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          SAMR Infant Formula Milk Powder Registration

          Infant,Registration,China,Food,Milk,Regulation,SAMR

          Under the Administrative Measure on Product Formula Registration of Infant Formula Milk Powder (CFDA Order No. 26) released in 2016, companies shall submit registration of imported infant formula milk powder to the State Administration for Market Regulation (SAMR). The registration not only applies to domestic infant formula milk powder produced and marketed in China, but also imported infant formula milk powder produced abroad and put on the Chinese market.

          Who Shall Register?

          • Manufacturers of infant formula milk powder in China.

          • Foreign manufacturers selling infant formula milk powder to China.

          Who Can Be The Applicant (The Certificate Owner) of Registration?

          Domestic infant formula milk powderManufacturers of infant formula milk powder in China
          Imported infant formula milk powderManufacturers of infant formula milk powder abroad

          Manufacturers in China can submit an infant formula milk powder registration or appoint a local agent to do so. Foreign manufacturers must appoint a local Chinese agent such as CIRS China to submit the infant formula milk powder registration. The local agent should be knowledgeable and qualified to carry out the registration.

          Our Services

          CIRS China fulfils all the qualifications and requirements of being a local Chinese agent (registered capital, expertise, etc). We provide all the necessary services in one package to complete registration at the most competitive price in the market.

          Our services include:

          Formula Compliance Review
          (Registration Feasibility Analysis)

          • Evaluation of whether the recipe is compliant with Chinese regulations

          • Preparation of an infant formula milk powder registration proposal

          Health Food Registration

          • Data evaluation and data gap analysis

          • Writing testing proposal, sending sample to certified labs

          • Translation and notarization of certifying documents

          • Dossier preparation and submission

          • Tracking the registration status and communication with SAMR

          Label Review

          • Review the Chinese packaging/label and provide modification suggestions

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