FDA officials said that the draft guidance is meant to address recommendations from two reports on the agency's response to COVID-19.
Years of research have showed that pulse oximeters yield less accurate readings for people with darker skin tones, and now ...
A Food and Drug Administration (FDA) draft guidance would require manufacturers of pulse oximeters to gather far more ...
After nearly a decade of machine learning innovations, the FDA has issued its first draft guidance on the use of AI in drug ...
Rather than relying on those testing the devices to judge skin tones, the draft guidance suggests manufacturers should either ...
Recognizing the increased use of artificial intelligence in the development of new therapies, the U.S. FDA on Monday released ...
The four new guidance documents are designed to help industry and other interest holders understand and comply with FDA ...
Priority review granted for CUTX-101 with PDUFA target action date set for June 30, 2025Cyprium is eligible to receive royalties and up to $129 ...
A proposed rule would require makers of talc-containing cosmetic products to test for asbestos via an analytical approach ...
The U.S. Food and Drug Administration isn’t just making a suggestion—it’s drawing a line in the sand. Last week, the FDA ...
TransOhio and Equitas Health host a monthly virtual legal clinic to help people within the LGBTQ+ community change names and gender markers on their birth certificates. But this month, they helped ...
The US Food and Drug Administration has declined to approve an injectable version of Johnson & Johnson's drug Rybrevant for a type of lung cancer, the drugmaker said on Monday. The FDA's so-called ...