ISO 13485 Quality management system
Are you a supplier to medical device manufacturers?
Do your customers demand the ISO 13485 quality standard?
Then you should deal with the implementation of this standard. The requirements of ISO 13485 are relevant for suppliers who supply medical device manufacturers with products or services. Through the application of ISO 13485, organizations are able to demonstrate their compliance with regulatory requirements, manage risks and ensure best practice to promote quality and safety and improve processes.
Interested in gaining certification?
Do not hesitate to arrange a meeting with us. On the basis of your information as communicated to us in strict confidence, we will draw up a personalised, clearly formulated offer for you. We offer our services worldwide with the exception of USA and Canada.