Free Webinar: How to Register Medical Devices in China 101
Are you planning to bring your medical device to the Chinese market but unsure how to navigate the regulatory landscape?
On Thursday, November 13 2025, Cisema’s regulatory experts delivered a focused, 45-minute webinar that unpacks the complexities of medical device registration in China under the NMPA (National Medical Products Administration).
Tailored for professionals in regulatory affairs and market access, this session provided expert guidance, practical strategies, and real-world case studies to support your next steps in China's evolving market.
What You'll Learn
By viewing the session, you’ll gain valuable insights into the medical device registration process:
Understand China’s regulatory framework and registration pathway
- Gain clarity on China’s key authorities and regulatory processes.
Navigate classification, testing and clinical requirements with confidence
- Move through regulatory checkpoints without delay.
Secure long-term success with essential post-registration insights
- Gain clarity on China’s key authorities and regulatory processes.
Meet the Speakers
Further Information
Explore how Cisema can help you streamline medical device registration and NMPA approval in China on our service page