Post-market surveillance as a medical device requirement in the EU
12:41
Short course on PRRC - Person responsible for regulatory compliance
17:40
Medical Device Regulation codes
1:25:47
EU Postmarket Surveillance Requirements for Medical Devices
14:55
Short course on the Medical Device Regulation (EU) 2017/745
21:42
Nobody Complained! Post market reporting under MDR
28:40
Short course on SaMD (Software as a medical device), IEC 62304 and IEC 82304-1
31:04
How to do Postmarketing Surveillance the right way?
1:30:28