IQVIA MedTech’s post-market safety solutions help meet rising global regulatory demands for continuous device monitoring across the lifecycle. Services span RWE generation, surveillance, clinical follow-up, and physician experience studies. Post-market evaluations highlight real-world risks, benefits, and usage patterns, enabling early detection of safety signals and performance improvements. IQVIA offers prospective and retrospective study designs, enriched methods, and both primary and secondary data collection. Compliance covers FDA CDRH, EU MDR/IVDR, and ISO 14155:200. Leveraging digital platforms, NextGen capabilities, and global-local expertise, IQVIA accelerates recruitment, ensures smarter evidence generation, and supports regulatory reporting requirements.

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