Miranda van Bodegom

Miranda finished her master’s degree in Medical Biology in 2017 at the Radboud University in Nijmegen. In early 2018, she joined the Regulatory Affairs department at DADA, where she works as a Consultant Regulatory Affairs. She coordinates marketing authorisation processes (DCP, MRP and national applications) in Europe, starting at the marketing authorisation application (MAA), and providing procedural support during eCTD lifecycle management. She furthermore specialises in writing product information texts and she supports DADA’s Pharmaceutical Safety and Efficacy team in preparing the clinical and non-clinical overviews of the pharmaceutical dossier. Besides this, Miranda acts as a client manager for various clients, providing support for diverse projects.