Decree of the Ministry of Agriculture No. 451 / 2000 Coll.
Decree of the Ministry of Agriculture implementing Act No. 91 / 1996 Coll., on Feed, as amended by Act No. 244 / 2000 Coll.
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Effective from 01.01.2001
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451
DECLARATION
Ministry of Agriculture
of 11 December 2000
implementing Act No. 91 / 1996 Coll., on feedingstuffs, as amended by Act No. 244 / 2000 Coll.
The Ministry of Agriculture provides, pursuant to § 3 (13), § 4 (12), § 5 (8), § 6 (3), § 7 (4) and (5), § 8 (13), § 8a (6) and § 13 of Act No. 91 / 1996 Coll., on feedingstuffs, as amended by Act No. 244 / 2000 Coll., ("the Act '):
Prohibited substances and products, warehouse pests
(1) This decree (1a) incorporates the relevant provisions of the European Community (1b) and regulates the details and requirements for the production, import, use, packaging, labelling, transport and putting into circulation of feed, additives and premixtures.
(2) In the manufacture of feed, additives and premixtures and for the feeding of livestock and pet animals which are kept by man, are not used and are not farmed animals other than fur animals (hereinafter referred to as "pet animals'), prohibited substances and products listed in Annex 1, Part A shall not be used.
(3) In the manufacture of feed, additives and premixtures and for the feeding of ruminants and other farmed animals which are kept, reared or fattened for food production, prohibited substances and products are to be classified
(a) animal waste derived from animals unfit for animal health assessment for human consumption as referred to in Annex 1, Part B; and
(b) further processed animal waste derived from low-risk confiscates of animal origin, (1) except feed materials listed in Part C of Annex 1, applicable to certain animal species under the conditions set out in that Part of the Annex; the prohibition does not apply to the use of processed animal waste derived from low-risk animal confiscates (1) for the production of feed and feed of domestic animals under specified conditions.
(4) The list of warehouse pests is set out in Annex 2.
The requirements for the production and conditions for the use of processed animal waste derived from low-risk confiscates of animal origin, i.e. processed animal proteins, blood products and blood meal, the use of which is not prohibited for the production of feed, feed additives and premixtures, shall be laid down in the immediately binding provisions of the European Communities (hereinafter referred to as the "European Community Regulations') .2).
Adverse Substance 1) and Products
(1) The undesirable substances, including their maximum permitted contents in products intended for animal feed, are listed in Annex 3. Products intended for animal feed (hereinafter referred to as "feed products') shall mean feed materials, premixtures, feed additives, feed and all other products intended for use in or used for animal feed, including wild farmed game.
(2) The content of undesirable substances is tolerated in feed products only if the limits and conditions laid down in Annex 3 are complied with.
(3) Products for feeding for which the undesirable substance or undesirable substance content exceeds the maximum content set out in column 3 of Annex 3 may not be mixed for dilution with the same or other feed products.
(4) In the absence of specific provisions in Annex 3 for the maximum content of an undesirable substance concerning feed additives or compound feed, the maximum content of the relevant undesirable substance, taking into account the prescribed proportion of the complementary feed or compound feed in the daily ration, shall not exceed the maximum content of that undesirable substance set out in Annex 3 for complete feed.
Radioactive contamination of feed, additives and premixtures
(1) The maximum levels of radioactive contamination expressed by the sum of the mass of the activities of caesium 134 and caesium 137 are:
(a) for complete feedingstuffs for pigs, 1 250 Bq.kg-1;
(b) for complete feedingstuffs for poultry, lambs, calves 2 500 Bq.kg-1, and
(c) for other feedingstuffs 5 000 Bq.kg-1
(2) Those values apply to feed intended for direct animal feed.
(1) The requirements for production equipment for manufacturers of additives, certain protein feed, premixtures, complete and complementary feedingstuffs are laid down in the directly applicable Regulation of the European Communities (2a).
(2) In feed additives containing additives classified as growth promoters, coccidiostats and histomonostats or vitamins A, vitamin D2 or D3, copper, selenium or zinc, classified as nutritional additives, the proportion of the dosage of the complementary feed in complete feed is determined by the concentration factor of the additive in the feed additive (hereinafter "concentration factor"). The maximum concentration factor values for each additive shall be the limit for the composition and dosage of the complementary feed in complete feed.
