We have established a complete quality management system according to the requirements of ISO 13485, QSR820 and NMPA GMP, covering all stages of IVD and CDx product design and development, clinical trials, registration and manufacturing. We can support the development and registration of companion diagnostic kits for global pharmaceutical companies. We have obtained EU ISO 13485 certification and NMPA production license.
If you have any of the following needs, feel free to contact us or email us at inquiry@MEDxTMC.net . We will reply within 24 hours.
1. Customized or bulk orders of IVD/CDx products.
2. Get a quote for IVD/CDx products
3. Become our distributor
4. Get customized pharmaceutical service solutions
5.Learn more about our technology and R&D