This course provides a comprehensive overview of China's medical device regulatory framework, including both pre-market and post-market requirements. China’s medical device regulations have evolved rapidly over the past two decades. This two-hour course covers the changes and key aspects of the regulations relevant to manufacturers wanting to market and sell in China.
By the end of this course you will be able to:
This course is vital for any medical device professional looking to bring products to market, or to manufacture or audit products in China. This course is particularly helpful for employees responsible for regulatory compliance, including developing pre-market submissions for entry into China.
By completing/passing this course, you will attain the Medical Device Certificate.