4.应当建立健全产品质量管理制度，包括采购、进货验收、仓储保管、出库复核、质量跟踪和不良事件的报告制度等；
5.应当具有与其经营的医疗器械产品相适应的技术培训和售后服务的能力，或者约定由第三方提供技术支持；
6.经营无菌和植入类产品的公司需建立计算机管理系统及计算机管理制度，能够保证产品从购进到销售整个过程的有效质量跟踪和追溯。
申请医疗器械经营许可证所需材料：
医疗器械经营许可证办理依据《北京市实施细则（2017年修订版）》，具体提交材料如下：
1．《 医疗器械经营许可申请表》（原件1份）
2．《营业执照》复印件（交验原件）；（复印件1份）
3．法定代表人、企业负责人、质量负责人的身份证明（查验原件）、学历或者职称证明复印件（对于统一采购渠道，采取连锁经营的非法人零售企业，提供连锁企业总部质量负责人身份证明、学历或者职称证明复印件）；（交验原件） （复印件共3份）
product quality management system shall be established and improved, including procurement, purchase acceptance, storage, warehouse delivery review, quality tracking and adverse event reporting system; 5. It shall have the ability of technical training and after-sales service suitable with the medical device products it operates, or agree to provide technical support by a third party; 6. Companies operating sterile and implanted products shall establish a computer management system and a computer management system to ensure the effective quality tracking and traceability of the whole process of products from purchase to sales. Materials required for applying for the Medical Device Busine
