The Medical Device Master File (MFs) registration system is a key initiative. It provides an excellent pathway for global suppliers of raw materials, critical components, software, and manufacturing processes to protect their intellectual property and efficiently support their Chinese clients in completing product registration.

중국NMPA 수입의료기기 등록

In this webinar, we will summarize the regulation updates and regulatory activities in 2022, to assist the companies keep up with the new regulation updates and know more about how to register the medical device under the new regulations.

The overview of medical device regulatory activities in 2021 The data analysis of medical device registration in 2021 Summary of medical device regulation updates in 2021 The new medical device rules in 2022

Free Webinar-Overview of Chinese Medical Device Regulations-Korea Branch