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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

First of the Cisema Webinar Series: NMPA Registration of Medical Devices in China
DIT, CBBC and Cisema To Host Webinar on Developments in China’s Healthcare and Life Sciences Sector
Webinar: China NMPA Registration of Medical Devices, IVDs, and Medical Software

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