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This Document Has Been Superseded
A newer publication replaces it: BSI BS EN ISO 17351
Packaging. Braille on packaging for medicinal products
This European Standard specifies requirements and provides guidance for the application of Braille to the labelling of medicinal products.
NOTE 1: The labelling of medicinal products placed on the market and incorporating Braille in accordance with this European Standard meets the requirements of European Directive 2001/83/EC, Article 56, (a) as amended by Directive 2004/27/EC [1].
NOTE 2: The principles in this European Standard can be applied in other sectors, as appropriate.
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