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The document ceased to be valid since  November 30, 2015 according to Item 1 of the Order of the Government of the Republic of Kazakhstan of October 31, 2015 No. 870

ORDER OF THE GOVERNMENT OF THE REPUBLIC OF KAZAKHSTAN

of December 21, 2011 No. 1576

About approval of Rules of sampling of the moved (transported) objects and biological material

(as amended of the Order of the Government RK of 07.08.2012 No. 1030)

According to the subitem 17) of article 5 of the Law of the Republic of Kazakhstan of July 10, 2002 "About veterinary science" the Government of the Republic of Kazakhstan DECIDES:

1. Approve the enclosed Rules of sampling of the moved (transported) objects and biological material.

2. This resolution becomes effective after ten calendar days from the date of the first official publication.

 

Prime Minister

Republic of Kazakhstan K. Masimov

Approved by the order of the Government of the Republic of Kazakhstan of December 21, 2011 No. 1576

Rules of sampling of the moved (transported) objects and biological material

1. General provisions

1. These rules of sampling of the moved (transported) objects and biological material (further - Rules) are developed according to the subitem 17) of article 5 of the Law of the Republic of Kazakhstan of July 10, 2002 "About veterinary science" and determine procedure for sampling of the moved (transported) objects and biological material.

2. In these rules the following concepts are used:

1) selection - set of tests, are selected - from the transported (moved) object for determination of compliance of batch to veterinary health requirements and safety requirements;

1-1) biological materials - the part of viable fabric or biologically active liquids which are selected for the purpose of performing diagnosis of diseases of animals (the blood, slime, cerebrospinal fluid, bile, pus, urine, excrements, scrapings, materials taken by method of biopsy and another);

1-2) pathological materials - the biological material taken from live or dead animals, containing or m contain the activator of infectious or parasitic diseases, intended for sending to veterinary laboratory

2) check sample - the part of average sample which is stored in the laboratory conducting researches, intended for repeated research in case of discrepancy or emergence of disputes over results of the conducted researches;

3) stern - the products of plant, animal, mineral, microbiological, chemical origin used for feeding of animals, which are containing nutritive matters in assimilable form and not making harmful effects on health of animals;

4) feed additive - the substances of organic, mineral and (or) synthetic origin used as sources of missing nutritive and mineral substances and vitamins B diet of animals;

5) laboratory test (final test) - the part of average sample intended for forming of the test sample directed to researches (brought to laboratory), determined by regulating documents for the purpose of confirmation of conformity of controlled object to the established requirements;

6) quartation method - method of creation of average sample of the joint test by its division (after careful hashing) on four equal parts and consecutive selections of two quarters on diagonal before receipt of the product quantity required for the laboratory analysis;

7) envelope method - the scheme of selection of pointed tests piece, bulk in display outer or without it and put by embankment, stack, ranks. Depending on the size of unit of the vehicle, display outer or storage with products, the method of single, double or triple envelope with sampling from the lower, average and upper layers is applied;

8) hinge plate - the part of average sample allocated for determination of separate quality factors of products;

9) the joint test - the set of the pointed tests which are selected from selection, intended for creation of average sample;

10) test - sample, the transported (moved) object which is selected from;

11) batch - the quantity of the homogeneous transported (moved) object made (made) by one producer in identical conditions on one regulating document, with identical date of development, which is drawn up by one veterinary accompanying document and brought at the same time;

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