(3) The concentration factor of the additive in the feed additive is the ratio of the additive content in 1 kg of the additive and the maximum content of the additive authorised by the relevant legislation2b) in 1 kg of the complete feedingstuff with a moisture content of 12%.
(4) The method of calculation of the concentration factor and the maximum concentration factor value for the specified additives are set out in Annex No 8A for additional feedingstuffs for the relevant species and categories of animals.
(5) The provisions of paragraph 2 shall not apply to complementary feed supplied in blocks or in the form of a lick and to complementary feed for non-food producing animals.
Requirements for suppliers or importers putting into circulation additives or premixtures or certain protein feed
(1) Manipulation with a supplier or importer means the holding of additives, premixtures or certain protein feedingstuffs associated with the change of packaging, labelling or other method of adjustment which does not change the composition or quality of the products.
(2) The requirements, including the registration requirements, for suppliers or importers of additives and certain protein feedingstuffs referred to in Article 4 (3) (a) are set out in Annex 6, points 4, 5, 6A and 8, where they make changes to packaging, point 3 and Annex 4, Part A, point 2.
(3) The requirements, including the formalities for keeping records, for suppliers or importers of premixtures containing additives referred to in Section 4 (3) (b) are set out in Annex 7, points 4, 5, 6B and 8, where they make changes to packaging, point 3 and Annex 4, Part A, point 2.
(4) The requirements, including the registration requirements, for suppliers or importers of additives or their premixtures referred to in points (d) and (e) of Section 4 (3) of Annex 10 are set out in points 4, 5, 6A, 6B and 7, where they carry out a change in packaging, in point 3 and in Annex 4 (A) (2).
Registration requirements for distributors and importers not in possession and putting into circulation additives or premixtures or certain protein feed
(1) The distributor and the importer shall keep a register when putting additives or certain protein feedingstuffs into circulation:
(a) the names and addresses of the manufacturers and users to which the feed additives or certain protein feedingstuffs have been supplied,
(b) the types of products, their quantities delivered, including production dates, batch numbers or production specific part-time data for continuous production products; and
(c) the registration of origin for the additives delivered.
(2) The distributor and importer shall keep a register of premixtures when putting into circulation:
(a) the names and addresses of the producers and customers to whom the premixtures have been supplied;
(b) the origin and quantity of premixtures delivered, the date of delivery, the type and the indication of the premixture, the number of the production lot or the specific part of production in respect of continuous production products.
(3) Distributor and importer
(a) it shall draw up a complaint order showing how any complaint will be dealt with, including how the product can be withdrawn rapidly from both the distribution network and users;
(b) keep a record of any withdrawal of the product, indicating the weight and reason for returning the additive, the protein feed or the premixture; where the additive, certain protein feed or premixture is intended for disposal, the method of disposal must be registered. 2)
FISH RAW AND CERTAIN PROTEIN FEED (3)
Feed materials
(1) The feed materials for the production of compound feed and for feeding, their names, description, technological presentation and the mandatory characteristics of the declaration are set out in Annex 11. The precondition is that feed materials must be of sound, genuine, marketable quality and must therefore not pose a risk to human or animal health or the environment.
(2) The feed materials contained in Annex 11, Part B, may be put into circulation only under the names indicated therein.
(3) The requirements for chemical and botanical purity of feed materials are as follows:
(a) it shall not contain chemical impurities, excipients or, where appropriate, relevant additives derived from the manufacturing process to the extent permitted by good manufacturing practice, unless a certain maximum content for that feed material is specified in Part B of the Annex;
(b) the botanical purity shall not be less than 95% unless a different value is specified in Annex 11, Part B or C;
(c) they shall be regarded as botanical impurities;
1. natural harmless impurities, i.e. straw, fragments thereof, husks, seeds of other cultivated species, seeds of weeds, unless they are among the harmful impurities referred to in points 3 and d);
2. harmless other oilseeds or oleaginous fruits or their residues from previous processing, the content of which may not exceed 0,5%;
3. harmful impurities and harmful oil seeds for cereals, legumes, oil seeds and other grains, i.e. seeds and weeds listed in Annex 3,
(d) the content of the seeds of the asparagus or parts thereof may not exceed 0,5%;
(e) the limit values laid down in points (a) to (d) shall apply to the weight of the feed material.
