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JapanesePharmacopoeia(JP)isestablishedandpublishedtoregulatethepropertiesandqualityofdrugsbytheMinisterofHealth,LabourandWelfareafter ...
Japanese Pharmacopoeia (JP) is established and published to regulate the properties and quality of drugs by the Minister of Health, Labour and Welfare after hearing the opinion of the Pharmaceutical Affairs and Food Sanitation Council (PAFSC). The JP consists of General Notices, General Rules for Crude Drugs, General Rules for Preparations, General Tests, Processes and Apparatus and Official Monographs. Items selected for entry in the JP must be those important in health care based on the necessity of the drug in medical practice, wide application and experience of use. Since it was first published in June 1886, the JP has been revised many times periodically. The 18th edition of the JP came into effect on June 7, 2021.
The Japanese Pharmacopoeia 18th editionページの先頭へ戻る[1]
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