United States drugmaker Moderna has applied for an Emergency Use Authorization for its mRNA-1273 coronavirus disease 2019 (Covid-19) vaccine, the Food and Drug Administration said on Monday.
FDA Director-General Rolando Enrique Domingo said that the agency is checking the documents submitted by Moderna.
Already have an active account? Log in here.
Continue reading with one of these options:
Continue reading with one of these options:
Premium + Digital Edition
Ad-free access
P 80 per month
(billed annually at P 960)
- Unlimited ad-free access to website articles
- Limited offer: Subscribe today and get digital edition access for free (accessible with up to 3 devices)
TRY FREE FOR 14 DAYS
See details
See details
If you have an active account, log in
here
.