I.S. EN 15823:2010
Superseded
View Superseded by
PACKAGING - BRAILLE ON PACKAGING FOR MEDICINAL PRODUCTS
Hardcopy , PDF
English
01-01-2010
08-02-2014
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.
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.
| DocumentType |
Standard
|
| Pages |
20
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Superseded
|
| SupersededBy |
| Standards | Relationship |
| EN 15823:2010 | Identical |
| DIN EN 15823:2010-11 | Equivalent |
| BS EN 15823:2010 | Equivalent |
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