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EMPIRICAL EVALUATION OF THE NEED FOR ‘ON-GOING CONSENT’ IN CLINICAL RESEARCH

OBJECTIVE: Some commentators argue that informed consent for clinical research should be an on-going process, which begins, rather than ends, with participants’ initial consent. Lacking, however, are empirical data on whether there is a need for ‘on-going consent’. DESIGN: Two self-administered surv...

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Autors principals: Smith, William, Grady, Christine, Krohmal, Benjamin, Lazovski, Jaime, Wendler, David
Format: Artigo
Idioma:Inglês
Publicat: 2011
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2995831/
https://ncbi.nlm.nih.gov/pubmed/21076272
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/QAD.0b013e328340fec7
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