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Clinical Evaluations for Medical Devices — How to Optimize Existing Clinical Evaluation Reports in Order to Fulfill the Requirements of the EU MD

Dr. Isabelle Lang-Zwosta (Group Leader Clinical Safety and Global Regulatory Affairs, knoell Germany)

Location: Tech Theater, Booth 637, Hall E

Date: Thursday, February 7

Time: 10:30am - 11:15am

Track: Tech Theater

Vault Recording: TBD

Audience Level: All

The new EU MDR brought many challenges to medical device manufacturers especially in regards to the clinical evaluation. This session will focus on how to optimize your clinical evaluation strategies and reports in order to meet the updated requirements and how to utilize existing data sets most efficiently.