EZFDA Consulting, ndi notice, gras NOtice, Inci, NMPA

EZFDA Consulting

EZFDA ConsultingEZFDA ConsultingEZFDA Consulting
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    • Home Page
    • FOOD & Supplement
      • GRAS Application
      • NDI Notification
      • FSVP Service
      • Label Review
      • FDA Registration
    • cosmetics
      • INCI Application
      • China CSAR
    • Beverage
    • Contact
    • 中文

EZFDA Consulting

EZFDA ConsultingEZFDA ConsultingEZFDA Consulting
  • Home Page
  • FOOD & Supplement
    • GRAS Application
    • NDI Notification
    • FSVP Service
    • Label Review
    • FDA Registration
  • cosmetics
    • INCI Application
    • China CSAR
  • Beverage
  • Contact
  • 中文

Site Content cosmetic ingredient registration in china

China CSAR Registration Services

Launch Your Cosmetics in China with Confidence


As China’s Cosmetic Supervision and Administration Regulation (CSAR) reshapes the regulatory landscape, cosmetic brands and raw material suppliers must navigate strict compliance standards to enter the Chinese market. At EZFDA Consulting, we specialize in guiding you through the full lifecycle of cosmetic product and ingredient registration with the NMPA (National Medical Products Administration).


What We Cover

We provide comprehensive support for both finished products and raw materials:


Cosmetic Products

  • General Cosmetics (e.g. creams, lotions, lipsticks) – NMPA Notification
  • Special Cosmetics (e.g. sunscreen, whitening, anti-hair loss) – NMPA Registration


Cosmetic Ingredients

  • New Cosmetic Ingredients (NCI) – Notification or Registration
  • Compliance support for existing ingredients under IECIC


Our Full-Service Approach

We offer end-to-end regulatory consulting, ensuring your products meet every CSAR requirement:

  • Product classification & gap assessment
  • Chinese Responsible Person (RP) designation
  • Formula & safety data review
  • Toxicology testing and animal testing coordination (if needed)
  • Translation of documentation & labeling
  • Online submission to NMPA
  • Response to NMPA inquiries
  • Post-market surveillance and annual reporting



Why EZFDA?

  • 10+ years regulatory experience
  • Deep understanding of China’s NMPA framework
  • In-country regulatory team for fast-track processing
  • Trusted by global beauty and biotech brands

  • Privacy Policy
  • Terms and Conditions

EZFDA consulting

400 West Capitol Avenue, Suite 1700, Little Rock, AR, 72201

+501-800-4108

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