EMA – CTIS: Update of training materials

EMA provides an online modular training programme to help clinical trial sponsors, national competent authorities, ethics committees, European Commission and EMA staff use the Clinical Trials Information System (CTIS). The programme contains modules and audience-targeted materials covering all clinical trial lifecycle stages, from submission through authorisation to supervision. The EMA published updated version of the following CTIS training materials: Clinical Trials Information System (CT...