WEBINAR

RIM for medical devices - challenges and opportunities for automation

Replay

Join Rimsys Director of Product Management and former Head of Post-Market at Philips, Adam Price for a live “fireside chat” about the regulatory challenges medtech teams are facing, some of the adoption hurdles that come with RIM systems, and the opportunities for automation across the regulatory lifecycle from pre-market submissions to post-market surveillance.

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RIM for medical devices - challenges and opportunities for automation

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Here's some additional content you may find helpful
Quick reference guide - global medical device UDI requirements and timelines
Quick reference guide - global medical device UDI requirements and timelines
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
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Check out these additional resources
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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