Up to 0%
First-pass yield
Solutions by function
Quality
Control quality from supplier material to customer delivery.
Quality is not only a final inspection. It starts with the right material, the correct certificate, an approved process and live production evidence. Aivhy connects supplier information, machine parameters, operator checks, Industrial Vision, laboratory results and quality workflows, so teams can act earlier and release with confidence.
Up to 0%
Lower scrap rate
Up to 0%
Fewer customer rejections
Reference outcomes from individual World Economic Forum Global Lighthouse sites. Results depend on the site, process and scope.
Connected quality
Where quality needs control
Explore the eight connected stages. Each point shows where evidence is missing, what Aivhy connects and what changes in practice. They are a selection from many practical ways Aivhy can improve your quality process. Use the button below to discuss the priorities in your operation.
Aivhy connects the information already available in ERP, MES, QMS, LIMS, supplier certificates, machines, measuring equipment and quality records. BOS provides the shared quality record. BAS guides inspections, approvals, actions and documentation where work still relies on email, spreadsheets or paper.
Quality priorities
The issues that turn into hidden quality loss
A deviation without a clear affected-product scope
When process conditions change, quality needs to know what was made during that exact window. Aivhy connects the deviation to the relevant product, batch, serial number or defined production quantity, so action stays proportionate and traceable.
Quarantine that needs a decision
A blocked item needs evidence, ownership and a clear next step. Aivhy guides the decision to release, rework, return, reuse, scrap or destroy it, preventing quarantined material from becoming forgotten inventory.
Corrective actions that do not reach the process
A complaint or non-conformance should improve the next production run, not only close a ticket. Aivhy links containment, root cause, CAPA and effectiveness evidence back to the relevant control plan and work instruction.
Operational result
What changes in practice
Inspect by risk, not by habit. Supplier evidence, process conditions, vision results and laboratory tests show where additional inspection is actually needed.
Faster containment and release. The issue, affected product, owner and next action are clear while production is still running.
Less scrap, rework and waste. Deviations are identified closer to their source, before they spread through the process.
A smaller recall scope. Product genealogy identifies the exact supplier lot, process window and shipment that need action.
The operation in practice
From first sample to final release
Quality works when every check, measurement, deviation and release is linked to the product and the responsible action.
Inspection at the point of work
Measurements, photos and operator checks become evidence in the product quality record.
Inspection and release
Test results and approvals reach Quality in time for a controlled release decision.
Start where quality risk begins
You do not need to replace the systems already in place. Start with one quality issue — incoming material, in-process control, inspection, non-conformance, release or traceability — and connect the missing workflow around it.