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Titlebook: Humanizing Healthcare – Human Factors for Medical Device Design; Russell J. Branaghan,Joseph S. O’Brian,L. Bryant F Book 2021 Springer Nat

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41#
發(fā)表于 2025-3-28 17:25:08 | 只看該作者
Humanizing Healthcare – Human Factors for Medical Device Design
42#
發(fā)表于 2025-3-28 19:13:54 | 只看該作者
43#
發(fā)表于 2025-3-29 02:09:20 | 只看該作者
44#
發(fā)表于 2025-3-29 05:17:54 | 只看該作者
Qualitative Human Factors Research Methods,research involves a human-centered approach—that is, keeping the user at the heart of all design decisions regardless of scope. This chapter begins by exploring what it means to follow a human-centered design (HCD) approach. It then provides the foundation for conducting qualitative HFE research, ad
45#
發(fā)表于 2025-3-29 09:29:59 | 只看該作者
46#
發(fā)表于 2025-3-29 11:25:08 | 只看該作者
47#
發(fā)表于 2025-3-29 15:40:37 | 只看該作者
Visual Perception,chapter focuses on visual perception, since we humans rely so heavily on vision, and because technology includes so many visual displays. Once we have discussed the mechanisms of visual perception, we can apply this knowledge to the design of visual displays that are useful, usable, and desirable.
48#
發(fā)表于 2025-3-29 20:03:25 | 只看該作者
Hearing,rves as a first line of defense in threat detection. It also has the potential to add hedonic value to our experience as humans. This chapter addresses what sound is, and how our auditory systems transform it into perceivable, localized, actionable information. The conclusion of this chapter discuss
49#
發(fā)表于 2025-3-30 01:06:18 | 只看該作者
Use-Error,oorly designed device, the user often takes the blame. Accident investigations often assign the blame on user error, a term that is not only overused, but that is just plain wrong. Often, the design poorly matches the capabilities and limitations of the users it was designed for in the first place,
50#
發(fā)表于 2025-3-30 04:46:22 | 只看該作者
Human Factors Regulations for Medical Devices,To ensure these products have the positive effect intended and protect the public from potentially harmful products, government agencies around the world regulate how they are developed, manufactured, labeled, and sold. Manufacturers of devices that have the potential to cause serious harm to users
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