Webinar - Cybersecurity, AI, and PCCPs: Navigating Regulatory Requirements When Developing Next-Gen Medical Devices

Next generation medical devices must navigate an increasingly complex regulatory landscape — from cybersecurity and AI governance to structured change management frameworks like PCCPs. This webinar will cover practical, actionable guidance on the most important regulatory topics shaping next generation devices and solutions for medtech companies.

Registrants will get complex requirements distilled into clear frameworks, real-world examples, and practical steps your team can apply immediately. Whether you’re designing AI-enabled features, strengthening cybersecurity, or planning predictable device updates, this series provides the clarity and structure needed to move faster, reduce risk, and develop next generation medical devices that remain safe and compliant over time.

Ideal for R&D, regulatory, quality, and product teams building connected, software-driven devices and solutions.
In this webinar, you will learn:

• Practical guidance covering cybersecurity, AI, and PCCPs.
• Clear frameworks aligned with FDA, EU MDR, EU AI Act, ISO/IEC standards, and global expectations.
• Practical steps to reduce regulatory risk and accelerate development.
• What regulators expect in pre submission and post market phases.