The US Food and Drug Administration is seeking feedback on a draft guidance on tests that will enable medical device manufacturers to understand and optimise how people interact with technology, thereby helping them improve the safety and effectiveness of products and reduce use error1,2
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Regulatory Affairs Medtech
US FDA consults on human factors testing guidance to improve device safety
24 June 2011
Vibha Sharma
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21September 2009
Minneapolis (MN), US
