Abstract
This paper identifies the major trends that will affect the future of the classic pharmaceutical dossier broker, among them: the possibility of the single bioequivalence (BE) study between the USA and the European Union providing for interchangeable final approved Abbreviated New Drug Applications with granted marketing authorisations; current dossier fee waivers; and, the forward integration of active pharmaceutical ingredient suppliers in Europe. This paper offers a look at the impact of these trends on brokers, and suggests several strategies to help business development professionals in the generic dossier broker industry (who read the
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