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Commission Implementing Regulation (EU) 2025/2091 of 17 October 2025 laying down good manufacturing practice for veterinary medicinal products in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council
Metadata for publikationen
- Offentliggjort:
- Forfatter(e): Directorate-General for Health and Food Safety (Europa-Kommissionen) , European Commission
- Emne: drug surveillance , health control , market approval , marketing standard , mode of production , product quality , quality standard , technical specification , veterinary legislation , veterinary medicinal product
- CELEX : 32025R2091
- ELI : reg_impl/2025/2091/oj
- OJ : L_202502091
- IMMC : C(2025)3700/4020748
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| ISSN 1977-0677 | ISBN | DOI | Katalognummer FXL2502091EN |
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