As the worlds first new digital cross-border SaaS+Data medical device CRO, we carry on regulatory compliance business with service networks in countries and regions including mainland China, the United States, the United Kingdom, Germany, Netherlands, Poland, Malta and Hong Kong.


Supported by a world-class professional team who possesses the requisite expertise in regulatory compliance, clinical trials and market access, we provide one-stop solutions accordingly for medical devices, in vitro diagnostics, AI medical software, etc. We boast consulting services for accessing 100+ counties market with 1,000+ successful cases of overseas registration and certification empowered by the database of 600,000+ global distributors, 1 million+ global clinical trials and 3 million+ global registration of medical devices. We are looking forward to ensuring a satisfactory certification procedure for all medical devices from marketing strategy to regulatory compliance.