Providing Key COVID-19 Response Technology
FDA EUA Antigen POC Solution
Our FDA/EUA-approved Antigen POC Solution provides results in 10 minutes with 88.4% sensitivity and 100% specificity.
Antigen lateral flow assay cassette test
FDA EUA approved CE Marked
Results in 10 minutes with less than 12% false-negatives and 0% false-positives.
Immediate volume available, despite 26-million-unit backlog
CE Marked Antigen POC Solution
Upcoming - Rapid Digital Saliva Test
CE Marking estimated March 1, 2021.
Not yet authorized by the FDA; undergoing FDA EUA process and subject to such regulatory approval.
In-country manufacturing and strategic alliance potential.
Contact us today to learn more about our leading technologies!