AAMI TIR50:2014/(R)2017

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This document will address the issue of use error detection for medical devices from clinical, manufacturer, and regulatory perspective regarding human factors assessment. The goal is to provide guidance on how clinicians and manufacturers can best collect and leverage post-market use error data to improve product safety and usability.

Product Details

Edition:

1st

Published:

03/10/2014

ISBN(s):

1570205140

Number of Pages:

46

File Size:

1 file , 740 KB