Deviation and quality management
Orchestratequality processes
Deviations, corrective actions, complaints, change control and approval workflows: CIPA drives deviation handling through to closure, then turns it into lasting gains.
Classified deviations
Tracked CAPA
Versioned workflows
Quality use cases
One flow, from deviation to closure
Deviations, actions, complaints, changes and approvals follow on from each other in the same tool, with no retyping and nothing lost.
01Quality
Deviations & non-conformities
Every deviation gets a reference and keeps its origin: audit, production check or shop-floor event. It is tied to an area and to a problem from the classification.
Before CIPA
- Deviations reported verbally or by email
- The origin of the deviation gets lost
- Causes described differently every time
- No consolidated view of open deviations
With CIPA
- Unique reference for each deviation
- Origin traced: audit, production, event
- Area and problem category
- Status tracked: created, in progress, closed
Deviations & non-conformitiesPreview
CIPA · Quality
Deviations & non-conformities
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- Unique reference for each deviation
- Origin traced: audit, production, event
- Area and problem category
- Status tracked: created, in progress, closed
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Schematic preview of the CIPA interface.
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The three pillars of CIPA
Structure shop-floor data, orchestrate quality processes, drive performance: one platform.
Let’s see what CIPA can orchestrate for you
A 45-minute demo focused on your processes, your challenges and your industry.