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Safety Risk Management for Medical Devices

Specificaties
Paperback, blz. | Engels
Elsevier Science | 2021
ISBN13: 9780323857550
Rubricering
Elsevier Science e druk, 2021 9780323857550
€ 158,20
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Samenvatting

Safety Risk Management for Medical Devices, Second Edition teaches the essential safety risk management methodologies for medical devices compliant with the requirements of ISO 14971:2019. Focusing exclusively on safety risk assessment practices required in the MedTech sector, the book outlines sensible, easily comprehensible, state-of the-art methodologies that are rooted in current industry best practices, addressing safety risk management of medical devices, thus making it useful for those in the MedTech sector who are responsible for safety risk management or need to understand risk management, including design engineers, product engineers, development engineers, software engineers, Quality assurance and regulatory affairs.

Graduate-level engineering students with an interest in medical devices will also benefit from this book. The new edition has been fully updated to reflect the state-of-the-art in this fast changing field. It offers guidance on developing and commercializing medical devices in line with the most current international standards and regulations.

Specificaties

ISBN13:9780323857550
Taal:Engels
Bindwijze:Paperback

Inhoudsopgave

<p>1 Introduction <br>2 What Is A Medical Device? <br>3 Why Do Risk‐Management?<br>4 The Basics <br>5 Understanding Risk <br>6 Risk Management Standards <br>7 Requirements of the Risk Management Process <br>8 Quality Management System <br>9 Usability Engineering and Risk Analysis <br>10 Biocompatibility and Risk Management <br>11 Influence of Security on Safety<br>12 The BXM Method<br>13 Risk Management Process <br>14 Risk Analysis Techniques <br>15 Software Risk Management<br>16 Integration of Risk Analysis<br>17 Risk Estimation<br>18 Risk Controls <br>19 Verification of Risk Controls<br>20 On Testing <br>21 Risk Evaluation<br>22 Risk Assessment and Control Table (RACT)<br>23 Benefit‐Risk Analysis<br>24 Risk Management Review <br>26 Traceability <br>27 Lifetime of a Medical Device <br>28 Safety versus Reliability <br>29 Risk Management for System of Systems <br>30 Risk Management for Clinical Investigations <br>31 Risk Management for Legacy Devices<br>32 Risk Management for Combination Medical Devices <br>33 Basic Safety and Essential Performance <br>34 Relationship between ISO 14971 and other Standards <br>35 Risk Management Process Metrics <br>36 Risk Management and Product Development Process<br>37 Risk Management for Suppliers <br>38 Axioms <br>39 Special Topics <br>40 Critical Thinking and Risk Management <br>41 Advice and Wisdom <br>Appendix A ‐ Glossary <br>Appendix B – Templates <br>Appendix C – Example Device – Vivio <br>Appendix D – Useful References</p> <p><br> </p>
€ 158,20
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        Safety Risk Management for Medical Devices