Introduction to different classifications rules for medical device software
![](https://i.ytimg.com/vi/l2Aq3tEqiwA/mqdefault.jpg)
10:44
Managing and documenting SOUP and OTS in medical device software
![](https://i.ytimg.com/vi/1dOr_QvaPMo/mqdefault.jpg)
28:40
Short course on SaMD (Software as a medical device), IEC 62304 and IEC 82304-1
![](https://i.ytimg.com/vi/yZAG51ogVhE/mqdefault.jpg)
16:47
FDA Regulation of Medical Devices (Part 1 of 3)
![](https://i.ytimg.com/vi/TUV6fLio_FU/mqdefault.jpg)
8:23
Classification Medical Device in EU (Medical Device Regulation MDR 2017/745)
![](https://i.ytimg.com/vi/Bg0LHOF0sTg/mqdefault.jpg)
1:30:26
Understanding the Medical Device Classification System
![](https://i.ytimg.com/vi/oOCzO-tLs2E/mqdefault.jpg)
45:52
An introductory guide to medical device Clinical Evaluation & Clinical Evaluation Reports (CER)
![](https://i.ytimg.com/vi/O9nV7rJMicQ/mqdefault.jpg)
14:55
Short course on the Medical Device Regulation (EU) 2017/745
![](https://i.ytimg.com/vi/-MoG7TFJBdI/mqdefault.jpg)
12:25