11724 results in Medical Law, Ethics and Forensic Medicine
Acknowledgments
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- The Future of Medical Device Regulation
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Contents
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Part III - Designing Medical Device Regulations
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7 - AI, Explainability, and Safeguarding Patient Safety in Europe
- from Part II - European Regulation of Medical Devices
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9 - IP and FDA Regulation of De Novo Medical Devices
- from Part III - Designing Medical Device Regulations
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12 - Clouded Judgment
- from Part IV - The Impact of Medical Device Regulation on Patients and Markets
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![](https://assets.cambridge.org/97810091/25765/cover/9781009125765.jpg)
Vaccines as Technology
- Innovation, Barriers, and the Public Health
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- 14 April 2022
6 - The Interaction of the Medical Device Regulation and the GDPR
- from Part II - European Regulation of Medical Devices
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18 - Professional Self-Regulation in Medicine
- from Part V - Medical and Legal Oversight of Medical Devices
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Part II - European Regulation of Medical Devices
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1 - Lifecycle Regulation and Evaluation of Artificial Intelligence and Machine Learning-Based Medical Devices
- from Part I - AI and Data as Medical Devices
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2 - Product Liability Suits for FDA-Regulated AI/ML Software
- from Part I - AI and Data as Medical Devices
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19 - Regulating Posttrial Access to In-Dwelling Class III Neural Devices
- from Part V - Medical and Legal Oversight of Medical Devices
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Dedication
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20 - Strengthening the Power of Health Care Insurers to Regulate Medical Device Risks
- from Part V - Medical and Legal Oversight of Medical Devices
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17 - Compulsory Medical Device Registries
- from Part V - Medical and Legal Oversight of Medical Devices
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11 - Digital Home Health During the COVID-19 Pandemic
- from Part III - Designing Medical Device Regulations
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5 - The mHealth Power Paradox
- from Part II - European Regulation of Medical Devices
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3 - Are Electronic Health Records Medical Devices?
- from Part I - AI and Data as Medical Devices
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Part V - Medical and Legal Oversight of Medical Devices
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