Neue Untersuchungs- und Behandlungsmethoden erfordern ein hohes Maß an klinischer Evidenz, bevor sie den Europäischen Markt betreten können. In einem Unterausschuss für die Methodenbewertung hat der Gemeinsame Bundesausschuss eine Instanz zur Bewertung der Sicherheit und des Nutzen einer neuen Methode und übernimmt zudem die Klassifizierung, ob es sich um eine Sprunginnovation, Schrittinnovation oder Scheininnovation handelt. Der G-BA bietet regelmäßig und auf Antrag Beratungsgespräche für Hersteller von Medizinprodukten und Pharma an.

Die Unterausschüsse bestehen aus einer oder einem unparteiischen Vorsitzenden, sechs Vertreterinnen oder Vertretern der Spitzenorganisationen der gesetzlichen Krankenkassen sowie insgesamt sechs Vertreterinnen oder Vertretern der Spitzenorganisationen der Leistungserbringer (DKG, KBV, KZBV). Die Zusammensetzung der Leistungserbringerseite erfolgt paritätisch, sofern das Plenum angesichts des Aufgabenbereichs des Unterausschusses keine andere Zusammensetzung bestimmt.Auszug von der G-BA Website, 05.06.2017

Zuletzt geändert am Mittwoch, 07 Juni 2017 14:58
Mehr aus dieser Kategorie: « Erstattung von Medizinprodukten

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