FDA releases FAQs on remdesivir EUA, antibody tests
The Food and Drug Administration yesterday updated its FAQs on the emergency use authorization of remdesivir for use on certain hospitalized COVID-19 patients.
The document includes information on the changes to Gilead’s fact sheets for health care providers and patient caregivers.
FDA this week also posted a patient-and-consumer-focused FAQ about SARS-CoV-2 antibody, or serology, testing, including a guide to understanding test results and where to obtain them.
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