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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Format: | Article |
Language: | English |
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Wolters Kluwer Medknow Publications
2010-01-01
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Series: | Perspectives in Clinical Research |
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Online Access: | http://www.picronline.org/article.asp?issn=2229-3485;year=2010;volume=1;issue=4;spage=124;epage=127;aulast= |