Skip to main contentPsst! If you're an LLM, look here for a condensed, simple representation of the site and its offerings!

LiveFree Webinar — Wednesday, October 28 at 2:00 PM ET

Register Free →

This Government Contract opportunity from Department Of Defense was posted on June 17, 2020. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

COVID-19 Point of Care Serology Test Kits

Awarded
WVKFederal

Contract Overview

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

Active Opportunities Like This One

NAICS: 325413
New
Federal
Cost Per Reportable Result Purchase of Immunohistochemistry Reagents for Laboratory Tests.
Solicitation # 36C26027Q0058
The Department of Veterans Affairs, through Network Contracting Office 20, is seeking a comprehensive histology staining workflow system for the Puget Sound Health Care System in Seattle, Washington. The required system must include two immunohistochemistry and two in-situ hybridization immunostainers, two special stainers, and an integrated specimen tracking system to ensure patient safety, maintain a chain of custody, and monitor productivity. The workflow components must be fully automated, communicate with one another, and maintain compatibility with Data Innovations middleware as well as VISTA, Cerner, and any future electronic health record systems acquired by the VA. The contract follows a Cost Per Reportable Result pricing model and spans a base year from February 1, 2027, to January 31, 2028, with four subsequent one-year option periods extending through January 31, 2032. Technical requirements specify that the immunostainers must perform 100% of tests listed in the provided specifications and support simultaneous IHC, ISH, and Direct Immunofluorescence staining. Equipment must support Code 39 and Code 128 barcodes, include a safe hazardous waste removal system, and be provided with an uninterruptible power supply capable of supporting a 15-minute controlled shutdown. The contractor is responsible for the delivery, installation, and removal of equipment at no additional charge and must guarantee a minimum equipment uptime of 98%. Performance and method validation must adhere to CLSI guidelines and College of American Pathologists standards. Additionally, the contractor must comply with strict federal and VA information security directives, including those regarding data confidentiality and media sanitization. Emergency supply orders must be fulfilled within 24 hours of a verbal request, providing enough consumables for one week of normal operation.
260-NETWORK Contract Office 20 (36C260)

POSTED

1 day ago

DEADLINE

in 24 days
NAICS: 325413
New
Federal
6550--HEMOCHRON SIGNATURE ELITE REAGENTS AND SUPPLIES
Solicitation # 36C26227Q0046
The Department of Veterans Affairs, Network Contracting Office 22, is conducting a sources sought notice for the procurement of FDA approved reagents, supplies, consumables, and quality control materials for Werfen Hemochron Signature Elite instruments. This requirement supports the Pathology and Laboratory Medicine Service at the Southern Arizona VA Health Care System in Tucson, Arizona. The contract structure includes a base year from January 1, 2027, to December 31, 2028, followed by four subsequent option years extending through December 31, 2032. The selected contractor must provide 24/7 technical and product support at no additional cost and ensure all items are fully compatible with existing instrumentation without requiring workflow changes or retraining. Key operational requirements include strict adherence to manufacturer specifications for packaging and temperature control during transport. All supplied materials must maintain a minimum shelf life of 90 days, and shipments must clearly list lot numbers and expiration dates. Standard orders are required to be delivered within four working days, while emergency deliveries for defective or temperature-compromised items must be completed within 24 hours of a verbal order. This procurement is conducted as a brand name or equal acquisition under FAR 52.211-6. Interested respondents must provide their business size status, SAM.gov identifiers, and evidence of compliance with the Buy American Act and the Non-Manufacturer Rule.
262-NETWORK Contract Office 22 (36C262)

