Maria has more than 10 years of experience in Life Science research, with a PhD in Pharmaceutical Technologies and a MSc in Biomedical Engineering.
For over 5 years, she has worked as clinical evidence evaluator and covered all aspects of products’ life cycle—from product ideation, to market, to end of life—for a variety of medical devices by providing input as clinical evaluation expert. Currently as Clinical Development Consultant at GBA Key2Compliance, Maria supports companies with all activities in clinical development of medical devices with focus on clinical evaluations, post-market clinical follow-up and post-market surveillance.