Detect Your Risks. Take the Right Action.
Managing risk and ensuring patient safety during a clinical trial are shared goals for researchers. Whether you are transitioning to a risk-based approach or are experienced with risk-based monitoring (RBM), Bioclinica's ClearSiteTM helps you:
Gain a holistic view of your RBM plan and:
- Enhance patient safety
- Improve data quality
- Mitigate risk
- Optimize resource allocation and utilization
- Comply with the revised International Council on Harmonization guidelines (ICH E6(R2), Section 5)
See how our solutions help you develop strategies to leverage your data for continual success and to provide actionable insights for improved RBM.
ClearSite Professional Support Services
If you are new to RBM or need help developing a plan, Bioclinica's experts offer support on various levels. Our ClearSite professional support services team uses best practices to help you achieve the highest level of organizational efficiency and regulatory compliance, while doing so in a cost-efficient manner.
Choose the level of assistance you need.
ClearSite Monitoring Technology
The ClearSite solution was built to not only facilitate traditional RBM activities — including centralized statistical monitoring — but also to support you in the fundamentals of overseeing site quality and patient safety. Unlike other solutions, the ClearSite technology system adapts to your processes as your experience and comfort with RBM grows.
Our system is the only system that aggregates qualitative and quantitative data to assess clinical and operational risk so you can make more informed decisions and act on potential issues before they happen.
Built on a Strong Foundation of Data
Aggregate: ClearSite technology integrates data from multiple sources — both qualitative and quantitative.
Assess: Then, our technology applies the software’s predictive analytics algorithm to identify the areas of greatest risk.
Act: Finally, we create a unique risk profile you can use to set initial target performance and monitoring recommendations for you protocol, site or a complete portfolio of studies.