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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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Dettagli Bibliografici
Pubblicato in:PLoS Negl Trop Dis
Autori principali: Diemert, David J., Lobato, Lucas, Styczynski, Ashley, Zumer, Maria, Soares, Amanda, Gazzinelli, Maria Flávia
Natura: Artigo
Lingua:Inglês
Pubblicazione: Public Library of Science 2017
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Accesso online: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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