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EU MDR MIR Electronic Reporting Solution New Product Icon 

ASSURX

Booth: 610

The new EUDAMED database, due to be live in December 2020, will be a much larger database structured from six interconnected modules and a public website. The design will improve the collection and coordination of information with additional requirements for adverse event reporting. To address the current and future automated reporting required for Post-market surveillance and Market Surveillance, AssurX is provides a solution for MIR report creation that enables compliance with current EU MDR requirements today that will also meet the future integration requirements with the new EUDAMED system.

Other product: AssurX Complaint Management Solution

Other product: Change Management Solution

Other product: FDA eMDR Electronic Medical Device Safety Reporting

Other product: The AssurX QMS Platform

EU MDR MIR Reporting Data Sheet Watch Video

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