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Germany - HTA Country/Area Profile ... Available Resources ... These results come from the 2020/2021 WHO Global Survey on HTA and Health Benefit Packages. “N/A” stands for ‘not applicable’ and 'N/R' stands ‘no reply’.
The German Benefit Assessment White Paper focuses on the current methodological requirements of the German HTA process, emphasizing its importance not only in assessing drug benefits but also in determining drug pricing.
Health technology assessment (HTA) has been discussed in Germany since the late 1990s, closely related to the advent of evidence-based medicine. The idea of technology assessment was initially discussed in Germany by the “technology assessment office of the parliament.”
It completely revises pricing regulations for newly authorized medicinal products and their reimbursement by statutory health insurance providers.
21 thg 6, 2024 · Learn about the comprehensive process for Health Technology Assessments (HTAs) in Germany, including key steps, regulatory bodies involved, and the importance of HTAs in healthcare decision-making.
Die Berichte treffen als systematische Bewertungen wissenschaftlicher Informationen Aussagen zu Nutzen, Risiko, Kosten und Auswirkungen von Verfahren und Technologien mit Bezug auf die gesundheitliche Versorgung der Bevölkerung.
The implementation of the EU Health Technology Assessment (HTA) Regulation in January 2025 introduces significant shifts in how pharmaceutical products gain market access in Germany.
Comprehensive overview of the HTA system in Germany, explaining everything you need to know to get started in simple terms
With country-specific data curated by local experts, it provides a comprehensive and up-to-date overview of relevant HTA and P&R documents as available per country, to support you with preparation for EU HTA assessments and all European and local market access activities.
1 thg 1, 2011 · Every pharmaceutical product with a new chemical entity (NCE) that received its marketing authorization on or after 1 January 2011 is subject to an HTA in Germany. In addition, new indications of products that were first approved on or after 1 …
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