The Medical Device Approval Process in China (video)

The medical device market in China continues to attract more and more foreign manufacturers, but the country's medical device approval process can be challenging. Careful preparation is required to successfully commercialize your product in China. Our free one-hour webinar will cover the major requirements involved in Chinese medical device approval, quality management system compliance, and more. Specific issues the webinar will cover include:

• CFDA (formerly the State Food and Drug Administration, or SFDA) device classification rules
• China Legal Agent and After Sales Agent representation
• Testing and clinical trial requirements
• Quality management system requirements in China
• Import Medical Device Registration Certification (IMDRC)
• How long it takes to register a medical device, and how much it costs

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