Biosimilars in Europe

This reprint examines regulatory, pricing and reimbursement issues related to the market access and uptake of off-patent biologics, biosimilars, next-generation biologics and competing innovative medicines in European countries.

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Dades bibliogràfiques
Format:	Online
Idioma:	anglès
Publicat:	MDPI - Multidisciplinary Digital Publishing Institute 2023
Matèries:	infliximab etanercept TNFα inhibitors biologics biosimilars Germany policies incentives uptake market dynamics biosimilar market biosimilar/supply and distribution biosimilar sustainability Delphi technique pricing reimbursement utilization biosimilar biological information education communication patient Europe adalimumab biosimilarity assessment quality attributes (QAs) potentially critical quality attributes (pCQAs) European public assessment reports (EPARs) clinical governance Spain barriers regulatory review approval clinical queries regulatory science budget impact analysis savings pharmaceutical spending cost containment reference biological competitive market Belgium trastuzumab intravenous subcutaneous HER2-positive breast cancer drug costs healthcare costs cost simulation tender procurement off-patent award criteria switching interchangeability sustainability competition n/a thema EDItEUR::M Medicine and Nursing thema EDItEUR::K Economics, Finance, Business and Management::KN Industry and industrial studies::KND Manufacturing industries
Accés en línia:	ONIX_20230202_9783036565750_185
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Biosimilars in Europe

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