Learn how to ensure EU-CTR compliance

Our panel of industry experts will present practical scenarios and discuss the implications of substantial modification (SM) submissions, to explore best future practices for navigating EU-CTR compliance. 

If your company has challenges or queries about next steps for transitioned trials, CTIS system alignment or first SM content, please use this opportunity to connect with our experts. Share your questions ahead of time (via the registration form) – or ask “live” during the event!