Is Your Team Prepared for China NMPA UDI Requirements?

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?

LS-China NMPA UDI Card Nov 2021

Register here to unlock explanatory videos concerning NMPA UDI database compliance.

  • With Reed Tech, leverage expertise from UDI experts in US FDA and other health authorities around the globe
  • Centralize product data in a single data hub for all the health authorities in your product markets
  • Integrate in-country users (subsidiary or affiliate, agent or distributor)
  • Share product data internally or externally with downstream customers
  • Learn more about SingleSource™ for Medical Devices, a flexible, centralized product data hub that allows for the type of interface needed – direct input, guided assistance or integrated options via API

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. 

See webinar recordings on China NMPA UDI regulations, requirements, data attributes and timeline