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This short interactive e-learning provides an overview of the new European Medical Device Regulation (MDR 2017/745) which will come into force in 2020
Description
Barco’s distributors of medical devices, will be directly affected by this new Medical Device Regulation
This e-learning will provide details of the responsibilities and the actions needed in order to prepare for compliance with this new regulation and will draw attention to the particular points, that may require immediate action.
This regulation only applies to those who make Barco’s Medical Devices available on the EU market
Target Audience
Barco Partners: Barco customers who make our devices available on the EU market
Barco Employees: Barco Belgium Healthcare product management, marketing & sales, services and QARA employees
Prerequisites
None
Objective
To ensure Healthcare Distributors who make Barco’s medical Devices available on the EU market are aware of the new Medical Device regulation and the responsibilities and actions required to be compliant