IQVIA leverages Nordic countries’ unique ecosystem linking registries, EMRs, and primary data to generate robust real-world evidence for medical devices. This combination provides insights on patient pathways, device utilization, outcomes, and safety. Applications span pre-approval studies on disease burden and treatment patterns, and post-approval monitoring for performance and regulatory compliance. With 70+ studies conducted, IQVIA’s local relationships and EMR access enable secure data integration. A 140-strong Nordic RWE team brings deep expertise in post-market safety, enhancing study quality and reliability.

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