Operational control of your homologation
Manage test scope, test readiness and dates across your target markets.
We develop AI-supported workflows for operational homologation: from agreed test scope and test preparation to evidence status for submission. So your team can see what is missing, who needs to act and which date is at risk.
A new type approval, an extension or an additional target market: we develop the workflows with your specialist teams. Tests, prerequisites, responsibilities and approvals should share a common basis for each approval case.
Target markets and variants are defined. Product data and requirements from the regulatory feed need to become an agreed test scope.
A proposal for tests and evidence by market and variant, with source revisions, assumptions and outstanding clarifications.
Expert approval: The responsible people confirm the scope following agreement with specialist teams and, where needed, the technical service or authority.
A test date is agreed. The vehicle, configuration, modifications and test request need to be ready in time.
Open prerequisites for each test, responsible people, outstanding responses and required readiness dates.
Expert approval: The responsible people confirm the configuration and test readiness. You can see which response or approval is still missing.
A new software revision, product configuration or requirement affects an ongoing programme. The test scope has already been approved.
A proposal identifying affected tests, evidence and modifications, with source references and consequences for dates.
Expert approval: The responsible specialists decide whether repeat testing and changes to the plan are needed.
Submission is approaching. Test reports and other evidence need to match the approved product configuration.
The status of the required evidence: available, reviewed or approved, with the associated product configuration and outstanding queries.
Expert approval: The responsible people approve the handover. Document contents and submission remain in your designated systems.
Changes in an ongoing programme
The fictional XR 01 programme illustrates how a change affects testing, the schedule and the next task.
Software revision 1.1 is announced. Which ongoing approval cases are affected?
The link to the test, reasoning and open questions are ready for expert assessment.
The emissions test needs the new revision. The EU buffer until market launch falls from four weeks to three.
After expert approval: update the target revision and modifications, assign tasks and confirm test readiness again.
Fictional programme with synthetic data. The AI assessment is simulated.
Three markets, shared test vehicles, one market launch.
View episode 1
From a software revision to expert assessment and schedule impact.
View episode 2Planning across programmes and target markets
With XORPunkt, we are developing a shared basis for homologation management. Which test needs which vehicle? What shifts when something changes? And how much time remains until market launch?
Product configuration, test vehicle, modifications and approvals belong with the relevant test. Open prerequisites need to be visible before the test date.
Sequence, lead times and resources determine dates. Planning needs to show which approval cases consume the buffer for each target market.
Source, data revision, reasoning and approval remain traceable within the case. Your team can see the basis for each decision.
A rule-based product preview with synthetic data. No live AI or connected customer systems. Interface in German.
Together, we select a specific case: an upcoming test, a change or a handover for submission. Existing exports and documents may be enough for the first comparison.
Which date is approaching? What needs to be ready by then? We record the people involved, sources, approvals and current coordination effort.
Using agreed cases, your specialists compare completeness, technical quality, handling time and rework. Review and corrections count towards the total effort.
Once value is demonstrated, we agree integrations, responsibilities and operation. Your existing specialist systems and approval routes provide the framework.
Within your system landscape
Market plans and product data come from your sources. Requirements remain in the regulatory feed, documents in the document system and submission in its designated solution. Between them, we connect approval cases, test vehicles, dates and approvals.
For technology and delivery partners: XOR Digital adds operational homologation management to your customer offering and supports implementation and operation. XORPunkt is the reusable product core under development.
Let’s discuss your programme, the outstanding prerequisites and the workflow that takes most of your team’s time.