ISO 13485:2016 Quality system certification
4 months ago
ISO 13485 is the standard created to ensures the consistent design, development, production, installation and delivery through to disposal of medical devices that are safe for their intended purpose. This standard allows to reduce safety and legal risks while creating more economical work environments. As an internationally recognized standard of quality and safety for medical device manufacturing, having ISO 13485 certification helps be recognized as more reputable, trustworthy partners.