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Patient representatives’ views on patient information in clinical cancer trials
BACKGROUND: Patient enrolment into clinical trials is based on oral information and informed consent, which includes an information sheet and a consent certificate. The written information should be complete, but at the same time risks being so complex that it may be questioned if a fully informed c...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2016
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736467/ https://www.ncbi.nlm.nih.gov/pubmed/26831330 http://dx.doi.org/10.1186/s12913-016-1272-2 |