• Scientific support and assistance during oral explanations at EMA
    • Pharmacovigilance Risk Assessment Committee (PRAC)
    • Committee for Medicinal Products for Human Use (CHMP)
    • Co-ordination Group for Mutual Recognition and Decentralised Procedures - Human (CMDh)
  • For medicinal products in the approval or the post approval phase
  • Knowhow of the former Member of the Committee for Medical Products for Human Use at EMA
  • Extensive experience with safety-related referrals