Prof. Dr. Michael Imhoff is a board-certified specialist in general surgery and intensive care medicine with 18 years of clinical experience at a tertiary care university hospital in Germany.
For over 20 years, Prof. Imhoff has worked as an independent medtech consultant, providing scientific and clinical expertise for product specifications, marketing, and management in areas such as patient monitoring, intensive care ventilation, anesthesia systems, and clinical information systems for major medical device manufacturers across Europe, the U.S., and Israel.
He has extensive experience in preparing clinical evaluation reports (CERs) in line with the Medical Devices Directive (MDD) and the Medical Device Regulation (MDR), as well as clinical risk assessments for a wide range of medical device product lines, including life-sustaining systems across all risk classes.
As a trainer for the qtec Academy, he educates medical device manufacturers, pharmaceutical companies, authorities, and Notified Bodies in the fields of clinical evaluation, literature searches, and clinical investigations.
What matters most to him as a speaker: "My goal is to equip participants with valuable insights, tips, and practical tools to help them confidently implement the many requirements of the MDR within their organizations."
