Thursday, June 9, 2011
Tuesday, May 10, 2011
THE PROCEDURE OF INFORMED CONSENT IN INDIAN CLINICAL TRIALS
Directions towards improving the Quality of Informed Consent
Saturday, May 7, 2011
Informed Consent
Introduction
Federal code states that "[a]ny research project utilizing human subjects requires the informed consent of those subjects." The first step in the process is detailing the specifics of your study that are important to communicate to participants and to the IRB.
IRB Approval has to be considered
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