TR IEC/TR 62366-2:2018

Medical devices - Part 2 : Guidance on the application of usability engineering to medical devices

OVERVIEW

Contains background information and provides guidance that addresses specific areas that experience suggests can be helpful for those implementing a usability engineering (human factors engineering) process both as defined in SS IEC 62366-1:2018 and as supporting goals other than safety.

Also can be useful for other healthcare products (e.g. drug packaging and drug labelling, drug-medical device combination products and health IT software).

COMMENTS

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PRODUCT DETAILS

Status Current
Edition 2018
No. of Pages 112
ICS Classification 11.040.01 Medical equipment in general
Committee Biomedical and Health Standards Committee
Available for Purchase Global
Adoption IEC/TR 62366-2 : 2016 IDT