Manufacturing
Manufacturing ERP & MRP Software
Connect MRP, production scheduling, shop-floor execution, quality and production costing in Tellency AI-native manufacturing ERP. Explore the complete workflow.
Tellency manufacturing
Keep quality decisions connected to the production record.
Inspect against a specification, control the lot’s status and follow a nonconformance through its resolution. Tellency brings quality records into the same manufacturing workflow as materials, production and finished goods.
By the Tellency team · Reviewed
Define what an acceptable result looks like.
Quality specifications and inspection plans provide the checks behind the inspection. Configure the measurements and limits that matter to the item and process.
- Use inspection plans and required test results in production workflows.
- Record numeric or other supported result types against their specification.
- Review sampling-plan requirements for the intended inspection scenario.
Control receiving and production quality.
Receiving inspections and production checks connect quality outcomes to lot availability. A rejected or held lot must remain visible to the team that would otherwise consume or ship it.
- Review quarantine, acceptance, rejection and release workflows.
- Connect failed checks to nonconformance records and disposition decisions.
- Trace material lots into production output and investigate affected orders.
Move beyond recording a defect.
Nonconformance, rework, scrap and corrective actions help the team follow a quality problem through to an accountable decision. CAPA records include owners, due dates and an effectiveness review.
- Assign corrective or preventive actions and record the root-cause investigation.
- Review effectiveness before closure, with separation of duties at the closure step.
- Use supplier corrective-action workflows and supplier-quality views for purchasing discussions.
Review process variation and supplier performance.
Statistical process control views help a quality team investigate numeric measurements over time. Control charts and capability calculations should be evaluated using a representative data set and an agreed baseline.
- Review supported X-bar/R and individuals/moving-range charts.
- Inspect control limits, flagged rules and Cp/Cpk outputs against the specification.
- Compare received, inspected and rejected supplier lots alongside open corrective actions.
Demonstrate a failed inspection from end to end.
A quality demo should include the exception, not just a passing measurement. Bring your own item, limits and sample data so the quality and operations teams can agree the outcome.
- Reject an incoming lot and inspect its inventory availability.
- Fail an in-process check and review the order’s hold and disposition path.
- Trace a finished lot back to inputs, then close the associated corrective action with the appropriate reviewer.
Before the demo
Questions worth asking.
Does Tellency replace a specialist quality-management system?
It includes connected manufacturing quality workflows. Compare your document control, calibration, validation, regulatory and supplier requirements individually before deciding the complete scope.
Do quality features establish ISO, GMP or FDA compliance?
No certification is implied by these features. Compliance depends on the configured system, validated processes, organisational controls and applicable requirements.
What is the benefit of connected lot traceability?
It lets the team investigate which input lots contributed to production output and follow quality decisions alongside the affected inventory and orders. Validate the depth and reports your operation needs.