# 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 2.1.1

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

If the removed tissues and cells are to be stored or cultured, the same minimum set of biological testing requirements must apply as for an allogeneic living donor. Positive test results will not necessarily prevent the tissues or cells or any product derived from them being stored, processed and reimplanted, if appropriate isolated storage facilities are available to ensure no risk of cross-contamination with other grafts and/or no risk of contamination with adventitious agents and/or mix-ups.

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Source: https://www.legislation.gov.uk/eudr/2006/17/annex/I/division/2/division/2.1/division/2.1.1 (the official version)
Page: https://openlegislation.uk/eu-directive-2006-17/annex-I/division-2/division-2.1/division-2.1.1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.