NEWS
QUIDEL RECEIVES EMERGENCY FDA AUTHORIZATION FOR FIRST RAPID COVID-19+A/B FLU ANTIGEN TEST
DALLAS - Quidel said late on Friday that it has received an Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) to market it's 15-minute, influenza A, influenza B and COVID-19, also known as the "ABC Test". This ABC test is a rapid...
*BREAKING NEWS* Huskers Partner with Vivature, Quidel for COVID-19 Testing
UN announced on Thursday, their COVID-19 Testing solution, by
NAIA announces COVID-19 guidelines
On July 1, 2020, the NAIA announced
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