Learn more about clinical trials and the most frequently asked questions and answers.
Learn the benefits of participating in a clinical trial.
Learn about your before enrollment patient rights and after enrollment patient rights.
An informed consent is a written agreement required by the FDA for all people enrolling in a clinical trial. Learn more about the information it contains, the process and the purpose of the informed consent.
Most people have heard myths about clinical trials, such as not being able to drop out after enrolling in a clinical trial. Learn the facts about these common clinical trial myths.
Learn about common clinical trial terminology.