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The ACT EU workplan for 2026-2027 outlines the initiative's revised objectives and areas of focus, informed by feedback from stakeholders.
Following consultation with the Multi-stakeholder platform Advisory Group, new documents have been published to support sponsors in the implementation of the Clinical Trials Regulation (CTR).
The ACT EU workplan for 2025-2026 outlines the initiative's areas of focus, which reflect feedback from stakeholders.
ACT EU has published two new webpages with information of interest to the network and clinical trial stakeholders.
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.
