Clinical Trials Information System (CTIS) Bitesize talk: Redesign of the CTIS training material for sponsor users, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 9 July 2025, 15:30 (CEST) to 9 July 2025, 17:00 (CEST)
CTIS is the business tool of the EU Clinical Trials Regulation (Regulation (EU) No 536/2014) and it acts as a single entry point for clinical trial authorisation and supervision in the European Union (EU) and the European Economic Area (EEA).
This CTIS Bitesize Talk presents an opportunity to become acquainted with the revised Sponsor Handbook, which will serve as the definitive reference for sponsor users operating within CTIS. Effective 9 July, it will supersede the existing sponsor training modules.
The event is open to all sponsor organisations, including pharmaceutical companies, contract research organisations, small and medium-sized enterprises (SMEs) and academic organisations. EMA cannot provide attendees certificates of attendance for this event.
To be better prepared for this event, sponsors are encouraged to have a quick look at the current:
A video recording is made available after the event. Processing and publication of the video recording typically take up to 60 days. Please subscribe to the clinical trials newsletter for updates on the availability of CTIS event video recordings.
