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  • China Regulatory 2021 Deep-dive: Major Updates, IVD Regulatory Landscape, evolving Digital Health Frameworks

China Regulatory 2021 Deep-dive: Major Updates, IVD Regulatory Landscape, evolving Digital Health Frameworks

Monday, 23 August 2021 / Published in Webinars

China Regulatory 2021 Deep-dive: Major Updates, IVD Regulatory Landscape, evolving Digital Health Frameworks

On September 14, 2021, Cisema, NAMSA and China Med Device will cohost a webinar session during the RAPS Convergence 2021, a four-day online event, to talk about the China medtech regulations with a deep-dive into the must-know trends, major changes and key product focus areas in 2021.

Learning Objectives of the session:

Latest trends and major NMPA regulatory updates in China
Latest overarching Order #739 and its implications on overseas medical device manufacturers.

Current regulatory landscape for IVDs
Case studies will also be available.

Evolving digital health framework in China
There will also be a particular focus on AI/ML products as regulations respond to an exploding global growth in software products and capabilities.

The webinar session is a must watch for all regulatory professionals covering medtech products in or entering the Chinese market.

Contact Cisema if you would like to learn more.

What you can read next

Webinar: Masterclass in China Registration for Medical Device & IVD
Medical Device Registration in China (NMPA)
Quality assurance in purchasing China products
IHK for Bavaria & Cisema Webinar: Online Procurement in China – Quality assurance in purchasing

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