This flyer highlights IQVIA’s device utilization electronic survey, a cost-effective method to capture real-world evidence (RWE) for medical device post-market surveillance under EU MDR Article 83. The solution provides real-time data access, on-demand reporting, and supports device usability, safety, and performance evaluation. Key features include rapid setup timelines, multilingual support, stakeholder consent capture, and PRO integration options. It is designed for ease of use by physicians, surgeons, and sponsors, enabling streamlined compliance and continuous monitoring of device effectiveness. By maximizing data generation, the tool accelerates regulatory readiness and enhances product lifecycle management.

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