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For more advice on the cosmetics industry and related issues of skin care products processing, you can consult online customer service or call the manufacturer directly or checkGuangzhou Lianying Cosmetics Co., LtdOther column articles related to the website

Precautions

1. Domestic ordinary cosmetics shall be put on record with the drug regulatory department of the people's government of the province, autonomous region or municipality directly under the Central Government where the filing person is located.

2. The general cosmetics filer shall complete the filing after submitting the filing materials stipulated in these regulations through the online government service platform of the drug regulatory department of the State Council.

3. The drug supervision and administration department of the people's government at or above the provincial level shall publish the relevant information for the record to the public within 5 working days from the date when the general cosmetics record-keeping person submits the record-keeping materials.

Filing procedures

1. After the filing application is submitted by the domestic ordinary cosmetics filer, the administrative examination and approval office of the provincial bureau shall guide him to submit the filing materials through the "https://zwfw.nmpa.gov.cn" (hereinafter referred to as the service platform) of the online service hall of the State Drug Administration in accordance with the relevant requirements of the Regulations on the Administration of Cosmetic Registration and Filing Materials (Announcement No. 32 of 2021 of the State Drug Administration), and accept relevant consultation from the cosmetics filer.

2. Data collation and publicity The administrative examination and approval office of the provincial bureau shall, within 5 working days from the date when the cosmetics filer submits the filing data, collate the filing data in accordance with the filing data collation requirements, and publicize those that meet the filing data collation requirements. For ordinary cosmetics that have been filed but the filing information has not been released to the public, the administrative examination and approval office of the provincial bureau may require the filing person to correct and publish the filing information to the public after meeting the requirements.

3. Information Inquiry After the cosmetic filer submits the information on the service platform to complete the filing, the publicly announced filing information can be queried in the "Data Inquiry" column "Domestic Ordinary Cosmetics Filing Information" on the official website of the State Drug Administration. Business-related departments should inform cosmetics filers and the public of the filing information query path.

Verification after filing

1. Data Review The Provincial Drug Evaluation Center (hereinafter referred to as the Evaluation Center) conducts technical review of the filing data in accordance with relevant laws, regulations, and technical specifications issued by the State Food and Drug Administration, and the review opinions are entered into the National Drug Intelligence Supervision Platform (referred to as the Supervision Platform).

2. On-site verification The inspection branches of the provincial bureau and the drug regulatory departments at the city and county level shall review the authenticity, reliability and consistency of the filing materials in accordance with the relevant laws, regulations and technical specifications issued by the State Food and Drug Administration. When the authenticity, reliability, consistency or product quality and safety cannot be ensured, on-site verification can be carried out, and sampling inspection can also be carried out if necessary. If it is found that the filing person has violated laws and regulations, it shall be disposed of in accordance with the law. The verification results and disposal opinions shall be entered into the supervision platform.

3. Verification of efficacy claims Verification of efficacy claims submitted by the filer shall be subject to post-mortem supervision and verification by the inspection branches of the provincial bureau and the drug regulatory departments at the city and county levels in accordance with the law in combination with the filing situation.