Fundamental ECTR Course to Submit Clinical Drug Trials in Europe

Deep dive into preparing and submitting submission packages with our Fundamental ECTR Course to Submit Clinical Drug Trials in Europe e-learning course, as well as the fundamentals of the new ECTR 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 ECTR.

• 5,5 hours
• 3 Learning Modules
• Online ECTR certificate
• Knowledge Test
• Available on desktop, smartphone or tablet. 
• Accredited in the Netherlands: GAIA and NVFG 5 CPE points

The e-learning Fundamental ECTR Course to Submit Clinical Drug Trials in Europe is intended for everyone 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.