February 2022: CTIS Training Update

European Medicines Agency (EMA) updated the page Clinical Trials Information System (CTIS): online modular training program on February 03, 2022, by adding the below documents in Modules 07 – Management of Registered Users and Role Matrix:

  1.  Member states (MS) business processes and roles – Module 07: It explains in detail the roles within the CTIS MS workspace. It provides an overview of MS CT processes and summarizes permissions/tasks by role and process with diagrams for a better understanding
  2.  Roles and permissions matrix summary – Authority workspace – Module 07: It defines roles and permission, types of permissions, the concept of saving, sharing, and submitting in the authority workspace. It also provides information on the roles of the Member States and the European Commission
  3. Notices and alerts per role – Module 07: It provides a list of notices and alerts for each role in CTIS
  4.  Sponsors business processes and roles – Module 07: It explains in detail the roles within the CTIS sponsor workspace. It provides an overview of sponsor CT processes and summarizes permissions/tasks by role and process with diagrams for a better understanding
  5. Roles and permissions matrix summary – Sponsors workspace – Module 07: It defines roles and permission, types of permissions, the concept of saving, sharing, and submitting in the sponsor workspace. It also provides information on sponsor roles

For more information, please click here.