# Council Directive of 26 June 1964 on animal health problems affecting intra-Community trade in bovine animals and swine (64/432/EEC), Division 4.1: Tasks and responsibilities

Extent: E+W+S+N.I.

National reference laboratories designated in accordance with Article 6a shall be responsible for:
(a) the approval of the results of the validation studies demonstrating the reliability of the test method used in the Member State;
(b) determination of the maximum number of samples to be pooled in ELISA kits used;
(c) calibration of working standards as referred to in point 2.1.6;
(d) quality checks of all antigens and ELISA kits batches used in the Member State;
(e) following recommendations of, and cooperating with the Community reference laboratory for brucellosis.

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Source: https://www.legislation.gov.uk/eudr/1964/432/annex/C/division/4/division/4.1 (the official version)
Page: https://openlegislation.uk/eu-directive-1964-432/annex-C/division-4/division-4.1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.