The US FDA’s policy rule changes for medical device manufacturing will require more attention to device security. From October 2021, manufacturers are required to design devices with security in mind and to include software bills of materials (SBOMs), identifying the location of potential vulnerabilities. While challenging for some, it is generally agreed that regulations increase medical device security and accountability. Its full implications may take years to see, but the target is a safer healthcare infrastructure overall.
Bridging the Gap – CISOs and CIOs Driving Tech-Driven Security
In today’s digital landscape, collaboration between Chief Information Security Officers (CISOs) and Chief Information Officers (CIOs) is crucial. Their partnership enhances security strategies and fosters
