Regulations of Permission on Manufacture and Import of Feed and Feed Additives｜第 2 條｜畜牧｜Regulation｜In Force
農業部｜v1.0
Last Amended: 2016-01-21
2.1 For the license to manufacture and/or process feed/feed additives according to Section 10.1 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/feed additives before the deadline. 2.1.1 Four photocopies of the applicant’s Identity card (ID). Non-natural-person applicants shall submit four photocopies of the certificate of incorporation or registration. 2.1.2 Four photocopies of registration certificate for the feed/ feed additives factory. 2.1.3 Two copies each of product description, ingredient specification, manufacture flowchart, testing method and the test report, formulation basis, and reference material or literature. Such documents are not required for feed/additive for which national standards already exist. 2.1.4 Two photos of the feed/ feed additives package or container, if any. 2.1.5 For reuse-entity applicants, four copies of the one-time or general-purpose permit, or the industrial waste disposal plan. 2.1.6 For applicants that are public/private waste clearance/disposal organization, four copies of the waste clearance/disposal permit, its attached list and appendices. 2.1.7 For feed in the animal-fat category, the proof of raw material source, and one color photo of the material. 2.1.8 For feed used as mineral supplements, two copies of proof of raw material source. 2.1.9 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. 2.1.10 For feed/ feed additives claiming special benefits, two copies of post-feeding test report about the benefit. 2.1.11 Four copies of the affidavit stating that the entity name and/or trademark are not a likeness, duplicate, counterfeit, or allusion of any existing entity name or trademark. 2.1.12 Other information or objects specified by the central competent authority. 2.2 For the license to repackage feed or feed additives according to Section 10.1 of the Act, applicants shall submit the application 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 feed additives. 2.2.1 Two photocopies of manufacture/import license registration for feed and additives. 2.2.2 Two copies of written consent by the holder of the registration described in Section 2.2.1. 2.2.3 Information or objects specified in Sections 2.1.1~2.1.4, 2.1.11, and 2.1.12. However, the formulation basis and reference material in Section 2.1.3 are not required. 2.2.4 Other information or objects specified by the central competent authority.