首页> 美国政府科技报告 >Manufacture, Distribution, and Promotion of Adulterated, Misbranded, orUnapproved New Drugs for Human Use by State-Licensed Pharmacies. FDA Compliance Policy Guides. Chapter 32-Drugs General
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Manufacture, Distribution, and Promotion of Adulterated, Misbranded, orUnapproved New Drugs for Human Use by State-Licensed Pharmacies. FDA Compliance Policy Guides. Chapter 32-Drugs General

机译:制造,分发和推广由国家许可的药房供人用的掺假,贴错标签或未经批准的新药。 FDa合规政策指南。第32章 - 药物总则

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Pharmacies engaged in promotion and other activities analogous to manufacturingand distributing drugs for human use are subject to the same provisions of the Act as manufacturers. The guide sets forth regulatory action guidance in such cases.

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