In this free webinar on June 23rd at 15:00-16:00 Finnish time by Hohot Consulting and J MedTech you will receive comprehensive insights on China National Medical Products Administration’s updated regulations and medical device registration essential information (e.g. product performance test, testing labs in China, registration processes for Class I/II/III products, clinical trials in China and alternatives, etc.).
Register here.
China’s medical device market revenue reached 103 billion € in 2020, making up 20%f the global medical device market. It is a market one cannot ignore. However, China has its own distinctive regulatory system set by National Medical Products Administration (NMPA), the language of which also adds more challenges to international medical device manufacturers and solution providers.
Hohot Consulting together with the China medical device regulatory expert partner, J MedTec, are determined to lower the knowledge and strategy barrier for your organization to enter the China market by providing comprehensive insights on NMPA’s updated regulations and medical device registration essential information (e.g. product performance test, testing labs in China, registration processes for Class I/II/III products, clinical trials in China and alternatives, etc.).