10）申报材料真实性的自我保证声明,包括申请材料目录和企业对材料作出如有虚假承担法律责任的承诺(原件1份).

三、现场提交成功后约去现场勘察，现场需提交材料

1）岗位职责

2）工作程序

3）公司制度

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。

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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。

那么在北京如何办理三类医疗经营许可证，办理许可证又有哪些条件及流程，小编今天带着满满的干货知识与您分享。

三类医疗器械常见产品有哪些：

mpany registration | agent Beijing three types of medical equipment company registration | agent Beijing class medical equipment for the record certificate | Beijing food business license | Beijing medical equipment network for the record | Beijing radiation safety license qualification 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 business license of third class medical devices according to the procedures. So in Beijing how to apply for the three types of medical business license in Beijing, what are the conditions and procedures for the license, Xiaobian today with full of dry