Hamburg, 19.02.2020, Juliane Celik
NSF PROSYSTEM – new eLearning Course Regulatory Requirements China
Learn flexibly for your advancement!
With our eLearning you learn at your own pace and you can fit it in anywhere.
With our new eLearning Course Regulatory Requirements China you learn more about
- Identify key dates and changes to China’s medical device regulation
- Recognize key differences in China’s medical device classification system
- Explain the approach of the registration process in China for domestic manufacturers
- The importance of the Clinical Evaluation Report (CER) for approval of most class II & III medical devices
- Recognize the increasing importance of Post-Market Surveillance activities
- Recognize the importance of complying with NMPA guidelines for labeling and instruction for use
China’s medical device regulation program has evolved rapidly over the past two decades. This 2 hours overview covers the changes and key aspects of the regulations as they pertain to domestic manufacturers.
Would you like to learn more about the requirements for medical devices in the Asian region?
Then you are welcome to attend our seminar in Hamburg: 21-22 April 2020 Asia Pacific Requirements – Registration types and regulatory requirements for the Asia Pacific region