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).
Southern 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 | 00:07:27 |
| Croatia | 00:00:43 |
| Greece | 00:00:32 |
| Italy | 00:00:33 |
| Malta | 00:00:36 |
| Portugal | 00:00:35 |
| Cyprus | 00:00:29 |
| Slovenia | 00:00:29 |
| Spain | 00:00:47 |
Exam and Certifications
- Final Test – Southern Europe Market Access
- Certification
Description
What I will learn?
You will learn about applicable regulations and medical device registration in countries in Southern 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 these Southern EU countries:
- Croatia
- Greece
- Italy
- Malta
- Republic of Cyprus
- Portugal
- Slovenia
- Spain
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