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- CFDA Issued Ten New Medical Device Registration Guidelines...tration GuidelinesEar Cavity Type Medical Infrared Thermometer Registration...2017-12-07 13:56:01
- keting Supervision-- Medical Device Quality Sampl...In order to strengthen Medical devices quality supervision and ensure the product safety and effec...2017-12-07 13:32:26
- tration for overseas Medical devices that are app... initial registration of imported Medical devices II. Contents of licensing...2017-12-07 12:48:37
- tration for overseas Medical devices that are app... initial registration of imported Medical devices II. Contents of licensing...2017-12-07 12:48:27
- Clinical Trials for Medical Devicesinical trials for the higher risk Medical devices in China. They are divide...2017-10-02 17:15:36
- t and Compliance for Medical device...Medical devices manufacturer and distributor must establish and follow the ...2017-10-02 17:02:41
- Medical Device CFDA RegistrationFor all Medical devices and in vitro diagnostic reagents(IVD), companies who plan t...2017-10-02 16:50:58
- 英国MHRA医疗设备新法规系列之一: 关键要求摘要 90/385/EEC on active implantable Medical devices (EU AIMDD) (2)Directive 9...2021-01-09 22:27:17
- 解读MDR新规 之MDR标签和说明书新规定MDR标签和说明书新规定解读: 德国欧通商务咨询 欧盟新法规MDR(Medical Device Regulation 2017/745)和IVDR(...2018-12-16 11:30:32
- 不会写510K注册报告怎么办?别慌,这些指南文件能帮到你list:http://www.fda.gov/downloads/Medicaldevices/deviceregulationandguidanc...2017-11-18 16:46:26