Southern Europe Market Access


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).

  • Course Type: Video Lecture
  • Language: English
  • Level: Beginner
  • Session: year 2020
  • Time: 0 - 1 Hour
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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


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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