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China Medical Devices Regulations Executive Leadership Training Program
Date: July 25, 2017
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USTDA is hosting a training for 22 senior officials from China's Food and Drug Administration (CFDA). The itinerary will feature global best practices on approving imported medical devices. The delegates will meet with U.S. government agencies, medical device industry associations, and U.S. companies interested in accessing this market in China. As part of the program, USTDA will host a Public-Private Workshop for U.S. companies looking for business opportunities in China's healthcare sector. Topics of discussion will include: 

  • Building a Cooperative Regulatory Environment in China
  • Medical Device Regulatory Issues China
  • Clinical Trials Requirements 
  • Unique Device Identification
  • Harmonization and Classification

Click here to view the event flyer.

PHM International is organizing this program and logistics on behalf of USTDA and in cooperation with HCP. For more information on the Business Briefing and to register, please contact Hank Kearney at hankk@phmintl.com or visit: www.phmintl.com/China-FDA