Please be sure to bring the proper identification to your initial visit along with any medications that you may be taking. During this visit you will be handed an Informed Consent Form. You will sit in a private room with the doctor or a member of the study team to go over the purpose of the study, the risks, benefits, known side effects, as well as all procedures that will be required during the trial. 

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Once the consent form has been explained, discussed and signed by all applicable parties (some studies require a caregiver or other such individual to be present during this process) you will begin the procedures of the actual study or be scheduled to come in another day depending study requirements.

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CONTACT US  today, if you have any questions.