# Commission Decision of 10 December 2008 amending Annex C to Council Directive 64/432/EEC and Decision 2004/226/EC as regards diagnostic tests for bovine brucellosis (notified under document number C(2008) 7642) (Text with EEA relevance) (2008/984/EC), Division 2: In Annex C to Directive 64/432/EEC point 4.1 is replaced by the following:

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

‘4.1.
Tasks and responsibilities
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/eudn/2008/984/annex/division/2 (the official version)
Page: https://openlegislation.uk/eu-decision-2008-984/annex/division-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.