Making quick and accurate decisions during a clinical trial is critical for keeping patients safe and studies on track. However, increasing trial complexity, new data types, and a growing reliance on contract research organizations (CROs) can make it difficult for sponsors to access and analyze the data they need, when they need it.
This article examines data challenges faced by sponsors and the underlying problems driving those challenges. It also details fast and flexible new processes and solutions designed to help overcome these challenges by serving sponsors’ ever-increasing need to analyze complex data. These solutions provide actionable insights that make safety signals easy to detect and investigate while easing the burden of meeting regulatory requirements.