Northern 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 00:07:30
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


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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