The quality and origin of our raw materials, our production processes and the safety of our staff, clients and end users are out top priorities. Our operations go beyond simply complying with internationally recognized ISO 13485:2016 quality standard and CE marking. Through these activities, we ensure that we aren’t just ticking boxes, but we are doing the right things, as you demand and expect.
By meeting these standards, not only are we free to move and trade our products locally and internationally, including the European Economic Area, but we have committed to a quality management system that establishes and maintains the effectiveness of our processes, providing medical devices and related services that consistently meet customer and regulatory requirements. Ultimately, this gives you peace of mind that the traceability, design verification, materials validation, supplier controls, risk assessments, production control and delivery activities, for example, are an indispensable and integral part of our business.
What this means to you – Our first-class approach ensures consistently safe and high-quality products and service regardless of location.
TAKE ADVANTAGE OF WORKING WITH A COMPANY THAT TRULY LIVES BY ITS MOTTO – PERFORMANCE. BEYOND. EXPECTATIONS.