Over 15 years of experience in the pharmaceutical industry in Regulatory Affairs, Clinical Trial Project Management and Pharmacovigilance.

His career spans the generic industry, the global market for biological medicines, and the CRO sector.

Academic path: studied at the University of Göttingen in Germany, earned a Ph.D. at the Helmholtz Centre for Infection Research in Braunschweig, and completed the Master of Drug Regulatory Affairs (DGRA/University of Bonn) with an award-winning thesis on regulatory compliance.

Founder of the knowledge platform regulatory-affairs-manager dot com