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
$49.00
- Course Type: Video Lecture
- Language: English
- Level: Beginner
- Session: year 2020
- Time: 0 - 1 Hour
Course Breakdown
| Section | Time |
|---|---|
| Introduction | 00:07:30 |
| Croatia | 00:00:53 |
| Greece | 00:00:51 |
| Italy | 00:00:34 |
| Malta | 00:00:44 |
| Portugal | 00:00:41 |
| Cyprus | 00:00:40 |
| Slovenia | 00:00:57 |
| Spain | 00:00:50 |
Exam and Certifications
- Final Test – Northern Europe Market Access
- Certification
Description
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:
- Denmark
- Finland
- Sweden
- UK
- Estonia
- Ireland
- Latvia
- Lithuania
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