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A Comparison of the Quality of Informed Consent for Clinical Trials of an Experimental Hookworm Vaccine Conducted in Developed and Developing Countries

Informed consent is one of the principal ethical requirements of conducting clinical research, regardless of the study setting. Breaches in the quality of the informed consent process are frequently described in reference to clinical trials conducted in developing countries, due to low levels of for...

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Detalles Bibliográficos
Publicado en:PLoS Negl Trop Dis
Main Authors: Diemert, David J., Lobato, Lucas, Styczynski, Ashley, Zumer, Maria, Soares, Amanda, Gazzinelli, Maria Flávia
Formato: Artigo
Idioma:Inglês
Publicado: Public Library of Science 2017
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5289607/
https://ncbi.nlm.nih.gov/pubmed/28114401
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pntd.0005327
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