|Date & Time||29 November 2021 at 09:00-13:15 CEST|
We would like to inform you that the European Medicines Agency is organising a Webinar for SMEs and Academia on the Clinical Trial Regulation (Regulation (EU) No 536/2014) and the Clinical Trials Information System (CTIS) that will take place on Monday, 29 November 2021 from 09:00 to 13:15 (timing to be confirmed).
The webinar is being organised as a training event and will present:
- an overview of the Clinical Trials Regulation
- an introduction to the new process for submitting clinical trial information in the European Union/European Economic Area
- functionalities of CTIS, including transparency aspects and safety reporting requirements
- guidance and training material available for sponsors
The draft agenda can be found here.
Attendance at the webinar is by registration only and open to companies that have been assigned SME status by EMA, academia and representatives of stakeholder organisations. There is no registration fee for this event.
If you wish to register for this webinar, please click here by 8 October 2021, e.o.b. (registration deadline). Presentations will be published on the EMA website shortly before the event. Recordings of the event will be available on the EMA website in the weeks after the event.
For any questions in relation to this event, please contact firstname.lastname@example.org.