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Reaping the Bounty of Publicly Available Clinical Trial Consent Forms

Public access to clinical trial consent forms, beyond those individuals involved in reviewing, conducting, or participating in a trial, has been notoriously poor, resulting in missed opportunities for empirical analysis and improvement, among other benefits. However, recent changes to the Common Rul...

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Bibliografski detalji
Izdano u:IRB
Glavni autori: Lynch, Holly Fernandez, Largent, Emily A., Zarin, Deborah A.
Format: Artigo
Jezik:Inglês
Izdano: 2017
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5985974/
https://ncbi.nlm.nih.gov/pubmed/29881132
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