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This is a Sources Sought Notice for specimen validity and drug of abuse reagent supplies required by the Minneapolis VA Health Care System. The Department of Veterans Affairs, Veterans Health Administration, Veterans Integrated Service Network 23 is seeking market research information from potential vendors. Responses must be submitted via email to theresa.thunder@va.gov by May 7, 2026, at 5:00 PM Central Time. The solicitation number is 36C26326Q0650, and the product service code is 6640 (reagents for clinical use).

The Minneapolis VA Health Care System's Forensic Toxicology Laboratory requires FDA-approved specimen validity and Fentanyl reagents to support the federal workplace urine drug-of-abuse testing program. Required items include Creatinine Perfect reagent, Fentanyl reagent, Nitrite Perfect reagent, calibrators, and validity calibrators with estimated annual quantities ranging from 6 to 25 units per product. The anticipated contract would be a five-year, brand-name-only award effective October 1, 2026, through September 30, 2031, on an on-demand, as-needed basis limited to MVAHCS use. Delivery must occur within five calendar days of order placement to the VA Medical Center warehouse in Minneapolis, with deliveries between 8:00 AM and 3:30 PM Monday through Friday. Vendors must respond with their socio-economic category, proof of capability or authorized distributor status, country of origin certification per FAR 52.225-2(b), information on existing government contracts, small business compliance documentation per 13 CFR 121.406, and estimated shipping/delivery lead times. Technical support must be available Monday through Friday, 8:00 AM to 5:00 PM, with telephone response within four hours.

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Sources Sought Notice Sources Sought Notice

SUBJECT*
Specimen Validity and Drug of Abuse of Abuse Reagent Supplies for the Minneapolis VA Health Care System

GENERAL INFORMATION

CONTRACTING OFFICE’S ZIP CODE*
58102
SOLICITATION NUMBER*
36C26326Q0650
RESPONSE DATE/TIME/ZONE
05-07-2026 17:00 CENTRAL TIME, CHICAGO, USA
ARCHIVE
15 DAYS AFTER THE RESPONSE DATE
RECOVERY ACT FUNDS
N

SET-ASIDE

PRODUCT SERVICE CODE*
6640
NAICS CODE*
325413
CONTRACTING OFFICE ADDRESS
DEPARTMENT OF VETERANS AFFAIRS

NETWORK CONTRACTING OFFICE 23

2101 NORTH ELM STREET (04-S)

FARGO ND 58102

POINT OF CONTACT*

Contracting Specialist Theresa (Tess) Thunder theresa.thunder@va.gov

PLACE OF PERFORMANCE

ADDRESS
Department of Veteran Affairs

Minneapolis VA Health Care System

One Veterans Drive

Minneapolis MN

POSTAL CODE
55417
COUNTRY
USA

DESCRIPTION

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. *

Statement of Work

Specimen validity and drugs of abuse reagents

1. Basic Requirement:

The Minneapolis VA Health Care System Toxicology Laboratory, located at 1 Veterans Drive, Minneapolis, MN 55417, hereinafter referred to as MVAHCS, needs to establish a contract which provides FDA approved specimen validity and Fentanyl reagents which are specified in the schedule of items. These reagents will be used to verify the validity of specimens, including nitrite and creatinine assays, as well as perform Fentanyl testing in our highly specialized Forensic Toxicology Laboratory. MVAHCS is certified by the Department of Health and Human Services (HHS), Substance Abuse and Mental Health Services Administration (SAMHSA) under the National Laboratory Certification Program (NLCP) to conduct the Federal Workplace Urine Drugs of Abuse Testing Program for all the VA hospitals and their affiliated CBOCs. These products are used to support that program.

The MVAHCS requires a nitrite specific colorimetric assay that uses the Griess test which detects nitrites through formation of a diazonium salt, as opposed to a general oxidant assay. Urine nitrite validity requires a calibrator availability of 0 µg/mL and 500 µg/mL. Fentanyl requires a cutoff value of 1.0 ng/mL and cross-reactivity with Nor-fentanyl ≥5%. In addition, these reagents must be compatible for use with the Beckman AU480 analyzer.

