BS EN 15823:2010
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Packaging. Braille on packaging for medicinal products
Hardcopy , PDF
31-10-2014
English
31-07-2010
Important note : Users cannot be edited or removed once added to your Multi user PDF.
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.
| Committee |
PKW/0/-/5
|
| DevelopmentNote |
Supersedes BS DD264(2007) & 08/30180499 DC. (07/2010)
|
| DocumentType |
Standard
|
| Pages |
22
|
| PublisherName |
British Standards Institution
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
This European Standard specifies requirements and provides guidance for the application of Braille to the labelling of medicinal products.
NOTE 1 The labelling of medicinal products placed on the market and incorporating Braille in accordance with this European Standard meets the requirements of European Directive 2001/83/EC, Article 56, (a) as amended by Directive 2004/27/EC [1].
NOTE 2 The principles in this European Standard can be applied in other sectors, as appropriate.
| Standards | Relationship |
| EN 15823:2010 | Identical |
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