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.

Webinar: Medical Device Pathways to Market for China 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

Register here.