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Qiagen Molecular Biology Reagents, Kits, and Consumables

Health & Human Services (HHS) > Center For Drug Evaluation & Research (Cder) > Division of Applied Regulatory Science (DARS)
FFP
$11K – $109K per task order
Quick Brief

The U.S. Food and Drug Administration (FDA) is procuring QIAGEN molecular biology reagents, kits, and consumables through a sole-source IDIQ contract with QIAGEN LLC to support the Division of Applied Regulatory Science. The contract will include Firm-Fixed-Price task orders over a five-year period to ensure consistency with validated laboratory methods and maintain the integrity of research data. This acquisition is essential for various omics analyses involving DNA, RNA, and proteins.

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Scope & Requirements

The work involves supplying QIAGEN molecular biology reagents, kits, and consumables to support various laboratory analyses.

Contract Details

Contract Typei
FFP
Contract Vehiclei
IDIQ
Estimated Value
$11K – $109K per task order
IDIQ ceiling: $2.5M, 1 awardee
Similar contracts award $11K to $109K (median $32K, 5,870 awards)
Period of Performance
5 years
Incumbent Contractor
QIAGEN LLC
Expected Awards
1
NAICS Codes
Place of Performance
Rockville, MD, US

Qualifications & Eligibility

NAICS Size Standard
$16.5M

Agency & Contact

Contracting Organization

Agency
HEALTH AND HUMAN SERVICES, DEPARTMENT OF
Sub-Agency
Center for Drug Evaluation and Research (CDER)
Office
Division of Applied Regulatory Science (DARS)

Point of Contact

John A. Smith
Contracting Officer
(202) 555-0100

Key Dates

Published4d ago
Jul 20, 2026
Last Updated4d ago
Jul 20, 2026
Became Solicitation3d ago
Jul 21, 2026
Tracked
Notice Response Datein 5d
Jul 29, 202610:00 AM EDT
Response Duein 10d
Aug 3, 2026

Description

for Purchase of QIAGEN Molecular Biology Reagents, Kits, and Consumables Announcement No.: FDA-26- 1289149 The U.S. Food and Drug Administration (FDA) hereby provides notice of its intent to award a sole-source, single-award Indefinite Delivery/Indefinite Quantity (IDIQ) contract to QIAGEN LLC for the supply of QIAGEN molecular biology reagents, kits, consumables, and related products in support of the Division of Applied Regulatory Science (DARS), (OCP/OTS), Center for Drug Evaluation and Research (CDER). Individual Firm-Fixed-Price (FFP) Task Orders will be issued throughout the ordering period based on program

requirements and the availability of funding. The anticipated ordering period consists of a Base Year and four (4) Option Years, for a total potential ordering period of five (5) years. The North American Industry System (NAICS) code for this acquisition is 325413, In-Vitro Diagnostic Substance Manufacturing. The FDA intends to procure QIAGEN reagents, kits, consumables, and related products supporting genomics, transcriptomics, proteomics, metabolomics, and other omics analyses, including the isolation, purification, amplification, sequencing, characterization, and analysis of DNA, RNA, proteins, and related biomolecules. This acquisition is being conducted on a sole-source basis pursuant to FAR 6.302-1, Only One Responsible Source and No Other Supplies or Services Will Satisfy Agency

Requirements. DARS has standardized, validated, and implemented laboratory protocols, standard operating procedures (SOPs), workflows, and analytical frameworks using QIAGEN reagents and associated technologies. Continued use of QIAGEN products is necessary to maintain consistency with validated laboratory methods, preserve the integrity and comparability of historical and future research data, and avoid the time, cost, and scientific risk associated with redevelopment, validation, and verification of laboratory methods using alternative products. The Government intends to solicit and negotiate directly with QIAGEN LLC. The determination not to compete this proposed contract action is solely within the discretion of the Government. This notice is not a request for competitive quotations or proposals. However, responsible sources that believe they can satisfy the Government's

requirements may submit a written capability statement demonstrating their ability to provide products that meet the Government's

requirements. Information received will be considered solely for the purpose of determining whether to conduct a competitive procurement. A determination by the Government not to compete this proposed acquisition based upon responses to this notice is solely within the discretion of the Government. Any response to this notice must demonstrate clear and convincing evidence that the respondent can satisfy the Government's

requirements without adversely affecting FDA's validated laboratory methods, ongoing scientific research, data integrity, or mission

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