Roles and permissions matrix summary - Authority workspace - CTIS Training Programme - Module 07

Step-by-step guide: How to respond to requests for information received during the evaluation of a Clinical Trial Application - CTIS Training Programme - Module 11

Step-by-step guide : Create, submit and withdraw a clinical trial application and nonsubstantial modifications - CTIS Training Programme - Module 10

Checklist of required fields per application type - CTIS Training Programme - Module 10

Clinical Trials Information System (CTIS) common features - CTIS Training Programme - Module 02

EMEA-003376-PIP01-22

Industry Update webinar on Regulatory Procedure Management for Product Lifecycle Management on IRIS, Online, European Medicines Agency, Amsterdam, the Netherlands, from 13 June 2024, 10:00 (CEST) to 13 June 2024, 11:30 (CEST)

EMEA-003374-PIP01-22

EMEA-003373-PIP01-22

EMEA-003372-PIP01-22