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 pharmaceutical regulatory affairs consultant. She manages registration and variation procedures and advises clients on their regulatory strategies. Furthermore, she is specialised in the national regulations ofBeNeLux countries and in the preparation of the national product information texts and artworks for these countries. Marissa also supports DADA’s Pharmaceutical Safety and Efficacy team, writing clinical and non-clinical overviews. Besides this, she has experience in various areas, such as compassionate use programs, market access, SPOR/IDMP implementation and the consultation procedure for medical devices.
