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Sources sought

Urinalysis Analyzer Cost-Per-Reportable-Result (CPRR)

36C25725Q0255

Department of Veterans Affairs, 257-Network Contract Office 17. In-Vitro Diagnostic Substance Manufacturing.

Response deadline

January 30, 2025 at 5:00 PM EST

Closed 640 days ago. Posted January 27, 2025. Scheduled to archive April 30, 2025.

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This one closed in 2025

13 like it are open now in in-vitro diagnostic substance manufacturing

All 13 open in in-vitro diagnostic substance manufacturing

Description

As published on SAM.gov.

This notice is for planning purposes only and shall not be considered an invitation for bid, request for quotation, request for proposal, or an obligation of the government to acquire any products or services. Responses to this notice will be used for informational purposes only. No entitlement to payment of direct or indirect costs from the government will arise from a response to this announcement. No contract will be awarded from this notice.

The information requested in this notice will be used to determine if there are sufficient socioeconomic small business concerns capable of performing the work described for the requirement. The Department of Veterans Affairs, Veterans Health Administration, Network Contracting Office (NCO) 17 seeks sources for the following procurement: Urinalysis Cost-Per-Reportable-Result (CPRR).

The contractor shall provide Urinalysis CPRR to the Veterans Affairs (VA), El Paso VA Clinic, Pathology & Laboratory Medicine Services (P&LMS) 5001 North Piedras Street, El Paso, TX 79930-4210, in accordance with the attached Statement of Work. DESCRIPTION OF SERVICES. The El Paso VA Clinic requires Automated Clinical Laboratory Urinalysis Testing for urine dipstick chemistries and urine microscopic analysis using the CPRR invoicing method.

The CPRR pricing shall include all equipment, comprehensive maintenance, software and hardware upgrades, workstations, servers, training, a quality control program, reagents, calibrators, controls, supplies, consumables, disposable items, parts, accessories, printers, uninterruptable power supply (UPS), and any other item required for the proper operation of its' contractor-owned automated urinalysis testing instruments and peripherals necessary for the generation of accurate automated urinalysis results.

The urinalysis analyzers, reagents, controls, and calibrators must be FDA-approved. The Contractor retains the title of the equipment. The contractor must hold and maintain a certificate of accreditation from the Centers for Medicare & Medicaid Services (CMS) as meeting the requirements of the Clinical Laboratory Improvement Amendments (CLIA) of 1988 and must hold and maintain accreditation by the College of American Pathologists (CAP) to perform the services. RESPONSE. If interested, please provide the following information in a response:

1. Name of Company 2. Point of Contact: name, phone number, and email address 3. DUNS number 4. Company socioeconomic status (i.e., Small Business) 5. Capability Statement 6. Description and specifications of proposed analyzers, reagents, controls, and calibrators. Interested parties are responsible for adequately marking any proprietary or competitive sensitive information that is provided in a response. Interested firms must respond to the notice to be considered. For any questions regarding this notice email the Contracting Point of Contact no later than Thursday, January 30, 2025, 4:00 PM Central Time.

Publications

Every notice SAM.gov issued under this solicitation number, oldest first. Each is a separate record on SAM.

  1. January 27, 2025

    Sources sought

    Due January 30, 2025 at 5:00 PM EST. SAM.gov, notice cc690ae67c2f47bb9a7a0a5c0f0e8027

Points of contact