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Northern 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 Eastern Europe.

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

 

TOPICS

  • Introduction (00:07:30)
  • Market Access in Northern Europe (00:00:53)
  • Finland (00:00:51)
  • Sweden (00:00:34)
  • United Kingdom of Great Britain and Northern Ireland (00:00:44)
  • Estonia (00:00:41)
  • Ireland (00:00:40)
  • Latvia (00:00:57)
  • Lithuania (00:00:50)

  • Final Test – Northern Europe Market Access
  • Certification

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