Miranda van Bodegom MSc
Consultant Regulatory Affairs
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 advises clients on national regulations regarding registration and variation procedures mainly in BeNeLux countries, and supports DADA’s Pharmaceutical Safety and Efficacy team in preparing the clinical and non-clinical overviews of the pharmaceutical dossier. She also offers assistance to the Promotion & Compliance Services. Besides this, Miranda acts as a client manager for various clients, providing support for diverse projects.
