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    • Market Access
      • Market Access US & International
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      • AI Medical Devices
      • And more…
    • Quality System
      • Quality management systems (ISO 13485)
      • ISO 13485 audits
      • Quality management representative
      • Quality management system as a service
    • Technical Documentation
      • Software (IEC 62304, FDA)
      • Risk Management (ISO 14971)
      • Clinical Evaluation
      • Performance evaluation of IVDs
      • Electrical Safety & IEC 60601
      • Human Factors / Usability (IEC 62366 and FDA)
      • FDA relevant documents
    • Product test
      • Human Factors Research
      • Safety and EMC test laboratory
      • Biological safety
      • Computer System Validation
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      • Seminar Overview
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  • Medical Device University
  • Regulatory Intelligence
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      • Current Vacancies
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February 25, 2025


Design change: Requirements, including MDCG 2020-3

By Janos HackenbeckFebruary 25, 20252 Comments

A design change is a change in the design of a product. It is important to understand what regulatory implications arise from this and where there may be an impact on the validity of the product’s declaration of conformity. This article provides an overview and thus resolves many currently common misconceptions.

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