Accessing EudraCT v.8

Access to EudraCTEudraCT (European Union Drug Regulating Authorities Clinical Trials) is the European Clinical Trials Database of all interventional clinical trials of medicinal products commencing in the European Union from 1 May 2004 onwards. The EudraCT database has been established in accordance with Directive 2001/20/EC.

To access EudraCT the following is applies:

For unregistered roles, access to the Internet.
For registered roles, registration for the role for NCANational Competent Authority employees through your NCA responsible contact or, for EMAEuropean Medicines Agency users, using the EMA service desk portal: https://servicedesk.ema.europa.eu.
Third country data provider users are normally registered at the time of a PIP application. If you need another person in your organisation to carry out the task of the third country data provider in relation to EudraCT, submit a signed letter to the EMA Service desk requesting authorisation of a person to upload third country clinical trial information to EudraCT. Please Note: The third country data provider role encompasses two roles, namely the PIP addressee and the Article 46 data provider.
For results users you must be registered in the Eudra Common Directory (ECD).