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Early scientific advice from regulators is crucial to the long haul process of developing medicines. It saves precious time and costs for each of industry, health systems, and patients when we get early input on the science and design of clinical studies. For the current drive towards regulatory simplification in Europe to be effective, it will need for each of the relevant disciplines and decision bodies to be included. #EU Pharma Legislation. #SixBoldActions

Very helpful! Thank you for sharing this paper!

Interesting!

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