Tag: USFDA
Philips AI-powered, software-defined magnetic resonance software receives 510(k) clearance
Philips has announced that its SmartSpeed artificial intelligence (AI)-powered magnetic resonance (MR) acceleration software has received US Food and Drug Administration (FDA) 510(k) clearance....
Highlights from the CX 2019 session, Paclitaxel: the last word
Watch the video roundup from the CX2019 Highlight Session, Paclitaxel: The last word.
Filmed onsite at the Charing Cross Symposium (15–18 April 2019, London, UK).
