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药品流通包括生产、经营和使用三个环节。《药品管理法》规定,药品生产企业、药品经营企业、医疗机构配制制剂必须分别取得《药品生产许可证》、《药品经营许可证》、《医疗机构制剂许可证》方可从事药品生产、经营、配制制剂。但对医疗机构使用药品实施许可证制度比较放松,助长了“以药养医”之风。实际上,医疗机构自行配制制剂应该属于药品生产范畴,而不仅限于使用范畴。我国已经有《药品管理法》,近期又公布了《药品管理法实施条例》,应当不折不扣地执行《条例》第四章的规定,严格医疗机构的药剂管理工作。
Drug circulation, including production, operation and use of the three links. The Drug Administration Law stipulates that pharmaceutical manufacturers, pharmaceutical companies and medical institutions must obtain “Drug Production License”, “Drug Business License” and “Medical Institution License” respectively before engaging in drug production and operation , Preparation of formulations. However, the medical institutions to use drugs to implement the permit system more relaxed, contributed to the “medicine and medicine” style. In fact, the preparation of medical institutions to prepare their own products should belong to the category, not just the scope of use. China already has the Drug Administration Law and recently promulgated the Regulations for the Implementation of the Drug Administration Law. It should strictly implement the provisions of Chapter 4 of the Regulations and strictly regulate the administration of pharmaceuticals in medical institutions.