If the FDA follows an advisory committee’s vote, it can potentially be a transformative step in the delivery of mental health ...
WASHINGTON – To earn the vote he needed to become the nation's top health official, Robert F. Kennedy Jr. made a special ...
With President Trump back in the Oval Office and Robert F. Kennedy possibly to follow at the Department of Health and Human Services, it’s hard to say what’s in store for the Food and Drug ...
The FDA isn’t bound to follow the PDAC’s advice, but the resounding verdict from the panel suggests Lykos is heading for disappointment when the regulator makes its final decision by 11th August.
A key Senate committee supports Robert F. Kennedy Jr., President Trump's pick to head the Department of Health and Human ...
Nuplazid (pimavanserin) is already FDA-approved to treat psychosis caused by Parkinson's disease, but Acadia's hope to expanding that use to the Alzheimer's population were shot down by a complete ...
The U.S. Food and Drug Administration has pulled draft guidance from its website requiring companies to test medicines and devices in diverse populations as part of a purge of diversity, equity and ...
"Roche’s STI assay panels gain FDA 510(k) clearance and CLIA waiver" was originally created and published by Medical Device Network, a GlobalData owned brand. The information on this site has ...
The FDA specifically noted these key areas need ... America grapples with—it’s considered a global issue. A joint panel from the United Nations and World Health Organization declared in ...
Roche announced that the US Food and Drug Administration (FDA) has granted 510(k) clearance and Clinical Laboratory Improvement Amendments of 1988 (CLIA) waiver for its cobas liat sexually transmitted ...