Salma Boushaba is a professional in regulatory affairs for medical devices, currently serving as a consultant at Abylsen since November 2021. Prior experience includes a role at LISI MEDICAL, where Salma implemented the 2017/745 regulation requirements for labeling and regulatory notices, and managed quality assurance tasks. Educational qualifications encompass a Master 2 in Regulatory Affairs from the Université de Technologie de Compiègne and an engineering degree in Biomedical Engineering from Polytech Marseille and École Normale Supérieure de l'Enseignement Technique de Rabat. Salma also possesses a range of internship experiences in biomedical engineering, quality compliance, and technical assessments, further contributing to a solid foundation in the medical device sector.