Press "Enter" to skip to content

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

Find out more regarding post-market monitoring right here:

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:

This is a passage from the training course “Intro to the Medical Tool Policy (EU) 2017/745” which is readily available at: