by John Nycz | Sep 24, 2020 | Diagnostics, Rapid Antibody Testing, Uncategorized
McMinnville TN— September 24, 2020 — Yesterday, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the first serology (antibody) point-of-care (POC) test for COVID-19. Point-of-Care Delivers More Timely and Convenient Results...
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