Right after graduating as a veterinarian at Ghent university (BE) I've worked for 4 years as practitioner in France. Moving back to Belgium I then started working for the Belgian OMCL for the quality control of immunological veterinary medicines. After passages in Regulatory Affairs in Pfizer Animal Health (now Zoetis) and again the Belgian authorities I have been working for Huvepharma since 2014.
My role as Regulatory Affairs Director is to take projects from pre - or post- Proof Of Concept (POC) and take them through registration trials in order to be able to submit compliant registration dossiers. Therefore my interest in new and promising projects.
development and commercialisation of immunologicals for food producing species (from early R&D over POC through clinical trials and registration)