Informed consent: Are we doing enough?

The process of informed consent is an ethical mandate for all clinical trials. The principles of ethics in research involving human beings decrees the conduct of a process where the prospective research subjects should be informed of all aspects of the research study and after complete comprehension...

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Bibliographic Details
Main Author: Pranati
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=4;spage=124;epage=127;aulast=