Federica Mori

Federica is a senior consultant in regulatory affairs with more than 14 years of experience in translational and clinical research. She specializes in recombinant vaccines and gene therapy across rare diseases and oncology, with a proven ability to manage multiple projects with efficiency and accuracy.

Federica has extensive expertise in clinical protocol development and clinical trial-related activities coordination. With more than 9 years of regulatory strategy consulting experience, she has prepared multinational cell and gene therapy and vaccines clinical trial applications.

Education
She holds a master's degree in biological sciences.