Quality inspection, predictive maintenance, line operations, and documentation — designed for environments where the system has to keep working when the network goes down.
Visual and document-based inspection augmentation for incoming, in-process, and outgoing quality.
Anomaly detection on equipment telemetry with operator-grade alerting and root-cause workflows.
Shift summarization, exception reporting, and hand-off documentation that survives the operator turning off.
Search and refresh of standard work documents, training materials, and corrective-action records.
Supplier document review, change-order analysis, and obsolescence tracking.
Incident write-up assistance, near-miss synthesis, and regulatory submission drafting.
Plants where IT and OT networks are intentionally separated and where the system has to work when neither cloud nor mobile data are available. The architectures we ship reflect that.
ISO 9001, IATF 16949, and industry-specific quality systems that constrain what counts as a valid record.
Regulated environments such as medical device manufacturing (21 CFR Part 820, EU MDR) and food/pharma (cGMP) where every system change is a documented change.