(4) Requirements for moisture content and insoluble ash content in hydrochloric acid
(a) for feed materials, where no other limit moisture content is laid down in Annex 11, Part B or C, a content exceeding 14,0% shall always be declared. At the request of the customer, moisture shall be declared even if it does not exceed 14,0%,
(b) in the case of feed materials, where no other limit content for the insoluble proportion of ash in hydrochloric acid is laid down in Annex 11, Part B or C, a content exceeding 2,2% expressed in dry matter shall always be declared.
(5) Feed materials not listed in Part B of Annex 11 may be put into circulation, used for the production of compound feed and for feeding only provided that:
(a) belong to the groups of feed materials listed in Part C of the Annex;
(b) bear names other than those listed in Part B of Annex 11; and
(c) they shall bear the quality characteristics indicated in column 3 of Part C of Annex No 11 and comply with the requirements of paragraphs 1 to 4.
(6) Feed materials listed in Annex 11, Part B, meeting the requirements of paragraphs 1 to 4, other than those of groups 9 and 10 and dicalcium phosphate from defatted bones may be mixed in different proportions when put into circulation provided that the percentage of each feed material is always indicated. Feed materials from groups 9 and 10 of Part B of the Annex and dicalcium phosphate from defatted bones and from groups 15 and 16 of Part C of the Annex shall not be mixed in or between groups.
(7) Where feed materials are used as denaturing or binding substances in the manufacture of other feed materials, only feed materials listed in Annex 11 (B) or (C) may be used, except feed materials from groups 9 and 10 and dicalciumphosphate from bones and the proportion of feed materials used as binding substances shall not exceed 3% of the total weight of the product to which they were used.
(8) Fats originating from ruminants may be used for the production of feed for farmed animals, except ruminants, if they are cleaned in such a way that the total insoluble impurities do not exceed 0,15% of material.3)
(9) Feed materials obtained by means of genetically modified organisms or containing genetically modified organisms shall comply at all stages of putting into circulation with the requirements laid down by the European Community.4)
Certain protein feed
(1) Certain protein feedingstuffs authorised for production, putting into circulation and feeding are listed in Annex 12.
(2) Certain protein feed (2) must be of sound, unfalsified and marketable quality and must not pose a risk to human, animal and environmental health and may only be put into circulation under the names listed in Annex 12 in columns 2 and 7 and provided that they comply with the description in column 3 and the requirements in column 5 and, in the case in question, have been produced on a substrate as specified in column 4 of that Annex.
(3) Certain protein feedingstuffs may be processed into compound feedingstuffs and put into circulation only under the conditions laid down in Annex 12, columns 6 and 7.
(4) Certain protein feed obtained by means of genetically modified organisms or containing genetically modified organisms must meet the requirements laid down in the European Communities at all stages of putting into circulation. 4)
(5) The protein feed groups listed in Annex 12, point 2.1. Urea and its derivatives, in point 3. Amino acids and their salts and in point 4. Hydroxyanalogues of amino acids are to be classified in the group "Nutritional additives' according to the Regulation of the European Communities. 5)
(1) In the case of feed materials and certain protein feedingstuffs, the data of the limit and declared characteristics tested are considered satisfactory if they do not exceed the minimum tolerances laid down in Annex 13.
(2) If tolerance is not set for the limit and declared characters in Annex 13, the data of the test values shall be considered satisfactory if they do not deviate from that value by more than the analytical tolerance derived from the uncertainties of the measurement (5a), (1) of the test character.
(3) If no tolerance is set in Annex 13 and no analytical tolerance derived from measurement uncertainties is established, (5a) a quality character shall not be evaluated.
Feed materials with hygroscopic properties when treated with granulation, agglomeration or cultivation shall not be considered as hygroscopic.
ADDITIONAL SUBSTANCES, PREMIXES AND STANDARDS
Additives
(1) The data of the test values of additives are also considered satisfactory if they do not exceed the tolerance values of Annex 14, Part A, taking into account the analytical tolerance derived from the uncertainties of measure5a), as set out in Annex 30.
(2) Additives for which analytical tolerance values derived from uncertainties of measure5a) are not determined are not evaluated.
(3) The maximum permitted content of undesirable substances in additives is set out in Annex 3.
(4) Additives obtained by means of genetically modified organisms or containing genetically modified organisms must meet the requirements laid down in European Community4 at all stages of putting into circulation.
The requirements for the authorisation, putting into circulation and use of additives and premixtures are laid down in the European Communities. 5)
Premixes and carriers
(1) Only additives listed in column 3 of Part C of Annex No 14, or amino acids listed in column 2 of Annex No 12, and carriers complying with the provisions of Sections 7 and 14 of the Decree are used for the manufacture of premixtures intended for circulation, provided that they are physically-chemically tolerated in premixtures.
