Shenzhen Jitong Medical Co., Ltd. (referred to as “Jitong Medical”) is a professional company specializing in the integration and service of the medical device industry chain. We are committed to providing comprehensive solutions for medical device companies, covering all aspects from engineering development, inspection and testing, animal experiments, clinical trials, registration and certification, contract manufacturing, brand building, to financing.

As a comprehensive technical service provider, Jitong Medical offers the following key services:

 • Product Testing and Certification: Includes domestic registration testing, international registration testing, and product quality testing.

 • Clinical Trials: Supports both domestic and international clinical trials, providing high-quality technical support.

 • Regulatory Registration Consulting and Certification: Provides global regulatory registration services for medical device companies, including but not limited to NMPA (China), CE (EU), FDA (USA), ANVISA (Brazil), RZN (Russia), Southeast Asia, South Africa, TGA (Australia), and other market registration and compliance consulting.

 • System Guidance and Training: Offers guidance for system certifications such as MDSAP, ISO13485, QSR820, GMP, and provides related regulatory training.

 • Local Authorized Representative Services: Provides authorized representative services for regions such as the EU, USA, UK, Hong Kong, etc.

 • Free Sales Certificate (FSC): Assists clients in obtaining the Free Sales Certificate, facilitating smooth market entry for products worldwide.

Our goal is to integrate global resources and create an efficient, one-stop technical service platform to help medical device and in-vitro diagnostic product companies successfully launch and quickly comply with regulations in global markets, ensuring product quality and market competitiveness.