Medical Device Usability and IEC 62366 2012 2366 is a course that covers topics such as:
- Design guidance in ANSI/AAMI HE75: 2009
- The steps to achieve compliance with IEC 62366: 2007
- Testable requirements for usability
- Usability techniques
- Development of a usability engineering process
- Management of the risk of use-error
- Document usability activities in the usability engineering file and HFE report (US)
Medical Device Usability and IEC 62366 2012 2366 brings together Project managers, Product design engineers, R&D personnel, Regulatory managers, Quality assurance managers, Risk management staff and Clinical trial managers.
