Your online EU CTR course
Your online EU CTR course on your tablet
EU CTR course on the go
Our all inclusive EU CTR Expert course for clinical drug trials in Europe helps you understand all the vital aspects of the EU CTR regulation. You’ll learn all strategic elements, from study design, to submission, to clinical conduct in our course, making you the EU CTR expert. This course teaches you everything you need to know about this new regulation, and you’ll walk away with a complete deep dive into EU CTR regulation.
The e-learning EU CTR Expert is intended for everyone who is responsible for product development and management, drug research design and / or strategic decisions. The e-learning offers a comprehensive insight into working according to the requirements of the new European legislation for clinical drug research, the EU CTR. The e-learning is perfect for research and science coordinators, principal investigators (Investigator initiated research), Sponsors, Medical Directors, Head of ClinOps, Study Directors, Project Managers, CRAs, Monitors and people responsible for submitting dossiers.