CoMeCT Workshop - Breaking Barriers Streamlined Approvals for Multi Arm, Adaptive Clinical Trials
Автор: ECRIN - Clinical Research Infrastructure
Загружено: 2025-11-24
Просмотров: 43
🔍 What we covered:
• Experiences from major European platform trials, including Remap-Cap and ECRAID-Prime, presented by Denise van Hout and Alike Van der Velden (UMC Utrecht)
• Insights from EU-SolidAct with Inge Christoffer Olsen (University of Oslo)
• Feedback from the Norwegian Medical Products Agency, shared by Anette Solli Karlsen
• A regulators’ perspective on CTIS and technical aspects, presented by Monique Al (Vice-Chair of the Clinical Trials Coordination Group)
• A rich panel discussion bringing together all speakers as well as methodologists and representatives from DG RTD, ECRIN, EFPIA, Medical University of Vienna, University of Oslo, UMC Utrecht and the Norwegian Medical Products Agency
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