As part of MedTech Digital Week, Executive vice-president Oliver Christ and senior consultant of regulatory affairs and project management Berkin Guler at NSF’s PROSYSTEM discusses taking advantage of the EU Medical Devices Regulation (MDR) post-market surveillance (PMS).
NSF International, Medical Devices
Subscribed
You have successfully submitted your enquiry. Someone from our company will respond ASAP
Taking Advantage of the New EU MDR PMS Requirements
