Dokumenty (168)
RSSZobrazujú sa výsledky 20 až 40
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
Hlavné témy
ACT EU workshop on paediatric clinical trials report
Report to monitor the European clinical trials environment (July - September 2025)
Hlavné témy
EU clinical trials during the 3 year CTR transition period
Core Dossier - opportunities for increasing efficiency and future proofing the CT ecosystem in Europe - M.OKane (EFPIA)
Update on EU clinical trials metrics - L.Pioppo (EMA)
Update on policy development at the EU level - E.Szepessy (EC)
Pre-read - Update on ACT EU progress - L.Pioppo (EMA)
Cross-border clinical trials and arrangements to take part in a trial abroad - F.Houyez (EURORODIS) - I.Klingmann (EFGCP)
Proposals on content for ACT EU Clinical trials curriculum - A.Michon (ECRIN)
PA11 Regulatory flexibility for CTs during Public health - G.Capone (EMA) - C.Mihaescu (EMA)
Reducing review timelines to 60 days - enhancing competitiveness through faster CTA approval - Blanca Garcia Ochoa (EuropaBio)
