Q301--Transplant Rejection Detection Molecular Genetic Testing
Overview
Buyer
Place of Performance
NAICS
PSC
Set Aside
Original Source
Timeline
Qualification Details
Fit reasons
- NAICS alignment with historical contract wins in similar service areas.
- Scope strongly matches core technical capabilities and delivery model.
Risks
- Past performance thresholds may require one additional teaming partner.
- Potential clarification needed on staffing minimums before bid/no-bid.
Next steps
Validate eligibility requirements, assign capture owner, and schedule partner outreach to confirm teaming strategy before submission planning.
Quick Summary
The Department of Veterans Affairs (VA), Network Contracting Office 19 (NCO 19), is conducting market research to identify potential sources for Transplant Rejection Detection Molecular Genetic Testing for the Salt Lake City VA Medical Center. This is a Sources Sought Notice for information and planning purposes only. Responses are due by June 30, 2026, at 15:00 MST.
Scope of Work
The requirement involves providing comprehensive molecular genetic testing services to monitor transplant patients and detect organ rejection. Key services include:
- Diagnostic laboratory services for molecular expression genetic blood testing.
- Molecular Expression Transplant Assessment Testing, Molecular Assessment for Kidney Disease, and Molecular Genetic Prenatal Screening Test.
- Laboratory testing, analysis, and result interpretation, performed entirely on contractor premises.
- Provision of individual patient-chartable test result reports meeting CLIA requirements.
- Supply of requisition forms and unique supplies for sample collection at no additional charge.
- Maintenance of patient record confidentiality.
Performance Standards & Requirements
- Tests must be performed and reported within established vendor turnaround times, with a maximum TAT of three weeks from specimen submission.
- Encrypted and/or secured electronic transmission of all completed results.
- Laboratories must be fully licensed and accredited (e.g., CAP, state regulatory agencies) and CLIA certified.
- Compliance with all local, state, and federal laws, including CLIA, HIPAA, OSHA, and CDC regulations.
- Maintenance of quality assurance programs meeting federal regulations and CAP certification.
- Contractor personnel must meet CLIA qualifications and be proficient in English.
Key Information Requested from Industry
Interested contractors must submit:
- An overview of proposed solutions and a description of products in accordance with the draft Statement of Work (SOW).
- Responses to a market research table questionnaire, including company details (Name, Address, UEI, Contact), business size information (Small Business categories, Large Business), FSS/GSA Contract details, proposed solution availability, and pricing structure.
- Responses to Federal Acquisition Regulation (FAR) Market Research Questions (e.g., Buy American Act).
- Specific questions for Small Businesses regarding Limitations on Subcontracting and the Nonmanufacturer Rule.
Contract & Timeline
- Type: Sources Sought / Request for Information (RFI)
- Set-Aside: None specified (market research stage, but includes small business questions)
- Primary NAICS Code: 621511 – Medical Laboratories (Small Business size standard: $41.5 Million)
- Response Due: June 30, 2026, 15:00 Mountain Standard Time (MST)
- Published: June 10, 2026
- Submission Method: Email to Lindsey.Zwaagstra@va.gov
- Page Limit: Maximum of 8 pages, including cover letter.
Important Disclaimers
This is not a solicitation or request for proposal and does not constitute an obligation or commitment by the Government. No award will be made based on responses, and the Government will not pay for any information received or costs incurred in developing responses.