# 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 1.5.3

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

Any accompanying tissue or blood samples for testing must be accurately labelled to ensure identification with the donor, and must include a record of the time and place the specimen was taken.

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Source: https://www.legislation.gov.uk/eudr/2006/17/annex/IV/division/1/division/1.5/division/1.5.3 (the official version)
Page: https://openlegislation.uk/eu-directive-2006-17/annex-IV/division-1/division-1.5/division-1.5.3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.