Due to the strict and very specific performance criteria which have been established per NLCP guidelines, the MVAHCS has determined that only the reagents listed below meet our needs for this regulated testing. The products listed below have been validated and certified for use at the MVAHCS. Any deviation would require revalidation and recertification from the NLCP.

2. Contract Type and Terms:

The MVAHCS will award a five-year, brand name only contract for all items listed in the Schedule of Items. Contract use will be limited to the MVAHCS. The effective period of the contract shall be from 10/1/26-9/30/31.

3. Estimated Quantities:

The quantities listed in the “Schedule of Items” are estimated annual requirements. The MVAHCS attempts to be as accurate as possible when providing estimated quantities, however, actual quantities required may vary from quantities listed. All products will be requested on an “on demand, as needed” basis.

Schedule of Items:

Description
Stock #
Est Annual QTY
Creatinine perfect - RGT - 900 ml / 200 ml
10445265
15
Fentanyl 2 - RGT- ARK - 500ml
11554029
6
Nitrite perfect - RGT - 500 ml / 500 ml
10445266
25
Fentanyl ARK Cal Cutoff - SYVA- CAL - 2 x 10 ml
11354476
10
Nitrite Validity Calibrator 500 mg - Syva - CAL - 14 ml
10445275
20
Validity Neg Calibrator - Syva - CAL 14 ml
10445268
20

4. Customer Service/Technical Support:

A company representative shall be available to the MVAHCS during the contract period to review the account, provide product information, handle problems or defective merchandise (if required) and address any other issues or concerns that may arise. Technical telephone support must be available Monday through Friday between 8:00am and 5:00pm. Telephone response time shall be within four (4) hours of notification.

5. Ordering Procedures:

Orders will be placed via contractor’s preferred method on an on-demand, as-needed basis by the MVAHCS. A list of approved personnel will be provided at the request of the contractor. Contractor shall provide the following preferred ordering information:

6. Delivery All supplies shall be delivered FOB Destination to the MVAHCS (unless otherwise indicated on the response to the solicitation) and shall arrive at the MVAHCS no later than 5 calendar days after receipt of an order.

Deliveries shall be made to:

VA Medical Center, Bldg. 70
Warehouse (90D), PO# _________
One Veterans Drive
Minneapolis MN 55417
Delivery Times: Between 8:00am and 3:30pm
(Monday-Friday except Federal Holidays)

All deliveries shall be accompanied by a packing slip which shall contain contractor’s name, purchase order number, date of order, date of delivery, itemized list of products furnished including product description and quantity shipped.

7. Product Quality All products offered to the MVAHCS must be of the same consistent high quality as would be offered to the general commercial public in the United States.

A. All products are purchased subject to acceptance by the MVAHCS. Products will be rejected if found unsatisfactory by the MVAHCS when they are received, or later if deterioration of the product occurs before the outdate. The MVAHCS will not be financially liable for unacceptable materials.

B. Any substitutions of product must have the written approval of the MVAHCS and the VISN 23 Contracting Officer.

C. All defective or inferior products must be replaced within 48 hours at no cost to the MVAHCS.

D. The MVAHCS is not required to return unacceptable product.

E. It is the contractor’s responsibility to provide the MVAHCS with recall notices on any product that has been delivered to this facility that may be defective. Notification shall be made via the most expedient method. The contractor shall replace and/or reimburse recalled or defective products at no cost to the government.

F. The contractor shall provide MVAHCS with a listing of the contractor’s products that are considered hazardous. The listing should also include a determination as to what can be considered harmless to be disposed of by normal methods, such as disposing in the sink or trash. SDS shall be available upon request.

G. To assure rotation of stock at the distributor, each lot of a product received must have an outdate later than previously received.

H. Only one lot number per product may be shipped per order. Multiple lot numbers per product per order will not be accepted.

I. All products must be delivered with at least 2/3 of the shelf-life remaining. The manufacturer will provide a shelf-life list (time from production to outdate), for each product, if requested.

8. Changes/Modifications:

Changes in the pricing, terms or conditions of this agreement may only be made by written agreement of the parties. All modifications for changes in the prices, terms or conditions of this agreement will be prepared for signature by the VISN 23 Contracting Officer.

*= Required Field
Sources Sought Notice

Sources Sought Notice

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