FDA panel to discuss emergency authorization for Moderna vaccine
A Food and Drug Administration panel is set to meet Thursday to discuss Moderna’s COVID-19 vaccine, and if they’ll give it emergency authorization.
A Food and Drug Administration panel is set to meet Thursday to discuss Moderna’s COVID-19 vaccine, and if they’ll give it emergency authorization.
This January, you will be able to buy a COVID-19 test to take home.
On Thursday, an advisory committee to the Food and Drug Administration recommended approving the Pfizer BioNTech vaccine.
The Food and Drug Administration has granted an emergency use authorization for the first non-prescription, over-the-counter COVID-19 test kit for at-home use.
U.S. health regulators have posted a positive review of Pfizer’s COVID-19 vaccine as they near a decision on whether to allow use of the shot.
President Trump’s Chief of Staff Mark Meadows is scheduled to meet with the head of the Food and Drug Administration to discuss a coronavirus vaccine.
The Food and Drug Administration has sent warning letters to companies selling products that falsely claim to treat COVID-19.
The United States Food and Drug Administration is authorizing Regeneron’s antibody cocktail for some patients who test positive for COVID-19.
The Food and Drug Administration has a new way of getting information out about outbreaks of foodborne illnesses.
As COVID-19 cases continue to climb here in the U.S., the FDA has just approved Remdesivir to treat coronavirus patients, though it was only used in hospitals in cases of emergency.