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Challenges and possible options when designing a Platform Trial - F. Houyez (EURORDIS)
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Challenges in performing mult-country Investigator Initiated Trials in EU - M. Zuidgeest (UMC Utrecht)
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CTA review process and CTR implementation - L. Leyens (EFPIA)
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Enabling CTIS Public Data Use - F. Sweeney (CDDF)
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Enhancing and harmonizing Regulatory process for clinical trials- M. Heath (Vaccines Europe)
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Innovative Study Designs in Paediatrics - D. Bonifazi (TEDDY)
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Limited Scientific advice for academic developers - D. Coppens (KWF)
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Low-intervention clinical trials - S. Kromar (EORTC)
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Paediatric patients involvement in the drug development - B. Nafria (eYPAGnet)
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Presentation of ACT EU workplan and deliverables - A. Zanoletty (EMA), L. Pioppo (EMA)
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This document outlines the 2024-2026 meeting dates for the MSP Advisory group and the MSP annual meetings.
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