Engineering medical devices for the IEC 62304 and CRA era

IEC 62304 still anchors the medical software lifecycle, but cybersecurity-by-design, EU Cyber Resilience Act reporting, and evolving FDA expectations have changed what teams must deliver. The fastest medical device teams aren't doing more compliance work, they're building it into how they engineer.

This webinar shows engineering leaders how TÜV SÜD-certified toolchains, integrated security, and CI/CD workflows turn compliance from an end-of-cycle obstacle into continuous, audit-ready evidence, preparing your team for IEC 62304 audits and CRA reporting.

What you’ll learn

• How IEC 62304, FDA cybersecurity, and the CRA fit together
• Generating submission-ready evidence inside your build pipeline
• Secure update and provisioning patterns regulators accept
• What "compliance-left" looks like in practice

Join us to learn how medical device teams turn regulatory complexity into faster, safer releases, on a proven, TÜV SÜD-certified, vendor-agnostic foundation built for decade-long product lifecycles.