New regulations impact the more than 500,000 types of medical devices and in vitro diagnostic (IVD) medical devices in Europe. What do these regulations mean for device manufacturers? European Union Medical Devices Regulation (2017/745/ EU) (MDR) represents a major update to the Medical Devices Directive (93/42/EEC) (MDD) and the Active Implantable Medical Devices Directive (90/385/EEC) … Continue reading EU MDR: Update to Medical Device Regulations in Europe