This Sources Sought opportunity from Department Of Veterans Affairs was posted on July 15, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.
6640-- Blood Bank Cost Per Test
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The Department of Veterans Affairs, VA North Texas Health Care System in Dallas, Texas, is conducting market research to identify qualified vendors capable of providing a fully automated gel-based blood bank analyzer and associated reagents on a cost-per-test basis. The system must support a broad range of transfusion medicine tests including ABO/RH typing, antibody screening and identification with selected cell panels, direct antiglobulin testing, immediate spin and AHG crossmatches, antigen testing, and antibody titration with automated serial dilutions. The analyzer must be compatible with government-owned Ortho Workstations and located in Room 1B-306 of the Pathology and Laboratory Medicine Service. The vendor must deliver the instrument and reagents within 60 days of award, along with installation, setup, test validation guidance, and a manual testing platform. The system must operate with continuous readiness, provide up to 24 hours of walkaway time, prevent sample carryover, avoid proprietary liquids, and include advanced features like automatic cap, clot, and liquid level detection, as well as 5-megapixel imaging of gel cards with digital result storage. The anticipated annual test volumes include approximately 7,800 ABO/RH tests, 4,000 antibody screens, 200 DATs, 400 AHG crossmatches, and other supporting assays, with corresponding consumable and reagent demands. The system must be bidirectionally interfaced with VistA via Data Innovations to eliminate manual data entry and comply with modern operating system requirements, excluding outdated platforms like Windows XP or Server 2003. Reagent and consumable volumes are specified in detail, including group-specific reagents, buffered gel cards, diluents, and daily QC kits. Vendors must submit a voluntary capability statement via email by July 27, 2026, including the place of manufacture for all equipment and reagents. This notice is strictly for market research and does not constitute a solicitation, obligation to award, or reimbursement for submissions. Responses will inform future acquisition planning, including potential small business set-asides, but no contract will result directly from this request.
General Info
Agency
NAICS
Place of Performance
Department of Veterans Affairs Dallas VA North Texas Health Care System, Dallas, TX, 75216, USASet-Aside
Timeline
Submission Closed
Organization & Contact Information
Full Description
I. General Information
- Agency/Office: Department of Veterans Affairs (VA), VA North Texas Health Care System (VANTHCS), Dallas, TX. - Place of Performance: VA North Texas Health Care System, Pathology and Laboratory Medicine Service (P&LMS), Microbiology Laboratory, Dallas, Texas. - Anticipated NAICS: 541380 Testing Laboratories and Services - Anticipated PSC: 6640 Laboratory Equipment and Supplies.
The Government is seeking to identify responsible vendors capable of providing Blood Bank Cost Per Test Reagents, brand name or equal, configured and supported with Government owned Ortho Workstations in the Transfusion Medicine Unit Room 1B-306, Pathology and Laboratory Medicine Services at VANTHCS. II. Description of Requirement Transfusion Medicine Unit, Pathology and Laboratory Medicine Services (P&LMS) at the VA North Texas Health Care System (VANTHCS), Dallas, TX is seeking a fully automated gel instrument and reagents to perform Type & Screen testing with antibody ID panels, Direct Antiglobulin test, IS and AHG crossmatches and the capability to test for antigens. Contract type will be cost per test with analyzer included. The contemplated purchase includes, at a minimum: The Contractor shall provide reagents, consumables, and supplies as requested by VANTHCS staff to perform blood bank testing for the analyzer. Estimated quantities shown below are for annual requirements. Group I Estimated Yearly Test Volume: Assay Est. Annual Test Volume ABO/RH 7,800 Antibody Screen 4,000 Antibody Identification (with Selected Cell Panels capabilities) 60 Direct Antiglobulin Test-IgG, C3d 200 Immediate Spin Crossmatch 100 AHG Crossmatch 400 ABD Group Forward type 500 O Group Forward type 500
Group II Estimated Yearly Reagents & Consumables Requirements: Reagents & Consumables Est. Annual Volume A/B Group 500 A/B/D Group 500 A/B/D Mono & Reverse Group 7,800 DAT Card (IgG & C3d) 200 Anti-IgG Card 4,000 Buffered Gel Card 200 7% Bovine Serum Albumin 32 Evaporation Caps for Reagent Red Cells 2 Diluent 2 4 Diluent 2 Plus 7
Group II Estimated Yearly Traditional Reagents Requirements: Traditional Reagents Standing Order with Scheduled Delivery Schedule. Est. Annual Volume 0.8% A1 Cell and B Cell (0.8% Affirmagen) 78 0.8% Panel B 13 0.8% Panel C 13 0.8% Antibody Screen Cells 3 Cells (0.8% Surgiscreen) 78 Daily QC Kit 52
Location: The analyzer shall be located, and testing will be performed in Transfusion Medicine Unit, Room 1B-306, Pathology & Laboratory Medicine Service, VA North Texas Health Care System, 4500 S. Lancaster Rd., Dallas, TX 75216. Delivery: Within 60 days of the contract award the vendor will deliver the analyzer and reagents to VA North Texas Health Care System, 4500 S. Lancaster Rd., Dallas, TX 75216. III. Performance requirements: Performance Requirements: The following are required: Installation Requirements: Deliver, install, and set up the instrument (automated analyzer) and components. Deliver one manual testing platform (equipment) Provide test validation guidance and validation supplies.
Testing Requirements: ABO/RH Antibody Screen (3 Cells) Direct Antiglobulin Test (DAT) Antibody Identification (with Selected Cell Panels Capabilities) Immediate Spin Crossmatch AHG Crossmatch Antigen Testing Capabilities Antibody Titration (with automated serial dilutions) Capabilities
System Requirements: The system must contain continuous, random and STAT access technology. The system must have minimal daily maintenance and tracking capabilities when maintenance has been completed. The system should have technology to prevent sample carryover. The system must feature error-proof reagent and commodity design with built-in safeguards to prevent reagent mix-ups, probe crashes and unnecessary downtime. Sample carriers must be capable of utilizing different tube sizes in one carrier, thus avoiding the need for pre-analytic sorting. The system must have automatic cap, clot and liquid level detection capabilities. The system must not utilize proprietary system liquids. The system must offer up to 24 hours of walkaway time. When operational, the system must always be in a ready mode and at no time go into a hibernation or sleep state. The system must be able to run selected cell antibody identification panels. The optical resolution of the onboard camera must be at least 5-megapixel resolution down to 32 x 32 microns and store a digital image of both the front and back of each gel card to record test results. A fully loaded waste container shall not weigh more than 11 lbs. and be accessible at waist height.
Connectivity Requirements: (Note: Does not use the following software: Windows XP Embedded Service Pack 3, Windows Server 2003 or Windows XP.) System is fully interfaced (bidirectional) with VistA via Data Innovations: System accommodates reporting through Data Innovations (DI) to eliminate the need for manual data entry.
IV. Submission Instructions Interested and capable vendors should submit an electronic capability statement and include the place of manufacture for all equipment and reagents via email in PDF or Word format by July 27, 2026, by 9:00 AM Central Standard Time.
- Teresa Arzola  - Email: Teresa.arzola@va.gov  - Subject line: Sources Sought Blood Bank Cost Per Test Reagents VA North Texas HCS Â
No telephone inquiries will be accepted. Responses received will be used solely for market research and planning purposes to assist the Government in determining an appropriate acquisition strategy (e.g., small business set aside or unrestricted).
Submission of a capability statement is voluntary and shall not be construed as a commitment by the Government to issue a solicitation or award a contract, nor will the Government pay for information submitted in response to this Sources Sought.
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