Informed consent is formal acceptance of the volunteer participant of the clinical trial. Informed consent in the clinical trial details that is required for the volunteer to participate in the clinical trial, but still there is some more information that the participant should know before participating in the clinical trial.You should know about the preclinical tests that have been published, reviewed and repeated by other experts. Know if the provider has acceptance from IRB Institutional review board to make sure that the risks of the clinical trials are very low and the benefits are high. The clinical trial also should have the approval from FDA for safe conduct of the clinical trials.
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