Implementing a centralised pharmacovigilance service in a non-commercial setting in the United Kingdom

The implementation of a pharmacovigilance service compliant with the legal and regulatory responsibilities of clinical trial sponsors presents particular challenges for sponsors in a non-commercial setting. In this paper we examine these challenges in detail. We identify and discuss the key steps in...

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Detalles Bibliográficos
Autores principales: Dinnett, Eleanor M, Kean, Sharon, Tolmie, Elizabeth P, Ronald, Elizabeth S, Gaw, Allan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695787/
https://www.ncbi.nlm.nih.gov/pubmed/23758677
http://dx.doi.org/10.1186/1745-6215-14-171

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695787/
https://www.ncbi.nlm.nih.gov/pubmed/23758677
http://dx.doi.org/10.1186/1745-6215-14-171

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