What is Integrated Clinical Research?

Integrated Clinical Research is the process of testing the safety and efficacy of newly developed drugs. It involves volunteers to participate in carefully conducted trials. All medications currently prescribed today have once been in a Integrated Clinical Research.

All volunteers entering a study will be given an approved Informed Consent that explains the study procedures, risks, and benefits. All of our volunteers are given ample time to review the consent form along with the opportunity to ask questions. Volunteers will then be randomly assigned to different groups as outlined in the study protocol. Volunteers are carefully monitored for treatment and safety throughout the course of the study. All studies are routinely monitored and audited by both the FDA and other regulatory authorities.

All study related products are provided at no cost to you. Compensation for time and travel is provided and medical insurance is not required.