With Medicines for Europe’s director general Adrian van den Hoven having spoken to Generics Bulletin about his early days with the association as well as reflecting on achievements and challenges over the past ten years (see sidebars), the final part of his exclusive three-part interview looks ahead to the opportunities that are on the horizon for generics, biosimilars and value added medicines in Europe.
First of all, van den Hoven was asked about the potential for value added medicines to gain ground in future, especially given recent EU legislative efforts to recognise the value of repurposing with a proposed four-year period of data exclusivity protection for new indications
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