Bianca Pauly, MSc studied Analytical Chemistry at the Radboud University Nijmegen. She has worked in the pharmaceutical industry for over 25 years in the fields of Quality Assurance, Clinical Trial Management and the last 18 years in Regulatory Affairs. By obtaining worldwide marketing authorizations via DCP, MRP, RUP, and national procedures, full life cycle management of multiple product formulations, and the preparation of registration files, she has built up extensive strategic regulatory expertise and gained knowledge in (generic) drug development. Since two years she is working as a Consultant Regulatory Affairs at 3D-PharmXchange, a leading consultancy firm specializing in drug development, where she is helping clients with regulatory strategic questions and became an expert in drug repurposing.