建立管理制度：
(1)企业各部门、组织和人员的职责权限制度;
(2)质量安全管理责任追究制度;
(3)首营企业资质审核管理制度;
(4)首营品种资质审核管理制度;
(5)产品购进及质量验收管理制度;
(6)产品养护和储存管理制度;
(7)产品陈列管理制度;
(8)效期产品管理制度;
(9)不合格产品管理制度;
(10)质量跟踪及不良事件报告制度;
(11)产品售后服务及投诉处理制度;
(12)问题产品协助召回制度;
(13)仪器、设备、计量器具管理制度;
(14)营业员管理制度;
(15)计算机信息化管理制度;
How to handle the business license of class III medical devices
1. The business license of Class III medical devices is handled as follows:
(1) The applicant shall submit the application materials to the relevant departments;
(2) Relevant departments shall accept the application of the applicant;
(3) Investigate the actual site and audit the products;
(4) Grant the issuance of a class III medical device license.