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San Francisco Bay Area Chapter Webcast: Applying Human Factors Engineering in Medical Device Development Regulatory Expectations and Trends will .. Read more review a general introduction to human factors engineering (aka usability engineering) as it pertains to Class II medical devices that are subject to design controls. There will be a clarification on the importance of meeting the US Food and Drug Administration’s (FDA) human factors expectations in advance of making a submission, and how it may also improve a medical device’s chance of commercial success.
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