Following China National Medical Products Administration’s (NMPA) announcement to implement filing system of first imported non-specials cosmetics nationwide, on Nov. 13, Zhejiang Medical Products Administration (MPA) first released its practical provincial enforcement rules along with a detailed filing service guidance, stipulating post-reform regulatory requirements for cosmetic stakeholders.
The guidance specifies the filing conditions, required dossiers and their criterions, process and duration of filing for first imported non-specials cosmetics, coupled with filing renewal requirements, providing step-by-step instructions for stakeholders and is applicable to the application for and handling of filing business of first-imported non-special use cosmetics in Zhejiang province.
The guidance mainly includes 21 chapters, as shown below:
Scope of Application
Review Types
Basis for Handling
Filing Agency
Handling Agency
Filing Conditions
Quantity Limit
Filing Conditions
Filing Materials
Receiving Methods
Basic Procedures
...


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Original regulatory document
