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    • All pharmacovigilance questions could be a bit vague, so find below a (non-exhaustive) list

      • QPPV tasks
      • Advice on post authorisation studies
      • Advice on answers to list of questions
      • Advice on inspections
      • Advice on other questions regarding pharmacovigilance
      • Create and/or review Risk Management Plan
      • Create and/or review wordings for the Summary of Product Characteristics (SmPC), sections 4.4 and 4.8
      • Write and/or review (parts of) PSUR
      • Handle and assess adverse events reports