Fourteen years of ISO 13485 certification
Maverick’s long-standing certification reflects an ongoing commitment to controlled processes, traceability and consistent quality.
Maverick Biomaterials first achieved ISO 13485 certification in 2012. Fourteen years later, that quality management system remains central to how materials are sourced, processed, documented and supplied.
Maverick is currently certified to ISO 13485:2016 for the manufacture of bovine and porcine serous membranes in accordance with EN ISO 22442-2:2020.
For customers, certification is more than a document. It provides confidence that materials are handled through controlled procedures by trained personnel, with records that support traceability, review and ongoing supplier qualification.
Maverick also holds ISO 9001 certification for the supply of biological materials to the medical device and pharmaceutical industries across its Australian and New Zealand operations.
Supporting documentation can include certificates of analysis, BSE/TSE risk statements, origin and traceability records, material specifications and other information required for supplier review, audits and regulatory submissions.
Quality is not treated as a final check. It is built into the process from source selection through preparation, packaging and delivery.
