《药品管理法》及其《实施办法》明确规定药品必须建立健全严格的质量检验和入库验收,在库保养、出库验发等制度。药品入库验收,是药品进入贮存、保管或销售之前必须经过的一个程序,是有效地把住药品质量关的一个重要保证。目前,我国药品经营企业和医疗单位普遍建立了药品入库验收制度,设立了一定数量的质检员,并进行认真的验收登记。验收的内容一般应检查品名、规格、数量、生产厂家、批准文号、批号、有效期、注册商标以 The “Drug Administration Law” and its “Implementation Measures” clearly stipulate that medicines must be established and perfected strict quality inspection and storage acceptance, in the library maintenance, delivery and inspection system. Drug storage and acceptance, is a drug must enter the storage, storage or sale must pass before a procedure, is to effectively control the quality of medicines is an important guarantee. At present, China’s pharmaceutical enterprises and medical units have generally established drug storage and acceptance system, set up a certain number of quality inspectors, and serious acceptance of registration. Acceptance of the content should generally check the name, size, quantity, manufacturer, approval number, lot number, expiry date, registered trademark