What we can help with, and what is done by partner laboratories

Jinshang Testing organizes cosmetics filing and registration for the China mainland market: path review, dossier compilation, Chinese name and label checks, safety-assessment document organization, platform submission and follow-up on supplementary requests. Testing and some evaluation steps are coordinated with partner laboratories. The laboratory that performs a test issues that report. We are not a CMA/CNAS laboratory of our own, and we do not advertise ourselves as a cosmetics testing lab.

Published 11 November 2026 · Updated 11 November 2026

What we organize

We help foreign brands decide between import and local manufacture, and between ordinary filing and special registration. We list the documents the brand, the factory and the Domestic Responsible Person should supply. We review consistency among the formula, standard and artwork, and we guide the official submission. Related documentation work, such as MSDS authoring or assistance with EU CPNP notification and US FDA facility and listing files, is available when clients need it. US FDA assistance is documentation support, not a certification and not a “seven-day approval.”

What partner laboratories do

Partner laboratories accept samples, run agreed microbiological, physicochemical, toxicological or human studies, and issue reports under their own qualifications. Which laboratory will issue a given report is confirmed before the work starts. A list of frequent partners appears on the about page; those companies are not Jinshang subsidiaries.

Cautions

Organizing a dossier does not make us the filer, registrant or Domestic Responsible Person. Those legal roles remain with the companies named in the file. See how we work for the project sequence.

Questions we are often asked

Will the report bear Jinshang’s logo?

The test report bears the name of the laboratory that performed the test. Our role is to organize the project around that report.

Can you guarantee that a submission will pass without supplementary requests?

No. We work to make the file consistent and complete, but supplementary requests depend on the authority’s review of the actual product and documents.