FDA issues emergency use authorisation for third COVID-19 vaccine

FDA

27 February 2021 - Action advances fight against COVID-19, follows comprehensive evaluation of available safety, effectiveness and manufacturing quality information by FDA career scientists, input from external experts.

Today, the U.S. FDA issued an emergency use authorisation for the third vaccine for the prevention of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). 

Read FDA press release

Michael Wonder

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Michael Wonder

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Outcome , US , Vaccine , COVID-19