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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...
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| Publicat a: | BMC Med Ethics |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4668674/ https://ncbi.nlm.nih.gov/pubmed/26630924 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12910-015-0073-1 |
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