国家食品药品监督管理局发布《医疗机构药品监督管理办法(试行)》日前,国家食品药品监督管理局发布了《医疗机构药品监督管理办法(试行)》(以下简称《办法》),对加强医疗机构药品监督管理方面从严要求。《办法》指出,医疗机构必须从具有药品生产、经营资格的企业购进药品,由专门部门统一采购,并禁止其他科室和医务 Recently, the State Food and Drug Administration released the Measures for the Supervision and Administration of Drugs in Medical Institutions (Trial Implementation) (the Measures) (hereinafter referred to as the Measures), which have been issued by the State Food and Drug Administration to strengthen the medical supervision and management of medical institutions (Trial Implementation) Institutional drug supervision and management of the strict requirements. The Measures state that medical institutions must purchase medicines from enterprises that have the capacity to produce and manage pharmaceuticals, purchase them in a unified way by special departments, and prohibit other departments and medical institutions