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All Federal Contract Awards
Delivery Order HHSN275201300025I-HHSN27500004
Award Date
9/24/14
Potential Completion Date
12/31/17
Potential Value
$770K
Overview
Contacts
Activity
4
Transactions
4
Subawards
Opportunity Stack
Similar Awards
Federal Agency
National Institute of Child Health and Human Development
Awardee
University Of Washington HD1WMN6945W6
Ultimate Awardee
Not listed
NAICS Category
541712 - Research and Development in the Physical, Engineering, and Life Sciences (except Biotechnology)
PSC Category
AN12 - Health R&D Services; Health Care Services; Applied Research
Federal Contract Vehicle
NICHD Contraceptive Clinical Trials Network
Set-Aside Type
No Set-Aside Used
Extent Competed
Full and Open Competition
Major Defense Program
Not listed
Pricing Type
Cost No Fee
Place of Performance
Seattle, WA 98125, USA
Solicitation Procedures
Multiple Award, Fair Opportunity
Number Of Offers Received
2
Legislative Mandate
Not listed
National Interest Action
Not listed
Research Type
Not listed
Primary Consortia Member
Not listed
NICHD Contraceptive Clinical Trials Network
Master IDIQ
HHSN275201300025I
Indefinite Delivery Contract
HHSN275201300025I-HHSN27500004
Delivery Order
Update #1
Update #2
NES TES DAY STUDY CLINICAL TRIAL FOR MALE CONTRACEPTION
Posted 9/24/14
5
1
Name
Description
Solicitation Number
FederalAgency
Type
PostedDate
NICHD Contraceptive Clinical Trials Network - Male Sites
Added: Apr 02, 2012 4:27 pm THIS IS NOT A REQUEST FOR PROPOSALS (RFP). THIS IS A PRE-SOLICITATION ANNOUNCEMENT ONLY. A REQUEST FOR PROPOSALS WILL BE ISSUED VIA FEDBIZOPPS ON OR ABOUT APRIL 17, 2012.The National Institutes of Health (NIH), Eunice Kennedy Siver 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 tough 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 tough the CRHB formulation and testing facilities or tough 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 male sites that will operate under an Indefinite/Delivery, Indefinite/Quantity (IDIQ) Task Order contracts. The male 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 male sites contractors will evaluate systematically the safety and efficacy of new male contraceptive drugs and devices as well as drug treatments for 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 tough 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 4 sites capable of performing male contraceptive clinical trials and up to 16 female sites. Please be advised that the NICHD is issuing separate RFPs for each CCTN Topic Area (Male Contraceptive Clinical Trials & Female Contraceptive Clinical Trials) and the SCCC for the CCTN. This Pre-Solicitation announcement is for the RFP for the Male Sites for the 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.
NIH-NICHD-CRHB-2012-04
Department of Health and Human Services National Institutes of Health
Award Notice 1/1
4/2/12, 4:27 PM
5
1
Mod #
Description
ReasonForModification
Federal Obligation
Date
3
NES TES DAY STUDY CLINICAL TRIAL FOR MALE CONTRACEPTION
Supplemental Agreement for work within scope
$0
6/30/17
2
NES TES DAY STUDY CLINICAL TRIAL FOR MALE CONTRACEPTION
Supplemental Agreement for work within scope
$407.0k
12/9/16
1
NES TES DAY STUDY CLINICAL TRIAL FOR MALE CONTRACEPTION
Supplemental Agreement for work within scope
$0
6/29/16
Not listed
NES TES DAY STUDY CLINICAL TRIAL FOR MALE CONTRACEPTION
Not listed
$362.6k
9/24/14