EUDAMED – European Database for Medical Devices

EUDAMED is an upcoming part of the newly enforce European (EU) Regulations 2017/745. EUDAMED database will be a transparent system aiming at coordinating information regarding medical devices available in the EU market. EU Commission in co-ordination with MDCG is currently working on the database planning, creation, and implementation. The new MDR based requirements will be imposed once EUDAMED becomes fully function in the market.
Please find our blog discussing upcoming information on MDR EUDAMED.

EU MDR 2017/745

The European Economic Area (EEA), inclusive of the European Union (EU) and European Free Trade Association (EFTA), has been contemplated as one of the largest global medical device markets. The obvious aspiration for device manufacturers is gaining an approval and maintaining access to this important market. It requires abiding by the regulatory changes to assure…