Pharmaceutical Industry Biologist, MBA
During her 20 years of professional life, she has always been linked to the pharmaceutical industry, managing projects related with basic research, clinical trials, quality assurance, compliance with GXP standards, regulatory affairs and pharmacovigilance, both from the technical side and from the business side.
During the last years Marta Rodríguez has also led several Medical Cannabis projects globally, acting as a consultant and a project manager, providing GACP/GMP support, licensing and regulatory affairs support.
Marta Rodríguez currently leads the IT Quality Assurance area in the vaccines manufacturing plant of a pharmaceutical company, from where she manages digitalization projects and handles GMP/GDP relevant computerized systems to achieve compliance with regulatory requirements and company data integrity policies.
She is board member of the board in the Spanish Association of Pharmacists in Industry (AEFI), lecturer in courses and conferences and associate professor in Pharma Business Schools. She also provides support to Life Sciences companies helping them to understand the applying regulation to their specific product, and to align their business strategy with the regulatory strategy.