Interactive ISO 13485:2016 infographic for medical device manufacturers

Get your company certified to ISO 13485:2016 in 7 steps

ISO 13485:2016 (Medical Devices – Quality Management Systems – Requirements for Regulatory Purposes) was officially published by the International Organization for Standardization (ISO) on 1 March 2016, and is the international standard that defines quality management system (QMS) requirements for medical device manufacturers and suppliers. 

Check out this interactive infographic to see how your medical device company can get certified to ISO 13485:2016 in 7 steps.