Research Forum: Inspection Ready Every Day

This webinar focuses on how strong day-to-day study practices lead to successful FDA clinical trial inspections. Using real examples from FDA trends and internal review findings, we will cover common compliance gaps, how to assess and manage protocol deviations, and practical ways to stay audit-ready. Attendees will learn simple, risk-based approaches to documentation, oversight, and self-monitoring, along with how to implement effective CAPAs that address root causes.