Define & implement the European Health Authorities consultation strategy for a US-based client

November 25, 2020
  • Drug Development
  • Drug Registration
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BlueReg made recommendations to a US based client on which Health Authorities in the European Union (EU) would be most relevant to consult throughout the development of their product.

Following these recommendations, the client subsequently entrusted to BlueReg the authoring of a Briefing Package and the management of the regulatory procedure for a national Scientific Advice consultation on its behalf.

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