IQVIA’s eTMF solutions strengthen compliance, transparency, and inspection readiness by addressing challenges like ad-hoc processes, poor indexing, and delayed uploads. Using the IMPACT framework—Integration of KPIs, Meticulous standardization, Proficient knowledge, Audit experience, Comprehensive change management, and Training excellence—IQVIA optimizes trial documentation globally. Benefits include harmonized SOPs, continuous performance monitoring, and expert-led audit readiness for agencies like FDA and MHRA. With proven onboarding, training, and change management, sponsors achieve streamlined workflows, improved visibility, and efficient, inspection-ready Trial Master Files.

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