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 ...

Moderna is seeking emergency use authorization from the FDA for its Covid-19 vaccine for children 6 months through 5 years of age. 24/7 Live San Francisco East Bay South Bay Peninsula North Bay.

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 ...

Fresh off of the heels of a shakeup at the CDC over vaccine recommendations, many Americans still question the necessity and ...

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.

Moderna, Inc. (MRNA) on Thursday announced that the U.S. Food and Drug Administration (FDA) has fully approved its COVID-19 ...

--BD, a leading global medical technology company, and CerTest Biotec have announced Emergency Use Authorization from the U.S. Food and Drug Administration for a molecular polymerase chain ...

The FDA this week fully approved Moderna’s COVID-19 vaccine for children aged 6 months to 11 years but limited the approval ...

Portugal has granted emergency use authorization (EUA) for Vestaron’s groundbreaking bioinsecticide SPEAR® LEP, enabling farmers to protect tomato crops from devastating infestations ...