EN ISO 17351:2014

Foreword
Introduction
1 Scope
2 Terms and definitions
3 General requirements for medicinal product packaging
4 Determination of Braille legibility
Annex A (normative) - Methods of verification
Annex B (informative) - Braille characteristics and
        recommendations
Annex C (informative) - Technology for the application
        of Braille to packaging for medicinal products
Annex D (informative) - Guidance on Braille specifications
        and artwork generation
Annex E (informative) - Braille character sets
Bibliography

ISO 17351:2013 specifies requirements and provides guidance for the application of Braille to the labelling of medicinal products.