Claudia-Rose Mastrobuoni

Claudia-Rose Mastrobuoni has a strong background in regulatory affairs and quality assurance within the medical devices and pharmaceutical industry. Claudia-Rose has experience working with various companies in roles such as QARA Manager, Regulatory Compiler, and Medical Devices Manager Regulatory Affairs. Claudia-Rose's educational background includes a Master of Science in Regulation and Evaluation of Medicines and Health Products.