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European Union

Welcome to EudraCT

EudraCT is a database of all clinical trials which commenced in the Community from 1 May 2004, and also includes clinical trials linked to European paediatric drug development.

The following tasks can be performed from this page:

Create a EudraCT number

Before any functionality of EudraCT can be used for a given clinical trial, a EudraCT number must be created in order to provide a unique reference for that trial.

Protocol-related information

Sponsors can:

  • Create, save XML/PDF files of clinical trial applications locally.
  • Load locally saved clinical trial applications to complete, validate, compare, or to prepare a package for submission to a National Competent Authority.

Third country data providers can:

  • Create, save XML/PDF files of third country files locally.
  • Create and post third country files to the EudraCT database.
  • Load locally saved third country files to complete, validate or post to the EudraCT database. To post third country files you will need to be registered as a third country data provider and log in.

    Contact:EMA Service Desk portal telephone: (+31) (0) 88781 6000

Result-related information

To use result related functionality you will need to be registered as a results user, and log in.

Results users can:

  • Create, update, validate and post result data sets, and load summary attachments to the EudraCT database.
  • Save locally XML/PDF files of result data sets.
  • Load locally saved result data sets to update, validate, or to post to the EudraCT database.

As of 1.2.2020, the UK is no longer an EU Member State. However, EU law still applies to the UK during the transition period

Application hosted on behalf of the European Commission http://ec.europa.eu

For technical support, visit the EMA Service Desk portal: https://servicedesk.ema.europa.eu

Domenico Scarlattilaan 6, 1083 HS Amsterdam, The Netherlands