WEBINAR

Why UDI is a regulatory concern - and not just an operational process

Replay

The introduction of new UDI requirements in the EU MDR/IVDR regulations has fueled an increased focus by regulatory affairs teams. However, Europe is not the only region that is adding UDI requirements for medical technology products. This session helps to simplify UDI complexity by exploring requirements across several major markets, including the types of devices that are covered and the expected implementation timelines.

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Why UDI is a regulatory concern - and not just an operational process

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Quick reference guide - global medical device UDI requirements and timelines
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Check out these additional resources
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
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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