Clinical Trials Information System (CTIS): Information day

The European Medicines Agency (EMA) is organising this webinar to provide an in-depth overview of the Clinical Trials Information System (CTIS), its optimisations, best practices, and upcoming developments.

• Date:
  Thursday, 22 May 2025, 12:30 - 17:30 Amsterdam time (CEST)
• Location:
  Online
  European Medicines Agency, Amsterdam, the Netherlands
  Live broadcast

Event summary

Since its launch on 31 January 2022, CTIS has undergone significant updates to enhance its functionality and improve user experience. This webinar aims to:

• Provide insights into the current of CTIS and an overview of implemented optimisations;
• Feedback on progress on CTIS and CTCG/CTAG guidance;
• Highlight key support initiatives and tips to help users navigate CTIS effectively, and discuss upcoming developments aimed at enhancing system functionality, user experience, and planned developments.

This EMA-hosted webinar is open to all sponsor organisations, including pharmaceutical companies, contract research organisations (CROs), small and medium-sized enterprises (SMEs), and academic institutions.

No certificates of attendance will be issued for this event.

Presentations from various sessions will be available on this webpage after the event.

Documents

Agenda - Clinical Trials Information System (CTIS): Information day (22/05/2025)

Live broadcast - 12:30 - 17:30 (CET)

 
A video recording will be available on this webpage afterward. The processing and publication of the video recording may take up to 60 days.

Participation via Slido

We encourage event participants to use Slido and to submit questions in advance of the webinar (use code: #CTISInfo2025). 

The most popular questions submitted in advance of the event will be answered by speakers during the panel session.

Please provide your questions between 6 April 2025 and 7 May 2025 at 12:00.

Attendees are invited to fill out a short feedback survey via Slido that will be available after the event.