##  [Need a NMPA Legal Agent? Freyr has your back!](/medical-devices/need-a-nmpa-legal-agent-freyr-has-your-back) 

# Complexities to clearance

Medical device registration in China requires a local agent to act as the NMPA Legal Agent for foreign companies. Partner with Freyr as your NMPA Legal Agent for unmatched global and local Regulatory support.





### Talk to our Regulatory expert today











## Freyr’s Capabilities







 

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Want help with China medical device registration? Freyr can help you with NMPA medical device Regulation and more.

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## WHY FREYR?





 ![Quality Benchmarks and Accelerators](/sites/default/files/MDV%20ADD%20Icon/MDV_China%20NMPA-Infographic_Icon7.svg)



Quality Benchmarks and Accelerators



 ![ptimized Cost Benefits](/sites/default/files/MDV%20ADD%20Icon/MDV_China%20NMPA-Infographic_Icon6.svg)



ptimized Cost Benefits



 ![One Stop Regulatory Shop](/sites/default/files/MDV%20ADD%20Icon/MDV_China%20NMPA-Infographic_Icon5.svg)



One Stop Regulatory Shop



 ![Strategic Regulatory Partnership](/sites/default/files/MDV%20ADD%20Icon/MDV_China%20NMPA-Infographic_Icon4.svg)



Strategic Regulatory Partnership



 ![Combinations Improvement Initiative](/sites/default/files/MDV%20ADD%20Icon/MDV_China%20NMPA-Infographic_Icon3.svg)



Combinations Improvement Initiative



 ![ ISO Certified Regulatory Practices](/sites/default/files/MDV%20ADD%20Icon/MDV_China%20NMPA-Infographic_Icon2.svg)



ISO Certified Regulatory Practices



 ![Global Regulatory Intelligence Network](/sites/default/files/MDV%20ADD%20Icon/MDV_China%20NMPA-Infographic_Icon1.svg)



Global Regulatory Intelligence Network





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#### Get seamless market access with Freyr as your China NMPA agent. Freyr represents many global Medical Device company as China Agent for NMPA registration.

[Book A Meeting](javascript:void(0))







120

\+



Countries





2100

\+



Global Customers





2500

\+



In-house Regulatory Experts





850

\+



In-country Regulatory Affiliates





10



Global Delivery Hubs

















 









## Meet our Regulatory Experts





  

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### Summer Xia

Associate Director







With over 20 years of experience, including 15 years in medical device regulatory affairs, Summer has excelled in navigating both pre-market and post-market requirements. Her expertise has been instrumental in guiding numerous foreign and local manufacturing companies entering the Chinese market. Summer’s leadership has been demonstrated through her roles heading multinational Quality Assurance and Regulatory Affairs teams. She holds an MBA and is a certified Lead Auditor by BSI, enabling her to proficiently manage complex compliance landscapes.









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### Layla Tan

Specialist







With over 8 years of experience, including 5 years in the medical device industry, focusing on 2 years in medical device regulatory affairs. Layla has excelled in file submission and preservation both pre-market and post-market. She keep eyes on any change/update from NMPA and provides support for numerous foreign and local manufacturing companies entering the Chinese market.









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### Allan Zhang

Manager







With 10 years experience of medical device registration. Allan has rich experience in active and non-active medical device, guiding numerous foreign and local manufacturing companies and helping them to get more than 100 certificates approved by NMPA. He had participated in drafting CMDE guideline and industry standards. He can guide manufacture with fast and compliant registration strategy.















[Book a meeting ](javascript:void(0))  
with our Regulatory experts today to achieve swift compliance with all China Medical Device Regulations.