In order to provide new medications to the public, pharmaceutical companies must test their investigational drugs through medical research studies (also called clinical trials). The United States Food and Drug Administration (FDA) reviews the data collected in these studies before determining if a new medication can be approved for the public.
Study doctors are required to follow strict rules to protect the safety of the people who volunteer to participate in clinical trials. All researchers must follow a detailed plan, called a protocol, which explains all study procedures and has been reviewed and approved by an independent board (or group of people) that oversees the safety and welfare of all study participants. Additionally, before enrolling individuals into a study, researchers must fully explain the study to the individual and answer any questions he or she may have. Participation in a clinical trial is voluntary, and participants may withdraw from the study at any time for any reason.
B.E.D. - Binge Eating Is A Disorder are research studies located in Akron, OH.