A biologist by training, Beate has 20 years of experience in the international development and licensing of pharmaceuticals. She has worked for biotech and pharmaceutical companies in Europe (Micromet AG) and North America (Aspreva Pharmaceuticals) before joining the European Medicines Agency (EMA) as a Scientific Administrator (2009-2012).
A biologist by training, Beate also holds Master’s degrees in Drug Regulatory Affairs (MDRA) and in Health Economics, Policy and Management (London School of Economics). Beate is RAC (EU, US) certified (Regulatory Affairs Professional Society, RAPS) and obtained a Market Access Certificate (European Business School).
Since 2012, Beate is a freelance regulatory consultant to the pharma and biotech industries, based in Mannheim, Germany. She is a lecturer for various regulatory affairs and market access programs.
IFAPP Academy provides an online, continuing professional development course, Medical Affairs in Medicines Development, resulting in the Professional Certification, Certified Medicines Development (CMD).