Ghent Metropolitan Area
Development and regulatory affairs for veterinary vaccines, therapeutics and feed additives: - Managing and coordinating people in multifunctional global projects - Project management for international development and regulatory programs - Regulatory affairs: compilation of dossiers, follow-up of regulatory procedures, life cycle management - Clinical development: design and follow-up of safety and efficacy studies - Medical writing - Member of several working groups within AHE and FEFANA
Lead manager in several projects for veterinary pharmaceuticals, vaccines and feed additives: - Managing and coordinating people in multifunctional projects - Regulatory affairs: compilation of dossiers, follow-up of regulatory procedures, life cycle management - Clinical development; design and follow-up of safety and efficacy studies - Medical writing - Member of several working groups within IFAH and FEFANA
Project management for veterinary medicinal products and feed additives. This includes: - Identification, protocol development and follow-up of the required regulatory studies (Part III and IV) - Preparation of the dossier, submission and follow-up of the regulatory procedures (MRP, DCP, ...) for both VMPs and feed additives - Variations, etc…