论文部分内容阅读
省、自治区、直辖市药品监督管理部门是药品广告审查机关,负责本行政区域内药品广告的审查工作。县级以上工商行政管理部门是药品广告的监督管理机关。国家食品药品监督管理局对药品广告审查机关的药品广告审查工作进行指导和监督,对药品广告审查机关违反本办法的行为,依法予以处理。药品广告批准文号的申请人必须是具有合法资格的药品生产企业或者药品经营企业。药品经营企业作为申请人的,必须征得药品生产企业的同意。申请人可以委托代办人代办药品广告批准文号的申办事宜。
The drug regulatory department of a province, autonomous region or municipality directly under the Central Government shall be the agency for the examination of drug advertisements and be responsible for the examination of drug advertisements within its own administrative area. The administrative department of industry and commerce above the county level is the supervisory authority of pharmaceutical advertising. The State Food and Drug Administration will supervise and supervise the review of drug advertisements by the drug advertisement examination authority, and handle the violation of the present Measures by the drug advertisement review authority in accordance with the law. Applicants for drug advertisement approval number must be legally qualified pharmaceutical manufacturers or pharmaceutical companies. Pharmaceutical companies as an applicant, must obtain the consent of pharmaceutical manufacturers. The applicant may entrust the agent to sign up for the drug advertisement approval number.