Cristina Lopez

Pharmacist with over 15 years of experience in the pharmaceutical industry, specialized in quality, regulatory affairs, and project development within GMP environments. Throughout her career, she has held roles as Qualified Person and Head of Quality, leading teams and complex projects in both sterile and non-sterile manufacturing. Additionally, she performed audits and GMP projects as a consultant across the entire pharmaceutical value chain. Currently Chief R&D Officer at Qualipharma, she drives innovation projects around GMP Pharmaceutical equipment compliance.