Webinar

Rethinking Device Design: Where Data and Compliance Align

H2 Title

November 20, 2025 | 1 PM ET | 10 AM PT

In today’s connected medical device ecosystem, data, traceability and compliance are no longer separate disciplines — they’re converging imperatives that must be addressed from the very start of design. Yet many development teams still approach serialization, labeling and life cycle data capture as afterthoughts, leading to costly redesigns and approval delays.

This webinar brings together experts in FDA regulatory strategy and RFID-enabled device intelligence to explore how early integration of identification and data systems builds compliance into the foundation of product design. Participants will gain a practical understanding of how to bridge R&D, regulatory and operational priorities to improve device performance and market readiness.

Discussion topics include:

How early RFID integration supports UDI compliance, traceability and global labeling consistency
Strategies for reducing redesign and rework costs through proactive regulatory planning
Building supply chain and lifecycle visibility to enhance post-market performance and safety
Using device-generated data to inform smarter design, maintenance and AI-driven insights

By approaching device development through the lens of data-enabled compliance, organizations can uncover and address R&D blind spots before they become barriers — designing devices that are not only compliant but intelligent, efficient and ready for the future of connected healthcare.

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