Marissa Benne MSc
Senior Manager Regulatory Affairs
Marissa finished in 2015 her Master Molecular Life Sciences at the Radboud University of Nijmegen. She started working at DADA soon after graduation and became an experienced regulatory affairs consultant. She manages European registration and variation procedures and advises clients on the national regulations in BeNeLux countries. When needed, she also supports DADA’s Pharmaceutical Safety and Efficacy team. She is involved in projects on implementation of the Falsified Medicines Directive and IDMP/SPOR. Since January 2021 Marissa is responsible for management of the regulatory affairs team.
