This brief focuses on reducing timelines between database lock and clinical study report (CSR) completion, a critical bottleneck in clinical development. It outlines common challenges such as fragmented workflows, manual processes, and late-stage data issues. IQVIA presents integrated approaches that combine advanced analytics, automation, standardized templates, and proactive data review to improve speed and quality. By streamlining collaboration across clinical, statistical, and medical writing teams, organizations can shorten submission timelines, reduce rework, and accelerate regulatory and market milestones.

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