Healixia symposium: Strengthening the landscape for Early Phase clinical studies in Belgium
Join us for an insightful afternoon.
Now open for registration!
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Registration
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Welcome & introduction with pre-symposium survey results
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The impact of EU-CTR on clinical vaccine research in Belgium by Isabel Leroux-Roels (UZ Gent)
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Early phase studies with genetically modified (GMO) vaccines, a case study by Bruno Speder (AstriVax)
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Early phase achievements & proposed improvements from regulatory perspective by Katelijne Anciaux (CT College)
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How to consolidate Belgium as an early clinical trial hub: challenges and opportunities in an evolving landscape by Nathalie Lambot (pharma.be)
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Panel discussion
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Coffee break
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Modus operandus and role of BAREC in the Belgian landscape by Pieter Moons (BAREC)
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Data transparancy rules from regulatory perspective by Nele Steens (FAMHP)
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EU Clinical Trial Regulation and Data Transparency: Implications for protecting our Innovation by Maarten Timmers (Johnson & Johnson)
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Panel discussion
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CTR and academic research by Minne Casteels & Ruth Storme (KU Leuven)
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Symposium wrap-up
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Closing drink
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