Inspection, documentation and accredited external laboratory coordination for medical nonwoven products.
We maintain product quality through documented inspection activities, process controls, batch traceability and testing coordination.
Where accredited laboratory evidence is required, tests are coordinated with qualified external laboratories and the related reports are included in the product documentation as applicable.
Request DocumentationMaterial, workmanship, packaging and labeling checks.
Traceability for product batches and release documentation.
Bioburden, sterility and related microbiological testing coordination.
Accredited laboratory reports when required by product or customer.
Typical controls and external testing support for sterile and non-sterile medical nonwoven products.
Our documentation package can support customer audits, export requests and medical device file requirements where applicable.
Send us the product name, target market and required documentation. Our team will guide you to the available product documents and testing support.
Contact Quality Team