IMPORTANT MESSAGE FROM ACT EU
All clinical trials expected to continue beyond 30 January 2025 must be transitioned to the EU Clinical Trials Regulation (CTR) via the Clinical Trials Information System (CTIS). This date marks the end of a three-year transition period that began when the CTR became...
Update from ACT EU: ACT EU Helpdesk For Non-Commercial Sponsors
[ 💡 🔔 Updates from ACT EU: ACT EU Helpdesk For Non-Commercial Sponsors] ACT EU has established a dedicated helpdesk, which employs different measures to support non-commercial sponsors in navigating the clinical trial landscape in the EU. Currently, the...
ACT EU: ACT EU Helpdesk For Non-Commercial Sponsors
ACT EU: Stakeholder Presentation on Critical Use-Cases at MSP Advisory Group Meeting (4 July 2024)
On 4 July 2024, CDDF participated in a stakeholder presentation focused on critical use-cases at Multi-Stakeholder Platform (MSP) Advisory Group meeting. The session aimed to identify and discuss real-world challenges faced by stakeholder groups within the European...