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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).
500 authorised multinational clinical trials to be added over five years
COMBINE “all-in-one” coordinated assessment pilot: call open for expressions of interest until 31 August 2025.
Designation facilitates data sharing, promotes transparency and trust in clinical research
Patients can locate trials for potential enrolment in their area
The report from the annual Multi-stakeholder platform meeting in October 2024 is now available.
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 revised ICH guideline on good clinical practice (principles and Annex 1) have been published.
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.
