The IQVIA LMS streamlines training for sites and study teams with cross-trial functionality. Sponsors and CROs can assign training across trials, roles, and therapeutic areas, eliminating redundant training. A centralized dashboard tracks compliance, completion, and reporting, reducing manual effort and costs. For sites, previously completed training is recognized across new studies, saving time and ensuring consistency. The system builds audit-ready documentation by tracking all user actions, ensuring compliance with regulatory requirements. Designed with PI and coordinator usability in mind, it reduces workload, improves oversight, and accelerates training while maintaining quality and efficiency.

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