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Requirements for Applying for Manufacturing and Marketing Approval of Quasi-drugs

Local Title
「医薬部外品原料規格」の改正に伴う医薬部外品等の製造販売承認申請等の取扱いについて
Country/Region
Japan
Competent Authority
Ministry of Health, Labour and Welfare
Type
Notice
Status
In force
Release Date
2021-03-25
Implementation Date
2021-03-25
Expert Translation AI Translation View Official Documents

Along with the revisions to the Japanese quasi-drug ingredient standards on March 25, 2021, Japan Ministry of Health, Labour and Welfare (MHLW) also revised the relevant application requirements for the manufacture and sale of quasi-drugs.

The revised requirements came into effect on the date of promulgation.

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