SS-EN-15823 › Packaging - Braille on packaging for medicinal products
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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.
To find similar documents by classification:
11.120.99 (Other standards related to pharmaceutics Including equipment for pharmaceutical industry)
55.020 (Packaging and distribution of goods in general)
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Designation Name
SS-EN 15823:2010
Revision Level
2010 EDITION
Status
Superseded
Publication Date
July 14, 2010
Language(s)
English
Page Count
28
International Equivalent
EN 15823:2010(IDT)