The future of medical device regulation: innovation and protection
Regulators have been more permissive for medical devices compared to their drug and biologic counterparts. While innovative products can thereby reach consumers more quickly, this approach raises serious public health and safety concerns. Additionally, the nature of medical devices is rapidly changi...
Gespeichert in:
Weitere beteiligte Personen: | , , , , |
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Format: | E-Book |
Sprache: | Englisch |
Veröffentlicht: |
Cambridge
Cambridge University Press
2022
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Links: | https://doi.org/10.1017/9781108975452 |
Zusammenfassung: | Regulators have been more permissive for medical devices compared to their drug and biologic counterparts. While innovative products can thereby reach consumers more quickly, this approach raises serious public health and safety concerns. Additionally, the nature of medical devices is rapidly changing, as software has become as important as hardware. Regulation must keep pace with the current developments and controversies of this technology. This volume provides a multidisciplinary evaluation of the ethical, legal, and regulatory concerns surrounding medical devices in the US and EU. For medical providers, policymakers, and other stakeholders, the book offers a framework for the opportunities and challenges on the horizon for medical device regulation. Readers will gain a nuanced overview of the latest developments in patient privacy and safety, innovation, and new regulatory laws. This book is also available as Open Access on Cambridge Core. |
Umfang: | 1 Online-Ressource (xiv, 280 Seiten) |
ISBN: | 9781108975452 |
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520 | |a Regulators have been more permissive for medical devices compared to their drug and biologic counterparts. While innovative products can thereby reach consumers more quickly, this approach raises serious public health and safety concerns. Additionally, the nature of medical devices is rapidly changing, as software has become as important as hardware. Regulation must keep pace with the current developments and controversies of this technology. This volume provides a multidisciplinary evaluation of the ethical, legal, and regulatory concerns surrounding medical devices in the US and EU. For medical providers, policymakers, and other stakeholders, the book offers a framework for the opportunities and challenges on the horizon for medical device regulation. Readers will gain a nuanced overview of the latest developments in patient privacy and safety, innovation, and new regulatory laws. This book is also available as Open Access on Cambridge Core. | ||
700 | 1 | |a Cohen, I. Glenn | |
700 | 1 | |a Minssen, Timo | |
700 | 1 | |a Price, W. Nicholson |b II | |
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700 | 1 | |a Shachar, Carmel |d 1985- | |
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spelling | The future of medical device regulation innovation and protection edited by I. Glenn Cohen, Timo Minssen, W. Nicholson Price II, Christopher Robertson, Carmel Shachar Cambridge Cambridge University Press 2022 1 Online-Ressource (xiv, 280 Seiten) txt c cr Regulators have been more permissive for medical devices compared to their drug and biologic counterparts. While innovative products can thereby reach consumers more quickly, this approach raises serious public health and safety concerns. Additionally, the nature of medical devices is rapidly changing, as software has become as important as hardware. Regulation must keep pace with the current developments and controversies of this technology. This volume provides a multidisciplinary evaluation of the ethical, legal, and regulatory concerns surrounding medical devices in the US and EU. For medical providers, policymakers, and other stakeholders, the book offers a framework for the opportunities and challenges on the horizon for medical device regulation. Readers will gain a nuanced overview of the latest developments in patient privacy and safety, innovation, and new regulatory laws. This book is also available as Open Access on Cambridge Core. Cohen, I. Glenn Minssen, Timo Price, W. Nicholson II Robertson, Christopher T. 1975- Shachar, Carmel 1985- Erscheint auch als Druck-Ausgabe 9781108838634 Erscheint auch als Druck-Ausgabe 9781108972055 |
spellingShingle | The future of medical device regulation innovation and protection |
title | The future of medical device regulation innovation and protection |
title_auth | The future of medical device regulation innovation and protection |
title_exact_search | The future of medical device regulation innovation and protection |
title_full | The future of medical device regulation innovation and protection edited by I. Glenn Cohen, Timo Minssen, W. Nicholson Price II, Christopher Robertson, Carmel Shachar |
title_fullStr | The future of medical device regulation innovation and protection edited by I. Glenn Cohen, Timo Minssen, W. Nicholson Price II, Christopher Robertson, Carmel Shachar |
title_full_unstemmed | The future of medical device regulation innovation and protection edited by I. Glenn Cohen, Timo Minssen, W. Nicholson Price II, Christopher Robertson, Carmel Shachar |
title_short | The future of medical device regulation |
title_sort | future of medical device regulation innovation and protection |
title_sub | innovation and protection |
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