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Eastern 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 Eastern 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:

  • Bulgaria
  • Czech Republic
  • Hungary
  • Poland
  • Romania
  • Slovakia

 

TOPICS

  • Introduction (00:07:28)
  • Bulgaria (00:01:08)
  • Czech Republic (00:00:58)
  • Hungary (00:01:02)
  • Poland (00:01:03)

  • Final Test – Eastern Europe Market Access
  • Certification

Additional information

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