Indefinite Delivery Contract 75N93023D00017

Award Date 6/20/23
Last Date to Order 6/19/30
Awardee
Mriglobal
Ultimate Awardee
Not listed
Federal Contract Vehicle
Pricing Type
Order Dependent (IDV only)
Legislative Mandate
Employment Eligibility Verification
National Interest Action
None
Award Type
Single
Primary Consortia Member
Not listed
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  • 75N93023D00017
    Indefinite Delivery Contract
  • 2
    Federal Contract Awards

This federal contract award is an Indefinite Delivery, Indefinite Quantity (IDIQ) contract for the Diagnostics Pre-Clinical Services Program, awarded by the Department of Health and Human Services' National Institutes of Health, National Institute of Allergy and Infectious Diseases to the prime contractor MRI Global, also doing business as Midwest Research Institute. The contract has a potential value of $24,000,000 and a period of performance through June 2030. Under this IDIQ, MRI Global will provide a broad range of services to support the development of in vitro diagnostic products for the detection, identification, and characterization of human infectious agents, including product development processes, reagents, clinical specimens, and manufacturing services. Two specific task orders have been awarded to date, each valued at $3,500 on a firm fixed price basis, for MRI Global to deliver diagnostics pre-clinical services in support of the agency's program to develop medical countermeasures against infectious diseases. The work will be performed in Kansas City, Missouri, and no set-asides were applied to this acquisition.

The original solicitation was a pre-solicitation notice seeking capability statements from qualified small businesses to potentially provide these diagnostic pre-clinical services under an IDIQ contract. The agency indicated it anticipated making multiple IDIQ contract awards with a 7-year ordering period starting in June 2023. The goal is to offer a comprehensive array of capabilities to product developers, helping them obtain critical data and complete studies to advance new in vitro diagnostic products toward regulatory clearance.

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