1994年药品监督管理工作要点

• 出 处: 中国药事
• 发表日期: 1994年03期
• 关键词: 人民用药安全 新药审批 直辖市卫生厅 劣药 组织修订 伪劣商品 制剂许可证 进口药品注册 法制建设 法律尊严

１９９４年药品监督管理工作要点１９９４年的药品监督管理工作，要认真贯彻落实党的十四届三中全会精神，强化和完善药品监督管理的法制建设，进一步建立健全适应社会主义市场经济的药品法律体系，深入宣传贯彻《药品管理法》，依法行政，廉洁自律，维护法律尊严，保证人...

Essentials of Drug Supervision and Management in 1994 The drug regulatory work in 1994 must conscientiously implement the spirit of the Third Plenary Session of the 14th CPC Central Committee, strengthen and improve the legal system for drug supervision and administration, and further establish and improve the drug law that is applicable to the socialist market economy System, in-depth publicity and implementation of the “Drug Administration Law”, according to the law, clean and self-discipline, safeguarding the dignity of the law, the guarantor ...