Connected, integrated, compliant. Build, scale, and optimize your quality and regulatory workflows with SmartSolve®, IQVIA's transformative Enterprise Quality Management System, built for Life Sciences.
Postmarket Surveillance is the keystone of a strong vigilance program. It ensures that even after a medical device is released into the market, developers continue to monitor its safety and effectiveness in the real world. Activities range from reactive reviews of complaints and adverse events, to proactive tracking of device performance via customer surveys, interviews and focus groups.
This process ensures medical devices perform as expected, and provide opportunities to improve future iterations. However, it's a costly and time-consuming aspect of the life sciences operation, and demands on postmarket surveillance teams continue to increase.
Connected, integrated, compliant. Build, scale, and optimize your quality and regulatory workflows with SmartSolve®, IQVIA's transformative Enterprise Quality Management System, built for Life Sciences.
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