What it Means to be a Study Participant
Steps Involved
1. More than likely your personal physician recommended you for a clinical trial with our center.
2. You will meet with a professional staff member, Medical professional or a study coordinator to discuss the study and requirements. At such a point you will be given an Informed Consent Form which will be explained thoroughly and will outline your responsibilities for the trial. There are other instructions that follow along with the consenting to ensure we follow Good Clinical Practices as well that are explained and followed at this visit.
3. You are compensated for your time and effort for each visit completed at the time of your visit, including your screening visit which may be the very first visit you meet with us.
4. During the course of the clinical trial you are carefully monitored and overseen by our Principal Investigator a board certified Medical Doctor that has been thoroughly trained on the protocol and he/she utilizes their medical expertise to evaluate your information at each visit.
5. We provide open sessions to the general public to learn more about being a study participant and you can call us directly to learn more at 772-242-7112.