ISO 10993-7:2026 resets EO residual compliance with new risk-based limits, parametric release, and tighter reassessment rules. Learn how it impacts batch release, imports, and sterile consumables.

UK MHRA Tightens EO Residue Rules for Sterile Imports: learn how the 2026 MHRA EO/ECH testing rule affects exporters, importers, shipment planning, and customs readiness.

CPHI & PMEC China 2026 highlights EO sterilization, Tyvek compliance, and ISO 11135:2014 validation. See why FDA, CE, and JP document readiness is becoming critical for buyers and exporters.

EO sterilization cycle validation: uncover key risks, control points, residual concerns, and packaging factors that impact compliance, product safety, and faster market release.