
is a 'Regulatory Strategist' in the Medical Device business unit of TÜV SÜD Product Service GmbH in Munich. His responsibilities in this organization include the communication with European authorities and the contribution to the work in associations, and he mainly deals with the regulation of digital medical devices, AI and combination products. Previously, Mr. Fischer held a similar position at Merck Healthcare KGaA in Darmstadt, where he was also responsible for the regulation of paediatric drug development and the regulatory environment in Japan.
Mr. Fischer worked in research for the MPIs for Medical Research and Intelligent Systems and studied molecular biomedicine (B.Sc.), molecular and cell biology (M.Sc.) as well as Drug Regulatory Affairs (MDRA) in Bonn and Heidelberg. He is also a lecturer on the medical technology programme at the Baden-Wuerttemberg Cooperative State University in Mannheim.