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FBO DAILY ISSUE OF MAY 04, 2012 FBO #3814
MODIFICATION

A -- NICHD Contraceptive Clinical Trials Network - Female Sites - Solicitation 1

Notice Date
5/2/2012
 
Notice Type
Modification/Amendment
 
NAICS
541712 — Research and Development in the Physical, Engineering, and Life Sciences (except Biotechnology)
 
Contracting Office
Department of Health and Human Services, National Institutes of Health, National Institute of Child Health and Human Development, Contracts Management Branch, 6100 Executive Blvd., Suite 7A07, MSC7510, Bethesda, Maryland, 20892-7510
 
ZIP Code
20892-7510
 
Solicitation Number
NIH-NICHD-CRHB-2012-03
 
Response Due
8/3/2012 4:00:00 PM
 
Point of Contact
Alice M. Pagán, Phone: 301-435-6959, Katharine Minker, Phone: 301-402-7571
 
E-Mail Address
alice.pagan@nih.gov, km571h@nih.gov
(alice.pagan@nih.gov, km571h@nih.gov)
 
Small Business Set-Aside
N/A
 
Description
RFP No. NIH-NICHD-CRHB-2012-03 - Female Sites THIS IS A REQUEST FOR PROPOSALS (RFP). The National Institutes of Health (NIH), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) is planning to issue an RFP for multiple Indefinite/Delivery, Indefinite/Quantity (IDIQ) Task Order contracts for the NICHD Contraceptive Clinical Trials Network (CCTN). The NIH, NICHD is the lead Federal agency for the conduct of basic, clinical and epidemiological research to develop new contraceptives and to evaluate existing methods of contraception and reproductive health. The Center for Population Research (CPR), within NICHD, was established in 1968 by the Secretary of Health Education and Welfare, with the important goal of developing new contraceptives through the use of contracts and grants. Within CPR, the Contraception and Reproductive Health Branch (CRHB) has long supported several preclinical contraceptive testing facilities, as well as facilities for chemical and peptide synthesis. To further expand their contraceptive development capabilities, in 1996 CRHB established the initial NICHD CCTN in order to conduct Phase I, II, and III clinical trials of new contraceptive methods. The NICHD CCTN is an important component of the CRHB contraceptive development capability. Products that have undergone formulation and successful pre-clinical testing, either through the CRHB formulation and testing facilities or through outside sources, are candidates for clinical testing in the NICHD CCTN. The NICHD CCTN is particularly valuable for providing a venue for testing new contraceptive drugs and devices that have been developed by small companies that lack the resources to support large-scale clinical trials. This acquisition is for a re-competition of the female sites that will operate under an Indefinite/Delivery, Indefinite/Quantity (IDIQ) Task Order contracts. The female sites will be able to work with the CCTN Statistical and Clinical Coordinating Center (SCCC) and NICHD to rapidly develop protocols and initiate clinical trials shortly after candidate products have completed the necessary preclinical testing. The resultant IDIQ contracts will be for a seven (7) year period of performance. The CCTN female sites contractors will evaluate systematically the safety and efficacy of new female contraceptive drugs and devices as well as drug treatments of gynecologic conditions in Phase I, II, III and IV trials. The results of these clinical trials would be the basis for advancing candidate drugs and devices through development with the ultimate goal of submission to the FDA in support of a New Drug Application (NDA), Premarket notification 510k, Premarket Approval (PMA) or Investigational Device Exemptions (IDE). It is estimated that the new NICHD CCTN will consist of up to 16 sites capable of performing female contraceptive clinical trials and up to 4 male sites. Please be advised that the NICHD is issuing separate RFPs for each CCTN Topic Area (Female Contraceptive Clinical Trials & Male Contraceptive Clinical Trials) and the SCCC for the CCTN. This RFP is for the Female Sites only. The RFP will be made available electronically only via the FedBizOpps website (http://www.fbo.gov). Offerors are responsible for routinely checking the FedBizOpps website for any possible solicitation amendments that may be issued.
 
Web Link
FBO.gov Permalink
(https://www.fbo.gov/spg/HHS/NIH/NICHD/NIH-NICHD-CRHB-2012-03/listing.html)
 
Record
SN02736856-W 20120504/120502235053-ff7ed6ed91dd0e249c1911bdc6c3f670 (fbodaily.com)
 
Source
FedBizOpps Link to This Notice
(may not be valid after Archive Date)

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