China represents a vast market for medical devices, but its regulatory system can be difficult to navigate. A recent report published by China’s medical device regulator, National Medical Products Administration (NMPA), indicates that medical device approvals decreased by 38% in 2018 compared to 2017, possibly as a result of the depth and breadth of medical device regulatory changes underway in China. Manufacturers who are considering accessing this market will benefit from understanding the ever-changing regulatory landscape in the country.
In this free webinar, market experts Janet Zhang and Annika Chen will discuss key medical device registration requirements in China, including:
This webinar was recorded on December 12, 2019.
Below you will find basic demographic and healthcare market data on China, plus specific information about the medical device and healthcare indust
read moreShown below are some important regulatory documents impacting medical device companies. Unfortunately, the NMPA only makes these available in Chine
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