Japanese Pharmacopoeia 18th Edition

Product Description

The Japanese Pharmacopoeia (JP) is an official document that defines the specifications, criteria and standard test methods necessary to properly assure the quality of medicines in Japan.

2022; 2876 pages; A4 Format (210 x 297 mm); Hardback; Published by Pharmaceutical and Medical Device Regulatory Science Society of Japan

The JP XVIII comprises the following items in order: The Ministry of Health, Labour and Welfare Ministerial Notification; Contents; Preface; General Notices; General Rules for Crude Drugs; General Rules for Preparations; General Tests, Processes and Apparatus; Official Monographs, including Monographs for Crude Drugs; Infrared Reference Spectra; Ultraviolet-visible Reference Spectra; General Information; Appendix ; Cumulative Index (English, Latin and Japanese titles); and Addenda.

General Tests, Processes and Apparatus which were newly added is 2.05 Size-Exclusion Chromatography

General Tests, Processes and Apparatus which were revised are
Preamble; 2.46 Residual Solvents; 2.48 Water Determination; 2.51 Conductivity Measurement; 2.52 Thermal Analysis; 2.66 Elemental Impurities; 4.06 Sterility Test; 5.01 Crude Drugs Test; 9.01 Reference standards; 9.41 Reagents, Test Solutions; and 9.62 Measuring Instruments, Appliances.

Official Monographs provides 2033 articles, including 33 articles newly added, 8 articles deleted and 168 articles revised.