Excellence in Clinical Monitoring

Our Clinical Research Associates (CRAs) have abundant experience in various therapeutic areas. Our CRAs are continually trained to ensure top quality monitoring for pharmaceutical development.

 

Flow of operation

Monitoring

Service line-up

  • Development protocol (PRT)/ Case Report Form (CRF) and draft trial design
  • Screen prospective trial sites and Investigators
  • Prepare Informed Consent form, CRF completion guide and other essential documents
  • Monitoring
    1. GCP compliance review of medical institutions and investigators
    2. Process trial requests for medical institutions, monitoring and trial termination
    3. Source Data Verification (SDV)
    4. Case monitoring
    5. Submit Safety Information