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Tag Archives: Medsafe

Proposed updates to GVP Module VI and what this might mean for our clients

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 and medicines regulatory authorities in EU Member States. The … Continue reading

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New Zealand Pharmacovigilance Guidelines Edition 2, effective in the New Year

In April this year, Medsafe released the new draft guidelines for pharmacovigilance (PV) in New Zealand. Interested parties were invited to provide comment and Medsafe provided feedback on these on their website. Part 8 of the Guideline of Therapeutic Products … Continue reading

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