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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...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
הוצא לאור ב:PLoS Negl Trop Dis
Main Authors: Diemert, David J., Lobato, Lucas, Styczynski, Ashley, Zumer, Maria, Soares, Amanda, Gazzinelli, Maria Flávia
פורמט: Artigo
שפה:Inglês
יצא לאור: Public Library of Science 2017
נושאים:
גישה מקוונת: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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