FDA advisors recommend emergency use authorisation of Moderna Covid-19 vaccine

The US Food and Drug Administration’s advisory panel, comprising external experts, has given an emergency use approval to Moderna COVID-19 vaccine, making it the second drug after Pfizer to receive such an authorisation in less than a week.
The US Food and Drug Administration’s advisory panel, comprising external experts, has given an emergency use approval to Moderna COVID-19 vaccine, making it the second drug after Pfizer to receive such an authorisation in less than a week.

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