Conference Description:

This training program will examine how human factors/usability is the analysis of how people interact with medical devices. The process of conducting rigorous human factors studies throughout the design process, integrating it with the device risk analysis and design process, and validating the effectiveness of the studies will be explained. The various types and methods of human factors analysis will be explained. This process conforms to the new ISO 62366 standard and the new FDA guidance document.

For More Info:
https://www.complianceonline.com/human -factors-usability-studies-following-iso -62366-and-new-fda-guidance-webinar-trai ning-704496-prdw?channel=worldconference calendar