Quality Management System
Audits and ISO/QS built on real evidence — not disconnected documents
In IVR 5.0 AI, the Management System is no longer a document repository. It becomes a traceable evidence system, connected to product, process, dimensional characteristics and measurement history — objectively and consistently.
What the DMS delivers
- Product, process and system audits with traceable evidence
- ISO / QS / IATF linked to real execution
- Complete history by part, process and time window
- Direct integration with QIF, MSA and SPC
- Less interpretation, more objective data reading
Management System as an evidence system
In IVR 5.0 AI, the Management System is not treated as a collection of files. It operates as a structured evidence system, where every requirement is connected to real process execution.
Standards, procedures and records stop living in isolation and become linked to products, operations, dimensional characteristics, measurement resources and historical results.
Evidence is generated by execution — not by the audit.
Product, Process and System Audits
IVR 5.0 AI supports product, process and system audits directly connected to real manufacturing and measurement data.
Each audit is associated with:
- Product, batch and revision
- Process and operation
- Dimensional characteristics (QIF)
- Measured results and historical data
The focus shifts from “filling checklists” to reading objective evidence.
ISO, QS and IATF connected to process reality
In IVR, requirements from standards such as ISO, QS and IATF are mapped directly to processes, measurements and results.
Documentation is no longer only descriptive — it becomes demonstrable, with traceability between requirement, execution and dimensional evidence.
Compliance stops being interpretation and becomes demonstration.
Integration with QIF, MSA and SPC
The IVR 5.0 AI Management System is built on the same foundation that supports Quality:
- QIF as the structure for characteristics and requirements
- MSA to validate measurement system reliability
- SPC for continuous statistical process control
This ensures audits and analyses are always performed on consistent, comparable and technically valid data.
Audits stop being events and become a continuous process
With structured and traceable data, audits stop being isolated events and become part of the normal management cycle.
There is no need to “prepare the factory for an audit”: evidence is already present in the system, ready for analysis.
A mature organization does not prepare for audits. It simply operates with reliable data.