On Demand Webinar: Revolutionizing Risk-Based Monitoring Through Real-Time Analytics
Since being officially condoned by the FDA in 2013, Risk-Based Monitoring (RBM) has progressed to become a viable clinical monitoring technique, leveraging the latest technology to proactively identify challenges to trial safety, data analysis, and compliance. With clinical trial resources prioritized by risk, RBM has brought study sponsors, CROs, and other stakeholders greater oversight into how trials are conducted.