(2) In the premixture, only one growth promoter and only one additive may be used to prevent coccidiosis (an anticoccidic) or histomoniasis (a chemotherapeutic agent).
(3) Where vitamin D is included in the premixture, it may only be used in one of the forms listed in Annex 14, Part C.
(1) For premixtures, data of test values are also considered satisfactory
(a) for additives, if they comply with the tolerances laid down in Annex No 14, Part A, taking into account the analytical tolerance derived from the uncertainties of measurement (1c) in Annex No 30,
(b) in the case of declared quality characteristics outside the feed additives, provided that they do not exceed the tolerance given in Annex 13, including additives of amino acid groups, their salts and analogous products, urea and its derivatives,
(c) for quality characteristics other than additives for which tolerances are not laid down in Annex 13, taking into account the analytical tolerance derived from uncertains5a).
(2) Where tolerances are not set out in Annex 13 for quality characteristics other than additives, nor the analytical tolerance values derived from uncertainties of measurement (5a), the characteristics are not evaluated.
(1) For the manufacture of premixtures intended for circulation, media are used which do not adversely affect the quality and stability of premixtures and the quality characteristics of complete, complementary and dietary feedingstuffs to which premixtures of additives are processed.
(2) The maximum permissible content of undesirable substances in the carrier is set out in Annex 3.
COMPLETE AND ADDITIONAL FEED
(1) Complete and complementary feedingstuffs shall also be considered
(a) molasses feed containing at least 14% of all sugars expressed as sucrose and for which molasses has been used, among other feed materials,
(b) milk compound feedingstuffs administered in a dry state or after dilution by the appropriate amount of liquid intended for feeding to the young as an addition or substitute for post-colostral milk or for feeding to calves in fattening;
(c) mineral feed consisting primarily of minerals and containing more than 40% ash;
(d) feed for particular nutritional purposes (hereinafter referred to as "dietary feed"), which are feedingstuffs which, with their specific composition or method of manufacture, clearly distinguish them from normal feedingstuffs, are intended to provide the specific nutritional and physiological purposes set out in Annex 15 for certain categories or species of livestock or domestic animals and are not veterinary medicinal products or preparations.
Complete and complementary feedingstuffs must be of sound, genuine and marketable quality and must not pose a risk to human, animal and environmental health.
(2) For the manufacture of complete or complementary feed, compound feed and dietetic feed for farmed animals, feed materials referred to in Annex 11 (B) or (C) or mixtures thereof, certain protein feed as referred to in Annex 12, feed additives as referred to in Annex 14 (C), columns 2 and 3 and premixtures corresponding to the requirements laid down in Sections 12 and 14 and, for dietary feed, feed materials as set out in Annex 15.
(3) In the case of a mixture of feed materials in accordance with Article 7 (6) corresponding to their composition to complementary feed and intended for direct feeding in combination with other feed, the provisions for complementary feed shall apply.
(4) For the manufacture of complete or complementary feedingstuffs and dietetic feedingstuffs for domestic animals intended for putting into circulation, the feed additives referred to in Annex No 14, Part C, columns 2 and 3 and premixtures conforming to the requirements laid down in Sections 12 and 14 shall be used. In addition, feed materials as referred to in Annex 11 and certain protein feed as referred to in Annex 12 and, where appropriate, other feed products to be indicated in the labelling and, for dietary feed, feed materials as referred to in Annex 15 are used for the manufacture.
(5) Only one growth promoter and only one additive may be used in complete and complementary feed to prevent coccidiosis (an anticoccidic) or histomoniasis (a chemotherapeutic agent).
(6) For complete or complementary feed for farmed animals which are kept, reared or fattened for the production of food, other than feed for carnivorous fur animals and fish, feed materials which are animal protein derived from low-risk confiscates of animal origin, (1) which have been treated in accordance with specific legislation1 (hereinafter "processed animal proteins'), blood products, blood meal, gelatine of ruminants and other protein products the use of which is prohibited pursuant to § 1 (2) and Annex 1 (B) shall not be used. The prohibition on the use of certain feed materials of animal origin also applies to feed, feed additives and premixtures containing those proteins. The conditions for the use of fishmeal, hydrolysed proteins, dicalcium and tricalcium phosphate, blood products and blood meal are laid down in Annex 1, Part C.
