# Council Directive 2009/156/EC of 30 November 2009 on animal health conditions governing the movement and importation from third countries of equidae (codified version) (Text with EEA relevance), Division: Real-time Reverse-Transcription Polymerase Chain Reaction (rRT-PCR)

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

Agent identification tests based on nucleic acid methods must detect reference strains from the nine virus serotypes of the AHSV.
The method described in point 2.1 is based on point 1.2 of Section B in Chapter 2.5.1 of the Manual of Diagnostic Tests and Vaccines for Terrestrial Animals, Edition 2016 as adopted by the World Assembly of Delegates of the OIE in May 2012.
Any RT-PCR detection method used for the testing of samples, either blood or spleen, in the context of Directive 2009/156/EC must perform equal to or exceed the sensitivity of the methodologies described in point 2.
Inactivated virus of serotypes 1 to 9 reference strains may be obtained from the European Union Reference Laboratory or the OIE Reference Laboratory for African horse sickness, Algete, Spain.

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Source: https://www.legislation.gov.uk/eudr/2009/156/annex/IV/part/B/division/1 (the official version)
Page: https://openlegislation.uk/eu-directive-2009-156/annex-IV/part-B/division-1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.