Informed consent is the process of learning the key facts about a clinical trial before an individual decides whether or not to participate. When an individual is considering joining a clinical trial, the research staff will provide informed consent documents that include details about the study. But informed consent is more than just signing a form. It is a continuous process, with the research team providing information throughout the course of the trial. Since joining a clinical trial is an important decision, people are encouraged to discuss all their questions and concerns with the research team before deciding whether to participate.
Patient’s Corner
Introducing Patient’s Corner, a place for you, the patient, to share your stories. If you have a story you would like to share please contact us below.
Pituitary Patient Tool Kit
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Downloadable Pituitary Brochures
Our print quality brochures are now available for download.