FDA Sets Its Sights On AI And Big Data For Medical Device Innovation
In the FDA’s annual Focus Areas of Regulatory Science report, the agency lays out its areas of interest for the use of medical device advancement in public health and the research and development of medical devices.
You may also be interested in...
FDA’s new website emphasizes CDRH’s responsibility for bringing antimicrobial susceptibility tests to market.
Widespread implementation of rapid diagnostic tests is critical for decreasing antimicrobial resistance.
The US FDA has labelled a recall of intensive care ventilators from Hamilton Recall as class I, the agency’s most serious. A hardware issue could cause the machines to shut down.