Clinical Trials Information System (CTIS) webinar: Six months of CTIS and looking forward

Table of contents

Date: 01/07/2021
Location: Online, 09:30-13:30 Amsterdam time (CEST)

Event summary

Clinical Trials Information System (CTIS) acts as the single-entry point for clinical trials authorisation and supervision in the EEA. CTIS was created as part of the EU Clinical Trials Regulation (Regulation (EU) No 536/2014).

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

Topics presented during the webinar include 

  • system usage metrics, 
  • member state and sponsor experience and reflections
  • user support feedback, and 
  • training environment.

No certificates of attendance will be issued for this event.

We encourage event participants to submit questions related to sponsor preparedness in advance of the webinar (use code:#info22). The most popular questions submitted in advance of the event will be answered by speakers during the panel session. Please provide your questions by 24 June 2022

The event will be broadcast live. 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 Highlights newsletter for updates on the availability of CTIS event video recordings.

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


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