Marielle Calderini

Marielle Calderini is an experienced Regulatory Affairs manager with a background in Pharmaceutical Sciences and Pharmaceutical Management. Marielle has worked in various companies, including Vectura Group and SFM Ltd, specializing in regulatory strategy and global approval of drug-device combination products and drug-delivery devices. With a strong foundation in Quality Control and Technical Documentation, Marielle's expertise also includes handling regulatory filings for medical devices and pharmaceutical products. Marielle's continuous pursuit of knowledge is evident through multiple certifications in areas such as risk analysis, biocompatibility for medical devices, and sterilization techniques.