Training
Training and supporting materials are available from the European Medicines Agency (EMA) on how to use the Clinical Trials Information System (CTIS). 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 are using the system.
Training materials for sponsors
Training and support materials for clinical trial sponsors and other organisations involved in running clinical trials are available on EMA’s website. They include:
- a handbook for clinical trial sponsors on how to use CTIS.
- reference materials for sponsors to help them set up their business processes in the system as well as practical guidance on how to work in CTIS;
Online training modules for authorities
Online training modules for authorities covering the applicable stages of a clinical trial are available on EMA’s website.
Support


