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Part 1: Why biocompatibility and material science are so important

Editorial, News
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4. September 2024
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The right to treatment with artificial intelligence (AI)?

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16. July 2024
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The Higher Regional Court of Hamburg on the risk classification of medical device software

Editorial
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29. February 2024
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Extension of the transitional arrangements for in-vitro diagnostics in the European Union

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26. January 2024
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Can ChatGPT be classified as a medical device in the sense of EU law?

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23. August 2023
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One audit, five markets: Opportunities of the Medical Device Single Audit Program (MDSAP)

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29. September 2022
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Regulatory backlog: why medical device manufacturers should not delay MDR implementation

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25. February 2022
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MDR and IVDR: differences and similarities of the regulations

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3. February 2022
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Artificial intelligence: 4 questions you should have an answer to

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20. January 2022
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