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Interested stakeholders may express their interest in becoming a member of the Multi-stakeholder platform Advisory Group by 24 November 2023.
EMA revised rules to give faster access to information in the EU Clinical Trials Information System (CTIS).
The summary report has been published as an outcome of the first ACT EU MSP workshop held in June 2023.
A workshop report outlines proposed actions for improved clinical trials in the EU during public health emergencies.
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).
