Table of Contents

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

Abstract

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

General Product Information

Published
Document Type	Standard
Status	Current
Publisher	International Organization for Standardization
Pages
ISBN
Committee	TC 122
Supersedes	ISO/DIS 17351 : 50.00 (2012)