Customers are responsible for paying all customs duties, taxes, and tariffs levied for importation of PMRJ Reference Standards.

医薬品・医療機器・再生医療等製品の承認審査・安全対策・健康被害救済の3つの業務を行う組織。

JP Reference Standards & Other Reference StandardsOur Products

PMRJ produces and distributes compendial reference standards represented by the Japanese Pharmacopoeia Reference Standards.

PREFACE 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. d at least every 10 years. Since the JP 9th edition, full-fledged revisions ha

Pharmaceutical and Medical Device Regulatory Science Society of Japan (PMRJ) is a non-profit general incorporated foundation formerly known as Society of Japanese Pharmacopoeia established in June 1956. Our mission is to promote better quality, efficacy, and safety of drugs and medical devices by advancing their regulatory sciences. new !

In July 2016, the Committee on JP established the basic principles for the preparation of the JP 18th Edi- tion, setting out the roles and characteristics of the JP, the definite measures for the revision, and the date of the revision.

医薬品・医療機器・再生医療等製品の承認審査・安全対策・健康被害救済の3つの業務を行う組織。

Please visit PMRJ Pharmaceutical Reference Standards Center website <https://www.pmrj-rs.jp/en> to check the ordering instruction. In addition, please find a leaflet of each reference …

The Japanese Pharmacopoeia Reference Standards are reference standards used for the tests of drugs specified in the Japanese Pharmacopoeia and for the General Tests.