Medical Device Regulation (MDR): Why Cybersecurity And Fuzz Testing Are No Longer Optional
The MDR came into full effect in 2021, but many devices are still certified under MDD and will need to transition. As a result, Europe is facing a period of regulatory limbo. The MDR outlines what manufacturers must achieve but not how to do it, creating a gap between regulatory intent and practical implementation. To help bridge this gap, manufacturers rely on.