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Quality Management Module

Under control at every stage, from receiving to shipping.

The Quality module unifies inspection plans, control records and nonconformity management on one data model. It makes incoming, in-process and final control traceable and links corrective actions to root cause.

Illustrative screenKalite YönetimiKontrol PlanıÖlçü toleransı (±0,1mm)UygunYüzey pürüzlülüğüUygunSertlik testi (HRC)UygunsuzKaplama kalınlığıBekliyorGörsel muayeneUygunUygunluk%804/5 madde1 uygunsuzluk · düzeltici işlem açıkParti #A-2041

Control plans and nonconformance tracking.

Overview

What it does

A traceable single flow instead of scattered control forms and delayed feedback. The Quality module brings inspection onto the same data as production and stock; nonconformities surface instantly and corrective actions link to root cause.

Scope

Sub-categories of Quality Management

Each sub-category manages a part of this process — all on the same data.

Quality Management

Manage quality plans, nonconformities and corrective/preventive actions in one place.

Quality plansNonconformity managementCAPARoot cause analysis

Quality Control

Record incoming, in-process and final inspections against criteria and produce decisions.

Incoming inspectionIn-process inspectionFinal inspectionMeasurement & sampling

Roles

Who is it for?

The same data, a different view for each role.

Quality Engineer

Define inspection plans, analyze nonconformities and launch corrective actions.

Quality Inspector

Record measurement and sampling results on the floor; make accept/reject decisions fast.

Quality Manager

Track nonconformity trends and CAPA closure live; compare supplier quality.

Connection

How quality runs across the process

Quality is not a separate step; it lives inside the flow. From incoming to final control every stage is recorded and each nonconformity links to root cause.

Incoming Control

Received material is inspected.

In-process Control

Measured during production.

Final Control

Approved before shipping.

Nonconformity & CAPA

Action opened on root cause.

Capabilities

Key features

Incoming, in-process and final inspection plans
Measurement, sampling and acceptance criteria
Nonconformity and quarantine management
Corrective/preventive action (CAPA)
Supplier quality scorecard
Traceability and audit trail

Compliance

Compliant with local regulation

Muayene PlanıDÖF / CAPAİzlenebilirlikSertifika YönetimiKVKK

Enterprise architecture that supports common quality management standards through inspection plans, traceability and corrective-action processes.

Quality Management with Sonia AI

Describe it, Sonia prepares it.

Describe your quality tasks in natural language; Sonia analyzes the records, prepares the report and brings it for your approval — the final decision is always yours.

Group this month’s top nonconforming products by root cause
List overdue open CAPA records
Compare accept/reject rates by supplier

Frequently Asked Questions

Which control stages does it cover?

It covers incoming (goods receipt), in-process (during production) and final control; each stage can have its own plan, criteria and sampling rule.

Are nonconformities linked to root cause?

Yes. Each nonconformity links to root cause analysis and a corrective/preventive action; closure status and recurrence are tracked.

Does it support compliance with quality standards?

Through inspection plans, traceability and CAPA processes it supports the records and audit trail required by common quality management standards.

See AinosERP on your own processes

Let’s schedule a short demo and walk through the screens and Sonia AI using your flows.