Table of contents
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1. Introduction
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2. Is AAL technology a medical device or consumer product?
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3. European regulatory framework
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3.1. Medical devices regulation
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3.1.1. The definition of a medical device
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3.1.2. The information security standards of MDR
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3.2. General Data Protection Regulation
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3.3. The Network and Information Security Directive
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3.3.1. AI Act – projected impact
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3.4. National rules
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4. Liability issues
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4.1. Liability for product malfunction
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4.2. Liability for breach information safety or security
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5. Conclusion
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6. Funding