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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Bibliographic Details
Main Author: Anvita Pandiya
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2010-01-01
Series:Perspectives in Clinical Research
Subjects:
Online Access:http://www.picronline.org/article.asp?issn=2229-3485;year=2010;volume=1;issue=3;spage=98;epage=100;aulast=Pandiya