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Methodological quality and reporting of ethical requirements in clinical trials

Objectives—To assess the relationship between the approval of trials by a research ethics committee (REC) and the fact that informed consent from participants (ICP) was obtained, with the quality of study design and methods. Design—Systematic review using a standardised checklist. Main measures—Meth...

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Detalhes bibliográficos
Main Authors: Ruiz-Canela, M., de Irala-Estevez, J., Martinez-Gonzalez, M. A., Gomez-Gracia, E., Fernandez-Crehuet, J.
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2001
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1733392/
https://ncbi.nlm.nih.gov/pubmed/11417024
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jme.27.3.172
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