本刊讯为了解辖区药品生产企业不良反应监测工作的现状,查找存在的问题和难点,近日,昌平区食品药品监督管理局对该区药品生产企业(不包括原料药、体外诊断试剂、医用气体、中药饮片生产企业)开展调查。调查围绕企业基本情况;企业药品不良反应(ADR)体系建设情况;企业ADR工作开展情况;企业ADR相关培训及档案管理;品种情况;企业对相关法律责任方面 Recently, Changping District Food and Drug Administration of the pharmaceutical production enterprises in the area (excluding APIs, in vitro diagnostic reagents, medical gases , Chinese Herbal Pieces production enterprises) to carry out investigations. The investigation focused on the basic situation of the enterprise; the establishment of enterprise adverse drug reaction (ADR) system; the development of enterprise ADR; the training and file management of enterprise ADR; the variety situation;