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Clinical trial procedure guidelines
  • Test participant clinical trial procedure
    • Establish schedule
    • 임상시험문의
    • Planning development
    • Research plan contract engagement
    • Clinical trial schedule
    • Contract
    • Provide test sample
    • Clinical trial monitoring
    • Receive clinical trial result reports
    • Clinical trial completion
  • 센타 임상시험 절차
    • Test plan review and consultation
    • Planning development
    • Contract
    • Recruiting and screening test participants
    • Receive test samples
    • Conduct clinical trials
    • Submission of clinical trial result reports
    • Internal quality-control management
    • Clinical trial completion
  • If IRB approval is required, clinical testing will be conducted after IRB approval.
  • If IRB approval is required, research papers are prepared and submitted according to guidelines of domestic and foreign journals and export/import country regulations.