Is your medical packaging line keeping pace with today’s compliance, production, and quality demands? Discover the seven key warning signs that indicate it may be time for an upgrade—from rising downtime and packaging defects to traceability gaps and increasing operating costs. Learn how modern packaging solutions can improve throughput, support regulatory readiness, reduce waste, and enhance sterile barrier integrity. This practical guide shares real-world insights from packaging specialists to help medical device manufacturers identify risks early and make informed decisions about upgrading packaging systems for long-term performance and compliance.

Sterility doesn’t happen by chance—it’s engineered. This insightful guide unpacks ISO 11607, the global standard ensuring medical devices remain sterile from production to patient use. Discover how packaging materials, design, and validation processes work together to prevent contamination, meet strict regulatory demands, and build trust in healthcare settings. Whether you're a manufacturer, packaging engineer, or quality professional, this breakdown highlights why compliance isn’t just a requirement—it’s critical to patient safety and product integrity in 2026 and beyond.