Contract Clinical Trial Site Management Services (CRO)

Service providers supports clinical trials with expert clinical research coordinators (CRCs) that help improve the quality of clinical trials, while reducing the workload of clinical staff. Companies offer a range of services that can include: patient eligibility support, informed consent support, manage patients’ hospital visit/testing schedule, manage clinical trial materials, support case report form (CRF) preparation, support clinical research associates, and support medical institution with audit/regulatory inspection.