Regulations of Permission on Manufacture and Import of Feed and Feed Additives｜第 3 條｜畜牧｜Regulation｜In Force
農業部｜v1.0
Last Amended: 2016-01-21
For the license to import feed/feed additives according to Section 11.1 of the Act, the application shall be submitted to the central competent authority along with the following information or objects and, upon subsequent notice of the central competent authority, provide the fee receipt, two copies of the list for lab tests, and four 300-gram samples of the feed or additive before the deadline. 3.1 Four photocopies of the applicant’s ID paper. Non-natural-person applicants shall submit four photocopies of the certificate of incorporation or registration. 3.2 Four photocopies of registration certificate for feed sale. 3.3 Two copies each of product description, ingredient specification, manufacture flowchart, inspection method and the inspection report, formulation basis, and reference literature. Such documents are not required for feed/feed additives for which national standards already exist. 3.4 Two photos of the feed/feed additives package or container, if any. 3.5 One original and three photocopies of notarized/certified Power of Attorney (POA) by the foreign supplier and manufacture/sales permit issued by the exporting country; if the foreign supplier is not the original manufacturer, additional documents are required: one original and two photocopies of notarized/certified POA by the original manufacturer to the supplier. No need to submit such a POA if the manufacturer has been verified by the central competent authority to be officially recognized by the exporting country. 3.6 For feed in the animal-fat category, the proof of raw material source, and one color photo of the material. 3.7 For feed additives containing peptide, protein, or nucleic acid that are produced with genetically modified (GM) or molecular biotechnology, the characteristics of the GM additives, safety assessment, a list of relevant research papers and such papers listed. 3.8 For feed/additives claiming special benefits, two copies of post-feeding test report about the benefit. 3.9 Four copies of the affidavit stating that the entity name and/or trademark are not a likeness, duplicate, counterfeit, or imitation of any existing entity name or trademark. 3.10 Other information or objects specified by the central competent authority.