RAPS Florida: EU MDR – Are You Ready?

Come engage with professionals from your local regulatory community for an interactive presentation on how to prepare for the implementation. The new regulation introduces more stringent clinical and post-market surveillance requirements for medical device manufacturers, regardless of risk classification. Come join us and learn strategies that can help your medical device company navigate the higher level of scrutiny. Find Senior Director of Client Relations Chick Maffei for information on RCA.

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