Post-market surveillance as a medical device requirement in the EU

This is an excerpt from the course "Introduction to the Medical Device Regulation (EU) 2017/745" which is available at:
medicaldevicehq.com/medical-d...
Read more about post-market surveillance here:
medicaldevicehq.com/articles/...
Chapters:
00:00 Introduction
00:25 About the instructor
01:08 Article 83: Post-market surveillance system of the manufacturer
01:47 The PMS system
03:43 Actively and systematically collecting data
08:42 The post-market surveillance plan
10:05 Sources the PMS plan must include
11:09 PMS plan coverage according to MDR requirements
19:14 Reporting PMS activities
21:00 Additional resources
Don't forget to follow Medical Device HQ on LinkedIn:
/ medicaldevicehq

[@hajranaashkar2103]

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[@pontusgedda]

Hi Hajrana,
Thanks a lot for that. Glad to hear that you find them helpful.
Take care
/Pontus

[@krishnareddy7076]

Very usefull video on PMS learnt a lot. Thankq.