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Clinical Graft Monitoring Tool Prototyping

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Contract Overview

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

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This subcontract opportunity with the Department of the Army USAMRRA involves the development of assays, devices, and technology for clinical graft monitoring in support of Defense Health Agency research projects. The selected provider will prototype monitoring devices and integrate biomarkers into tools specifically designed for the human use factors associated with vascularized composite allotransplantation recipients. The project requires the delivery of a functional prototype or a validated assay kit. To qualify, providers must possess bio-engineering facilities and adhere to ISO 13485 or FDA Quality System Regulation standards. The work falls under NAICS code 541715 and is focused on advancing clinical monitoring capabilities for the Department of Defense.

General Info

Army subcontract for developing clinical graft monitoring assays and devices for DHA research.

Agency

Department Of Defense → Department Of The Army -- Usamraa

NAICS

541715 - Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)

Place of Performance

Not specified

Set-Aside

NONE

Documents

This scope was carved out of HT942526RTRPCA.

The full solicitation package (2 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

DoW Reconstructive Transplant, Concept Award

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Timeline

PostedMay 29

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Organization & Contact Information

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AgencyDepartment Of Defense → Department Of The Army -- Usamraa

ContactsNo contacts available

OfficeN/A

Organization / AgencyDepartment Of Defense → Department Of The Army -- Usamraa

Office AddressN/A

ContactsNo contact information available

Full Description

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Develops assays, devices, or technology for clinical graft monitoring for prime contractors on Defense Health Agency (DHACA) research projects. Prototypes monitoring devices and integrates biomarkers into tools designed for human use factors unique to VCA recipients. Requires ISO 13485 or FDA QSR standards and bio-engineering facilities. Delivers a functional prototype or validated assay kit.

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