Nelson Labs’ MedTech Lifecycle Seminar: Design, Validation & Regulatory Compliance

Nelson Labs and Sterigenics, both members of the iia, are hosting MedTech Lifecycle Seminar: Design, Validation & Regulatory Compliance October 13 – 15, 2026, in San Jose, Costa Rica.

This three-day seminar delivers a practical, end-to-end overview of sterile medical device validation, combining regulatory strategy with hands-on technical training. Attendees will explore evolving requirements such as QMSR, ISO standards, and global market regulations while learning how to build compliant, risk-based systems.

The program also provides in-depth coverage of key validation areas—including biocompatibility, packaging, and sterilization—along with real-world application through case studies and a facility tour. Overall, participants will gain the tools and insights needed to ensure product safety, regulatory compliance, and successful global commercialization. Find the full agenda here.

To learn more and register for the seminar, visit the Nelson Labs website →