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This European Standard specifies requirements and provides guidance for the application of Braille for the labelling of medicinal products. In the first place it is focussed on supporting the implementation of Braille on medicinal products available in the European Union (EU) and in the European Economic Area (EEA). On the European level Working Group CEN/TC 261/SC 5/WG 12 "Marking" is responsible for the works. The secretariat of this Working Group is held by Packaging Standards Committee (NAVp) of DIN. The work was accompanied by German Mirror Committee NA 115-01-03 AA "Markierung" ("Marking").
This document has been replaced by: DIN EN ISO 17351:2014-10 .