Deep dive into preparing and submitting submission packages with our EU CTR Submission e-learning course, as well as the fundamentals of the new EU CTR regulation. Bring your strategies, roles, dossier contents, patient information and study feasibility, plus other important changes in line with the new regulation, as well as learning the fundamentals of the EU CTR.

• 5 hours
• 3 modules (Introduction, preparing for a submission, submitting and assessing)
• Knowledge test with 30 questions and 3 attempts
• Available in Dutch and English
• Accreditation 
• Focussed on clinical research in Europe
• Online EU CTR certificate with a testscore of 80 or higher

The e-learning EU CTR Submission is intended for everyone in Europe involved in the design, preparation and submission of clinical drug research dossiers. The e-learning offers a complete overview of the impact of the new regulation on the submission of dossiers in for medical-ethical review. The e-learning is perfect for start-up specialists, start-up departments in drug companies and CROs and research coordinators in hospitals responsible for submission of dossiers.

Are you involved in clinical drug trials in the Netherlands? See our EU CTR in the Netherlands courses