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Improving the Safety of Medicines in the European Union: From Signals to Action

Pharmacovigilance and risk minimization must be planned during drug development and forms a critical part of the regulator's decision on whether a medicinal product can be authorized. Pharmacovigilance systems should ensure proactive monitoring of all authorized medicines throughout their lifec...

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Detalhes bibliográficos
Publicado no:Clin Pharmacol Ther
Main Authors: Potts, Joanne, Genov, Georgy, Segec, Andrej, Raine, June, Straus, Sabine, Arlett, Peter
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7027976/
https://ncbi.nlm.nih.gov/pubmed/31621897
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cpt.1678
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