Are you ready for QMSR? Live AMA with FDA compliance experts

QMSR goes live in February 2026. Are you prepared?

The FDA’s new Quality Management System Regulation is replacing 21 CFR Part 820 and aligning US regulations with ISO 13485. Enforcement begins February 2, 2026. This webinar will help you validate your readiness, refine your strategy, and get clear answers to your biggest compliance questions from two of the most trusted voices in the industry.

Join Greenlight Guru’s Etienne Nichols and FDA compliance expert Eric Henry for a live AMA session focused on QMSR readiness. Whether you’re still trying to decode what the final rule means or you’re knee-deep in documentation updates, this is your chance to ask anything.

What you’ll learn

• What the QMSR final rule means for medical device companies
• How to prepare your quality system, risk processes, and inspection readiness before February 2nd
• Compliance strategies, documentation alignment, and inspection pitfalls to avoid
• Live answers to your questions about QMSR, ISO 13485 alignment, and what the FDA will expect