GCP Clinical Research advocates for its patients to ensure safety, protection and confidentiality for all patients participating in our clinical trials. These include the Patient Bill of Rights and Hospital Accreditation to ensure that an international review board must approve every new study at a hospital or medical facility before it can begin. Our bilingual staff meets with each patient to present all the facts and details about the clinical trial and explain the informed consent process before deciding to participate. At GCP, you never have to wait when you arrive for your study visits and you can feel reassured that our Patient Support throughout your participation in the study is Continuous.