How Europe Is Using Regulations to Harden Medical Devices Ag

Manufacturers need to document a medical device's intended use and operational environment, as well as plan for misuse, such as a cyberattack.

Related Keywords

, International Electrotechnical Commission , Association For The Advancement Of Medical Instrumentation , Device Coordination Group , European Union , European Union Medical Device Regulation , Product Development Framework , European Union In Vitro Diagnostic Regulation , Medical Instrumentation , Secure Product Development Framework ,