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Russell J. Branaghan,Joseph S. O'Brian,Emily A. Hildebrand,L. Bryant Foster

Humanizing Healthcare - Human Factors for Medical Device Design

Humanizing Healthcare - Human Factors for Medical Device Design

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This book provides an introduction to human factors engineering (HFE) principles, guidelines, and design methods for medical device design. It covers physical, perceptual, and cognitive abilities and limitations, and applies them to input controls, visual displays, auditory displays, and human-computer interaction. It also discusses specific challenges and solutions for various medical device domains and includes a human factors design lifecycle and regulatory requirements.

Format: Paperback / softback
Length: 395 pages
Publication date: 23 February 2022
Publisher: Springer Nature Switzerland AG


This comprehensive book delves into the realm of human factors engineering (HFE), providing a comprehensive framework for designing medical devices that prioritize human safety, effectiveness, and usability. It begins by exploring the physical, perceptual, and cognitive abilities and limitations of humans, shedding light on their implications for medical device design. Through a rigorous analysis, a set of human factors principles is established, serving as a guiding framework for addressing various design challenges. These principles are then applied to specific guidelines for designing input controls, visual displays, auditory displays (alerts, alarms, warnings), and human-computer interaction.

The book goes beyond general principles and offers in-depth discussions of specific medical device domains, including robotic surgery, laparoscopic surgery, artificial organs, wearables, continuous glucose monitors, and insulin pumps. It addresses the unique challenges and solutions associated with each domain, highlighting the importance of human factors in ensuring safe and effective use of these devices.

Furthermore, the book integrates human factors research and design methods into a human factors design lifecycle, emphasizing the importance of integrating these aspects throughout the development process. It provides a detailed discussion of regulatory requirements and procedures, including guidance on when and how human factors activities should be conducted and documented. This hands-on professional reference is invaluable for students and practitioners in HFE, biomedical engineering, industrial design, graphic design, user-experience design, quality engineering, product management, and regulatory affairs.

By mastering the principles and methodologies outlined in this book, readers will gain the skills necessary to design medical devices that are safer, more effective, and less error-prone. They will also gain a deeper understanding of the role and responsibilities of regulatory agencies in medical device design, as well as the analysis and research methods employed to evaluate the usability and safety of medical devices. With its comprehensive coverage and practical insights, this book serves as a valuable resource for anyone seeking to excel in the field of human factors engineering in medical device design.

Weight: 646g
Dimension: 235 x 155 (mm)
ISBN-13: 9783030644352
Edition number: 1st ed. 2021

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