Total 48Articles, Present Page 1/5
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48Korean Pharmacopoeia (Twelfth Edition)Korean Pharmacopoeia (Twelfth Edition)
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01_KP Cover.pdf
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02_[Appendix 1] General Notices.pdf
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03_[Appendix 2] General Requirements for Pharmaceutical Preparations.pdf
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04_[Appendix 3] Monographs_Part1.pdf
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05_[Appendix 4] Monographs_Part2.pdf
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06_[Appendix 5] General Tests.pdf
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07_[Appendix 6] General Information.pdf
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08_Index.pdf
2024-01-31 -
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47Enforcement Rule of the Regulations on Relief of Injury from Side Effects of Drugs(No. 1783)Enforcement Rule of the Regulations on Relief of Injury from Side Effects of Drugs(No. 1783)
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Enforcement Rule of the Regulations on Relief of Injury from Side Effects of Drugs(No. 1783).pdf
2023-08-29 -
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46The Enforcement Rule of the Narcotics Control Act (No. 1781)The Enforcement Rule of the Narcotics Control Act (No. 1781)
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The Enforcement Rule of the Narcotics Control Act (No. 1781).pdf
2023-08-07 -
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45Regulations on the Criteria for Classification of Drugs(MFDS Notification No.2019-55, July 1, 2019)Regulations on the Criteria for Classification of Drugs(MFDS Notification No.2019-55, July 1, 2019)
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Regulations on the Criteria for Classification of Drugs (No. 2019-55).pdf
2023-05-31 -
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44Designation of Drugs Not Eligible for Allowances for Relief of Injury from Adverse Drug Reaction(MFDS Notification, No.2017-62, 25 July 2017)Designation of Drugs Not Eligible for Allowances for Relief of Injury from Adverse Drug Reaction(MFDS Notification, No.2017-62, 25 July 2017)
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Designation of Drugs Not Eligible for Allowances for Relief of Injury from Adverse Drug Reaction (No.2017-62).pdf
2023-05-31 -
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43Guideline on Re-Examination Affairs of New Drug,etc.Guideline on Re-Examination of New Drug,etc.(Nov 18, 2021)
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Guideline on Re-Examination of New Drugs etc. (Nov 18,2021).pdf
2023-03-27 -
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42Regulation on the Labeling of Medicinal Products,etc.Regulation on the Labeling of Medicinal Products,etc.(No.2020-82, Sep 7, 2020)
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Regulation on the Labeling of Medicinal Products, etc.(No.2020-82, Sep 7,2020).pdf
2023-03-27 -
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41Regulation on Good Manufacturing Practices (GMP) for Medicinal ProductsRegulation on Good Manufacturing Practices (GMP) for Medicinal Products.(No.2021-87, Nov 4, 2021)
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Regulation on Good Manufacturing Practices (GMP) for Medicinal Products (No.2021-87, Nov 4,2021).pdf
2023-03-27 -
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40Regulation on Fees for Pharmaceutical Approval, etc.Regulation on Fees for Pharmaceutical Approval, etc.(No.2022-46, Jun 27, 2022)
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Regulation on Fees for Pharmaceutical Approval, etc.(No.2022-46, Jun 27, 2022).pdf
2023-03-27 -
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39Regulation on Approval for Investigational New Drug Application of Drugs.Regulation on Approval for Investigational New Drug Application of Drugs.(No.2022-81, Nov 23, 2022)
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Regulation on Approval for Investigational New Drug Application of Drugs(No.2022-81, Nov 23, 2022).pdf
2023-03-27 -