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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...

詳細記述

保存先:
書誌詳細
出版年:BMC Med Ethics
主要な著者: Ebile, Akoh Walter, Ateudjieu, Jerome, Yakum, Martin Ndinakie, Djuidje, Marceline Ngounoue, Watcho, Pierre
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2015
主題:
オンライン・アクセス: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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