Five Steps To Streamline Your Trial

Data lie at the heart of clinical trials, necessary to prove safety and efficacy—and increasingly to demonstrate value in the real world. Today, with the growing use of wearables, remote devices, and other novel data collection modalities, researchers have more information sources to tap into. Yet, much of the data is irrelevant to the study at hand—and all the data is meaningless if it isn't adequately verified and analyzed, an increasingly daunting task.

The solution: Use risk-based quality management (RBQM) as a key organizational principle for study conduct.