{"topic_id":"cn_vet_gmp_2020","category":"cn-vet-regulation","context":"---\ntopic_id: cn_vet_gmp_2020\ntitle: China — 兽药生产质量管理规范（2020年修订） (Veterinary GMP, MOA Order 2020 No.3): quality-system baseline for veterinary drug makers\ncategory: cn-vet-regulation\nlang: en\nsource_file: pdf-raw/cn-vet-regulation/vet_gmp_2020.txt\nsource_url: https://fgs.moa.gov.cn/flfg/202005/t20200515_6344129.htm\ndate_parsed: 2026-07-24\ntokens_estimated: 0\nrecovered: false\n---\n\n# China — 兽药生产质量管理规范（2020年修订） (Veterinary GMP, MOA Order 2020 No.3): quality-system baseline for veterinary drug makers\n\nThe <Good Manufacturing Practice for Veterinary Drugs (2020 Revision)> (兽药生产质量管理规范（2020年修订）, i.e. 兽药 GMP) was deliberated and adopted at the 6th executive meeting of the Ministry of Agriculture and Rural Affairs on 2020-04-02 and took effect 2020-06-01. It sets the basic requirements for veterinary-drug production management and quality control, requires enterprises to implement the standard in good faith and prohibits any falsification or deception, and outlines the general requirements of veterinary-drug production quality management. It is the manufacturing-layer companion to the veterinary-drug regulatory topics in this category.\n\n## Verified claims (C1 — exact substrings of first-hand Chinese official source)\n\n1. 中文原文：兽药生产质量管理规范（2020年修订）\n2. 中文原文：第一章 总则 第一条 为加强兽药生产质量管理，根据《兽药管理条例》，制定兽药生产质量管理规范（兽药 GMP ）。\n3. 中文原文：第二条 本规范是兽药生产管理和质量控制的基本要求，旨在确保持续稳定地生产出符合注册要求的兽药。\n4. 中文原文：第三条 企业应当严格执行本规范，坚持诚实守信，禁止任何虚假、欺骗行为。\n5. 中文原文：已经农业农村部 2020 年 4 月 2 日第 6 次常务会议审议通过，现予公布，自 2020 年 6 月 1 日起施行。\n6. 中文原文：第九条 兽药生产质量管理的基本要求：\n","sources":[],"tokens_estimated":236,"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."}