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This Government Contract opportunity from Department Of Defense was posted on May 10, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Reverse Blood Grouping Test Kit Supply

Closed
Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

Active Opportunities Like This One

NAICS: 325414
New
Federal
iNDI FA13.1J Cell Lines Expansion and Distribution for the iPSC Neurodegenerative Disease Initiative (iNDI) ProjectThe Department of Health and Human Services, through the National Institutes of Health's National Institute on Aging, intends to award a sole source contract to The Jackson Laboratory for the expansion, quality control, biobanking, and distribution of isogenic Alzheimer’s disease and related dementias induced pluripotent stem cell lines as part of the iPSC Neurodegenerative Disease Initiative (iNDI) Project. This contract will focus on providing up to 936 specific iPSC lines, including 486 FA13.1J female SNV lines and 450 lines across 25 high-priority SNV trios, adhering to iNDI protocols for quality and expansion. The Jackson Laboratory is uniquely qualified for this contract as it currently houses the existing distribution infrastructure and has demonstrated successful past performance in supporting NIH’s iNDI requirements. The contract is planned to be a firm-fixed-price agreement with a performance period starting September 1, 2026, for a base year and up to three option years, ending August 31, 2030. The primary place of performance will be the contractor’s facility in Bar Harbor, Maine. While this notice signals the intent for a sole source award, other capable sources may submit capability statements demonstrating their ability to meet the outlined requirements, including supply of the specific cell lines, adherence to quality protocols, product and web content creation, and public distribution via an established platform. Responses must be submitted electronically by June 23, 2026, and the Government reserves the right to consider all responses but is under no obligation to initiate a competitive procurement.
National Institutes Of Health Olao

POSTED

6 days ago

DEADLINE

in 7 days

AI Contract Overview

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This contract involves the supply of reverse blood grouping test kits branded as AFFIRMAGEN, each unit containing two 10 mL bottles. The test kits must adhere to FDA regulations and federal medical product standards, ensuring compliance and quality for medical use. The contract is issued by the Department of Defense under the Medical Supply Chain MD SURG FSF agency, specifying delivery to a location in Perry Point, with a ZIP code of 21902. The solicitation was posted on May 10, 2026, with responses due by May 18, 2026, indicating a relatively short window for bids or proposals. It is classified as a subcontract opportunity within the NAICS code 325414, related to biological product manufacturing. While no specific set-aside or organization type is mentioned, the focus is clearly on securing compliant test kits for reverse blood grouping to support medical supply needs within the defense sector.

General Info

Supply of FDA-compliant AFFIRMAGEN reverse blood grouping test kits for Department of Defense delivery.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

NAICS

325414 - Biological Product (except Diagnostic) Manufacturing View NAICS

Place of Performance

PERRY POINT, MD, 21902, US

Set-Aside

NONE

Documents

(0)

No documents available

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Timeline

PhaseClosed
Posted

subcontract

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF
Office AddressN/A
ContactsNo contact information available

Full Description

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Supply of reverse blood grouping test kits (AFFIRMAGEN) consisting of two 10 mL bottles per unit, compliant with FDA and federal medical product regulations.