Manufacturers and other stakeholders are invited to take part in the training on the European Medical Device Nomenclature organised by the SMEMDN consortium, which will take place on 4 June 2026.
The European Medical Device Nomenclature (EMDN) plays an increasingly important role in the regulatory framework for medical devices in Europe. In particular, it supports registration in EUDAMED (European Database on Medical Devices), certification activities, market surveillance and the development of data-driven policies.
On 4 June 2026, the SMEMDN consortium will hold a third EMDN training event for manufacturers and other stakeholders.
This event will bring together representatives from the competent authorities, notified bodies and industry to share experiences, challenges and best practices in the use of EMDN.
The programme will cover both regulatory and operational aspects, with particular emphasis on practical experience and real-life case studies.
Themes
• Case studies on the allocation of EMDN codes.
• Key points for manufacturers and Persons Responsible for Regulatory Compliance (PRRC).
• Impact on certification, consistency and data quality.
• Feedback on data governance and data classification.
Practical information
• Date: 4 June 2026
• Time: 10:00 - 16:00
• Venue: Trieste (Italy) - online participation possible
• Target audience: manufacturers and other stakeholders
• Programme
• Language: English
• Register using this link.