Very interesting developments in Europe with the increased regulation around medical devices whereby manufacturers must establish, document, implement and maintain a risk management system (RMS) as part of their QMS. : https://medcitynews.com/2020/01/what-will-the-medtech-sector-look-like-under-eu-mdr-law/?rf=1
I like the goal for the EUDAMED database to become publicly available in May 2022 so patients will be able to make more informed decisions about devices by researching them ahead of usage