Die bisherigen Beratungen und Stellungnahmen seien eine "wertvolle Orientierung" für die Überlegungen zum AMNOG 2.0, schrieb Thomas Müller, der Leiter der Abteilung Arzneimittel, Medizinprodukte, Biotechnologie des Bundesgesundheitsministeriums (BMG), in der Einladung für die vierte und wohl vorerst letzte Pharmadialog-Sitzung der AG 3 zu Nutzenbewertung und EU-HTA am Donnerstag. Die Reform-Debatten dürften in den kommenden Wochen Fahrt aufnehmen.
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Weitere Vorschläge des G-BA
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Pharma: AMNOG-Anpassungen reichen nicht
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Kosten-Nutzen-Bewertung, aber ohne neue Hürde
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Unsicherheit managen
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Arzneimittel auch im Versorgungskontext bewerten
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