泰国土耳其许可证书领事认证
只需要CE副本扫描件一份
营业执照副本一份清晰地，拍照也可以
出单时间是9个工作日哦
出单地点：IN beijing
CFDA强制性规定，从2018年1月1日起，所有医疗器械制造商应满足《规范》的要求，即从2018年1月1日起，医疗器械GMP全面实施，仍无法实现《规范》如果必须停止生产，并向当地市食品药品监管部门报告。
CFDA mandates that as of January 1, 2018, all medical device manufacturers shall meet the requirements of the Code, namely, as of January 1, 2018,
Full implementation of GMP medical devices, still unable to achieve the "specification" if must stop production, and to the local municipal food and drug regulatory authorities report.
此外，CFDA总局将继续加强对三流医疗器械制造商的飞行检查和投诉举报，及时对一流和二等医疗器械制造商进行飞行检查
In addition, CFDA will continue to strengthen flight inspections and complaints against third-tier medical device manufacturers, and conduct timely flight inspections on first-class and second-tier medical device manufacturers
。如同在当地[0x9A8B的实施工作的监督和抽查，所以公司需要提前做好准备，以满足检查
As in local [0x9A8B] implementation of work supervision and spot checks, so the company needs to be prepared in advance to meet the inspection
