You will receive a confirmation email with a link to view the EU MDR Preparedness webinar. Be sure to check your SPAM folder.
If you do not receive an email please contact us at firstname.lastname@example.org.
Download the AssurX Automated Process for EU MIR Submissions Datasheet
The AssurX EU MDR enables electronic reporting of medical device vigilance events required by manufacturers, user facilities and importers in compliance with European Union Medical Device Regulation (EU MDR) and requirements of the Manufacturing Incident Report form (MIR).