$QLGN (reminder) We have recently been in communication with the FDA on our Emergency Use Authorization (EUA) submission for our FastPack® SARS-CoV-2 IgG test for COVID-19 antibodies. We remain confident that the data meet or exceed the FDA guidelines for an EUA. As vaccines are deployed, we believe the FastPack COVID-19 antibody test has the ability to provide an accurate rapid solution in the marketplace.
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