据李文报道 :近日 ,安徽省药监局作出决定 ,对通过GMP认证药品生产企业进行跟踪检查。本次跟踪检查分为二级检查 :省局统一组织对无菌药品生产企业的跟踪检查 ;各市局负责组织对口服制剂、外用制剂生产企业的跟踪检查 ,省局进行督察和抽查 ;对同时生产无菌制剂及口服、外用制剂 According to Li Wen reports: Recently, Anhui Province Food and Drug Administration made a decision to track through the GMP certified drug manufacturers. The follow-up inspection is divided into two levels: the provincial unified organization of aseptic drug manufacturers follow-up inspection; the Municipal Bureau is responsible for organizing the oral preparations, topical preparations manufacturers tracking inspection, the provincial bureau inspector and spot checks; simultaneous production Sterile preparations and oral, topical preparations