EMA Clinical Trials Information System (CTIS)
As of January 2022, only 9 months from now, all scientific research with
medicinal products in the EU need to be submitted via the Clinical
Trial Information System, the CTIS. To make sure all future users of the
CTIS system, both sponsors and member states, are familiar with the
settings and way-of-working in the system, the EMA has setup a training
program.