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A New Look at Informed Consent for Cancer Clinical Trials

Informed consent is fundamental to the conduct of clinical trials. Prospective participants need to be adequately informed and given the opportunity to ask questions and consult with relatives or friends without feeling pressured or rushed.

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Detalhes bibliográficos
Main Authors: Baer, Allison R., Good, Marge, Schapira, Lidia
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Clinical Oncology 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3140452/
https://ncbi.nlm.nih.gov/pubmed/22043194
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1200/JOP.2011.000347
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