Date

Thursday, 20 June 2024, 15:30 (CEST) - 17:00 (CEST)

Location

European Medicines Agency, Amsterdam, the Netherlands
Live broadcast

Event summary

CTIS is the business tool of the EU Clinical Trials Regulation (Regulation (EU) No 536/2014) and acts as a single entry point for clinical trial authorisation and supervision in the European Union (EU) and the European Economic Area. 

This bitesize talk provides an opportunity for sponsors to familiarize themselves with the revised transparency rules that will become applicable on 18 June 2024. Furthermore, sponsors will also be able to familiarize themselves with the new CTIS Public portal, that will be live as of 18 June. 

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 consult the CTIS training and support materials:

Please note that the training material is currently being updated and will be made available shortly before the event.

Live participation via Slido

We encourage event participants to submit questions related to sponsor preparedness in advance of the webinar (use code: #bt20jun). The most popular questions submitted in advance of the event will be answered by speakers during the panel session. Please provide your questions by 13 June 2024, noon.

Live broadcast

 

You should see the live broadcast on pressing the 'play' icon in the video window, or a message stating that the event has not started yet.

To optimise video quality, once the video is playing we recommend clicking on the ‘Wheel’ symbol in the video window then selecting the Quality Option up to 1080p.

If the video window is blank, or if you experience other difficulties viewing the broadcast, please try connecting directly to the EMA's Vimeo Channel 1.

For technical information about the required network security settings, please see this Vimeo help page.

For further assistance, please consult the EMA Service desk.


A video recording will be 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.

 

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