论文部分内容阅读
在药品生产企业所在地和进口药品代理机构所在地以外的省、自治区、直辖市发布药品广告的(以下简称异地发布药品广告),在发布前应当到发布地药品广告审查机关办理备案。异地发布药品广告备案应当提交如下材料(一)《药品广告审查表》复印件;(二)批准的药品说明书复印件;(三)电视广告和广播广告需提交与通过审查的内容相一致的录音带、光盘或者其他介质载体。上述材料的复印件,需加盖证件持有单位印章。对按照本办法第十二条、第十三条规定提出的异地发布药品广告备案申请,药品广告审查机关在受理备案申
The drug advertisement shall be issued in the place where the drug manufacturer locates and the province, autonomous region or municipality directly under the Central Government where the imported drug agency is located (hereinafter referred to as the drug advertisement issued in different places) shall be put on record at the place where the drug advertisement examination authority at the place of issue is to be released. (2) The photocopy of the approved drug specification; (3) The tapes consistent with the content of the review shall be submitted for television commercials and radio commercials; , Optical disk or other media carrier. Copies of the above-mentioned materials shall be stamped with the seal of the certificate holder. In accordance with the provisions of Article XII, Article XIII of the proposed release of drug advertising applications filed in remote places, the drug advertisement examination authority in the acceptance of the record