Our webinar series “Practical guidance on EU CTR and CTIS” for clinical trials in Europe help you learn the most crucial information of the EU CTR and its innovations as well as the main preparatory steps to use CTIS portal. You will get practical expert advice starting from the preparation of clinical trial documents for submission, the submission process and its timelines as well as submission of substantial amendments, communication between sponsor, investigators and Member States during the study and notification of study closure. The smooth transition from trials conducted according to the former Directive will be another main topic, enabling you to run the process in the most effective way.