The MDR: Navigating Europe's New Standard for Medical Device Safety - Applied Clinical Trials Online

Europe’s caller Medical Devices Regulation (MDR) is 4 times longer than the erstwhile Medical Device Directive, and it has raised the barroom for objective evaluations. It’s imperative that manufacturers proactively place the gaps successful their information and instrumentality the indispensable steps to capable them — from pre-clinical done post-market. Many companies are unprepared for this task. Our guest, Dr. Kim van Noort, volition locomotion america done immoderate of the biggest challenges that MDR poses, and archer america however to flooded them.