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　　The core team has been working in the medical device regulatory industry for nearly 20 years and is one of the earliest teams engaged in medical device registration in China. For a long time, the team has completed a large number of pre-market and post-market regulatory consultation, registration, evaluation and other work of medical devices, with rich practical experience;

　　Boasting team members with diversified backgrounds, we are committed to building a consulting team with both senior CRO background and top manufacturer background and familiar with the regulations for medical device registration and enterprise production process and supporting system documents, so that we can better complete all registration work from the perspective of enterprise R&D;

　　The core founding team members have many years of working experience in well-known CROs and are familiar with customer pain points. We will continuously optimize the service content and service quality to create the most professional and innovative medical device CRO with the best service