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.