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The limitations of clinical evidence from trials when data presented for HTA: Immature survival data, selected patient populations, phase II data for uncommon cancers etc...
Presenter: Nathan Cherny
Session: How does real-world evidence inform decision making for new drug funding?
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Real-world evidence and regulatory drug approval
Presenter: Christopher Booth
Session: How does real-world evidence inform decision making for new drug funding?
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Webcast
RWE: When should it be used by EMA?
Presenter: Francesco Pignatti
Session: How does real-world evidence inform decision making for new drug funding?
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Challenges of collecting RWE: Limitations of administrative data sets, complex methodological issues, responsibility for collecting data
Presenter: Valery Lemmens
Session: How does real-world evidence inform decision making for new drug funding?
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Introduction
Presenter: Solange Peters
Session: Beating cancer at the EU level: Influential policies changing the paradigm of the cancer (treatment) lifecycle
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ESMO’s blueprint to tackle cancer
Presenter: Rosa Giuliani
Session: Beating cancer at the EU level: Influential policies changing the paradigm of the cancer (treatment) lifecycle
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Webcast
EMA/HMA strategy 2025
Presenter: Ralf Herold
Session: Beating cancer at the EU level: Influential policies changing the paradigm of the cancer (treatment) lifecycle
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Webcast
Europe's Beating Cancer Plan
Presenter: John F. Ryan
Session: Beating cancer at the EU level: Influential policies changing the paradigm of the cancer (treatment) lifecycle
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Pharmaceutical strategy for Europe and how to combine a thriving pharmaceutical landscape with affordable drug prices
Presenter: Ferenc Marofka
Session: Beating cancer at the EU level: Influential policies changing the paradigm of the cancer (treatment) lifecycle
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Industry perspective
Presenter: Nathalie Moll
Session: Beating cancer at the EU level: Influential policies changing the paradigm of the cancer (treatment) lifecycle
Resources:
Webcast