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根据《药品管理法》的规定和国家药品监督管理局有关文件的要求,北京市药品监督管理局(以下简称市药监局)决定自2000年8月至12月开展2000年药品生产企业换发许可证工作。 这次换证的范围为:凡在北京市行政区域内具有北京市卫生局颁发的1995至1999年药品生产企业许可证和1995至1999年原北京市医药管理局颁发的1995至1999年药品生产企业合格证的药品生产企业、保健药品生产企业、中药饮片生产企业、中药材加工点、医用氧气等兼产生产企业及具有北京市卫生局颁发的1999至2000年药品生产企业许可证的生物制品、体外诊断试剂等生产企业,均需在规定时限内换发许可证。
According to the provisions of the “Drug Administration Law” and the requirements of the relevant documents of the State Drug Administration, the Beijing Municipal Drug Administration (hereinafter referred to as the SFDA) decided to carry out the 2000 re-issue of the pharmaceutical manufacturing enterprises from August 2000 to December 2000 Permit work. The scope of the renewal is: where in Beijing’s administrative region with the Beijing Municipal Health Bureau issued 1995-1999 pharmaceutical manufacturing license and 1995-1999 issued by the Beijing Municipal Bureau of Medicine 1995-1999 drug production Enterprise certificate of the pharmaceutical manufacturers, health-care pharmaceutical manufacturers, Chinese Herbal Pieces production enterprises, Chinese herbal medicine processing point, medical oxygen and other production-producing enterprises and the Beijing Municipal Health Bureau issued by the 1999-2000 pharmaceutical manufacturing enterprises permit biological products , In vitro diagnostic reagents and other manufacturing enterprises, are required within the prescribed time limit for the renewal of permits.