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  • Home
  • SERVICES
    • TRAINING
      • About EUDAMED Training
      • Live EUDAMED Training 25th January 2022
      • Live EUDAMED Training 23rd February 2022
      • Live EUDAMED Training 29th March 2022
      • EUDAMED Simplified (Self-paced)
      • EUDAMED Registration (Self-paced)
      • Understanding EUDAMED (Self-paced)
    • SUPPORT
      • About EUDAMED Support
      • EudaMed (5 Incident)      Support Package
      • EudaMed (25 Incident)      Support Package
    • EUDAMED REGISTRATION
    • TEMPLATES
      • About EUDAMED Templates
      • MDR Template Package
      • IVDR Template Package
      • Authorised Representative Template
      • Distributor Template
      • Importer Template
    • SOFTWARE
      • About EUDAMED Software
      • EudaMed+
      • EudaMed SaaS
      • EudaMed SaaS 100 UDI DI’s
      • EudaMed SaaS 300 UDI DI’s
  • Resources
    • EUDAMED DI Generator
    • Eudamed Articles
    • EC & MDCG Updates
    • MDR and IVDR Regulations
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We are the EUDAMED specialists here to assist you with your medical device data and European Commission EUDAMED compliance.

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LINKS
  • What is MDR (Medical Device Regulation)?
  • MDR Eudamed Regulatory Framework
  • Market surveillance and vigilance
  • European MDR and IVDR Regulations
  • European Commission MDR Updates
ARTICLES
  • EUDAMED Device Module is Live
  • Add my device data to EUDAMED
  • Medical Device Regulations and EUDAMED 2021
  • Authorised Reps, Distributors, Importers, solution.
  • How to prepare your EUDAMED spreadsheets.
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