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Latest Past Events
Learn the Ins and Outs of China NMPA E-Filing – Day 2
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 […]
Learn the Ins and Outs of China NMPA E-Filing
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 […]
Medical Device Clinical Trials in China Latest Regulatory Developments
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 […]