Handbook of Medical Device Design

Author:   Richard C. Fries
Publisher:   Taylor & Francis Ltd
ISBN:  

9780367249403


Pages:   774
Publication Date:   07 May 2019
Format:   Hardback
Availability:   In Print   Availability explained
This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us.

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Handbook of Medical Device Design


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Overview

First published in 2001: This handbook has been written to give those professionals working in the development and use of medical devices practical knowledge about biomedical technology, regulations, and their relationship to quality health care.

Full Product Details

Author:   Richard C. Fries
Publisher:   Taylor & Francis Ltd
Imprint:   CRC Press
Weight:   0.453kg
ISBN:  

9780367249403


ISBN 10:   0367249405
Pages:   774
Publication Date:   07 May 2019
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   In Print   Availability explained
This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us.

Table of Contents

"Section 1: Standards and Regulations 1. FDA Regulations 2. Preparing an FDA Submission 3. European Standards and Regulations 4. The Medical Device Directives 5. The Basis of ISO 9001 6. Design of Medical Devices for the Canadian Market 7. Pacific Rim Standards and Regulations 8. Overview of Software Standards Section 2: Determining and Documenting Requirements 9. Defining the Device 10. Documenting Product Requirements 11. Medical Device Records Section 3: The Design Phase 12. Hazard and Risk Analysis 13. Hardware Design 14. Software Design 15. Human Factors Engineering 16. Biocompatibility 17. Reliability Assurance 18. Product User Guides 19. Translation: ""It’s a Small World After All"" 20. Liability 21. Intellectual Property Section 4: Verification and Validation 22. Testing 23. Overview of Verification and Validation for Embedded Software in Medical Systems 24. Software Verification and Validation 25. Reliability Evaluation 26. Analysis of Test Results Section 5: The Manufacturing/Field Phase 27. Quality System Regulation and Manufacturing 28. Configuration Management 29. The Quality System Audit 30. Analysis of Field Data"

Reviews

a worthwhile reference and source. . ..Biomedical and engineering libraries would benefit from this addition to their reference collections. ---E-Streams


Author Information

Richard C. Fries is Manager of Reliability Engineering, Datex-Ohmeda, Inc., Madison, Wisconsin.

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