ISO 13485:2016 Medical Device Training (Live, Online, In-House)
The ISO 13485:2016 standards specify requirements for a quality management system where an organization needs to demonstrate its ability to provide medical
devices that meet customer and regulatory requirements.
Major regulatory bodies worldwide require certification to ISO 13485 to allow organizations to market their products and services.
Our courses are offered both open public classes and in-house. To maximize the effectiveness of the sessions, both options include practical examples, templates, and simulations. Classes are conducted by experts in the field. Free after-class support by email.