Need for this

In regulated industries like pharmaceuticals, stage labelling is critical for ensuring product traceability, reducing errors, and complying with standards such as USFDA and EU GMP. Stage labelling helps manufacturers track materials, ongoing manufacturing status, and finished goods as they move through the various phases of production. Without stage labelling, there is a higher risk of mislabelling, batch confusion, and compliance violations, particularly during audits by regulatory bodies like the USFDA or EU regulatory authorities.
Real-time Production Tracking
Error Reduction
Audit-Readiness
Customisable Labels
Process Diagram
Quarantine Labels
Under test labels
Approved/Rejected labels
Dispensed material status label
Stage Label with Process XE®
Process XE® Stage Labelling integrates seamlessly with the MES/ERP. Here’s how Process XE® is leveraging the stage labelling feature:
Automated Label Updates: As batches move through predefined production stages, their labels are automatically updated based on triggers within the system, reducing manual intervention.
Integration with Quality Modules: The stage labelling system can be integrated to quality management features ensuring that production status reflects any issues encountered during quality checks.
Customizable Workflows: The solution allows users to define custom production workflows, with stage labels that match the specific needs of their manufacturing processes.
Data Logging and Reporting: All label updates are updated, providing a detailed record that can be accessed for audits, compliance reporting, and process optimization.