Reliable Design of Medical Devices

Reliable Design of Medical Devices
Author: Richard C. Fries
Publisher: CRC Press
Total Pages: 490
Release: 2005-11-21
Genre: Medical
ISBN: 1420027948

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As medical devices increase in complexity, concerns about efficacy, safety, quality, and longevity increase in stride. Introduced nearly a decade ago, Reliable Design of Medical Devices illuminated the path to increased reliability in the hands-on design of advanced medical devices. With fully updated coverage in its Second Edition, this practical guide continues to be the benchmark for incorporating reliability engineering as a fundamental design philosophy. The book begins by rigorously defining reliability, differentiating it from quality, and exploring various aspects of failure in detail. It examines domestic and international regulations and standards in similar depth, including updated information on the regulatory and standards organizations as well as a new chapter on quality system regulation. The author builds on this background to explain product specification, liability and intellectual property, safety and risk management, design, testing, human factors, and manufacturing. New topics include design of experiments, CAD/CAM, industrial design, material selection and biocompatibility, system engineering, rapid prototyping, quick-response manufacturing, and maintainability as well as a new chapter on Six Sigma for design. Supplying valuable insight based on years of successful experience, Reliable Design of Medical Devices, Second Edition leads the way to implementing an effective reliability assurance program and navigating the regulatory minefield with confidence.

Reliable Design of Medical Devices, Third Edition

Reliable Design of Medical Devices, Third Edition
Author: Richard C. Fries
Publisher: CRC Press
Total Pages: 505
Release: 2012-09-06
Genre: Medical
ISBN: 1439894914

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As medical devices become even more intricate, concerns about efficacy, safety, and reliability continue to be raised. Users and patients both want the device to operate as specified, perform in a safe manner, and continue to perform over a long period of time without failure. Following in the footsteps of the bestselling second edition, Reliable Design of Medical Devices, Third Edition shows you how to improve reliability in the design of advanced medical devices. Reliability engineering is an integral part of the product development process and of problem-solving activities related to manufacturing and field failures. Mirroring the typical product development process, the book is organized into seven parts. After an introduction to the basics of reliability engineering and failures, it takes you through the concept, feasibility, design, verification and validation, design transfer and manufacturing, and field activity phases. Topics covered include Six Sigma for design, human factors, safety and risk analysis, and new techniques such as accelerated life testing (ALT) and highly accelerated life testing (HALT). What’s New in This Edition Updates throughout, reflecting changes in the field An updated software development process Updated hardware test procedures A new layout that follows the product development process A list of deliverables needed at the end of each development phase Incorporating reliability engineering as a fundamental design philosophy, this book shares valuable insight from the author’s more than 35 years of experience. A practical guide, it helps you develop a more effective reliability engineering program—contributing to increased profitability, more satisfied customers, and less risk of liability.

Designing Usability into Medical Products

Designing Usability into Medical Products
Author: Michael E. Wiklund
Publisher: CRC Press
Total Pages: 285
Release: 2005-02-11
Genre: Medical
ISBN: 1040063756

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Advocating a user-centered approach to medical technology design, Designing Usability into Medical Products covers the essential processes and specific techniques necessary to produce safe, effective, usable, and appealing medical systems and products. Written by experts on user-centered research, design, and evaluation, the book provides a range o

Design Controls for the Medical Device Industry

Design Controls for the Medical Device Industry
Author: Marie Teixeira
Publisher: CRC Press
Total Pages: 258
Release: 2002-09-20
Genre: Medical
ISBN: 9780203909386

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This reference provides real-world examples, strategies, and templates for the implementation of effective design control programs that meet current ISO 9000 and FDA QSR standards and regulations-offering product development models for the production of safe, durable, and cost-efficient medical devices and systems. Details procedures utilize

Engineering Open-Source Medical Devices

Engineering Open-Source Medical Devices
Author: Arti Ahluwalia
Publisher: Springer Nature
Total Pages: 275
Release: 2022-02-23
Genre: Medical
ISBN: 303079363X

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This book focuses on the challenges and potentials of open source and collaborative design approaches and strategies in the biomedical field. It provides a comprehensive set of good practices and methods for making these safe, innovative and certifiable biomedical devices reach patients and provide successful solutions to healthcare issues. The chapters are sequenced to follow the complete lifecycle of open source medical technologies. The information provided is eminently practical, as it is supported by real cases of study, in which collaboration among medical professionals, engineers and technicians, patients and patient associations, policy makers, regulatory bodies, and citizens has proven beneficial. The book is also supported by an online infrastructure, UBORA, through which open-source medical devices can be collaboratively developed and shared for the democratization of medical technology and for promoting accessible biomedical engineering education.

