Southern Europe Market Access
Europe Market AccessDuration: Unlimited
Cost: 49 USD
VIDEO LECTURE
Level: All Levels
Time: 15 Minutes
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).
Level: All Levels
Time: 15 Minutes
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).
Version: 01
Release Date: 29 April 2020
Eastern Europe Market Access
Europe Market AccessDuration: Unlimited
Cost: 49 USD
VIDEO LECTURE
Level: All Levels
Time: 15 minutes
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).
Level: All Levels
Time: 15 minutes
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).
Version: 01
Release Date: 29 April 2020
Western Europe Market Access
Europe Market AccessDuration: Unlimited
Cost: 49 USD
VIDEO LECTURE
Level: All Levels
Time: 15 minutes
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).
Level: All Levels
Time: 15 minutes
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).
Version: 01
Release Date: 29 April 2020
Northern Europe Market Access
Europe Market AccessDuration: Unlimited
Cost: 49 USD
VIDEO LECTURE
Level: All Levels
Time: 15 minutes
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).
Level: All Levels
Time: 15 minutes
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).
Version: 01
Release Date: 29 April 2020