clinicalevaluation-report7 天
Proactive and Reactive Post Market Surveillance Activities: A Dual Approach to Device Safety
According to the European Union Medical Device Regulation (EU MDR 2017/745) Post-market surveillance (PMS) are set of activities conducted by manufacturers, to collect and evaluate experience gained ...
clinicalevaluation-report7 天
Proactive and Reactive Post Market Surveillance Activities
According to the European Union Medical Device Regulation (EU MDR 2017/745) Post-market surveillance (PMS) are set of activities conducted by manufacturers, to collect and evaluate experience gained ...