China Regulatory Affairs
How to register your medical device in China
As the second largest healthcare market in the world, China offers immense opportunities for medical device companies. However, regulatory affairs in this market can be complex and challenging to navigate, making it crucial to understand the regulatory process and requirements set out by the National Medical Products Administration (NMPA) to ensure compliance for medical device products in China.
In this webinar, we will provide you with an introductory but detailed guide on how to register your medical device in China. Our speakers will cover the entire NMPA registration process, requirements, legal frameworks, and regulatory pathways involved in obtaining market approval.
Date: Wednesday 31 May 2023
Time: 2:00pm-2:30pm CET / 8:00pm-8:30pm CST
Presenter: Hamish King, Anna King and Cristina Ribo
Language: English
The 30 minutes webinar will cover the following topics:
- Regulatory pathways
- Clinical pathways and feasibility
- Recent registration trends
- NMPA Legal Agent
- Localization trends
Sign up for the webinar even if you are in a different time zone, a replay will always be available at a time convenient for you
Presenters
Hamish King
Webinar Host
Anna King
Webinar Host
Cristina Ribo
Webinar Host
, ,