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"Unclear proposal from the EU Commission on how to solve the MDR challenges"

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Marie Gårdmark: Potential step change – EU regulators get to play with data

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Marie Gårdmark: New incentives for orphan products on its way

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Marie Gårdmark: Finally, it’s time for a revision of the EU pharma legislation

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Column: Repurposing as a golden ticket to approval

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Marie Gårdmark: Do EMA and FDA talk to each other?