Introduction to the European Medical Devices Regulation MDR EU 2017 745
Webinar recording
The new Regulation (EU) 2017/745, called MDR was published on May 5, 2017 and entered into force on May 25, 2021. What does this mean for medical device manufacturers?
In our free webinar recording, we will review the new Regulation (MDR) that replaced the previous Medical Device Directive MDD 93/42/EEC and the Active Implantable Medical Devices Directive AIMD 90/385/EEC. This webinar, presented by Andreas Geringer, will give you a brief introduction into the procedures and possible obstacles on the way to the certification.
The webinar at a glance:
New requirements under MDR (EU) 2017/745
Legacy device information and requirements
Timeline for transition and your next steps
Duration: 32:00 min
How to get to the webinar recording
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