The Medical Device R&D Handbook

The Medical Device R&D Handbook
Author: Theodore R. Kucklick
Publisher: CRC Press
Total Pages: 376
Release: 2005-11-21
Genre: Medical
ISBN: 1420038354

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The Medical Device R&D Handbook presents a wealth of information for the hands-on design and building of medical devices. Detailed information on such diverse topics as catheter building, prototyping, materials, processes, regulatory issues, and much more are available in this convenient handbook for the first time. The Medical Device R&D Ha

Reliability and Regulatory Compliance Design for Medical Devices

Reliability and Regulatory Compliance Design for Medical Devices
Author: Reinaldo Perez
Publisher: Academic Press
Total Pages: 350
Release: 2002-06
Genre: Medical
ISBN: 9780125507127

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This text addresses all of the major design considerations in making a device reliable including electromagnetic interference, noise and environmental considerations such as temperature, radiation and moisture. The second major issue is the ability of the device to meet with the codes, standards and regulations necessary for approval. This text addresses both the reliability and the regulations from the standpoint of the design.

Design of Biomedical Devices and Systems, 4th edition

Design of Biomedical Devices and Systems, 4th edition
Author: Paul H. King
Publisher: CRC Press
Total Pages: 508
Release: 2018-10-03
Genre: Medical
ISBN: 0429786069

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This fourth edition is a substantial revision of a highly regarded text, intended for senior design capstone courses within departments of biomedical engineering, bioengineering, biological engineering and medical engineering, worldwide. Each chapter has been thoroughly updated and revised to reflect the latest developments. New material has been added on entrepreneurship, bioengineering design, clinical trials and CRISPR. Based upon feedback from prior users and reviews, additional and new examples and applications, such as 3D printing have been added to the text. Additional clinical applications were added to enhance the overall relevance of the material presented. Relevant FDA regulations and how they impact the designer’s work have been updated. Features Provides updated material as needed to each chapter Incorporates new examples and applications within each chapter Discusses new material related to entrepreneurship, clinical trials and CRISPR Relates critical new information pertaining to FDA regulations. Presents new material on "discovery" of projects "worth pursuing" and design for health care for low-resource environments Presents multiple case examples of entrepreneurship in this field Addresses multiple safety and ethical concerns for the design of medical devices and processes

Materials and Coatings for Medical Devices

Materials and Coatings for Medical Devices
Author:
Publisher: ASM International
Total Pages: 453
Release: 2009-01-01
Genre:
ISBN: 1615031359

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"The Materials Information Society, MPMD-Materials and Processes for Medical Devices."

Design of Biomedical Devices and Systems, 4th edition

Design of Biomedical Devices and Systems, 4th edition
Author: Paul H. King
Publisher: CRC Press
Total Pages: 725
Release: 2018-10-03
Genre: Medical
ISBN: 0429786050

Download Design of Biomedical Devices and Systems, 4th edition Book in PDF, Epub and Kindle

This fourth edition is a substantial revision of a highly regarded text, intended for senior design capstone courses within departments of biomedical engineering, bioengineering, biological engineering and medical engineering, worldwide. Each chapter has been thoroughly updated and revised to reflect the latest developments. New material has been added on entrepreneurship, bioengineering design, clinical trials and CRISPR. Based upon feedback from prior users and reviews, additional and new examples and applications, such as 3D printing have been added to the text. Additional clinical applications were added to enhance the overall relevance of the material presented. Relevant FDA regulations and how they impact the designer’s work have been updated. Features Provides updated material as needed to each chapter Incorporates new examples and applications within each chapter Discusses new material related to entrepreneurship, clinical trials and CRISPR Relates critical new information pertaining to FDA regulations. Presents new material on "discovery" of projects "worth pursuing" and design for health care for low-resource environments Presents multiple case examples of entrepreneurship in this field Addresses multiple safety and ethical concerns for the design of medical devices and processes