Learn to navigate China’s regulatory, cultural and economic landscape for medical devices to improve the efficiency of your regulatory processes

Develop or market your medical devices in China more effectively with a deep understanding of the Chinese medical device regulatory landscape. During this course, you will learn fundamental Chinese regulatory requirements for medical devices and how they relate to the country’s economic and cultural background. Guided by our expert course leader you will:

• Unlock an Introduction to China Medical Device Regulations covering the regulatory bodies and regulatory requirements & updates
• Unearth the intricacies of the medical device registration and submission processes in China and leverage learnings for future submissions in the US/EU
• Hone in on best practices to liaise with regulators in your products region to enhance understanding of regulatory processes
• Dive into market assessment and entry strategies
• Explore 4 different case studies where participants will:
  • Work in groups to analyze a case study related to China medical device registration challenges
  • Each group will present their analysis and discuss with the facilitator and other participants