The CE mark signifies that products sold in the European Economic Area have been assessed to meet high safety, health, and environmental protection requirements. The mark is the medical device manufacturer’s claim that a product meets the essential requirements of all relevant European Medical Device Directives.

Oxford’s Medical CE Marking Forum aims to bring interested parties from academia and industry in Oxford together to discuss CE marking related issues and to learn from each other.

The forum is open to anyone who is interested in CE marking. A case study will be presented by Dr Toni Day from OrganOx during this session.