One area in the clinical trial process that has been identified for
improvement is risk-based planning and management. Monitoring
and managing risk has always been a critical piece of clinical research,
as it directly relates to the safety and evaluation of the efficacy of a
drug. This article, written by Justin Stark, Head/Director Risk Based
Monitoring & Standards, UCB, spotlights a modern, risk-based
approach to the design, planning and management of clinical trials,
exploring its key attributes.