Defining Requirements for AI Enabled Medical Devices: What Next in Cybersecurity and Supplier Relations?
Time: 10:01 am
day: Pre-Conference Day
Details:
Building safe and trustworthy AI systems in the medical device industry, covering essential questions, regulatory expectations, and quality considerations. Through practical examples and a template-based case study, participants will learn how to lead AI decision-making in healthcare, understand global regulatory landscapes, and address key quality considerations for AI-enabled devices. The session aims to equip participants with cross-functional critical thinking techniques, risk-based approaches, and specific regulatory questions essential for AI model development and deployment in a healthcare context. In the second half of the workshop, we will be exploring agentic AI for mitigating cybersecurity risks.
Part 1: Defining Requirements for AI Enabled Medical Devices.
- Requirements for AI enabled medical devices. Supplier selection best practices
Part 2: Agentic Artificial Intelligence for Mitigating Cybersecurity Risks.
- Automated vulnerability monitoring and handling via Agentic AI systems and other Automated tools
