EN ISO 17351:2014
Current
The latest, up-to-date edition.
Packaging - Braille on packaging for medicinal products (ISO 17351:2013)
16-07-2014
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.
| Committee |
CEN/TC 261
|
| DevelopmentNote |
Supersedes EN 15823. (07/2014)
|
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| UNI EN ISO 17351 : 2014 | Identical |
| SN EN ISO 17351:2014 | Identical |
| I.S. EN ISO 17351:2014 | Identical |
| NF EN ISO 17351 : 2014 | Identical |
| NBN EN ISO 17351 : 2014 | Identical |
| DIN EN ISO 17351:2014-10 | Identical |
| PN EN ISO 17351 : 2014 | Identical |
| NS EN ISO 17351 : 2014 | Identical |
| NEN EN ISO 17351 : 2014 | Identical |
| BS EN ISO 17351:2014 | Identical |
| DIN EN ISO 17351 E : 2014 | Identical |
| ISO 17351:2013 | Identical |
| UNE-EN ISO 17351:2014 | Identical |
Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.