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Integration of Real-World Data into Clinical Trials: An Interdisciplinary Discussion from Regulatory and Practical Perspectives

Köppe, J.; Schiel, A.; Gerlinger, C.; Götte, H.; Edelmann, D.; Erdmann, S. · Das Gesundheitswesen · Ausgabe EFirst/2026 · S. 1 bis 1

DOI 10.1055/a-2736-6561

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Autor:innenKöppe, J.; Schiel, A.; Gerlinger, C.; Götte, H.; Edelmann, D.; Erdmann, S.
ZeitschriftDas Gesundheitswesen
AusgabeEFirst/2026
Jahrgang / SeitenJg. 88 · S. 1 bis 1

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Abstract-Vorschau

Increasing efforts are required to integrate the growing volume of so-called real-world data (also named routine practice data), which are data generated outside of randomized controlled trials, into regulatory studies. Various stakeholders anticipate that such integration could save time and financial resources during the approval process of new therapies, and ethical considerations also partially support such an a…

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Zitierempfehlung

Köppe, J.; Schiel, A.; Gerlinger, C.; Götte, H.; Edelmann, D.; Erdmann, S (2026) Integration of Real-World Data into Clinical Trials: An Interdisciplinary Discussion from Regulatory and Practical Perspectives. Das Gesundheitswesen, 88 (EFirst), 1 bis 1. https://doi.org/10.1055/a-2736-6561

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