质量跟踪制度和不良事件的报告制度等。
(五)应当具备与其经营医疗器械产品相适应的技术培训和售后服务的能力，或者约定第三方提供
技术支持(六)具有能够满足企业所在地食品药品监督管理部门实施电子监管的条件(七)其他条件
详见《新疆医疗器械经营企业现场检查验收标准》。
第五条医疗器械经营企业跨区设置仓库，应具备以下条件: (一)具有与经营企业本部互联的能
够时时交换医疗器械储存、出入库数据的计算机管理系统和能够满足仓库所在地食品药品监管部门实施
电子监管的条件互联网药品信息服务许可证需要哪些材料广告(一)企业营业执照复印件(二)网站域名证
书及服务器所在地址(三)网站负责人相关材料(一名)(四)两名药品及医疗器械相关技术人员除此之外从
事互联网药品信息服务网站...查看全文精品 感谢下载载(二)仓库设置条件应符合《新疆医疗器械经
Three kinds of medical devices as the highest risk in the medical device classification category, strictly by the supervision and management, but for many families of three kinds of medical devices, many basic problems is not fully grasp, today we will take a look, what are three business scope of medical devices? How to apply for the three types of medical equipment business license again!
Beijing for the medical device business license process of Beijing medical device second class record network record