1. Where to apply for drug advertising approval in Hezhou

Window No. 38, Autonomous Region Food and Drug Administration, 2nd Floor, Autonomous Region Government Service Center, No. 6 Yibin Road, Qingxiu District, Nanning City

2. Hezhou Drug Advertising Approval and Acceptance Conditions

According to Article 47 of the "Drug Advertising Law of the People's Republic of China", advertisers applying for advertising review shall comply with laws and administrative regulations Submit relevant supporting documents to the advertising review authority.

According to the provisions of Article 8 of the "Measures for the Examination of Drug Advertisements" (State Food and Drug Administration Order No. 27 on March 13, 2007, effective from May 1, 2007), the application To obtain the drug advertising approval number, the "Drug Advertisement Review Form" (Appendix 1) should be submitted, along with samples (samples, sample tapes) consistent with the published content and electronic files of drug advertising applications. At the same time, the following authentic, legal, and Valid supporting documents:

(1) A copy of the applicant's "Business License";

(2) The applicant's "Drug Production License" or "Drug Business License" 》Copy;

(3) If the applicant is a pharmaceutical trading enterprise, the original document proving that the pharmaceutical manufacturing enterprise agrees to be the applicant shall be submitted;

(4) The agent shall act on his behalf When applying for a drug advertising approval number, the applicant's original power of attorney and a copy of the agent's business license and other subject qualification certification documents shall be submitted;

(5) Drug approval documents (including the "Imported Drug Registration" Certificate", "Pharmaceutical Product Registration Certificate"), a copy of the approved instructions and the actual labels and instructions;

(6) Over-the-counter drug advertisements must submit a copy of the non-prescription drug review and registration certificate or related Copies of certification documents;

(7) If applying for an imported drug advertising approval number, a copy of the relevant qualification certification document of the imported drug agency shall be provided;

(8) If the advertisement involves drug product names, registered trademarks, patents, etc., copies of relevant valid certification documents and other certification documents confirming the authenticity of the advertising content must be submitted.

Copies of the certification documents stipulated in this article must be affixed with the seal of the document holder.