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Regulatory Ask Us Anything: Medical Device submission strategy in China for imported devices

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Rimsys' panel of regulatory experts, Bruce McKean, Director of Regulatory and Karen Cohn, Regulatory Specialist, will answer attendees' pressing questions about medical device submissions in China for imported devices during our next "ask-us-anything" webinar. Bring your questions!

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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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