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Clinical Trials Information System (CTIS): training programme


In order to prepare for the implementation of the new Clinical Trials Regulation, the State Agency of Medicines  of Latvia is inviting Clinical Trial sponsors to apply for Clinical Trials Information System (CTIS) training programme organized by the European Medicines Agency (EMA).

Training is available from EMA on how to use the 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.

Read more:here.