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Evidence
Testing, safety assessment and efficacy evaluation
China cosmetics filing and registration require test reports and safety-assessment materials that match the product type and claims. Jinshang Testing coordinates this work; partner laboratories perform the tests and issue those reports.
Who this is for
Foreign brands usually need a combination of microbiological and physicochemical tests, toxicology unless a legal waiver applies, a cosmetic safety assessment prepared under current Chinese guidelines, and efficacy evaluation where claims require it. Special cosmetics add category-specific safety or human studies.
How the path works
Tests should be performed by institutions that meet the qualifications required for cosmetics registration and filing inspection, following the Safety and Technical Standards for Cosmetics and the inspection rules in force. Safety assessment follows the Technical Guidelines for Cosmetic Safety Assessment (2021) and, after NMPA Announcement No. 50 of 2024, the classified submission approach in the relevant submission guide. Efficacy evaluation follows the Efficacy Claim Evaluation Standard: different claims require human tests, consumer-use tests, laboratory tests, or literature and research-data analysis.
A Material Safety Data Sheet is not a substitute for a China cosmetic safety assessment.
What Jinshang organizes, and what partner labs do
We identify which evidence the chosen path requires, keep the test plan aligned with the formula and claims, and place the reports in the dossier. Partner laboratories design and run the tests they accept and issue the corresponding reports. We do not claim those reports as Jinshang’s own CMA/CNAS output.
Next step
Discuss your China market path
Tell us whether you plan to import finished goods or manufacture in mainland China, and what the product claims. We will outline the likely filing or registration path. Testing, where needed, is arranged with partner laboratories.
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