Dr. Martin Neumann

Dr. Martin Neumann is an experienced consultant in regulatory affairs at infoteam Software AG, focusing on European medical device and in-vitro diagnostic regulations, cybersecurity, risk management, and FDA market access. Prior roles include Regulatory Affairs Manager at a small consultancy, Product Development Lead and Scientist at QIAGEN, and a PostDoc Biomarker Research Scientist at Bayer, where coordination of international projects and biomarker research was emphasized. Academic credentials include a Dr. rer. nat. in Biology/Biomedical Sciences from the University of Düsseldorf, a Master of Science in Cell Biology from Ruhr University Bochum, and various undergraduate degrees in Applied Biology and Virology. Expertise spans product development, project management, and advanced molecular techniques.