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Securing Regulatory Approval in China
11/20/2018

Dec. 11 and 12 | Washington, D.C.
This course will cover CMDE/CFDA's perspective on submissions, from processes to approval to modifications of submissions. In this program, industry experts will provide an in-depth guide to how you as an organization can secure regulatory approval in the China market. Closely paralleling the topics covered during AdvaMed's 510(k) and PMA Submission Strategy Workshops, you will walk away with actionable insights and strategies for assembling and streamlining your submissions. Learn more.

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