Get certified to ISO 13485:2016 in 6 steps!

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

Download this info-graphic and discover 6 simple steps that can help you get certified to ISO 13485:2016 then maintain and optimize your certification.

Get certified to ISO 13485 2016 in 6 steps