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Assessing the detection, reporting and investigation of adverse events in clinical trial protocols implemented in Cameroon: a documentary review of clinical trial protocols

BACKGROUND: International guidelines recommend ethical and scientific quality standards for managing and reporting adverse events occurring during clinical trials to competent research ethics committees and regulatory authorities. The purpose of this study was to determine whether clinical trial pro...

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Detalles Bibliográficos
Autores principales:	Ebile, Akoh Walter, Ateudjieu, Jerome, Yakum, Martin Ndinakie, Djuidje, Marceline Ngounoue, Watcho, Pierre
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2015
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589194/ https://www.ncbi.nlm.nih.gov/pubmed/26420169 http://dx.doi.org/10.1186/s12910-015-0061-5

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