Several monitoring and control activities are arranged in the production chain, starting from the incoming until the final release. Accurate visual and dimensional inspections, functional and resistance testings are performed during all production phases.

To obtain these results, all business processes are designed to ensure compliance with regulatory requirements and regulatory reference. All companies in the group apply and keep updated the quality management system as certified by ISO 13485 / ISO 9001, as well as their CE certification for different families of medical devices.