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Documents (157)
RSSTiek rādīts(i) 1 līdz 20 rezultāti
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
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ACT EU workshop on paediatric clinical trials report
Report to monitor the European clinical trials environment (July - September 2025)
