Controlled project pathway
Make quality requirements part of the engineering input
Inspection, cosmetic zones, traceability and change control need to be defined alongside the display stack rather than added after the first build.
Proof belongs next to the claim
For supplier qualification, project teams need more than broad statements. We organise the relevant process scope, inspection approach and available evidence around the assembly being reviewed.
A practical five-stage route
Topics to define
Visual and cosmetic
- Active and non-active cosmetic zones
- Particle, bubble and edge criteria
- Reference lighting and viewing conditions
Process and change
- Revision control and approved inputs
- Material or supplier changes
- Non-conformance and deviation handling
Traceability
- Batch and component identification
- Inspection records
- Packaging and shipment references
Testing responsibility
- Assembly-level inspection
- Touch and optical checks
- System validation by the responsible party
Supplier qualification. Quality teams can request the evidence relevant to their assessment. Availability and scope are confirmed before documents are shared, with confidential information handled through an agreed route.
Frequently asked questions
What inspection evidence can you provide?
Availability and scope are confirmed before documents are shared. Quality teams can request the evidence relevant to their specific assessment.
Is your cleanroom certified?
Certification documents and cleanroom scope will be published once formal company approval is complete. Please request current status directly for an active project.
How is traceability handled?
Through batch and component identification, inspection records and packaging or shipment references defined for the project.
NEED QUALIFICATION EVIDENCE?
Select “Supplier qualification” in the assessment form.
Describe the documents your process requires and we will confirm availability and scope.