Redacted J&A or a Cost-Per-Test (CPT) Agreement to include reagents, instrument/equipment, consumables, controls, and any necessary services to conduct Flow Cytometry Requirement

JustificationActive

Key Takeaways

  • No response deadline specified - contact the agency for details
  • Full and open competition - all businesses eligible to bid
  • Work to be performed in JBSA FT SAM HOUSTON, TX
  • Industry: In-Vitro Diagnostic Substance Manufacturing

Contract Details

Notice ID
23-P-0054
Opportunity Type
Justification
Sub-Agency
DEPT OF THE ARMY
Office
W40M MRC0 WEST
Posted Date
Wednesday, January 21, 2026
Response Deadline
Not specified
PSC Code
6550
Set-Aside
Full & Open Competition
Status
Active

Description

This requirement was for a FDA Approved Flow Cytometry Instrumentation must be able to have fully automated discrete random-access capabilities; be able to store reagents at the Food and Drug Administration (FDA) storage levels; be capable of barcode identification; be able to print patient results as one per page; have the ability to interface with the Military Health System (MHS) Genesis and the Risk Management Framework (RMF) and Health Insurance Portability and Accountability Act (HIPAA) compliant.

Why This Opportunity Matters

The Department of DEFENSE is seeking responses for in-vitro diagnostic substance manufacturing in JBSA FT SAM HOUSTON, TX.