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  • Home
  • SERVICES
    • TRAINING
      • About EUDAMED Training
      • Live EUDAMED Training 23rd June 2022
      • Live EUDAMED Training 26th July 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 EUDAMED Templates
      • IVDR EUDAMED Templates
      • Authorised Representative Template
      • Distributor Template
      • Importer Template
    • SOFTWARE
      • About EUDAMED Software
      • EudaMed+ UDI Submission Tool
      • EudaMed SaaS UDI Submission Tool
      • EudaMed SaaS 100 UDI DI’s
      • EudaMed SaaS 300 UDI DI’s
      • EUDAMED UDI DI Bulk Search Service
      • EUDAMED UDI DI, SRN & Basic UDI Search Tool
  • Resources
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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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