It occurs to me That we don't need hc or fda approval to sell in asia.
Perhaps that's why the k-one tone was full speed ahead...
With our primary Asia-based manufacturing partner, K-One MediTech, in place we are ready to begin production of our CE-approved AcuVid™ COVID-19 Rapid Antigen Saliva Test....and
K-One MediTech will be granted the primary manufacturer rights for Asia of the Company's AcuVid™ COVID-19 Rapid Antigen Saliva Test Kits for a period of two (2) years commencing from the 1st production batch for the commercial market