Clinical Trials Information System (CTIS): online training modules

EMA provides an online modular training programme to help clinical trial sponsors, national competent authorities, ethics committees, European Commission and EMA staff use the Clinical Trials Information System (CTIS). The programme contains modules and audience-targeted materials covering all clinical trial lifecycle stages, from submission through authorisation to supervision. 

The online training modules are all available on this page. EMA regularly updates and enhances its training materials. 

Please consult the documents below for:

  • a full catalogue of available training modules, organised by clinical trial lifecycle stage;
  • the latest new or updated training materials;
  • technical system requirements for the best experience with using CTIS. 

Users can provide feedback to help EMA enhance its CTIS training materials, by completing a short survey, at any time:

Introduction to CTIS

Sponsor workspace

Common functionalities for all registered users

Authority workspace

Searching CTIS as a public user

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