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Readability and Comprehensibility of Informed Consent Forms for Clinical Trials

The signed informed consent form provides documentary evidence that the patient has given informed consent to participate in a clinical trial and that the patient has been given the requisite information. However, this document must not only provide the necessary information, it must also be provide...

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Détails bibliographiques
Auteur principal: Pandiya, Anvita
Format: Artigo
Langue:Inglês
Publié: Medknow Publications Pvt Ltd 2010
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3146080/
https://ncbi.nlm.nih.gov/pubmed/21814628
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