Conditions and requirements for application for examination of health food advertisements: (1) Conditions 1. The applicant who publishes the advertisement of health food must be the holder of the approval document of health food or the citizen, legal person and other organization entrusted by him. The applicant may advertise health food by himself or by entrusting other legal persons, economic organizations or citizens. 2. An application for publishing domestic health food advertisements shall be submitted to the (food) drug supervision and administration department of the province, autonomous region or municipality directly under the Central Government where the holder of the health food approval certificate is located. An application for publishing an advertisement for imported health food shall be submitted by the China office of an overseas production enterprise of the product or the agency entrusted by the enterprise to the local (food) drug supervision and administration department of the province, autonomous region or municipality directly under the Central Government. 3. The advertising application for health food whose production and sale are explicitly prohibited by the relevant departments of the State Council will not be accepted. The relevant departments in the State Council have cleaned up and rectified the cancelled health care function, and no longer accept the application for product advertisement of this function. (2) Electronic materials and paper materials submitted by the applicant. Electronic materials 1. Download the filling procedure of the Health Food Advertising Review Form from the website of the US Food and Drug Administration and install it on the computer. 2. Fill in and print the Health Food Advertisement Review Form according to the instructions, and check whether the data check codes of electronic documents and paper documents are consistent. 3. Make the certification documents and samples of the advertising content to be published into electronic documents. Paper material 1. Health food advertising review form; 2. Samples (samples, tapes) and electronic documents consistent with the published contents; 3. Copy of health food approval certificate; 4. A copy of the hygiene license of the health food production enterprise; 5 copies of the business license or qualification certificate and identity certificate of the applicant and the advertising agent; If there is an entrustment relationship, the original power of attorney shall be submitted; 6. Quality standards, instructions, labels and actual packaging of health food; 7. If there are trademarks, patents and other contents in health food advertisements, copies of relevant supporting documents shall be submitted; 8. Other relevant documents to confirm the authenticity of the advertising content; 9 declaration of the authenticity of the substantial contents of the application materials. The cover and advertising content page of the Health Food Advertising Review Form shall be stamped with the signature of the applicant; To submit a copy of the above information, the signature of the applicant is required. (3) Form requirements of application materials: 1. The application materials shall be made according to the requirements of the Interim Provisions on the Examination of Health Food Advertisements, and numbered in sequence. 2. Use A4 paper and print it with No.4 ~ No.5. 3. Each item should be bound separately, and the following items should be printed on the cover in turn: item number, name of health food, name of item, name of trustee (with official seal), name and telephone number of contact person and name of applicant (with official seal). 4. The materials should be put into an envelope, and the cover of the envelope should indicate the advertisement and the name of the health food for which the application is made. In the upper right corner, the original 1 set/copy 1 set of materials attached to this bag (including 5 review forms), the contact telephone number of the applicant and the name of the applicant's organization (with official seal) should be indicated. Licensing procedures: 1. Data receiving standard: 1, and the application items and contents are correct; 2. All kinds of materials are complete; 3. The form is standardized and the supporting documents are valid; 4. Whether the relationship between the form and the supporting documents is correct; 5. The application materials shall be complete and clear, signed and stamped with the official seal of the enterprise. Print or copy on A4 paper, and bind them into volumes in the order of the application materials catalogue; 6. If the application materials need to be copied, the applicant (unit) shall indicate the words "this copy is consistent with the original" or a written explanation on the copy, indicate the date and affix the official seal of the unit. Person-in-charge: Acceptance Office of Provincial US Food and Drug Administration; Responsibilities and authority: 1. Check the application materials according to the standards; 2. Sign for those that meet the standards, and send the written and electronic data to the drug registration office within 1 working day; 3, does not meet the standards, returned to the applicant. II. Acceptance criteria: The handed-over materials are standardized, complete and effective. Person in charge: Provincial Drug Registration Office of US Food and Drug Administration Acceptance Criteria: 1. Whether the application items and contents are correct; 2. All kinds of information are complete; 3. The form is standardized and the documents are valid; 4. Whether the relationship between the form and the supporting documents is correct; 5. The application materials shall be complete and clear, signed and stamped with the official seal of the enterprise. Print or copy on A4 paper, and bind them into volumes in the order of the application materials catalogue; 6. If the application materials need to be copied, the applicant (unit) shall indicate the words "this copy is consistent with the original" or a written explanation on the copy, indicate the date and affix the official seal of the unit. Person-in-charge of the post: the accepting personnel of the Drug Registration Office of the US Food and Drug Administration of the province; post responsibilities and authority: 1. Check the application materials according to the standards. 2. If the application materials are complete and meet the requirements of formal examination, it shall be accepted within 5 working days, and the Notice of Acceptance of Health Food Advertisement shall be filled out and submitted to the applicant as an acceptance certificate. 3. If the application materials submitted by the applicant are incomplete or do not meet the requirements of formal examination, the accepting personnel of the Drug Registration Office shall fill in the Notice of Supplementary Materials, indicate the contents that need to be supplemented, and submit them to the applicant through the accepting office. 4. If the application matters do not fall within the scope of functions and powers of the department or the application matters do not need administrative license, it will not be accepted, fill in the notice of inadmissibility, explain the reasons, and inform the applicant of the right to apply for administrative reconsideration or bring an administrative lawsuit according to law and the complaint channels.