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INDIANAPOLIS, April 16, 2021 /PRNewswire/ -- Eli Lilly and Company (NYSE: LLY) has requested the U.S. Food and Drug Administration (FDA) revoke the Emergency Use Authorization (EUA) for ...
The FDA has issued an emergency use authorization for left-sided Impella heart pumps to support to COVID-19 patients suffering from heart and lung issues. Skip to main content. BHR; ...
Siemens Healthineers announces FDA Emergency Use Authorization for CLINITEST® Rapid COVID-19 Antigen Self-Test for unsupervised self-testing for the SARS-CoV-2 virus by individuals age 14 and ...
Before treatments were available. During the early days of the pandemic, there were no treatments approved, not even for emergency use authorization, by the U.S. Food and Drug Administration.
GenMark Receives FDA Emergency Use Authorization for its ePlex® SARS-CoV-2 Test. COVID-19 diagnosis in under two hours now available globally in hospitals on company’s ePlex System.
EVANSTON, Ill.--(BUSINESS WIRE)--Minute Molecular Diagnostics today announced that the U.S. Food and Drug Administration (FDA) granted an Emergency Use Authorization (EUA) for its rapid DASH SARS ...
Trump administration officials are exploring options to quickly fix its plan to make the vaccine free for all Americans.
Pfizer will seek emergency use authorization from the FDA for a third booster shot of its Covid-19 vaccine, specifically intended to increase the immune response to the delta variant of the virus ...
The agency issued an emergency use authorization for that test, a process it can use to speed up authorization. It did the same for other combination tests approved afterward, such as the FlowFlex ...
There is no data from well-controlled, randomized clinical trials that demonstrate the efficacy and safety of convalescent plasma for treating COVID-19, according to a statement issued Sept. 1 by ...
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