FDA Authorizes COVID-19 Vaccine For Emergency Use In U.S.
December 14, 2020
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 a statement. "Vaccines will help bring this pandemic to an end, which is all the more reason to double down on the public health measures we need to stay safe in the coming months."