How Meta Achieves Best-in-Class Engineering in Regulated Environments
June 30, 2026
,
11:00 am
EST
•
60
mins
Recorded on
June 30, 2026
•
60
mins
When Meta’s Reality Labs set out to bring AI-enabled smart glasses to market, the goal was clear: preserve its world-class engineering culture while applying medical-grade rigor to the software components classified as medical devices. Balancing rapid iteration with regulatory rigor required changes to collaboration, tooling, and quality management.
In this rebroadcast of one of our most popular sessions, Lucas Fernandez, Director, Medical Devices at Meta, and Erez Kaminski, CEO of Ketryx, walk through how Meta aligned AI-driven development practices with FDA and IEC 62304 requirements without slowing teams down.
What you'll learn
- How embedding quality processes into existing tooling with automated checks let engineers across hardware and software teams stay in their native tools
- How simplifying QMS management by unifying training and approvals strengthened compliance
- How automating documentation workflows within existing tools enhanced consistency and speed without adding manual overhead
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