Proposed partical amendments to the "Standard on Pharmaceutical Equivalence Test"; (41 page(s), in Korean)
Partial Revision to the Miscellaneous Manufactured Goods Quality Labeling Regulation; (1 page(s), in English)
Draft Food and Drug Administration (FDA) Circular "Guidelines for the Importation and Exportation of Finished Drug Products and Raw Materials"; (6 page(s), in English)
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