After several months of document reviewing, auditing and implementing, Delft is proud to announce their certification in EN ISO 13485:2012.
The EN ISO 13485:2012 Quality Management Standard for the medical devices industry represents the requirements for a comprehensive management system for the design, development, production and distribution of medical devices and related activities and services.
“With this quality management system Delft shows its commitment to quality to our (potential) clients & customers and all stakeholders in the company. The focus of Delft is to maintain and improve the quality management system, enabling us to provide products and services that meet administrative and regulatory requirements and also the needs of our customers”, said Guido Geerts, CEO of Delft Imaging Systems.
