Are you a medical device manufacturer?
According to the new Regulation (EC) 2017/745 on medical devices (MDR), medical device manufacturers must demonstrate to notified bodies that all critical suppliers conform with the ISO 13485 standard covering quality management systems.
As a critical supplier of high-quality toxicological services, SAXOCON is ISO 13485 certified, which means that there will be one less thing to worry about at the next audit.
Having confidence in your suppliers allows you to focus on your manufacturing processes and get your products approved and ready for market as quickly as possible.
Find out how we can help you here.