Fayuan
Party regulationsLawsDepartmental documentsAbout
中文English
西藏自治区实施《中华人民共和国药品管理法》办法/Chapter 4 药品生产企业的管理

Article 31

Repealed

药品生产企业必须具备与所生产药品相适应的厂房、设施和卫生环境。配制输液剂、粉针剂的,必须具备超净条件,达到洁净标准。

Local Regulations · 西藏自治区人民代表大会常务委员会 · In force from —

Article 30Back to full textArticle 32

Texts on this site are reproduced from theParty Regulations Library on 12371.cn, theNational Database of Laws and Regulations(General Office of the NPC Standing Committee), and the official libraries of the State Council departments: STA Policy and Regulations Library, MOHRSS Rules Library, MEE Rules Library, MOE Rules Library, MCT Departmental Rules, NRTA Rules Library, MEM Rules Library, MOHURD Rules Library. Party regulations and national law are two separate bodies of rules: this site searches them separately and never merges the results. Departmental rules and normative documents rank below laws and administrative regulations and are likewise kept in their own corpus.

Where an electronic text differs from the standard text of the law, the standard text governs. All texts here are in Chinese, the language in which they were officially promulgated; this interface is translated but the legal texts are not. The content of this site is for reference only and does not constitute legal advice— consult a practising lawyer about any specific matter.