![[News from ACT EU] – Clinical Trials Information System (CTIS): training and support](https://cddf.org/wp-content/uploads/2026/04/Copy-of-PUBLICATION-Annual-Repport-2024-Is-available-4-1080x675.jpg)
Interim Report: ACT EU pilots on consolidated scientific and regulatory advice
The interim results from the ACT EU pilots on consolidated scientific and regulatory advice have been published and available to stakeholders. These pilots were launched to offer harmonised advice on how to improve the quality of applications for clinical trials and...
ACT EU: MSP AG – Call for Expressions of Interest
📢 🔔Take a look at the below ‘Call for Expressions of Interest’ from the Multi-stakeholder Platform Advisory Group (MSP AG) under ACT EU: ▶️ Message from ACT EU: MSP AG “Call for Expression of Interest – Focus Group on the review of the Guideline for...
ACT EU:Workshop on the Use of External Controls for Evidence Generation in Regulatory Decision-Making
ACT EU is pleased to announce a hybrid workshop on 3 November 2025: “Workshop on the Use of External Controls for Evidence Generation in Regulatory Decision-Making” Registration: Please register via the ACT EU website here: Workshop Registration The Methodology...
Upcoming ACT EU Multi-Stakeholder Platform Advisory Group in June
Upcoming ACT EU Multi-Stakeholder Platform Advisory Group in June The Multi-stakeholder Platform Advisory Group (MSP Advisory Group) forms part of the ACT EU multi-stakeholder platform (ACT EU MSP), which aims to provide regulators and stakeholders with a...