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...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:BMC Med Ethics
Asıl Yazarlar: Ebile, Akoh Walter, Ateudjieu, Jerome, Yakum, Martin Ndinakie, Djuidje, Marceline Ngounoue, Watcho, Pierre
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2015
Konular:
Research Article
Online Erişim: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
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller