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Accelerate your global expansion with the ultimate Chinese regulatory affairs resource for medical device and IVD manufacturers. Our newsletter delivers real-time updates on China's National Medical Products Administration (NMPA) guidelines, registration dossiers, and localized country strategies. Join a community of MedTech innovators receiving exclusive compliance advice, e-learning opportunities, and expert guidance directly to their inbox.

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Newsletter Nr. 5, 2025

Chinese restricts EU manufacturers back

AI tool for Chinese registration


PTR tool for change registration

Tool for Chinese instruction for use


Key Takeaways for Project Management in China

A list of recalls of medical device

Non-compliances of 5 manufacturers

Attractive international fairs in China in 2025

Incubator for Chinese market