Founded in 1992, we are an independent and dedicated clinical research company located in Evansville, Indidana. We conduct a comprehensive study of the safety and effectiveness of the most promising advances in patient care for pharmaceutical, nutritional and medical device trials for phase 2, 3 and 4 studies. MediSphere provides a bridge between scientific breakthroughs and new standards of medical care. The trials are carefully controlled and regulated by the federal standards of the Food and Drug Administration, National Institutes of Health, and Institutional Review Boards (IRB). These boards govern clinical trials to protect the rights and welfare of clinical research participants.
Your rights are protected in two important ways when you volunteer for a clinical trial. First, any physician who is awarded a research study by a pharmaceutical company must obtain approval to conduct the study from the Institutional Review board. The review board is responsible for examining the study to ensure that all volunteers' rights are protected and the study does not present any undue or unnecessary risk to the patient. Secondly, anyone who volunteers to participate in a clinical trial in the United States is required to sign a "Informed Consent" form. The purpose of this form is to provide details about the study, the risks associated with the study medication, and what procedures the volunteer will undergo during the course of the study.
In a clinical research study, the participants may receive study related care from a doctor/research team for the duration of the study. Reasonable payments will be made for participation. No health insurance or doctor referral is needed.
To see if you qualify for one of our current studies, visit or call us today. It's quick and easy and there is no obligation to participate.
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Mon-Fri: 7:30am - 5:00pm
Sat-Sun: CLOSED