FDA Authorizes COVID-19 Vaccine For Emergency Use In U.S.
Pfizer and BioNTech's vaccine is the first to receive an emergency authorization from the Food and Drug Administration. Officials say it may be ready for widespread inoculations within days.
Federal officials have authorized emergency use of the COVID-19 vaccine produced by Pfizer and BioNTech in a landmark decision that promises to alter the fight against the coronavirus radically in the United States.
The Food and Drug Administration released its letter to Pfizer granting the authorization Friday evening.
"It is nothing short of a medical miracle to have FDA authorization of a vaccine for COVID-19 just over 11 months since the virus was made known to the world," said Health and Human Services Secretary Alex Azar in
