to listen, with call-ins
limited to the number of telephone lines available. Individuals who
plan to call in and need special assistance, such as TTY, assistive
listening devices, or materials in alternative format, should inform
Ericka Alston, Executive Assistant, PCPID, Telephone--202-619-0634,
Fax--202-205-9519, E-mail: ealston@acf.hhs.gov, no later than March 10,
2006. Efforts will be made to meet special requests received after that
date, but availability of special needs accommodations to respond to
these requests cannot be guaranteed.
Agenda: Committee members will be briefed on the outcome of the March
22, 2006 Roundtable on Personal and Economic Freedom for People with
Intellectual Disabilities: An Exploration of Asset Development for
People with Intellectual Disabilities that will be jointly sponsored by
PCPID, the Administration for Children and Families' Office of
Community Services, and the U.S. Department of Health and Human
Services' Office of the Assistant Secretary for Planning and Evaluation
(ASPE).
FOR FURTHER INFORMATION CONTACT: Sally Atwater, Executive Director,
President's Committee for People with Intellectual Disabilities,
Aerospace Center Office Building, Suite 701, 901 D Street, SW.,
Washington, DC 20447, Telephone--202-619-0634, Fax--202-205-9519, E-
mail: satwater@acf.hhs.gov.
SUPPLEMENTARY INFORMATION: PCPID acts in an advisory capacity to the
President and the Secretary of Health and Human Services on a broad
range of topics relating to programs, services and supports for persons
with intellectual disabilities. The Committee, by Executive Order, is
responsible for evaluating the adequacy of current practices in
programs, services and supports for persons with intellectual
disabilities, and for reviewing legislative proposals that impact the
quality of life experienced by citizens with intellectual disabilities
and their families.
Dated: March 1, 2006.
Sally Atwater,
Executive Director, President's Committee for People with Intellectual
Disabilities.
[FR Doc. E6-3642 Filed 3-14-06; 8:45 am]
BILLING CODE 4184-01-P
