Integration Of Clinical & Analytical Instruments With MES For A Biopharma In-Process QC

Integration Of Clinical & Analytical Instruments With MES For A Biopharma In-Process QC

A global biopharmaceutical manufacturing organization faced growing inefficiencies in its in-process QC laboratories due to manual data transcription from analytical instruments into the Körber PAS-X Manufacturing Execution System. Offline data capture increased the risk of errors, delayed batch operations, and created compliance concerns. This case study highlights how integrating laboratory instruments with PAS-X MES using Logilab SDMS transformed QC workflows, improved data integrity, and enabled scalable, audit-ready operations.

Inside this case study, you’ll learn

• How Logilab SDMS eliminated manual data entry by automating real-time data capture from QC instruments
• How seamless integration between Logilab SDMS and PAS-X MES accelerated batch record updates and release timelines
• How metadata-driven workflows and REST APIs ensure traceable, tamper-proof data flow into MES
• How instrument auto-locking through Logilab SDMS improved equipment utilization and compliance control
• How a scalable middleware architecture supports regulatory requirements such as 21 CFR Part 11, ALCOA+, and GMP