PPD
Ana Sofia Cruz is a highly experienced regulatory affairs professional with a progressive career spanning over a decade in the pharmaceutical industry. Currently serving as Principal Regulatory Affairs Specialist at PPD since April 2019, Ana has held various roles within the company, including Senior Regulatory Affairs Specialist and Country Approval Specialist. Prior experience includes clinical project assistance at AstraZeneca and a decade in community pharmacy focusing on quality management, inventory control, and patient care. Educational qualifications include a Master’s degree in Pharmaceutical Sciences from the Faculty of Pharmacy of the University of Lisbon and a Master in Pharmaceutical Industry from CESIF. Additionally, Ana has pursued health management studies at Universidade Católica Portuguesa.
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PPD
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PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Their customers include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 46 countries and approximately 23,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help customers bend the cost and time curve of drug development to deliver life-changing therapies that improve health.