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The Cetec ERP all-in-one SaaS model helps in the implementation of FDA and CFR Part 11 measures by streamlining and automating quality tracking and error-proofing material traceability for medical devices and life sciences in the cloud, from manufacturing to inventory, document revision control, NCRs, CAPAs, and inspection management.
The Cetec ERP inventory management platform offers intelligent, system-dictated processes to ensure complete traceability, satisfying the need to trace back through the supply chain all the parts and components in an end product to source lot code. The FIFO inventory methodology with bin level routing guides warehouse users to parts and barcodes, with iPad support, to facilitate the put-away and pick-parts processes. The pick-parts process simultaneously relieves inventory and captures date-code/lot-code data for each order, achieving total traceability for customer purchase orders.
With Cetec ERP softare, lot/serial data collection for manufactured components for auditing, recall, and customer deliverables takes less than an hr, and often is instant. Every click, transaction, and action in Cetec ERP is 100% auditable and traceable, and ties back to an electronic signature, with required documents like CoCs or CoAs attached for easy access.
The software streamlines traceability requirements of certification bodies like ISO 9001, ISO 13485, UL, and the FDA, and enables businesses to compete effectively in regulated markets with strict customer and certification requirements. The system features built-in automated quality tools to meet requirements more efficiently and helps companies stay competitive.
All Cetec ERP modules, support, maintenance, and upgrades are included in a monthly subscription, with three comprehensive service plans to choose from.
