38688 Federal Register / Vol. 70, No.
127 / Tuesday, July 5, 2005 / Notices
in the GPD 2.04 [http://198.102.218.46/
doc/gpd204.doc]. The application
review will be performed by CDC
employees within the agency’s CIOs. In
addition, the following factors may
affect the funding decision:
(a) Funding preference will be given
to organizations that have a recent
history of collaborating with the CDC on
public health student training programs.
(b) Preference will be given to
institutions with at least a five-year
track record of implementing public
health internship and fellowship
programs for minority students.
(c) Funding preference will be given
to institutions that have appropriate
staff expertise and other sources of
support for implementing public health
internship and/or fellowship programs.
(d) At least one organization will be
funded from each academic group (i.e.,
HBCU, HSI/HSHPS, TCU).
CDC will provide justification for any
decision to fund out of rank order.
V.3. Anticipated Announcement and
Award Dates
Anticipated Award Date: August 31,
2005.
VI. Award Administration Information
VI.1. Award Notices
Successful applicants will receive a
Notice of Award (NoA) from the CDC
Procurement and Grants Office. The
NoA shall be the only binding,
authorizing document between the
recipient and CDC. The NoA will be
signed by an authorized Grants
Management Officer, and mailed to the
recipient fiscal officer identified in the
application.
Unsuccessful applicants will receive
notification of the results of the
application review by mail.
VI.2. Administrative and National
Policy Requirements
Successful applicants must comply
with the administrative requirements
outlined in 45 CFR Part 74 and Part 92
as Appropriate. For more information
on the Code of Federal Regulations, see
the National Archives and Records
Administration at the following Internet
address: http://www.access.gpo.gov/
nara/cfr/cfr-table-search.html.
An additional Certifications form
from the PHS5161-1 application needs
to be included in your Grants.gov
electronic submission only. Refer to
http://www.cdc.gov/od/pgo/funding/
PHS5161–1 Certificates.pdf. Once the
form is filled out attach it to your
Grants.gov submission as Other
Attachments Form.
The following additional
requirements apply to this project:
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• AR–7 Executive Order 12372
• AR–10 Smoke-Free Workplace
Requirements
• AR–11 Healthy People 2010
• AR–12 Lobbying Restrictions
• AR–15 Proof of Non-Profit Status
• AR–16 Security Clearance
Requirement
• AR–21 Small, Minority, and
Women-Owned Business
Additional information on these
requirements can be found on the CDC
web site at the following Internet
address: http://www.cdc.gov/od/pgo/
funding/ARs.htm.
VI.3. Reporting Requirements
You must provide CDC with an
original, plus two hard copies of the
following reports:
1. Interim progress report, due no less
than 90 days before the end of the
budget period. The progress report will
serve as your non-competing
continuation application, and must
contain the following elements:
a. Current Budget Period Activities
Objectives.
b. Current Budget Period Financial
Progress.
c. New Budget Period Program
Proposed Activity Objectives.
d. Budget.
e. Measures of Effectiveness.
f. Additional Requested Information.
2. Annual progress report, due 90
days after the end of the budget period.
3. Financial status report due no more
than 90 days after the end of the budget
period.
4. Final financial and performance
reports, no more than 90 days after the
end of the project period.
These reports must be mailed to the
Grants Management or Contract
Specialist listed in the ‘‘Agency
Contacts’’ section of this announcement.
VII. Agency Contacts
We encourage inquiries concerning
this announcement.
For general questions, contact:
Technical Information Management
Section, CDC Procurement and Grants
Office, 2920 Brandywine Road, Atlanta,
GA 30341. Telephone: 770–488–2700.
For program technical assistance,
contact: Yvonne Lewis, HBCU Project
Officer, Centers for Disease Control and
Prevention, 1600 Clifton Road MS E67,
Atlanta, GA 30333. Telephone: 404–
498–2320. E-mail: YLewis@cdc.gov.
