Implementing Risk Based Monitoring
Clinical trial costs and complexity have risen considerably in recent years. The conventional on-site evaluation of trial data accounts for one-third of the study's expense. This method, which relies primarily on comprehensive source data verification, has shown to be both resource-intensive and restricted in its capacity to detect and avoid problems. It is widely acknowledged that the procedure for clinical trial monitoring needs to alter in order to ensure the well-being of trial participants and retain the integrity of final results.
- Data Integrity
- Detection of Critical Data and Processes
- Risk Assessment
Related Conference of Implementing Risk Based Monitoring
November 25-26, 2025
4th World Congress on Medicinal Chemistry and Computer Aided Drug Design
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Implementing Risk Based Monitoring Conference Speakers
Recommended Sessions
- Adaptive Trial Model
- Biomarkers&Biomarker Discovery and Drug Development
- Cancer Clinical Research
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- Clinical Trial Auditing
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