This is an excerpt from the course "Introduction to the Medical Device Regulation (EU) 2017/745" which is available at:
https://medicaldevicehq.com/medical-d...

Chapters:
00.00 Introduction
00.11 About the instructor
00.57 The goals of the short course
02.08 The main aspects
07.30 Manufacturer and the Notified bodies
09.43 Conformity assessment and the intended purpose
10.51 Clinical evaluation and clinical investigation
11.18 CE-marking
11.49 The MDR
14.52 Additional resources

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