FDA Emergency Use Authorization

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Roche’s Elecsys Anti-SARS CoV-2 Antibody Test Receives Emergency Use Authorization by FDA: To Ship Double-Digit Millions Per Month

The U.S. Food and Drug Administration issued an Emergency Use Authorization (EUA) for Roche’s Elecsys® Anti-SARS-CoV-2 antibody test. Designed to help assess if a patient has been exposed to the novel coronavirus as well if the patient has developed any antibodies,...

Los Alamos National Laboratory-based COVID-19 Test Receives Emergency Use Authorization from the FDA

San Diego-based Meso Biotech received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for its Accula™ SARS-CoV-2 Test, which purportedly generates COVID-19 diagnostic results in 30 minutes. Apparently affordable and designed for the...

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