?浙江省医疗机构药品和医疗器械使用监督管理方法?(省238号令) of rural drinking water sources, protection of drinking water sources in rural疗器械的使用负全面责任。 医疗机构应当根据其规模和管理需要，设置药品、医疗器械管理组织或者配备管理人员，建立管理制度，明确并落实职责。 第二章 药品、医疗器械的采购与储存 第七条 医疗机构应当建立药品、医疗器械进货查验制度,对相关证明文件进行查验： 〔一〕从药品、医疗器械生产企业首次采购药品、医疗器械的，应当查验?药品生产许可证?、药品批准证明文件或者?医疗器械生产企业许可证?、医疗器械产品注册证书； of rural drinking water sources, protection of drinking water sources in rural areas by the end of the delimitation of the scope of protection, complete with warning signs, isolating network protection facilities of rural drinking water sources, protection of drinking water sources in rural areas by the end of the delimitation of the scope of protection, complete with warning signs, isolating network protection facilities5 of rural drinking water sources, protection of drinking water sources in rural areas by the end of the delimitation of the scope of protection, complete with warning signs, isolating network protection facilities 〔二〕从药品批发企业、医疗器械经营企业首次采购药品、医疗器械的，应当查验?药品经营许可证?、药品批准证明文件或者?医疗器械经营企业许可证?、医疗器械产品注册证书； 〔三〕采购进口药品，应当查验药品进口批准证明文件和进口检验质量报告书；采购进口医疗器械，应当查验医疗器械进口注册证书，有进口质量检验要求的，应当同时查验进口检验质量报告书。 第八条 医疗机构对购进的药品和医疗器械应当逐批进行验收，并作记录。 医疗机构接受捐助、赠送药品和医疗器械，从其他医疗机构调入急救需要药品和医疗器械，或者从药品零售企业直接购进急救需要药品的，应当按照前款规定进行验收，并作记录。 第九条 药品验收记录应当包括药品通用名称、规格、批号、有效期、生产厂商、供货单位、购货数量、购进价格、购货日期、验收日期、验收结论等内容。 医疗器械验收记录应当包括产品名称、规格型号、产品批号〔生产日期〕、生产厂商、供货单位、购货数量、购进价格、购货日期、验收日期、验收结论等内容；有灭菌批号、有效期的，应当记录灭菌批号、有效期；医疗仪器、设备的验收记录还应当包括相关配置和技术性指标。 of rural drinking water sources, protection of drinking water sources in rural areas by the end of the delimitation of the scope of protection, complete with warning signs, isolating network protection facilities of rural drinking water sources, protection of drinking water sources in rural areas by the end of the delimitation of the scope of protection, complete with warning signs, isolating network protection facilities5 of rural drinking water sources, protection of drinking w
