Risk Management For Medical Devices: A Data-driven Approach To Comply With ISO 14971

ISO 14971 is the gold standard for managing medical device risks. It is critical for ensuring patient safety and securing faster market approval. But traditional, manual risk management slows teams down and leaves room for costly mistakes.

Watch the recording to see how the 3DEXPERIENCE platform makes risk management smarter, faster, and fully integrated into your product development process.

You’ll learn how to:

• Reuse proven risk and hazard libraries to save time and ensure consistency.
• Link risks directly to requirements and design activities for true safety-by-design.
• Automate risk thresholds, spot critical issues early, and take fast action.
• Use real-time analytics and up-to-date reports to streamline regulatory submissions.

Why View This Session?

• Reduce recalls and improve device safety.
• Harmonize best practices across teams and products.
• Eliminate manual data entry and always work with the latest information.
• Turn ISO 14971 compliance into a competitive edge.