Date
- Monday, 22 February 2021, All day
Location
- OnlineEuropean Medicines Agency, Amsterdam, the Netherlands
Event summary
This training webinar provides essential information on CTIS for micro, small and medium-sized enterprises (SMEs) and non-commercial (academic) sponsors. 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, European Commission, 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.