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).
Northern Europe Market Access
- Course Type: Video Lecture
- Language: English
- Level: Beginner
- Session: year 2020
- Time: 0 - 1 Hour
Exam and Certifications
- Final Test – Northern Europe Market Access
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:
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