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    • Market Access
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      • AI Medical Devices
      • And more…
    • Quality System
      • Quality management systems (ISO 13485)
      • ISO 13485 audits
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      • Quality management system as a service
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      • Software (IEC 62304, FDA)
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      • Clinical Evaluation
      • Performance evaluation of IVDs
      • Electrical Safety & IEC 60601
      • Human Factors / Usability (IEC 62366 and FDA)
      • FDA relevant documents
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      • Safety and EMC test laboratory
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November 20, 2025


Regulatory requirements for medical devices with machine learning

By Prof. Dr. Christian JohnerNovember 20, 20251 Comment

Manufacturers who use machine learning (ML) in their medical devices or IVDs must comply with numerous regulatory requirements. This article provides an overview of the most important regulations and best practices for implementation. It saves you the trouble of researching and reading hundreds of pages and helps you prepare perfectly for your next audit.

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Combination products: Applicable law and regulatory requirements (EU law)

By Mario KlessascheckNovember 20, 2025Leave a comment

Combination products consist of the combination of a medical device and a medicinal product. Since both medical device and medicinal product law could be applicable here, there are some special features that must be taken into account for products of this type. In this article, you learn more about

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