OpenLegislation

Division 2

United Kingdom

Original text. Later amendments are not shown.

The labelling system for the collected blood, intermediate and finished blood components and samples must unmistakably identify the type of content, and comply with the labelling and traceability requirements referred to in Article 14 of Directive 2002/98/EC and Commission Directive 2005/61/ECf1. The label for a final blood component shall comply with the requirements of Annex III to Directive 2002/98/EC.

Annotations

Footnotes

f1

See page 32 of this Official Journal.