VMD FOI/EIR Requests May 2026

FOI2026/00812 - Librela adverse effects

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FOI2026/00818 - Assessment/approval/and/or post-authorisation monitoring of Librela and Solensia

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PDF, 415 KB, 5 pages

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FOI2026/00821 - Adverse event reporting line in operation

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FOI2026/00822 - Usage of non-disclosure agreements

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FOI2026/00904 - Private healthcare cover

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FOI2026/00905 - Adverse event report line

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FOI2026/00921 - Secondments, Consultancy and Post-Employment Movement of VMD staff

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FOI2026/00929 鈥� Neonicotinoids sales

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FOI2026/00964 - Librela adverse event reports

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FOI2026/00967 鈥� Information on Leptospirosis

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FOI2026/00980 - Use of spotinor in lactating mares and foals.

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FOI2026/00987 - SIC's for Bronopol (active ingredient) 2025-2026

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FOI2026/00993 鈥� Information on a specific adverse event report

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FOI2026/00995 - Librela and Solensia Specific Fees and Estimated Animals Treated

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FOI2026/01029 鈥� Veterinary Safety Communication

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