The U.S. Food and Drug Administration has announced the availability of its final guidance on AI medical devices. The document – Marketing Submission Recommendations for a Predetermined Change Control ...
The U.S. Food & Drug Administration issued select updates to premarket cybersecurity guidance on March 13, including who is required to comply, the types of devices that fall under certain agency ...
CyberActa medical device software design and development expertise minimizes vulnerabilities and reduces attack surface of every phase of the development cycle ...
Due to the increasing concerns about medical devices' cybersecurity risks, European Union regulators put forward a new set of market entry requirements for medical devices and in vitro diagnostic ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback