AppSens is ISO 13485 certified

ISO 13485:2016 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. Such organizations can be involved in one or more stages of the life-cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities Safety and quality are essential in this business.


ISO 13485 covers all aspects of the production of products and services – from development and marketing to manufacturing, maintenance and related services such as sterilization, validation, testing and customer supportLorem ipsum dolor sit amet, consectetur adipiscing elit. Ut elit tellus, luctus nec ullamcorper mattis, pulvinar dapibus leo.