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Application documents for disinfectant China NHFPC(MOH) register

 
For disinfectant Products, the follow application documents must be collected and submitted to the NHFPC(MOH):

1, The import disinfectant NHFPC(MOH) Permit Application Form
2, product R&D report
3, the product formula
4, the main active ingredient content and test methods
5 Production process and chart
6 product internal quality standards
7, the testing report conducted in the Country of Origin
8, Testing reports issued by the NHFPC(MOH) designated lab
9, the product label (including manual)
10, Authorization letter of NHFPC(MOH) registration angent in china  issued by the applicant manufacturer/ company.
11 Country (region)  of Origin to allow the production and sales documents ( Free sale certificate, etc.)
12 The disinfectantt samples

 
 

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Important Note
Due to the reorganization of the Chinese government in 2018,
CFDA (China Food and Drug Administration) was renamed to NMPA (National Medical Product Administration), and its food supervision function has been transferred to SAMR (State Administration for Market Regulation of China);
GACC (General Administration of Quality Supervision, Inspection and Quarantine of China) was abolished, and its import and export trade supervision function has been transferred to GACC (General Administration of Customs of China),
Therefore, all
CFDA and SFDA on this website default to NMPA, GACC defaults to GACC; 
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