has over 15 years’ experience in the pharmaceutical industry, specialising in CMC Regulatory Affairs and Lifecycle Management. She currently works as Global Submission Lead at Sanofi, coordinating complex global submissions. Previously, she worked in CMC Regulatory Affairs at Boehringer Ingelheim and MSD, where she was responsible for various regulatory projects. Her focus: communicating drug regulatory affairs in a practical way. In her training sessions, she uses real-life case studies to demonstrate how regulatory requirements can not only be understood but also successfully implemented under real-world conditions.