Healthcare Sep 28, 2020 10:06 AM (GMT+8) · EqualOcean
National Medical Products Administration (NMPA), China's Food and Drug Administration, updated the policy about the application process for local manufacturing of registered imported medical devices. For registered imported medical devices in Class II and III, NMPA recognizes part of the importing registration application files if the primary materials, manufacturing technique, quality management system keep consistent. This policy update can improve the review and approval efficiency and accelerate the industry development.

Source: National Medical Products Administration