{"topic_id":"cn_vet_drug_gsp_2010","category":"cn-vet-regulation","context":"---\ntopic_id: cn_vet_drug_gsp_2010\ntitle: Veterinary drug Good Supply Practice (GSP) (MOA Order 2010, No. GSP)\ncategory: cn-vet-regulation\nlang: en\nsource_file: pdf-raw/cn-vet-regulation/vet_drug_gsp_2010.txt\nsource_url: https://public.zzgx.gov.cn/attachment/%E4%B8%AD%E5%8D%8E%E4%BA%BA%E6%B0%91%E5%85%B1%E5%92%8C%E5%9B%BD%E5%86%9C%E4%B8%9A%E9%83%A8%E4%BB%A4%E5%85%BD%E8%8D%AF%E8%B4%A8%E9%87%8F%E7%AE%A1%E7%90%86%E8%A7%84%E8%8C%83.docx?FQRYR-6v6tNh2YPWTJHP0PlpL7PNpfoEjMsp8dQj5goOxXXU4I-D_EgtvbDQ68xARkw5nB0XFIhcSqsBUuVnCN2Vg6wKQJr7WA==\ndate_parsed: 2026-07-24\ntokens_estimated: 0\nrecovered: false\n---\n\n# Veterinary drug Good Supply Practice (GSP) (MOA Order 2010, No. GSP)\n\nThe Ministry of Agriculture Order (dated 2010-01-15) enacted the <Good Supply Practice for Veterinary Drugs> (兽药经营质量管理规范, abbreviated GSP). It applies to veterinary-drug trading enterprises within the territory of the PRC and is built on the Veterinary Drug Administration Regulation. Key requirements: trading enterprises must have fixed premises and warehouses whose area meets provincial veterinary-administration rules, with living/diagnosis areas separated to avoid cross-contamination; the business location must match the Veterinary Drug Trading License (displayed prominently), and a change of location requires re-issuing the license while changes to premises/warehouse area are filed with the issuing authority within 30 working days; warehouses must separate qualified / unqualified / pending-inspection / returned-drug zones; enterprises must appoint quality personnel (quality managers need secondary-school-or-above veterinary-related education or junior-or-above technical title). This GSP layer pairs with the human-drug-ban and prescription-drug topics in this category.\n\n## Verified claims (C1 — exact substrings of first-hand Chinese official source)\n\n1. 中文原文：《兽药经营质量管理规范》英文缩写为GSP\n2. 中文原文：第一条为加强兽药经营质量管理，保证兽药质量，根据《 兽药管理条例 》，制定本规范。\n3. 中文原文：第二条 本规范适用于 中华人民共和国 境内的兽药经营企业。\n4. 中文原文：第三条 兽药经营企业应当具有固定的经营场所和仓库，其面积应当符合省、 自治区 、直辖市人民政府兽医行政管理部门的规定。\n5. 中文原文：兽药经营企业应当配备与经营兽药相适应的质量管理人员。有条件的，可以建立质量管理机构。\n6. 中文原文：兽药经营企业的经营地点应当与《兽药经营许可证》载明的地点一致。《兽药经营许可证》应当悬挂在经营场所的显著位置。\n7. 中文原文：变更经营场所面积的，应当在变更后30个工作日内向发证机关备案。\n8. 中文原文：兽药经营企业主管质量的负责人和质量管理机构的负责人应当具备相应兽药专业知识，且其专业学历或技术职称应当符合省、自治区、直辖市人民政府兽医行政管理部门的规定。\n","sources":[],"tokens_estimated":279,"generated_at":null,"tip":"Use /api/v1/topics to discover more topics. /api/v1/nutrient for precise single-point queries. /api/v1/cross_compare for 2-3 standard comparisons."}