The medtech industry is experiencing a huge proliferation in AI-powered tools that are driving predictive medicine. Gain actionable insights on navigating the pre- and post-market regulatory landscape and creating a process focused on patient safety for AI-enabled medical devices with a focus on:
• Building a more efficient AI post-market surveillance - best practices and modern tools
• Achieving regulatory success in Adaptive AI
• Prioritizing safety by knowing when and how to engage with regulatory authorities for AI-related modifications