Medical Device Software in Europe: Get Ready with TÜV Italia Akademie
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Learn more about essential regulatory requirements by joining our online course on February 28th!
What you will learn:
- ️How to classify standalone and embedded software according to MDR and IVDR.
- ️Key concepts of risk management, clinical assessment and cybersecurity.
- ️Best practices for software lifecycle management (IEC 62304 and IEC 82304-1).
- ️How to prepare a complete Technical File to ensure compliance.
This course is designed for anyone who wants to gain a solid understanding of European regulations for medical device software, with the aim of ensuring compliance and enhancing their professional skills.