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Informed Consent for Phase I Oncology Trials: Form, Substance and Signature
BACKGROUND: Federal regulations state consent information should be understandable to participants; concerns have been voiced about the quality of informed consent forms (ICFs) in oncology trials. METHODS: The content of ICFs for phase I studies that were conducted at a tertiary care cancer center o...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elmer Press
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985563/ https://www.ncbi.nlm.nih.gov/pubmed/24734147 http://dx.doi.org/10.14740/jocmr1803w |