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SESSION 16: CHANGES IN VIGILANCE AND POST-MARKET REQUIREMENTS IN THE NEW MEDICAL DEVICE REGULATION
Speaker(s)
SESSION 16: CHANGES IN VIGILANCE AND POST-MARKET REQUIREMENTS IN THE NEW MEDICAL DEVICE REGULATION
Reinhard Berger, DRSc, MSc
Regulatory Affairs Medical Devices, Consulting-Advising, Austria
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Ways to register
Registration fee includes refreshment breaks, lunches and training course material.
This course has limited capacity. Register early!