Mike Snesrud, TCU Project Officer,
Centers for Disease Control and
Prevention, 1600 Clifton Road MS E67,
Atlanta, GA 30333. Telephone: 404–
498–2320. E-mail: PSnesrud@cdc.gov.
Ana Rivera, HSI Project Officer,
Centers for Disease Control and
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Prevention, 1600 Clifton Road MS E67,
Atlanta, GA 30333. Telephone: 404–
498–2320. E-mail: ARivera@cdc.gov.
For financial, grants management, or
budget assistance, contact: Mattie B.
Jackson, Grants Management Specialist,
CDC Procurement and Grants Office,
2920 Brandywine Road MS K14,
Atlanta, GA 30341. Telephone: 770–
488–2696. E-mail: mij3@cdc.gov.
Dated: June 27, 2005.
Alan A. Kotch,
Acting Deputy Director, Procurement and
Grants Office, Centers for Disease Control
and Prevention.
[FR Doc. 05–13133 Filed 7–1–05; 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 (SEP): Breast and
Prostate Cancer Data Quality and
Patterns of Care Study, Request for
Applications (RFA) DP–05–071
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)
announces the following meeting:
Name: Disease, Disability, and Injury
Prevention and Control Special Emphasis
Panel (SEP): Breast and Prostate Cancer Data
Quality and Patterns of Care Study, Request
for Applications (RFA) DP–05–071.
Times and Dates: 6:30 p.m.–9:30 p.m., July
27, 2005 (Closed), 8:30 a.m.–5:30 p.m., July
28, 2005 (Closed).
Place: Doubletree Hotel-Buckhead, 3342
Peachtree Road, NE., Atlanta, GA 30326,
Telephone Number 404.231.1234.
Status: The meeting will be closed to the
public in accordance with provisions set
forth in Section 552b(c)(4) and (6), Title 5
U.S.C., and the Determination of the Director,
Management Analysis and Services Office,
CDC, pursuant to Public Law 92–463.
Matters to be Discussed: The meeting will
include the review, discussion, and
evaluation of applications received in
response to: Breast and Prostate Cancer Data
Quality and Patterns of Care Study, Request
for Applications (RFA) DP–05–071.
Contact Person for More Information:
Gwen Cattledge, Ph.D., Scientific Review
Administrator, National Center for Chronic
Disease Prevention and Health Promotion,
CDC, Chamblee Campus 4770 Buford Hwy,
Mailstop K92, Atlanta, GA 30341, Telephone
770.488.4655.
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
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 Federal Register / Vol. 70, No. 127 / Tuesday, July 5, 2005 / Notices
both CDC and the Agency for Toxic
Substances and Disease Registry.
Dated: June 28, 2005.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 05–13131 Filed 7–1–05; 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: Diagnostics of Fungal
Infections; Correction
In the notice document appearing on
page 33905 in the Federal Register
issued on Friday, June 10, 2005, Vol. 70,
No. 111, make the following correction:
On page 33905 under Centers for
Disease Control and Prevention, change
the title ‘‘Prospective Grant of Exclusive
License: Diagnostics of Fungal
Infections’’ to ‘‘Prospective Grant of
Exclusive License: System and Methods
for Aerosolized Delivery of Vaccines’’
(remove previous title ‘‘Diagnostics of
Fungal Infections’’).
All other information in the document
remains unchanged.
Dated: June 24, 2005.
James D. Seligman,
Associate Director for Program Services,
Centers for Disease Control and Prevention.
[FR Doc. 05–13132 Filed 7–1–05; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Cellular, Tissue and Gene Therapies
Advisory Committee (formerly
Biological Response Modifiers
Advisory Committee); Notice of
Meeting
AGENCY: Food and Drug Administration,
HHS.
ACTION: Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). At least one portion of the
meeting will be closed to the public.
Name of Committee: Cellular, Tissue
and Gene Therapies Advisory
Committee.
