Annick accumulated 15 years of experience in ethylene oxide sterilization field, quality management and pharma manufacturing. In her role as Technical Director, EO Pharma, Annick leads the Ethylene Oxide (EO) sterilization projects at numerous Sterigenics facilities and supports the facilities as the technical expert with pharmaceutical project responsibility. She’s now also supporting the development and validation of NO2 projects in Sterigenics European facilities. A seasoned speaker, Annick presents at industry conferences—such as CPhI and the A3P Congress—and hosts webinars. Annick has also been published in Medical Design & Outsourcing. Annick often presents on innovative and customized solutions for terminal sterilization of pharmaceuticals.
Education: Biochemistry Graduate of Haute Ecole Liège (Belgium), DES Total Quality from Faculté Polytechnique (Belgium), Management of Pharmaceutical Quality Systems from the ECA Academy
Certifications: Certified Trainer, EO Sterilization Validation
Expertise: EO Sterilization Validation of Medical Devices and Pharma Applications (API, drug products, combination products), Cycle Design and Development, Process Definition and Performance Qualification Studies, PCD Development, D-Value Determination, EO Residues