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Length and Complexity of US and International HIV Consent Forms from Federal HIV Network Trials

BACKGROUND: Informed consent is required in most clinical research with humans. While federal regulations state consent information should be understandable to participants, concerns have been raised that consent forms are overly long and complex. DESIGN: Consent forms from 2006 HIV network trials s...

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Detalhes bibliográficos
Main Authors: Kass, Nancy E., Chaisson, Lelia, Taylor, Holly A., Lohse, Jennifer
Formato: Artigo
Idioma:Inglês
Publicado em: Springer-Verlag 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3208469/
https://ncbi.nlm.nih.gov/pubmed/21748435
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11606-011-1778-6
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