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    • Market Access
      • Market Access US & International
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      • And more…
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      • Quality management systems (ISO 13485)
      • ISO 13485 audits
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      • Quality management system as a service
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      • Performance evaluation of IVDs
      • Electrical Safety & IEC 60601
      • Human Factors / Usability (IEC 62366 and FDA)
      • FDA relevant documents
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      • Computer System Validation
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June 20, 2025


Brexit: How you can still sell your medical devices in the UK

By Luca SalvatoreJune 20, 2025Leave a comment

Brexit was completed in January 2021. What was a cause for celebration for some means an additional burden for many – including medical device manufacturers. For manufacturers, it is important to understand which regulatory requirements they will have to fulfill and which transition periods they will benefit from if they want to continue selling their…

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