Medical software Chronicle™

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Chronicle™ automation software provides a unified digital platform to monitor facility manufacturing operations and supply chain logistics Overview Chronicle™ automation software connects Cytiva and third-party instruments. From process development through commercial GMP manufacturing, pre-GMP and GMP plans have been designed to support you. Digitize records to reinforce GMP compliance and improve sample security with Chronicle™ automation software. eSOPs manage deviations, promote adherence, and provide training. Chronicle™ automation software has been independently audited against GAMP5, 21 CFR Part 11 and EU Annex 11. Plus, Chronicle™ automation software can support two different environments—the cell therapy and the biologics environment—to better fit your specific needs. Implement electronic batch records that comply with regulatory requirements, reviewing deviations efficiently with automated workflows to support release by exception. Optimize operators’ time and help reduce mistakes with electronic standard operating procedures (eSOPs). Schedule procedures by reserving instruments and checking availability on a built-in calendar. Trace all your products and consumables with stock control, barcode label printing, and scanning. Obtain a Certificate of Analysis (COA) automatically for many Cytiva cell therapy reagents and plastics. Connect third-party instruments to upload and visualize instruments data. Chronicle™ automation software provides a unified digital platform to monitor your facility manufacturing operations and supply chain logistics. Plus, electronic batch records will trace every manufacturing step.