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Regulations for Registration of Medicinal Products - Article 2

Regulations for Registration of Medicinal Products|第 2 條|Food and Drug Administration|Regulation|In Force

第 一 章|衛生福利部|v1.0

Effective Date: 2024-01-01|Last Amended: 2023-04-27

Content

The registration of drugs, and the post-approval change, transfer, extension, or reissue of damaged or lost drug licenses should follow the Regulations. Matters not included in the Regulations are subject to other regulations, orders or announcements made by the central health competent authority.

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