General Function of the Committee:
To provide advice and
VerDate jul<14>2003 18:41 Jul 01, 2005 Jkt 205001
recommendations to the agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held, via teleconference, on July 29,
2005, from 12:30 p.m. to 2:30 p.m.
Location: National Institutes of
Health, Bldg. 29B, conference room C,
8800 Rockville Pike, Rockville, MD.
This meeting will be held by
teleconference. The public is welcome
to attend the meeting at the previously
mentioned location. A speakerphone
will be provided at the specified
location for public participation in the
meeting.
Contact Person: Gail Dapolito, Center
for Biologics Evaluation and Research,
Food and Drug Administration, 1401
Rockville Pike, Rockville, MD 20852,
301–827–0314, or FDA Advisory
Committee Information Line, 1–800–
741–8138 (301–443–0572 in the
Washington, DC area), code
3014512389. Please call the Information
Line for up-to-date information on this
meeting.
Agenda: In open session, the
committee will hear brief opening
remarks and allow time for public
participation and comments related to
individual FDA research programs
during the open public hearing. The
committee will not hear presentations or
discuss individual research programs in
the open session (see Closed Committee
Deliberations below).
Procedure: On July 29, 2005, from
12:30 p.m. to 1:30 p.m., the meeting is
open to the public. Interested persons
may present data, information, or views,
orally or in writing, on issues pending
before the committee. Written
submissions may be made to the contact
person by July 21, 2005. Oral
presentations from the public will be
scheduled between approximately 12:30
p.m. to 1:30 p.m. Time allotted for each
presentation may be limited. Those
desiring to make formal oral
presentations should notify the contact
person before July 21, 2005, and submit
a brief statement of the general nature of
the evidence or arguments they wish to
present, the names and addresses of
proposed participants, and an
indication of the approximate time
requested to make their presentation.
Closed Committee Deliberations: On
July 29, 2005, from approximately 1:30
p.m. to 2:30 p.m., the meeting will be
closed to permit discussion where
disclosure would constitute a clearly
unwarranted invasion of personal
privacy (5 U.S.C. 552b(c)(6)). The
committee will discuss a review of
individual FDA research programs.
Persons attending FDA’s advisory
committee meetings are advised that the
PO 00000 Frm 00045 Fmt 4703 Sfmt 4703 E:\FR\FM\05JYN1.SGM
38689
agency is not responsible for providing
access to electrical outlets.
FDA welcomes the attendance of the
public at its advisory committee
meetings and will make every effort to
accommodate persons with physical
disabilities or special needs. If you
require special accommodations due to
a disability, please contact Gail Dapolito
at least 7 days in advance of the
meeting.
Notice of this meeting is given under
the Federal Advisory Committee Act (5
U.S.C. app. 2).
Dated: June 23, 2005.
Sheila Dearybury Walcoff,
Associate Commissioner for External
Relations.
[FR Doc. 05–13122 Filed 7–1–05; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2004D–0333]
Draft Guidance; Emergency Use
Authorization of Medical Products;
Availability
AGENCY: Food and Drug Administration,
HHS.
ACTION: Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
availability of draft guidance entitled
‘‘Emergency Use Authorization of
Medical Products.’’ The draft guidance
explains FDA’s policies for authorizing
the use of an unapproved medical
product or an unapproved use of an
approved medical product during a
declared emergency. The draft guidance
is not final and is not in effect at this
time. FDA also is announcing an
opportunity for public comment on the
proposed collection of information
related to emergency use authorizations
by the agency.
DATES: Submit written or electronic
comments on the draft guidance and the
proposed collection of information by
September 6, 2005.
ADDRESSES: Submit written requests for
single copies of the draft guidance to the
Office of Counterterrorism Policy and
Planning (HF–29), Food and Drug
Administration, 5600 Fishers Lane, rm.
14C–26, Rockville, MD 20857. Send a
self-addressed adhesive label to assist
that office in processing your request, or
fax your request to 301–827–5671.
Submit written comments on the draft
guidance and the proposed collection of
information to the Division of Dockets
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