Kostenloses Webinar: Wie man Medizinprodukte in China registriert – Grundlagen
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
Live Broadcast Details
- Date: Thursday, 13 November 2025
- Time: 9:15–10:00 CET | 16:15–17:00 HKT
Further Information
Explore how Cisema can help you streamline medical device registration and NMPA approval in China on our service page
CONNECT WITH CISEMA
With more than 20 years of experience and a team of over 100 specialists, Cisema helps global companies achieve compliance across Asia Pacific with confidence and accelerate market entry.
Stay Informed with Monthly News and Analysis
Stay informed with the latest regulatory changes, expert insights, and market opportunities across APAC, delivered straight to your inbox.
