IQVIA integrates pharmacovigilance and regulatory affairs to streamline compliance, enhance drug safety, and support faster approvals. By combining ADR monitoring, risk-benefit assessment, and regulatory filings, IQVIA ensures lifecycle management with global reach. Advanced analytics, a global safety database, 24/7 monitoring, and regulatory intelligence strengthen oversight. The FSP model drives cost efficiency, vendor consolidation, and consistent governance through a unified team and shared KPIs. With localized expertise and scalable resources, IQVIA enables rapid market entry, optimized budgets, real-time insights, and continuous safety monitoring, delivering unmatched quality, compliance, and faster regulatory action.

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