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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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Detaylı Bibliyografya
Yayımlandı:PLoS Negl Trop Dis
Asıl Yazarlar: Diemert, David J., Lobato, Lucas, Styczynski, Ashley, Zumer, Maria, Soares, Amanda, Gazzinelli, Maria Flávia
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2017
Konular:
Online Erişim: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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