Ricardo Cunha is a scientific and regulatory strategist with over 12 years of experience in the R&D field, holding a PharmD and an MSc in Pharmaceutical Medicine. He specializes in supporting sponsors by establishing compliant non-clinical and clinical development plans and study designs, both for innovative and generic medicines. Ricardo ensures full regulatory compliance with worldwide authorities, including the US FDA, EMA, and ANVISA. He leads the preparation of scientific and regulatory advice packages to streamline proposals, minimizing overall investment and time to market.
