Documents

Report to monitor the European clinical trials environment (January - March 2026)

ACT EU multi-annual workplan 2026-2027

Helpdesk for non-commercial sponsors: 15-month report

Executive summary of ACT EU matrix meeting 1 October 2025

Recommendations by the Coalition for Reducing Bureaucracy in Clinical Trials_R. Doeswijk (EHA)

eConsent initiative_H.Vanaken (EFGCP)

Framework for shared patient input in a specific indication across products_F.Houyez (EURORDIS)

Update on FAST-EU (Facilitating and Accelerating_M.Lunzer (CTCG , AGES)

Pre-CTA and SAWP-CTCG pilots_B.Garcia-Ochoa (EuropaBio)

EU model template for “Clinical site agreements” between sponsors and clinical sites_M.Matei (ECRIN)

Consolidated pilots in clinical trials-status update_M.Sarra (EMA)

Clinical Research Investment Plan_Romina Escobar (EC, DG RTD)

Update on MedEthicsEU_M.Al (MedEthicsEU)

Update on CTR Collaborate_M.Lunzer_M.Al (CTR Collaborate)

Consolidated advice pilots interim report - March 2026

ACT EU roadmap of clinical trial methodology guidance

Agenda MSP Advisory Group meeting 20 March 2026

Report to monitor the European clinical trials environment (October - December 2025)

Helpdesk for non-commercial sponsors: 6-month report

Meeting highlights MSP Advisory Group 18 September 2025