Clinical Trials Information System (CTIS): training programme

11th February 2021

Training is available from the European Medicines Agency (EMA) on how to use the Clinical Trials Information System (CTIS) ahead of its planned launch. EMA’s training resources are tailored for clinical trial sponsors and staff of the European Union (EU) Member States, European Commission and other organisations who will use the system. 

The training materials aim to help users comply with their obligations under the Clinical Trial Regulation (Regulation (EU) No 536/2014), which apply once the CTIS goes live.

More information on the CTIS and the Clinical Trial Regulation is available on Clinical Trial Regulation.

Click here to access training material

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