DIN EN ISO 17351 E : 2014

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

Defines requirements and provides guidance for the application of Braille to the labelling of medicinal products.