of pharma supply leaders cite “lack of end-to-end visibility” as their biggest bottleneck
is lost annually across pharma due to inefficient manufacturing and supply planning
Real-time production tracking with contextual QA annotations and regulatory traceability
Unified dashboard across production, testing, and environmental monitoring
Adaptive algorithms using sales, clinical trials, and market data to drive manufacturing plans
Instant alerts, root-cause mapping, and traceable remediation workflows
Temperature and integrity monitoring across storage and transit — with alert thresholds
Dynamic risk models using delivery trends, compliance history, and geopolitical data
Built-in FDA, EMA, and WHO reporting frameworks, including CFR Part 11 compliance
Controlled access and audit logs for CMO, 3PL, QA, and internal ops teams
Unified data flows from lab to line to logistics — enabling full-lifecycle traceability and faster release cycles
Predictive analytics tuned to your product class, market dynamics, and regional compliance
Build or bolt-on modules for batch monitoring, QA approvals, deviation capture, or regulatory reporting
GxP-aligned, CFR Part 11-ready, and validated systems approach with automated audit trails
Native connectors to your ERP, QA, and shop floor systems without ripping existing infrastructure
Visualize cycle time bottlenecks, material waste trends, equipment reliability, and supplier disruptions in one place
Let’s map your current manufacturing and supply network against global best practices.
You’ll receive:
We go beyond maintaining operations—we empower businesses with data, insights, and best practices to stay ahead in an ever-evolving digital landscape.
