EU CTR Expert Course
For Sponsors, CROs and Freelancers
- Interactive eLearning
- approx. 6.5 h
- Certificate of Attendance
Intense training on EU Clinical Trials Regulation
Our expert training on the EU regulation "Clinical Trials Regulation" (EU CTR, also EU Regulation No. 536/2014) supports you in understanding all important aspects of the new regulation. The online e-learning takes you from the study design to the clinical trial application and the actual execution of the clinical trial, thereby providing you with in-depth knowledge. In our course, you will learn what you need to know about the EU CTR in order to be well equipped for the preparation and conduct of a clinical trial under the new law.
Our online e-learning "EU CTR Expert" is aimed at all employees of sponsors and CROs, freelancers and academic sponsors who want to conduct clinical trials with medicinal products in accordance with the new EU regulation "EU CTR". Since 31 January 2023, the submission of new clinical drug trials under the EU CTR is mandatory!
eLearning on smartphone, tablet or PC in self-selected stages!
Our interactive course can be started, interrupted and resumed anytime, anywhere. Learn at your own pace! Please note that this e-learning is only available in English.
The modular structure and the associated division into content chapters enable an individual learning experience.
- Module 1: Basis
- Module 2: Preparing for a submission
- Module 3: Submitting and assessing
- Module 4: During and after the study
Who is this course for?
- For employees of sponsors, CROs or freelancers
- For all functions at Sponsor or CRO that deal with regulatory affairs, clinical operations, project management, clinical monitoring and related tasks