- 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)
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).
Why take this course
To learn how to successfully place a CE-Marked device on the market in many different countries in Western Europe.
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:
- Final Test – Western Europe Market Access
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