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  • Home
  • Shop
    • EUDAMED Training Self-paced
    • EUDAMED Training 25th/26th January 2022
    • EudaMed+
    • EudaMed SaaS
    • EudaMed SaaS 100 UDI DI’s
    • EudaMed SaaS 300 UDI DI’s
    • EudaMed (25 Incident)      Support Package
    • EUDAMED Company Registration and User Management
    • MDR Template Package
    • IVDR Template Package
    • Authorised Representative Template
    • Distributor Template
    • Importer Template
  • Training
    • Eudamed Training Overview
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    • EUDAMED DI Generator
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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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