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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 33

Repealed

药品生产企业生产的各种药品,必须按照原核定的药品标准和工艺规程进行生产,如果改变药品生产工艺规程可能影响药品标准时,须报自治区药政管理局审核批准后方可进行。

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

Article 32Back to full textArticle 34

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