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EVS-EN 62366-1:2015+A1:2020

Medical devices - Part 1: Application of usability engineering to medical devices (IEC 62366-1:2015 + IEC 62366-1:2015/A1:2020)

General information
Valid from 17.08.2020
Base Documents
EN 62366-1:2015; IEC 62366-1:2015; EN 62366-1:2015/AC:2015; IEC 62366-1:2015/COR1:2016; EN 62366-1:2015/AC:2016-09; IEC 62366-1:2015/A1:2020; EN 62366-1:2015/A1:2020
Directives or regulations
None

Standard history

Status
Date
Type
Name
17.08.2020
Main + amendment
17.08.2020
Amendment
01.08.2018
Corrigendum
05.01.2016
Corrigendum
07.05.2015
Main
EVS-EN 62366-1 specifies a process for a manufacturer to analyse, specify, develop and evaluate the usability of a medical device as it relates to safety.

Medical practice is increasingly using medical devices for observation and treatment of patients. Use errors caused by inadequate medical device usability have become an increasing cause for concern. As healthcare evolves, less skilled users including patients themselves are now using more difficult devices.

Many of the medical devices developed without applying a usability engineering (human factors engineering) process are non-intuitive, difficult to learn and difficult to use. The usability engineering process is intended to identify and minimise use errors and thereby reduce risks.

EVS-EN 62366-1 describes a usability engineering process to provide acceptable risk related to usabilty of a medical device. It is intended to be useful for manufacturers of medical devices.
EVS-EN 62366-1 strictly focuses on applying usability engineering process to
optimize medical device usability as it relates to safety.

The text of IEC 62366-1:2015 has been approved in Europe as EN 62366-1:2015 without any modification.
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