Processing built around your product.

Prepared to the point your specification defines, which differs by material. For tissue, that might be selection, cleaning and cutting to dimension. For collagen, it might be extraction, purification and supply at a defined concentration and format.

Five stages: source, select, process, assure and deliver. At source, that means export-registered facilities, government veterinary inspection before and after slaughter, age verification and lot or batch traceability, with RFID available for bovine material. Then documented selection against your specification, controlled preparation, a certified quality system and validated temperature-controlled delivery.

No supplier can remove it, so we narrow it where it starts. Species, age, tissue and handling are set in the specification, and every step is documented, so your team can see what changed when something does.

No. Cleanroom processing is applied where the product requires it. Our ISO 7 cleanroom is in operation, and an ISO 5 expansion is under way.

Material characterisation and biological safety testing support each product. Tell us the tests your quality team expects and we’ll confirm what is available and how results are reported.

Yes. We plan for it from the start, so the material you qualify in development is the material you can order at commercial scale. Shipments range from 200 g samples to full container loads.

Yes. Bring a specification and we’ll build to it, or bring the problem and we’ll work through material options with your R&D, quality and regulatory teams.