About me


Dr. Michael Wolf-Pflugmann has more than 25 years of experience in the pharmaceutical industry (generics, biosimilars, cosmetics, OTCs, medical devices and food supplements). In his last position he served as Corporate Vice-President Research & Development for a multinational generic company. In this role Dr. Wolf-Pflugmann was responsible for the world-wide development activities including all strategic elements in this regard. After his graduation as a pharmacist at the university of Berlin in Germany he completed his studies with a PhD in pharmacology at the university of Frankfurt. Dr. Wolf-Pflugmann joined the pharmaceutical industry in 1986 and achieved valuable experience in Regulatory Affairs, Clinical Research and Pharmaceutical Development, as well as in General Management. After several leading positions in Regulatory Affairs and Clinical Research, he was promoted to General Manager of the German Research & Development subsidiary of a leading multinational generic company. In this position he was in charge of Regulatory Affairs, Pharmaceutical Development and Clinical Research. Thereafter, he was appointed as Vice-President Research & Development and took responsibility of worldwide development activities. Dr. Wolf-Pflugmann is member of TOPRA (The Organisation for Professionals in Regulatory Affairs) and has an additional qualification as pharmaceutical expert for drug information (Fachapotheker für Arzneimittelinformation).