The establishment and maintenance of that system should be done in such a way as to ensure coherence and compatibility with traceability requirements laid down in Directive 2004/23/EC in respect of human tissues and cells, and in Directive 2002/98/EC of the European Parliament and of the Council of 27 January 2003 setting standards of quality and safety for the collection, testing, processing, storage and distribution of human blood and blood components (11).
De mhaolú ar mhír #, beidh feidhm ag Airteagail #, #, #, #, #, # an dara fomhír, #, # agus # ón dáta a dtiocfaidh an Rialachán seo i bhfeidhmEurLex-2 EurLex-2