Is this just on a personal hunch or something based on fact?
It's hard to fathom why you'd go through the "normal FDA approval" when the medical device you're creating sits under the EUA specifications.
https://www.fda.gov/medical-devices/emergency-use-authorizations-medical-devices/coronavirus-disease-2019-covid-19-emergency-use-authorizations-medical-devices
- Forums
- ASX - By Stock
- SE1
- Ann: Half Year Accounts - Appendix 4D
Ann: Half Year Accounts - Appendix 4D, page-12
-
- There are more pages in this discussion • 4 more messages in this thread...
You’re viewing a single post only. To view the entire thread just sign in or Join Now (FREE)