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Volunteer experiences and perceptions of the informed consent process: Lessons from two HIV clinical trials in Uganda
BACKGROUND: Informed consent as stipulated in regulatory human research guidelines requires that a volunteer is well-informed about what will happen to them in a trial. However researchers are faced with a challenge of how to ensure that a volunteer agreeing to take part in a clinical trial is truly...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4668674/ https://www.ncbi.nlm.nih.gov/pubmed/26630924 http://dx.doi.org/10.1186/s12910-015-0073-1 |