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About This Item

 

Full Description

Specifies a process for a manufacturer to analyse, specify, design, verify and validate usability, as it relates to safety of a medical device. This usability engineering process assesses and mitigates risks caused by usability problems associated with correct use and use errors, i.e. normal use. It can be used to identify but does not assess or mitigate risks associated with abnormal use. If the usability engineering process detailed in this International Standard has been complied with and the acceptance criteria documented in the usability validation plan have been met, then the residual risks, as defined in ISO 14971, associated with usability of a medical device are presumed to be acceptable, unless there is objective evidence to the contrary. This International Standard does not apply to clinical decision-making relating to the use of a medical device.
 

Document History

  1. IEC 62366-1 Ed. 1.0 b:2015


    Medical devices - Part 1: Application of usability engineering to medical devices

    • Most Recent
  2. IEC 62366 Ed. 1.1 b:2014


    Medical devices - Application of usability engineering to medical devices CONSOLIDATED EDITION

    • Historical Version
  3. IEC 62366 Ed. 1.0 b:2007

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    Medical devices - Application of usability engineering to medical devices

    • Historical Version
 

Amendments & Errata

  1. IEC 62366 Amd.1 Ed. 1.0 b:2014


    Amendment 1 - Medical devices - Application of usability engineering to medical devices