IEC 62366:2007+A1:2014 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. This consolidated version consists of the first edition (2007) and its amendment 1 (2014). Therefore, no need to order amendment in addition to this publication.
Document identifier
IEC 62366 Ed. 1.1 b:2014 [ Withdrawn ]
Title
Medical devices - Application of usability engineering to medical devices CONSOLIDATED EDITION
IEC Category
SC 62A: Common aspects of electrical equipment used in medical practice
Publication date
2014-01-28
International Relationship
History of version
IEC 62366-1 Ed. 1.0 b:2015*IEC 62366 Ed. 1.1 b:2014 [ Withdrawn ] * IEC 62366-1 Ed. 1.0 b:2015 * IEC 62366 Ed. 1.1 b:2014 * IEC 62366 Ed. 1.0 b:2007
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484 vnd |