Office of the Director, National Institutes of Health; Amended Notice-Request for Public Comment, 14705-14706 [05-5671]
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Federal Register / Vol. 70, No. 55 / Wednesday, March 23, 2005 / Notices
Time: 8:30 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Jury’s Washington Hotel, 1500 New
Hampshire Avenue, NW., Washington, DC
20036.
Contact Person: Gayle M. Boyd, PhD,
Scientific Review Administrator, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3028–D,
MSC 7759, Bethesda, MD 20892, 301–451–
9956. gboyd@mail.nih.gov.
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.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Skeletal
Biological Pilot/Feasibility, AREA and Small
Grant Group 2.
Date: April 6, 2005.
Time: 8 a.m. to 8 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Virtual Meeting).
Contact Person: Daniel F. McDonald, PhD,
Chief, Renal and Urological Sciences IRG,
Center for Scientific Review, National
Institutes of Health, 6701 Rockledge Drive,
Room 4214, MSC 7814, Bethesda, MD 20892.
(301) 435–1215, mcdonald@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel,
Preadolescent Exposure to Tobacco Smoke.
Date: April 6, 2005.
Time: 9:30 a.m. to 10:30 a.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Gayle M. Boyd, PhD,
Scientific Review Administrator, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3028–D,
MSC 7759, Bethesda, MD 20892, 301–451–
9956. gboyd@mail.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Skin
Mutagenesis.
Date: April 7, 2005.
Time: 2 p.m. to 4 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Syed M. Quadri, PhD,
Scientific Review Administrator, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 6210,
MSC 7804, Bethesda, MD 20892, (301) 435–
1211. quadris@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Skeletal
Biology Pilot/Feasibility, AREA and Small
Grant Group 1.
Date: April 8, 2005.
Time: 8 a.m. to 8 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
VerDate jul<14>2003
19:44 Mar 22, 2005
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Contact Person: Daniel F. McDonald, PhD,
Chief, Renal and Urological Sciences IRG,
Center for Scientific Review, National
Institutes of Health, 6701 Rockledge Drive,
Room 4214, MSC 7814, Bethesda, MD 20892,
(301) 435–1215,mcdonald@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Disease
Recovery.
Date: April 8, 2005.
Time: 2 p.m. to 3 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Karen Lechter, PhD,
Scientific Review Administrator, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3128,
MSC 7759, Bethesda, MD 20892, (301) 496–
0726, lechterk@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Arial
Remodeling.
Date: April 18, 2005.
Time: 1 p.m. to 2 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Ai-Ping Zou, PhD, MD,
Scientific Review Administrator, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4118,
MSC 7814, Bethesda, MD 20892, (301) 435–
1777, zouai@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, 3D
Morphometry.
Date: April 19, 2005.
Time: 2:30 p.m. to 3:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Russell T. Dowell, PhD,
Scientific Review Administrator, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4128,
MSC 7814, Bethesda, MD 20892, (301) 435–
1850, dowellr@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Renal
Related Sciences.
Date: April 19, 2005.
Time: 12 p.m. to 1:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: M. Chris Langub, PhD,
Scientific Review Administrator, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4112,
MSC 7814, Bethesda, MD 20892, (301) 496–
8551, langubm@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Renal and
Urology Member Conflict.
Date: April 22, 2005.
Time: 2 p.m. to 4 p.m.
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Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Shirley Hilden, PhD,
Scientific Review Administrator, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4218,
MSC 7814, Bethesda, MD 20892, (301) 435–
1198, hildens@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Fatty Acids
and Colon Tumorigenesis.
Date: April 25, 2005.
Time: 11 a.m. to 12 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Angela Y. Ng, PhD, MBA,
Scientific Review Administrator, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 6200,
MSC 7804, (for courier delivery, use MD
20817), Bethesda, MD 20892, 301–435–1715,
nga@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Small
Business Orthopedic Medicine Applications.
Date: April 26–27, 2005.
Time: 6 p.m. to 4 p.m.
Agenda: To review and evaluate grant
applications.
Place: Wyndham Washington, DC, 1400 M
Street, NW., Washington, DC 20005.
Contact Person: Richard J. Bartlett, PhD,
Scientific Review Administrator, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4110,
MSC 7814, Bethesda, MD 20892, 301–435–
6809, bartletr@csr.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: March 16, 2005.
LaVerne Y. Stringfield,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 05–5672 Filed 3–22–05; 8:45 am]
BILLING CODE 4140–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Office of the Director, National
Institutes of Health; Amended Notice—
Request for Public Comment
Notice is hereby given of a change in
the submission date of public
comments. Comments will be accepted
until April 10, 2005, instead of March
31, 2005, as published in the Federal
Register on March 9, 2005, 70 FR 4568.
