[オンデマンドセミナー] NMPA medical device registration requirements in China


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:

The history and regulatory structure of the NMPA, formerly known as the China Food and Drug Administration (CFDA)
The regulatory pathway for market access
Recent initiatives to ease regulatory requirements for foreign manufacturers of medical devices
Details on implementation of the NMPA’s new electronic medical device registration management (eRPS) system
New Unique Device Identifier (UDI) requirements
And more

This webinar was recorded on December 12, 2019.