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Clinical Trial Regulation

The way clinical trials are conducted in the European Union (EU) will undergo a major change when the Clinical Trial Regulation comes into operation in 2018. The Regulation harmonises the assessment and supervision processes for clinical trials throughout the EU, via an EU portal and database. The European Medicines Agency (EMA) will set up and maintain the portal and database, in collaboration with the Member States and the European Commission.

Click on this link for more information.

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