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, 38688-38689 [05-13131]

Download as PDF 38688 Federal Register / Vol. 70, No. 127 / Tuesday, July 5, 2005 / Notices in the GPD 2.04 [https://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: https://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 https://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: VerDate jul<14>2003 18:41 Jul 01, 2005 Jkt 205001 • 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: https://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 PO 00000 Frm 00044 Fmt 4703 Sfmt 4703 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 E:\FR\FM\05JYN1.SGM 05JYN1 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 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 E:\FR\FM\05JYN1.SGM 05JYN1

Agencies

[Federal Register Volume 70, Number 127 (Tuesday, July 5, 2005)]
[Notices]
[Pages 38688-38689]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-13131]


-----------------------------------------------------------------------

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

[[Page 38689]]

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
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