EMA risk management information day
EventHumanPharmacovigilance
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This in-person information day will provide an overview of key developments in EU pharmacovigilance guidance related to the safe use of medicines during pregnancy and breastfeeding.
It will also provide updates on GVP module V risk management plans and GVP module VIII post authorisation safety studies (PASS).
The agenda and more information are available at the DIA website: