In 2018, CIRS has received many emails from overseas medical device companies about how to classify their products, how to register their products in one registration unit and what the cost and the duration are. As the one-stop service we always provide for global companies, in 2019, we start to open ‘Weekly Case Study’ column in our official website. Every week, we will choose 1-2 categories and issue case studies that we have well understood or have rich registration experience for domestic or imported medical devices. The contents include the introduction, registration unit, clinical trials, duration and cost, etc.
We are trying to cover the popular and advanced medical device categories in the world and provide reliable and professional registration guidelines, through the accumulation for near one decade and professional registration team. Hope ‘Weekly Case Study’ can help you preliminarily understand the registration condition in China.
If you have any suggestions or want to know the registration condition of a specific category, please contact to us firstname.lastname@example.org