A client needed to review legacy REMS program records covering about 2,500 patients to ensure no safety events were missed before a regulatory report. IQVIA’s Lifecycle Safety Services partnered with Vigilance Detect to deliver a compliance-focused, tech-enabled solution. The system automatically screened records, flagged potential adverse events, and provided a GxP-compliant workflow for centralized pharmacovigilance review. Within two months, 277K records were processed, 15K filtered out, and 54% of identified events validated by PV analysts. Supported by 40 global specialists and OCR technology, the solution reduced manual workload, improved compliance, and ensured faster, reliable results.

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