Operational systems for pharma & plastics-packaging manufacturers.
Traceability, batch-level costing, and audit-ready records — built for the most compliance-heavy manufacturing sectors in Egypt.
You can't produce a full batch record on demand for an audit.
Pharma manufacturers face hard compliance requirements from the Egyptian EDA and GMP-aligned practices. Plastics-packaging manufacturers serving pharma or food clients inherit similar traceability demands. In both cases, raw material lot traceability has gaps, QC data lives in separate paper forms per shift, and producing a full batch record for an auditor means days of assembly, not a single query.
Batch record assembly
Can't produce a full batch record on demand — audits mean days of paper assembly, not a single query.
Raw material lot gaps
Traceability breaks between the incoming lot and the finished product — fine until it isn't.
Disconnected QC data
Quality checks live in separate paper forms per shift — not linked to the batch, the operator, or the stage.
Enter through the module that hurts most — expand from there.
Quality Management & Traceability
Financial & Ops Backend
Manufacturing Execution System
Compliance frameworks: GMP-aligned batch record practices, Egyptian EDA documentation expectations.
Important: Trinova builds the system that supports compliance documentation — we do not certify GMP compliance itself.
Tell us how your production line actually runs.
We'll map it against these modules and tell you exactly where to start.