# Commission Directive 2006/17/EC of 8 February 2006 implementing Directive 2004/23/EC of the European Parliament and of the Council as regards certain technical requirements for the donation, procurement and testing of human tissues and cells (Text with EEA relevance), Division 2.1

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

The tests must be carried out by a qualified laboratory, authorised as a testing centre by the competent authority in the Member State, using EC-marked testing kits where appropriate. The type of test used must be validated for the purpose in accordance with current scientific knowledge.

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Source: https://www.legislation.gov.uk/eudr/2006/17/annex/II/division/2/division/2.1 (the official version)
Page: https://openlegislation.uk/eu-directive-2006-17/annex-II/division-2/division-2.1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.