Andrea Challand is working at F. Hoffmann-La Roche Ltd.’s Global Pharma Technical (CMC) Regulatory for Biologics in Basel, Switzerland, where she leads a group of regulatory professionals responsible for submissions of CMC regulatory documents for biological products at development and commercialization stage. Andrea has 14 year of experience in the regulatory affairs of biotechnological products (CMC aspects). Andrea has a Ph.D. in Cell Biology and a M.Sc. in Microbiology.