Western Europe Market Access


This tutorial intends to provide the requirements for placing CE-marked Medical Devices on the European market according to the Regulation (EU) 2017/745 on Medical Devices (MDR).

  • Course Type: Video Lecture
  • Language: English
  • Level: Beginner
  • Session: year 2020
  • Time: 0 - 1 Hour
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Course Breakdown

Section Time
Introduction 00:07:25
Austria 00:01:41
Belgium 00:01:00
France 00:00:55
Germany 00:01:17
Luxembourg 00:00:51
Netherlands 00:01:09

Exam and Certifications

  • Final Test -Western Europe Market Access
  • Certification


What I will learn?

You will learn about applicable regulations and medical device registration in countries in Western Europe, along with country specific requirements including: legislative framework and procedure for approval

Skills I will gain

You are going to explore how the main requirements of the Medical Device Regulation will be implemented in Western EU countries:

  • Austria
  • Belgium
  • France
  • Germany
  • Luxembourg
  • Netherlands


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