The BioMed Alliance, together with the European Society of Cardiology (ESC) and the European Federation of National Associations of Orthopaedics and Traumatology (EFORT), are organising a Joint Workshop on Medical Device Registries on 17 June in Brussels. 

As the EU prepares to implement the new Medical Devices Regulation in May 2020, the workshop will aim to explore what role clinical registries may play in informing regulators’ market surveillance activities, and to identify a possible “common framework” for EU registries responding to the needs of regulators, patients, physicians and industry alike. 

The event will bring together key experts in data collection, review and management, including European Commission officials, healthcare professionals, regulators and industry representatives. 

For more information, please find the programme here.

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