The examination and approval materials for drug advertisements in Qiandongnan Prefecture include an advertisement examination form, advertisement samples (samples, audio tapes) and electronic documents consistent with the published contents, and the applicant's Pharmaceutical Production License or Pharmaceutical Trading License. If the applicant is a pharmaceutical trading enterprise, it shall submit the certification documents that the pharmaceutical manufacturing enterprise agrees to be the applicant. The following questions about the examination and approval materials of drug advertisements in Qiandongnan Prefecture are answered in detail by Bian Xiao. 1. Approval materials for drug advertisements in Qiandongnan 1. Advertising review table 2. Three advertising samples (samples and tapes) and electronic documents consistent with the published content. 4. The applicant's pharmaceutical production license or pharmaceutical business license. 5. If the applicant is a pharmaceutical trading enterprise, it shall submit the certificate that the pharmaceutical production enterprise agrees to be the applicant. Where an agent applies for a drug advertisement approval number on his behalf, he shall submit the applicant's authorization certificate. 6 product registration certificate or filing certificate, registered or filed product labels and instructions, production license documents. 7. If the advertisement involves drug trade names, registered trademarks, patents, etc. Copies of relevant valid certification documents and other certification documents to confirm the authenticity of advertising content shall be submitted. 8. Enterprise authenticity assurance materials 2. Conditions for examination and approval of drug advertisements in Qiandongnan Prefecture. The holders of registration certificates or filing certificates of drugs, medical devices, health foods and formula foods for special medical purposes and their authorized production and operation enterprises are advertising applicants (hereinafter referred to as applicants). The applicant may entrust an agent to handle the application for advertisement examination of drugs, medical devices, health foods and formula foods for special medical purposes. 3. The examination and approval time of drug advertisements in Qiandongnan Prefecture is from Monday to Friday: 09: 00 am to 12: 00 am and from 13: 00 pm to17: 00 pm; Business is not handled on statutory holidays (except for reservation service). Four. The legal basis for the approval of drug advertisements in Qiandongnan Prefecture is Article 48 of the Regulations for the Implementation of the Drug Administration Law of People's Republic of China (PRC). Relevant materials shall be submitted to the pharmaceutical supervisory and administrative department of the people's government of the province, autonomous region or municipality directly under the Central Government where the pharmaceutical production enterprise is located. The pharmaceutical supervisory and administrative departments of the people's governments of provinces, autonomous regions and municipalities directly under the Central Government shall, within 10 working days from the date of receiving the relevant materials, make a decision on whether to issue the approval number of pharmaceutical advertisements; Where the approval number of drug advertisements is issued, it shall be reported to the drug supervision and administration department of the State Council for the record. The specific measures shall be formulated by the drug supervision and administration department of the State Council. To publish an advertisement for imported drugs, the applicant shall, in accordance with the provisions of the preceding paragraph, apply to the pharmaceutical supervisory and administrative department of the people's government of the province, autonomous region or municipality directly under the Central Government where the imported drug business organization is located for the approval number of the drug advertisement. Where a pharmaceutical advertisement is published in a province, autonomous region or municipality directly under the Central Government other than the place where the pharmaceutical production enterprise is located and the place where the imported pharmaceutical agency is located, the enterprise that publishes the advertisement shall file with the pharmaceutical supervisory and administrative department of the people's government of the province, autonomous region or municipality directly under the Central Government before the publication. If the pharmaceutical supervisory and administrative departments of the people's governments of provinces, autonomous regions and municipalities directly under the Central Government that accept the record find that the contents of the examination and approval of pharmaceutical advertisements do not conform to the Provisions on the Administration of Pharmaceutical Advertisements, they shall hand them over to the original publishing department for handling. Publishing drug advertisements requires advertisers to apply for approval of drug advertisements in advance, and can only publish advertisements in the media center after obtaining the approval procedures. It shall not be published without approval. I hope the above content can help you. If you have other legal problems, you can consult online.