I.S. EN ISO 17351:2014
Current
The latest, up-to-date edition.
PACKAGING - BRAILLE ON PACKAGING FOR MEDICINAL PRODUCTS (ISO 17351:2013)
Hardcopy , PDF
English
01-01-2014
For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
Only cited Standards give presumption of conformance to New Approach Directives/Regulations.
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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
Describes requirements and provides guidance for the application of Braille to the labelling of medicinal products.
| DevelopmentNote |
Supersedes I.S. EN 15823. (08/2014)
|
| DocumentType |
Standard
|
| Pages |
28
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| ISO 17351:2013 | Identical |
| EN ISO 17351:2014 | Identical |
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