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FAQs about the Required Materials for the Application of Manufacturing and Marketing Approval of Quasi-drugs and for Revised Requirements for Cosmetic Standards 2
Local Title:
医薬部外品の製造販売承認申請及び化粧品基準改正要請に添付する資 料に関する質疑応答集（Ｑ＆Ａ）について（その２）
Country/Region:
Japan
Competent Authority:
Ministry of Health, Labour and Welfare
Type:
FAQ
Status:
In force
Release Date:
2019-10-15
Implementation Date:
2019-10-15
Document
Language Source Title Access
JA
 Official FAQs about the Required Materials for the Application of Manufacturing and Marketing Approval of Quasi-drugs and for Revised Requirements for Cosmetic Standards 2
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Summary

On October 15, 2019, the Ministry of Health, Labour and Welfare (MHLW) released the FAQs about the Required Materials for the Application of Manufacturing and Marketing Approval of Quasi-drugs and for Revised Requirements for Cosmetic Standards 2.

The 2 FAQs including 4 questions, and the Q&A 14, 15 in the the first FAQs shall be deleted with the Second FAQs coming into force.

History
2019-10-15
FAQs about the Required Materials for the Application of Manufacturing and Marketing Approval of Quasi-drugs and for Revised Requirements for Cosmetic Standards 2
In force
Release Date: 2019-10-15
Implementation Date : 2019-10-15
2018-03-29
FAQs about the Required Materials for the Application of Manufacturing and Marketing Approval of Quasi-drugs and for Revised Requirements for Cosmetic Standards 1
In force
Release Date: 2018-03-29
Implementation Date : 2018-03-29
Noteworthy Information