Notice ID:36C26026Q0807
The VA Portland Healthcare System requires a contractor to provide FDA-cleared, next-generation sequencing-based Measurable Residual Disease (MRD) testing for blood and bone marrow samples from patients with multiple myeloma, chronic lymphocytic leukemia, and B-cell acute lymphoblastic leukemia. Testing must be performed at the contractor’s CLIA-certified and CAP-accredited reference laboratory, with results reported within an average turnaround time of six business days. The contract includes five ordering periods from September 1, 2026, through August 31, 2031. The place of performance is the contractor’s reference laboratory as defined at award. The contractor must also provide all necessary supplies, technical support, and secure electronic reporting to VA clinicians.