Serialization, aggregation and line integration for GS1 DataMatrix delivered and run by one accountable team, from code to TTAC report. The window to choose a vendor and implement is 2026.
Indonesia is moving pharmaceutical traceability from basic identification to full authentication. Prescription drugs and biologics must carry unique GS1 DataMatrix codes with TTAC lifecycle reporting by December 2027. The window to select a vendor and complete implementation is 2026 — not later.
Indonesia is moving pharmaceutical traceability from basic identification to full authentication. Prescription drugs and biologics must carry unique GS1 DataMatrix codes with TTAC lifecycle…
Read articleMost projects split that across a software vendor and separate integrators. We deliver and own the whole chain.
Five layers we supply and deploy as a single project, configured for Indonesian regulation.
Code generation and management, event model, reconciliation, reporting, integrations.
Indonesian rules, statuses, formats and the workflow for submitting data to TTAC.
Printers, vision, reject units, aggregation stations and operator workstations.
Line assessment, design, integration, FAT/SAT, validation and go-live.
Support, integration monitoring, regulatory updates, incident handling.
This section follows the newer structure while keeping the previous TraceWay navigation and footer patterns.
We supply the platform, the country pack, the hardware layer and the implementation scope as one accountable program.
Serialization logic, event model, reconciliation and regulatory reporting.
Printers, vision, reject units, aggregation stations and operator stations.
ERP, PLC, packaging hierarchy and brownfield adaptation with minimal disruption.
Line audit and SKU review.
Country pack and hardware integration.
Factory testing and pilot run.
Go-live, TTAC reporting and support.
The implementation model is aligned to BPOM TTAC requirements and operational lifecycle reporting.
TraceWay is the engineering arm of Original Group, founded in 2006. Since 2015 we have delivered mandatory pharmaceutical serialization at 20+ large pharma manufacturers, inside one of the world's most demanding national track-and-trace systems.
We build both the software and the hardware — from device firmware (L1) to national-system and ERP connectors (L3–L4). One supplier owns the code, the line and the reporting, instead of a chain of subcontractors.
Experience reaches well beyond pharma. We fit production lines with industrial automation, retrofit running lines and support third-party equipment — decisive for brownfield projects where the plant cannot stop.
Timing depends on line complexity, number of SKUs and aggregation design. A guide for a single line.
Line audit, SKU review, packaging hierarchy and data-flow mapping.
Platform setup, country pack, hardware and ERP integration.
Factory tests, pilot run on the line, operator training.
Production launch, stabilization, TTAC reporting.
Message Yunita directly on WhatsApp, or send the form — we'll map your line, SKUs and timeline to a clear compliance plan.
For pharmaceutical manufacturers, CMOs, importers and marketing authorization holders in Indonesia.