- Protocol development, including Case Report Form and Subject Informed Consent - Submission to Ethics Committee/Institutional Review Board and Regulatory Authority - Project management - Monitoring - Site management - Out-sourcing clinical research associate or study coordinator - Data Management, Statistical Analysis and Clinical Study Report - Clinical research and ICH GCP training: in cooperation with Vietnam MOH and quailfied experts - Investigational Product Handling: in cooperation with local drug distributor - Translation services