Developers of COVID-19 tests available through OTC sales in the US should look to two revised emergency use authorization templates from the Food and Drug Administration as they prepare their EUA applications to the agency.
The templates, “Molecular and Antigen Home Use Test Template” and “Supplemental Template for Molecular and Antigen Diagnostic COVID-19...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on HBW Insight for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?