Regulations of Medicament Manufacturer Inspection｜第 2 條｜Food and Drug Administration｜Regulation｜In Force
衛生福利部｜v1.0
Last Amended: 2014-02-21
Medicament manufacturers that shall be inspected in accordance with this set of regulations are as follows: (1) Firms in the manufacturing, processing of pharmaceutical products; (2) Firms in the manufacturing, assembling of medical devices; (3) Other firms related to the manufacturing, processing or assembling of medicaments, including firms that are approved by the central competent health authority to manufacture medicaments for development, firms that produce drug labeling, and firms related to the packaging of medicaments.