Revolutionizing IMDRF Coding with AI

Discover the Future of Medical Device Compliance!

Post-market surveillance is crucial for medical device manufacturers. However, traditional complaint handling systems often use inefficient manual processes. These systems also rely on inconsistent methods and fragmented workflows. Consequently, compliance risks and patient safety are compromised. Additionally, brand reputation is put at stake.

With growing regulatory complexities from frameworks like EU MDR and FDA guidelines, the stakes have never been higher.

During this webcast, Dr. Dharani, Chief Scientist, CEO, and Co-founder of 3Analytics, will guide you through the transformative power of the IMDRF Coding Solution. This modern platform automates complaint handling with unmatched accuracy, reducing processing times from 15 minutes to 4-6 seconds and achieving 95% accuracy.

Discover how the 3Analytics solution effortlessly integrates with systems like AssurX’s QMS for compliance, efficiency, and safety monitoring. Explore real-world success stories, such as a client who improved operations significantly by reducing manual efforts and ensuring coding consistency.

Gain actionable insights to streamline workflows, safeguard your brand, and excel in an evolving regulatory environment.