Supplier qualification
Ingredients, materials and components are procured only from suppliers that hold the relevant certifications and are able to support an audit. Incoming materials are accepted against a written specification.
Certified manufacturing
Skincare is produced under good manufacturing practice by contract manufacturers. Medical devices are manufactured in facilities certified to ISO 13485.
Regulatory approval
The nasal splint range is approved by the United States Food and Drug Administration, and the supporting documentation is available to institutional customers.
Product documentation
Each product is supported by specifications, certificates and, for medical devices, instructions for use, issued to hospitals, distributors and stockists as required.
Batch traceability
Every pack carries a batch number traceable to its production and quality records, so that any question concerning a specific pack can be answered.
Tender support
We prepare the documentation required by hospital purchase committees, tender authorities and distributors, including certificates, specifications and product literature.