Global Pharmacovigilance Benefit-Risk Management Graduate Certificate

Pharmacovigilance focuses on the detection, assessment, understanding and prevention of adverse effects associated with the use of health care products, including drugs, biologics, devices, vaccines, in vitro diagnostics, human cell and tissue products, and consume products. The health care industry is challenged with providing safety oversight throughout the product life cycle. This includes continually reviewing safety profiles and managing and accessing benefit and risk that arise during and after product development. While a company’s goal is to move products through all phases of development in a timely and cost-efficient manner, the obligation to protect public safety remains paramount. The discipline of pharmacovigilance is constantly evolving in a dynamic regulatory, economic, and scientific environment. The Global Pharmacovigilance: Benefit-Risk Assessment Certificate provides a strong foundation in pharmacovigilance principles to both experienced professionals and those seeking entry into this career field from within and outside of regulated industry. Its five courses explore pharmacovigilance in a global environment, combining key regulatory, scientific, demographic, and analytical concepts that define the field. Upon completing the certificate, students will better appreciate the need for continuous learning in this complex discipline.

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