CTTM02_Guide on CTIS common features
Roles and permissions summary - Sponsor workspace
Clinical Trials Regulation
EMA CTIS New Module & Updated docs made available today
CTTM10_Instructor guide
Interview met Marieke Meulemans, directeur GCP Central en lid EMA CTIS Training Expert Group - Dutch Clinical Research Foundation
CTTM05 - Step-by-step guide
EMA Clinical Trial Information System Summary Status - Acron
EMA Clinical Trial Information System - Sponsor user training programme
Guidance and Q&As - EMA
Guide to CTIS Training Catalogue
CTIS – M10 How to submit an initial CTA in the CTIS – Fill in the Form and the MSC sections. - YouTube
Introduction to CTIS for public users CTIS Training Programme – Module 22
EU Clinical Trials Regulation (EU-CTR) enters application on 31 January 2022
Six-month countdown to go-live for the Clinical Trials Information System ( CTIS)
CTTM03 - Quick Guide
Ontwikkeling CTIS Training Materiaal - update november 2020 - Acron
Training Archives | Ivowen Regulatory Affairs Specialists
The guide to the Clinical Trials Information System (CTIS)
The guide to the Clinical Trials Information System (CTIS)
Understanding the New EU Clinical Trials Regulation (2022)
CTIS - M02 CTIS Technical Environment - YouTube
EU Clinical Trial Regulation & the Clinical Trial Information System
