Automated molecular testing systems help labs cut turnaround time by reducing manual steps, improving workflow consistency, and speeding reporting. Discover how to boost efficiency.
EU CE rule adds tamper-evident RFID to IVD kits from Oct 1, 2026. Learn what MDCG 2026-12 means for packaging lines, UDI connectivity, traceability, and EU export compliance.
FDA UDI export log rule reshapes IVD shipments by requiring batch-level electronic traceability for U.S.-bound exports. Learn how it impacts clearance, inventory, and compliance.
Laboratory diagnostic systems for hospitals: avoid costly selection mistakes by comparing workflow fit, software integration, service support, and total operating cost before you buy.
FDA Tightens IVD Export Traceability for China Suppliers: learn how new batch-level UDI, real-time upload, and CDRH Gateway rules may impact customs, distributors, and lab procurement.
FDA Tightens UDI Traceability for IVD Exports: learn how real-time batch-level UDI and FDA Gateway rules impact compliance, customs clearance, distributors, and U.S. market access.
FDA Tightens UDI Batch Rules for IVD Exports: learn how new FDA batch-level UDI and GUDID requirements affect customs, inventory traceability, and U.S. market access for IVD exporters.
Hospital capacity planning laboratory teams can prevent bottlenecks with the right metrics. Learn how utilization, TAT, staffing, and downtime data drive smarter lab decisions.
FDA Tightens IVD Export Traceability for China Suppliers: learn how the new FDA CDRH Gateway batch-data rule affects customs clearance, importer acceptance, and U.S. market access.
FDA tightens IVD traceability rules for China suppliers: learn how the new FDA-recognized RTS requirement may affect customs clearance, delivery timelines, and U.S. market access.