Before joining IGBA, Susana was Clinical Development and Safety Director at Medicines for Europe. She has also overseen clinical trials in Europe and in North America, with her experience spanning positions at pharmaceutical companies and clinical research organisations. She earned her doctorate degree in Clinical Pharmacology from the Faculty of Medicine, Universidad Autònoma de Barcelona and has authored several scientific papers and patents.
Susana believes that generic and biosimilar medicines industries play a vital role in fostering worldwide patient access to quality-assured medicines and that a strong off-patent sector is essential to a healthy medicines ecosystem.