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

, -

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.

Documents

Video recording

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