Enhancing Pharmacovigilance from the US Experience: Current Practices and Future Opportunities

Veronique F. Kugener (), Eric S. Freedland (), Kenneth I. Maynard (), Omar Aimer (), Peggy S. Webster (), Maribel Salas () and Maxine Gossell-Williams ()
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Veronique F. Kugener: Takeda Pharmaceuticals International Co.
Eric S. Freedland: Takeda Pharmaceuticals International Co.
Kenneth I. Maynard: Takeda Pharmaceuticals International Co.
Omar Aimer: Brunel Canada
Peggy S. Webster: GlaxoSmithKline
Maribel Salas: University of Pennsylvania
Maxine Gossell-Williams: University of The West Indies

Drug Safety, 2021, vol. 44, issue 8, No 3, 843-852

Abstract: Abstract This review is intended to present perspectives from the US experience in enhancing pharmacovigilance on current practices and future opportunities. Best practices concepts could be applied worldwide through the presentation of how three pillars of pharmacovigilance: (1) medical and scientific excellence, (2) operational and compliance excellence, and (3) knowledge sharing and experts development in the field could serve as a framework for the establishment of an efficient and successful global pharmacovigilance system.

Date: 2021
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DOI: 10.1007/s40264-021-01078-8

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