From 31 January 2023 all clinical trials with medicines must be authorised, handled and reported according to the rules lined out in the Regulation EU No 536/2014 (Clinical Trials Regulation).

IFAPP offers you a free 2-day virtual training programme that will explain what you need to understand about the new processes, procedures and obligations of parties involved for updating your regulatory knowledge and for the preparation and conduct of your clinical trials in the EU. And the workshop will give you ample opportunities to ask your questions and discuss your concerns with experts in the fields.