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Document: Information on the Member States requirement for the nomination of a pharmacovigilance (PhV) contact person at national level-2025/10/1
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Page: In-use stability testing of veterinary medicinal products - Scientific guideline-2025/10/1
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Document: Guideline on in-use stability testing of veterinary medicinal products-2025/10/1
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Document: Veterinary pre-submission meeting request form - in accordance with Regulation (EU) No 2019/6-2025/9/30
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Page: Quality of medicines questions and answers: Part 1-2025/9/30
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Document: Minutes of the CAT meeting 12-14 August 2025 - written procedure-2025/9/30
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Document: Minutes of the CAT meeting 16-18 July 2025-2025/9/30
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Document: List of centrally authorised products with safety-related changes to the product information-2025/9/30
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Document: Members of the Coordinating group of European network of paediatric research at the European Medicines Agency (Enpr-EMA)-2025/9/30
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Page: Clinical evaluation of medicinal products intended for treatment of hepatitis B - Scientific guideline-2025/9/30
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