FDA Tightens qPCR Data Integrity Rules: learn how the new dual-control, 21 CFR Part 11-aligned requirements could reshape qPCR software compliance, FDA 510(k) planning, and U.S. market access.

Non-destructive inspection systems: learn how to choose the right solution for welds, castings, and composite parts based on defects, materials, speed, and compliance needs.

EU EN 13485:2026 takes effect for CT algorithm validation, requiring two independent scenarios and a Notified Body report. See how CE-MDR rules may impact certification, exports, and delivery plans.

EU updates EN ISO 17025 for CT and X-Ray calibration: learn the new EU report requirements, uncertainty and traceability rules, key compliance deadlines, and what importers, distributors, and end users must do now.