Clinical Trials

The Importance of "Informed Consent"

If you decide that you want to participate in a clinical study, the study doctor will review a very detailed document with you called the "Informed Consent", before any study procedure can be administered. The purpose of the Informed Consent is to make sure that you understand all the study procedures and the potential risks associated with the study procedures or the study. All questions or concerns that you have should be answered to your satisfaction at that time. If you decide to participate in the clinical study you will receive a copy of your signed "Informed Consent Form".

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