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This Sources Sought opportunity from Department Of Veterans Affairs was posted on May 1, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

6640--Specimen Validity and Drug of Abuse of Abuse Reagent Supplies for the Minneapolis VA Health Care System

Closed
36C26326Q0650Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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NAICS: 325413
New
DIBBS
TEST KIT, CHLAMYDIA TRA
Solicitation # SPE2DS-26-T-423P
Solicitation SPE2DS-26-T-423P, issued by the DLA Troop Support Medical Supply Chain, is a request for quotes for one test kit for the detection of Chlamydia trachomatis, identified by NSN 6550-01-725-3600. The kit is designed for in vitro diagnostic use to perform qualitative direct immunofluorescence tests on human urogenital and ophthalmic specimens, as well as for confirming Chlamydia in cell culture. Each kit must provide materials for 50 tests and include two positive control slides, mounting fluid, Chlamydia test reagent, and instructions for use. The required delivery date is September 14, 2026, with the place of performance and delivery located in San Antonio, Texas. The procurement falls under NAICS code 325413 and is subject to destination inspection and acceptance. Packaging must adhere to commercial standards, MIL-STD-2073-1E, and RP001, while marking must comply with Medical Marking Standard No. 1. The contract incorporates various FAR and DFARS clauses, including the Buy American and Balance of Payments Program and the Hazard Communication Standard for hazardous materials. Payment and invoicing are to be processed electronically through the Wide Area WorkFlow system. Quotes must be submitted via the DIBBS portal by September 16, 2026, and the award may be processed through an automated system, with a price evaluation preference applied to HUBZone concerns.
MEDICAL SUPPLY CHAIN MD SURG FSF

POSTED

2 days ago

DEADLINE

in 4 days

AI Contract Overview

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The Minneapolis VA Health Care System is conducting market research through a sources-sought notice to identify qualified vendors capable of supplying FDA-approved specimen validity and drug of abuse reagents, specifically for nitrite and fentanyl testing, to support its Forensic Toxicology Laboratory under the National Laboratory Certification Program. The required reagents must be compatible with the Beckman AU480 analyzer, meet precise performance standards including a 1.0 ng/mL fentanyl cutoff with at least 5% cross-reactivity to nor-fentanyl and a Griess method nitrite assay, and comply with shelf-life requirements ensuring at least two-thirds of the product’s original shelf life remains upon delivery. Each shipment must contain only one lot number per product, follow FOB Destination delivery terms to the Minneapolis VA Medical Center, and include a detailed packing slip with the contractor’s name, purchase order number, delivery date, and itemized listing. All products must be accompanied by Safety Data Sheets, and hazardous materials must be clearly labeled. The solicitation also mandates compliance with FAR 52.225-2(b) for country of origin certification, requiring vendors to state whether items are U.S.-made or imported, and to provide proof of authorization if acting as a distributor rather than the manufacturer. Vendors must respond via email to theresa.thunder@va.gov by 5:00 PM Central Time on May 7, 2026, providing their Unique Entity Identifier, socio-economic classification, and confirmation of compliance with 13 CFR 121.406(b) regarding small business size standards and subcontracting limitations. If the vendor is not the manufacturer, they must submit a letter of authorization from the manufacturer along with the manufacturer’s socio-economic status. Responses must also disclose whether the supplies are available under existing government contracts such as FSS or GSA. Delivery must occur within five calendar days of order receipt, and technical support must be available Monday through Friday, 8 a.m. to 5 p.m., with a guaranteed four-hour response time. The anticipated contract duration is five years, from October 1, 2026, to September 30, 2031, and the resulting award, if any, may be subject to set-asides for Veteran-Owned Small Businesses under VAAR 852.219-76 or Small Businesses under FAR 52.219-14, with additional restrictions against gray market items under VAAR 852.

General Info

Minneapolis VA seeks vendors for drug test supplies; submit info by May 7, 2026.

Agency

Department Of Veterans Affairs → Network Contract Office 23 (36C263)View Agency

NAICS

325413 - In-Vitro Diagnostic Substance ManufacturingView NAICS

Place of Performance

Department of Veteran Affairs Minneapolis VA Health Care System, Minneapolis, MN, 55417, USA

Set-Aside

NONE

Documents

(1)

Sources Sought 36C26326Q0650 Specimen Validity and Drug of Abuse Reagent Supplies

DOCXsources-sought

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Timeline

PhaseClosed
Posted

Sources Sought

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Veterans Affairs → Network Contract Office 23 (36C263)
Contacts1 person available
OfficeSaint Paul, MN, 55101, USA
Organization / Agency
Department Of Veterans Affairs → Network Contract Office 23 (36C263)
View Agency Profile
Office AddressSaint Paul, MN, 55101, USA
Contacts
Theresa (Tess) ThunderContracting Specialist

Full Description

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The Minneapolis Health Care System requires Specimen Validity and Drug of Abuse Reagen Supplies with the Salient Characteristics listed below. This is a sources sought looking for businesses to provide the supplies listed below for market research purposes. No awards of a contract will be made from this announcement. If you are a vendor that can provide the requested information above and required supplies described below with competitive pricing, send your information (to include your organization's Unique Entity Identifier number) with a description of proof of capability to: theresa.thunder@va.gov on or before May 7th, 2026. Only emailed responses will be considered. Additionally, please provide answers as appropriate to the following questions in the table below with your response to this sources sought. Failure to respond to the following questions may affect the acquisition strategy. 1. Identify your organization's socio-economic category. 2. Identify if your organization is the manufacturer of the requested supplies. If you are not the manufacturer, identify the manufacturer of the supplies that you will provide, their socio-economic category and a letter showing that your organization is an authorized distributor for the requested supplies.  3. Fill out the certificate under FAR Provision 52.225-2(b), identifying the item and its country of origin. ( https://www.acquisition.gov/far/part-52#FAR_52_225_2__d3401e52). If the product is a US domestic end product, write in USA for the item's country of origin. 4. State whether any of the requested supplies may be ordered against a government contract awarded to your organization (e.g Federal Supply Schedule (FSS), General Services Administration (GSA), etc.). 5. Address whether your organization meets the requirements of 13 CFR 121.406 (b)(1)(i), (b)(1)(ii) and (b)(1)(iii) (https://www.ecfr.gov/current/title-13/chapter-I/part-121/subpart-A/subject-group-ECFR0fca5207262de47/section-121.406#p-121.406(b)). 6. Provide estimated shipping and delivery information for the requested supplies (e.g. Expected lead time on delivery).   *If applicable, VAAR 852.219-76 VA Notice of Limitations on Subcontracting Certificate of Compliance for Supplies and Products, will apply to the potential solicitation if set-aside for Veteran Owned Small-Businesses.*   *If applicable, VAAR 852.212-71 Gray Market Items, will apply to the potential solicitation.* *If applicable, FAR 52.219-14 Limitations on Subcontracting, will apply to the potential solicitation if set-aside for Small-Businesses. *

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Solicitation # 36C26326Q1098
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