Bathroom pods are manufactured under ISO 9001 certified quality management procedures.
Quality control includes:
- Defined inspection stages during production
- Dimensional verification prior to dispatch
- Pre-packaging photographic documentation
- Structured non-conformity reporting
Additional management systems and certifications are implemented in line with project and market requirements.
Quality documentation is aligned with project-specific QA systems and can be integrated into digital information management platforms to support traceability and Golden Thread requirements.
Other FAQs
How are Testing & Inspection (T&I) stages structured?
Testing and inspection are carried out in two stages: factory verification before dispatch and on-site inspection and functional testing after installation and service connection. All inspection records are documented and can be integrated into the project’s digital QA system to ensure full traceability and accountability.
How are damages or non-conformities managed?
Damages or non-conformities are managed through a three-stage QA process including factory inspection, 360° photographic documentation before dispatch, and joint on-site delivery inspection. Any issues are recorded and resolved through defined rectification procedures aligned with project quality systems.
How is documentation managed to support the Golden Thread of information?
Documentation is managed across design, manufacture, and inspection stages, including drawings, QA records, testing results, material traceability, and as-built information. These records can be integrated into digital systems to support the Golden Thread of information.