EMA risk management information day

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Date

, -

Ort

European Medicines Agency, Amsterdam, the Netherlands

Event summary

This in-person information day provides:

  • overview of key developments in EU pharmacovigilance guidance related to the safe use of medicines during pregnancy and breastfeeding;
  • updates on GVP module V risk management plans and GVP module VIII post authorisation safety studies (PASS).

Doocuments

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