欧盟的药品管理概况曹立亚凌静萍程鲁榕（卫生部药品审评中心北京１０００５０）根据卫生部的对外合作协议，本着了解和学习欧盟药品管理先进经验的目的，我们三人于１９９６年１月至４月在比利时杨森公司进行了为期三个月的培训。现将欧盟药品管理法规、新药审评机构及程... According to the Ministry of Health’s cooperation agreement with foreign countries, in line with the purpose of understanding and studying the advanced experience of the EU drug administration, the three of us, from January to April 1996, Three-month training was conducted at Janssen in Belgium. Now the EU drug management regulations, drug review agencies and processes ...