FAQ

return to topWhat is a clinical research study?

A clinical research study is developed by a pharmaceutical company to evaluate new treatments. Physicians, also called clinical investigators, are chosen to conduct these studies. The clinical testing of a new drug is a step by step process that ensures you receive careful medical attention. All clinical trials are conducted with the approval of the US government's Food and Drug Administration (FDA) and the oversight of institutional review boards (IRBs).

return to topShould I volunteer for a research study?

There are several reasons why you should consider volunteering for a clinical research trial. Studies are necessary for the development of new medical therapies that offer better treatments and remedies. Taking part in a clinical trial is also a way to get free health care and often financial compensation for participating. You will always be given the opportunity to make an informed choice before beginning a study.

return to topWhat happens during a study?

At the start of a study you will have your history taken, undergo a physical exam, and sign an informed consent form. Your safety is the number one priority in a clinical trial. Therefore, it is important that you take all your medication as prescribed at the right times. It is important that you keep all your scheduled visits. If you miss your medication or you haven't taken it on schedule, tell your physician. Your input is valuable and important. When you participate in a study, your privacy is protected. Your medical records are confidential. Your name will not be listed on the study data that is submitted to the drug company. As a volunteer, you have the right to leave your study at any time.