Naming and labelling of biologicals – a survey of US physicians’ perspectives

Introduction: The US Food and Drug Association (FDA) released its requirements for the non-proprietary naming of biological products in January 2017. Before the FDA's release, the Alliance for Safe Biologic Medicines (ASBM) asked physicians for their views on the labelling and naming of biosimi...

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Veröffentlicht in:GaBI Journal 2017-03, Vol.6 (1), p.7-12
Hauptverfasser: Gewanter, Harry L, Reilly, Michael S
Format: Artikel
Sprache:eng
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