WEBINAR

Actionable regulatory insights and process optimization for MDR/IVDR compliance

Replay

The roll-out of new EU medical device regulations has been challenging for the global medtech community. How can regulatory intelligence tools be used to stay on top of frequently changing regulations and deadlines? This interactive panel discussion will feature regulatory experts from three technology companies working to provide solutions for the medical device industry and will include a Q&A session with the audience.

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Actionable regulatory insights and process optimization for MDR/IVDR compliance

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Here's some additional content you may find helpful
A primer on medical device classification
A primer on medical device classification
5 ways a RIM system can accelerate time-to-market for MedTech companies
5 ways a RIM system can accelerate time-to-market for MedTech companies
Quick reference guide - global medical device UDI requirements and timelines
Quick reference guide - global medical device UDI requirements and timelines
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Check out these additional resources
Quick reference guide - global medical device UDI requirements and timelines
Quick reference guide - global medical device UDI requirements and timelines
5 ways a RIM system can accelerate time-to-market for MedTech companies
5 ways a RIM system can accelerate time-to-market for MedTech companies
A primer on medical device classification
A primer on medical device classification
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