- Introduction (00:07:27)
- Croatia (00:00:43)
- Greece (00:00:32)
- Italy (00:00:32)
- Malta (00:00:33)
- Portugal (00:00:36)
- Cyprus (00:00:35)
- Slovenia (00:00:29)
- Spain (00:00:47)
Southern Europe Market Access
$49.00
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).
Description
Why take this course
To learn how to successfully place a CE-Marked device on the market in many different countries in Southern Europe.
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
TOPICS
- Final Test – Southern Europe Market Access
- Certification
Additional information
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