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Presentation: Pieter Neels

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Dr Pieter Neels, Member Committee for Medicinal Products for Human Use at the European Medicines Agency spoke at last year’s World Influenza Congress in Vienna on the reasoning behind regulatory standpoints in Europe.
And he did address the elephant in the room before getting started, saying that:
“Regulators cannot do any good:
  • If we are critical: we are delaying new medicinal products to the market
  • If we are pragmatic: we are not severe enough, and we are accused to work for bigpharma,…”
Setting the tone for the presentation, Pieter then continued to analyse the reasons behind why adjuvants should be used in influenza vaccines and what needs to be proven to achieve global approval.
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