Announcement of the general administration on matters related to the implementation of the filing management of imported non-special purpose cosmetics on a larger scale (2018 31st)-XJ

Announcement of the general administration on matters related to the implementation of the filing management of imported non-special purpose cosmetics on a larger scale (2018 31st) The filing management of imported non-special purpose cosmetics has achieved positive results since its pilot implementation in Pudong New Area of Shanghai. In accordance with the 'opinions of the State Council on promoting the pilot work of' license separation 'reform in a wider scope' (Guo Fa [2017] No. 45) It is required to further promote and replicate the pilot experience of Pudong New Area in Shanghai. Now it is in 10 pilot free trade zones in Tianjin, Liaoning, Zhejiang, Fujian, Henan, Hubei, Guangdong, Chongqing, Sichuan and Shaanxi, the announcement on matters related to the expansion of the pilot implementation of the filing management of imported non-special purpose cosmetics is as follows: 1. From the date of publication of this announcement to December 21, 2018, for the first time imported non-special purpose cosmetics imported from the above 10 pilot free trade zones and registered in the pilot free trade zone, the current examination and approval management shall be adjusted to filing management. 2. If an imported cosmetics manufacturer intends to import non-special purpose cosmetics for the first time from the above 10 pilot free trade zones, it shall, before the products are imported, entrust its domestic responsible person to go through the filing formalities through the national unified 'import non-special purpose cosmetics filing management system' network platform, and obtain the electronic version of the filing certificate before carrying out the import trade. The filing products are in accordance with the 'national makeup Network (Abbreviation of the province where the pilot free trade zone is located) The rule of 'four-digit year number, six-digit sequence number' is numbered. Products that have been submitted for the first time to import non-special purpose cosmetics according to the requirements of current laws and regulations can apply to the Food and Drug Administration for returning the application materials before the technical review is carried out, import according to the filing method. Three, in accordance with the requirements of the first import of non-special purpose cosmetics for the record, should be imported at the port of the free trade test area where the domestic responsible person is located. Follow-up need to import from other ports, should cancel the record product information, in accordance with the current 'cosmetics hygiene supervision regulations', apply for the first import of cosmetics after the approval of the administrative license, or go through the import filing formalities again in other free trade zones and import after obtaining the filing certificate. Four, Food and Drug Administration 'on the release of Shanghai Pudong New Area imported non-special purpose cosmetics record management procedures (Provisional)The announcement of (2017 10th) And other relevant documents are applicable in the above 10 free trade test zones. Five, responsible for the pilot implementation of the record management of the relevant provincial food and drug supervision departments, should be in accordance with the 'Food and Drug Administration General Office on in some provinces (City) Notice on matters related to the implementation of the pilot filing of imported non-special purpose cosmetics ( Food and Drug Administration drug administration [2017] No. 160) It is required to strengthen the capacity building of cosmetics filing, meet the requirements of the pilot work of filing, and timely formulate relevant guidelines for the pilot implementation of imported non-special purpose cosmetics filing management in the pilot free trade test zone within their respective administrative areas, and open it to the public. Six, food and drug supervision departments at all levels should increase the supervision of imported products in the event and after the event, strengthen coordination and cooperation with relevant departments such as entry-exit inspection and quarantine departments, and timely report product quality and safety information, in conjunction with the relevant departments to investigate and deal with relevant violations of laws and regulations. It is hereby announced. Food and Drug Administration March 8, 2018