Part 2 Measures for supervision and adminstration of medical device production (China GMP) and key aspects of onsite inspections.

To better understanding China GMP, the speaker used a tablle to list corresponding main items for ISO 13485:2016). Some key articles are listed in this section to explain medical device operation. It also summarized good quality practices for medical device business in order 58.

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UK-China Medical Device Access to China Webinar: Session 1-Navigating Medical Device Lifecycle and Compliance in China
UK-China Medical Device Access to China Webinar: Session 2 - Targeting Unmet Medical Needs in China's Growing Market

Previous: Part 1 Introduction the Webinar——Keep up with the Enhancement of Medical Device Post-Market Surveillance in China: GMP, GSP, and NMPA onsite inspections

Next: Part 3 Various types of NMPA inspections on the quality system of imported/domestic medical device manufactures

Part 2 Measures For Supervision And Adminstration Of Medical Device Production (China GMP) And Key Aspects Of Onsite Inspections.

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