I.S. EN 16679:2014
Withdrawn
View Superseded by
PACKAGING - TAMPER VERIFICATION FEATURES FOR MEDICINAL PRODUCT PACKAGING
Hardcopy , PDF
English
01-01-2014
04-30-2021
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
4 Categories of tamper verification features
Annex A (informative) - Additional information
regarding tamper verification features
Bibliography
Defines requirements and provides guidance for the application, use and check of tamper verification features to the packaging of medicinal products.
| DocumentType |
Standard
|
| Pages |
22
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Withdrawn
|
| SupersededBy |
| Standards | Relationship |
| EN 16679:2014 | Identical |
| BS EN 16679:2014 | Equivalent |
| CFR 21(PTS200-299) : 0 | FOOD AND DRUGS - FOOD AND DRUG ADMINISTRATION, CHAPTER 1 DEPARTMENT OF HEALTH AND HUMAN SERVICES - PARTS 200-299 |
| ISO 9000:2015 | Quality management systems — Fundamentals and vocabulary |
| EN ISO 9000:2015 | Quality management systems - Fundamentals and vocabulary (ISO 9000:2015) |
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