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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Dades bibliogràfiques
Publicat a:PLoS Negl Trop Dis
Autors principals: Diemert, David J., Lobato, Lucas, Styczynski, Ashley, Zumer, Maria, Soares, Amanda, Gazzinelli, Maria Flávia
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2017
Matèries:
Research Article
Accés en línia: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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