Public Meeting of the President's Council on Bioethics, 31692 [E8-12344]
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31692
Federal Register / Vol. 73, No. 107 / Tuesday, June 3, 2008 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Public Meeting of the President’s
Council on Bioethics
Department of Health and
Human Services, Office of Public Health
and Science, The President’s Council on
Bioethics.
ACTION: Notice.
AGENCY:
SUMMARY: The President’s Council on
Bioethics (Edmund D. Pellegrino, MD,
Chairman) will hold its thirty-third
meeting, at which it will discuss its
projected White Paper on newborn
screening and hear and discuss
presentations on the ethics of health
care reform. Subjects discussed at past
Council meetings (although not on the
agenda for the June 2008 meeting)
include: therapeutic and reproductive
cloning, assisted reproduction,
reproductive genetics, neuroscience,
aging retardation, organ transplantation,
personalized medicine, and lifespan
extension. Publications issued by the
Council to date include: Human Cloning
and Human Dignity: An Ethical Inquiry
(July 2002); Beyond Therapy:
Biotechnology and the Pursuit of
Happiness (October 2003); Being
Human: Readings from the President’s
Council on Bioethics (December 2003);
Monitoring Stem Cell Research (January
2004), Reproduction and Responsibility:
The Regulation of New Biotechnologies
(March 2004), Alternative Sources of
Human Pluripotent Stem Cells: A White
Paper (May 2005), Taking Care: Ethical
Caregiving in Our Aging Society
(September 2005), and Human Dignity
and Bioethics: Essays Commissioned by
the President’s Council on Bioethics
(March 2008). Reports on controversies
in the determination of death and on
organ donation, procurement,
allocation, and transplantation are
forthcoming.
The meeting will take place
Thursday, June 26, 2008, from 9 a.m. to
5 p.m. (CT); and Friday, June 27, 2008,
from 9 a.m. to 11:15 a.m. (CT).
ADDRESSES: Courtyard Marriott
Magnificent Mile, 165 East Ontario
Street, Chicago, IL 60611. Phone 312–
573–0800.
FOR FURTHER INFORMATION CONTACT: Ms.
Diane M. Gianelli, Director of
Communications, The President’s
Council on Bioethics, 1425 New York
Avenue, NW., Suite C100, Washington,
DC 20005. Telephone: 202/296–4669; email: info@bioethics.gov; Web site:
https://www.bioethics.gov.
SUPPLEMENTARY INFORMATION: The
meeting agenda will be posted at
ebenthall on PRODPC60 with NOTICES
DATES:
VerDate Aug<31>2005
14:18 Jun 02, 2008
Jkt 214001
https://www.bioethics.gov. The Council
encourages public input, either in
person or in writing. At this meeting,
interested members of the public may
address the Council, beginning at 11
a.m. (CT), on Friday, June 27. Comments
are limited to no more than five minutes
per speaker or organization. As a
courtesy, please inform Ms. Diane M.
Gianelli, Director of Communications,
in advance of your intention to make a
public statement, and give your name
and affiliation. To submit a written
statement, mail or e-mail it to Ms.
Gianelli at one of her contact addresses
given above.
Dated: May 22, 2008.
F. Daniel Davis,
Executive Director, The President’s Council
on Bioethics.
[FR Doc. E8–12344 Filed 6–2–08; 8:45 am]
BILLING CODE 4154–06–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2008–N–0313]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Requests for
Inspection Under the Inspection by
Accredited Persons Program
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the eligibility criteria and the process to
be followed by establishments when
requesting FDA’s approval to have an
accredited third party conduct a quality
systems regulation inspection of their
establishment instead of FDA, under the
new inspections by the Accredited
Persons Program.
DATES: Submit written or electronic
comments on the collection of
information by August 4, 2008.
ADDRESSES: Submit electronic
comments on the collection of
information to https://
PO 00000
Frm 00020
Fmt 4703
Sfmt 4703
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, M20852. All comments
should be identified with the docket
number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Denver Presley, Jr., Office of the Chief
Information Officer (HFA–250), Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301 827–
1472.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
Requests for Inspection Under the
Inspection by Accredited Persons
Program—21 U.S.C. 374(g) (OMB
Control Number 0910–0569)—Extension
Section 201 of the Medical Device
User Fee and Modernization Act of
2002, (Public Law 107–250), amended
section 704 of the Federal Food, Drug,
E:\FR\FM\03JNN1.SGM
03JNN1
Agencies
[Federal Register Volume 73, Number 107 (Tuesday, June 3, 2008)]
[Notices]
[Page 31692]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-12344]
[[Page 31692]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Public Meeting of the President's Council on Bioethics
AGENCY: Department of Health and Human Services, Office of Public
Health and Science, The President's Council on Bioethics.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The President's Council on Bioethics (Edmund D. Pellegrino,
MD, Chairman) will hold its thirty-third meeting, at which it will
discuss its projected White Paper on newborn screening and hear and
discuss presentations on the ethics of health care reform. Subjects
discussed at past Council meetings (although not on the agenda for the
June 2008 meeting) include: therapeutic and reproductive cloning,
assisted reproduction, reproductive genetics, neuroscience, aging
retardation, organ transplantation, personalized medicine, and lifespan
extension. Publications issued by the Council to date include: Human
Cloning and Human Dignity: An Ethical Inquiry (July 2002); Beyond
Therapy: Biotechnology and the Pursuit of Happiness (October 2003);
Being Human: Readings from the President's Council on Bioethics
(December 2003); Monitoring Stem Cell Research (January 2004),
Reproduction and Responsibility: The Regulation of New Biotechnologies
(March 2004), Alternative Sources of Human Pluripotent Stem Cells: A
White Paper (May 2005), Taking Care: Ethical Caregiving in Our Aging
Society (September 2005), and Human Dignity and Bioethics: Essays
Commissioned by the President's Council on Bioethics (March 2008).
Reports on controversies in the determination of death and on organ
donation, procurement, allocation, and transplantation are forthcoming.
DATES: The meeting will take place Thursday, June 26, 2008, from 9 a.m.
to 5 p.m. (CT); and Friday, June 27, 2008, from 9 a.m. to 11:15 a.m.
(CT).
ADDRESSES: Courtyard Marriott Magnificent Mile, 165 East Ontario
Street, Chicago, IL 60611. Phone 312-573-0800.
FOR FURTHER INFORMATION CONTACT: Ms. Diane M. Gianelli, Director of
Communications, The President's Council on Bioethics, 1425 New York
Avenue, NW., Suite C100, Washington, DC 20005. Telephone: 202/296-4669;
e-mail: info@bioethics.gov; Web site: https://www.bioethics.gov.
SUPPLEMENTARY INFORMATION: The meeting agenda will be posted at https://
www.bioethics.gov. The Council encourages public input, either in
person or in writing. At this meeting, interested members of the public
may address the Council, beginning at 11 a.m. (CT), on Friday, June 27.
Comments are limited to no more than five minutes per speaker or
organization. As a courtesy, please inform Ms. Diane M. Gianelli,
Director of Communications, in advance of your intention to make a
public statement, and give your name and affiliation. To submit a
written statement, mail or e-mail it to Ms. Gianelli at one of her
contact addresses given above.
Dated: May 22, 2008.
F. Daniel Davis,
Executive Director, The President's Council on Bioethics.
[FR Doc. E8-12344 Filed 6-2-08; 8:45 am]
BILLING CODE 4154-06-P