- 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

SMART Research Corp,

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Teams

Offices