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).
Western Europe Market Access
$49.00
- Course Type: Video Lecture
- Language: English
- Level: Beginner
- Session: year 2020
- Time: 0 - 1 Hour
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
Description
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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