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Home
Consulting Services
NMPA Registration/Filing
Medical Device and IVD
NMPA Medical Device and IVD Registration/Filing
NMPA Medical Device Classification Consulting
NMPA Product Technical Requirements Support
NMPA Clinical Trial Application Support
NMPA Periodic Risks Assessment Report Service
China Local Legal Agent Service
China Medical Device Advertising Management Service
Drug
NMPA Drug Registration
Cosmetic
NMPA Cosmetic Registration/Filing
NMPA New Cosmetic Ingredient Application
NMPA Cosmetic Ingredient Safety Information Code Application
SAMR Registration
China Health Food Registration
Special Equipment Manufacturing License Application Support
China Food for Special Medical Purposes Registration
CCC Certification Support
MARA Registration
China Veterinary Products Consulting
China Veterinary Drug Registration
China Veterinary Diagnostic Reagent Registration
China Pet Food Consulting
China Pet Food Registration
GACC Registration
GACC Admission Application Support
Overseas Production Enterprises of Imported Food Registration Support
CFSA Registration
China Three New Foods Registration
China New Food Ingredients Registration
China New Food Additive Registration
China Food-related Products Registration
Regulatory Consulting
Registration Certificate Management Service
Quality Management System (QMS) Establishment Consulting
China Operation and Production License Application Service
China Test Support
Other Services
China Market Research Service
China Logistics Transportation, Warehousing, Customs Clearance Service
Translation Service
About us
FAQ
Blog
Industry News
Regulatory News
Contact us
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NMPA Requirements for Post-Market Surveillance(PMS) of Medical Devices
2024-07-22
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