A lot factors into your monitoring decisions. Costs, patient safety and data quality. Not to mention other challenges like the complexity of managing international sites, resistance to business process change and variability according to clinical trial type.
New monitoring strategies can reduce costs, improve patient safety, help you meet regulatory requirements and limit on-site monitoring visits. And improve upfront identification of risk and trial performance expectations. In this complimentary Applied Clinical Trials e-book, learn about the challenges and rewards of risk-based monitoring based on a third-party research study and a recent webcast featuring industry experts.
This e-book helps explain:
- Why you should consider risk-based monitoring.
- What determines risk and how risk levels are determined.
- What technology is available for effective risk-based monitoring.
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