High Quality

• Experienced team leader, who have international GCP studies experience
• Experienced clinical monitoring staff trained on GCP and therapeutic area
• SOP, Confidentiality, QA System
• Adherence to ICH GCP and China GCP
• Pivotal data acceptable to the FDA

High Efficiency

• Quickly set up professional team
• Wide networking with clinical sites
  Quick sites initiation
  Quick patient enrollment
• Standardized Operating
  Less query
  Quick solution
  Quick data lock

Low Cost

• Strict cost control
• Time saving brings cost saving
• Flexible collaboration mode（Governmental fund, VC)