COVID-19 TESTING SOLUTIONS FOR SCHOOLS & ORGANIZATIONS

Helping Organizations Stay Open and Safe!

Cordant Health Solutions®️ is now offering fast and cost-effective RT-PCR COVID-19 nasal swab and saliva testing solutions, focusing on serving organizations in the Pacific Northwest through our laboratory located in Tacoma, Washington.

Cost Effective

Cordant’s program offers competitive pricing and includes robust reporting capabilities.

Fast Results

Test results are typically available within 24 hours of the sample being received by Cordant.

Convenient Test Options

Cordant offers both saliva and nasal swab tests that detects the virus that causes COVID-19, including the Delta variant.*

Testing Solutions

Pooled Sample Testing

Cordant offers cost-effective pooled testing for schools and business organizations. Pooled testing is a way to use the gold standard of testing at a cost comparable to instant or antigen testing. This technology allows for the testing of large groups rapidly and at a lower cost than a typical PCR diagnostic test.

Business Travel

Having a COVID-19 pre-flight screening plan in place for your employees will help save your business time and money that can be lost due to quarantine periods. Cordant is one of the only test providers able to deliver COVID-19 RT-PCR saliva test results within 24 hours, providing an ideal solution for your traveling workforce needs.

RT-PCR Test Processing

Cordant is able to accept overflow testing for organizations and laboratories experiencing high demand for testing.

Your Trusted Partner

For over 30 years, Cordant Health Solutions has operated as a high-volume clinical laboratory with scientific expertise and strict quality standards with a long history of supporting local and state agencies, employers, and community programs.

Cordant is certified under the Clinical Laboratory Improvement Amendment (CLIA)

Registered with the International Reagent Resource (IRR)

*Cordant uses the SalivaDirect™ Test qualitative detection of nucleic acid from SARS-CoV-2 in saliva. This test has not been FDA cleared or approved. This test has been authorized by FDA under an EUA for use by authorized laboratories. This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens; and this test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.