Shenzhen Jitong Medical Co., Ltd., abbreviated as Jitong Medical. We are a resource integration and service provider in the medical device industry chain, focusing on integrating engineering development, inspection and testing, animal experiments, clinical trials, registration and certification, commissioned production, brand building, financing and other resources for medical device customers. And provide comprehensive technical services such as high-quality clinical trials, global regulatory registration, and inspection and testing for medical device and in vitro diagnostic product enterprises.
As a professional comprehensive service provider, our main service projects include: product testing, domestic registration inspection, international registration inspection, domestic and international clinical trials, regulatory registration consultation (such as China NMPA, Brazil ANVISA registration, Southeast Asia registration, South Africa registration, Russia RZN, EU CE MDR&IVDR, US FDA&510K, Australia TGA, UK MHRA&UKCA, Canada MDL&MDEL, South Korea MFDS, Central Asia registration, etc.).We provide one-stop technical solution services for medical device customers, including product quality testing, free sales certificates, system guidance (MDSAP, ISO13485, QSR820, GMP, etc.), regulatory training, and local authorized representatives (European, American, British, Hong Kong, Russian, Pakistani, Southeast Asian licensees, etc.).
Includes: clinical trial research, analytical performance studies, regulatory registration consultation, certification consultation, whitelist registration in various countries, product quality testing, system guidance, regulatory training, local authorized representatives, etc.