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DB37/T 4825.3-2025   Management specification for daily supervisory inspection of drugs, medical devices and cosmetics enterprises―Part 3:Daily supervisory inspection (English Version)
Standard No.: DB37/T 4825.3-2025 Status:valid remind me the status change

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Standard No.: DB37/T 4825.3-2025
English Name: Management specification for daily supervisory inspection of drugs, medical devices and cosmetics enterprises―Part 3:Daily supervisory inspection
Chinese Name: 药品、医疗器械、化妆品企业日常监督检查管理规范 第3部分:日常监督检查
Chinese Classification: A90    Social and public safety in general
Professional Classification: DB    Provincial Standard
ICS Classification: 03.080.01 03.080.01    Services in general 03.080.01
Source Content Issued by: Shandong Provincial Administration for Market Regulation
Issued on: 2025-02-14
Implemented on: 2025-3-14
Status: valid
Target Language: English
File Format: PDF
本文件规定了药品、医疗器械、化妆品企业日常监督检查流程、检查实施过程以及检查后续工作等方面的要求。
本文件适用于对药品、医疗器械、化妆品企业的日常监督检查管理。
Code of China
Standard
DB37/T 4825.3-2025  Management specification for daily supervisory inspection of drugs, medical devices and cosmetics enterprises―Part 3:Daily supervisory inspection (English Version)
Standard No.DB37/T 4825.3-2025
Statusvalid
LanguageEnglish
File FormatPDF
Word Count words
Price(USD)
Implemented on2025-3-14
Deliveryvia email in business day
Detail of DB37/T 4825.3-2025
Standard No.
DB37/T 4825.3-2025
English Name
Management specification for daily supervisory inspection of drugs, medical devices and cosmetics enterprises―Part 3:Daily supervisory inspection
Chinese Name
药品、医疗器械、化妆品企业日常监督检查管理规范 第3部分:日常监督检查
Chinese Classification
A90
Professional Classification
DB
ICS Classification
Issued by
Shandong Provincial Administration for Market Regulation
Issued on
2025-02-14
Implemented on
2025-3-14
Status
valid
Superseded by
Superseded on
Abolished on
Superseding
Language
English
File Format
PDF
Word Count
words
Price(USD)
Keywords
DB37/T 4825.3-2025, DB37 4825.3-2025, DB37T 4825.3-2025, DB37/T4825.3-2025, DB37/T 4825.3, DB37/T4825.3, DB374825.3-2025, DB37 4825.3, DB374825.3, DB37T4825.3-2025, DB37T 4825.3, DB37T4825.3
Introduction of DB37/T 4825.3-2025
本文件规定了药品、医疗器械、化妆品企业日常监督检查流程、检查实施过程以及检查后续工作等方面的要求。
本文件适用于对药品、医疗器械、化妆品企业的日常监督检查管理。
Contents of DB37/T 4825.3-2025
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Keywords:
DB37/T 4825.3-2025, DB37 4825.3-2025, DB37T 4825.3-2025, DB37/T4825.3-2025, DB37/T 4825.3, DB37/T4825.3, DB374825.3-2025, DB37 4825.3, DB374825.3, DB37T4825.3-2025, DB37T 4825.3, DB37T4825.3