We have collected questions about the National Medical Products Administration Government Service Portal and translated them into English for your reference.

We have collected questions concerning the National Medical Products Administration Government Service Portal and translated them into English for your reference.

According to inquiries with the National Medical Products Administration(NMPA), five NMPA numbers have been deregistered this year. The possible reasons for deregistering newly registered ingredients may include: - Non-compliance with the definition of new ingredients: Some ingredients were registered, but in reality, they are already being used and managed as cosmetic ingredients, and are no longer considered new. - Functions exceeding the scope of cosmetics: Some ingredients have medicinal or other functions that go beyond the definition of cosmetics.

We have collected the latest FAQs on ordinary cosmetics filing from the Guangzhou Administration for Market Regulation and translated them into English for your reference.

We have collected the latest FAQs on ordinary cosmetics filing from the Beijing Cosmetics Review and Inspection Center and translated them into English for your reference.

On July 24, China's National Medical Products Administration (NMPA) held the inaugural meeting for the establishment of the Cosmetics Standardization Technical Committee (hereinafter referred to as the Committee). Attendees included officials from the NMPA’s Cosmetics Regulatory Department, the Medical Device Registration Department, relevant Committee leaders, and other concerned parties.

China's National Medical Products Administration (NMPA) has decided that starting from April 1, 2026, radio frequency therapeutic (non-ablative) equipment that has not obtained a medical device registration certificate in accordance with the law cannot be manufactured, imported, or sold. This decision aims to ensure the smooth and orderly advancement of work related to radio-frequency therapeutic devices and radio-frequency skin treatment devices, and takes into account the actual conditions of product development as well as the need to balance public safety and the orderly development of the industry. This refers to products classified under 09-07-02 radio frequency therapeutic (non-ablative) equipment in the annex of the "Announcement on Adjusting Parts of the Medical Device Classification Catalog" (No. 30, 2022).

We have collected the latest FAQs on ordinary cosmetics filing from the Guangzhou Administration for Market Regulation and translated them into English for your reference.

We have collected the latest FAQs on new cosmetic ingredients registration and filing in China and translated them into English for your reference.

China's National Medical Products Administration (NMPA) announced the full implementation of the electronic registration and filing for cosmetics and new ingredients. This comes as part of the NMPA's efforts to further improve government services and promote the digitization of archives for the registration and filing of cosmetics and new cosmetic ingredients (including toothpaste), thereby enhancing the efficiency of the process.