There are 205 resources available
Clinical drug development of radiotheranostics: Trial design, administered vs absorbed dose and the role of internal dosimetry
Presenter: Alessandra Gennari
Session: ESMO Colloquium supported by Novartis - Radiotheranostics in oncology: Optimising the science, building capacity and streamlining the regulation
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Current policy and regulatory hurdles for RLT implementation: Regulatory approval, centre accreditation and radioprotection, reimbursement
Presenter: Valentina Di Iorio
Session: ESMO Colloquium supported by Novartis - Radiotheranostics in oncology: Optimising the science, building capacity and streamlining the regulation
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Q&A and discussion
Session: ESMO Colloquium supported by Novartis - Radiotheranostics in oncology: Optimising the science, building capacity and streamlining the regulation
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Webcast
Concluding remarks
Presenter: Bart Cornelissen
Session: ESMO Colloquium supported by Novartis - Radiotheranostics in oncology: Optimising the science, building capacity and streamlining the regulation
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Introduction to the Keynote Speaker
Presenter: Anastasios Stathis
Session: Revolutionising cancer treatment: The transformative odyssey of tumour-agnostic drug development in precision medicine
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Webcast
Revolutionising cancer treatment: The transformative odyssey of tumor-agnostic drug development in precision medicine
Presenter: Vivek Subbiah
Session: Revolutionising cancer treatment: The transformative odyssey of tumour-agnostic drug development in precision medicine
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Regulatory frameworks for biomarker-driven drug development
Presenter: Pierre Démolis
Session: Hurdles in the regulatory and operational framework of early drug development in Europe
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The challenges of IVDR in Europe: Latest updates and potential solutions
Presenter: Olga Tkachenko
Session: Hurdles in the regulatory and operational framework of early drug development in Europe
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Combinations within the MAPkinase pathway: Does drugging within the same pathway work?
Presenter: Neeltje Steeghs
Session: MAPkinase
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Optimising the EU Clinical Trial Regulation and the Clinical Trials Information System to increase the attractiveness of the EU as a destination for clinical trials
Presenter: Martin O'Kane
Session: Hurdles in the regulatory and operational framework of early drug development in Europe
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Webcast