STEP 01
Preliminary Review
Review key materials such as product ingredients and test reports, identify applicable regulations, and determine the relevant authorities and requirements for registration.
STEP 02
Regulatory Analysis
Map target country standards (SFDA/MoIAT, etc.) and conduct a detailed feasibility review.
STEP 03
Document Preparation
Review and supplement essential documents such as product photos, artwork, CFS, COA/MSDS, and certificates to meet registration requirements.
STEP 04
Submission to Local Authorities
Official license application and feedback management via local official portals and partner networks
STEP 05
Certification Complete
Final certificate issuance and system registration complete, enabling immediate export and distribution