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SUMMARY:Florida Chapter In-Person Event: EU MDR Clinical and Post Market Surveillance Requirements for High Risk and Up-classified Devices in the Orthopedic Space, and Other Devices
DESCRIPTION:Event details: https://www.raps.org/learn-develop/events/florida-chapter-in-person-event-eu-mdr-clinical-and-post-market-surveillance-requirements-for-high-risk-and-up-classified-devices-in-the-orthopedic-space-and-other-devices.html
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