For more information on CTIS, see Clinical Trial Regulation.
This is the first day of a two-part webinar. It will cover:
- Overview of CTIS
- User access management, including how to register users
- Sponsor user management
- Sponsor roles and permissions in CTIS
Presentations are provided by EMA system experts and presenters from SME and academic institutions. These will be complemented by pre-recorded demonstrations of the system.
The second day of the webinar is on 4 March 2021. EMA advises participants to attend both days of this training webinar.
The webinar is free of charge for all attendees.