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The Impact of MDR transition period extensions

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Listen to a discussion of the recent extension to the MDR transition periods. It is important to understand what this means - and doesn't mean - for medtech companies marketing medical devices in the EU. Learn why this extension does not mean MDR certification should be delayed! Our panelists will include Rimsys experts - James Gianoutsos, founder and CEO; Bruce McKean, Director of Regulatory; and Adam Price, Director of Product for Post-Market.

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Check out these additional resources
Introducing Rimsys Intel: A Free, Centralized Global Regulatory Intelligence Hub for Medtech
Introducing Rimsys Intel: A Free, Centralized Global Regulatory Intelligence Hub for Medtech
A primer on medical device classification
A primer on medical device classification
Quick reference guide - global medical device UDI requirements and timelines
Quick reference guide - global medical device UDI requirements and timelines
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