The Secretary’s Advisory Committee
on Xenotransplantation (SACX) is
E:\FR\FM\23MRN1.SGM
23MRN1
14706
Federal Register / Vol. 70, No. 55 / Wednesday, March 23, 2005 / Notices
requesting public comment on two draft
reports on xenotransplantation. One is
on the state of the science of
xenotransplantation and the other is on
informed consent issued in clinical
trials involving xenotransplantation.
Before the reports are finalized and
transmitted to the Secretary, the SACX
is requesting comments on the draft
reports from members of the public. All
public comments received will be
considered in finalizing the reports.
Comments should be submitted by
March 31, 2005 [amended to April 10,
2005]. Received comments will be
available for public inspection at the
NIH Office of Biotechnology Activities,
Monday through Friday between the
hours of 8:30 a.m. and 5 p.m., at the
contact address noted below.
Information: The Secretary’s Advisory
Committee on Xenotransplantation,
Department of Health and Human
Services, considers the scientific,
medical, social, and ethical issues and
the public health concerns raised by
xenotransplantation and makes
recommendations to the Secretary on
policy and procedures. The Committee’s
charges include advising on the current
state of knowledge regarding
xenotransplantation and on the
potential for transmission of infectious
diseases as a consequence of
xenotransplantation; and deliberating
on medical, public health, ethical, legal
and socioeconomic issues, including
international policies and developments
that are relevant to xenotransplantation.
Overview of Drafts: The state of the
science report addresses the scientific
challenges in xenotransplantation, the
infectious disease risks associated with
xenotransplantation, public health
concerns associated with xenotourism,
knowledge gaps and resource
limitations, and alternative strategies to
xenotransplantation. The report also
proposes a series of recommendations
regarding these issues.
The report on informed consent issues
in clinical research involving
xenotransplantation addresses the
ethical foundations and functions of
informed consent, components of
informed consent, the informed consent
process, informed consent forms, and
special issues raised by
xenotransplantation. The report
proposes a series of recommendations
regarding informed consent in
xenotransplantation research.
A full draft reports are available
electronically at https://
www4.od.nih.gov/oba/Sacx.htm. A
paper or electronic copy can also be
requested by calling the NIH Office of
Biotechnology Activities at (301) 496–
VerDate jul<14>2003
17:54 Mar 22, 2005
Jkt 205001
9838 or by e-mailing Marcy Groesch at
groeschm@od.nih.gov.
Contact Person: March Groesch,
Executive Director, Secretary’s Advisory
Committee on Xenotransplantation,
Office of Biotechnology Activities,
Rockledge I, Room 750, Bethesda, MD
20892, (301) 496–9838.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.14, Intramural Research
Training Award; 93.187, Undergraduate
Scholarship Program for Individuals from
Disadvantages Backgrounds; 93.22, Clinical
Research Loan Repayment Program for
Individuals from Disadvantaged
Backgrounds; 93.232, Loan Repayment
Program for Research Generally; 93.39,
Academic Research Enhancement Award;
93.936, NIH Acquired Immunodeficiency
Syndrome Research Loan Repayment
Program, National Institutes of Health, HHS)
Dated: March 16, 2005.
LaVerne Y. Stringfield,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 05–5671 Filed 3–22–05; 8:45 am]
BILLING CODE 4140–01–M
DEPARTMENT OF HOMELAND
SECURITY
Citizenship and Immigration Services
Agency Information Collection
Activities: Extension of a Currently
Approved Information Collection;
Comments Request
30-Day Notice of Information
Collection Under Review: Application
for Status as Temporary Resident under
Section 245A of the Immigration and
Nationality Act, Form I–687.
ACTION:
The Department of Homeland
Security, U.S. Citizenship and
Immigration Services (USCIS) has
submitted the following information
collection request to the Office of
Management and Budget (OMB) for
review and clearance in accordance
with the Paperwork Reduction Act of
1995. The information collection was
previously published in the Federal
Register on March 24, 2004 at 69 FR
13865, allowed for a 60-day public
comment period. The USCIS did not
receive any comments on this
information collection.
The purpose of this notice is to allow
an additional 30 days for public
comments. Comments are encouraged
and will be accepted until April 22,
2005. This process is conducted in
accordance with 5 CFR 1320.10.
Written comments and suggestions
from the public and affected agencies
concerning the collection of information
PO 00000
Frm 00072
Fmt 4703
Sfmt 4703
should address one or more of the
following points:
(1) Evaluate whether the collection of
information is necessary for the proper
performance of the functions of the
agency, including whether the
information will have practical utility;
(2) Evaluate the accuracy of the
agency’s estimate of the burden of the
collection of information, including the
validity of the methodology and
assumptions used;
(3) Enhance the quality, utility, and
clarity of the information to be
collected; and
(4) Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques, or
other forms of information technology,
e.g., permitting electronic submission of
responses.
Overview of this information
collection:
(1) Type of Information Collection:
Extension of a currently approved
collection.