Quality requirements
(1) The moisture content of complete, complementary and dietary feedingstuffs must be declared if it exceeds:
(a) 5% for mineral feed not containing organic feed materials;
(b) 10% for mineral feed containing organic feed materials;
(c) 7% for milk compound feedingstuffs, other complete and complementary feedingstuffs containing more than 40% milk products,
(d) 14% for other complete, complementary and dietary feedingstuffs.
(2) The content of the insoluble proportion of ash in hydrochloric acid in complete, complementary and dietetic feedingstuffs may not exceed 2,2% in the dry matter and, in the case of feedingstuffs containing mainly rice by-products, 3,3% in the dry matter. However, the content of 2,2% in the dry matter may be exceeded provided that the content is declared as a percentage of the feed as such, in the case of:
(a) complete, complementary and dietary feedingstuffs containing authorised mineral binders;
(b) mineral feed;
(c) complete, complementary and dietetic feedingstuffs containing more than 50% of sugar beet or sugar beet cuttings;
(d) complete and complementary feedingstuffs containing more than 15% fishmeal intended for farmed fish.
(3) The content of iron in compound feedingstuffs for calves weighing up to and including 70 kg must be at least 30 mg per kilogram of complete feedingstuff with a moisture content of 12%.
(4) Additives or premixtures, or complete and supplementary and dietary feed with additives or using premixtures, shall be homogeneous in the additive content. Homogeneity is a character that is expressed by the variability of the values of the additives contained and monitored. 1)
(6) Premixes or complete and complementary and dietary feedingstuffs must not be cross-contaminated and the manufacturer must prevent cross-contamination.
(1) For complete complementary and dietetic feedingstuffs, the data of the test values are considered satisfactory.
(a) for additives if they comply with the tolerances laid down in Annex 14, Part A, point 3;
(b) in the case of quality characteristics, excluding additives, declared in accordance with Annex No 26 for feed for farmed animals or Annex No 27 for feed for domestic animals and other declared quality characteristics, excluding additives, and in the case of limit quality characteristics, provided that they do not exceed the tolerance of that value in accordance with Annex No 16 or Annex No 17,
(c) for quality characteristics, other than additives for which tolerances are not laid down in Annex 16 or Annex 17, provided that they do not deviate from that value more than those of analytical tolerances derived from uncertains5a).
(2) Where tolerances are not set out in Annex No 16 or Annex No 17 for quality characteristics other than additives, or in Annex No 17 for analytical tolerances derived from uncertains5a), the characteristics are not evaluated.
PRODUCTION, PROCESSING, IMPORTATION AND INSTALLATION EXPERIENCE
(1) For the demonstration of competence, the following shall be required:
(a) for the production, import and putting into circulation of additives, successful completion of higher education studies, with the exception of Bachelor's study programmes (5), from the field of chemistry or biology or biotechnology or biotechnology or pharmacy or medicine or veterinary medicine or food or agriculture and professional practice relating to the manufacture or use of substances of a minimum duration of two years;
(b) for the manufacture of premixtures or complete and complementary feedingstuffs using additives or using premixtures or for the manufacture and processing of certain protein feedingstuffs or for the processing of feed with an excessive level of undesirable substances;
1. successful completion of higher education, with the exception of bachelor programmes (5) in the field of agriculture or veterinary medicine; or
2. the successful completion of the higher education studies referred to in point (a) with the exception of agriculture and veterinary medicine and the successful completion of post-graduate studies in the agricultural or veterinary university with a professional focus on animal feed and nutrition and professional experience relating to the production or putting into circulation or use of premixtures or complete and complementary feedingstuffs using additives or using premixtures of a minimum duration of three years;
(c) for the production of feed using additives or premixtures and processing of certain protein feedingstuffs, a secondary vocational examination in an agricultural or veterinary or food direction and professional experience in the manufacture of feed using additives or premixtures and processing of certain protein feedingstuffs of a minimum duration of four years;
(d) for the import and putting into circulation of premixtures or certain protein feedingstuffs or grains or oil seeds obtained by means of genetically modified organisms or containing genetically modified organisms, a graduation test. This activity shall not be required to demonstrate the competence of the practice.
