- Introduction (00:07:28)
- Bulgaria (00:01:08)
- Czech Republic (00:00:58)
- Hungary (00:01:02)
- Poland (00:01:03)
Eastern 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 Eastern 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:
- Czech Republic
- Final Test – Eastern Europe Market Access
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