Overview:
Various pathways are available to overseas manufacturers of medical devices and IVDs to register their products in China with the NMPA, but do you know which routes exist? What are their requirements? And do they even apply to the specific circumstances of your product?
 
Join us for our succinct 30-minute webinar designed to help you understand the options to choose the most appropriate pathway for your product market entry in China, the world’s second-largest medical device market.

Pathways covered:
- Standard NMPA Notifications & Registrations
- Hong Kong Listing
- Greater Bay Area Approvals
- Hainan Island Medical Tourism Zone Applications
- Innovative Medical Device / Green Route Applications
- Priority Registrations
- Emergency Registrations

Date: Thursday, February 15, 2024
Time: 14:00-14:30 CET / 08:00-08:30 EST /  21:00-21:30 CST

​​​​​​​​​​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
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Presenters