New Update on China CFDA Regulation and Registration for Medical Devices with Case Studies

You will get a deep understanding of the up-to-date China CFDA regulatory policies

Course objective and outcome
Chinese market becomes more and more important for medical device manufacturers due to its large volume. The CFDA registration process is very time and cost consuming. Also, China CFDA is updating the regulations very rapidly recently. 
This course aims to provide the participants a deep understanding of the up-to-date CFDA regulatory policies and practical solutions to the problems of frequent occurrence during Chinese market entry.

  • CFDA organization reform and regulation system
  • Important concepts for CFDA registration
  • Product registration III
  • “Made in China” Strategy: Registering a domestic device
  • Vigilance and inspection
  • Registration renewal and change
  • Green channel for innovative device and prioritized device

 Who should attend
This course is suitable for not only RA and clinical professionals who manage the product approval work, but also international marketing and C-level directors who are interested in Chinese marketing strategy.
Dr. Chao Xu, Co-Founder & Strategic investor, J MedTec Limited

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mp@medicoindustrien.dks billede
Morten Petersen