Medical Device Usability and IEC 62366 2012

  • 14-15 Nov 2012
  • Hotel Sofitel London Gatwick, Crawley, United Kingdom

Description

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.

Past Events

Important

Please, check "Medical Device Usability and IEC 62366" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device

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