How will latest QMS and PMS changes affect your medical device’s entry to China? China’s National Medical Products Administration (NMPA) — formally known as the China Food and Drug Administration
China has been increasing its surveillance on post market monitoring with more regulations and random inspections both inside China and outside of China. Find out how to meet the upcoming
The China IVD market has seen record growth recently and will continue to be an important market with the growing threat of cancer and COVID-19. Join us on Thursday, July
Hundreds of new regulations in the forms of policies, guidelines, standards, and announcements are released continuously as part of the NMPA transformational reform. These updates and changes have impacts not
FOLLOW THIS LINK TO VIEW THE SESSION ONLINE. Hundreds of new regulations in the forms of policies, guidelines, standards, and announcements are released continuously as part of the NMPA transformational
Learn new Hainan RWD program to use NMPA unapproved devices in China directly from the authorities. Find out how to cut years to months for initial clinical use in real
To keep up with international standards and help device manufacturers prepare for regulatory compliance, China’s National Medical Products Administration (NMPA) issued a number of regulations related to unique device identifiers
Want to reduce your device’s clinical trial costs and accelerate its time to market in China? It’s possible when you use the latest China National Medical Products Administration (NMPA) regulatory
This intensive, two-day workshop will provide an overview of electronic submissions to the China NMPA for devices and IVDs called electronic Regulated Product Submissions (eRPS), which are similar to eCTD
This intensive, two-day workshop will provide an overview of electronic submissions to the China NMPA for devices and IVDs called electronic Regulated Product Submissions (eRPS), which are similar to eCTD
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