Ilan has more than 16 years of experience in biopharmaceutical industry. He is involved in QA since 2005. Ilan worked first in CROs located in North-America and Europe. These CROs were providing a wide range of services (e.g. monitoring, regulatory, data management) for international clinical trials. The North-American CRO high quality system standards was recognized by the accreditation of the company by the Association for the Accreditation of Human Research Protection Programs (AAHRPP) – one of the top human research watchdog groups. Ilan joined Actelion Global Quality Management department at the beginning of 2010. He is currently an Associate Director GCP QA there. He is in charge of auditing all clinical trial stakeholders (e.g. clinical sites, CROs, internal processes), to provide training on GxP requirements and advices to clinical trial teams. He is also in charge of helping clinical trial teams to prepare, hosting and answering to international regulatory authority inspections (e.g. FDA, EMA, MHRA, Health Canada) Ilan has two master degrees: one in biology from Rene Descartes University (Paris-France) and one in administration sciences from Reims Management School (Reims-France).