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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Bibliografiske detaljer
Udgivet i:BMC Med Ethics
Main Authors: Ebile, Akoh Walter, Ateudjieu, Jerome, Yakum, Martin Ndinakie, Djuidje, Marceline Ngounoue, Watcho, Pierre
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2015
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4589194/
https://ncbi.nlm.nih.gov/pubmed/26420169
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12910-015-0061-5
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