Success in clinical trial conduct is reliant upon three critical factors: the strength and quality of relationships between the sponsor, the CRO, sites and clinical trial vendors; the proactive establishment of robust processes that build quality into activities from the start; and the ability to leverage technology to predict and support performance of trial activities. In this session, led by the WCG Avoca Quality Consortium, we will connect, collaborate and explore how building quality relationships, planning processes proactively and utilizing current technology solutions equates to inspection success in an environment where we are often doing more with less.