DIN EN 15823 E : 2010

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

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