Documents (178)
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MSP AG report on the most frequently reported and major issues
Report to monitor the European clinical trials environment (1-30 September 2024)
Member States participating in ACT EU pilots on consolidated advice
Agenda MSP Advisory Group meeting 27 September 2024
Meeting highlights - MSP Advisory Group 4 July 2024
Report to monitor the European clinical trials environment (1-31 August 2024)
Report to monitor the European clinical trials environment (1-31 July 2024)
Report to monitor the European clinical trials environment (1-30 June 2024)
Challenges and possible options when designing a Platform Trial - F. Houyez (EURORDIS)
Challenges and possible options when designing a Platform Trial - F. Houyez (EURORDIS)
Challenges in performing mult-country Investigator Initiated Trials in EU - M. Zuidgeest (UMC Utrecht)
Challenges in performing mult-country Investigator Initiated Trials in EU - M. Zuidgeest (UMC Utrecht)
CTA review process and CTR implementation - L. Leyens (EFPIA)
CTA review process and CTR implementation - L. Leyens (EFPIA)
Enabling CTIS Public Data Use - F. Sweeney (CDDF)
Enabling CTIS Public Data Use - F. Sweeney (CDDF)
Enhancing and harmonizing Regulatory process for clinical trials- M. Heath (Vaccines Europe)
Enhancing and harmonizing Regulatory process for clinical trials- M. Heath (Vaccines Europe)
Innovative Study Designs in Paediatrics - D. Bonifazi (TEDDY)
Innovative Study Designs in Paediatrics - D. Bonifazi (TEDDY)
Limited Scientific advice for academic developers - D. Coppens (KWF)
Limited Scientific advice for academic developers - D. Coppens (KWF)
Low-intervention clinical trials - S. Kromar (EORTC)
Low-intervention clinical trials - S. Kromar (EORTC)
Paediatric patients involvement in the drug development - B. Nafria (eYPAGnet)
Paediatric patients involvement in the drug development - B. Nafria (eYPAGnet)
Presentation of ACT EU workplan and deliverables - L. Pioppo (EMA)
Presentation of ACT EU workplan and deliverables - A. Zanoletty (EMA), L. Pioppo (EMA)
Report on the 2023 survey on the implementation of the Clinical Trials Regulation
MSP Advisory Group Agenda 04 July 2024
