Filter by
News (9)
RSS
The Clinical Trials Information System now supports submission, assessment and oversight of all trials in the EU
The ACT EU workplan for 2025-2026 outlines the initiative's areas of focus, which reflect feedback from stakeholders.
The enhanced portal aims to benefit the public by making it easier to search for publicly available information on clinical trials in the EU and EEA.
Revised rules for Clinical Trials Information System (CTIS) become applicable.
Pilots are part of ACT EU collaboration to foster high-quality clinical research in the EU.
The revised transparency rules for the Clinical Trials Information System (CTIS) will become applicable on 18 June 2024, with the launch of a new version of the CTIS public portal.
All ongoing clinical trials in the EU must be transitioned to the Clinical Trials Information System (CTIS) by 31 January 2025.
EMA revised rules to give faster access to information in the EU Clinical Trials Information System (CTIS).
EMA has opened a public consultation to review the transparency rules for the publication of information on clinical trials submitted through the Clinical Trials Information System (CTIS) in the European Union (EU).
