About Task Force Lab
Task Force Lab (TFL) was formed to address the shortage of COVID-19 testing in the United States. We offer a solution - not just a test - by bringing testing on site for corporate clients and returning results within 24 - 48 hours.
When you buy through TFL, the test spot is yours, whereas other labs have a queue. There is no overbooking - we understand that you depend on these results to get your team back to work safely.
Tell us when and where you'd like your team to be tested.
We come to you to collect samples.
Results are sent securely and privately within 24 - 48 hours.
Available On Site Tests
Antibody Test (IgG/IgM)
Blood draw to test for COVID-19 antibodies
PCR (Swab) Test
Nasal or throat swab to detect COVID-19 virus
Certified. Responsive. Professional.
TFL has partnered with a CLIA certified and CAP accredited clinical laboratory
FDA EUA PCR Test
TFL uses the BGI RT-PCR test which was one of the first 20 to receive an FDA EUA
Licensed Registered Nurses
Qualified registered nurses with hospital experience arrive to collect sample
Rapid Result Turnaround
You rely on these results so we don't overbook; results returned within 48 hrs
Contact us today to discuss your on site testing
Volume discounts available
Frequently Asked Questions
What does TFL's full-service, on site testing include?
Task Force Lab brings everything required to setup testing at your location, including tents (with privacy walls), tables, chairs and, of course, registered nurses trained to collect samples.
Which FDA-EUA PCR test is TFL running?
PCR FDA EUA ( link)
Amended PCR FDA EUA ( link)
PCR Patient Factsheet ( link)
PCR Provider Factsheet ( link)
Where is TFL currently providing on site testing?
TFL is already providing full-service, on site testing throughout Southern California (including in Altadena, Santa Monica, Rancho Palos Verdes, Aliso Viejo and Irvine), and Northern California (San Jose).
How do I know TFL's turnaround time will not exceed 48 hours?
About the Antibody (IgG/IgM) Test
The Healgen Scientific COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) is authorized for the detection of IgG and IgM antibodies against SARS-CoV-2 in human serum, plasma (EDTA, lithium heparin, and sodium citrate), or venous whole blood.
About the RT-PCR Test
FIND conducted independent evaluations at the Hôpitaux Universitaires de Genève, to verify the limit of detection (LOD) and the clinical performance of the BGI RT-PCR test. The BGI test received 100% (95%CI: 93, 100) clinical sensitivity, and 99% (95%CI: 95, 100) clinical specificity.
-FIND (The Foundation for Innovative New Diagnostics. FIND is a WHO Collaborating Centre for Laboratory Strengthening and Diagnostic Technology Evaluation. Source)