Incoming Raw Material Inspection
Raw material selection is driven by our suppliers’ production processes to ensure stable, reproducible quality across all incoming products. Upon arrival, each batch undergoes a rigorous conformity inspection against defined specifications, guaranteeing the stability, reliability, and performance of our formulations.
In-Process Control
Before packaging, samples are taken and subjected to two complementary control protocols
Analytical Control
An autonomous, software‑driven method — aligned with pharmaceutical industry standards — enabling titration and chromatography‑based measurement of:
- Water content, Blowing agent content
- Hydroxyl value and basicity index (Polyols)
- NCO content (Isocyanates)
Physico-chemical Control
A pragmatic, complementary approach designed to validate analytical results. For each Polyol/Isocyanate pair, the following parameters are checked:
- Viscosity
Reactivity (cream time, string time, end of rise) - Free foam density.
- Molding Control
Archiving
During packaging, samples from each production batch are collected and archived for 12 months, ensuring full traceability and long‑term quality monitoring.
All batch production sheets are digitally archived. For each component, they record the reference, supplier batch number, introduced weight, and the complete set of production parameters: – temperature, – introduction speed, – mixer type, – agitation time, – tank number.
This archiving protocol guarantees complete process transparency and supports reliable quality audits over time.
All batch production sheets are digitally archived. For each component, they record the reference, supplier batch number, introduced weight, and the complete set of production parameters: – temperature, – introduction speed, – mixer type, – agitation time, – tank number.
This archiving protocol guarantees complete process transparency and supports reliable quality audits over time.
