China is the third largest medical device market in the world. In China, regulating medical device clinical trials is still in the beginning stages; changes are being made in order to improve the regulatory system. Medical device executives are striving to understand merging regulatory requirements across the continent. At the same time, challenges in completing studies within a specific time frame, clinical trial design and statistics analysis are also trouble areas for medical device executives.

China's 2nd Medical Trials and Safety Surveillance is designed to provide you with knowledge of changing government regulations. The conference will dig deep into the device clinical trial process, helping you build a practical clinical strategy to successfully introduce your products quickly into the market. With eminent speakers from regulatory departments, clinical trial hospitals, leading manufacturers, CROs and other industry stakeholders, Noppen presents the most influential information gathering for the medical device industry

"It was a good way to learn about the Chinese healthcare market, the reforms and prospects. The event was excellently prepared."
-Hirtz & Co. KG

"Excellent presentations combined with a perfect match of clients offered a great forum for participation. Thank you!"
-Pall Corporation

"I found your speakers' excellent. This was an outstanding forum for us to attend to hear from experts and to share and listen to other people's experiences in a same situation as us."
-BSI

"Excellent event, I've learned a lot."
-GE Healthcare

"Your conference had a lively and relaxing vibe throughout, but also allowed me to meet a lot people in this industry."
-Sunray

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