Human Factors/Usability Studies following ISO 62366 and the new FDA Guidance

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Human Factors/Usability Studies following ISO 62366 and the new FDA Guidance

Website https://www.complianceonline.com/human-factors-usability-studies-following-iso-62366-and-new-fda-gui | Edit Freely

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Deadline: November 03, 2022 | Date: November 03, 2022

Venue/Country: Online, U.S.A

Updated: 2022-10-11 23:47:27 (GMT+9)

Call For Papers - CFP

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.

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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