The EU Clinical Trials Information System (CTIS) will be operational by December 2021, creating a single portal for #clinicaltrial management across all Member states.

The CTIS will “increase the efficiency of all trials in Europe with the greatest benefit for those conducted in multiple Member States. It aims to foster innovation and research, while helping avoid unnecessary duplication of clinical trials or repetition of unsuccessful trials.

The key benefits include:

1. harmonised electronic submission and assessment process for clinical trials conducted in multiple Member States;
2. improved collaboration, information-sharing and decision-making between and within Member States;
3. increased transparency of information on clinical trials;
highest standards of safety for all participants in EU clinical trials.

Link to more detail here: https://lnkd.in/g9rEaQ5