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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

  • 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)

  • Final Test – Southern Europe Market Access
  • Certification

Additional information

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