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Good pharmacovigilance practices (GVP) are a set of measures drawn up to facilitate the performance of pharmacovigilance in the European Union (EU). GVP apply to marketing-authorisation holders, the European Medicines Agency (EMA) and medicines regulatory authorities in EU Member States. They cover medicines authorised centrally via the Agency as...
The European Medicines Agency (EMA) ensures accurate information is available on medicine use during pregnancy and breastfeeding. EMA identifies gaps in related data and implements strategies to improve evidence on medicine safety. These initiatives enable healthcare providers and patients to make informed decisions about treatment options during...