Ensayos clínicos y consentimiento informado: visión de investigadores, pacientes y médicos de familia

OBJECTIVE: Adequate information for patients and respect for their autonomy are mandatory in research. This article examined insights of researchers, patients and general practitioners (GPs) on the informed consent process in clinical trials, and the role of the GP. DESIGN: A cross-sectional study u...

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Detalles Bibliográficos
Autores principales: Giménez, Nuria, Pedrazas, David, Redondo, Susana, Quintana, Salvador
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Originales
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877861/
https://www.ncbi.nlm.nih.gov/pubmed/26777978
http://dx.doi.org/10.1016/j.aprim.2015.10.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877861/
https://www.ncbi.nlm.nih.gov/pubmed/26777978
http://dx.doi.org/10.1016/j.aprim.2015.10.008

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