The EU Medical Devices Regulation (MDR) Date of Application (DoA) is imminent. Do you understand what your regulatory obligations will be as of May 26, 2021? This webinar will define the different categories of products covered under MDR and will outline noteworthy requirements and deadlines. Analysis will include legacy devices registered under the Medical Devices Directive (MDD), as even these need to be compliant to relevant aspects of MDR. The presentation will focus on aspects of MDR applying to all devices which are to be imported after the DoA. Attendees will receive practical guidance and the opportunity to pose questions relating to their own products at the end of the session.
This webinar was recorded on April 8, 2021.
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