Digitalise Biotech Production. Without the Complexity.
BatchLine streamlines Electronic Batch Records (EBR) and Manufacturing execution system (MES) workflows for biotechnology and vaccines manufacturing.
Managing, monitoring, and optimising complex production processes in real time, accelerating time to market,
and ensuring GxP compliance.
"BatchLine MES has transformed the way we manage manufacturing operations. By digitising our processes, our operators, supervisors, and QA teams can focus on activities that truly improve product quality, efficiency, and compliance.
We are very pleased with the results and the measurable improvements achieved."
Wasin Palabunma,
Production Manager, Global Biotech Products
With BatchLine MES
With Traditional MES
Traditional MES
Platforms are heavily customised to deeply integrate with process automation systems.
This makes them complex to implement and costly to maintain. Project scale and cost blow up Deep process automation integration Implementation period of 2+ years
- Project scale and cost blow up
- Deep process automation integration
- Implementation period of 2+ years
Built Different
Offers a highly efficient, GxP-ready solution for teams still reliant on paper and those struggling with full scale MES.
- Affordable pricing with quick time to value
- Configured to your process, not the other way
- Shorter implementation period
- Compliance with industry guidelines (ISPE) in response to regulatory changes
This Is What
“Better” Looks Like.
Measured outcomes from
manufacturers already running on ![]()
%
Reducing in review time
%
Remarkable reduction in product release time
10 -
%
Gain in operator efficiency
Key benefits of BatchLine MES in Biotechnology

Electronic Batch Records (EBR)
Go paperless, accelerate batch release through review by exception, reduce batch cycle times, and optimize production efficiency.

Manufacturing Execution System (MES)
Connect and control manufacturing operations in real time to enhancing traceability, and shop floor visibility.

Regulatory Compliance
Designed for FDA/GMP compliance with 21 CFR Part 11 compliant e-signatures, data integrity, and digital audit trails built in.

Rapid Deployment
Achieve go live within months using robust, lean, out of the box functionalities.
Core capabilities
1
Batch Management
Coordinates production from Batch creation to Final product release and approval.
2
Process Control
Monitors and controls critical process parameters (CPP) and critical quality attributes (CQA) in real time, flagging out of specification conditions before they impact the batch.