Thursday, 5, March, 2026 / Published in Blog, China, IVDs, Medical Devices

China Medical Device and IVD Registration FAQs: What Foreign Manufacturers Need to Know About NMPA Requirements

While China’s regulatory framework is well defined, many overseas companies still encounter uncertainty around classification rules, Chinese technical standards, Product…

Thursday, 12, February, 2026 / Published in Blog, China, IVDs, Medical Devices

China IVD Risk Classification Explained: How NMPA Class Shapes Registration Pathways

China IVD risk classification is the first and most consequential regulatory decision foreign manufacturers face when bringing an in vitro…