This fact sheet highlights IQVIA’s SmartSolve Postmarket Surveillance (PMS), a comprehensive system for MedTech companies to manage PMS from planning to reporting. It ensures compliance with tightening regulations like the EU MDR while enhancing product safety and lifecycle management. The solution centralizes workflows, integrates with CAPA and risk management, and enables real-time task tracking, evidence access, and report generation. Benefits include improved product performance, reduced recalls, better compliance, and lower costs. With dashboards, template-based reporting, and ISO 14971/20416 alignment, SmartSolve PMS empowers continuous improvement, proactive risk mitigation, and robust oversight across the entire device surveillance journey.

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