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Join the third webinar in our series on Tuesday September 27th as we focus on China Alternative Registration Pathways for Medical Devices and IVDs. Our regulatory experts will share an overview of the latest changes in alternative registration pathways. in such a fast-moving regulatory landscape for medical device and IVD manufacturers, we help you stay informed about requirements to stay fully compliant in China.

The webinar will cover the following topics:

  • Fast track pathways with NMPA: emergency approval, innovative approval, and priority review and approval
  • Trend in approvals via the green channels
  • Hainan Pilot Zone & medical device clinical real-world data applications
  • Hong Kong listing
  • Greater Bay Area approval, importing and contract manufacturing
  • Q&A session live with the audience

Click here to register