UDI data requirement experts Gary Saner and John Lorenc of Reed Tech will discuss best practices for UDI preparations and the future potential impacts to medical device manufacturers as global health authorities publish mandates.
This session will give suggested best practices concerning EU EUDAMED preparation, what we have learned via testing and a Q&A session. Bring your specific questions concerning medical device registration scenarios, data elements and requirements. The speakers will review and provide clarity on currently posted guidance and answer your questions concerning EUDAMED and other health authority timelines.
KEY TAKEAWAYS - Best practices and recent learnings for EU UDI preparation - Regulatory Health Authority update on UDI timelines and requirements - Leveraging UDI data internally/externally
WHO SHOULD ATTEND -Global Strategy Business Managers - Regulatory Affairs/Operation Leaders - Product Managers and Business Analysts - Manufacturing, Operations, and Supply Chain Leaders - Quality Leaders - IT Support