日前,为进一步贯彻学习《药品管理法》和国家药品监督管理局下发的《药品包装用材料、容器管理办法》,北京市药品监督管理局召开了实施《药品包装用材料、容器管理办法》的专项工作会议。 北京市药品监督管理局根据国家药监局的有关会议精神和工作通知,在本次会议上向与会者布置了下一步药包材注册工作的程序、要求和安排,包括Ⅰ、Ⅱ、Ⅲ类药包材生产企业核、换证申请工作的开始,进口药包材的注册申请,具体药包材品种调 Recently, in order to further implement the “Drug Administration Law” and the “Measures for the Administration of Materials and Containers for Pharmaceutical Packaging” issued by the State Drug Administration, Beijing Municipal Administration of Drug Control held the “Measures for the Administration of Materials and Containers for Pharmaceutical Packaging” Special working meeting. According to the SFDA’s meeting spirit and working notice, Beijing Municipal Bureau of Drug Administration arranged the procedures, requirements and arrangements for the registration of drug packaging materials to the participants at this meeting, including categories I, II and III Pharmaceutical packaging material manufacturer nuclear, replacement of the beginning of the application process, the registration of imported drug packaging materials, the specific drug packaging material species