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.