Giada Di Leo has a strong background in regulatory affairs, quality assurance, and pharmacovigilance, with experience working in various roles within the pharmaceutical industry. Giada has proactively managed project operations, handled regulatory submissions, and played a key role in clinical trial coordination. With a Master's degree in Chemistry and Pharmaceutical Technology, as well as specialized training in regulatory affairs and pharmaceutical marketing, Giada is well-equipped to handle the complexities of the pharmaceutical industry.
Current role