Peter J. Ogrodnik (Award Leader MSc Medi Partner in Metaphysis LLP
Medical Device Design
Innovation from Concept to Market
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Peter J. Ogrodnik (Award Leader MSc Medi Partner in Metaphysis LLP
Medical Device Design
Innovation from Concept to Market
- Broschiertes Buch
Provides a reference to standards and regulations that have been updated, including ISO 13485:2016, FDA regulations and the European Medical Device Regulation Includes new case studies in the areas of classifying medical devices, the design process, quality, labeling, instructions for use, and more Presents additional content around software and biocompatibility concerns
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Provides a reference to standards and regulations that have been updated, including ISO 13485:2016, FDA regulations and the European Medical Device Regulation Includes new case studies in the areas of classifying medical devices, the design process, quality, labeling, instructions for use, and more Presents additional content around software and biocompatibility concerns
Produktdetails
- Produktdetails
- Verlag: Elsevier Science Publishing Co Inc
- 2 ed
- Seitenzahl: 538
- Erscheinungstermin: 26. Oktober 2019
- Englisch
- Abmessung: 236mm x 193mm x 32mm
- Gewicht: 1066g
- ISBN-13: 9780128149621
- ISBN-10: 0128149620
- Artikelnr.: 57881578
- Verlag: Elsevier Science Publishing Co Inc
- 2 ed
- Seitenzahl: 538
- Erscheinungstermin: 26. Oktober 2019
- Englisch
- Abmessung: 236mm x 193mm x 32mm
- Gewicht: 1066g
- ISBN-13: 9780128149621
- ISBN-10: 0128149620
- Artikelnr.: 57881578
Professor Ogrodnik is a Chartered Mechanical Engineer, a Member of the Institution of Engineering Designers and a Fellow (regional) of the Royal Society of Medicine, an Honorary Consultant at the Royal Stoke University Hospital. For over 20 years he has conducted research into optimising the treatment of tibial fractures. Using this research base he has enhanced the application of engineering design principles to the solution of medical devices, his book Medical Devices Design is a core text in core R&D departments. He has founded two medical devices companies (one manufactures and sells medical devices to the NHS and beyond) and is named inventor on numerous patents. He was a founding director of the University spinout Intelligent Orthopaedics Ltd, and is a founding partner of Metaphysis LLP. Through this corporate involvement Professor Ogrodnik has an understanding of the realities of applied research for industry; for example he was a member of the AWM Healthcare Technologies cluster opportunity group.
1. Introduction2. Classifying Medical Devices3. The Design Process4.
Implementing Design Procedures5. Developing Your Product Design
Specification6. Generating Ideas and Concepts7. Enhancing Quality in
Design8. Design Realisation/Detailed Design9. Risk Management, Risk
Analysis and ISO 1497110. Evaluation (Validation and Verification)11.
Manufacturing Supply Chain12. Labelling and Instructions for Use13. Post
Market Surveillance14. Protecting Your IP15. Obtaining Regulatory Approval
to Market
Appendix A. Useful WebsitesAppendix B. TablesAppendix C. ISO 14971 Annex C
Pre-Risk Analysis QuestionnaireAppendix D. Generic Codes for Class I
Medical Devices (MHRA)Appendix E. Basic Materials Properties for Materials
SelectionAppendix F. Standard Materials in Medicak Devices
Implementing Design Procedures5. Developing Your Product Design
Specification6. Generating Ideas and Concepts7. Enhancing Quality in
Design8. Design Realisation/Detailed Design9. Risk Management, Risk
Analysis and ISO 1497110. Evaluation (Validation and Verification)11.
Manufacturing Supply Chain12. Labelling and Instructions for Use13. Post
Market Surveillance14. Protecting Your IP15. Obtaining Regulatory Approval
to Market
Appendix A. Useful WebsitesAppendix B. TablesAppendix C. ISO 14971 Annex C
Pre-Risk Analysis QuestionnaireAppendix D. Generic Codes for Class I
Medical Devices (MHRA)Appendix E. Basic Materials Properties for Materials
SelectionAppendix F. Standard Materials in Medicak Devices
1. Introduction2. Classifying Medical Devices3. The Design Process4.
Implementing Design Procedures5. Developing Your Product Design
Specification6. Generating Ideas and Concepts7. Enhancing Quality in
Design8. Design Realisation/Detailed Design9. Risk Management, Risk
Analysis and ISO 1497110. Evaluation (Validation and Verification)11.
Manufacturing Supply Chain12. Labelling and Instructions for Use13. Post
Market Surveillance14. Protecting Your IP15. Obtaining Regulatory Approval
to Market
Appendix A. Useful WebsitesAppendix B. TablesAppendix C. ISO 14971 Annex C
Pre-Risk Analysis QuestionnaireAppendix D. Generic Codes for Class I
Medical Devices (MHRA)Appendix E. Basic Materials Properties for Materials
SelectionAppendix F. Standard Materials in Medicak Devices
Implementing Design Procedures5. Developing Your Product Design
Specification6. Generating Ideas and Concepts7. Enhancing Quality in
Design8. Design Realisation/Detailed Design9. Risk Management, Risk
Analysis and ISO 1497110. Evaluation (Validation and Verification)11.
Manufacturing Supply Chain12. Labelling and Instructions for Use13. Post
Market Surveillance14. Protecting Your IP15. Obtaining Regulatory Approval
to Market
Appendix A. Useful WebsitesAppendix B. TablesAppendix C. ISO 14971 Annex C
Pre-Risk Analysis QuestionnaireAppendix D. Generic Codes for Class I
Medical Devices (MHRA)Appendix E. Basic Materials Properties for Materials
SelectionAppendix F. Standard Materials in Medicak Devices