Services - Clinical Trial Management

Clinical Trial Management

           CRF Completion Instruction

           Investigator Selection and Grant Management

           Patient Enrollment Tracking

           Study Initiation, Monitoring, and Close-out Visits

           CRF Review and Data Query Resolution

           Adverse Event, Medication, and Disease Terminology Coding

           Safety Monitoring and Serious Adverse Event Report Tracking

           Service on IRB

We provide full service in clinical trial management. Our clinical operation group consists of experienced clinicians and site monitors, follows ICH guidelines for Good Clinical Practice in conducting trials, and provides professional outcomes in clinical trial data collection and review.