Part 6 Adverse event reporting management under order 739

This session of the webinar introduces the adverse event reporting management under order 739. The speaker list article 62, article 65 to support this regulation. The speaker also shares some cases. After that, it shows principles for the exemption of medical device adverse events.

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UK-China Medical Device Access to China Webinar: Session 1-Navigating Medical Device Lifecycle and Compliance in China
UK-China Medical Device Access to China Webinar: Session 2 - Targeting Unmet Medical Needs in China's Growing Market

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Part 6 Adverse Event Reporting Management Under Order 739

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