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

Find out more regarding post-market monitoring right here:
https://medicaldevicehq.com/articles/post-market-surveillance-medical-device-requirement-eu/

Phases:
00:00 Introduction
00:25 About the trainer
01:08 Article 83: Post-market security system of the maker
01:47 The PMS system
03:43 Actively and also methodically accumulating information
08:42 The post-market monitoring strategy
10:05 Sources the PMS strategy should consist of
11:09 PMS strategy insurance coverage according to MDR demands
19:14 Reporting PMS tasks
21:00 Additional sources

Do not neglect to comply with Medical Device HQ on LinkedIn:
https://www.linkedin.com/company/medicaldevicehq/

This is a passage from the training course “Intro to the Medical Tool Policy (EU) 2017/745” which is readily available at:
https://medicaldevicehq.com/medical-device-regulation