To market medical devices in China, the regulatory process to comply with NMPA UDI may be unfamiliar, requiring experienced help. Does your team have a checklist of all the necessary attributes and other process steps?
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Reed Tech helps Life Sciences professionals gain control over their own and their industry’s data. With subject-matter expertise and product data management capabilities, Reed Tech serves manufacturers and distributors of medical device products and those who support them in consulting and IT roles. They provide the means to efficiently collect, transform, submit and analyze regulatory data. We believe that when people and organizations are enabled with technologies that help them achieve regulatory compliance, manage product data and gain insights backed by analytics, the potential to positively impact patient outcomes is unlimited.
We welcome you to contact us to discuss your questions about UDI database submissions to China NMPA and other Health Authorities.