CRO Services
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.