REQUIREMENTS FOR THE MARKETING AUTHORISATION OF PRODUCERS, SUPPLIERS, IMPORTERS AND DISTRIBUTORS AND TECHNICAL PARAMETERS OF BIOLOGICAL TESTING
Registration of producers, importers and suppliers
(1) The application for registration of the manufacturer or persons referred to in Article 3 (11) of the Act or persons operating the production facilities of mobile feed manufacturers or importers or suppliers contains:
(a) if the person is a legal, business or name, registered office, type of legal person, identification number, if assigned, and tax identification number, and if the person is a natural, name or surname (s), address (s), date of birth, identification number and tax identification number of the applicant, if assigned;
(b) if there is a legal person residing abroad, the registered office of that person's organisational unit in the Czech Republic or the name and place of permanent residence of the person responsible in the Czech Republic; if the person is a natural person having his registered office abroad, the name, date of birth, place of permanent residence or the name and place of permanent residence of the person responsible in the Czech Republic,
(c) an extract from the Commercial Register, if it is a person registered in it, or a trade licence or an establishment certificate issued by a competent authority;
(d) the name and address of the manufacturing plant, the type of production and its specification;
(e) data subject to the protection of patent law (6) and disclosure of data classified as trade secrets (7)
(f) proof of compliance with the requirements laid down in Sections 4 and 7 of the Act and the dosage limit of the premixture, if applicable,
(g) for applicants for the production of additives or certain protein feedingstuffs or premixtures or feedingstuffs using additives or feedingstuffs using premixtures, the name, surname and address of the person responsible for the manufacture and the certificate of professional competence referred to in Article 6 (2) of the Act;
(h) applicants for import or entry into circulation (suppliers) handling additives or certain protein feed or premixtures, the name and address of the person responsible and the certificate of professional competence referred to in Article 6 (2) of the Act;
(i) proof of entry in the list of genetically modified organisms and products approved for circulation in the Czech Republic;
(j) methods of testing, unless specified in specific legislation, 1)
(k) proof of the right to manufacture the additive by the person responsible for putting it into circulation, in the case of a feed additive listed in Annex No 14, Part C 1 or C 2,
(l) in the case of the production, processing, putting into circulation, import or use of genetically modified organisms, feed products containing or consisting of genetically modified organisms or feed products produced from genetically modified organisms, proof of their authorisation in accordance with European Community rules, 4)
(m) for import applicants, proof of entry in the list of manufacturing establishments located in third countries authorised in accordance with specific legislation (7) and European Communities Regulation (7) which are authorised to put additives or premixtures or feedingstuffs into circulation in the States of the European Communities.
(2) The application for registration, including further particulars, is submitted in the Czech language.
(3) Further details on the application for authorisation are provided in Annex 18.
Registration of production plants
(1) The application for registration of production operations pursuant to Sections 4 and 8b of the Act contains:
(a) if the person is a legal, business or name, registered office, type of legal person, identification number, if assigned, and tax identification number, if any, if any, of the natural person, name or surname (s), address (s), date of birth, identification number and tax identification number of the applicant, if any;
(b) if the person is a legal person having his head office abroad, the registered office of that person in the Czech Republic or the name and address of the person responsible in the Czech Republic; if the person is a natural person with a place of business abroad, the name, date of birth, residence or the name and address of the person responsible in the Czech Republic,
(c) an extract from the Commercial Register, if it is a person registered in it, or a trade licence or an establishment certificate issued by a competent authority;
(d) the name and address of the production operation, the type of production and the scope of the activity.
(2) The application for registration, including further particulars, is submitted in the Czech language.
Registration of distributors
The application shall contain:
(a) if the person is a legal, business or name, registered office, type of legal person, identification number, if assigned, and tax identification number, and if the person is a natural, name, address, date of birth, identification number and tax identification number of the applicant;
(b) an extract from the Commercial Register, if it is a person registered in it, or a trade license or an establishment certificate issued by a competent authority;
(c) groups of additives or premixtures or feed referred to in Article 4 (3) (a) and (b) of the Act;
(d) a written declaration by the applicant to ensure that the documentation and records of the products the placing into circulation of which he makes available in accordance with Article 6 are kept;
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Regulation Information
| Citation | Decree of the Ministry of Agriculture No. 451 / 2000 Coll., implementing Act No. 91 / 1996 Coll., on Feed, as amended by Act No. 244 / 2000 Coll. |
|---|---|
| Regulation Type | Order |
| Author | - |
| Collection | Code of Laws |
| Date of Promulgation | 29.12.2000 |
|---|---|
| Effective from | 01.01.2001 |
| Effective until | - |
| Status | Valid |
The regulation text is for informational purposes only.
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