Maverick Biomaterials is making solid progress towards probable attainment of ISO 13485 certification for Q1 2012.

A Notify body audit will be completed late in the year with Mavericks Quality Manager quietly confident of a successful outcome. This will be well received by clients soon to progress beyond animal trials for device’ utilising Mavericks custom sourced and produced materials. Some clients choose and approve Mavericks custom sourced produced materials for their manufacturing of Percutaneous Valves, among other devices.