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UDI/EUDAMED: Processes, modules, and practical requirements

This course is dedicated to the practical management of UDI requirements and the use of EUDAMED, with a focus on processes, modules, and information flows required by the MDR.

This course belongs to the “Regulatory core” line: Core regulatory expertise in the MD field.

Contact our team if you would like a complete training package covering all related topics, or to request a tailored solution.

Abstract

This course is dedicated to the practical management of UDI requirements and the use of EUDAMED, with a focus on processes, modules, and information flows required by the MDR. Through examples and hands-on simulations, it provides concrete guidance to prevent common errors and ensure proper device traceability.

Key Points

  • UDI requirements (MDR)

  • EUDAMED modules and processes

  • UDI/EUDAMED information flows

  • Device traceability and common pitfalls

Structure

8-hour course.

Live streaming or on-site at your company, based on your needs.

 

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