Market access for medical devices in Europe with reference to the U.S. FDA requirements and the differences between Europe and the U.S. Benefits of attending: Understand the progress of a device from concept to marketing. Discover how regulatory, quality, clinical, and other aspects of device development are joined into a continuous process. Learn what devices are and how they are developed. Access lectures and workshops. Listen to case studies covering each process applicable to device development, marketing, and eventually the postmarket procedures.
Medical Device Autumn School
Sep 27th, 2009Oct 1st, 2009
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