FDA and the University IRB recognize there may be circumstances for a health care provider to use an unapproved or investigational device to save the life of a patient or to help a patient suffering ...
The COVID-19 public health emergency’s end doesn’t affect the U.S. Food and Drug Administration’s authority to issue new emergency use authorizations related to the novel coronavirus. That’s because a ...
MANILA, Dec 2 (Reuters) - Philippines President Rodrigo Duterte issued an executive order on Wednesday granting the Food and Drug Administration (FDA) the power to clear COVID-19 drugs and vaccine for ...
(Reuters Health) - U.S. emergency rooms are increasingly running short on medications, including many that are needed for life-threatening conditions, a recent study documents. Since 2008, the number ...
SHELTON, CT / ACCESS Newswire / October 20, 2025 / NanoViricides, Inc., a publicly traded company (NYSE American:NNVC) (the “Company”), announced that its clinical lead drug NV-387 has shown strong ...
The US Food and Drug Administration approved the first nasal spray epinephrine drug for severe allergic reactions known as ...
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