4）供应商档案

5）培训记录

6）新法律法规

7）员工档案等

现场核查成功后一周内就可以拿证了。

我公司主要经营代办北京医疗器械公司注册|代办北京三类医疗器械公司注册|代办北京二类医疗器械备案凭证|代办北京食品经营许可证|代办北京医疗器械网络备案|代办北京辐射安全许可等资质专项审批服务

三类医疗器械指的是植入人体，用于支持、维持生命，对人体具有潜在危险，对其安全性、有效性必须严格控制的医疗器械。现行制度规范下，经营三类医疗器械的经营主体需要按程序办理三类医疗器械经营许可证。

alification special examination and approval services Class III medical devices refer to the medical devices implanted in human body to support and maintain life, with potential danger to human body, and their safety and effectiveness must be strictly controlled. Under the current system and norms, the business entities of third class medical devices need to apply for the