- Introduction (00:07:30)
- Market Access in Northern Europe (00:00:53)
- Finland (00:00:51)
- Sweden (00:00:34)
- United Kingdom of Great Britain and Northern Ireland (00:00:44)
- Estonia (00:00:41)
- Ireland (00:00:40)
- Latvia (00:00:57)
- Lithuania (00:00:50)
Northern 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 Eastern Europe.
What I will learn
You will learn about applicable regulations and medical device registration in countries in Northern 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 Northern EU countries:
- Final Test – Northern Europe Market Access
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