Martine Draguet brings 30 years of experience in pharmaceutical regulatory affairs. After 10 years in academic research, she joined the pharmaceutical industry where she has developed and implemented international and regional regulatory strategies for several blockbuster drug products. Since 2010, Martine has consulted with pharmaceutical companies to,develop and/or implement their regulatory/quality strategy. Martine, is a qualified Pharmacist and Industrial Pharmacist (QP) and holds a PhD, both from University of Louvain (UCL). She joined ASIT biotech in November 2014 as a consultant and is now Head of Regulatory Affairs and Quality Assurance.
- Head of Regulatory Affairs and Quality Assurance