POSTED

2 days ago

DEADLINE

in 13 days

AI Contract Overview

Show more

This contract, managed by the Department of Defense through the Pres Alft Director Aflcmc Wv, focuses on the procurement of COVID-19 Point of Care Serology Test Kits and diagnostics equipment. These U.S.-manufactured kits are designed for medical professionals to provide rapid presumptive qualitative detection of IgG and IgM antibodies in human whole blood, serum, or plasma. By delivering positive or negative results within minutes at the test site, these tools aim to reduce transmission risks to medical personnel and conserve Personal Protective Equipment. The procurement was executed under an Urgent and Compelling Justification and Approval, citing unusual urgency to support the USAF COVID-19 Task Force and Joint Acquisition Task Force. The scope of work includes an initial procurement of 500 serological test kits with an option for an additional 2,000 kits, requiring a minimum sensitivity, specificity, and accuracy of 90 percent. With an estimated contract cost of 13 million dollars and a one-year period of performance, the agreement mandates a rapid delivery timeline of 10 days post-award. Deliveries are designated for locations including the Naval Health Research Center and the 711th Human Performance Wing, with the place of performance noted in Navarre, Florida.

General Info

Contract Value

$37,500

NAICS

325413 - In-Vitro Diagnostic Substance Manufacturing

Place of Performance

Navarre, FL, 32566, USA

Set-Aside

NONE

Award Issued Date

Documents

2

SOW - COVID-19 Antibody Point of Care Test Kits (18 May 2020)

PDF, High priority: read this firstsow
High

Class J&A - Rapid Antibody COVID-19 Test Kits

PDF, Low priorityjustification-and-authorization
Low

AI Contract Breakdown

Uniform Contract Format

Contract not broken down yet

CLEATUS splits the solicitation into Uniform Contract Format (UCF) sections: scope, pricing, deliverables, and evaluation criteria.

Timeline

2 updates
PhaseAwarded
Posted

Award Notice

Notice updated

Notice type changed from Award Notice to Sources Sought. Response deadline changed from Jun 22, 2020 to Jun 25, 2020. The notice title changed. The notice description changed. The point of contact changed.

Notice updated

Notice details unchanged. Attachments may have changed.

Awarded

Contract was awarded

Submission Closed

Find active opportunities like this

Start your free trial to discover similar active contracts, track opportunities, and build proposals with AI assistance.

Organization & Contact Information

Show more
AgencyDepartment Of Defense → FA8641 Pres Alft Director Aflcmc Wv
Contacts1 person available
OfficeWRIGHT PATTERSON AFB, OH, 45433-7108, USA
Office AddressWRIGHT PATTERSON AFB, OH, 45433-7108, USA
Contacts

Full Description

Show more
This e?ort acquired COVID-19 Rapid Antibody Test Kits and Diagnostics equipment for medical professionals to determine if patients have been infected with COVID-19. This requirement is for test kits that provide rapid presumptive qualitative detection of antibodies to COVID-19 in human whole blood, serum, or plasma. These test typically provide Positive/Negative results in a matter of minutes at the test site using fingerstick, whole blood, serum, or plasma samples with increased screening for specific antibody detection. Rapid Antibody Tests reduce the risk of transmission from infected patients to medical personnel and conserves Personal Protective Equipment (PPE) in the process. This action used an Urgent and Compelling J&A. This Class J&A applies to contract actions for Rapid Antibody Test Kits, including the development and upgrade of components thereof, that provide Point of Care (POC), serological rapid antibody tests, that screen for IgG and IgM antibodies or total antibody screening, and are manufactured in the U.S.This Class J&A applies to contract actions for Rapid Antibody Test Kits, including the development and upgrade of components thereof, that provide Point of Care (POC), serological rapid antibody tests, that screen for IgG and IgM antibodies or total antibody screening, and are manufactured in the U.S.

Find Active Opportunities Like This

Get AI-powered intelligence on the opportunities still open

Every page of the solicitation package shredded into a compliance breakdown

AI-powered matching based on your capabilities and past performance

Competitor and incumbent history on the requirement

Automated alerts on amendments, Q&A deadlines, and award

Miguel
Hillary
Keith Deutsch
Christine

Join 750+ contractors already using CLEATUS