EudraCT (European Union Drug Regulating Authorities Clinical Trials Database) is the database for all interventional clinical trials on medicinal products that were conducted in the European Union (EU)/European Economic Area (EEA) between 1 May 2004 and 30 January 2025 under Directive 2001/20/EC, as well as for all trials conducted outside of the EEA that are part of a Paediatric Investigation Plan (PIP) and/or are conducted under Article 45 or 46 of Regulation (EC) No 1901/2006. As of 31 January 2025, the conduction of trials in the EU/EEA is no longer allowed under Directive 2001/20/EC and should be performed under Regulation (EU) 536/2014 only. Submissions of new clinical trial applications must be performed through the Clinical Trials Information Systemas well as submissions of modifications of existing CTIS applications. EMA Website