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Marketing Authorisations Information Service (MAVIS) Hub edition 128
The process for the simultaneous review of veterinary medicine submissions by New Zealand’s Ministry for Primary Industries (MPI) and the UK's Veterinary Medicines Directorate.
Information on how to delete a report of an adverse event to an animal medicine.
Marketing Authorisations Veterinary Information Service (MAVIS) edition 102
VMD Published Standards for regulatory work 2020-2021 against Key performance indicators (KPIs)
Information for reporting adverse events involving residues from animal medicine.
Apply to make changes (a variation) to an existing animal stem cell centre authorisation.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 April to 30 June 2024.
How we use information you give us when you submit an adverse event report.
Marketing Authorisations Information Service (MAVIS) Hub edition 114
Marketing Authorisations Veterinary Information Service (MAVIS) edition 109
Information required for reporting an adverse event in an animal.
Marketing Authorisations Veterinary Information Service (MAVIS) edition 106
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 July to 30 September 2024.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Jan - 31 Mar 2024.
VMD Published Standards for regulatory work 2021-2022 against Key performance indicators (KPIs)
Information on reporting suspected adverse events to animal medicines in the environment.
The published standards relate to a number of KPIs in the VMD Deliverables.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 July - 30 September 2023.
Marketing Authorisations Veterinary Information Service (MAVIS) edition 107
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