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Informa

Christopher Bravery, Ph.D.
Principal Consultant at Consulting on Advanced Biologicals

Agenda Sessions

  • Target audience: those in late stage clinical trials, planning for MAA/BLA or beginning to think about it. Also useful for others involved in the preparation of clinical trials dossiers at any stage.

    09:00
  • Target audience: those in late stage clinical trials, planning for MAA/BLA or beginning to think about it. Also useful for others involved in the preparation of clinical trials dossiers at any stage.

    11:00
  • Target audience: regulatory professionals and anyone interested in regulatory strategy and the reasons for success or failure at approval

    13:30
  • Target audience: regulatory professionals and anyone interested in regulatory strategy and the reasons for success or failure at approval

    16:00
  • Chairperson’s Opening Remarks

    11:10
  • Breakfast Surgery – FDA, EMA and PMDA Pinch Points

    09:00