“Anyone doing design, development, or postmarket surveillance for a medical product that humans use should be considering human factors and usability,” Shannon Hoste, chief scientific officer at ...

DUBLIN--(BUSINESS WIRE)--The "Human Factors and Usability Engineering in the Development of Drug Delivery Products Training Course 24" conference has been added to ResearchAndMarkets.com's offering.

The U.S. FDA recently posted the regulation for software used to derive vital signs from optical camera images thanks to a successful de novo petition by Oxford, U.K.-based Oxehealth Ltd., a ...

To err is human. We have short attention spans and get distracted easily. We have unreliable memories and forget. We have a limited ability to process information, and we overgeneralize rules-of-thumb ...

The wheels of medical device regulation turn slowly at times. But just like The Little Engine That Could, it usually reaches its destination eventually. One of the slowest moving regulations was FDA's ...

Brandy Guarda, Regulatory Analyst in Washington, D.C., contributed to the drafting of this post. If you are a device manufacturer, what human factors and usability information should you include in ...

Over the next year, the term human factors must become very important to those who develop and market medical devices (if the term is not already). Developers must take a look at some common ...

If you are interested in understanding people—how they think, behave, and interact with other people, technology, or the world around them—in order to improve their personal and professional ...

Effectively incorporating human insight and oversight is critical to implementing artificial intelligence systems. However, the use of AI tools in real-world environments introduces new challenges.