Medical Devices And Human Engineering
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Medical Devices And Human Engineering
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Author : Donald R. Peterson
language : en
Publisher: CRC Press
Release Date : 2017-08-30
Known as the bible of biomedical engineering, The Biomedical Engineering Handbook, Fourth Edition, sets the standard against which all other references of this nature are measured. As such, it has served as a major resource for both skilled professionals and novices to biomedical engineering. Medical Devices and Human Engineering, the second volume of the handbook, presents material from respected scientists with diverse backgrounds in biomedical sensors, medical instrumentation and devices, human performance engineering, rehabilitation engineering, and clinical engineering. More than three dozen specific topics are examined, including optical sensors, implantable cardiac pacemakers, electrosurgical devices, blood glucose monitoring, human�computer interaction design, orthopedic prosthetics, clinical engineering program indicators, and virtual instruments in health care. The material is presented in a systematic manner and has been updated to reflect the latest applications and research findings.
The Biomedical Engineering Handbook
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Author : Joseph D. Bronzino
language : en
Publisher:
Release Date : 2015
Handbook Of Human Factors In Medical Device Design
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Author : Matthew Bret Weinger
language : en
Publisher: CRC Press
Release Date : 2010-12-13
Developed to promote the design of safe, effective, and usable medical devices, Handbook of Human Factors in Medical Device Design provides a single convenient source of authoritative information to support evidence-based design and evaluation of medical device user interfaces using rigorous human factors engineering principles. It offers guidance
Applied Human Factors In Medical Device Design
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Author : Mary Beth Privitera
language : en
Publisher: Academic Press
Release Date : 2019-06-15
Applied Human Factors in Medical Device Design describes the contents of a human factors toolbox with in-depth descriptions of both empirical and analytical methodologies. The book begins with an overview of the design control process, integrating human factors as directed by AAMI TIR 59 and experienced practice. It then explains each method, describing why each method is important, its potential impact, when it's ideal to use, and related challenges. Also discussed are other barriers, such as communication breakdowns between users and design teams. This book is an excellent reference for professionals working in human factors, design, engineering, marketing and regulation. Focuses on meeting agency requirements as it pertains to the application of human factors in the medical device development process in both the US and the European Union (EU) Explains technology development and the application of human factors throughout the development process Covers FDA and MHRA regulations Includes case examples with each method
Medical Devices And Human Engineering
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Author : Joseph D. Bronzino
language : en
Publisher: CRC Press
Release Date : 2018-10-08
Known as the bible of biomedical engineering, The Biomedical Engineering Handbook, Fourth Edition, sets the standard against which all other references of this nature are measured. As such, it has served as a major resource for both skilled professionals and novices to biomedical engineering. Medical Devices and Human Engineering, the second volume of the handbook, presents material from respected scientists with diverse backgrounds in biomedical sensors, medical instrumentation and devices, human performance engineering, rehabilitation engineering, and clinical engineering. More than three dozen specific topics are examined, including optical sensors, implantable cardiac pacemakers, electrosurgical devices, blood glucose monitoring, human–computer interaction design, orthopedic prosthetics, clinical engineering program indicators, and virtual instruments in health care. The material is presented in a systematic manner and has been updated to reflect the latest applications and research findings.
Usability Engineering And Human Factors For Medical Devices
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Author : Bernadette White
language : en
Publisher: Independently Published
Release Date : 2022-02
A short introduction to Usability in paperback- the perfect pocket book- Recent changes in regulation (e.g. MDR 2017/745) have increased the focus on usability requirements for medical devices. With stronger references to risks associated with use error and foreseeable misuse now requiring manufacturers to respond to foreseeable misuse. This short book introduces Usability Engineering and Human Factors Engineering providing a grounding in the principles of UE/HFE and the deliverables expected by manufacturers. As medical device vary in classification, complexity, cost and intended use, it is not feasible to provide a ready-made solution for device usability. However, if usability is integrated into the product development processes and risk management processes it can achieve devices that have minimal use related hazards. If medical devices are designed and developed without applying a usability engineering or human factors engineering, their use can be non-intuitive, difficult to learn, difficult to complete tasks and difficult to use. Furthermore, as technology and medical devices offer more innovative solutions, patients can now be tasked with using medical devices or administering their treatments, therefore usability becomes more important. While the goal of design should aim to provide medical devices that are inherently safe, as with most medical devices, residual risks remain once a product is designed, manufactured and validated clinically. Use errors or Usability errors contribute to those potential risk scenarios where medical device usability is an issue for the user. With the increasing abundance of medical devices is the observation, treatment and monitoring of patients, use errors must be assessed for medical devices and reduced to an acceptable level. In contrast to safety inherited by design, the least and often the last protective measures are warnings or contraindications provided on labelling or instructions for use. The strength of applying usability engineering principles (aka human factors engineering) medical devices is that use errors can be identified and mitigated through design and engineering practices, early-on in the product development and product realization cycle. Medical devices designed and developed devoid of usability engineering, are less intuitive, difficult to use and require focus and attention to learn to use them effectively. In addition, usability is a growing requirement from a regulatory perspective. A strength of this short book is its focus on the themes of usability, risk management and design control which interact together and if managed early-on in projects can benefit the user and deliver medical devices optimised for usability and human factors. At approx. 73 pages, this book does not intend to provide an expensive textbook solution to Usability, alternatively, it is a concise guide offering a 'to-the-point' reference at great value.
Human Factors Engineering Guidelines And Preferred Practices For The Design Of Medical Devices
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Author : Association for the Advancement of Medical Instrumentation
language : en
Publisher: Association for the Advancement of Medical Instrumentation (AAMI)
Release Date : 1988