4.應當建立健全產(chǎn)品質(zhì)量管理制度，包括采購、進(jìn)貨驗收、倉儲保管、出庫復核、質(zhì)量跟蹤和不良事件的報告制度等；

5.應當具有與其經(jīng)營(yíng)的醫療器械產(chǎn)品相適應的技術(shù)培訓和售后服務(wù)的能力，或者約定由第三方提供技術(shù)支持；

6.經(jīng)營(yíng)無(wú)菌和植入類(lèi)產(chǎn)品的公司需建立計算機管理系統及計算機管理制度，能夠保證產(chǎn)品從購進(jìn)到銷(xiāo)售整個(gè)過(guò)程的有效質(zhì)量跟蹤和追溯。

申請醫療器械經(jīng)營(yíng)許可證所需材料：

醫療器械經(jīng)營(yíng)許可證辦理依據《北京市實(shí)施細則（2017年修訂版）》，具體提交材料如下：

1．《 醫療器械經(jīng)營(yíng)許可申請表》（原件1份）

2．《營(yíng)業(yè)執照》復印件（交驗原件）；（復印件1份）

3．法定代表人、企業(yè)負責人、質(zhì)量負責人的身份證明（查驗原件）、學(xué)歷或者

d improved, including procurement, purchase acceptance, storage, warehouse delivery review, 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 tracking and traceability of the whole process of products from purchase to sales. Materials required for ap