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EN ISO 17351:2014

(Main)

Packaging - Braille on packaging for medicinal products (ISO 17351:2013)

Packaging - Braille on packaging for medicinal products (ISO 17351:2013)

ISO 17351:2013 specifies requirements and provides guidance for the application of Braille to the labelling of medicinal products.

Verpackung - Blindenschrift auf Arzneimittelverpackungen (ISO 17351:2013)

Diese Internationale Norm legt Anforderungen fest und stellt Anleitungen bereit für die Aufbringung der Blindenschrift zur Kennzeichnung von Arzneimitteln.
ANMERKUNG   Die Anforderungen dieser Internationalen Norm können in anderen Bereichen, wenn zutreffend, angewendet werden.

Emballage - Braille sur les emballages destinés aux médicaments (ISO 17351:2013)

L'ISO 17351:2013 spécifie les exigences et fournit les lignes directrices relatives à l'application du braille sur l'étiquetage des médicaments.

Embalaža - Braillova pisava na embalaži za zdravila (ISO 17351:2013)

Standard EN ISO 17351 določa zahteve in podaja smernice za uporabo Braillove pisave pri označevanju medicinskih izdelkov.

General Information

Status
Published
Publication Date
15-Jul-2014
Withdrawal Date
30-Jan-2015
ICS
55.020 - Packaging and distribution of goods in general
Technical Committee
CEN/TC 261 - Packaging
Drafting Committee
CEN/TC 261/SC 5 - Primary packaging and transport packaging
Current Stage
6060 - Definitive text made available (DAV) - Publishing
Start Date
16-Jul-2014
Due Date
02-Sep-2015
Completion Date
16-Jul-2014
Ref Project
SIST EN ISO 17351:2014 - Packaging - Braille on packaging for medicinal products (ISO 17351:2013)

Relations

Replaces
EN 15823:2010 - Packaging - Braille on packaging for medicinal products
Effective Date
23-Jul-2014

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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 17351:2014
01-oktober-2014
1DGRPHãþD
SIST EN 15823:2010
Embalaža - Braillova pisava na embalaži za zdravila (ISO 17351:2013)
Packaging - Braille on packaging for medicinal products (ISO 17351:2013)
Verpackung - Blindenschrift auf Arzneimittelverpackungen (ISO 17351:2013)
Emballage - Braille sur les emballages destinés aux médicaments (ISO 17351:2013)
Ta slovenski standard je istoveten z: EN ISO 17351:2014
ICS:
11.180.30 3ULSRPRþNLLQSULODJRGLWYH]D Aids and adaptations for
EUDQMH reading
55.020 Pakiranje in distribucija blaga Packaging and distribution of
na splošno goods in general
SIST EN ISO 17351:2014 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 17351:2014

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SIST EN ISO 17351:2014

EUROPEAN STANDARD
EN ISO 17351

NORME EUROPÉENNE

EUROPÄISCHE NORM
July 2014
ICS 55.020 Supersedes EN 15823:2010
English Version
Packaging - Braille on packaging for medicinal products (ISO
17351:2013)
Emballage - Braille sur les emballages destinés aux Verpackung - Blindenschrift auf Arzneimittelverpackungen
médicaments (ISO 17351:2013) (ISO 17351:2013)
This European Standard was approved by CEN on 10 July 2014.

CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European
Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national
standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN member.

This European Standard exists in three official versions (English, French, German). A version in any other language made by translation
under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management Centre has the same
status as the official versions.

CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania,
Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United
Kingdom.





EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2014 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 17351:2014 E
worldwide for CEN national Members.

---------------------- Page: 3 ----------------------

SIST EN ISO 17351:2014
EN ISO 17351:2014 (E)
Contents Page
Foreword .3
2

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SIST EN ISO 17351:2014
EN ISO 17351:2014 (E)
Foreword
The text of ISO 17351:2013 has been prepared by Technical Committee ISO/TC 122 “Packaging” of the
International Organization for Standardization (ISO) and has been taken over as EN ISO 17351:2014 by
Technical Committee CEN/TC 261 “Packaging” the secretariat of which is held by AFNOR.
This European Standard shall be given the status of a national standard, either by publication of an identical
text or by endorsement, at the latest by January 2015, and conflicting national standards shall be withdrawn at
the latest by January 2015.
Attention is drawn to the possibility that some of the elements of this document may be the subject of patent
rights. CEN [and/or CENELEC] shall not be held responsible for identifying any or all such patent rights.
This document supersedes EN 15823:2010.
According to the CEN-CENELEC Internal Regulations, the national standards organizations of the following
countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech
Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece,
Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal,
Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom.
Endorsement notice
The text of ISO 17351:2013 has been approved by CEN as EN ISO 17351:2014 without any modification.

3

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SIST EN ISO 17351:2014

---------------------- Page: 6 ----------------------

SIST EN ISO 17351:2014
INTERNATIONAL ISO
STANDARD 17351
First edition
2013-01-15
Packaging — Braille on packaging for
medicinal products
Emballage — Braille sur les emballages destinés aux médicaments
Reference number
ISO 17351:2
...

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