Medical Device Usability and IEC 62366 2012

Key Topics

• 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)

Who should Attend

Project managers, Product design engineers, R&D personnel, Regulatory managers, Quality assurance managers, Risk management staff and Clinical trial managers.