European Medicines Agency (EMA) updated the page Clinical Trials Information System (CTIS): online modular training program on January 31, 2022, by adding new and updated documents in Modules 03 – User Access Management:
- Step-by-step guide: User access management – Module 03 (v1.0): It includes step-by-step guidance for sponsor users for obtaining user credentials to access CTIS, logging into the system, managing the user profile, and requesting a role
- Instructor’s guide: User access management – Module 03 (v1.1): It includes steps to organize a webinar for understanding the process of self-registration, CTIS landing page, managing user profile, and roles and permissions
- Quick guide: User access management – Module 03 (v1.2): Updated by adding detailed guidance for sections related to self-registration, steps to log-in and log-out, introduction to CTIS landing page, managing user profile, and roles and permissions that the users can be assigned in CTIS
For more information, please click here.