Public Health Conference Grant Program; Notice of Availability of Funds Amendment, 3374 [05-1205]

Download as PDF 3374 Federal Register / Vol. 70, No. 14 / Monday, January 24, 2005 / Notices Request for Comments In accordance with the above-cited Paperwork Reduction Act legislation, comments on the AHRQ information collection proposal are requested with regard to any of the following: (a) Whether the proposed collection of information is necessary for the proper performance of functions of the Agency, including whether the information will have practical utility; (b) the accuracy of the Agency’s estimate of the burden (including hours and costs) of the proposed collection of information; (c) ways to enhance the quality, utility, and clarity of the information to be collected; and, (d) ways to minimize the burden of the collection of information on respondents, including the use of automated collection techniques or other forms of information technology. Comments submitted in response to this notice will be summarized and included in the request for OMB approval of the proposed information collection. All comments will become a matter of public record. Dated: January 7, 2005. Carolyn M. Clancy, Director. [FR Doc. 05–1187 Filed 1–21–05; 8:45 am] BILLING CODE 4160–90–M DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention Agency for Toxic Substances and Disease Registry [Program Announcement 05002] Public Health Conference Grant Program; Notice of Availability of Funds Amendment A notice announcing the availability of Fiscal Year 2005 funds to award a Grant Agreement to Support Public Health Conference Support Grant Agreement published in the Federal Register on November 2, 2004, Volume 69, Number 211, pages 63541–63546. The notice is amended as follows: On page 63543, second column, under III.3 Other, Special Requirements, second bullet, delete the bullet that reads, ‘‘Applicants who do not submit a LOI will not be eligible to submit an application for review or funding.’’ On page 63543, third column, under IV.2 Content and Form of Submission, Letter of Intent (LOI), first paragraph, delete the fifth sentence that reads, ‘‘If you do not submit a LOI, you will not be allowed to submit an application.’’ VerDate jul<14>2003 18:04 Jan 21, 2005 Jkt 205001 On page 63544, second column, under IV.3 Submission Dates and Times, delete the fourth paragraph that reads, ‘‘Applicants who do not submit an LOI will not be eligible to submit an application for review or funding.’’ Dated: January 14, 2005. William P. Nichols, Director, Procurement and Grants Office, Centers for Disease Control and Prevention. [FR Doc. 05–1205 Filed 1–21–05; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention Early Hearing Detection and Intervention (EHDI) Tracking, Surveillance, and Integration; Correction In the notice document announcing the ‘‘Early Hearing Detection and Intervention (EHDI) Tracking, Surveillance, and Integration,’’ Funding Opportunity Number: RFA 05028, appearing on page 357 in the Federal Register issue of Tuesday, January 4, 2005, the notice is amended as follows: On page 357, third column under DATES, and page 360, second column under Section IV.3. Submission Dates and Times: amend to reflect Letter of Intent Deadline (LOI) Date: February 10, 2005, and Application Deadline Date: March 14, 2005. On page 359, second column under Section III.3. Other: fourth bullet delete the semicolon and the word and [; and]; delete fifth bullet ‘‘Have previously been awarded a CDC Cooperative Agreement for EHDI Tracking, Surveillance, and Integration (Program Announcements 00076, 01048, or 03055).’’ Dated: January 14, 2005. William P. Nichols, Director, Procurement and Grants Office, Centers for Disease Control and Prevention (CDC). [FR Doc. 05–1219 Filed 1–21–05; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Cardiovascular and Renal Drugs Advisory Committee; Notice of Meeting AGENCY: Food and Drug Administration, HHS. ACTION: PO 00000 Notice. Frm 00020 Fmt 4703 Sfmt 4703 This notice announces a forthcoming meeting of a public advisory committee of the Food and Drug Administration (FDA). The meeting will be open to the public. Name of Committee: Cardiovascular and Renal Drugs Advisory Committee (CRDAC). General Function of the Committee: To provide advice and recommendations to the agency on FDA’s regulatory issues. Date and Time: The meeting will be held on February 24, 2005, from 8 a.m. to 5 p.m. Location: Food and Drug Administration, Center for Drug Evaluation and Research Advisory Committee Conference Room, rm. 1066, 5630 Fishers Lane, Rockville, MD. Contact Person: Cathy Groupe, Center for Drug Evaluation and Research (HFD– 21), Food and Drug Administration, 5600 Fishers Lane, (for express delivery, 5630 Fishers Lane, rm. 1093) Rockville, MD 20857, 301–827–7001, e-mail: groupec@cder.fda.gov, or FDA Advisory Committee Information Line, 1–800– 741–8138 (301–443–0572 in the Washington, DC area), code 3014512533. Please call the Information Line for up-to-date information on this meeting. Agenda: The committee will discuss supplemental new drug applications (sNDAs) S–022, S–024, and S–025 to approved new drug application (NDA) 20–838, ATACAND (candesartan cilexetil) Tablets (4 milligrams (mg), 8 mg, 16 mg, and 32 mg), AstraZeneca LP, for the use in the treatment of patients with congestive heart failure, specifically in the following ways: (1) S–022, reducing the risk of cardiovascular mortality or heart failure hospitalization when added to an angiotensin-converting enzyme inhibitor-containing regimen in congestive heart failure patients with left ventricular systolic dysfunction; (2) S–024, reducing the risk of cardiovascular mortality or heart failure hospitalization in congestive heart failure patients with left ventricular systolic dysfunction, as a primary reninangiotensin-aldosterone system modulating treatment; and (3) S–025, reducing the frequency of hospitalizations for heart failure in congestive heart failure patients with preserved left ventricular systolic dysfunction. ATACAND is currently approved for use in the treatment of hypertension. The background material will become available no later than the day before the meeting and will be posted on FDA’s Web site at https:// www.fda.gov/ohrms/dockets/ac/ acmenu.htm under the heading E:\FR\FM\24JAN1.SGM 24JAN1

Agencies

[Federal Register Volume 70, Number 14 (Monday, January 24, 2005)]
[Notices]
[Page 3374]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-1205]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

Agency for Toxic Substances and Disease Registry

[Program Announcement 05002]


Public Health Conference Grant Program; Notice of Availability of 
Funds Amendment

    A notice announcing the availability of Fiscal Year 2005 funds to 
award a Grant Agreement to Support Public Health Conference Support 
Grant Agreement published in the Federal Register on November 2, 2004, 
Volume 69, Number 211, pages 63541-63546. The notice is amended as 
follows:
    On page 63543, second column, under III.3 Other, Special 
Requirements, second bullet, delete the bullet that reads, ``Applicants 
who do not submit a LOI will not be eligible to submit an application 
for review or funding.''
    On page 63543, third column, under IV.2 Content and Form of 
Submission, Letter of Intent (LOI), first paragraph, delete the fifth 
sentence that reads, ``If you do not submit a LOI, you will not be 
allowed to submit an application.''
    On page 63544, second column, under IV.3 Submission Dates and 
Times, delete the fourth paragraph that reads, ``Applicants who do not 
submit an LOI will not be eligible to submit an application for review 
or funding.''

    Dated: January 14, 2005.
William P. Nichols,
Director, Procurement and Grants Office, Centers for Disease Control 
and Prevention.
[FR Doc. 05-1205 Filed 1-21-05; 8:45 am]
BILLING CODE 4163-18-P
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