Netorus, Inc. Information

Netorus is a cloud-based ERP software system with a focus on companies who have to comply with FDA regulations We offer a complete integration of the QC/LIMS, MES, Warehouse, Sales/Purchase, Accounting, and HR. FDA audited (USFDA, CFDA, EMA) and approved to detail the whole flow of electronic batch production and quality records and corresponding cGMP validation documentation. Typically, legacy LIMS systems are limited to save data or charts from detecting instruments and input Test Reports manually. The Netorus™ system integrates LIMS with MRP and Production. It automatically acquires data from laboratory instruments and generates Test Records and Reports. You can also use barcodes for lab materials and link it together with the warehouse and production to create an organic network. It includes a whole QA/QC process workflow. By setting up the Netorus™ PAT, we ensure quality control of every stage of the production process, including pre-release inspections of raw materials and packaging materials, production process control, quality test, intermediate inspection, finished production inspections, until the final product audit and release. You can have real-time control of all production process, parameter analysis and release. Based on research of the TOP 14 pharmaceutical companies in the world, Netorus system has been developed in accordance with cGMP CSV (Computer System Validation) criteria: 21 CFR PART 210, 21 CFR PART 211 21 CFR PART 11, Q7, Q8, Q9, Q10, GAMP 5.  Netorus™ software complies with all cGMP regulations