GCP compliance and readability of informed consent forms from an emerging hub for clinical trials

BACKGROUND: The rapid expansion of trials in emerging regions has raised valid concerns about research subject protection, particularly related to informed consent. The purpose of this study is to assess informed consent form (ICF) compliance with Good Clinical Practice (GCP) guidelines and the read...

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Detalles Bibliográficos
Autores principales: Nair, Satish Chandrasekhar, Ibrahim, Halah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394576/
https://www.ncbi.nlm.nih.gov/pubmed/25878956
http://dx.doi.org/10.4103/2229-3485.154012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394576/
https://www.ncbi.nlm.nih.gov/pubmed/25878956
http://dx.doi.org/10.4103/2229-3485.154012

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