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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