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Discover the Future of Medical Device Compliance Post-market surveillance is a critical responsibility for medical device manufacturers, yet traditional complaint handling systems rely heavily on inefficient and inconsistent manual processes, compounded by fragmented workflows.

These challenges not only increase compliance risks but also jeopardize patient safety and brand reputation. With growing regulatory complexities from frameworks like EU MDR and FDA guidelines, the stakes have never been higher.

Join our exclusive webinar, presented by Dr. Dharani, Chief Scientist, CEO, and Co-founder of 3Analytics. A thought leader in leveraging AI for compliance and safety, Dr. Dharani will guide you through the transformative power of our IMDRF Coding Solution. This revolutionary platform automates complaint handling with unmatched accuracy, reducing processing times from 15 minutes to 4-6 seconds and achieving 95% accuracy. Learn how our solution integrates seamlessly with existing systems like QMS to ensure compliance, enhance efficiency, and support proactive safety monitoring.

In this webinar, Dr. Dharani and AssurX will also showcase real-world success stories, including how one client drastically improved operations by cutting manual efforts and achieving coding consistency. Gain actionable insights to streamline workflows, safeguard your brand, and excel in an evolving regulatory environment. Don’t miss this opportunity to learn from an industry pioneer—register now to secure your spot and take the first step towards enhanced efficiency and patient safety!