(2) Title of the Form/Collection:
Application for Status as Temporary
Resident under Section 245A of the
Immigration and Nationality Act.
(3) Agency Form Number, if Any, and
the Applicable Component of the
Department of Homeland Security
Sponsoring the Collection: Form I–687.
U.S. Citizenship and Immigration
Services.
(4) Affected Public Who Will be Asked
or Required to Respond, as Well as a
Brief Abstract: Primary: Individuals and
Households. The collection of
information on Form I–687 is required
to verify the applicant’s eligibility for
temporary status, and if the applicant is
deemed eligible, to grant him or her the
benefit sought.
(5) An Estimate of the Total Number
of Respondents and the Amount of Time
Estimated for an Average Respondent to
Respond: 100,000 responses at 1 hour
and 10 minutes (1.16 hours) per
response.
(6) An Estimate of the Total Public
Burden (in Hours) Associated With the
Collection: 116,000 annual burden
hours.
If you have comments, suggestions, or
need a copy of the information
collection instrument, please contact
Richard A. Sloan, Director, Regulatory
Management Division, Department of
Homeland Security, 111 Massachusetts
Avenue, NW., Washington, DC 20529;
202–272–8377.
E:\FR\FM\23MRN1.SGM
23MRN1
Agencies
[Federal Register Volume 70, Number 55 (Wednesday, March 23, 2005)]
[Notices]
[Pages 14705-14706]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-5671]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Office of the Director, National Institutes of Health; Amended
Notice--Request for Public Comment
Notice is hereby given of a change in the submission date of public
comments. Comments will be accepted until April 10, 2005, instead of
March 31, 2005, as published in the Federal Register on March 9, 2005,
70 FR 4568.
The Secretary's Advisory Committee on Xenotransplantation (SACX) is
[[Page 14706]]
requesting public comment on two draft reports on xenotransplantation.
One is on the state of the science of xenotransplantation and the other
is on informed consent issued in clinical trials involving
xenotransplantation.
Before the reports are finalized and transmitted to the Secretary,
the SACX is requesting comments on the draft reports from members of
the public. All public comments received will be considered in
finalizing the reports. Comments should be submitted by March 31, 2005
[amended to April 10, 2005]. Received comments will be available for
public inspection at the NIH Office of Biotechnology Activities, Monday
through Friday between the hours of 8:30 a.m. and 5 p.m., at the
contact address noted below.
Information: The Secretary's Advisory Committee on
Xenotransplantation, Department of Health and Human Services, considers
the scientific, medical, social, and ethical issues and the public
health concerns raised by xenotransplantation and makes recommendations
to the Secretary on policy and procedures. The Committee's charges
include advising on the current state of knowledge regarding
xenotransplantation and on the potential for transmission of infectious
diseases as a consequence of xenotransplantation; and deliberating on
medical, public health, ethical, legal and socioeconomic issues,
including international policies and developments that are relevant to
xenotransplantation.
Overview of Drafts: The state of the science report addresses the
scientific challenges in xenotransplantation, the infectious disease
risks associated with xenotransplantation, public health concerns
associated with xenotourism, knowledge gaps and resource limitations,
and alternative strategies to xenotransplantation. The report also
proposes a series of recommendations regarding these issues.
The report on informed consent issues in clinical research
involving xenotransplantation addresses the ethical foundations and
functions of informed consent, components of informed consent, the
informed consent process, informed consent forms, and special issues
raised by xenotransplantation. The report proposes a series of
recommendations regarding informed consent in xenotransplantation
research.
A full draft reports are available electronically at https://
www4.od.nih.gov/oba/Sacx.htm. A paper or electronic copy can also be
requested by calling the NIH Office of Biotechnology Activities at
(301) 496-9838 or by e-mailing Marcy Groesch at groeschm@od.nih.gov.
Contact Person: March Groesch, Executive Director, Secretary's
Advisory Committee on Xenotransplantation, Office of Biotechnology
Activities, Rockledge I, Room 750, Bethesda, MD 20892, (301) 496-9838.
(Catalogue of Federal Domestic Assistance Program Nos. 93.14,
Intramural Research Training Award; 93.187, Undergraduate
Scholarship Program for Individuals from Disadvantages Backgrounds;
93.22, Clinical Research Loan Repayment Program for Individuals from
Disadvantaged Backgrounds; 93.232, Loan Repayment Program for
Research Generally; 93.39, Academic Research Enhancement Award;
93.936, NIH Acquired Immunodeficiency Syndrome Research Loan
Repayment Program, National Institutes of Health, HHS)
Dated: March 16, 2005.
LaVerne Y. Stringfield,
Director, Office of Federal Advisory Committee Policy.
[FR Doc. 05-5671 Filed 3-22-05; 8:45 am]
BILLING CODE 4140-01-M