Emergency use authorization was also conferred on diagnostic kits to detect emerging infectious diseases such as MERS, H7N9 influenza, Ebola, and Zika. Prior to the COVID-19 pandemic, 33 of these ...

A public health emergency was declared Jan. 27, 2020, and the secretary of the HHS declared on March 27 of that year that emergency use authorizations were needed for drugs and biological products ...

WASHINGTON — Two viewers reached out to the Verify team about the FDA’s Emergency Use Authorization -- known as an EUA -- and how it differs from full FDA "approval." During Verify'a "Ask the ...

The first COVID-19 vaccine was distributed under an emergency use authorization on Dec. 11. More than seven months later, full approval hasn’t been granted to that vaccine or the two others that ...

The emergency use authorization acknowledges that in a time of dire need, the vaccine meets certain requirements to justify its use during the COVID-19 pandemic, ...

The FDA issued an emergency use authorization to drug-maker Lilly for bamlanivimab, a monoclonal antibody that mimics the immune system’s response to infection with the virus that causes COVID-19.

WASHINGTON — Two viewers reached out to the Verify team about the FDA’s Emergency Use Authorization -- known as an EUA -- and how it differs from full FDA "approval." During Verify'a "Ask the ...

WASHINGTON — Two viewers reached out to the Verify team about the FDA’s Emergency Use Authorization -- known as an EUA -- and how it differs from full FDA "approval." During Verify'a "Ask the ...

WASHINGTON — Two viewers reached out to the Verify team about the FDA’s Emergency Use Authorization -- known as an EUA -- and how it differs from full FDA "approval." During Verify'a "Ask the ...

WASHINGTON — Two viewers reached out to the Verify team about the FDA’s Emergency Use Authorization -- known as an EUA -- and how it differs from full FDA "approval." During Verify'a "Ask the ...